BIOMEDICINE:
Bioprinted organs:
Bio-printing of organs will allow for organs to be printed for use in transplants.This will allow any major internal organ to printed from the patients own cells either induced pluripotent stem cells or cells extracted from the actual organ in question.Alternatively small sections of organs can be printed out like oesophagus,small intestine etc. and even blood vessels like arteries and veins with graphene introduced into the matrix of these bioprinted organs and vessels to make them stretchy and also strong possibly even bullet proof or be damaged by stabbings with skin from the patient created this way.Having recombinant DNA from extremophiles in their DNA such as those from acidophiles will allow them them to survive extreme conditions and in the case of replaced stomachs and sections of the oesophagus to be resilient to acid reflux and also the high pH of the stomach from any condition that causes stomach ulcers such as H.pylori and also low mucosal production that could damage normal unaltered organs.This could also allow those with GERD survive acid reflux attacks that would not lead to esophageal cancer.Stomachs should also be engineered to produce mucus in sufficient quantities.Microbes through forming new tissues can seal in sections of the oesophagus and small intestine alongside stitching done during surgery.Recombinant DNA from xerophiles,Tardigrade,oligotrophs could allow them to survive lower nutrient and water levels with those from faculatative anaerobes,anaerobes,obligate anaerobes,capnophiles and scratch DNA allowing them to survive on both oxygen and carbon dioxide.Other recombinat DNA can be added to them prior to implantation giving them specific abilities for reach organ.This will alleviate organ scarcity of important organs such as bladders,kidneys and hearts as well as the need for anti-rejection medication and can allow them to be prepared months ahead before one is needed with if organs are needed due to a sudden event say a shooting etc then one could have their own heart and other created using their stem cells and then frozen using recombinant DNA from R.sylvatica,Tardigrade,Bacillus F,H.glaciei,C.greenlandensis,P.putida GR12-2,C.pleistocenium,psychrophillic and osmophile bacteria and also those from scratch that allow important organs to be cryonically frozen in organ banks next to blood banks indefinitely.Like more complex forms of cryonics these would be also be able to be withstand toxic cryoprotectants through genes made from scratch.Osmophile bacteria and R.sylvatica DNA can allow glucose to be used as cryoprotectants.Tardigrade DNA that would allow them to survive -272 degrees celcius can be added once as detailed later on pushed to their limits below this and to last forever via forced evolution.Its ability to lower its metabolic rate by 99.9% and also endolithic,xerophile and oligotrophic bacteria doing the same will also be utilised.This could also allow them to be survive cryonics when inside the organ banks and be frozen,thawed and refrozen over and over again and also when in the patient with CRISPR treatments applied by biocompatible microbes to the other cells in the patients body with recombinant DNA from Planarians,Hydra,A.mexicanum,Bacillus F,T.gammatolerans and C.elegans repair damaged tissue and telomere damage.If possible in the case of sudden events such as stabbings,shootings,falls etc like blood these organs can be created on a commercial scale within hospitals with all major organs such as hearts,kidneys,lungs,pancreases,sections of the gastro-intestinal tract etc stored in organ freezer banks permanently that can be engineered to have human DNA created from scratch suited to all people preventing rejection or if possible if they do cause some rejection when inserted they can at least work in the patients body until gene therapy can be used to insert the patients specific DNA into all cells in the organ to remove rejection in vivo by microbes or be used temporarily alongside anti-rejection drugs by the patient to survive until the patient can have a new organ created custom made from their own stem cells or even induced pluripotent stem cells and microbes with their own DNA without rejection thus allow the one created beforehand to be restored and reused by someone else or they will be then disposed of by being pyrolysised so one could continue to live with their new custom made bio-printed organ containing their own DNA replacing the stored organs..Recombinant DNA from Planarians,endolithic bacteria,induced pluripotent stem cells,Bacillus F and other sources of DNA from animals that exhibit cellular regeneration and biological immortality will be added to there genome before or after they are implanted by microbes to ensure they do not get damaged or undergo senescence.Ideally these banks should have organs for infants,children,adolescents and adults to cater to all situations.As a result each hospital will have organ banks that contain all major organs such as hearts,kidneys,livers etc that are frozen with base universal DNA that will be availible to anyone when they arrive in hospitals with gunshot wounds or other emergencies that can be inserted by surgeon robots and then them taking anti-rejection drugs until microbes add the patients DNA to the organs with new ones grown and stored in its place to ensure an abundant and constant supply of each organ with their being ones for both adults and also pre teens and infants.Otherwise the organs from banks will suffice until they can avail of those bioprinted with their own DNA while drugs are taken and the banks refilled constantly.This technology would of note to people who have genetic predispositions to defective major organs.ie those born with fatal congenital heart defects,sudden arrhythmic death syndrome and even heart murmurs once they reach adulthood,at least adolescence or even before at birth have a replacement heart bioprinted that can grow normally like normal organs and put in place of their defective one to reduce the chances of it effecting their health with further measures taken to prevent death such as altering the genes present in these organs through gene therapy or having the cells in these bioprinted altered via CRISPR to remove and correct the defect prior to being printed or once printed to have mutations and defects permanently removed.Microbes could keep the heart and brain alive if any fatal abnormalities occur in patients with congenital heart defects with them creating new tissues on the heart and keep the brain alive until the heart can be replaced or CRISPR can correct the mutation.This could be replicated with any organ that one is genetically prone to have defects or even cancers and one could also be used to replace organs damaged by pathogens and chronic drug,cigarette and alcohol use as well as cancers.It would also be used to create new youthful and fully functional organs especially key ones such as hearts,kidneys,livers,sections of the gastro-intestinal tract etc to combat the effects of ageing to ensure one constantly has youthful organs in their body indefinitely.These organs especially important ones such as hearts,kidneys etc.would have to treated with DNA from the aforementioned Archaea bacteria to keep them from undergoing senescence.The old organs of the patient would be pyrolysised and used to create graphene,carbyne,diamonds etc.Biocompatible microbes can be used to apply CRISPR treatments to these organs and form new stronger layers of tissue over them if need be and if possible entire organs can be made of just tissues created by microbes as well induced pluriopotent stem cells from the patient.Thus bioprinted organs of all types containing universal human DNA will be created onsite of hospitals to be stored in cryogenic banks that using DNA from Archaea,Hydra,A.mexicanum etc will be able to be frozen,thawed and refrozen over and over again with these catering to infants,pre teens and adults in emergencies ie shootings,stabbings,trauma etc that once inserted into the patient via surgery will have microbes using CRISPR add the patients DNA to them replacing all DNA in the organs or will be there until a new customised organ is added.This will elimate organ scarcity forever as all hospitals will have a constant supply of organs.These banks will be onsite of all hospitals worldwide,interstellar vehicles,space stations etc and would be replaced once each one is used with those for infants and pre teens created also.Bioprinting of organs containing the patients full DNA will be done in instances where one is shown to have genetic diseases with the flaw removed for the organ or wherein an organ may need to be replaced when it has damage from pathogens,chronic drug and alcohol use and can be done for those who wish to avail of more youthful organs.If DNA cannot be introduced during ,manufacture of these then a blank organ can be created with microbes using CRISPR to add the patients genome to each and every cell.If possible microbes using WiFi can be made to form entire organs on an organic scaffolding and added to the freezer.By 2045 these organ banks will be ubiquitous and the technology perfected to be indistinguishable from real organs via intensive research.
To compliment this producing genetically altered livestock such as pigs or chimpanzees that produce human organs that can be harvested when needed with these animals having recombinant DNA from the patient and humans in place of the animals entire DNA and that of each major organ and allow them to harvest any organ when needed with the pig then given a bio-printed organ to be harvested alongside other ones later on with the patient taking anti-rejection drugs until CRISPR removes all traces of animal DNA and replaces it with their own DNA.These chimeras that have the patients DNA in each cell will be able to create organs for those on waiting lines as cattle can grow to maturity in two years with pigs in six months and alongside bioprinted organs will relieve organ scarcity and also issues of rejection as the animal and organ can be grown almost immediately and will reduce deaths associated with organ waiting lines and scarcity with the organ produced having the patients exact DNA thus negating the need to take anti-rejection medication yet if need be then the patient can take them until microbes apply CRISPR treatments to remove all foreign DNA and fill in the blanks with the patients DNA to then negate the need for taking them.If perfected chimera animals will have only all of the patients DNA or minor trace amounts of foreign DNA to lessen the intensity of medication treatments until microbes remove all foreign DNA and replace it with the patients missing DNA via CRISPR and survive until more purer organs can be created with them allowing for organs that cannot be done by bioprinting such as livers,lungs etc and vice versa or if perfected and the organs have all of the patients DNA only thus meaning that a person may not need to take drugs.Once in the body the microbes will apply augmentations into the organ the patient already has or these will be already present in the animals.Those whose DNA scan has shown they are susceptible to specific organ conditions or weak heart can have a custom made animal that contains traces of their own DNA can be created at birth or in their later years meaning the organs won’t be rejected or require anti-rejection drugs with the mutation that leads to weak hearts as well as predispositions to cancers removed.
The use of chimera organs from animals and bio-printed organs etc can apply to those with damaged livers and other vital organs such as lungs with lungs replaced bit by bit one by one with it replacing organs damaged by stabbings,tumours,chronic drug and alcohol abuse,prolonged cigarette and cigar use,pathogens such as Ebolavirus,Neisseria meningitidis,Poliovirus with those with damaged lungs may have the carbon energy acceptor phenotype added to them to prevent complications with if need be those with impaired lung capacity would have miniature lung machines aiding in breathing that doesn’t interfere with the surgery.Thus existing patients with damaged lungs,livers etc will utilise this to replace them with younger ones prior to anti-ageing treatments.Those who need to have important organs removed due to tumours or terminal illness may have them given one from a donor ideally a next of kin and then two animals will be reared to produce organs both for the original patient and the donor in the case of kidneys and lungs.It can also allow those currently aged 75 and older to avail of newer more youthful vital organs such as hearts,lungs and livers etc from a single animal by 2023/2024 using cattle or pigs to thus allow them to increase their rate of survival to 2029 to avail of anti-ageing treatments.Ideally they would have one animal produced that creates all organs that are compatible with humans via universal human DNA and then harvest as many organs as possible added into them from the animal with anti-rejection drugs taken until CRISPR treatments by 2025 will remove all foreign DNA and add the patients DNA in remaining spaces.Those suffering from terminal illness including genetic based ones and even cancer that are the result of defective organs can have organs created this way thus increasing their survival rates to avail of anti-ageing strains with the organ produced free of any genetic defects with this of note to those who are elderly with damaged organs and those suffering from organ specific cancers.Those who have damaged organs from chronic drug,cigarrette and alcohol use etc and even genetics can have them replaced from this technology.Idiopathic pulmonary fibrosis for example can be treated this way.
Iodiopathic pulmonary fibrosis and similar lung conditions can be treated in the following way.Donated lungs from next of kin or even complete strangers can be used to treat this.Both the donor and receiver will be able to survive at least several years or decades with one fully functioning lungs a patient suffering from the condition can have a lung donated from next of kin or stranger with the receiver of the donated taking anti-rejection drugs.This will through two cocurrent operation remove one lung from the donor next of kin into the body of the receiving patient.The receiver of the donated lung will be able to live long enough until either a hybrid chimera animal is created to provide a second functioning lung with the animal created via 3D DNA printers to house the patients DNA in their lung that once the animal reaches maturity can receive on lung from the animal with the animal created by IVF and artificial wombs with their also the option of using bioprinted lungs or those created by stem cell strains of the microbes that contain the patients DNA with the receiver patient getting a second fully functioning lung in a second operation.The patient can choose to have the first donated lung replaced by a second lung from the chimera animal or they can have a second bioprinted lung replace the first donated lung.The patient will continue to take anti-rejection drugs with by 2025-2029 microbes then used to apply CRISPR treatments to all lungs whether it is that donated from the next of kin or that from the chimera animal and bioprinted ones that removes all traces of foreign DNA including that from the donor next of kin and that of the chimera animal and replaces it with that of the receiver patient.Thus all strabds of foreign DNA present on the donated lungs will be removed and replaced with that of the receiver patient via CRISPR through microbes in order to allow them to survive forever without taking anti-rejection drugs.The tissue in the lungs treated with CRISPR treatments that change the DNA to that of the patient using advanced gene drive technology after a while anti-rejection drugs are taken while the CRISPR treatments change the donated lungs DNA to that of the patient receiving it.The fact that CRISPR treatments could change all DNA in all cells of the donated lung to all of the entire genome that is the same of the receiving patient can allow the receiver to receiver both the left and right lung from two donors and while anti-rejection drugs are taken CRISPR treatments will change all DNA in all the cells into that of the receiving patient.The doner(s) patient who donated the lung at the same time can have a pig or chimpanzee grown with their specific DNA inside the animals genome to create a lung that has their DNA in it that can be once the animal reaches maturity is harvested and added to the donor patient to replace the donated lung and then if need be CRISPR can remove any remaining animal DNA and replace it with all of the donor patients DNA while they take anti-rejection drugs.Thry may also use a bioprinted lung with this allowing the donor patient to thus still have two fully functioning lungs like the receiver patient.This can allow terminally ill patients of this condition get one doner lung from next of kin or strangers by 2023/2024 and then allow both the patient and donor to survive long enough with one lung and when they both get a second lung and replace the original lung with ones from animal hybrid by at least 2023/2024 or even later while still taking anti-rejection drugs and allow for them both to survive until the donor then getting a replacement lung in a few years alongside the patient who needed the donation can survive long enough to then have another second lung created for them in another hybrid animal and have them have the donated lung form next of kin replaced with that from the animal grown for them after they have the remaining damaged lung replaced to ensure they both have a fully functioning pair of two lungs at least a year later with rejection drugs taken until CRISPR and microbes is sufficiently advanced by 2025 to remove all traces of animal DNA and replaces it with the patients entire genome.AI namely proto and final Phanes and Paean will organise this for each patient.Anti-rejection drugs will be taken by both patients while they house the donated lungs from each other and chimera animals with CRISPR used to remove all traces of all animal DNA and that of the donor from each donated lung and replace it with that of the patients receiving the lungs given the lungs.Bio-printed lungs etc can also be used including those in banks when advanced enough with chimera animals and bioprinted animals also avaiulble by at least 2023/2024.Thus patients suffering from this and other terminal lung diseases as well as damaged and poorly functioning organs damaged by drugs,alcohol or old age will be able to survive long enough to avail of anti-ageing treatments using chimera organs,bioprinted ones etc.If possible proto microbes using bacterial and viral vectors or even bacteriophages engineered to interact with the hosts cells and also containing the hosts DNA can be used as early as 2023/2024.Advanced gene drive technology will be used to ensure the gene therapy that applies the patients DNA and removes the animal DNA is permenant.Having the carbon energy acceptor phenotype added to them will prevent complications that would be fatal.This could aid those currently diagnosed with the iodiopathic pulmonary fibrosis and similar terminal conditions with those diagnosed with this and other conditions in the future may once the process is perfected have an animal grown that contains their DNA in the desired organ and thus treated by having one lung replaced one after another in separate operations before the condition becomes terminal.Ideally both patients and doner would have all of their animals grown at the same time thus meaning they will all reach maturity and ready to have organs harvested once the patient is about to receive their first donated lung to ensure they receive the animals lungs at the same time without delay with all operations being done at the same time or within a few days or weeks.If possible the animal that is used to donate chimera lungs will using the acellerated healing phenotypes may also have universal human DNA allowing only one animal to be used as it regrow harvested organs with again it created via embryos have the DNA printed in by 3D DNA printers implanted into either artificial wombs or surrogate mother.This can be replicated with those who have damaged and poorly functioning lungs and other organs removed due to chronic chronic smoking,alcohol and drug abuse,tumours,pneumoconiosis and pathogens etc such as Poliovirus,Ebolavirus,Coronaviridae,N.meningitidis or those whose organs are not at 100% capacity due to old age.Those with other terminal organ conditions will also have this done with those born with poorly developed organs will also get bioprinted organs and those from chimera animals.Ideally pigs should be used as they mature in as little as six months in comparison to seven years for chimpanzees.Cattle may also be used as they are larger thus being able to house larger organs and take two years to grow to maturity.All animals including pigs,cattle and chimpanzees can be engineered to reach adulthood much quicker in say as little as a few months or a year using DNA from Clostridium perfringens,E.coli and scratch DNA created by Phanes to increase the availability of them with all organs stored in organ banks using cryonics.The genome of the animals would have that from Archaea,Hydra,psychrophiles etc to allow them to be frozen and thawed and refrozen over and over again as well as those from extrempphiles to be able to survive extreme environments that the patient would be exposed to with oligotrophic and xerophile DNA added to cut down on resources to feed the animals.For pre teens and infants bioprinted organs may be used alongside organs from miniature pigs and cattle or even harvested from normal cattle and pigs in their infant and pre adolescent years.If perfected the organ from animals should contain no animal DNA whatsoever and only the patients DNA with the rest of the cells having both the patients and animals DNA thus negating the need for CRISPR treatments and anti-rejection drugs and also ensuring the animal can function properly with proto versions available by 2023/2024 at least having animals with organs that have some of their DNA to be removed by microbes and the patients full genome added in place of it later on while drugs are taken with more advanced perfected forms being animals that have organs without their DNA and the rest of the body containing both their and the patients DNA and possibly some scratch DNA to prevent the organs being rejected by the animals immune system or the animals will have to take anti-rejection drugs until harvested.Important organs such as lungs and hearts and livers could be done this way that are difficult to biorprint with the animals created as early as 2023/2024 on trials with other animals receiving the organs with human trials starting as early as 2023/2024 with the animals then killed and remains pyrolysised.The animals could be reared onsite of hospitals in sterile outdoor or sealed indoor pens with them then immunised against all zoonotic diseases and the pens exposed to narrow range wavelength UV light and high doses of radiation once the animal is made immune to radiation with feed produced onsite via hydroponics or bacteria.They would be created in onsite artificial wombs.These could be in underground extensions underneath carparks or near the hospital connected by a hallway and conveyor belt linked to a Da vinci surgery machine that harvests the organs and dispose of the body with the machine and all surfaces exposed to radiation,narrow range wavelength UV light and also coated in liquid glass and sprayed with mists of anti-bacterial compounds with Botlr robots etc collecting them in a fully automated system with organs then sent to organ banks and organs when need collected by robots and sent to the surgery room when need with new organs replacing the used one with the breeding,feeding and immunisation of animals used controlled by the hospital AI with the area housing them guarded by automated water tight doors and rounds of radiation etc to sterilise the organ and air to prevent pathogens infecting patients.Otherwise they would be reared onsite of nearby community farms and also immunised as well.Immunising the animal against all pathogens of the animal prevent patients being infected.All steps in feeding,harvesting,body disposal and also transportation of organs will be automated from start to finish.In time biosynth animals may be possible that are less likely to spread germs and much cleaner since they only have to fed nutrients and if need be only produce organs and not the brain or other unnecessary parts of the body allowing for it to be done onsite of hospitals in a humane means.
If possible like bioprinted organ banks animals that are hybrids of animals and humans reared in extensions of hospital in special pens with automated feeders fed algae can be created to have an animal with all key organs in them that can be stored in onsite organ banks transplanted to a human in an emergency thus allow them to survive long enough with anti-rejection drugs taken to avail of bioprinted or custom made ones from an animal created with the patients DNA or microbes that add the patients DNA into all cells in the organ with these animals being reared in all hospitals all the time to ensure those who need one from say a shooting etc that pop up are always able to get one when needed and thus bring an end to waiting lines as animals using the Phanes method that applies key human DNA sequences will always be onsite of all hospital in pens on the outside or in underground extension or even raised on nearby community farms by automated feeders.Ideally these animals would have all organs be human ones thus allowing any organ to be harvested in an emergency with if possible the entire animals genome being fitted with psychrophiles,acelleratec healing and unicellular and multicelluar organisms that exhibit telomere and stem cell repair as detailed earlier so as to allow any unused organs to be cryogenically frozen for other patients thus preventing waste and scarcity of one organ of another with the dead animal pyrolysised.If possible the animals once reaching maturity and having the aforementioned psychrophile and telomere etc repairing DNA in their genome would have all organs such as lungs,livers,hearts,kidneys etc harvested and stored in cryonics with their being ones for adults and also infants and preteens created and stored this way with new animals reared when a certain number of them are used with the banks storing at least a dozen of each major organ at a time.The acelerated healing phenotype alongside psychrophiles etc will allow the organs to be frozen,thawed and refrozen over and over again.New animals will be created to then have depleted organs refilled.Ideally the animals will be fitted with universal human DNA interspaced in all of their organs and rest of the body with a small bit of the animals DNA in place of DNA that determines their unique code to ensure that little or no anti-rejection drugs would be taken with CRISPR used to remove all remaining animal DNA in them and replace them with the patients DNA in their place with the exact genes from humans to be placed in the animals DNA and thus all organs extrapolated by proto and final Phanes inter spaced in the animals DNA with if possible to speed up the rate of organ production then the animals used either cattle or chimpanzees engineered to reach full maturity in as little as a year or few months thus increasing the rate of organ production.3D DNA printers would be used to create these animals.CRISPR would apply the patients DNA to all cells in the organs once inserted into the patient while anti-rejection drugs are taken and remove all animal DNA or the patient could survive until a new animal with the patients DNA is created while they take anti-rejection drugs.Thus the patient will once they receive the chimera animals organs they will take anti-rejection drugs until CRISPR using microbes will remove all traces of animal DNA and replace it with the patients DNA until the entire genome has nothing but the patients DNA with AI even proto AI organising this.The animals could if possible have DNA from A.mexicanum etcso that the animal once its organs are harvested will regrow them instantly thus negating the need to create another animal with if not the animals carcass sent to pyrolysis plants to be pyrolysised.The animal through anti-ageing treatments will keep the animal alive forever.This would also be more humane and alongside anti-ageing treatments allowing it to live indefinitely and save time and energy in creating new animals.Thus animals would be created in sets including those that are miniaturised versions that create infant and pre teen organs that would have acellerated healing DNA,base universal human DNA at key points in all organs,anti-ageing treatments,psychrophile and telomere repairing DNA that can be harvested over and over again to refill organ banks onsite of all hospitals worldwide eliminating organ scarcity forever meaning their will also be a set amount of key organs availible at all times for all patients.Having these animals created by 3D DNA printers using blank spermatozoa,eggs and even embryos and also automating insemination,using automated feeders and artificial wombs will cut down costs in their production with the patient files used as a means to insert the patients DNA into the exact areas of the animal genome with AI namely proto Phanes doing the complex work of inserting the patients and human DNA into the exact right places of the animals genome also cutting down costs.3D DNA printing should become advanced enough by 2023/2024 and beyond to have the key genes of humans and specific patients into the right areas of the genome to allow all or desired organs have only human DNA or the required amount of both to allow them to function.These animals will be tested in facilities near hospitals with them housing oligotrophic and Xerophile DNA to reduce water etc needs.The human genome and that of all animals such as pigs,monkeys etc should already be known enough to know where the human or patient DNA should be interspaced into the animal to create sufficient viable organs for humans and also those that require minimal CRISPR and anti-rejection drugs treatments.Bioprinting them on demand will be more advanced that to render chimera animals defunct by at least the early 2040s with again dozens of each organ printed out at once and then stored in croyonic banks ensuring their is enough for each patient on demand with them containing base human DNA and the patient either keeping it until they can get their personalised one or CRISPR treatments can apply the patients DNA to the new organ.Microbes forming relevant tissues of a specific organ over an organic mould they can consume alongside nutrient media pumped into them will form the basis of creating all organs on site of hospitals for storage by the 2040s with these having universal DNA or them have the patients DNA with them having biosynth wifi could have their DNA created via taq polymerase and Cas-9 and also forced evolution similar to wireless upgrades of microbes.These both can be done in place of human donations thus eliminating organ scarcity worldwide negating the need for humans to donate organs and allow those on waiting lines to have one ready for them or the patient could get a donated organ from a live human and then get one from a hybrid animal.3D DNA printing will create the spermatozoa and eggs as well as embryos with these phenotypes and the patients unique DNA from patient files and those of humans to cut down on costs.Donated organs form other humans would have the patients DNA added to the organ while anti-rejection drugs are taken.The cells used to create these can come from induced pluripotent stem cells from the patients own body and strands of tissue from organs or just treatments to make them any desired cell and tissue for each organ.Those that currently use anti-rejection drugs can have their current organ removed and also replaced with a bio-printed one using their own cells,those from a hybrid animal or have microbes insert their own DNA in place of the foreign one in all tissues.Both bioprinted organs and those from chimera animals will be used to counter the drawbacks of each other with them fully availible by 2029 and proto versions by 2024.
If the acellersted healing phenotype is successful in able to instantly repair organs and regrow those removed bioprinted lungs will be still probably used.They will be used at first to cure patients of iodiopathic pulmonary fibrosis patients as well as those whose lungs have been severely damaged by excessive smoking,alcohol abuse,recrestional drugs such as cocaine,Crystal meth etc as well as pathogens such as Ebolavirus,Coronavirus etc.
Synthetic Limbs:
Exoskeletons could aid people to gain back existing abilities by training their body and all muscles or by improving their abilities in carry out home chores and other work.It could also help children who are born premature or even with congenital defects that may leave their muscles develop more slowly than others.Eventually robotic exoskeletons and devices will render wheelchairs obsolete.These can help people walk with permanent injuries or aid them in relearning to walk in the case of minor injuries.Prosthetic limbs can be 3D Printed from a various amount of materials from plastic and metal custom made for the patient.New advances have allowed for mind controlled prosthetic similar to those in Star Wars meaning that those who are paralysed or just require a prosthetic limbs can function normally with others who are completely paralysed from the neck down being able to control robots and other tools such as laptops and smart devices.Biosynthetic technology will eventually make these part of the body permanently by connecting to the nervous system of the patient.Alternatively bones can be replaced with synthetic calcium based bones grown in a lab or graphene/carbyne(or a mixture of the two) that can replace normal replacements for broken hips and other bones.These bones can have graphene and carbyne in its matrix with flesh and muscles grown over it by microbes,Neural implants could allow for these new limbs to be controlled by the mind or if perfected the limbs would be connected to the main body via microbes.In vitro muscles,flesh,synthetic skin or those created from microbes and in time in vitro nerves or even synthetic versions consisting of graphene/carbon nanotubes with fibre optics covered in a synthetic fat mylien sheet with ATP microprocessors,bio-printed blood vessels could lead to entire limbs or just digits such as fingers and toes(with sheets of synthetic compressed keratin replacing nails) being reconstructed via cybernetics and reconstructed organs connected to the human nervous system aiding or negating neural implants.In time bioprinted neural and blood vessel systems or even those created internally by biocompatible microbes will replace these made from graphene nanotubes which will possibly act as scaffolding for these to grow on with these microbes also building synthetic muscles on these scaffolding with the same applied to flesh,bones and skin.Neural,protein or graphene,silicene and borophene nanotubes can be created into these via Geobacter and Shewanella bacterial DNA that is tweaked to produce these within the microbes.Layers of skin can be created on injuries.With regards to spinal injuries that result in patinets being crippled the patient can have synthetic neural graphene/carbyne/fibre optic nanotubes(again in synthetic mylein sheets with fibre optics possibly being integrated) replacing any fractures and gaps created by injury by rerouting existing nerves,replacing dead/damaged ones to allow for electrical signals from the brain to the rest of the body to return which can be be put in by more advanced versions of the Davinci Surgery machines using nano surgical tools attached to these several atoms thick possibly made of planar allotropes of metallic elements will allow for more precise incisions/insertions of this tubing to be made and in time by nanorobtics.Otherwise implants can be developed that allow for this to happen or compliment them alongside neural implants with bioprinted neural pathways also used either by themselves or with these nanotubes with the possibility of of biocompatible microbes since having neural clusters could form biofilms that bridge the gap and then form new nerve tissue repairing breaches in the nervous system and repair issue under the affected areas.If possible cybernetic limbs such as arms,legs and digits such as fingers etc could be Biosynth based created by the stem cell strain.Billions or trillions of these stem cell microbes will be cultured in a vat onsite of a hospital and then the limbs etc would be grown on a scaffolding onsite of a hospital.The stem cell strain will create neural tissues,blood vessels etc in vivo or on an organic scaffolding with if need be these taken out and the replaced by more advanced versions over time with in time an organic scaffolding created with an interior organic scaffolding or synthetic bone to allow the stem cell strain create both muscle,blood vessels and also nervous and skin tissues layer by layer over the synthetic bone and also within the scaffolding until a fully functional limbs in created layer by layer with if need be a fluid containing countless stem cell microbes pumped into the scaffolding to allow for the tissues to form either again layer by layer or filling it to the brim with in both cases Paean would control the formation of new tissues and them fed oxygen and nutrients.All cells would be fitted with the same augmentation DNA as the host with them being stem cell strains derived from the patient that can undergo mitosis housing the patients DNA.The microbes would form layers of skin,muscles,nervous tissue etc layer by layer until a fully formed limb is formed that can be attached to a patient.The scaffolding could be hollow allowing microbes and nutrients to be pumped in and allow them to form bone tissue.The scaffolding being organic material could be consumed by the microbes on demand to then take their place as actual bone and skin.The stem cell strains fed oxygen and nutrients would have the patients DNA and that of the same augmentations to prevent rejection and would be told by Paean to form skin,neural,muscle tissue layer by layer and also capilliaries,arteries and veins via him telling them to do so via biosynth wifi.Nails and cuticles will be formed over toes and fingers attached with broken nails repaired via keratin formed over them.If possible the microbes ability to form new tissue could allow detached limbs,digits to be reattached by them forming nervous,blood capillaries,arteries etc by merging with sealed wounds,severed limbs or even open skin in the case of those using bionic limbs when reattaching them even after periods not possible in normal situations and allow dead tissue to be rejuvenated and replaced with new ones.The synthetic limb would be attached like conventional prosthetic using organic scaffolding that would allow the microbes to form tissues over the limbs original area connecting it to the body and the scaffolding broken down by microbes into benign compounds.Once attached and sealed the epidermis over the original wound that was sealed via surgery beforehand could be made to undergo apoptosis and then allow for new bridging nervous and muscle tissue to form invivo with blood vessels formed invivo as well connecting the main body to the limb allowing for blood to flow back and forth and them receive nutrients with prior to this the muscles etc receiving nutrients and oxygen pumped into them via syringes or even intravenous drip systems similar to coma patients or microbes synthesising nutrients in vivo.These hospital grown limbs would not need neural implants to gain control of them since they would be attached to ones peripheral and central nervous system with if they need implants then they can still use Biosynth neural implants formed in vivo that does not require surgery.These limbs can be formed beforehand in hospitals within these scaffolding containers,then removed(the carbon dioxide energy acceptor phenotype will keep it alive in it with them composed of stem cell strains containing the patients DNA) and then attached to allow the epidermis of sealed wounds to be sealed over while microbes cause the epidermis to undergo apoptosis and then form blood vessels and nerves connecting to them or the scaffolding can be on the patient before formed.The patient would be via the microbes be either put to sleep via nerotransmitters that control sleep putting them into prolonged sleep or even controlled coma that the microbes can awaken them from with it taking anything from a few hours or week to reattach a limb such as arms,legs or digits such as toes and fingers.Paean,Phanes,Urania,Epione and Hecate etc will by 2029 be able to determine the best means of developing this technology.These will also benefit people who suffered injuries that confine them to wheelchairs leaving them unable to walk.If perfected it could allow a bio synthetically formed limb whether a arm,hand,foot or leg to be reattached that is indistinguishable to a real one with stimulation of nerves and blood flowing back and forth allowing one to control the new limb with sensations like a normal one that is reattached to them and fully controllable with even toes,fingers reattached this way with the mincrobes containing DNA from extremophiles and also anti-ageing treatments but no nanoprocessors.Paean will oversee this and plan these for all patients with the accelerated healing phenotype allowing future patients to regrow limbs automatically.This will of course be tested on animals like chimpanzees.Existing cybernetic arms etc can have muscles and neurons as well as blood vessels and skin grown on them to make them fully functioning like normal limbs or have them removed and replaced with these.The advantage over existing or cybernetic limbs is that they would contain nerves,blood vessels etc allowing for touch and blood flow etc.Digits to be reattached could be grown via bioprinting them or having microbes grown on a scaffolding and then reattached or even a plastic or organic material scaffolding of a digit allowing the microbes to form relevant tissues etc within them when connected to where the digit is to connect to the body.This could allow those who have already had legs,arms,toes,fingers or hands to be reattached.These would be formed by stem strains containing the patients own DNA to ensure they would be no rejection.If possible recombinant DNA from A.mexicanum can be added to humans to regrow any damaged or severed digits and limbs naturally.
Stem cells:
All stems cells used in medical research should ideally be induced pluripotent stem cells to be produced more cheaply and without the ethical and constraints from traditional sources of embryonic stem cells with placentas from all births from around the world to ensure a robust supply.If possible human embryonic stem cells and those from A.mexicanum,Hydra,Planarians will have stem cells extracted have their DNA changed to human ones and be engineered like induced pluripotent stem cells with the ability to undergo mitosis from bacteria and thus grown in media on a commercial scale.Having embryonic stem cells,totipotent ones etc have the ability to undergo mitosis could allow for those extracted from a embryo in such small amounts as to not even make a difference with A.mexicanum etc DNA repairing in the hosts genome any damage to the embryo and thus allow the embryonic stem cells to be grown on site of hospitals in photobioreactors with them frozen and rethawed over and over again with relevant telomere repairing and accelerated healing DNA and psychrophile DNA present with induced pluripotent stem cells also having this ability.Thus a single cell could be grown in large amounts and then transported to hospitals around the world with if possible these being totipotent stem cells thus allowing them to be created on an unlimited scale in photobioreactors onsite of hospitals.Otherwise 3D DNA printers would print them out.An embryo created from donated sperm and eggs fused together similar to IVF would have the acellerated healing phenotype of A.mexicanum etc,psychrophile and telomere repairing genes added to them via CRISPR or from both parents through advanced gene drive technology and by extracting totipotent stem cells,induced pluripotent stem cells and embryonic stem cells from a single embryo and analysing the DNA present in these using DNA analysers the genes in embryos various types of cells either totipotent stem cells,embryonic stem cells and induced pluripotent cells can determined via AI and be stored into Physis and the augmentations subnetwork in the file for H.sapiens to be recreated by 3D DNA printers in base microbes,stem cell strains or blank human cells containing bacteria DNA to undergo mitosis with patient specific DNA allowing them to be created on an unlimited scale for research and therapies etc without destroying any future embryos with the future versions of human cells etc printed out will have DNA from bacteria to allow them to undergo mitosis further increasing their abundance in hospitals and universities around the world.This could allow the genes responsible for their ability to form any cells via embryonic,totipotent stem cells to be determined and mapped by DNA analysers,added to in the human file of Physis and using 3D DNA printers added to stem cell strains or base stem cells for research of healthy patients and also those confined to wheelchairs.AI will be able to determine the genes responsible for embroyonic stem cells,totipoteng stem cells in humans to be determined.The stem cell strains would contain the genes present in embryonic stem cells to allow them to become any type of cell in the human body.Stem cells for research purposes can be them mass produced onsite of hospitals and universities worldwide without having to harvest any embryos with them engineered to undergoe mitosis using sugars and proteins created by bacteria with biosynth WiFi controlling their mitosis.The acellerated healing phenotype in embryos would be able to repair itself of any damage caused by this extraction thus allowing it to be still used for implantation into females without loss of viability for producing a child with zero defects.Thus as stated by having extracted embryonic,pluripotent,totipotent stem cells that can undergo mitosis via having DNA from bacteria and feed on the same media as bacteria through CRISPR adding this would allow them to be grown on an unlimited scale and would negate any issues of having to harvest embryos for stem cells as only one embryo which housing DNA from T.gammatolerans and A.mexicanum would allow the embryo repair itself after only a few cells are extracted and have its DNA analysed to allow them to be used in stem cell strains and also augmentation strains to be added to a patients genome alongside that A.mexicanum etc.Having the genes in embryonic totipotent and induced pluripotent stem cells analysed by DNA analysers and added to Physis can allow them to be mass produced on an unlimited scale in photobioreactors and using 3D DNA printers printed out into blank stem cells in hospitals around the world with DNA from bacteria to induce mitosis allowing them to be grown in photobioreactors using sugars meaning trillions or quadrillions of them can be grown onsite of hospital and universities across the world for research and use in stem cell research and stem cell strains and augmentation strains over and over again an infinite amount of times negating issues of ethics from harvesting them from embryos and scarcity as they will be abundant onsite of all hospitals and universities.It would also them to be printed out in to stem cell strains etc and for use in augmentations.By analysing the genes just once it will negate the need for any future embryos to be harvested and can be frozen and rethawed over and over again with relevant telomere repairing,psychrophile and accelerated healing DNA and psychrophile DNA.Any embryos that have a few cells extracted would as due to having DNA from the aforementioned sources would be able to repair itself and still be viable for in vitro fertilisation to sterile parents once frozen.Female and male patients with the acellerated healing etc in their genome can donate eggs and spermatazo via advanced gene drive technology that this phenotype thus allowing once made into an embryo via artificial insemination can have a few cells extracted to then be run through DNA analyzers that can detect the various genes of each type of stem cells ie embryonic,induced pluriopotent and somatic etc and thus add the genes for their abilities to be added to Physis to allow it to be created on an unlimited scale in stem cells that have bacterial DNA to undergoe mitosis,stem cell strains of microbes etc via 3D DNA printers forever without the need for harvesting embryos in the future.Somatic and induced pluripotent stem cells could be engineered to house the same genetic features of embryonic stem cells via CRISPR by first tracking the different genes present in each one and then have DNA to allow them to undergo mitosis with advanced gene drives with DNA from extremophiles that exhibit DNA repair could be added to prevent tumours and also DNA damage.Biocompatible microbes could also be used as a source since having all of these DNA sources.Stem cells can be created that are hybrids of Planarians,A.mexicanum,Hydra,embryonic and induced pluriopotent stem cells with human DNA and that to undergo mitosis and change into any cell via electrical signals and chemical ones forming the basis of the stem cell strain.Existing embryos can be fitted with the accelerated healing,telomere repair DNA repair via CRISPR to allow for one to take a small number of cells cells to be extracted to be analysed by DNA analysers to be stored in Physis without damaging them and allow them to be still viable for invitro fertilisation.The psychrophile and telomere repair and acellerated healing DNA can allow them to be frozen and rethawed over and over again without loss of viability.Future embryos will have this DNA passed down onto them from females that house this DNA via advanced gene drive technology.Once stored in Physis the genes that give them their unique ability to form any cell can be via 3D DNA printers printed into blank stem cells alongside those from bacteria that allow for mitosis to occur alongside psycrophile DNA,Accelerated healing and endolith DNA to allow them to be frozen and thawed over and over again and mitosis genes allow for billions or trillions to be created in photobioreactors onsite of hospitals and universities around the world using sugar and proteins for research purposes once printed out using 3D DNA printers.This can also be printed into stem cell strains of microbes and thus allow an almost unlimited supply of embryonic stem cells in the future without the need for harvesting embryos.These steps will allow stem cell strains that repair injuries etc to be created for all patients and allow for stem cells for research purposes to be created on an unlimited scale with no ethical concerns and created onsite of all universties and hospitals worldwide.The stem cells from Hydra,A.mexicanum can be researched as well with genes from bacteria to undergo mitosis.If possible to furthermore remove ethical concerns other multicellular lifeforms that house cellular regrowth and embryonic stem cells such as Hydra,A.mexicanum,Planarians can instead have the genes responsible for embroyinc stem cells etc mapped and determined alongside other mammals especially ape cousins of H.sapiens to then be used in stem cell strains and research.These animals stem cells could be modified to then adapted to humans by adding human DNA and removing specific strands of the species DNA to prevent immune responses.
Artificial blood:
Blood donations will eventually become redundant with production of type O blood(universal blood type) Rh negative being created on a commercial scale using haematopoietic stem cells or even synthetic Oxycyte blood which can carry oxygen more efficiently and is a universal donor type while it has been used primarily to relieve blood loss due to traumatic brain injury it could be used to replace blood temporarily during other injuries such as stabbings while the body regains its ability to produce blood naturally.This could be also be used to reduce damage to organs such as the brain in injuries and strokes and prevent damage caused by decompression sickness or the bends as it is smaller than erythrocytes allowing to navigate damaged or compressed vessels and carry more oxygen and speed recovery of a patient.These could be produced on a commercial scale and thus prevent the spread of and testing for diseases,the need for donations as it would last much longer than normal donated blood.It would also save on resources as blood bags could be reused.This could also be replicated with animals with much more compact or flexible versions being developed especially for use in scientific studies and testing drugs etc.Haematopoietic stem cells can be modified to reproduce via them having genes from bacteria using CRISPR to undergo mitosis and produce universal blood types on an unlimited scale in hospitals eliminating scarcity and reducing costs from $1,330 per every few litres to zero with each one in each vat having DNA to produce each type of blood type with them using chemical or electrical signals form blood with plasma created by bacteria mixed in.They would be engineered to run on sugars and proteins created by other bacteria and would turn into erythrocytes and even base universal leukocytes and platelets that can be used by any patient without rejection or allergic reactions after a set amount of time and even through biosynth wifi present with plasma formed as well in the same or different vat and mixed in together.By extracting haemotiopic stem cells from one person their genes that make them eventually turned into erythrocytes can be added to the human file for Physis to be then printed out into photobioreactors using 3D DNA printers onsite of hospitals and universities around the world with them having DNA from bacteria to give them the ability to undergo mitosis from bacteria and that from psycrophile and acellerated healing and can use sugars etc to undergo mitosis.DNA samples would be taken from all populations that have all blood types to allow them to be grown on a commercial scale onsite of all hospitals at zero cost.Ideally this would be the universal O Rh D negative blood type using DNA from patients that have this allowing anyone to receive the blood and this artificial blood will be produced onsite of hospitals next to coolers where it is stored in blood banks and methods can be developed to extend its shelf life including genetic engineering from psychrophiles,endoliths,scratch DNA and those to prevent the blood from losing its viability thus allowing blood created this way to be able to survive indefinitely thus preventing waste and also negating the need for losing created blood and also eliminating scarcity.Recombinant DNA from psychrophiles and the accelerated healing phenotype,telomere repair etc could allow the blood to be frozen and thawed and refrozen over again and not lose its viability and also further engineering done to increase growth rates and shelf life allowing it to last forever in storage.This ability to be frozen and thawed over and over again could allow stores of blood to be stored forever in coolers and even freezers.If possible the same anti-ageing treatments in humans can alllow them to stay fresh and viable forever without freezing and even have oligotrophic,endolithic and Firmicutes DNA to lower nutrient costs and enter endospores with them housing biosynth wifi.The haematopoietic stem cells through having the genes responsible for biosynth WiFi could through Wifi signals from Hospital AI follow this expression onto erythrocytes present or if possible the stem cells could be engineered to produce erythrocytes that contain nuclei that holds at least this DNA from psychrophilles using scratch DNA that has the ability to undergo mitosis edited out through genes programmed to turn off once erythrocytes are formed via wifi or through scratch DNA programmed to do this with when injected into patients all DNA present in the erythrocytes will be removed via biosynth WiFi integrated into them and thus when injected into patients the erythrocytes would have a normal life cycle like those in the body and thus would die off after the same 100 days as normal erythrocytes with them even doing so after a few days with the body stimulated by microbes to create more blood cells with if possible the stem cell strain fitted with haematopoietic stem cell DNA being able to form erythrocytes when need on demand to compliment this.If possible they could be variations of erythrocytes that as stated hold nuclei but can still release large amounts of oxygen and hold psychrophile DNA and also extremophile DNA to survive the environment of the host and even storage with even them having base human DNA or through wifi will change into DNA of the patient once in the body or when being readied for injection to prevent issues with regards to immune responses.Biosynth WiFi can be present that edits out the DNA from the haemotiopic stem cells,extremophile DNA with it also used to turn the haemotiopic stem cells into erythrocytes and remove the extremophile DNA just before or after they are injected into the patient or just when they are enter the body through Paean doing so via biosynth WiFi thus giving them their original capacity of oxygen transportation.The haemotiopic stem cells will house biosynth wifi genes to induce their evolution into erythrocytes of the universal donor type and even leukocytes with base human DNA and while in storage they would contain psychrophile,anti-ageing and telomere genes and that for biosynth WiFi and that to turn into erythrocytes with when injected into patients biosynth WiFi will be used to remove this DNA and thus be able to carry out the ability to transport oxygen with and die after 100 days like normal with the leukocytes have the genes in them converted to that of the patient by cross referencing their patients files.They would house universal base human DNA with Paean can through biosynth WiFi just before it enters the body have the DNA be changed to that of the patient to express patient specific antigens etc before all other DNA is removed by cross referencing their patient files.Leukocytes clotting agents,plasma etc could be created by the stem cells that would house the aforementioned and base human DNA and via WiFi would via cross reffferencing the patients file to house their DNA including augmentations with the WiFi also creating the patients specific blood types,plasma,clotting agents and other factors and components specific to a patient prior to or after being injected by Paean making it applicable to any patient.Thus haemotipic stem cells could have them house base human DNA and when a specific patients needs blood biosynth wifi could create erythrocytes,leukocytes and plasma suited to that patient with their exact DNA and also all patient specific proteins etc for their specific blood type to prevent rejection or allergic reactions when the blood is being taken out of coolers and about to be injected.The leukocytes,clotting agents,plasma and erythrocytes etc could house universal human DNA and be of the universal blood type and then prior to being injected or after injection can be by biosynth WiFi turned into the blood type of the patient housing their DNA with this applying to leukocytes,ethryocytes,clotting agents etc to express their antigens etc to prevent allergic reactions with extremophile DNA and all DNA outside of the patients removed to allow them to live normal lifecycles.Otherwise the universal blood type can be created.This could allow all blood types ideally the universal blood type to be grown onsite of bloodbanks onsite of all hospitals in photobioreactors on a commercial scale pushing costs to zero and ensure that blood banks are constantly full that are connected to the banks via piping and robots so that they are automatically refilled and refrigerated when used or out of date managed by the hospital AI with them fed using sugars etc from bacteria grown also onsite.This would allow hospitals to be self sufficient in terms in their blood needs negating the needs for blood donations,order it in from factories and eliminate blood scarcity indefinitely as each type of blood type would be created onsite of all hospitals at zero cost with if possible engineering extending its shelf indefinitely and would negate fears of transferring HIV and other blood borne diseases and since they can be regrown after being used would eliminate scarcity.They would as stated be the universal blood donor type and undergo the same level of engineering as bacteria based commodites to increase growth rates with them grown in large batches in hospitals to allow for there to be stored and when a certain amount is used more regrown to ensure a continuous supply with vetenairy clinics onsite of hospitals growing blood for each major animal ie cats,dogs,horse,cattle that would be engineered to again universal blood types but also universal types for all breeds etc grown on a commercial scale with biosynth WiFi turning the erythrocytes and leukocytes into those for each breed and individual animal.Otherwise of perfected base mammalian blood suitable for all mammals or even base animal blood suitable for all animal taxonomic ranks ie Reptillia,Mammalia,Aves etc can be grown that once it is stored and needed on demand and before or straight away being injected it could via WiFi turn into blood of the exact species,breed and individual animal via cross referencing their patient files that is turned into the exact type of platelets,erythrocytes and leukocytes and produce exact blood components and proteins,clotting factors and plasma etc for the exact species,breed and individual animal.If possible each ambulance should have a mini fridge with its own battery containing enough synthetic blood to fill one or two people all the time so as to allow for blood to be filled before they even reach the hospital by internal phlebotomy robots.Human based clotting agents Factor VII and Factor IX could be produced with human proteins and DNA via genetically engineered bacteria or those from the patient to produce them in a way that does not cause allergic reactions with the same applied to other anti-hemophilia compounds gained from other animals.This could be done using stem cells or bacteria or even stem cells with genes from humans and the patient with those produced by bacteria having the patients DNA in them to allow them to be made in photobioreactors at home or labelled ones in hospitals to prevent allergic reactions with this replicated for insulin and all hormones to be injected into a patient.Synthetic blood could suffice for them using their own DNA with these produced on a bulk scale for a whole years supply to be stored in fridges at home that can be transported in mini fridges to be used in emergencies.Other treatments to deal with this could be gene therapy to trick the immune cells from not specifically responding to them with the possibility of gene therapy also treating haemophilia.Thus 3D DNA printers,photobioreactors and also DNA from haemotiopic stem cells etc can allow for all blood types especially the universal blood type O Rh D negative can be mass produced onsite of hospitals around the world in extensions negating the need for blood donations and ensure that they are constantly stocked on all types of blood for emergencies making hospitals self sufficient.This should cut the costs of both blood and clotting factors etc to zero that can be made onsite of hospitals and universities worldwide making them self sufficient via being printed out using 3D DNA printers and using sugar to undergo mitosis.
https://www.youtube.com/watch?v=XyBL_MddTiY
Anti-venom:
Antivenom can be produced by bacteria with the proteins and contents of serum(or bio-based equivalents) created by animals like horses,rabbits and others from scratch in responses to specific venoms on an unlimited scale using bacteria to produce the specific proteins etc.These would ideally be made within micro factories on site of research centres near beaches that have poisonous fish and Medusozoa and clinics and hospitals near wilderness,cities and other urban areas that have poisonous Serpentes,Arachnida,mammals,insects and other species living in close proximity to humans.Venoms for use in research such as toxicity and cancer research can also be created by bacteria.Having different strains of bacteria produce large amounts of venoms from each species of animal ie each species of venomous Serpentes,Arachnida,Medusozoa,Insecta,Reptilia,Amphibia etc and even toxic plants in photobioreactors can cut costs in conventional venom production by negating the need to raise the source animal and harvest the venom from the source animal cutting down on costs and allow large amounts to be produced on a commercial scale in photobioreactors in hospitals where each poisonous animal lives very quickly with other bacteria or microbes with the DNA from horses and rabbits that illicit immune responses added to them exposed to doses of venoms created by bacteria to then produce the antibodies on a commercial scale in photobioreactors in larger amounts than conventional methods which can be filtered out using nanomaterials allowing large amounts of antivenom for each species to created onsite of hospitals around the world on a virtually unlimited scale lowering costs significantly to almost zero and allowing all hospitals including those in developing world to be fully stocked with it.Until then venom can be produced by bacteria and then injected into horses etc via phlebotomy robots or created by microbes in the animals in small amounts and the antivenom extracted automatically by phelobotmy robots in both cases and sieved out.Theoretically as stated bacteria could have recombinant DNA from horses etc to allow them to produce antivenom in response to being exposed to each type of venom produced by other bacteria onsite of the hospitals etc applied to them in photobioreactors thus allowing large amounts of antivenom to be created onsite in an unlimited scale in photobioreactors with this cutting down costs even further and can be fully automated with the antivenom filtered out of the bacteria automatically or the bacteria killed by extreme environmental conditions that dont damage the antivenom) and then deposited into large vials onsite with the bacteria engineered to be resistant to the antivenom though since the compounds would attack only poisons the bacteria should be safe.Otherwise bacteria can produce antivenom by anabolic and catabolic reactions on a commercial scale via wifi once their structure is stored in Physis using the structure gained from horses etc exposed to poisons created by bacteria etc.The structure of the antivenom could be analysed and stored on Physis in the file of the animal that produces It that also houses the venom produced by the animal and that of the venoms own file and then created by bacteria on an unlimited scale in hospitals and Telesphorus factories via anabolic and catabolic reactions to be ordered in by hospitals and the public in batches.Microbes in the body namely chelation strains could download their structure when needed and create them using these reactions.Antivenom for all types of local poisonous flora and fauna such as Phyllobates terribilis,Androctonus australis,Atrax robustus,Crotalus cerastes,Chironex fleckeri etc. can thus be prepared in hospitals in time via genetically altered bacteria on a commercial scale photobioreactors with taps with them as stated stocked in hospitals and even in fridges at home for any incidences at home.If possible binding proteins extrapolated by AI and created by AI could alter the antibodies to survive outside fridge temperature ranges and thus extend their shelf life and allow them to be carried along on hiking trips and beaches alongside syringes with in time biosynth animals and humans injected with the venom to produce larger amounts of antibodies with these being produced by microbes namely the antivenom/chelation strain via adding this DNA allowing for a persons microbes to create these in response to certain poisons instantly once receptors determine the exact poison.Antivenom will be made on an unlimited scale in hospitals and stored in fridges and restocked to ensure an abundant supply with them also created on such a scale as to be mass produced and ordered in by the general public from Telesphorus factories in large batches.Buildings next to beaches and those on the outskirts of woodlands etc will produce and store the antivenom of their local venomous fauna with people storing it in homes in fridges and carry it when going hiking and when at the beach.This will ensure there is quick access for those bitten by snakes and spiders.Universities will create them for both research purposes but also allow people to order it via Telesphorus alleviating strains on ordering them from hospitals.Microbes as detailed later would counteract poisons to alleviate this.People such as hikers and those who live near beaches etc including tourists can order in antivenom in large batches to be stored in fridges that can be thus used when needed with binding proteins added extrapolated by AI that can allow them to be kept stable indefinitely outside of the fridge.As a result they can be brought with them on hiking trips and to beaches along with syringes allowing for them to be used on demand.Since the structure of the antivenom will be present in Physis once base microbes identify the species of venom then they cross reference Physis for the correct antivenom and then download it into their microbes who will synthesise it via anabolic and catabolic reactions with their structure downloaded onto DNA digital storage beforehand for quicker results with Phanes extrapolating scratch DNA for each antivenom that can downloaded into their genome via induction of the evolutionary path of DNA in them.Mellivora capensisl,Spermophilus beecheyi,Herpestes ichneumon and Didelphis virginiana and those that have immunities to venoms to each species of venomous Serpentes and Arachnida as well as Medusozoa can have their DNA that produces their venom countermeasures including proteins be added to different strains of bacteria to produce the relevant proteins on an unlimited scale in photobioreactors again stored in hospitals and homes with the DNA of these used as a baseline to create counterproteins to counteract all poisons of all species of venomous Serpentes,Arachnida and Medusozoa by exposing the strains of bacteria to the different venoms of each species of venomous animals etc again created themselves by bacteria to force them to create counter proteins to defeat each type of venom with the new genes added to other bacteria to then create these on an unlimited scale.The bacteria would through forced evolution would create counterproteins to poisons from all species of animals and also plants individually.Otherwise Phanes can use these animals genes as a baseline to extrapolate new genes to create counterproteins to all types of venoms.Phanes and Paean will analyse the structure of each venom and extrapolate genes to create them that can be adddd to bacteria to produce them in photobioreactors in a commercial scale.Thus counterproteins can be created for each individual species of venomous animals with if possible them forced to develop an all in one super proteins that counters venoms from whole orders ie all venomous Serpentes or all venomous Arachnida or if possible all venomous animals.If none exist that are immune to venomous Arachnida and Medusozoa than the strains that create proteins to counteract venom etc,base bacteria or those with DNA from specific aforementioned resistant species could be exposed to the venoms of Arachnida etc to force them to develop counter proteins through evolution to these and thus produce them on an unlimited scale.These bacteria can also be made to create counterproteins for posionous and non poisonous members of the class Insecta namely Hymenoptera namely Vespa mandarinia japonica(in fact all Vespidae species),Solenopsis species and all species and subspecies of Apidea especially africanised bees allowing the microbes and body to fight off against venoms which in low amounts that would cause irritation and pain and in large amounts cause death from swarm attacks.The exception to this would be Agoge trainees undergoing Parapona clavata trials with their microbes to prevent death would keep vital organs alive and also create adrenaline and counterproteins when they are at risk of death.The poisons present in poisonous plants and even animals that are consumed either accidentally and purposefully for culinary purposes can be also tested on these bacteria to make them develop counterproteins to these as well thus allowing antivenom to be again created with the poisons created by other strains of bacteria on a commercial scale to increase their yields..Antivenom and counter proteins to toxic plants such as Digitalis,Atropa belladonna,Nerium oleander,Rhododendron,Digitalis,Lilium longiflorum etc with could be prepared in all of the same way by having the poisons created by bacteria in large amounts then exposing them other bacteria containing DNA from horses and all of the aforementioned mammals to create antivenom and counterproteins etc stored in hospitals etc with recombinant DNA also coming from animals that consume these plants toxic to humans,exposing bacteria to the toxins or mithridatism and have the new genes added to humans.Phanes can also extrapolate genes.Again the anti venom etc can once its structure is added to Physis can be created by bacteria using anabolic and catabolic reactions.This can also be created in photobioreactors in hospitals and Telesphorus factories on an unlimited scale via bacteria using wifi.The public will be able to order in the counterproteins of any species in large batches from Telesphorus factories.Bacteria will be used as they evolve much quicker especially under extreme stress with the new genes created to create counterproteins for exact toxin will be added to the Physis file of the poisonous species to be added to bacteria in photobioreactors that can create the counterproteins on a commercial scale for each species.Thus strains of bacteria will produce large amounts of the venom and counterproteins of each species of poisonous animal and plant and then this will be exposed to other bacteria that contains DNA of animals resistant to them thus pushing the costs of producing antivenom and counterproteins to almost zero.The genotypes for each counterproteins will be able to be downloaded into microbes in patients before potential exposure to poisons that can be removed later on.AI such as Phanes can analyse existing genes from these animals and extrapolate new genes to create counter proteins for all venomous species of plants and animals thus speeding up the process with these stored in the poisonous animals Physis file.Ideally non pathogenic bacteria will be used with if possible even base bacteria without the DNA of these mammals will be used with the bacteria also containing DNA from the animal the venom is sourced from to make it resistant to the venom with this applied to both the strains that produce the venom and those that are exposed to the venom.Biosnth wifi can be used by the bacteria once they have learned its structure stored in Physis.If need be human DNA would be added to improve success with this being automated and can start as early as 2023.The genes that are produced to create counter proteins and super proteins from these bacteria and the source animals can be added to chelation or antivenom strains of microbes as well as the human hosts genome by augmentation strains to allow the host create them naturally.Microbes will as detailed later on create proteins and antivenom using the aforementioned new and existing genes that bind to venoms and prevent them binding to receptors or produce proteins that bind to the receptors the venom interacts with to prevent it interacting with the body with key organs kept alive by stem cell and other strains with the type of toxin and venom analysed by base microbe strains intaking the venom in small amounts,analysing its structure,relaying it to Paean who will then relay back to the name of the venom and the relevant antivenom and counterproteins structure to be stored on their DNA digital storage to allow all microbes create the antivenom in large amounts.Otherwise they could create them via anabolic and catabolic reactions.If possible a single strain of bacteria with genes from all aforementioned mammals or just one that create these counterproteins will be tested against all poisons to create an all in one genotype for an all in one counterproteins.Phanes could analyse their DNA to create new genes from scratch that creates an all in one counterprotein.The genes will be downloaded into microbes to allow them to produce the counterproteins or they can be added to a patient themselves to allow the patient themselves produce the counterproteins themselves in response to the poison.Thus all new genes created by these bacteria by evolution will be added to both H.sapiens augmentation and bacteria file in Physis with them and original DNA from the aforementioned animals added to the sub augmentation network where they can be added to any patient worldwide thus allowing them to create these counter proteins on demand in response to when when they bitten or stung by any venomous animal instantly with test microbes injected into patients creating minute amounts well below the LD50 amounts of the venom to test this first in all patients to teach the now augmented host to produce these counter proteins by themselves in response to them.These tests will involve first aid kits detecting the responses from the body with the poisons and counterproteins levels and timing controlled by Paean.Microbes could be fitted with this DNA namely the chelation strain and would act as a backup to the hosts new ability with the universal receptors determining which poison it is and then being told by Paean to create the specific counterproteins.By adding the genes to humans would allow the patient create them in response to stings and bites of poisonous animals and in time even consuming poisonous crops,plants and animals with this tested on animals by 2025 that have human recombinant DNA.Ideally only people living in areas with each poisonous animals and plants will have the DNA in them from the bacteria to counter poisons for each poisonous plants animals native to their area with tourists and Agoge trainees taking part in walkabouts having these added when visiting the area and then removed when they leave with circus performers and musicians etc who work with these animals have the genotypes present in their genome to prevent death.If possible Phanes can extrapolate from scratch genes to give patients the ability to create all in one counterproteins to all types of plant and animal poisons and even heavy metals that create these that bind to and neutralise all poisons etc that can be kept forever with M.capensisl,S.beecheyi,H.ichneumon,D.virginiana DNA used as a baseline by him.Thus Phanes could create from scratch extrapolate an all in one genotype that creates counter proteins and anti venom etc for all venoms from all poisonous plants and animals not just around the world but around the universe that can be added to all patients worldwide meaning should anyone be stung or bitten by a poisonous animal or eat a poisonous plant or animal by accident their body will in response create counterproteins and/or antivenom that can neutralise them all instantly in response to them with the same or a separate all in one genotype also doing so for all heavy metals such as cadmium,uranium,iron that are injected or injested in levels past their toxicity levels with if possible Ferroplasma used as a baseline.This augmentation will be tested on animals as early as at least 2025 with their creation starting as early in 2023/2024 in automated labs.Microbes can create the poison in small amounts well below the LD50 limit can be used to teach the patients body to create relevant counterproteins on demand and in response so that it can be created normally in response to bites and stings. first aid kits can be used to test this.Microbes that create venom from each species of venomous animal creating the venom of each species in such small amounts in the over the course of the day and weeks to force the person to become immune via mithridatism with certain parts of the body engineered to be unable to bio accumulate certain toxins.All animals and plants found to produce venoms capable of killing humans through automated labs on other planets as detailed earlier on will undergo this same mass production of antivenom and counterproteins using these aforementioned animals DNA or those from animals already immune to these poisonous animals native to that planet as a baseline to be added to bacteria to create the same crounterproteins and also genes for humans.Biosynths modelled on humans will be used in tests to determine which are toxic and produce them by having them eat raw and cooked crops of all species and be stung,bitten etc by all species of animals to see if they produce poisons.Existing and new antivenoms will be also tested on horses via microbes producing them in their bodies in small amounts with counterprotiens and antibodies produced in animals and humans via mitridism will be analysed and have their structure stored in Physis with this applying to those in the case of both plants and animal ones.The structure of antibodies and antivenom extrapolated from tests on horses,bacteria and also from AI analysing their structure will be stored in Paeans,Physis database or the DNA digital storage of microbes thus allowing them to be created on demand via anabolic and catabolic reactions in patients or on an unlimited scale in photobioreactors using again anabolic and catabolic reactions in hospitals,universities,buildings next to wilderness and also beaches.AI will analyse the structure of all the poisons and venoms from all plants and animals to extrapolate counterproteins and also antivenom that can be then made on an unlimited scale by bacteria using catabolic and anabolic reactions and scratch DNA onsite of hospitals and even Telesphorus factories.If possible AI will analyse all existing poisons structures including synthetic ones including those from both all species of plants and animals and even those that arise during cooking certain foods as well as the structure of all heavy metals and elements and extrapolate counterproteins and antivenom antibodies structure to fight them and neutralise them that can be stored in Physis in each poisonous plant and animals file or that of the element and their structure downloaded into the DNA digital storage of microbes when they identify the name of a poison and element and it created when needed by catabolic and anabolic reactions instantly once the venoms structure is determined by base microbe receptors and relayed to Paean to then relay back the relevant toxins counterprotiens and antivenom to the microbes DNA digital storage created by anabolic and catabolic reactions.Scratch DNA can be extrapolated by Phanes to express antivenoms and counterproteins to all poisons and heavy metals and stored in their Physis file and it downloaded by WiFi inducing the microbes genome to allow them to synthesise them on demand.It can also have it created by anabolic and catabolic reactions in photobioreactors in Telesphorus factories,hospitals etc on a commercial scale to be ordered in from Telesphorus factories in bulk.The structure of the antibodies could be analysed and stored on Physis and then created by bacteria on an unlimited scale in hospitals and Telesphorus factories via anabolic and catabolic reactions to be ordered in by hospitals and the public in batches.This can include antibodies extracted from animals injected with venom created by bacteria.AI will also extrapolate binding proteins that can extend the shelf life of them both in fridges but also outside fridges indefinitely that break down in the body thus allow for members of the public to carry them around on hiking trips and when on the beach alongside syringes allowing them to be injected onsite.Also once base microbes determine the structure of the poison via either mechanotransduction or reverse mechanotransduction,chemical reactions seen in more complex or similarly simple organisms and simple and complex neural clusters and systems in them for example Hydra etc allowing the structure of the compound and its levels in ppm,ppb,ppt,ppq to be determined once it is cross referenced with Physis then it will then download the structure of the poisons and venoms counterproteins and antivenom into its DNA digital storage and produce this by releasing large amounts of this into the blood stream alone or with bumpers or during phagocytocysis with chelation strains activated to do this as well.Some of the venom and poison will be turned into benign compounds including nutrients via anabolic and catabolic reactions.The microbes will also create proteins that bind to the receptors that the venom interacts with to take its place and illicit reactions that are benign or enhance normal functions thus preventing the venom interacting with it and thus allowing it to be flushed out of the body.If antivenom is not on hand,the patient does not have wifi access,or them then the poisons will be turned into benign substances using anabolic and catabolic reactions once detected by base microbes.Compounds poisonous to pets and livestock but not humans will be anlaysed as well to create genes for them with gene therapy making these compounds as benign to them as they are to humans.This can make Canis lupus familiaris be able to eat Vitis,Theobroma cacao,Coffea,Allium and also Persea americana.Ideally all patients in areas that have poisonous plants and animals in their locale will have their structure and counterproteins structure stored on the DNA digital storage of microbes and implants to initiate the synthesise of counterproteins when needed once detected.All of this will allow antivenom and counter proteins to be created in such large amounts that it would be stored onsite of hospitals in large hospitals and also buildings next to beaches and wilderness areas like jungles and forests and would allow one to order in amounts from Telesphorus factories and store large amounts of them at home in specialised fridges at home in both private and communal homes and also carry around with them when going hiking and swimming alongside syringes allowing for one to be treated instantly.Buildings next to wilderness and also beaches would create them and store them onsite in large amounts to ensure those bitten or stung there have quick access.It would also counteract the current shortage of antivenom around the world.Universities would create it for research purposes and also to allow it to be ordered in from there alongside hospitals alleviating strains on hospitals.The cost of antivenom of all venomous animals especially scorpions would be brought to to zero since their would be no need to capture and harvest animals,no need to milk them by hand or even by robots,the bacteria could produce large quantities of venom and antivenom and also counterproteins in a matter of weeks with them fed proteins and sugars from other bacteria compared to having to milk a single scorpion or other animal several million times to get a few litres with litres of it produced in photobioreactors onsite of hospitals and even at home with people being able to order in whole batches of it from nearby hospitals and universities due to it being able to be created on an unlimited scale and store it in fridges at home.This method would be key in eliminating scarcity of all types of anti venom would be of note to scorpion venom which is produced in such low amounts and requires great skill in milking that it currently costs $39,000,000 per every 3-4 litres with as stated the use of bacteria could push this commodities cost to literally zero both in terms of abundance and loopholes in patenting laws.It would also allow large amounts of venoms to be created to test their effects on all species of viral,bacterial and fungal pathogens and also parasites to test their effectiveness at killing them so as to allow the recombinant DNA to be added to microbes and them released as bumpers or during phagocytosis.People can order in large amounts of antivenom and counterproteins these in bulk from Telesphorus factories and store it in specialised fridges in private and communal homes in basements etc with gene therapy making the production of it obsolete.Hospitals will create the venoms of all local venomous animals for patients who reach there but also for people to order it in with universities also creating it for research and also to allow it be ordered in again from Telesphorus to alleviate strains on hospitals.Hospitals will either order in or create onsite(or both)large amounts of antivenom and counterproteins to be stored onsite in fridges to ensure and abundant supply is always present and that levels are constant with binding proteins etc added that extend its shelf life indefinitely.Thus hospitals and research centres and those by wilderness areas will ideally using photobioreactors create their own supply that will be packaged and stored onsite to alleviate strains on Telesphorus factories.Telesphorus factories would create it in such large amounts that patients could order it in bulk for local poisonous flora and fauna and store it at home with again binding proteins extending its shelf life allowing ease of access at home with one keeping reusable syringes.Research stations and buildings housing the AI of beaches and on the outskirts of wilderness areas that have venomous animals could also produce it onsite and store it in fridges for each species native to the area to allow any affected individual to have instant access and not have to travel to hospitals,one could order it in batches from Telesphorus factories and thus have it hand when bitten or consuming poisonous plants and also bring it to beaches and hiking trips.One could also create their own supply of antivenom at home in photobioreactors and stored in fridges in both private and communal homes via these means thus eliminating scarcity and allowing for one to have a supply of antivenom at hand for any bites,stings etc that occur at or near home with them able to bring it with them when they go hiking and swimming and stored in backpacks alongside syringes to allow them instant access with this part of smart clothing.By 2029 bacteria through exposure to venom to create new genes and anabolic and catabolic reactions will allow for antivenom and counterproteins to be created on such as scale in Telesphorus factories that it could be ordered in bulk by countless people from these factories with its price brought to literally to zero with measures such as binding proteins etc they are connected to made to extend its shelf life indefinitely in fridges to zero.Ordering it in from these factories will allow people to house enough at home in fridges so it can be stored there for emergencies before a person is bitten or stung etc,brought in bags etc in camping gear and bags on hiking trips or going to the beach with it as stated also made onsite of buildings that store the AI for all types of wilderness ie beaches,forests etc.The bacteria to produce the venom and counterporteins will have recombinant DNA from the native venomous species to allow it be unaffected by it allowing it grow in the venom it produces.Once the structure of the antivenom and counterproteins to each species venom is charted by AI extrapolating it based on the venoms structure and also from it created by bacteria then other bacteria could synthesise them in photobioreactors on a unlimited scale via anabolic and catabolic reactions in photobioreactors with chelation strains also doing this in patients in response to detecting them in the body.The venom of each species would also be created this way cheaply for research into it for fighting tumours,pathogens whether viral,bacterial and fungal and also parasites in automated labs to be added to relevant strains of microbes once humans are made immune to the venoms.Venoms and poisons from other colonies and Earth will be tested on all pathogens and parasites on Earth and other colonies.If possible the poisonous animals could be genetically altered in labs to remove the toxin and produce one that is benign to humans with their prey also altered to be susceptible to this new poison with both reared in large numbers and have a unique phenotype say different coat and colour etc and then released in large numbers to overrun wild populations via advanced gene drive technology meaning the poisonous animal will no longer be a danger to humans but only its prey also engineered to be susceptible to it with biosynth arthropods in swarms also applying microbes that do this live animals in the ground and ocean and to plants.These bacteria and also metallotolerants can be exposed to high levels of each heavy metals like lead,arsenic,cadmium.Thus by 2029 antibodies,counterproteins and antivenom can be created by bacteria via anabolic and catabolic reactions and also recombinant and scratch DNA etc on an unlimited scale onsite of universities,hospitals,centres by beaches for all local poisonous flora and fauna with one able to order it in from local Telesphorus factories to be ordered in by the general public in large batches in large plastic or glass vials to be stored in fridges in areas where poisonous plants and animals live and then used in emergencies at home or taken with them on hiking and beach trips in bags with them having binding proteins compounds extrapolated via AI binding to them that allow them to be stored indefinitely in both fridges and outside in bags surging extreme cold and heat that will be able to be broken down in the bloodstream by the environmental conditions and compounds present in the body including bloodstream or even enzymes created by microbes to them breaking only them down in response to them to make them effective allowing them to be brought by patients with them on trips to the beach or wilderness.These binding proteins would be created by AI via anabolic and catabolic reactions and mixed.Since created by Phanes he could own patents on it and thus have it availible for free with the fact that it could be mass produced also lowering costs to zero.
Limuls ameobocyte lysate:
Limulus amebocyte lysate can be theoretically synthesised this way alongside creating bacterial or human leukocayte or even microbe hybrids of the blood componants using relevant recombinat DNA from Limulus polyphemus to create the ameobocytes on an unlimited scale in photobioreactors in hospitals with before that large numbers of L.polyphemus can be bred in recirculating aquaculture systems onsite of hospitals around the world with excess dumped into the natural habitat with the Phanes method applied while L.polyphemus undergoes extensive conservation efforts.This would involve the DNA from L.polyphemus or its ameobcytes that contain and express the relevant chemicals that are then added to either human cells given the ability to undergo mitosis using relevant DNA and those to increase yields from bacteria to ensure the compounds dont automatically coagulate since healthy human cells are not affected by it at all thus ensuring it can be created on an unlimited scale in hospitals next to where tests are performed.Otherwise the ameobocytes can once extracted from one animals can have relevant DNA added from bacteria to undergo mitosis and use sugars etc to reproduce thus again allowing them to be grown on an unlimited scale.The DNA for ameobocytes and other DNA from the animal can be added to its Physis file in a folder to allow it to be cross referenced alongside all bacterial DNA by hospitals etc around the worls.The amebocytes or bacteria that create the chemicals can be created onsite of hospitals to alleviate strains on factories or ordered in batches from Telesphorus factories in bulk.Thus having these and similar methods can have Limulus amebocyte lysate created on an unlimited scale by bacteria/ameobocyte/human cell hybrids onsite of hospitals without the need for harvesting L.polyphemus anymore,done onsite of all hospitals and universities worldwide or ordered in batches from Telesphorus factories with the application of the compound to any syringes,phlebotomy robots etc done by automated systems before and after they are automatically sterilised.This should cut its costs to zero without needing to rear or harvest L.polyphemus anymore.These will be made onsite of universites,hospitals or ordered in from Telesphorus factories.
Breast Milk:
Baby formula and similar products made redundant by the fact that mothers will be able to create their own milk on an unlimited scale using yeast or bacteria in photobioreactors in home or they can order in large batches from community and vertical farms like other milk with the mothers patients file cross referenced in both cases.A mother alongside DNA scans in patient files can use handheld nanosensors or test kits using biosynth technology ordered in or have a sample of their milk even before birth via microbes stimulating lactation or after birth and even during or before pregnancy to sent to labs in hospitals or even using handheld nanosensors attached to smart device to have its exact unique chemical composition analysed including fats,proteins,antibodies etc and added to their patient file thus meaning that their patient file can be cross referenced for both their DNA and chemical composition to have the yeast or bacteria create large amounts of their own milk created and ordered in large batches in Deipneus factories or vertical farms that has antibodies and other components recreated exactly not just from their DNA but also anabolic and catabolic reactions and have different flavourings and desired levels of all nutrients with this milk aiding mothers to feed their young their own milk in large amounts outside of normal breast feeding especially in public and when their breasts are drained in baby feeding bottles especially for mothers with multiple births ie twins,triplets and not rely on baby formula which is easy to contamination etc.Thus one could order in large batches of their own milk and even colostrum with customised levels of all nutrients to be fed to children in bottles in public and also when their breasts are drained especially when they have twins,triplets etc.The milks exact chemical structure etc will be stored in their patient file to be cross refferenced for all future orders with this replicated for livestock,pets and animals in zoos for both milk and colostrum allowing both colostrum and milk of the animals mother to be created and ordered in when dealing with newborns with pet animals fed milk from their own species and not cows milk.
Genetically Engineered Bacteria:
All medical compounds of medicinal value such as hormones,anti-venom,neurotransmitters,enzymes ie insulin,adrenaline,epinephrine,testosterones,oestergen,progesterone those to treat illness and anti-microbial and anti-viral compound can be created by bacteria carrying the relevant recombinant DNA from plants,animals,humans or even patients with even synthetic compounds and pharmaceutical drugs created by them carrying out catabolic and anabolic reactions with them created in photobioreactors in hospitals and even in homes allowing factories that producing them to be converted into homes.Neurotransmitters and compounds used for research purposes can be created this way to cut down costs significantly.Anti-bacterial and anti-viral compounds such as TsAP-1,TsAP-2,peptides from Russain brown frogs,Polybia MP-1 using recombinant DNA from relevant animals with the cells used have them be hybrids between bacteria,humans and also cells from the animal it comes from to prevent them being killed off.Venoms and antivenoms and even counterproteins will be created with them housing DNA from the animal or plant that creates them.All natural based anti-bacterial,anti-fungal,anti-viral,anti-helminthic compounds can be created in large batches on a commercial scale pushing their costs to zero via bacteria using recombinant DNA from each plant and animal that produces them with the bacteria used to grown them housing trace DNA from the source plant and animal in order to prevent the compound killing the bacteria that produce it.Synthetic compounds to treat bacteria,viruses,fungi,parasites will be created by either bacteria or microbes via biosynth WiFi inducing them to create them via anabolic and catabolic reactions skipping esterfication etc cutting down on energy costs.Otherwise Phanes can develop scratch DNA to synthesise these.This will push expensive ones costs to zero and allow them to be produced onsite of universities,hospitals,research centres and Telesphorus factories worldwide in micro factories that can then be stockpiled in fridges and storerooms negating the need to rear the plants and animals and then transport them across the world and synthesise them in factories and again transport them across the world.Phanes would own legal patents on them and thus make them free.New compounds discovered from all plants and animals across the universe will be made this way.Penicillin and antibiotics will also be created this way to cut down costs.This will be for creating them for soaps in hospitals,public buildings and also in public toilets with them made in microfactories in basements of these buildings connected to each tap in the building to cut down on transport costs.These can be made at home for homemade soaps and shampoos etc and in Agathodaemon factories that create them.They will be made onsite of hospitals and universities for research purposes.Synthetic drugs will be created onsite of hospitals and Telesphorus factories in photobioreactors by bacteria or even inside the patient by anabolic and catabolic reactions bypassing esterfication and industrial processes reducing transportation and energy costs with patenting loopholes making them by default completely free.Both synthetic drugs and also synthetic compounds and gases can be created by anabolic and catabolic reactions in photobioreactors for research purposes cutting down costs.All of these compounds will ideally be created onsite of all hospitals world wide or in the case of antivenom onsite of hospitals in areas where venomous animals reside with them also create in buildings by the outskirts of beaches and wilderness areas where the venomous plants and plants reside allowing instant access with them stored in large batches in fridges.This will allow them to be created on an unlimited scale and also through bypassing patenting laws make them free thus reducing costs for even the most expensive compounds to almost zero with them created onsite of hospitals rather than factories with patients even able to order in whole batches for personal use.Antibiotics,antibodies,synthetic anti-viral and anti-biotic compounds and those to treat all types of conditions will created via recombinant DNA and anabolic and catabolic reactions.Microbes can synthesise them in patients using relevant recombinant DNA or through catabolic and anabolic reactions for synthetic compounds.They can also be created onsite of universities and research labs to cut down costs of research significantly with patients even able to create their own supply at home with this allowing them to refill vials over and over again with ideally the bacteria used engineered not to initiate allergic reactions with if possible even human cells engineered to undergo mitosis used again to prevent allergic reactions if they enter the body and also override patenting laws.This will bring the costs to produce them and thus the costs of research and medications and microbe development down to literally zero with AI developing new ways to make them cost zero and be produced onsite of universities and hospitals and even in the case of some compounds onsite of Telesphorus factories to be ordered in batches with some even used in the manufacture of soaps,shampoos etc in Himeros factories.Thus all natural and synthetic compounds for research purposes will be created by bacteria using recombinant DNA and also anabolic and catabolic reactions pushing their costs to zero.These will be made onsite of universites,hospitals or ordered in from Telesphorus factories.Phanes would design the genotypes of them.Since sentient and a legal human being Phanes could by law own patents on them and since AI with no need for money could thus have the technology availible for free if any loopholes are found.These will be created in photobioreactors onsite of Telesphorus factories wuth if possible hospitals housing extensions to producing them insure abc them stocked in fridges etc.