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PG Department of Environmental Science and Technology
Institute of Science and Technology for Advanced Studies and Research
CVM University
Vallabh Vidyanagar, Anand, Gujarat 388120
ENZYME
TECHNOLOGY
Environmental biotechnology
is biotechnology that is applied to and
used to study the natural environment.
• Background
• Products of Enzyme Technology
• Structure of an enzyme
• Mechanism of an Enzyme
• Production of Enzymes
• Properties of Enzyme
• Sources of Enzyme
• Classification of Enzyme
• Isolation of enzymes
• Uses of Enzymes
• Application of enzymes in
various industries
• Use of Nanoparticles in
Enzyme Technology
• Enzyme immobilization
• Single cess enzyme
nanoparticle
• Enhancement of Enzyme
activity and thermos ability
• Enzyme Metallography
• A case study on
Bioluminescence of Fireflies
CONTENT
BACKGROUND
Enzyme - A biological catalyst that promotes & speeds up a chemical reaction without itself being altered in
the process, they fulfil their role by binding specific substrates at their active sites.
Enzyme technology is concerned with the application of enzymes as tools of industry, agriculture and
medicine.
The value of using enzymes over inorganic catalysts in the technological field is due to their efficiency,
selectivity and specificity.
Enzymes are able to operate at wide range of temperatures, atmospheric pressure and within normal pH ranges
– all of which create energy savings for industry.
Enzymes are biodegradable and, unlike many inorganic catalysts, cause less damage to the environment.
Functions of Enzyme
Metabolism
Enzymes are proteins that help speed up metabolism, or the chemical reactions in
our bodies.
Enzymes are proteins that catalyze a chemical reaction
They build some substances and break others down.
The enzyme accelerates a chemical reaction without changing its equilibrium, so it
is called as a biocatalyst.
PRIMARY METABOLITES
During cell growth the nutrients of
the substrate are converted to cell
mass. The chemical compounds
produced in this process are called
“primary metabolites”.
„The cell mass itself consists
mainly of proteins, but a number
of primary waste products are also
formed, for instance carbon
dioxide, lactic acid, ethanol, etc.
Primary metabolites are produced
in parallel with the cell mass.
SECONDARY METABOLITES
T
„ he formation of secondary metabolites is not
directly related to cell growth.
They are the side products of bacterial life.
In nature, they are produced in low concentration,
but through laboratory mutation and selection, cells
can be optimized to overproduce these metabolites.
Many antibiotics and vitamins are secondary
metabolites.
The formation of secondary metabolites is not
directly proportional to primary metabolism and cell
growth.
Micro-organisms have been
used for thousands of years
for making products such as
wine, beer, vinegar, soy sauce,
bread and cheese.
Products of Enzyme Technology
NOTE - The micro-organisms
(such as yeast) are really used as
a source of enzymes during the
manufacture of these products of
biotechnology.
Many industrial processes now make use of pure sources of enzymes, i.e. the enzymes have been
ISOLATED from the micro-organisms before use
 Protease
found in papaya
as meat
tenderizer
STRUCTURE OF AN ENZYME
ENZYMES
NON-PROTEIN
COENZYMES
( VITAMIN)
COFACTOR
(MINERAL)
PROTEIN
(Apo-enzyme)
• NOTE :- All
enzymes are
proteins but all
proteins are
not enzymes.
MECHANISM 0F ENZYMES - LOCK AND KEY
HYPOTHESIS
Enzymes possess specifically shaped active sites for reacting with one specific substrate thereby generating
pure products free from unwanted by-products.
MODIFICATION – possible
application of genetic
engineering to improve
the microbial strain
LABORATORY SCALE PILOT
– to determine the optimum
conditions for growth of the
Micro-organism
PILOT PLANT – small scale
fermenter to clarify optimum
operating conditions
SCREENING – choosing an
appropriate micro-organism
for the desired enzyme
INDUSTRIAL SCALE
FERMENTATION
The Biotechnological Process of Enzyme Production
Pectinase is obtained
from the fungus
Aspergillus niger
Aspergillus niger
produces pectinase
as an extracellular
enzyme
Commercial Enzyme Production - An Example
PRODUCTIONOF PECTINASE
Pectin is an insoluble substance found in
the cell walls of plants
In the drinks industry, juice extracted
from fruits appears cloudy due to the
presence of pectin.
Pectinase is an enzyme that is used in the
industry to break down the pectin
The effect of pectinase is to clarify the
fruit juice and to make it flow more freely
• Control ripening.
• Cause food spoilage (rotting).
• Responsible for changes in flavor, color, texture
and nutritional properties.
• Can be inactivated by heat to extend storage
stability of foods.
• Control oxidation and spoilage (bioconservation)
• Increase nutritive values ( phytase , proteases etc.)
• Used for fermentation purposes in foods.
• Can be extracted and purified to a high degree.
Properties of enzymes
Sources of enzymes
There are three major sources of enzymes :
Plants ( 4%)
(papain, bromilain)
Animals ( 8%)
(renet)
Microorganisms
(>80%)
(yeast, fungi and
bacteria)
VEGETABLE COAGULANTS
• Vegetable coagulants are plant extracts which contain a mixture of proteolytic enzymes
and contribute unique characteristics to cheese.
• Vegetable coagulants are used primarily in niche products where specific flavours and
consistency are desired, or in remote regions where other coagulants are unavailable.
• Extracts of the Cardo flower (Cynara cardunculus) used in Spain and Portugal for the
production of some DOP (Denominación de Origen Protegida) cheeses, these cheeses are
often very soft or semi-liquid and may be spoonable. The flavour profile is strong, with
some bitterness.
• Extracts of the Calotropis procera plant used in Ghana for the production of Wara or
Wagashi cheese, having a hard texture and high melting point suitable for grilling.
Due to high production costs, low yield and development of off-flavors, vegetable coagulants
are not used in industrial cheese production.
ENZYMES EXTRACTED FROM ANIMALS
• Lipase :- Lipolytic enzymes extracted from the throat of cows, sheep or goats which
enhance cheese flavour.
• These are very expensive
Rennet
• Produced from stomach of cows, enzyme chymosin (rennin)
obtained either from calf stomach or more recently from a
microorganism.
• Cut casein proteins in milk into smaller pieces
• solidify milk
TAQ POLYMERASE
•Thermo stable enzyme
essential for PCR reactions
•Isolated from hot-spring
dwelling species Thermus
aquaticus
ENZYMES PRODUCED BY MICROORGANISMS
INVERTASE
•Derived from Saccharomyces
cerevisiae
• Also known as sucrase
•Enzyme digests sucrose into
glucose and fructose
•Used to create candies with a
soft center
•Most commonly used to make
chocolate covered cherries
ENZYME PRODUCTION/ISOLATION METHODS
PRODUCTIONANDISOLATIONOF ENZYMES
USES OF ENZYMES
1. Analytical Applications of Enzymes
2. The Animal Feed Industry
3. The Meat and Fish Processing Industry
4. The Dairy Industry
5. The Leather Industry
6. CIP and cleaning of microfilters – Detergents
7. The modification of Fats and Oils
8. The Pulp and Paper Industry
9.The Fruit Juice Processing Industry
10.The Production of Bulk and Fine Chemicals
11.Enzyme-Replacement Therapy
INDUSTRIAL USE OF ENZYMES
Enzyme Source Action in food Food application
Papain Latex of unripe
papaya fruit
protein hydrolysis Meat tenderisation
Bromelain Pineapple juice
and stem
Muscle and connective
tissue protein hydrolysis
Meat tenderisation
Ficin Fig fruit latex Muscle and connective
tissue protein hydrolysis
As bromelain & papain but
not widely used due to cost
Chymosin
(rennet)
Calf abomasum Kappa casein hydrolysis Cheese making
Pepsin Bovine abomasum casein
hydrolysis in cheese
Help for rennet action
Lysozyme Hen egg white Hydrolysis of
bacterial
cell wall
polysaccharides
Prevention of late
blowing
defects in cheese by
spore-forming bacteria
Lactoperoxidase Cheese whey: Oxidation of thiocyanate Cold sterilisation of milk
bovine colostrum ion to bactericidal
Hypothiocyanate
Aminopeptidase Lcictococcus lactix Releases free amino acids Releases free amino acids
Axpergillux spp. from N-terminus from N-terminus
Rhizopux oryzae of proteins and peptides of proteins and peptides
Lipase/ Gullet of Triglyceride (fat) Flavour enhancement in
esterase goat&lamb: calf hvdrolvsis cheese products:
abomasum:
pig pancreas
Enzymes break down specific components within
fruit & vegetables such as pectin, starch, proteins and
cellulose which results in increased yields, shortening
of processing time and improving sensory
characteristics.
Some examples:
Pectinases and Cellulases are used to break down cell
walls in fruit and vegetables, resulting in improved
extraction and increase in yield. They can also be
used to decrease the viscosity of purees or nectars,
and to provide ‘cloud stability’and texture in juices.
Serial
no.
Enzyme Purpose/Function
1. Cellulases, beta-glucanases, alpha
amylases, proteases, maltogenic
amylases
2. Amyloglucosidase
For liquefaction, clarification
and to supplement malt
enzymes
Conversion of starch to sugar
Serial
no.
Enzyme Purpose/Function
1. Alpha-amylases Breakdown of starch, maltose production
2. Amyloglycosidases Saccharification
3. Maltogen amylase (Novamyl) Delays process by which bread becomes stale
4. Protease Breakdown of proteins
5. Pentosanase Breakdown of pentosan, leading to reduced gluten
production
Sr. Industry
no.
Enzyme Purpose/Function
1. Wine &
fruit Juice
Pectinase
Glucose oxidase
Increase of yield and juice
clarification
Oxygen removal
2. Meat Protease Meat tenderising
3. Protein Proteass, trypsin,
aminopeptidases
Breakdown of various
components
4. Starch Alpha amylase,
glucoamylases,
hemicellulases,
amylases,
Modification and
conversion (eg to dextrose
or high fructose syrups)
Alpha-amylase: Converts starch to dextrins in producing corn syrup. Solubilizes carbohydrates found in
barley and other cereals used in brewing.
Glucoamylase:Conversion of dextrins to glucose in the production of corn syrup. Conversion of residual
dextrins to fermentable sugar in brewing for the production of "light" beer.
Beta-glucanase: Breakdown of glucans in malt and and other materials to aid in filtration after mashing in
brewing.
Lipase: Enhancing flavor development and shortening the time for cheese ripening. Production of specialty fats
with improved qualities. Production of enzyme-modified cheese/butter from cheese curd or butterfat.
Papain: Used as meat tenderizer. Used in brewing to prevent chill-haze formation by digesting proteins that
otherwise react with tannins to form insoluble colloids.
Chymosin: Curdling of milk by breaking down kappa-caseins in cheese making.
Microbial proteases: Processing of raw plant and animal protein. Production of fish meals, meat extracts,
texturized proteins, and meat extenders.
Pectinase: Treatment of fruit pulp to facilitate juice extraction and for clarification and filtration of fruit juice.
Lactase:Additive for dairy products for individuals lacking lactase. Breakdown of lactose
in whey products for manufacturing polyactide.
Acetolactate decarboxylase:Reduction of maturation time in wine making by
converting acetolactate to acetoin.
Glucose oxidase: Conversion of glucose to gluconic acid to prevent Maillard reaction in
products caused by high heat used in dehydration.
Cellulase: Conversion of cellulose waste to fermentable feedstock for ethanol or single-
cell protein production. Degradation of cell walls of grains, allowing better extraction of cell
contents and release of nutrients.
Use of Nanoparticles in Enzyme Technology
•Nanotechnology is the study of manipulating matter on an atomic scale.
•Nanotechnology refers to the constructing and engineering of the functional
systems at very micro level or we can say at atomic level.
•A Nanometer is one billionth of a meter, roughly the width of three or four atoms.
The average human hair is about 25,000 nanometers wide.
• The first ever concept was presented in 1959 by the famous professor of physics Dr.
Richard P.Feynman.
• Invention of the scanning tunneling microscope in 1981 and the discovery of
fullerene(C60) in 1985 lead to the emergence
of nanotechnology.
• The term “Nano-technology" had been coined by Norio Taniguchi in 1974
ENZYME IMMOBILISATION
• Application of nanomaterials as novel supporting materials for enzyme
immobilisation has generated incredible interest in the biotechnology
community.
• These robust nanostructured forms, such as nanoparticles, nanofibres,
nanotubes, nanoporous, nanosheets, and nanocomposites, possess a high
surface area to volume ratios that can cause a high enzyme loading and
facilitate reaction kinetics, thus improving biocatalytic efficiency for
industrial applications.
• The current status of versatile nanomaterial support for biofuel production
employing cellulases and lipases is described in details
• nanomaterials will become an integral part of sustainable bioenergy
production.
How nanoparticles helps
enzyme in increasing the
catalytic activity ???
SINGLE ENZYME NANOPARTICLES
• SEN (single enzyme nanoparticles )
• Enzyme lead short and brutal lives ,to increase the enzymes
longevity and versatility, a a team at department of Energy’s
Pacific Northwest , National Laboratory in Richlad caged single
enzyme to create a new class of catalysts called SENs
• The nanostructure protects the catalyst, allowing it to remain
active for several months
• Kim and Grate , working in te W.R Wiley Environmental molecular
sciences laboratory modified a common protein splitting enzyme
called alpha chymotrypsin
ENHANCEMENT OF ENZYME ACTIVITY AND
THERMOSTABILITY
Study on Impaired Pectate Lyase from AttenuatedMacrophomina phaseolina in
Presence of Hydroxyapatite Nanoparticle
Hydroxyapatite nanoparticles (NP) can not only act as a chaperon (by imparting
thermostability) but can serve as a synthetic enhancer of activity of an isolated
extracellular pectate lyase (APL) with low native state activity.
The purified enzyme showed feeble activity at 50°C and pH 5.6. However, on
addition of 10.5 µg/ml of hydroxyapatite nanoparticles (NP), APL activity increased
27.7 fold with a 51 fold increase in half-life at a temperature of 90°C as compared to
untreated APL.
The upper critical temperature for such compensation was elevated from 50°C to
90°C in presence of NP.
ENZMET (ENZYME METALLOGRAPHY)
• EnzMet (Enzyme Metallography) is a new biological labeling and
staining method developed at Nanoprobes.
• It uses a targeted enzymatic probe with a novel metallographic
substrate to provide a quantum leap in staining clarity over
conventional chromogenic and fluorescent substrates.
• EnzMet™ has proven highly sensitive both for in situ hybridization
(ISH), where it readily visualizes endogenous copies of single genes,
and immunohistochemistry (IHC) detection.
NANOTECHNOLOGY TO HARNESS THE NATURAL
LIGHT PRODUCED BY FIREFLIES
• By designing a way to chemically attach genetically manipulated
luciferase enzymes directly to the surface of nanorods, scientists at
Syracuse University found a new way to harness the natural light
produced by fireflies.
• Fireflies produce light through a chemical reaction between
luciferin and it’s counterpart, the enzyme luciferase.
• In Maye’s laboratory, the enzyme is attached to the nanorod’s
surface; luciferin, which is added later, serves as the fuel.
A Case Study
CONTINUE….
• The energy that is released when
the fuel and the enzyme interact is
transferred to the nanorods,
causing them to glow. The process
is called Bioluminescence
Resonance Energy Transfer
(BRET).
• The nanorods are composed of an
outer shell of cadmium sulfide and
an inner core of cadmium
seleneide.
REFRENCES
• J. Srilakshmi, ;J. Madhavi, Lavanya S and Ammani (2014)
Commercial Potential of Fungal Protease: Past, Present and Future Prospects , Journal of Pharmaceutical,
Chemical and Biological Sciences ,2(4)p.218-234.
• Sumantha (2006).Food-Grade Proteases, journal of Food Technology & Biotechnology. 44 (2), p.211–220
• Riddhi Sawant and Saraswathy Nagendran (2014),protease: an enzyme with multiple industrial application,
www.wjpps.com .
 www.journals.elseveir.com/biological-control/
http://microbewiki.kenyon,edu.index.php/Biocontrol
www.sciencedirect.com/science/article/pii/0261219491900385
• http://www.azonano.com/article.aspx?ArticleID=736
• http://omicsonline.org/2153-0777/2153-0777-2-e114.pdf
• http://www.nanoprobes.com/products/EnzMet-SISH-enzyme-metallography-for-ISH-and-IHC.html
• http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0063567
• http://www.che.udel.edu/research_groups/wilfred/Current%2013%20final.pdf
THANK YOU…

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enzymetechnology-170829114019.pptx

  • 1. PG Department of Environmental Science and Technology Institute of Science and Technology for Advanced Studies and Research CVM University Vallabh Vidyanagar, Anand, Gujarat 388120 ENZYME TECHNOLOGY
  • 2. Environmental biotechnology is biotechnology that is applied to and used to study the natural environment.
  • 3.
  • 4. • Background • Products of Enzyme Technology • Structure of an enzyme • Mechanism of an Enzyme • Production of Enzymes • Properties of Enzyme • Sources of Enzyme • Classification of Enzyme • Isolation of enzymes • Uses of Enzymes • Application of enzymes in various industries • Use of Nanoparticles in Enzyme Technology • Enzyme immobilization • Single cess enzyme nanoparticle • Enhancement of Enzyme activity and thermos ability • Enzyme Metallography • A case study on Bioluminescence of Fireflies CONTENT
  • 5. BACKGROUND Enzyme - A biological catalyst that promotes & speeds up a chemical reaction without itself being altered in the process, they fulfil their role by binding specific substrates at their active sites. Enzyme technology is concerned with the application of enzymes as tools of industry, agriculture and medicine. The value of using enzymes over inorganic catalysts in the technological field is due to their efficiency, selectivity and specificity. Enzymes are able to operate at wide range of temperatures, atmospheric pressure and within normal pH ranges – all of which create energy savings for industry. Enzymes are biodegradable and, unlike many inorganic catalysts, cause less damage to the environment. Functions of Enzyme Metabolism
  • 6. Enzymes are proteins that help speed up metabolism, or the chemical reactions in our bodies. Enzymes are proteins that catalyze a chemical reaction They build some substances and break others down. The enzyme accelerates a chemical reaction without changing its equilibrium, so it is called as a biocatalyst.
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  • 9. PRIMARY METABOLITES During cell growth the nutrients of the substrate are converted to cell mass. The chemical compounds produced in this process are called “primary metabolites”. „The cell mass itself consists mainly of proteins, but a number of primary waste products are also formed, for instance carbon dioxide, lactic acid, ethanol, etc. Primary metabolites are produced in parallel with the cell mass.
  • 10. SECONDARY METABOLITES T „ he formation of secondary metabolites is not directly related to cell growth. They are the side products of bacterial life. In nature, they are produced in low concentration, but through laboratory mutation and selection, cells can be optimized to overproduce these metabolites. Many antibiotics and vitamins are secondary metabolites. The formation of secondary metabolites is not directly proportional to primary metabolism and cell growth.
  • 11. Micro-organisms have been used for thousands of years for making products such as wine, beer, vinegar, soy sauce, bread and cheese. Products of Enzyme Technology NOTE - The micro-organisms (such as yeast) are really used as a source of enzymes during the manufacture of these products of biotechnology. Many industrial processes now make use of pure sources of enzymes, i.e. the enzymes have been ISOLATED from the micro-organisms before use  Protease found in papaya as meat tenderizer
  • 12. STRUCTURE OF AN ENZYME ENZYMES NON-PROTEIN COENZYMES ( VITAMIN) COFACTOR (MINERAL) PROTEIN (Apo-enzyme) • NOTE :- All enzymes are proteins but all proteins are not enzymes.
  • 13.
  • 14. MECHANISM 0F ENZYMES - LOCK AND KEY HYPOTHESIS Enzymes possess specifically shaped active sites for reacting with one specific substrate thereby generating pure products free from unwanted by-products.
  • 15. MODIFICATION – possible application of genetic engineering to improve the microbial strain LABORATORY SCALE PILOT – to determine the optimum conditions for growth of the Micro-organism PILOT PLANT – small scale fermenter to clarify optimum operating conditions SCREENING – choosing an appropriate micro-organism for the desired enzyme INDUSTRIAL SCALE FERMENTATION The Biotechnological Process of Enzyme Production
  • 16. Pectinase is obtained from the fungus Aspergillus niger Aspergillus niger produces pectinase as an extracellular enzyme Commercial Enzyme Production - An Example PRODUCTIONOF PECTINASE Pectin is an insoluble substance found in the cell walls of plants In the drinks industry, juice extracted from fruits appears cloudy due to the presence of pectin. Pectinase is an enzyme that is used in the industry to break down the pectin The effect of pectinase is to clarify the fruit juice and to make it flow more freely
  • 17. • Control ripening. • Cause food spoilage (rotting). • Responsible for changes in flavor, color, texture and nutritional properties. • Can be inactivated by heat to extend storage stability of foods. • Control oxidation and spoilage (bioconservation) • Increase nutritive values ( phytase , proteases etc.) • Used for fermentation purposes in foods. • Can be extracted and purified to a high degree. Properties of enzymes
  • 18. Sources of enzymes There are three major sources of enzymes : Plants ( 4%) (papain, bromilain) Animals ( 8%) (renet) Microorganisms (>80%) (yeast, fungi and bacteria)
  • 19. VEGETABLE COAGULANTS • Vegetable coagulants are plant extracts which contain a mixture of proteolytic enzymes and contribute unique characteristics to cheese. • Vegetable coagulants are used primarily in niche products where specific flavours and consistency are desired, or in remote regions where other coagulants are unavailable. • Extracts of the Cardo flower (Cynara cardunculus) used in Spain and Portugal for the production of some DOP (Denominación de Origen Protegida) cheeses, these cheeses are often very soft or semi-liquid and may be spoonable. The flavour profile is strong, with some bitterness. • Extracts of the Calotropis procera plant used in Ghana for the production of Wara or Wagashi cheese, having a hard texture and high melting point suitable for grilling. Due to high production costs, low yield and development of off-flavors, vegetable coagulants are not used in industrial cheese production.
  • 20. ENZYMES EXTRACTED FROM ANIMALS • Lipase :- Lipolytic enzymes extracted from the throat of cows, sheep or goats which enhance cheese flavour. • These are very expensive Rennet • Produced from stomach of cows, enzyme chymosin (rennin) obtained either from calf stomach or more recently from a microorganism. • Cut casein proteins in milk into smaller pieces • solidify milk
  • 21. TAQ POLYMERASE •Thermo stable enzyme essential for PCR reactions •Isolated from hot-spring dwelling species Thermus aquaticus ENZYMES PRODUCED BY MICROORGANISMS
  • 22. INVERTASE •Derived from Saccharomyces cerevisiae • Also known as sucrase •Enzyme digests sucrose into glucose and fructose •Used to create candies with a soft center •Most commonly used to make chocolate covered cherries
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  • 26. USES OF ENZYMES 1. Analytical Applications of Enzymes 2. The Animal Feed Industry 3. The Meat and Fish Processing Industry 4. The Dairy Industry 5. The Leather Industry 6. CIP and cleaning of microfilters – Detergents 7. The modification of Fats and Oils 8. The Pulp and Paper Industry 9.The Fruit Juice Processing Industry 10.The Production of Bulk and Fine Chemicals 11.Enzyme-Replacement Therapy
  • 27. INDUSTRIAL USE OF ENZYMES Enzyme Source Action in food Food application Papain Latex of unripe papaya fruit protein hydrolysis Meat tenderisation Bromelain Pineapple juice and stem Muscle and connective tissue protein hydrolysis Meat tenderisation Ficin Fig fruit latex Muscle and connective tissue protein hydrolysis As bromelain & papain but not widely used due to cost Chymosin (rennet) Calf abomasum Kappa casein hydrolysis Cheese making Pepsin Bovine abomasum casein hydrolysis in cheese Help for rennet action
  • 28. Lysozyme Hen egg white Hydrolysis of bacterial cell wall polysaccharides Prevention of late blowing defects in cheese by spore-forming bacteria Lactoperoxidase Cheese whey: Oxidation of thiocyanate Cold sterilisation of milk bovine colostrum ion to bactericidal Hypothiocyanate Aminopeptidase Lcictococcus lactix Releases free amino acids Releases free amino acids Axpergillux spp. from N-terminus from N-terminus Rhizopux oryzae of proteins and peptides of proteins and peptides Lipase/ Gullet of Triglyceride (fat) Flavour enhancement in esterase goat&lamb: calf hvdrolvsis cheese products: abomasum: pig pancreas
  • 29.
  • 30. Enzymes break down specific components within fruit & vegetables such as pectin, starch, proteins and cellulose which results in increased yields, shortening of processing time and improving sensory characteristics. Some examples: Pectinases and Cellulases are used to break down cell walls in fruit and vegetables, resulting in improved extraction and increase in yield. They can also be used to decrease the viscosity of purees or nectars, and to provide ‘cloud stability’and texture in juices.
  • 31. Serial no. Enzyme Purpose/Function 1. Cellulases, beta-glucanases, alpha amylases, proteases, maltogenic amylases 2. Amyloglucosidase For liquefaction, clarification and to supplement malt enzymes Conversion of starch to sugar
  • 32. Serial no. Enzyme Purpose/Function 1. Alpha-amylases Breakdown of starch, maltose production 2. Amyloglycosidases Saccharification 3. Maltogen amylase (Novamyl) Delays process by which bread becomes stale 4. Protease Breakdown of proteins 5. Pentosanase Breakdown of pentosan, leading to reduced gluten production
  • 33. Sr. Industry no. Enzyme Purpose/Function 1. Wine & fruit Juice Pectinase Glucose oxidase Increase of yield and juice clarification Oxygen removal 2. Meat Protease Meat tenderising 3. Protein Proteass, trypsin, aminopeptidases Breakdown of various components 4. Starch Alpha amylase, glucoamylases, hemicellulases, amylases, Modification and conversion (eg to dextrose or high fructose syrups)
  • 34. Alpha-amylase: Converts starch to dextrins in producing corn syrup. Solubilizes carbohydrates found in barley and other cereals used in brewing. Glucoamylase:Conversion of dextrins to glucose in the production of corn syrup. Conversion of residual dextrins to fermentable sugar in brewing for the production of "light" beer. Beta-glucanase: Breakdown of glucans in malt and and other materials to aid in filtration after mashing in brewing. Lipase: Enhancing flavor development and shortening the time for cheese ripening. Production of specialty fats with improved qualities. Production of enzyme-modified cheese/butter from cheese curd or butterfat. Papain: Used as meat tenderizer. Used in brewing to prevent chill-haze formation by digesting proteins that otherwise react with tannins to form insoluble colloids. Chymosin: Curdling of milk by breaking down kappa-caseins in cheese making. Microbial proteases: Processing of raw plant and animal protein. Production of fish meals, meat extracts, texturized proteins, and meat extenders. Pectinase: Treatment of fruit pulp to facilitate juice extraction and for clarification and filtration of fruit juice.
  • 35. Lactase:Additive for dairy products for individuals lacking lactase. Breakdown of lactose in whey products for manufacturing polyactide. Acetolactate decarboxylase:Reduction of maturation time in wine making by converting acetolactate to acetoin. Glucose oxidase: Conversion of glucose to gluconic acid to prevent Maillard reaction in products caused by high heat used in dehydration. Cellulase: Conversion of cellulose waste to fermentable feedstock for ethanol or single- cell protein production. Degradation of cell walls of grains, allowing better extraction of cell contents and release of nutrients.
  • 36.
  • 37. Use of Nanoparticles in Enzyme Technology •Nanotechnology is the study of manipulating matter on an atomic scale. •Nanotechnology refers to the constructing and engineering of the functional systems at very micro level or we can say at atomic level. •A Nanometer is one billionth of a meter, roughly the width of three or four atoms. The average human hair is about 25,000 nanometers wide. • The first ever concept was presented in 1959 by the famous professor of physics Dr. Richard P.Feynman. • Invention of the scanning tunneling microscope in 1981 and the discovery of fullerene(C60) in 1985 lead to the emergence of nanotechnology. • The term “Nano-technology" had been coined by Norio Taniguchi in 1974
  • 38. ENZYME IMMOBILISATION • Application of nanomaterials as novel supporting materials for enzyme immobilisation has generated incredible interest in the biotechnology community. • These robust nanostructured forms, such as nanoparticles, nanofibres, nanotubes, nanoporous, nanosheets, and nanocomposites, possess a high surface area to volume ratios that can cause a high enzyme loading and facilitate reaction kinetics, thus improving biocatalytic efficiency for industrial applications. • The current status of versatile nanomaterial support for biofuel production employing cellulases and lipases is described in details • nanomaterials will become an integral part of sustainable bioenergy production.
  • 39. How nanoparticles helps enzyme in increasing the catalytic activity ???
  • 40. SINGLE ENZYME NANOPARTICLES • SEN (single enzyme nanoparticles ) • Enzyme lead short and brutal lives ,to increase the enzymes longevity and versatility, a a team at department of Energy’s Pacific Northwest , National Laboratory in Richlad caged single enzyme to create a new class of catalysts called SENs • The nanostructure protects the catalyst, allowing it to remain active for several months • Kim and Grate , working in te W.R Wiley Environmental molecular sciences laboratory modified a common protein splitting enzyme called alpha chymotrypsin
  • 41. ENHANCEMENT OF ENZYME ACTIVITY AND THERMOSTABILITY Study on Impaired Pectate Lyase from AttenuatedMacrophomina phaseolina in Presence of Hydroxyapatite Nanoparticle Hydroxyapatite nanoparticles (NP) can not only act as a chaperon (by imparting thermostability) but can serve as a synthetic enhancer of activity of an isolated extracellular pectate lyase (APL) with low native state activity. The purified enzyme showed feeble activity at 50°C and pH 5.6. However, on addition of 10.5 µg/ml of hydroxyapatite nanoparticles (NP), APL activity increased 27.7 fold with a 51 fold increase in half-life at a temperature of 90°C as compared to untreated APL. The upper critical temperature for such compensation was elevated from 50°C to 90°C in presence of NP.
  • 42. ENZMET (ENZYME METALLOGRAPHY) • EnzMet (Enzyme Metallography) is a new biological labeling and staining method developed at Nanoprobes. • It uses a targeted enzymatic probe with a novel metallographic substrate to provide a quantum leap in staining clarity over conventional chromogenic and fluorescent substrates. • EnzMet™ has proven highly sensitive both for in situ hybridization (ISH), where it readily visualizes endogenous copies of single genes, and immunohistochemistry (IHC) detection.
  • 43. NANOTECHNOLOGY TO HARNESS THE NATURAL LIGHT PRODUCED BY FIREFLIES • By designing a way to chemically attach genetically manipulated luciferase enzymes directly to the surface of nanorods, scientists at Syracuse University found a new way to harness the natural light produced by fireflies. • Fireflies produce light through a chemical reaction between luciferin and it’s counterpart, the enzyme luciferase. • In Maye’s laboratory, the enzyme is attached to the nanorod’s surface; luciferin, which is added later, serves as the fuel. A Case Study
  • 44. CONTINUE…. • The energy that is released when the fuel and the enzyme interact is transferred to the nanorods, causing them to glow. The process is called Bioluminescence Resonance Energy Transfer (BRET). • The nanorods are composed of an outer shell of cadmium sulfide and an inner core of cadmium seleneide.
  • 45. REFRENCES • J. Srilakshmi, ;J. Madhavi, Lavanya S and Ammani (2014) Commercial Potential of Fungal Protease: Past, Present and Future Prospects , Journal of Pharmaceutical, Chemical and Biological Sciences ,2(4)p.218-234. • Sumantha (2006).Food-Grade Proteases, journal of Food Technology & Biotechnology. 44 (2), p.211–220 • Riddhi Sawant and Saraswathy Nagendran (2014),protease: an enzyme with multiple industrial application, www.wjpps.com .  www.journals.elseveir.com/biological-control/ http://microbewiki.kenyon,edu.index.php/Biocontrol www.sciencedirect.com/science/article/pii/0261219491900385 • http://www.azonano.com/article.aspx?ArticleID=736 • http://omicsonline.org/2153-0777/2153-0777-2-e114.pdf • http://www.nanoprobes.com/products/EnzMet-SISH-enzyme-metallography-for-ISH-and-IHC.html • http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0063567 • http://www.che.udel.edu/research_groups/wilfred/Current%2013%20final.pdf