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By- HIMANSHU JAIN
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CONTENTS
• Introduction
• History
• SCP production in India
• Raw materials
• SCP production
• Advantages and Disadvantages
• Applications
• Conclusion
• References
Environmental Biotechnology may be referred as application of
biotechnological techniques to solve the problems and issues
of environment.
Biomass as the name suggests consists of all organic matter that
grows by photosynthetic conversion of solar energy.
This biomass is available abundantly and is estimated to contain
3x 10²¹ joules of energy, some 10 times the yearly worldwide
consumption.
Utilization of Biomass would lead to-
a. Help solve modern waste disposal problems.
b. Decrease in environmental pollution.
c. Help activate shortage of food and animal feed.
WHATARESINGLECELLPROTEINS?
• SCP are dried cells ofmicro organisms which can be used as
dietary protein supplement.
• They are used asanimal feed &can beused forhuman feed as
protein supplement.
• Also called ‘Novel Food’ & ‘Minifood’.
HISTORY
• Part of our diet since ancient times.
• Earlier known as ‘Microbial Protein’.
• Name was introduced byProf. Scrimshow ofMIT in1967
• In 1950’s British Petroleum initiated production of SCP on
commercial basis.
• Pruteen was the 1st commercial SCP used as animal feed
additive
• Pruteen was produced from bacteria Methylophilus
methylotrophus cultured onmethanol &had 72 protein
content.
SCPPRODUCTIONININDIA
• National Botanical Research Institute (NBRI).
• Central Food Technological Research Institute (CFTRI).
• In CFTRI, SCP is produced from algae cultured on
sewage.
RAWMATERIALS
• Production of SCP requires micro-organisms that serve as the
protein source and the substrate that is biomass on which they
grow.
• There is a variety of both the sources that can be used for the
production of SCP.
• The biomass used can be plant biomass or organic biomass.
• The micro-organisms used belong to the group of Algae, Fungi
and Bacteria.
MICROORGANISMS
•Micro-organisms used are fungi ,yeast, algae & bacteria.
•The following table shows average different compositions of main groups of
micro– organisms dry wt.)
OMPOSITON FUNGI ALGAE YEAST BACTERIA
PROTEIN 30- 40 % 40- 60 % 45- 55 % 50- 65 %
FAT 9-14 % 8-10 % 5-10 % 3-7 %
NUCLEIC
ACID
7-10 % 3-8 % 6-12 % 8-12 %
Alistofthemicro-organisms usedforSCPproduction
Fungi
• Aspergillus fumigatus
• Aspergillus niger
• Rhizopus cyclopium
Yeast
• Saccharomyces cerevisae
• Candida tropicalis
• Candida utilis
Algae
• Spirulina sps.
• Chlorella pyrenoidosa
• Chondrus crispus
Bacteria
• Pseudomonas fluroescens
• Lactobacillus
• Bacillus megaterium
FUNGI YEAST
ALGAE BACTERUA
COMPARISIONOFMICRO-ORGANISMS
ADVANTAGES DIS ADVANTAGES
FUNGI Easy to grow & harvest Lower growth rates & lower
protein content
ALGAE Easy to grow & harvest &
high
quality protein
Non –digestible cellulosic
cell wall, concentrate
heavy metals
YEAST Larger in size, lower NA
content
, familiarity & acceptability
Poor digestibility, low
protein content, slow
growth rate
BACTERIA High protein content,
digestible cell wall
High NA content, small in
size, low density
Biomass
• Biomass alsoplays averyimportant roleinthe
production of SCP.
• Selection of biomass depends on the micro-organisms
used for theproduction.
• For eg. Algae are cultivated on sewage whereas Yeast
are cultured on agro-industrial wastes.
Algal Biomass
• Algae grows auto-
tropically.
• Requires low intensity of
light.
• Temperature – 35 -40
C& pH – 8. 5 -10.5
• Cultivated inlarge
trenches of sewage
oxidation ponds.
Bacterial&Fungalbiomass
• Bacteria &fungi can
begrown easily on a
wide range of
substrates.
• They require a
minimum temperature
of 15º-34ºc & a pH of
5- 7.
Yeast biomass
• Cultivated on agro- industrial
wastes such asmolasses, starchy
materials, fruit pulp, wood pulp, etc.
• Requires a temperature of 30 -34
c & pH of 3.5- 4.5.
• Also requires addition of inorganic
acids & sulphur supplements in the
form of salts.
FACTORS AFFECTING BIOMASS PRODUCTION
• Illumination time
• Temperature
• .pH
• Suitable strains
• Agitation
• Sterile conditions
SCP PRODUCTION
• Selection of suitable
strain
• Fermentation
• Harvesting
• Post harvest treatment
• SCP processing forfood
Selection of strain
• Itavery critical step asthe quality ofprotein depends totally on the
microbe that is used for the production.
• Thus careful selection of the strain should be done.
• Care should be taken that the selected strain should not produce any
toxic or undesirable effects in the consumer.
Fermentation
• It can be carried out in the fermentor which is equipped with aerator,
thermostat, pH, etc. or in the trenches or ponds.
• Microbes are cultured in fed- batch culture.
• Engineers have developed deep lift fermentor & air lift
fermentor .
Harvesting
• When the colonies of microbes are fully
developed, they are then harvested.
• The bulk of cells are removed from the
fermentor by decantation.
Post harvest treatment
• After harvesting, the cells are subjected to
a variety ofprocesses.
• Post harvesting treatments includes steps
like separation by centrifugation,washing,
drying, etc.
PROCESSING FOR FOOD
It includes
1. Liberation of cell proteins by destruction of indigestible cell
wall.
A. MECHANICAL METHODS
• Crushing, crumbling, grinding, pressure homogenization, etc.
B. CHEMICAL METHODS
• Enzymes & salts are used to digest or disrupt the cell wall.
• Salts like NaCl, sodium dodecyl sulfate, etc. whereas nuclease
enzymes are used.
C. PHYSICAL METHODS
• Freeze- thaw, osmotic shock, heating & drying.
2. Reduction of nucleic acid content
• Chemical & enzymatic treatments are preferred.
• Chemicals which are used includes acidified alcohol, salts, acids &
alkalies.
• Use of such chemicals leads to formation of lygino-alanine which causes
hypersensitivity skin reactions.
• Enzymes which are used include ribonuclease & nuclease enzymes .
• These enzymes can be used exogenously or can be induced
endogenously.
ADVANTAGES
• Rapid successions ofgenerations.
• Easily modifiable genetically.
• High protein content of 43- in dry mass.
• Broad spectrum of original raw material used for production, which also
includes waste products.
• Production in continuous cultures
• consistent quality not dependant on climate in determinable amount
• low land requirements, economically beneficial.
• Utilization of solar energy
• Cellular, molecular and genetic alterations.
DISADVANTAGES
• High content of nucleic acids leading to elevated levels of uric
acid.
• Development of kidney stone and gout if consumed in high
quality.
• Possibility for the presence of secondary toxic metabolites.
• Poor digestibility
• Stimulation of gastro-intestinal
• Hypersensitivity skin reactions.
APPLICATIONS
1. As protein supplemented food-
• Also source of vitamins, amino acids,
minerals, crudefibers, etc.
• Supplemented food for undernourished
children.
2. As health food-
• Controls obesity
• Provides instant energy.
• Example- Spirulina- part of diet of US
Olympic team.
3. In therapeutic and natural medicines-
• Reduce body weight, cholesterol,
stress.
• Lowers blood sugar level in
diabetic(due topresence ofB-
linolenic acid)
• Prevents accumulation of cholesterol
in body.
• Healthy eyes and skin (beta carotene)
• Beta carotene ( anti cancer substance-
UN National Cancer Research Institute)
• Increase lactation.
4.In cosmetics-
• Important role in maintaining
healthy hair (vitamin A and B).
• Many herbal beauty products.
• Biolipstics and herbal face
cream(Phycocyanin).
• Capableofreplacing coaltardye
based cosmetics.
5. Poultry and cattle feed-
• Excellent, convenient source of
protein and other nutrients.
• Used to feed cattle, fishes etc.
CONCLUSION
• Atpresent SCPproduction isinitsinfancy. Oneofthe
ways toenhance productivity andquality isgenetic
improvements ofmicro-organisms.
• Using microbial biomass as a food source deserves
serious consideration because of insufficient world
food supply and high protein content of most micro-
organisms.
REFERENCES
Books -
• Biotechnology- Dubey
• Basic Biotechnology- Colin & Ratledge
• Molecular biotechnology- Channarayappa
• Biotechnology- Satyanarayana.
Websites -
• Wikipedia .com
THANK YOU

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SINGLE CELL PROTEINS

  • 2. CONTENTS • Introduction • History • SCP production in India • Raw materials • SCP production • Advantages and Disadvantages • Applications • Conclusion • References
  • 3. Environmental Biotechnology may be referred as application of biotechnological techniques to solve the problems and issues of environment. Biomass as the name suggests consists of all organic matter that grows by photosynthetic conversion of solar energy. This biomass is available abundantly and is estimated to contain 3x 10²¹ joules of energy, some 10 times the yearly worldwide consumption. Utilization of Biomass would lead to- a. Help solve modern waste disposal problems. b. Decrease in environmental pollution. c. Help activate shortage of food and animal feed.
  • 4. WHATARESINGLECELLPROTEINS? • SCP are dried cells ofmicro organisms which can be used as dietary protein supplement. • They are used asanimal feed &can beused forhuman feed as protein supplement. • Also called ‘Novel Food’ & ‘Minifood’.
  • 5. HISTORY • Part of our diet since ancient times. • Earlier known as ‘Microbial Protein’. • Name was introduced byProf. Scrimshow ofMIT in1967 • In 1950’s British Petroleum initiated production of SCP on commercial basis. • Pruteen was the 1st commercial SCP used as animal feed additive • Pruteen was produced from bacteria Methylophilus methylotrophus cultured onmethanol &had 72 protein content.
  • 6.
  • 7. SCPPRODUCTIONININDIA • National Botanical Research Institute (NBRI). • Central Food Technological Research Institute (CFTRI). • In CFTRI, SCP is produced from algae cultured on sewage.
  • 8. RAWMATERIALS • Production of SCP requires micro-organisms that serve as the protein source and the substrate that is biomass on which they grow. • There is a variety of both the sources that can be used for the production of SCP. • The biomass used can be plant biomass or organic biomass. • The micro-organisms used belong to the group of Algae, Fungi and Bacteria.
  • 9. MICROORGANISMS •Micro-organisms used are fungi ,yeast, algae & bacteria. •The following table shows average different compositions of main groups of micro– organisms dry wt.) OMPOSITON FUNGI ALGAE YEAST BACTERIA PROTEIN 30- 40 % 40- 60 % 45- 55 % 50- 65 % FAT 9-14 % 8-10 % 5-10 % 3-7 %
  • 10. NUCLEIC ACID 7-10 % 3-8 % 6-12 % 8-12 %
  • 11. Alistofthemicro-organisms usedforSCPproduction Fungi • Aspergillus fumigatus • Aspergillus niger • Rhizopus cyclopium Yeast • Saccharomyces cerevisae • Candida tropicalis • Candida utilis Algae • Spirulina sps. • Chlorella pyrenoidosa • Chondrus crispus Bacteria • Pseudomonas fluroescens • Lactobacillus • Bacillus megaterium
  • 13. COMPARISIONOFMICRO-ORGANISMS ADVANTAGES DIS ADVANTAGES FUNGI Easy to grow & harvest Lower growth rates & lower protein content ALGAE Easy to grow & harvest & high quality protein Non –digestible cellulosic cell wall, concentrate heavy metals YEAST Larger in size, lower NA content , familiarity & acceptability Poor digestibility, low protein content, slow growth rate
  • 14. BACTERIA High protein content, digestible cell wall High NA content, small in size, low density
  • 15. Biomass • Biomass alsoplays averyimportant roleinthe production of SCP. • Selection of biomass depends on the micro-organisms used for theproduction. • For eg. Algae are cultivated on sewage whereas Yeast are cultured on agro-industrial wastes.
  • 16. Algal Biomass • Algae grows auto- tropically. • Requires low intensity of light. • Temperature – 35 -40 C& pH – 8. 5 -10.5 • Cultivated inlarge trenches of sewage oxidation ponds.
  • 17. Bacterial&Fungalbiomass • Bacteria &fungi can begrown easily on a wide range of substrates. • They require a minimum temperature of 15º-34ºc & a pH of 5- 7.
  • 18. Yeast biomass • Cultivated on agro- industrial wastes such asmolasses, starchy materials, fruit pulp, wood pulp, etc. • Requires a temperature of 30 -34 c & pH of 3.5- 4.5. • Also requires addition of inorganic acids & sulphur supplements in the form of salts.
  • 19. FACTORS AFFECTING BIOMASS PRODUCTION • Illumination time • Temperature • .pH • Suitable strains • Agitation • Sterile conditions
  • 20. SCP PRODUCTION • Selection of suitable strain • Fermentation • Harvesting • Post harvest treatment • SCP processing forfood
  • 21. Selection of strain • Itavery critical step asthe quality ofprotein depends totally on the microbe that is used for the production. • Thus careful selection of the strain should be done. • Care should be taken that the selected strain should not produce any toxic or undesirable effects in the consumer. Fermentation • It can be carried out in the fermentor which is equipped with aerator, thermostat, pH, etc. or in the trenches or ponds. • Microbes are cultured in fed- batch culture. • Engineers have developed deep lift fermentor & air lift fermentor .
  • 22.
  • 23. Harvesting • When the colonies of microbes are fully developed, they are then harvested. • The bulk of cells are removed from the fermentor by decantation. Post harvest treatment • After harvesting, the cells are subjected to a variety ofprocesses. • Post harvesting treatments includes steps like separation by centrifugation,washing, drying, etc.
  • 24. PROCESSING FOR FOOD It includes 1. Liberation of cell proteins by destruction of indigestible cell wall. A. MECHANICAL METHODS • Crushing, crumbling, grinding, pressure homogenization, etc. B. CHEMICAL METHODS • Enzymes & salts are used to digest or disrupt the cell wall. • Salts like NaCl, sodium dodecyl sulfate, etc. whereas nuclease enzymes are used. C. PHYSICAL METHODS • Freeze- thaw, osmotic shock, heating & drying.
  • 25. 2. Reduction of nucleic acid content • Chemical & enzymatic treatments are preferred. • Chemicals which are used includes acidified alcohol, salts, acids & alkalies. • Use of such chemicals leads to formation of lygino-alanine which causes hypersensitivity skin reactions. • Enzymes which are used include ribonuclease & nuclease enzymes . • These enzymes can be used exogenously or can be induced endogenously.
  • 26. ADVANTAGES • Rapid successions ofgenerations. • Easily modifiable genetically. • High protein content of 43- in dry mass. • Broad spectrum of original raw material used for production, which also includes waste products. • Production in continuous cultures • consistent quality not dependant on climate in determinable amount • low land requirements, economically beneficial. • Utilization of solar energy • Cellular, molecular and genetic alterations.
  • 27. DISADVANTAGES • High content of nucleic acids leading to elevated levels of uric acid. • Development of kidney stone and gout if consumed in high quality. • Possibility for the presence of secondary toxic metabolites. • Poor digestibility • Stimulation of gastro-intestinal • Hypersensitivity skin reactions.
  • 28. APPLICATIONS 1. As protein supplemented food- • Also source of vitamins, amino acids, minerals, crudefibers, etc. • Supplemented food for undernourished children. 2. As health food- • Controls obesity • Provides instant energy. • Example- Spirulina- part of diet of US Olympic team.
  • 29. 3. In therapeutic and natural medicines- • Reduce body weight, cholesterol, stress. • Lowers blood sugar level in diabetic(due topresence ofB- linolenic acid) • Prevents accumulation of cholesterol in body. • Healthy eyes and skin (beta carotene) • Beta carotene ( anti cancer substance- UN National Cancer Research Institute) • Increase lactation.
  • 30. 4.In cosmetics- • Important role in maintaining healthy hair (vitamin A and B). • Many herbal beauty products. • Biolipstics and herbal face cream(Phycocyanin). • Capableofreplacing coaltardye based cosmetics. 5. Poultry and cattle feed- • Excellent, convenient source of protein and other nutrients. • Used to feed cattle, fishes etc.
  • 31. CONCLUSION • Atpresent SCPproduction isinitsinfancy. Oneofthe ways toenhance productivity andquality isgenetic improvements ofmicro-organisms. • Using microbial biomass as a food source deserves serious consideration because of insufficient world food supply and high protein content of most micro- organisms.
  • 32. REFERENCES Books - • Biotechnology- Dubey • Basic Biotechnology- Colin & Ratledge • Molecular biotechnology- Channarayappa • Biotechnology- Satyanarayana. Websites - • Wikipedia .com