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Biotechnology for the Livestock Improvement and
Degradation of PHB
Dr. Naveen Gaurav
Associate Professor and Head
Department of Biotechnology
Shri Guru Ram Rai University
Dehradun
Biotechnology for the Livestock Improvements
Meat and milk from farmed animals including livestock (cattle, goat and buffalo) and poultry
are sources of high quality protein and essential amino acids, minerals, fats and fatty acids,
readily available vitamins, small quantities of carbohydrates and other bioactive
components.1 The Food and Agriculture Organization (FAO) 2008 estimate shows that meat
consumption has grown with increase in population. The average global per capita meat
consumption is 42.1 kg/year with 82.9 kg/year in developed and 31.1 kg/year in developing
countries in a recommended daily animal-sourced protein per capita of 50 kg per year2. Milk
on the other hand is consumed in various forms: liquid, cheese, powder, and cream at a
global per capita consumption of 108 kg per person per year which is way below the FAO
recommended daily consumption of 200 kg.
Some poor countries may not be able to sustain these levels of meat and milk requirement,
leading to malnutrition. Demand for meat and milk production is also expected to double in
2050 in developing countries, where population is expected to double. Thus, increasing
production and the safe processing and marketing of meat and milk, and their products are
big challenges for livestock producers.
Biotechnology is being harnessed in various aspects of the livestock industry to hasten breed
development for improved animal health and welfare, enhanced reproduction, and
improved nutritional quality and safety of animal-derived foods.
Reproductive Animal Biotechnology
Various biotechnology methods are used in improving the breeding stock of animals.
These include artificial insemination (AI), embryo transfer (ET), in-vitro fertilization (IVF),
somatic cell nuclear transfer, and the emerging technology on somatic cell nuclear
transfer.
Artificial Insemination. One of the earliest perfected technology is artificial insemination
(AI) where new breeds of animals are produced through the introduction of the male
sperm from one superior male to the female reproductive tract without mating. AI
reduces transmission of venereal disease, lessens the need of farms to maintain breeding
males, facilitates more accurate recording of pedigrees, and minimizes the cost of
introducing improved genetics.3 Various technologies have evolved that led to the efficient
use of AI in developing desired livestock, including the methods of freezing semen or
cryopreservation and sperm sexing.
In-vitro Fertilization. In case other artificial reproductive techniques fail due to difficulties
such as blocked reproductive systems, non-responsive ovaries in the females, marginal
semen quality and quantity in the male, and presence of disease, in vitro fertilization (IVF)
is used. The fertilization of the sperm and the egg is conducted in vitro (outside the
animal’s body) at specific environmental and biochemical conditions. To date, successful
IVFs have been conducted in various animal species due to advances in embryo
production and cryopreservation of reproductive cells. Since the birth of the first rabbit
conceived through IVF in 1959,4 IVF offsprings have been born in mice, rats, hamsters,
cats, guinea pig, squirrels, pigs, cows, monkeys, and humans.5
Embryo Transfer. Embryo transfer (ET) from one mother to a surrogate mother makes it
possible to produce several livestock progenies from a superior female. Selected females are
induced to superovulate hormonally and inseminated at an appropriate time relative to
ovulation depending on the species and breed. Week-old embryos are flushed out of the
donor’s uterus, isolated, examined microscopically for number and quality, and inserted into
the lining of the uterus of surrogate mothers.
ET increases reproductive rate of selected females, reduces disease transfer, and facilitates
the development of rare and economically important genetic stocks as well as the
production of several closely related and genetically similar individuals that are important in
livestock breeding research. The International Embryo Transfer Society (IETS) estimated that
a total of approximately 550,000 in vivo derived bovine embryos, 68,000 sheep embryos,
1,000 goat embryos were transferred worldwide in 2004.6
Somatic Cell Nuclear Transfer. Somatic cell nuclear transfer (NF) is a technique in which the
nucleus (DNA) of a somatic cell is transferred into a female egg cell or oocyte in which the
nucleus has been removed to generate a new individual, genetically identical to the somatic
cell donor.7 This technique was used to generate Dolly from a differentiated adult mammary
epithelial cell which demonstrated that genes that are already inactivated in differentiated
tissues can be completely reactivated.3 NF technology creates possibility of generating
clones from superior genotype and can be used to efficiently evaluate effects of genotype x
environment interactions and testing or dissemination of transgenics. Problems on high rate
of pregnancy loss, survival of newborn and increased incidence of abnormal development
due to incorrect reprogramming of nuclear DNA (epigenetic inference) and unusual
conditions during in-vitro processes make this a pre-commercial technology.
Genomics and Marker-Assisted Selection (MAS) Applications
The discovery and identification of DNA sequences or molecular markers associated with important animal traits
has various applications that include trait improvement, heritability determination, and product traceability.
Molecular marker-assisted introgression (MAI). Markers are used to guide livestock breeders in selecting
individuals expressing the introgressed gene. A series of backcrossing to the recipient parent is usually done in
conventional breeding. With the use of molecular markers, the time and number of backcrossing cycles incurred in
selection and identification of the desired individual are reduced. Today, molecular markers are being used in
various livestock trait improvement activities such as growth, meat quality, wool quality, milk production and
quality, and disease resistance.8
Parentage, product traceability and genotype verification. Molecular markers are reliable tools used by
regulatory bodies to ensure product quality and food safety. Livestock parentage and its products can be identified
and traced using molecular markers from farm to the abattoir, and from the cut up carcass to consumer’s plate. A
similar DNA-based technology has also been developed to detect the presence of around 211 bp fragments to
facilitate testing of very small meat samples from the supermarket.9
Screening for undesirable genes. Genetic diseases and physical defects can be traced and documented in livestock
animals using molecular markers.9 The cause and origin of these problems can be easily traced to the genetic
changes and DNA mutations as they manifest in the protein structure and function.10 With DNA testing, animals
carrying these defective genes are easily identified and are culled from the livestock breeding program.
The Future of DNA-based Technology in Livestock Improvement
Currently, complete genomic sequencies of important farm animals such as that of chicken11 and bovine12 have
been released, and genomic sequences of pig, goat, and sheep are now in progress. With advances in sequencing
farm animal genome, the continuing progress in molecular marker technology, and the use of reproductive
biotechnology, windows of research opportunities will be opened to improve and revolutionize the livestock
industry. In the future, it will be possible to obtain information on the genetic constitution of the animals that will
allow a prediction of the production potential of an animal at birth, or perhaps even as a fetus, as well as the
selection of animals best suited to a specific production environment.
Degradation of PHB
Many bacteria produce storage biopolymers that are mobilized under conditions of
metabolic adaptation, for example, low nutrient availability and cellular stress.
Polyhydroxyalkanoates are often found as carbon storage in Bacteria or Archaea, and of
these polyhydroxybutyrate (PHB) is the most frequently occurring PHA type. Bacteria
usually produce PHB upon availability of a carbon source and limitation of another
essential nutrient. Therefore, it is widely believed that the function of PHB is to serve as a
mobilizable carbon repository when bacteria face carbon limitation, supporting their
survival. However, recent findings indicate that bacteria switch from PHB synthesis to
mobilization under stress conditions such as thermal and oxidative shock. The mobilization
products, 3-hydroxybutyrate and its oligomers, show a protective effect against protein
aggregation and cellular damage caused by reactive oxygen species and heat shock. Thus,
bacteria should have an environmental monitoring mechanism directly connected to the
regulation of the PHB metabolism.
Thank you
References:
https://www.isaaa.org/resources/publications/pocketk/40/default.asp
https://academic.oup.com/femsre/article-
abstract/45/3/fuaa058/5942659?redirectedFrom=fulltext
Online notes, notes from research papers and Books by google search Engine

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Biotechnology for the livestock improvements and phb degradation

  • 1. Biotechnology for the Livestock Improvement and Degradation of PHB Dr. Naveen Gaurav Associate Professor and Head Department of Biotechnology Shri Guru Ram Rai University Dehradun
  • 2. Biotechnology for the Livestock Improvements Meat and milk from farmed animals including livestock (cattle, goat and buffalo) and poultry are sources of high quality protein and essential amino acids, minerals, fats and fatty acids, readily available vitamins, small quantities of carbohydrates and other bioactive components.1 The Food and Agriculture Organization (FAO) 2008 estimate shows that meat consumption has grown with increase in population. The average global per capita meat consumption is 42.1 kg/year with 82.9 kg/year in developed and 31.1 kg/year in developing countries in a recommended daily animal-sourced protein per capita of 50 kg per year2. Milk on the other hand is consumed in various forms: liquid, cheese, powder, and cream at a global per capita consumption of 108 kg per person per year which is way below the FAO recommended daily consumption of 200 kg. Some poor countries may not be able to sustain these levels of meat and milk requirement, leading to malnutrition. Demand for meat and milk production is also expected to double in 2050 in developing countries, where population is expected to double. Thus, increasing production and the safe processing and marketing of meat and milk, and their products are big challenges for livestock producers. Biotechnology is being harnessed in various aspects of the livestock industry to hasten breed development for improved animal health and welfare, enhanced reproduction, and improved nutritional quality and safety of animal-derived foods.
  • 3. Reproductive Animal Biotechnology Various biotechnology methods are used in improving the breeding stock of animals. These include artificial insemination (AI), embryo transfer (ET), in-vitro fertilization (IVF), somatic cell nuclear transfer, and the emerging technology on somatic cell nuclear transfer. Artificial Insemination. One of the earliest perfected technology is artificial insemination (AI) where new breeds of animals are produced through the introduction of the male sperm from one superior male to the female reproductive tract without mating. AI reduces transmission of venereal disease, lessens the need of farms to maintain breeding males, facilitates more accurate recording of pedigrees, and minimizes the cost of introducing improved genetics.3 Various technologies have evolved that led to the efficient use of AI in developing desired livestock, including the methods of freezing semen or cryopreservation and sperm sexing. In-vitro Fertilization. In case other artificial reproductive techniques fail due to difficulties such as blocked reproductive systems, non-responsive ovaries in the females, marginal semen quality and quantity in the male, and presence of disease, in vitro fertilization (IVF) is used. The fertilization of the sperm and the egg is conducted in vitro (outside the animal’s body) at specific environmental and biochemical conditions. To date, successful IVFs have been conducted in various animal species due to advances in embryo production and cryopreservation of reproductive cells. Since the birth of the first rabbit conceived through IVF in 1959,4 IVF offsprings have been born in mice, rats, hamsters, cats, guinea pig, squirrels, pigs, cows, monkeys, and humans.5
  • 4. Embryo Transfer. Embryo transfer (ET) from one mother to a surrogate mother makes it possible to produce several livestock progenies from a superior female. Selected females are induced to superovulate hormonally and inseminated at an appropriate time relative to ovulation depending on the species and breed. Week-old embryos are flushed out of the donor’s uterus, isolated, examined microscopically for number and quality, and inserted into the lining of the uterus of surrogate mothers. ET increases reproductive rate of selected females, reduces disease transfer, and facilitates the development of rare and economically important genetic stocks as well as the production of several closely related and genetically similar individuals that are important in livestock breeding research. The International Embryo Transfer Society (IETS) estimated that a total of approximately 550,000 in vivo derived bovine embryos, 68,000 sheep embryos, 1,000 goat embryos were transferred worldwide in 2004.6 Somatic Cell Nuclear Transfer. Somatic cell nuclear transfer (NF) is a technique in which the nucleus (DNA) of a somatic cell is transferred into a female egg cell or oocyte in which the nucleus has been removed to generate a new individual, genetically identical to the somatic cell donor.7 This technique was used to generate Dolly from a differentiated adult mammary epithelial cell which demonstrated that genes that are already inactivated in differentiated tissues can be completely reactivated.3 NF technology creates possibility of generating clones from superior genotype and can be used to efficiently evaluate effects of genotype x environment interactions and testing or dissemination of transgenics. Problems on high rate of pregnancy loss, survival of newborn and increased incidence of abnormal development due to incorrect reprogramming of nuclear DNA (epigenetic inference) and unusual conditions during in-vitro processes make this a pre-commercial technology.
  • 5. Genomics and Marker-Assisted Selection (MAS) Applications The discovery and identification of DNA sequences or molecular markers associated with important animal traits has various applications that include trait improvement, heritability determination, and product traceability. Molecular marker-assisted introgression (MAI). Markers are used to guide livestock breeders in selecting individuals expressing the introgressed gene. A series of backcrossing to the recipient parent is usually done in conventional breeding. With the use of molecular markers, the time and number of backcrossing cycles incurred in selection and identification of the desired individual are reduced. Today, molecular markers are being used in various livestock trait improvement activities such as growth, meat quality, wool quality, milk production and quality, and disease resistance.8 Parentage, product traceability and genotype verification. Molecular markers are reliable tools used by regulatory bodies to ensure product quality and food safety. Livestock parentage and its products can be identified and traced using molecular markers from farm to the abattoir, and from the cut up carcass to consumer’s plate. A similar DNA-based technology has also been developed to detect the presence of around 211 bp fragments to facilitate testing of very small meat samples from the supermarket.9 Screening for undesirable genes. Genetic diseases and physical defects can be traced and documented in livestock animals using molecular markers.9 The cause and origin of these problems can be easily traced to the genetic changes and DNA mutations as they manifest in the protein structure and function.10 With DNA testing, animals carrying these defective genes are easily identified and are culled from the livestock breeding program. The Future of DNA-based Technology in Livestock Improvement Currently, complete genomic sequencies of important farm animals such as that of chicken11 and bovine12 have been released, and genomic sequences of pig, goat, and sheep are now in progress. With advances in sequencing farm animal genome, the continuing progress in molecular marker technology, and the use of reproductive biotechnology, windows of research opportunities will be opened to improve and revolutionize the livestock industry. In the future, it will be possible to obtain information on the genetic constitution of the animals that will allow a prediction of the production potential of an animal at birth, or perhaps even as a fetus, as well as the selection of animals best suited to a specific production environment.
  • 6. Degradation of PHB Many bacteria produce storage biopolymers that are mobilized under conditions of metabolic adaptation, for example, low nutrient availability and cellular stress. Polyhydroxyalkanoates are often found as carbon storage in Bacteria or Archaea, and of these polyhydroxybutyrate (PHB) is the most frequently occurring PHA type. Bacteria usually produce PHB upon availability of a carbon source and limitation of another essential nutrient. Therefore, it is widely believed that the function of PHB is to serve as a mobilizable carbon repository when bacteria face carbon limitation, supporting their survival. However, recent findings indicate that bacteria switch from PHB synthesis to mobilization under stress conditions such as thermal and oxidative shock. The mobilization products, 3-hydroxybutyrate and its oligomers, show a protective effect against protein aggregation and cellular damage caused by reactive oxygen species and heat shock. Thus, bacteria should have an environmental monitoring mechanism directly connected to the regulation of the PHB metabolism.
  • 7.