PROTEOLYTIC ENZYMES
Presented By:-
Saurabh Verma
M.Sc.
Biotechnology
Proteolytic Enzymes
Prof. Harshraj. S. Shinde
K. K. Wagh College of Agril. Biotech, Nashik. India
Proteolytic Enzymes
Enzymes involved in degradation of proteins are
called as proteases or proteolytic enzymes
Industrially available proteolytic enzymes
produced by microorganisms are usually
mixtures of endopeptidases and exopeptidases.
Polypeptides
Polypeptides amino acids
2
Proteins Endopeptidases
Exopeptidases
Because
Cont …
of the complex structures and high molecular
weights of proteins enzymic proteolysis is extremely
complicated.
Most proteases are quite specific with regard to which
peptide linkages they can split
3
List of proteolytic enzymes
a.
b.
c.
d.
e.
f.
g.
Papain
Ficain
Bromelain
Pepsin
Rennin
Cathepsin
Trypsin
4
A) Papain
◦
◦
◦
Found in papaya
papain,also known as papaya proteinase I
Broad pH (3-11) and temperature stability
 For this reason very popular for a variety of food
applications.
1. Used as a meat tenderizer on inferior meat cuts (can also use slice
of pineapple on meat)



The enzyme makes its way into the muscle and hydrolyzes
primarily connective tissue proteins (collagen etc.) and
softens muscle
Have to use low amount to prevent liquefaction of muscle
If you mix raw papaya into Jell-O it will not form a gel
Application of papain
MeatTenderizer- Papain ( a protease
found in papaya) is used as meat
tenderizer to soften meat for cooking
Papain
Cont…
can be used to dissociate cells in
the first step of cell culture preparations.
7
Ficain
Ficain also known as
ficin is an enzyme that is derived from figs latex
It is of a family of proteases known as
the cysteine endopeptidases
It is one of the most commonly used for
differentiating many blood group antigens
8
Bromelain
Bromelain is an enzyme generally found in the stems
and fruits of pineapples.
According their sources enzymes are divided into
A. Stem bromelain.
B. Fruit bromelain.
The proteolytic enzymes are sulfhydryl proteases, since
a free sulfhydryl group of a cysteine side chain is
required for function
9
Bromelain is present in all parts of the
pineapple plant but the stem is the most
common commercial source
10
Applications of bromelain
Along with papain,bromelain is one of the most popular
proteases to use for meat tenderizing
Cooked pineapple does not have a tenderizing effect, as
the enzymes are heat-labile
Preparation of meat balls
Systemic enzyme therapy (combinations of proteolytic
enzymes such as bromelain, trypsin and papain) has
been used in the treatment of breast cancer
11
Pepsin
 Pepsin is an enzyme whose zymogen (pepsinogen) is released by
the stomach and that degradesthe chief cells in
food proteins into peptides



It was discovered by Theodor Schwann who also coined its name
from the Greek word pepsis,meaning "digestion
Pepsin is one of three principal protein-degrading enzyme in the
digestive system,the other two being chymotrypsin and trypsin
Pepsin is most efficient in cleaving peptide bonds and
suchpreferably breaks at aromatic amino acids
as phenylalanine, tryptophan,and tyrosine
12



Cont…
Pepsin is most active in acidic environments Pepsin exhibits
maximal activity at pH 2.0 and is inactive at pH 6.5
In most cases Pepsinogen is activated by HCl
Pepsins should be stored at very low temperatures (between
−80 °C and −20 °C) to prevent autolysis (self-digestion
13
Applications of pepsin
Pepsin is commonly used in the
preparation of F(ab')2 fragments from
antibodies
14
Powder
Cont…
of pepsin is often used as a
dietary supplement to aid digestion
15
Rennin
 Rennin or Chymosin is a protease produced by


newborn ruminant in the fourth stomach to curdle the milk they
ingest
The native substrate of Chymosin is K-casein cleavaes at amino
acids like phenylalanine and methionine
Bovine chymosin is now produced recombinantly in E
coli, Aspergillus niger alternative resource.
16
Application of rennin
It is widely used in the production
of cheese
17
Cathepsin
Cathepsins are proteases that degrade proteins) found
in all animals as well as other organisms.
Enzyme cathepsins found only in the lysosome
Most of the members become activated at the low pH
found in lysosomes
18
There
Cont….
are approximately a dozen members of
this family, which are distinguished by their
structure
CathepsinA (serine protease)
Cathepsin B (cysteine protease)
Cathepsin C (cysteine protease)
Cathepsin D (aspartyl protease)
Cathepsin E (aspartyl protease)
Cathepsin F (cysteine proteinase)
19
Trypsin
Trypsin is a protease found in the digestive system of
many vertebrates,where it hydrolyses proteins.
Trypsin is produced in the pancreas as the inactive
protease trypsinogen.
Trypsin cleaves peptide chains mainly at
the carboxyl side of the amino acids lysine or arginine
20
Application of trypsin
In a Animal tissue culture lab, trypsin is used to re-
suspend cells adherent to the cell culture dish wall
during the process of harvesting cells
Used in proteomics experiments to digest proteins into
peptides for mass spectrometry analysis
As a baking enzyme to improve the workability of
dough;
in the extraction of seasonings and flavourings from
vegetable or animal proteins and in the manufacture of
sauces 21
To
To
Cont…
improve the texture of fish products
tenderize meat along with papain
For cold stabilization of beer
22
In
Cont…
the production of hypoallergenic food where trypsin
into nonbreak down specific allergenic proteins
allergenic peptides
23

Saurabh proteaseenzymes

  • 1.
  • 2.
    Proteolytic Enzymes Prof. Harshraj.S. Shinde K. K. Wagh College of Agril. Biotech, Nashik. India
  • 3.
    Proteolytic Enzymes Enzymes involvedin degradation of proteins are called as proteases or proteolytic enzymes Industrially available proteolytic enzymes produced by microorganisms are usually mixtures of endopeptidases and exopeptidases. Polypeptides Polypeptides amino acids 2 Proteins Endopeptidases Exopeptidases
  • 4.
    Because Cont … of thecomplex structures and high molecular weights of proteins enzymic proteolysis is extremely complicated. Most proteases are quite specific with regard to which peptide linkages they can split 3
  • 5.
    List of proteolyticenzymes a. b. c. d. e. f. g. Papain Ficain Bromelain Pepsin Rennin Cathepsin Trypsin 4
  • 6.
    A) Papain ◦ ◦ ◦ Found inpapaya papain,also known as papaya proteinase I Broad pH (3-11) and temperature stability  For this reason very popular for a variety of food applications. 1. Used as a meat tenderizer on inferior meat cuts (can also use slice of pineapple on meat)    The enzyme makes its way into the muscle and hydrolyzes primarily connective tissue proteins (collagen etc.) and softens muscle Have to use low amount to prevent liquefaction of muscle If you mix raw papaya into Jell-O it will not form a gel
  • 7.
    Application of papain MeatTenderizer-Papain ( a protease found in papaya) is used as meat tenderizer to soften meat for cooking
  • 8.
    Papain Cont… can be usedto dissociate cells in the first step of cell culture preparations. 7
  • 9.
    Ficain Ficain also knownas ficin is an enzyme that is derived from figs latex It is of a family of proteases known as the cysteine endopeptidases It is one of the most commonly used for differentiating many blood group antigens 8
  • 10.
    Bromelain Bromelain is anenzyme generally found in the stems and fruits of pineapples. According their sources enzymes are divided into A. Stem bromelain. B. Fruit bromelain. The proteolytic enzymes are sulfhydryl proteases, since a free sulfhydryl group of a cysteine side chain is required for function 9
  • 11.
    Bromelain is presentin all parts of the pineapple plant but the stem is the most common commercial source 10
  • 12.
    Applications of bromelain Alongwith papain,bromelain is one of the most popular proteases to use for meat tenderizing Cooked pineapple does not have a tenderizing effect, as the enzymes are heat-labile Preparation of meat balls Systemic enzyme therapy (combinations of proteolytic enzymes such as bromelain, trypsin and papain) has been used in the treatment of breast cancer 11
  • 13.
    Pepsin  Pepsin isan enzyme whose zymogen (pepsinogen) is released by the stomach and that degradesthe chief cells in food proteins into peptides    It was discovered by Theodor Schwann who also coined its name from the Greek word pepsis,meaning "digestion Pepsin is one of three principal protein-degrading enzyme in the digestive system,the other two being chymotrypsin and trypsin Pepsin is most efficient in cleaving peptide bonds and suchpreferably breaks at aromatic amino acids as phenylalanine, tryptophan,and tyrosine 12
  • 14.
       Cont… Pepsin is mostactive in acidic environments Pepsin exhibits maximal activity at pH 2.0 and is inactive at pH 6.5 In most cases Pepsinogen is activated by HCl Pepsins should be stored at very low temperatures (between −80 °C and −20 °C) to prevent autolysis (self-digestion 13
  • 15.
    Applications of pepsin Pepsinis commonly used in the preparation of F(ab')2 fragments from antibodies 14
  • 16.
    Powder Cont… of pepsin isoften used as a dietary supplement to aid digestion 15
  • 17.
    Rennin  Rennin orChymosin is a protease produced by   newborn ruminant in the fourth stomach to curdle the milk they ingest The native substrate of Chymosin is K-casein cleavaes at amino acids like phenylalanine and methionine Bovine chymosin is now produced recombinantly in E coli, Aspergillus niger alternative resource. 16
  • 18.
    Application of rennin Itis widely used in the production of cheese 17
  • 19.
    Cathepsin Cathepsins are proteasesthat degrade proteins) found in all animals as well as other organisms. Enzyme cathepsins found only in the lysosome Most of the members become activated at the low pH found in lysosomes 18
  • 20.
    There Cont…. are approximately adozen members of this family, which are distinguished by their structure CathepsinA (serine protease) Cathepsin B (cysteine protease) Cathepsin C (cysteine protease) Cathepsin D (aspartyl protease) Cathepsin E (aspartyl protease) Cathepsin F (cysteine proteinase) 19
  • 21.
    Trypsin Trypsin is aprotease found in the digestive system of many vertebrates,where it hydrolyses proteins. Trypsin is produced in the pancreas as the inactive protease trypsinogen. Trypsin cleaves peptide chains mainly at the carboxyl side of the amino acids lysine or arginine 20
  • 22.
    Application of trypsin Ina Animal tissue culture lab, trypsin is used to re- suspend cells adherent to the cell culture dish wall during the process of harvesting cells Used in proteomics experiments to digest proteins into peptides for mass spectrometry analysis As a baking enzyme to improve the workability of dough; in the extraction of seasonings and flavourings from vegetable or animal proteins and in the manufacture of sauces 21
  • 23.
    To To Cont… improve the textureof fish products tenderize meat along with papain For cold stabilization of beer 22
  • 24.
    In Cont… the production ofhypoallergenic food where trypsin into nonbreak down specific allergenic proteins allergenic peptides 23