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MICROBIAL
PRODUCTION OF
SINGLE CELL
PROTEIN
Presented by: Amandeep Kaur &
Sukhpreet Kaur (B.Sc. Biotech IV th sem)
Submitted to: Dr. Pardeep Kaur
BAEKER’S
YEAST
WHAT IS SINGE CELL
PROTEIN (SCP):-
 Protein that consist of processed
microorganisms ( such as yeast,
fungi, algae and bacteria ) grown in
culture and are used as source of
food especially for livestock.
 Edible protein which is extracted
from pure microbial culture, dead or
dried cell biomass.
 Also known as “Microbial Protein”.
 Also called ‘Novel Food’ & ‘Minifood’
HISTORY OF SCP:-
 The term was coined by Carol L.
Wilson in 1966.
 Earlier known as “Microbial
Protein”.
 During World War II, when there
were shortage in proteins and
vitamins in the diet, the Germans
produced yeast and moulds in some
quantity for food; this led to produce
edible proteins on large scale by
means of microorganism during
1970’s.
 Research on SCP technology was
started a century ago when Max
Delbruck & his collegues found out
the high value of surplus Brewer’s
yeast as a feeding supplement for
animals.
 In 1950’s British Petroleum initiated
production of SCP on commercial
basis.
 Considered as a part of our diet from
ancient times.
 Pruteen was the Ist commercial SCP
used as animal feed additives.
 Pruteen was produced from bacteria
Methyophilus methyotrophus
cultured on methanol & had 72%
protein content.
 SCP contains- fats, carbohydrates,
vitamins, nucleic acid & minerals. It
is also rich in essential amino acids
like Lysine & Methionine
LIST OF MICRO-ORGANISMS
UESD FOR PRODUCTION OF
SCP:-
 FUNGI :
i. Aspergillus fumigates
ii. Aspergillus niger
iii. Rhizopus cyclopium
 YEAST :
i. Saccharomyces cerevisae
ii. Candida tropicalis
iii. Candida utilis
 ALGAE :
i. Spirulina sps
ii. Chlorella pyrenoidosa
iii. Chondrus crispus
 BACTERIA:
i. Pseudomonas fluroescens
ii. Lactobacillus
iii. Bacillus megaterium
FUNGI: YEAS
T:
BACT
ERI;
ALGA
E:
TEMPRATU
RE:
25-30C 25-
26C
35-45C 25C
pH: 5-6 4-4.4 5-7 8-10
PROTEIN
(%age):
30-55% 45-
55%
50-85% 45-
65%
ADVANTA
GES:
Fast
growth,hi
gh protein
content
and
higher
penetrtion
power.
Bioma
ss can
be
easily
harves
ted
due to
large
size,
can
grow
in
highly
aciddi
c ph,
bioma
ss
produc
ed has
high
level
of
lysine.
Rapid
growth
, short
genera
tion
time,
utilisat
ion of
any
kind of
raw
materi
al.
Protei
n rich
bioma
ss is
produc
ed,
simple
& fast
growt
h.
DISVANTA
GES:
Risk of
contamin
ation,
produce
mycotoxin
s , some
have
slower
growth
rate.
Lower
growt
h rate
& low
protei
n
conten
t.
Grow
only
in
highly
basic
conditi
on.
OTHER SUBSTRATE FOR SCP
PRODUCTION:-
 SCP can be produce by :
 High Energy Sources Like:
i. Methanol
ii. Ethanol
iii. Methane
 Waste Products:
i. Molasses
ii. Whey
iii. Sewage
 Agricultural Sources:
i. Cellulose
ii. Lignin
 Carbon Dioxide:
i. Spirulina species
SCP PRODUCTION IN INDIA :-
1) National Botanical Research
Institute (NBRI).
2) Central Food Technological
Research Institute (CFTRI).
 In CFTRI, SCP is produced from
algae cultured on sewage.
RAW MATERIALS :-
 Production of SCP requires microbes
that serve as the protein source as
the substrate that is biomass on
which they grow.
 There is variety of both the source
that can be used for the production
of SCP.
 The biomass used can be plant
biomass or organic biomass.
 The microbes used belong to the
group of algae, fungi and bacteria.
MICRO-ORGANISMS:-
 Micro-organisms used are fungi,
bacteria, yeast an algae.
 The following table shows average
different composition of main groups
o microbes (% dry wt.):
COMPARISION OF MICRO-
ORGANISMS:-
MICROBE
S:
ADVANTAG
ES:
DISADVNTAG
ES:
FUNGI : Easy to grow
and harvest.
Lower growth
rate & lower
protein
content.
ALGAE : Easy to grow
and harvest
and high
quality
protein .
Non-digestible
cellulosic cell
wall
concentrate
heavy metals.
YEAST : Large in size,
lower NA
content,
familiarity &
acceptability
Poor
digestibility,
low protein
content, slow
growth rate.
BACTERI
A :
High protein
content,
digestible cell
wall.
High NA
content, small
in size, low
density.
PRODUCTION OF SCP:-
Production of SCP involves following
steps:
1. Selection of strain of microbe and
substrate.
2. Fermentation..
3. Harvesting.
4. Post harvest treatment.
5. Processing of SCP
1) SELECTION OF MICROBIAL
STRAIN & SUBSTRATE :-
 It is a very crucial step as the quality of
proteintotally depend upon the microbe
that is use for production.
 Microbe selected shouldn’t produce toxicity
in its biomass.
 It shouldn’t be harmful for a consumer to
consume.
 Selected microbe should produce a large
quantity of protein.
 Substrate should be cheap, effective, allow
favourable growth& ease of isolation.
2) PREPRATION OF MEDIA FOR
MICROBIAL GROWTH:
 Media formulation is important for
fermentation. The constituents of media
should satisfy the elemental requirements
of biomass & metabolite production.
 Different types of raw material are used in
different types of industrial fermentation
process. Mostly agricultural & industrial
wastes are used as raw material.
 Eg. : Molasses, Cassava, Cheese Whey,
Cellulosic Material (Wood molasses, Rice
straw).
3) FERMENTATION:-
 It is done in large chambers either of glass
or stainless steel called Fermentor.
 Fermentation should done under sterile
conditions.
 Controlled conditions are necessary e.g.
Temperature, Pressure, pH, Humidity etc.
 Usually fed-batch cultures are used for
this process.
 Deep lift fermentors & air lift fermentors
are used.
3) HARVESTING:-
 When the colonies of microbes are fully
developed , they are then Harvested.
 The bulk of cells are removed from the
fermentor by the method called
Decantation.
4) POST- HRVESTING
FERMENTATION:-
 Isolated microbial colonies are subjected to
variety of processes.
 It include steps like- Centrifugation,
Washing, Drying etc.
5) PROCESSING OF SCP:-
 Produced protein contain impurities like-
carbohydrates, nucleic acid, lipid content,
salts etc.
 Pure protein isolation can be done by
crushing, crumbling, cycles of freezing &
thawing, grinding & thermal shocks.
 Nucleic acid can be removed by:
a. By treatment with NaCl 10%.
b. By chemicals e.g. NaOH Thermal shocks.
c. Enzymes treatment e.g. Ribonuclease.
ADVANTAGES:-
 Microbes have rapid succession of
generation thus number o
generation can be obtained in very
short time (algae- 2-6 hrs, yeast- 1-3
hrs, bacteria- 0.5-2 hrs).
 They can easily be modified
genetically.
 Contain high protein content of 43-
85% in dry mass.
 Can be easily produced and isolated.
 Production in continuous culture.
 Economically beneficial
 Broad spectrum of original raw
material used for production which
include industrial.
 Low land requirements.
DISADVANTAGES:-
 Development of kidney stone & gout
if consumed in high quantity.
 Possibility of presence of secendory
toxic metabolites.
 Hypersenstivity skin reactions.
 Poor digestibility.
 High content of nucleic acid leading
to elevated levels of uric acid.
 Production of SCPs is very expensive
method & requires highly sterilized
conditions.
APPLICATIONS:-
As protein supplement food-
i. Also source of vitamins, amino acids, minerals,
crude fibers etc.
ii. Supplemented food for undernourished
children.
As health food-
i. Controls obesity.
ii. Provides instant energy.
In medicines-
i. Reduce body weight,cholesterol, stress.
ii. Prevents accumulation of cholesterol in
body.
iii. Increase lactation.
In cosmetics-
i. Important role in maintaining healthy
hair
ii. Used in lipstics & herbal face cream.
iii. Used in many cosmetic products.
CONCLUSION:-
 The development o SCP is just a
beginning of biotechnology.
 With the improvement in the
production o SCPs we can solve the
malnutritive conditions of the
progressing countries & can so
introduce better quality food & taste
with decrease chances of occurrence
o side effects. Moreover, genetic
modification in microorganisms can
lead to better future o SCPs in
biotechnology, medicines,
agriculture, poultry etc.
 One of the way to enhance
productivity and quality is genetic
improvements of micro-organisms.
Amandeep kaur

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Amandeep kaur

  • 1. Presentation on... MICROBIAL PRODUCTION OF SINGLE CELL PROTEIN Presented by: Amandeep Kaur & Sukhpreet Kaur (B.Sc. Biotech IV th sem) Submitted to: Dr. Pardeep Kaur BAEKER’S YEAST
  • 2. WHAT IS SINGE CELL PROTEIN (SCP):-  Protein that consist of processed microorganisms ( such as yeast, fungi, algae and bacteria ) grown in culture and are used as source of food especially for livestock.  Edible protein which is extracted from pure microbial culture, dead or dried cell biomass.  Also known as “Microbial Protein”.  Also called ‘Novel Food’ & ‘Minifood’
  • 3. HISTORY OF SCP:-  The term was coined by Carol L. Wilson in 1966.  Earlier known as “Microbial Protein”.  During World War II, when there were shortage in proteins and vitamins in the diet, the Germans produced yeast and moulds in some quantity for food; this led to produce edible proteins on large scale by means of microorganism during 1970’s.  Research on SCP technology was started a century ago when Max Delbruck & his collegues found out the high value of surplus Brewer’s yeast as a feeding supplement for animals.
  • 4.  In 1950’s British Petroleum initiated production of SCP on commercial basis.  Considered as a part of our diet from ancient times.  Pruteen was the Ist commercial SCP used as animal feed additives.  Pruteen was produced from bacteria Methyophilus methyotrophus cultured on methanol & had 72% protein content.  SCP contains- fats, carbohydrates, vitamins, nucleic acid & minerals. It is also rich in essential amino acids like Lysine & Methionine LIST OF MICRO-ORGANISMS UESD FOR PRODUCTION OF SCP:-
  • 5.  FUNGI : i. Aspergillus fumigates ii. Aspergillus niger iii. Rhizopus cyclopium  YEAST : i. Saccharomyces cerevisae ii. Candida tropicalis iii. Candida utilis  ALGAE : i. Spirulina sps ii. Chlorella pyrenoidosa iii. Chondrus crispus  BACTERIA: i. Pseudomonas fluroescens ii. Lactobacillus iii. Bacillus megaterium
  • 6. FUNGI: YEAS T: BACT ERI; ALGA E: TEMPRATU RE: 25-30C 25- 26C 35-45C 25C pH: 5-6 4-4.4 5-7 8-10 PROTEIN (%age): 30-55% 45- 55% 50-85% 45- 65% ADVANTA GES: Fast growth,hi gh protein content and higher penetrtion power. Bioma ss can be easily harves ted due to large size, can grow in highly aciddi c ph, bioma ss produc ed has high level of lysine. Rapid growth , short genera tion time, utilisat ion of any kind of raw materi al. Protei n rich bioma ss is produc ed, simple & fast growt h.
  • 7. DISVANTA GES: Risk of contamin ation, produce mycotoxin s , some have slower growth rate. Lower growt h rate & low protei n conten t. Grow only in highly basic conditi on.
  • 8.
  • 9. OTHER SUBSTRATE FOR SCP PRODUCTION:-  SCP can be produce by :  High Energy Sources Like: i. Methanol ii. Ethanol iii. Methane  Waste Products: i. Molasses ii. Whey iii. Sewage  Agricultural Sources: i. Cellulose ii. Lignin  Carbon Dioxide: i. Spirulina species
  • 10. SCP PRODUCTION IN INDIA :- 1) National Botanical Research Institute (NBRI). 2) Central Food Technological Research Institute (CFTRI).  In CFTRI, SCP is produced from algae cultured on sewage.
  • 11. RAW MATERIALS :-  Production of SCP requires microbes that serve as the protein source as the substrate that is biomass on which they grow.  There is variety of both the source that can be used for the production of SCP.  The biomass used can be plant biomass or organic biomass.  The microbes used belong to the group of algae, fungi and bacteria.
  • 12. MICRO-ORGANISMS:-  Micro-organisms used are fungi, bacteria, yeast an algae.  The following table shows average different composition of main groups o microbes (% dry wt.):
  • 13. COMPARISION OF MICRO- ORGANISMS:- MICROBE S: ADVANTAG ES: DISADVNTAG ES: FUNGI : Easy to grow and harvest. Lower growth rate & lower protein content. ALGAE : Easy to grow and harvest and high quality protein . Non-digestible cellulosic cell wall concentrate heavy metals. YEAST : Large in size, lower NA content, familiarity & acceptability Poor digestibility, low protein content, slow growth rate. BACTERI A : High protein content, digestible cell wall. High NA content, small in size, low density. PRODUCTION OF SCP:-
  • 14. Production of SCP involves following steps: 1. Selection of strain of microbe and substrate. 2. Fermentation.. 3. Harvesting. 4. Post harvest treatment. 5. Processing of SCP
  • 15. 1) SELECTION OF MICROBIAL STRAIN & SUBSTRATE :-  It is a very crucial step as the quality of proteintotally depend upon the microbe that is use for production.  Microbe selected shouldn’t produce toxicity in its biomass.  It shouldn’t be harmful for a consumer to consume.  Selected microbe should produce a large quantity of protein.  Substrate should be cheap, effective, allow favourable growth& ease of isolation.
  • 16. 2) PREPRATION OF MEDIA FOR MICROBIAL GROWTH:  Media formulation is important for fermentation. The constituents of media should satisfy the elemental requirements of biomass & metabolite production.  Different types of raw material are used in different types of industrial fermentation process. Mostly agricultural & industrial wastes are used as raw material.  Eg. : Molasses, Cassava, Cheese Whey, Cellulosic Material (Wood molasses, Rice straw).
  • 17. 3) FERMENTATION:-  It is done in large chambers either of glass or stainless steel called Fermentor.  Fermentation should done under sterile conditions.  Controlled conditions are necessary e.g. Temperature, Pressure, pH, Humidity etc.  Usually fed-batch cultures are used for this process.  Deep lift fermentors & air lift fermentors are used.
  • 18. 3) HARVESTING:-  When the colonies of microbes are fully developed , they are then Harvested.  The bulk of cells are removed from the fermentor by the method called Decantation. 4) POST- HRVESTING FERMENTATION:-  Isolated microbial colonies are subjected to variety of processes.  It include steps like- Centrifugation, Washing, Drying etc. 5) PROCESSING OF SCP:-  Produced protein contain impurities like- carbohydrates, nucleic acid, lipid content, salts etc.
  • 19.  Pure protein isolation can be done by crushing, crumbling, cycles of freezing & thawing, grinding & thermal shocks.  Nucleic acid can be removed by: a. By treatment with NaCl 10%. b. By chemicals e.g. NaOH Thermal shocks. c. Enzymes treatment e.g. Ribonuclease.
  • 20. ADVANTAGES:-  Microbes have rapid succession of generation thus number o generation can be obtained in very short time (algae- 2-6 hrs, yeast- 1-3 hrs, bacteria- 0.5-2 hrs).  They can easily be modified genetically.  Contain high protein content of 43- 85% in dry mass.  Can be easily produced and isolated.  Production in continuous culture.  Economically beneficial  Broad spectrum of original raw material used for production which include industrial.  Low land requirements.
  • 21. DISADVANTAGES:-  Development of kidney stone & gout if consumed in high quantity.  Possibility of presence of secendory toxic metabolites.  Hypersenstivity skin reactions.  Poor digestibility.  High content of nucleic acid leading to elevated levels of uric acid.  Production of SCPs is very expensive method & requires highly sterilized conditions.
  • 22. APPLICATIONS:- As protein supplement food- i. Also source of vitamins, amino acids, minerals, crude fibers etc. ii. Supplemented food for undernourished children. As health food- i. Controls obesity. ii. Provides instant energy. In medicines- i. Reduce body weight,cholesterol, stress. ii. Prevents accumulation of cholesterol in body. iii. Increase lactation. In cosmetics- i. Important role in maintaining healthy hair ii. Used in lipstics & herbal face cream. iii. Used in many cosmetic products.
  • 23.
  • 24. CONCLUSION:-  The development o SCP is just a beginning of biotechnology.  With the improvement in the production o SCPs we can solve the malnutritive conditions of the progressing countries & can so introduce better quality food & taste with decrease chances of occurrence o side effects. Moreover, genetic modification in microorganisms can lead to better future o SCPs in biotechnology, medicines, agriculture, poultry etc.  One of the way to enhance productivity and quality is genetic improvements of micro-organisms.