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Dr. R. Mallika
Associate professor
Department of Biochemistry
V.V.Vanniaperumal College for Women,
Virudhunagar.
 Immobilization is defined as the imprisonment of cell or
enzyme in a distinct support or matrix.
 The support or matrix on which the enzymes are
immobilized allows the exchange of medium containing
substrate or effector or inhibitor molecules.
 First immobilized enzyme was amino acylase of
Aspergillus oryzae for the production of L-amino acids in
Japan.
 Increased functional efficiency of enzyme
 Enhanced reproducibility of the process they are
undertaking.
 Reuse of enzyme
 Continuous use of enzyme
 Less labour input in the processes
 Saving in capital cost and investment of the process
 Minimum reaction time
 Less chance of contamination in products
 More stability of products
 Stable supply of products in the market
 Improved process control
 High enzyme substrate ratio
 High cost for the isolation, purification and recovery of active
enzyme (most important disadvantage)
 Industrial applications are limited and only very few industries are
using immobilized enzymes or immobilized whole cells.
 Catalytic properties of some enzymes are reduced or completely lost
after their immobilization on support or carrier.
 Some enzymes become unstable after immobilization.
 Enzymes are inactivated by the heat generated in the
system
 The matrix immobilizes the enzyme by holding it
permanently or temporarily for a brief period of time.
 A wide variety of matrixes or carriers or supports
available for immobilization are cheap and easily
available.
 Their reaction with the components of the medium or
with the enzyme should be minimum as possible.
 They are grouped into three major categories
 1. Natural polymers
 2. Synthetic polymers
 3. Inorganic materials
 Alginate: A natural polymer derived from the cell wall of
some algae. Calcium or magnesium alginate is the most
commonly used matrix.
 Chitosan and chitin: They are structural polysaccharides
occurring naturally in the cell wall of fungi and the
exoskeleton of Arthropods.
 Collagen: It is the proteinaceous support with good
porosity and water holding capacity.
 Carrageenan: It is a stellated polysaccharide obtained
from some red algae. Their good gelling properties makes
it as a good support for immobilizing enzymes.
 Gelatin: Gelatin is the partially hydrolyzed collagen with
good water holding capacity.
 Cellulose: Most abundant polymer of nature and it is the
cheapest support available as carrier of enzymes.
 Starch: A natural polymer of aniylose and amylo-pectin.
It has good water holding capacity.
 Pectin: It is a structural polysaccliaride of plants found in
their primary cell wall and they also acts as the inter-
cellular cementing material in plant tissues.
Synthetic polymers
 Synthetic polymers are ion exchange resins or polymers and are
insoluble supports with porous surface.
 Their porous surface can trap and hold the enzymes
 Examples: Diethylaminoethyl cellulose (DEAE cellulose),
Polyvinyl chloride (PVC), UV activated Polyethylene glycol (PEG)
Inorganic materials
 Zeolites extensively used for immobilizing enzymes
 Ceramics are nonmetallic solids. Its composition and bonding
pattern varies with different types.
 Diatomaceous earth or Celite are solicitous sedimentary rocks. It is
a good adsorbent and are resistant to high pH and temperature.
 Silica , Glass, activated carbon and charcoal.
 Based on support or matrix and the type of bonds involved, there
are five different methods of immobilization of enzyme or whole
cells.
 1. Adsorption
 2. Covalent bonding
 3. Entrapment
 4. Copolymerization
 5. Encapsulation
 Adsorption is the oldest and simplest method of enzyme
immobilization.
 Nelson & Griffin used charcoal to adsorb invertase for the
first time in 1916. In this method enzyme is absorbed to
external surface of the support.
 The support or carrier used may be of different types such
as:
 1. Mineral support (Eg. aluminum oxide, clay)
 2. Organic support (Eg. starch)
 3. Modified sepharose and ion exchange resins
There is no permanent bond formation between carrier and
the enzyme in adsorption method. Only weak bonds stabilize
the enzymes to the support or carrier.
Adsorption
The weak bonds (low energy bonds) involved
are mainly:
 Ionic interaction
 Hydrogen bonds
 Van der Waal forces
 Static process: Immobilization to carrier by allowing
the solution containing enzyme to contact the carrier
without stirring.
 Dynamic batch process: Carrier is placed in the
enzyme solution and mixed by stirring or agitation.
 Reactor loading process: Carrier is placed in the
reactor, and then the enzyme solution is transferred to
the reactor with continuous agitation.
 Electrode position process: Carrier is placed near to
an electrode in an enzyme bath and then the current is
put on, under the electric field the enzyme migrates to
the carrier and deposited on its surface.
Advantages
 No pore diffusion limitation
 Easy to carry out
 No reagents are required
 Minimum activation steps involved
 Comparatively cheap method of immobilization
 Less disruptive to enzyme than chemical methods
Disadvantages
 Pore size limitation
 Only small substrate molecule is able to cross the
membrane
 Widely used method of enzyme immobilization involves
the formation of covalent bonds between the chemical
groups in enzyme and to the chemical groups on the
support or carrier.
 Chemical groups in the support or carrier that can form
covalent bonds with support are amino groups, imino
groups, hydroxyl groups, carboxyl groups, thiol groups,
ethylthiol groups, guanidyl groups, imidazole groups
and phenol ring.
 enzyme and support
Carriers or supports commonly used for covalent bonding
are:
 Carbohydrates: Eg. Cellulose, DEAE cellulose, Agarose
 Synthetic agents: Eg. Polyacrylamide
 Protein carriers: Collagen, Gelatin
 Amino group bearing carriers: Eg. amino benzyl cellulose
 lnorg anic carriers: Porous glass, silica
 Cyonogen bromide (CNBr)-agarose and CNBr Sepharose
 Diazoation: Bonding between amino group of support and
tyrosine or histidine group of enzyme.
 Peptide bond: Bonding between amino or carboxyl groups
of the support and that of the enzyme.
 Poly functional reagents: Use of a bi- functional or
multifunctional reagent (glutaraldehyde) which forms
covalent bonds between the amino group of the support and
amino group of the enzyme.
Advantages
 Strong linkage of enzyme to the support
 No leakage or desorption problem
 Comparatively simple method
 A variety of support with different functional groups available
 Wide applicability
Disadvantages
 Chemical modification of enzyme leading to the loss of
functional conformation of enzyme.
 Enzyme inactivation by changes in the conformation
when undergoes reactions at the active site.
 Enzymes are physically entrapped inside a porous
matrix.
 Bonds involved in stabilizing the enzyme to the
matrix may be covalent or non-covalent.
 The matrix used will be a water soluble polymer.
 Pore size of matrix is adjusted to prevent the loss
of enzyme. Pore size can be adjusted with the
concentration of the polymer used.
Examples of commonly used matrixes for
entrapment are:
 Polyacrylamide gels
 Cellulose triacetate
 Agar
 Gelatin
 Carrageenan
 Alginate
 Inclusion in the gels: enzymes trapped inside the
gels.
 Inclusion in fibers: enzymes supported on fibers
made of matrix material.
 Inclusion in microcapsules: Enzymes entrapped in
microcapsules formed by monomer mixtures such
as polyamine and calcium alginate.
Advantages
 Fast method of immobilization
 Cheap (low cost matrixes available) k Easy to practice at
small scale
 Mild conditions are required
 Less chance of conformational changes in enzyme
 Can be used for sensing application
Disadvantages
 Leakage of enzyme
 Pore diffusion limitation
 Chance of microbial contamination
 Not much success in industrial process
 In this method of immobilization, enzymes are directly linked
by covalent bonds between various groups of enzymes via
polyfunctional reagents.
 There is no matrix or support involved in this method.
 Commonly used poly functional reagents are glutaraldehyde
and diazonium salt.
 This method is widely used in commercial preparations and
Industrial applications.
 The greatest disadvantage of this method is that the
polyfunctional reagents used for cross linking the enzyme
may denature leading to the loss of catalytic properties.
 This immobilization is done by enclosing the
enzymes in a membrane capsule.
 The capsule will be made up of semi permeable
membrane like nitro cellulose or nylon.
 In this method the effectiveness depends upon
the stability of enzymes inside the capsule
Advantages
 Cheap and simple method
 Large quantity of enzymes can be immobilized by
encapsulation
Disadvantages
o Pore size limitation
o Only small substrate molecule is able to
cross the membrane
 Industrial production: Industrial production of antibiotics,
beverages, amino acids etc. uses immobilized enzymes or whole
cells.
 Biomedical applications: Immobilized enzymes are widely used in
the diagnosis and treatment of many diseases. Immobilized enzymes
can be used to overcome inborn metabolic disorders by the supply
of immobilized enzymes. Immobilization techniques are effectively
used in drug delivery systems especially to oncogenic sites.
 Food industry: Enzymes like pectinases and cellulases immobilized
on suitable carriers are successfully used in the production of jams,
jellies and syrups from fruits and vegetables.
 Research: Research activity extensively uses many enzymes.
The use of immobilized enzyme allow researcher to increase
the efficiency of different enzymes such as Horse Radish
Peroxidase in blotting experiments and different Proteases for
cell or organelle lysis.
 Production of biodiesel from vegetable oils.
 Waste water management: treatment of sewage and
industrial effluents.
 Textile industry: scouring, bio-polishing and desizing of
fabrics.
 Detergent industry: immobilization of lipase enzyme for
effective dirt removal from cloths.
 THANK YOU

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Benefits of Immobilized Enzymes in Industry and Research

  • 1. Dr. R. Mallika Associate professor Department of Biochemistry V.V.Vanniaperumal College for Women, Virudhunagar.
  • 2.  Immobilization is defined as the imprisonment of cell or enzyme in a distinct support or matrix.  The support or matrix on which the enzymes are immobilized allows the exchange of medium containing substrate or effector or inhibitor molecules.  First immobilized enzyme was amino acylase of Aspergillus oryzae for the production of L-amino acids in Japan.
  • 3.  Increased functional efficiency of enzyme  Enhanced reproducibility of the process they are undertaking.  Reuse of enzyme  Continuous use of enzyme  Less labour input in the processes  Saving in capital cost and investment of the process  Minimum reaction time  Less chance of contamination in products  More stability of products  Stable supply of products in the market  Improved process control  High enzyme substrate ratio
  • 4.  High cost for the isolation, purification and recovery of active enzyme (most important disadvantage)  Industrial applications are limited and only very few industries are using immobilized enzymes or immobilized whole cells.  Catalytic properties of some enzymes are reduced or completely lost after their immobilization on support or carrier.  Some enzymes become unstable after immobilization.  Enzymes are inactivated by the heat generated in the system
  • 5.  The matrix immobilizes the enzyme by holding it permanently or temporarily for a brief period of time.  A wide variety of matrixes or carriers or supports available for immobilization are cheap and easily available.  Their reaction with the components of the medium or with the enzyme should be minimum as possible.  They are grouped into three major categories  1. Natural polymers  2. Synthetic polymers  3. Inorganic materials
  • 6.  Alginate: A natural polymer derived from the cell wall of some algae. Calcium or magnesium alginate is the most commonly used matrix.  Chitosan and chitin: They are structural polysaccharides occurring naturally in the cell wall of fungi and the exoskeleton of Arthropods.  Collagen: It is the proteinaceous support with good porosity and water holding capacity.  Carrageenan: It is a stellated polysaccharide obtained from some red algae. Their good gelling properties makes it as a good support for immobilizing enzymes.
  • 7.  Gelatin: Gelatin is the partially hydrolyzed collagen with good water holding capacity.  Cellulose: Most abundant polymer of nature and it is the cheapest support available as carrier of enzymes.  Starch: A natural polymer of aniylose and amylo-pectin. It has good water holding capacity.  Pectin: It is a structural polysaccliaride of plants found in their primary cell wall and they also acts as the inter- cellular cementing material in plant tissues.
  • 8. Synthetic polymers  Synthetic polymers are ion exchange resins or polymers and are insoluble supports with porous surface.  Their porous surface can trap and hold the enzymes  Examples: Diethylaminoethyl cellulose (DEAE cellulose), Polyvinyl chloride (PVC), UV activated Polyethylene glycol (PEG) Inorganic materials  Zeolites extensively used for immobilizing enzymes  Ceramics are nonmetallic solids. Its composition and bonding pattern varies with different types.  Diatomaceous earth or Celite are solicitous sedimentary rocks. It is a good adsorbent and are resistant to high pH and temperature.  Silica , Glass, activated carbon and charcoal.
  • 9.  Based on support or matrix and the type of bonds involved, there are five different methods of immobilization of enzyme or whole cells.  1. Adsorption  2. Covalent bonding  3. Entrapment  4. Copolymerization  5. Encapsulation
  • 10.  Adsorption is the oldest and simplest method of enzyme immobilization.  Nelson & Griffin used charcoal to adsorb invertase for the first time in 1916. In this method enzyme is absorbed to external surface of the support.  The support or carrier used may be of different types such as:  1. Mineral support (Eg. aluminum oxide, clay)  2. Organic support (Eg. starch)  3. Modified sepharose and ion exchange resins
  • 11. There is no permanent bond formation between carrier and the enzyme in adsorption method. Only weak bonds stabilize the enzymes to the support or carrier. Adsorption The weak bonds (low energy bonds) involved are mainly:  Ionic interaction  Hydrogen bonds  Van der Waal forces
  • 12.  Static process: Immobilization to carrier by allowing the solution containing enzyme to contact the carrier without stirring.  Dynamic batch process: Carrier is placed in the enzyme solution and mixed by stirring or agitation.  Reactor loading process: Carrier is placed in the reactor, and then the enzyme solution is transferred to the reactor with continuous agitation.  Electrode position process: Carrier is placed near to an electrode in an enzyme bath and then the current is put on, under the electric field the enzyme migrates to the carrier and deposited on its surface.
  • 13. Advantages  No pore diffusion limitation  Easy to carry out  No reagents are required  Minimum activation steps involved  Comparatively cheap method of immobilization  Less disruptive to enzyme than chemical methods Disadvantages  Pore size limitation  Only small substrate molecule is able to cross the membrane
  • 14.  Widely used method of enzyme immobilization involves the formation of covalent bonds between the chemical groups in enzyme and to the chemical groups on the support or carrier.  Chemical groups in the support or carrier that can form covalent bonds with support are amino groups, imino groups, hydroxyl groups, carboxyl groups, thiol groups, ethylthiol groups, guanidyl groups, imidazole groups and phenol ring.
  • 15.  enzyme and support
  • 16. Carriers or supports commonly used for covalent bonding are:  Carbohydrates: Eg. Cellulose, DEAE cellulose, Agarose  Synthetic agents: Eg. Polyacrylamide  Protein carriers: Collagen, Gelatin  Amino group bearing carriers: Eg. amino benzyl cellulose  lnorg anic carriers: Porous glass, silica  Cyonogen bromide (CNBr)-agarose and CNBr Sepharose
  • 17.  Diazoation: Bonding between amino group of support and tyrosine or histidine group of enzyme.  Peptide bond: Bonding between amino or carboxyl groups of the support and that of the enzyme.  Poly functional reagents: Use of a bi- functional or multifunctional reagent (glutaraldehyde) which forms covalent bonds between the amino group of the support and amino group of the enzyme.
  • 18. Advantages  Strong linkage of enzyme to the support  No leakage or desorption problem  Comparatively simple method  A variety of support with different functional groups available  Wide applicability Disadvantages  Chemical modification of enzyme leading to the loss of functional conformation of enzyme.  Enzyme inactivation by changes in the conformation when undergoes reactions at the active site.
  • 19.  Enzymes are physically entrapped inside a porous matrix.  Bonds involved in stabilizing the enzyme to the matrix may be covalent or non-covalent.  The matrix used will be a water soluble polymer.  Pore size of matrix is adjusted to prevent the loss of enzyme. Pore size can be adjusted with the concentration of the polymer used.
  • 20. Examples of commonly used matrixes for entrapment are:  Polyacrylamide gels  Cellulose triacetate  Agar  Gelatin  Carrageenan  Alginate
  • 21.  Inclusion in the gels: enzymes trapped inside the gels.  Inclusion in fibers: enzymes supported on fibers made of matrix material.  Inclusion in microcapsules: Enzymes entrapped in microcapsules formed by monomer mixtures such as polyamine and calcium alginate.
  • 22. Advantages  Fast method of immobilization  Cheap (low cost matrixes available) k Easy to practice at small scale  Mild conditions are required  Less chance of conformational changes in enzyme  Can be used for sensing application Disadvantages  Leakage of enzyme  Pore diffusion limitation  Chance of microbial contamination  Not much success in industrial process
  • 23.  In this method of immobilization, enzymes are directly linked by covalent bonds between various groups of enzymes via polyfunctional reagents.  There is no matrix or support involved in this method.  Commonly used poly functional reagents are glutaraldehyde and diazonium salt.  This method is widely used in commercial preparations and Industrial applications.  The greatest disadvantage of this method is that the polyfunctional reagents used for cross linking the enzyme may denature leading to the loss of catalytic properties.
  • 24.  This immobilization is done by enclosing the enzymes in a membrane capsule.  The capsule will be made up of semi permeable membrane like nitro cellulose or nylon.  In this method the effectiveness depends upon the stability of enzymes inside the capsule
  • 25. Advantages  Cheap and simple method  Large quantity of enzymes can be immobilized by encapsulation Disadvantages o Pore size limitation o Only small substrate molecule is able to cross the membrane
  • 26.  Industrial production: Industrial production of antibiotics, beverages, amino acids etc. uses immobilized enzymes or whole cells.  Biomedical applications: Immobilized enzymes are widely used in the diagnosis and treatment of many diseases. Immobilized enzymes can be used to overcome inborn metabolic disorders by the supply of immobilized enzymes. Immobilization techniques are effectively used in drug delivery systems especially to oncogenic sites.  Food industry: Enzymes like pectinases and cellulases immobilized on suitable carriers are successfully used in the production of jams, jellies and syrups from fruits and vegetables.
  • 27.  Research: Research activity extensively uses many enzymes. The use of immobilized enzyme allow researcher to increase the efficiency of different enzymes such as Horse Radish Peroxidase in blotting experiments and different Proteases for cell or organelle lysis.  Production of biodiesel from vegetable oils.  Waste water management: treatment of sewage and industrial effluents.  Textile industry: scouring, bio-polishing and desizing of fabrics.  Detergent industry: immobilization of lipase enzyme for effective dirt removal from cloths.