- A. Classification of the immobilized enzymes
- B. Techniques of immobilization
- C. Change in the properties of enzymes after Immobilization
- D. Basis of extensive research on immobilized enzymes
- E. Applications of immobilized enzymes
Main text
Classification of immobilized enzymes
The enzymes were first classified into two groups: “native enzymes” and “modified enzymes”. The immobilized enzymes belonged to the class of modified enzymes and are currently further divided into two groups: “entrapped immobilized enzymes” and “bound immobilized enzymes”.
Entrapped immobilized enzymes
“Entrapped enzymes are those enzymes that can be entrapped in a semi-permeable gel or enclosed in a semi-permeable polymer membrane”. For example, glucoamylase is entrapped by polyacrylic acid and invertase by polyvinyl alcohol (Zdarta et al. 2018)”.
“Entrapped enzymes are further divided into two sub-classes:
- (a) Matrix entrapped enzymes Matrix-entrapped enzymes are those which are entrapped within the interstitial spaces of cross-linked water-insoluble polymers, i.e., within a gel. For example, alcohol dehydrogenase is entrapped within polyacrylamide and invertase is entrapped within polyethylene glycol polymer (Godbole et al. 1980).
- (b) Micro-encapsulated enzymes These are the enzymes, which are enclosed within the semi-permeable polymer membranes.
Bound immobilized enzymes
Bound immobilized enzymes are also further sub-divided into two classes: adsorbed bound immobilized enzymes and covalently bound immobilized enzymes.
Adsorbed bound immobilized enzymes The adsorbed immobilized enzymes are those which are immobilized by binding with an adsorbent such as activated charcoal and micro-glass beads (Science, Direct)”.
Covalently bound immobilized enzymes
The covalently bound immobilized are those which are immobilized by attachment to a matrix through a covalent chemical linkage.
The author and his associates, in the light of their research in the field of immobilized enzymes, have proposed modification of classification of immobilized enzymes by Enzyme Engineering Conference (1971) because his groups have worked on cell bound proteases of medicinal seeds and have given them the name of “Naturally Immobilized Enzymes” (Khan and Bukhari 2008a, b; Khan et al. 2008). Thus, the author has proposed that the enzymes should be basically classified into “naturally immobilized enzymes” and “artificially immobilized enzymes”. The latter should be further sub-classified as done in 1971. That sounds logical and thus acceptable to the author and his associates (Khan 2021).
The author and his associates appreciate without any reservation the spectrum of applications of immobilized enzymes and breaking the news that the spectrum being broad, the field of immobilized enzymes deserves a close attention. It will open new vistas for broadening the spectrum of applications for the benefit of future generations. This encourages the author and his associates to give some suggestions based on the results of their research particularly on naturally immobilized enzymes on the basis that “Whatsoever is natural is safer to use as medical treatment”.
Changes in properties of enzymes after immobilization
Immobilization translates into certain changes in the characteristics of the enzymes, which form the basis for the determination of the applications of immobilized enzymes and for the explanation of structure and function, relationship between the enzyme and substrate, mechanics of enzymatic action, etc. Two factors are responsible for change of the enzyme characteristics: structural changes of enzyme itself and changes in physical and chemical characteristics of matrices used for immobilization.
Below are outlined the main properties of the enzymes that may or may not undergo a change after immobilization.
Substrate specificity When enzymes are immobilized, their activity often decreases and the substrate specificity also undergoes a change accordingly, for example, when enzymes such as proteases and amylases acting on certain substrates having higher molecular weight are immobilized by carrier binding method. For example, in peptide binding or diazo binding, significant changes of substrate specificity have been encountered.
It has been observed that “when an enzyme is immobilized using a water-insoluble polymer carrier, the enzyme activity toward substrates of higher molecular weight is markedly reduced due to steric hindrance which obstructs the approach of the substrate to the enzyme molecule (Zhong et al. 2014)”. However, the activity of the immobilized enzymes toward substrates of low molecular weight is not significantly changed, because the substrate can easily approach the enzyme (Science Direct Online).
Immobilized enzymes show better thermal and storage stability than the free enzymes. Increase in Km value only about 1.25 times has been reported, and enzyme activity behavior to pH and temperature function has been reported (Waterhouse and waterhouse 2020).
Temperature dependence of enzymatic reactions The catalytic activity of enzymes is dependent upon temperature, as it is observed in case of ordinary chemical catalysts. The activity is lost at temperature above a certain limit due to the denaturation of enzyme protein. Changes in the optimum temperature of the enzymatic reaction after immobilization occur in some cases. The optimum temperatures of immobilized enzymes were observed to be many times higher than those of native enzymes in case of trypsin and chymotrypsin immobilized by peptide binding with CM cellulose (Homaei et al. 2013).
There are, of course, many reports that “no change of optimum temperature occurs after immobilization. Examples are chymotrypsin immobilized with CNBr-activated cellulosic membrane, trypsin immobilized with CNBr activated agarose, etc. (Singh et al. 2013)”.
Markoglou and Wainer (2003) studied the effect of immobilization on the thermal stability of phenylethanolamine N-methyltransferase (PNMT), and the immobilized enzyme was observed to exhibit increase in thermal stability. The initial enzyme activity was lower for the immobilized PNMT, relative to the non-immobilized enzyme, and it remained comparatively stable over the range of experimental temperature. In their opinion, “increased stability may be a result of the fact that immobilization limits the thermal movement of the enzyme at higher temperatures. As a result, thermal denaturation may not occur at higher temperatures with an immobilized enzyme. Thermostable enzymes allow for higher reaction rate, lower diffusional restrictions, increased stability and greater yields”.
Homaei et al. (2013) have updated the techniques of immobilization compared to free enzymes in solution and reported that the immobilized enzymes are “more robust and more resistant to environmental changes”. In their opinion, the “heterogeneity of the immobilized enzyme systems allows an easy recovery of both enzymes and products, multiple re-use of enzymes, continuous operation of enzymatic processes, rapid termination of reactions, and greater variety of bioreactor designs”.
pH dependence of the enzymatic action The enzymes are proteinous in nature, and thus, their catalytic activity is markedly affected by the pH of the aqueous medium. Changes in activity to pH behavior caused by immobilization of enzymes help in the understanding of the structure–function relationship of enzyme protein. Suzuki and Ozawa (2014) prepared water-insoluble yeast invertase by binding native invertase with DEAE-cellulose and compared some of its characteristics with that of native enzyme and also described the continuous hydrolysis of sucrose by its use. “The activity of bound invertase corresponded to about half at pH 3.4 with shift to pH 2 “after binding when compared with the maximum activity of free form and it could hydrolyze sucrose into invert sugar perfectly”. Stability of bound invertase to temperature, of course, was slightly less compared to that of free invertase at pH 5.2”.
There are many cases of shift in optimum pH without showing any change in pH activity curve after immobilization. “The optimum pH of amino acylase immobilized by ionic binding with DEAE cellulose or DEAE sephadex shifted 0.5 to 1.0 pH unit to the acid side from the optimal pH of the native enzyme. Similar shifts in optimum pH have been encountered with invertase and ATP, d -aminase immobilized by ionic binding with DEAE cellulose and NADH dehydrogenase immobilized by cross-linking using glutaraldehyde (Homaei et al. 2013). “The current demand of the world’s biotechnological industries is enhancement in enzyme productivity and development of novel techniques for increasing their shelf life. These requirements are inevitable to facilitate large-scale economic formulations. Enzyme immobilization provides an excellent base for increasing availability of enzyme to the substrate with greater turnover over a considerable period of time. Several natural and synthetic supports have been assessed for their efficiency for enzyme immobilization. Nowadays, immobilized enzymes are preferred over their free counterparts due to their prolonged availability that curtails redundant downstream and purification processes. Future investigations should endeavor at adopting logistic and sensible entrapment techniques along with innovatively modified supports to improve the state of enzyme immobilization and provide new perspectives to the industrial sector (Datta et al. 2013)”.
Hassan et al. (2019) conducted covalent immobilization of glucoamylase on the chemically activated surface of κ-carrageenan. The authors reported that the immobilized enzyme showed enhancement in temperature profile as the optimal temperature for the free enzyme was 60 °C, which increased to the range of 60–80 °C: broader range and stability in acidic conditions. “The apparent Km of immobilized enzyme, 147.46 mM, became higher than Km of the free one, 110 mM and the maximum reaction velocity (Vmax) values for the immobilized enzyme decreased from 2.28 to 1.11 μmol min −1 . The immobilized enzyme could be reused and kept its activity (100%) till 11 successive cycles”. The conclusion was that the economic and biotechnical benefits of enzyme immobilization, particularly with reference to the number of enzyme reuses, would open the possibility of increase in different industrial applications.
There are also some reports that both shifts of optimum pH and the change of pH activity curve occur as a result of enzyme immobilization. An important example is of glucoamylase immobilized by alkylation with dichlorotriazinyl cellulose. The pH shifted to the acid side and the pH activity became narrow compared with that of the native enzyme (Homaei et al. 2013).
“Some immobilized enzymes show no shift of optimum pH but do exhibit changes of pH activity curve. In case of β-fructo furanosidase immobilized by diazo binding with poly amino polystyrene, for example, the optimum pH did not shift, but the pH activity curve became narrow (Filipusson and Hornby 1970)”.
Activation energy of immobilized enzymes Some enzymes do not undergo a change in the energy of activation. Some undergo an increase and some a decrease after immobilization. The activation energies of some immobilized enzymes are almost the same as those of the corresponding native enzymes. Examples may be invertase immobilized by physical adsorption on activated carbon, asparaginase and invertase immobilized by ionic binding with DEAE cellulose.
The activation energies of amino acylase immobilized by ionic binding with DEAE cellulose and DEAE-sephadex have been reported to increase compared to those of the native enzyme. The decreases of activation energy have also been observed. For example, “the Energy of Activation (Ea) of invertase from NOVO Nordisk immobilized in controlled pore silica particles by covalent binding with the silane-glutaraldehyde method. was found as pH dependent. It gave for free invertase, Ea = 7.0 and 6.86 kcal/mol at pH 5.0 and 5.5, respectively, whereas for the immobilized enzyme, Ea = 6.55 and 5.93 kcal/mol at pH 4.5 and 5.0, respectively, was found to be a function of pH, giving for free invertase, Ea = 7.0 and 6.86 kcal/mol at pH 5.0 and 5.5, respectively, whereas for the immobilized enzyme, Ea = 6.55 and 5.93 kcal/mol at pH 4.5 and 5.0, respectively (Bergamasco et al. 2000)”.
Stability An increase of stability of enzymes after immobilization has been encountered in many cases. The enhancement of stability leads to some advantages for the industrial applications of immobilized enzymes and is an important index of the feasibility of enzymes for specific applications. Different kinds of stabilities are briefly outlined below:
Stability towards regents Immobilization of enzymes causes changes in the stability of enzymes towards different reagents. Increase in stability towards protein denaturing agents or enzyme inhibitors has been encountered for some immobilized enzymes. For instance, immobilized amino acylase and immobilized trypsin are not inhibited by urea. Increased resistance towards inhibitors has also been reported for some immobilized enzymes. Immobilized trypsin prepared by peptide binding and carrier-cross-linking with CM-cellulose azide has been said to become resistant to trypsin inhibitor. It sounds quite convincing that the approach of high molecular weight trypsin inhibitor to the immobilized enzyme is interrupted by steric hindrance.
Levitsky et al. (1998) reported that the proteolytic enzymes immobilized by adsorption on a solid support were widely used for synthetic reactions in low water systems. However, stability of such products had to be optimized to avoid reversible and irreversible inactivation of enzyme by organic solvent. Immobilization of enzyme, previously involved in non-covalent complex with polyelectrolyte, could be a possible way to suppress inactivation processes. In the research work reported here, non-covalent complex between α-chymotrypsin and polycation Polybrene was immobilized on Celite and the stability of the resulted biocatalyst against irreversible inactivation by organic solvents as DMSO, DMFA and AcN at 30 °C was investigated. It was observed that the complexation with Polybrene could result into either stabilization or destabilization of enzyme depending on type and concentration of organic co-solvent. “Maximal protective effect, defined as ratio of half-life times of enzymes, immobilized in/out of complex with Polybrene, was about 50-fold for inactivation by dry DMFA and 30-fold for inactivation by dry AcN and 20% solution of DMSO”.
Stability towards proteolytic enzymes “In enzymatic reactions using crude enzyme preparation, inactivation of the enzyme is often encountered to accelerate by contaminating proteolytic enzymes. In some cases, resistance to various proteolytic enzymes is increased by immobilization (Kilbinov, On-line)”.
In case of proteolytic enzymes such as trypsin and papain, the stability is increased by a decrease of catalytic activity towards substrates of high molecular weight due to steric hindrance because of reduction of the extent of autolysis.
Heat stability “The catalytic activity of enzymes increases with elevation of temperature, as it happens in case of chemical catalysts. However, as enzymes are proteins and are generally heat sensitive, the enzymatic reactions cannot be carried out at high temperature. If the heat stability of enzymes is increased by immobilization, the potential utilization of such enzymes will be extensive”.
Operational stability “The operational stability of immobilized enzymes is one of the most important factors affecting the success of industrialization of the immobilized systems. A column of immobilized papain prepared by carrier cross-linking with porous glass retained full initial activity after 35 days of continuous operation at 45 °C with casein solution has been reported by Freeman and Lilly (1998)”.
Kinetic constants
Conformational changes of the enzyme protein may take place after immobilization (Hassan et al. 2019), and thus, the affinity between enzyme and substrate may also undergo a change. The authors have reported that little or no change occurs in Michaelis–Menten constant (Km) that indicates the presence of affinity between enzyme and substrate after immobilization.
In some cases, “significant changes, say up to twofold magnitude occur. The Km value for trypsin immobilized by a polyanionic carrier ethylene maleic anhydride co polymer was determined using positively charged benzoyl l -arginine amide as a substrate at various ionic strengths (Science Direct, Library)”. It is also reported that “Km for the immobilized enzyme decreased to 1/10th that of the native enzyme at lower ionic strength but approached that of native enzyme at higher ionic strength”. Thus, “the change in Km value was considered to be caused by electrostatic attraction between the carrier and the substrate”. Some experiments have also shown that “the Km values measured for asparaginase microencapsulated in nylon or polyurea membrane and immobilized by entrapping in poly acrylamide gel become greater than those of native enzyme by twofold magnitude”. In an earlier report by Mori et al. (1972), an astonishingly high value of increase that is about 200 times in Km for asparaginase trapped in poly acrylamide microcapsule has been reported.
Techniques of immobilization
Methods for enzyme immobilization have been basically classified into three categories as outlined below.
- 1. Carrier-binding method In this method, the linking of enzymes is accomplished with water-insoluble carriers: polysaccharide derivatives, synthetic polymers, and porous glass.
- 2. Cross-linking method This method involves the intermolecular cross-linking of enzymes by bi-functional or multifunctional reagents such as glutaraldehyde, bisdiazoben-zidine, and hexamethylene, diisocyanate.
- 3. Entrapping method Here the enzymes are incorporated into the lattice of a semipermeable gel or the enzymes are enclosed in a semipermeable polymer membrane: collagen, gelatin, cellulose triacetate, polyacryl-amide, and j-carrageenan, etc.
One of the methods being studied involves the immobilization of enzymes by trapping in certain active materials or by binding with specific matrices. The enzymes in the immobilized state are less subject to denaturation and thus can be preserved over time. Several techniques have been developed to prepare immobilized enzymes because they exhibit many advantages over enzymes in the solution state (Mohamad et al. 2015). An overview of technologies for enzyme immobilization and surface analysis techniques for immobilized enzymes has been presented by Biotechnology and Biotechnological Equipment (Mohamad et al. 2015). For instance, immobilization leads to ease of recoverability and reusability of the enzymes.
Proteolytic enzymes that hydrolyze and thus break down proteins into smaller units such as proteoses, peptones, amino acids can be immobilized on different materials. These can be subsequently applied for continuous hydrolysis of protein substrates. Enzymes are usually immobilized by binding them with some matrices filled in chromatographic columns and subsequently passing through them the buffered substrates and collection of products of hydrolysis eluting out of the column. Enzymes immobilized in this way may increase the stability of enzymes to thermal shocks and extremes of pH. The enzymes, after immobilization, undergo certain changes in the spectrum of their activity. Fortunately, many enzymes remain significantly active after their immobilization. Thus, immobilization leads to ease of recoverability and reusability of the enzymes. Proteases break down proteins into smaller units that may recombine to yield different proteins essentially required by the organic body. This process of breaking and reforming is in operation continuously in living organisms. The process of breakdown of proteins by proteases into peptides, amino acids, etc. is called proteolysis. Although the observations about the action of proteolytic enzymes on proteins made the discovery of the cleavage of the peptide bond in the nineteenth century, still at that time there was no clear map of the mode of action of enzymes. Later, when it became known that the amino acids were linked by the peptide bonds in proteins, the experts paid full attention to understand the mode of action of theses enzymes on protein to utilize proteases on commercial scale. The proteases have also found extensive applications in medicine as cures of diseases such as stomach disorder, fistulas, hyperacidity and cramps. They are being extensively used as anti-inflammatory agents. They digest dead cells of skin’s necrotic tissue and thus act as wound cleaners. Similarly, they are being widely applied as cleaners of contact lenses.
On the basis of the importance of proteases highlighted above, the proteases have been under extensive investigation in the past and, even, are currently being intensively studied, all over the world. The countries involved in this activity are USA, China, Australia and Japan and some developing countries including Pakistan. China, of course, is the leader to utilize plant proteases on commercial scale. Some significant reports have appeared which highlight the diversity of applications of proteases in Pakistan. Amino acids and other products of proteolysis have extensive applications in different fields. The mixture of amino acids can be transfused with the help of drips into the body of patients. The supply of these essential nutrients for the synthesis of structural and functional proteins, essentially required for the body, may be ensured. Amino acids may also be separated for use in Chemistry laboratories. There are also many other applications of amino acids. Considerable work has been carried in Pakistan to hydrolyze casein by proteases immobilized on different materials keeping in view the above-mentioned applications. An attempt was made to develop continuous proteolysis systems consisting of protease immobilized by combining with artificial and naturally occurring materials such as DEAE A-50 cellulose, Amberlite-50, Activated Charcoal (Khan and Talib 1986; Nawaz and Khan 2000). Later, the work was extended to the study of naturally immobilized proteases of vegetable origin such as Carum copticum, Allium sepa, Nigella sativa (Khan and Bukhari 2008a, b; Khan et al. 2008). The difficulty encountered was that there was also contained in the cells of the seeds the soluble protease component. Thus, the seeds were investigated for both soluble and immobilized proteases. The results, of course, revealed that the major component was the immobilized one, while soluble component was a minor one. This difference made a good ground for the study of naturally immobilized enzymes packed in chromatographic columns. Thus, the work was extended by the elution of soluble enzyme so that only the cell bond enzyme may react with the substrates.
The current demand of the world’s biotechnological industries is increase in enzyme productivity and development of innovative techniques for increasing their shelf life. These requirements are essential to facilitate large-scale and economic formulations. Enzyme immobilization provides an excellent basis for increasing availability of enzyme to the substrate with greater turnover over a considerable period of time. Several natural and synthetic supports have been evaluated for their efficiency for enzyme immobilization. Nowadays, immobilized enzymes are preferred over their free counterparts due to their prolonged availability that curtails redundant downstream and purification processes. Future investigations should aim at adopting logistic and sensible entrapment techniques along with innovatively modified supports to improve the state of enzyme immobilization and provide new perspectives to the industrial sector. The reviews such as by Datta et al. (2013) and others have the focus on the development of immobilization techniques with regard to their application in industry.
A number of techniques have been developed to bring the enzymes in the immobilized state. While making the choice of techniques for enzyme immobilization, it is desirable that the native enzymes retain most of their catalytic activity in the immobilized state. To that end, it is essential that the enzyme retains its native structure and conformation as far as possible. Therefore, immobilization should be carried out under very mild and appropriately controlled conditions.
The change in catalytic activity of the enzyme during immobilization largely depends upon certain structural changes in its active centers. If the amino acid residues involved in the tertiary structure of the active center are altered, the catalytic activity may decrease. The decrease may be accompanied by the changes of enzymatic properties such as substrate specificity.
The functional groups involved in the enzyme immobilization are free amino, carboxylic and the active groups contributed by different amino acids such as sulphydryl (-SH) provided by cysteine), imidazole by histidine, phenolic, and hydroxyl by serine and threonine.
In order to retain most of the catalytic activity after immobilization of the enzyme, it is essential that the functional groups in the active center may not be involved in the reaction leading to the immobilization of the enzyme.
Keeping in view, the retention highlighted above and development of certain characteristics of the immobilized enzymes that qualify them for applications in industry, an intensive research has been conducted and many reviews have been documented. The number of methods has also expanded particularly at the sub-class level. Methods recently and currently applied for enzyme immobilization are sub-classified below. A brief description of each method is also given.
Carrier binding method This is the oldest enzyme immobilization method. In this method, “the immobilization is accomplished by physical or chemical bonding of the enzyme with an appropriate carrier. The carriers mostly used for immobilization are physical adsorbents such as coal, porous glass, polyacrylamide gel, etc. (Jesionowski et al. 2014)”.
A lot of care is required while selecting of carriers as well as carrying out the binding technique. The selection of carrier depends on the nature of the enzyme itself with regard to the parameters: particle size, surface area molar ratio of hydrophobic groups and chemical composition of the carrier. The carrier binding methods may be further subdivided into three types.
A. Physical adsorption method The principle involved in this method is the physical adsorption of enzyme proteins on the surface of water-insoluble carriers. The physical adsorption causes little or no conformational change in enzyme molecule, which may lead to the destruction of its active center. The only disadvantage of this method is that the adsorbed enzyme may leak out of the carrier during its use as the binding force between the enzyme protein and the physical adsorbing carrier is weak. Usually employed as carriers are the inorganic materials: activated carbon, porous glass, acid clay, bleaching clay, alumina, silica gel, calcium phosphate, etc. Natural polymers such as starch and gluten have also been used.
The immobilization of invertase on charcoal was studied by Nelson and Griffin (1916). These workers observed that “the enzyme adsorbed on the activated carbon retained its catalytic activity towards sucrose. The immobilization of an enzyme lipoamide dehydrogenase by hydrophobic binding to a carrier has also been reported in literature (Lowe 1977). “The enzyme was immobilized by binding with carriers containing hydrophobic residues such as butyl or haxyl sepharose. It has been readily immobilized by using adsorbent containing tannin as a ligand”. The tannin amino haxyl cellulose can be used for immobilization of many enzymes and the hydrophobic forces play an important role in this immobilization.
B. Ionic binding method This method is based on the principle of ionic binding of the enzyme protein to the water-insoluble carrier containing ion exchange residues (Krishnamoorthi et al. 2015).
Polysaccharides and synthetic polymers having ion exchange residues have been successfully used as carriers for ionic binding. This method causes little or no change of conformation in the structure of active site of the enzyme protein and thus yields the immobilized enzymes having high activity in many cases. The disadvantage of the method is that the leakage of the enzyme from the carrier may occur in substrate solutions of high ionic strength upon variation of pH of medium because of the weakening of the ionic forces.
The results of immobilization of the enzyme by ionic binding method are reported by Mitz (1956). He prepared immobilized catalase by passing the enzyme solution through a column packed with DEAE cellulose. Highly active and stable immobilized protease has been prepared using anion exchange carriers such as DEAE cellulose (Khan and Talib 1986). Ionic binding to the carriers has also been reported after infusing the change in enzyme protein by chemical modification. For example, anionic glucoamylase was modified to a polyanionic derivative by covalent bonding with a water-soluble polymer of ethylene and maleic anhydride (Goldstein et al. 1964).
C. Covalent binding method This method involves the binding of enzymes and water-insoluble carriers by covalent linkages (Hartmeier 2016). “The functional groups which take part in covalent binding of enzyme to the carrier are given below.
- (i) α or 3-amino group
- (ii) α, β or γ carboxylic group
- (iii) Sulfhydryl group
- (iv) Hydroxyl group
- (v) Phenolic group
These functional groups react with carriers containing reactive groups such as diazonium, isocyanide, halides and acid azide”.
“The reaction conditions required for covalent binding are relatively complicated. The binding force between enzyme and carrier being strong, the leakage of the enzyme does not take place. This is an advantage of this method over physical adsorption and ion exchange methods”. This method can be further classified into types given below on the basis of the nature of the reaction involved.
- I. Peptide binding method: This method is based on the conformation of peptide bond between enzyme protein and water-insoluble carriers (Fu et al. 2011). In 1956, Brandenberger used a carboxychloride of Amberlite IRC-50 for the immobilization of lipase. It is considered to be the first of the peptide binding methods. Similarly, leucine amino peptide attached to the isocyanate derivative of fluorochrome was immobilized using CNBr-activated sepharose.
- II. Alkylation method (Tamer et al. 2016)
“This method involves the alkylation of amino, phenolic or sulphydryl groups of the enzyme protein with a reactive group (e.g., halide) in the water-insoluble carrier. Carriers possessing reaction halogens employed for the immobilization of enzyme are triazinyl derivative of cellulose, sephadex, sepharose, porous glass and bentonite. Enzymes such as aldolase glyceraldehyde phosphate dehydrogenase have been immobilized by using AE-cellulose and glutaraldehyde. Thiolation of enzymes containing no thiol group such as chymotrypsin and their subsequent immobilization through disulfide linkages has also been studied”.
“This method involves the diazocoupling of the enzyme protein and diazonium derivatives of water-insoluble carriers. The functional groups participating in diazocoupling include free amino group imidazole group of histidine and phenolic group of lysine. For example, catalase is immobilized on m-aminoanisole cellulose and papain is immobilized on p-amino-DL-phenyl alanine, l -leucine”.
2. Cross-linking method This method is based on the principle of formation of chemical bonds and intermolecular cross-linkages between the enzyme molecules by means of bifunctional and multifunctional reagents. Water-insoluble carriers are not used in this method. “Glutaraldehyde; isocyanate derivatives, bis-diazobenzelene. N,N-polyethylene, N,N′-ethylene, bis-malomide have been in practice as cross-linking reagents. The functional groups of the enzyme protein participating in the reactions are α amino group or 3-amino group of lysine, the phenolic group of tyrosine, sulfhydryl group of cystine and amindazole group of histidine. Severe conditions are required for the cross-linking of the enzymes. This results into the loss of activity due to change in the conformation of the active center of the enzyme. N,N′-polymethylene bis-iodo-acetamide have been employed for the immobilization of the aldolase in rabbit muscle and α amylase, etc.
3. Entrapping method (Luna and Verdugo-Escamilla Online) “This method depends upon the principle of confining the enzyme in the lattice of a polymer matrix or enclosing it in a semi permeable membrane”. The entrapping methods are of two types.
- i. Lattice type This method involves “entrapping of the enzyme within the interstitial spaces of a cross-linked water-insoluble polymer, i.e., within the gel matrix. Various synthetic polymers such as polyacrylamide, polyvinyl alcohol and natural polymers such as starch, and konjac powder have been used for the immobilization of the enzyme by this method. This technique was used by Bernfeld et al. (1963) who entrapped trypsin, papain, amylase, ribonuclease, etc., in a gel lattice of polyacrylamide.
- ii. Microcapsule type (Wikipedia) This method involves enclosing of enzyme within the semipermeable polymer membrane. The resulting enzyme microcapsules generally have a diameter of 1–100μ. Microcapsules are being extensively used in medicine, foods, cosmetics, dyes and fuels. Extremely well controlled conditions are required for the enzyme preparation.
The procedures for the micro capsulation of the enzyme can be classified into three categories.
- I. Interfacial polymerization (Okobira et al. 2015): “This procedure is based on the enclosing of the enzyme in a semi-permeable membrane of a polymer by applying the principle that hydrophobic and hydrophilic monomers polymerize the interface”. The micro-encapsulation of enzymes by this procedure was first reported by Chang et al. (2009); these workers microencapsulated asparaginase urease and carbonic anhydrase using a nylon membrane.
- II. Phases separation method (Sun et al. 2017) This method is based on the principle of one of the purification methods for polymers. “It involves dissolving the polymer in an organic solvent and re-precipitating it by adding another organic solvent which is miscible with the first but which does not dissolve the polymer”. Chang et al. (Online) succeeded in the microencapsulation of asparaginase, urease and catalase by this method. They also reported that more stable microencapsulated urease was obtained when the enzyme was microencapsulated after being adsorbed on silica gel.
- III. Liquid membrane method (Kimura et al. 1989): In this method, “the encapsulation of enzymes by means of liquid membrane instead of a water-insoluble semi-permeable membrane has been attempted. This new procedure involves encapsulation of the enzyme solution within an amphipathic liquid surfactant membrane (liposome), e.g., formed from surfactant and Lecithin. The most significant characteristic of liquid fraction microcapsules for the immobilization of glucoamylase is that the permeability of substrate and product across the liquid membranes is independent of pore size of membrane but depends on the solubility of the substrate and or product in the components of the membrane. Therefore, applications different from those of the conventional microcapsules are anticipated, and research on liquid membrane microcapsules is expected to increase in importance”.
Liquid drying method (Hossein et al. 2018)
This method is based on the “enclosing of the enzyme via processes of dispersion in polymers dissolved in water immiscible organic solvents followed by dispersion in aqueous solution and subsequent drying. The microcapsulation of catalase, lipase and other enzymes have been carried out by this method using ethyl cellulose and polyethylene”.
Applications
Immobilized enzymes have specific characteristics. Many efforts have been made to the development of immobilized enzymes for a number of applications. Their modified forms are applied in different fields as given below.
- Synthesis of radioactive compounds
- Analytical techniques
- Medical treatments
- Food processing such as hydrolysis of lactose before making milk fit for babies to drink, milk
- Processing for removal of hydrogen per oxide from chemically sterilized milk using immobilized oxidase, production of cheese
- Preparation of sweet liquor by hydrolysis of starch for continuous preprocessing of alcoholic fermentation using immobilized amylase from micro-organisms instead of malt, Affinity chromatography
- Fuel cells and bio-chemical batteries.
Sirisha et al. (1916) earlier reviewed the applications of immobilized enzymes and reported that the immobilized enzymes could be used in a wide range of processes. In recent years, a variety of new approaches have emerged for the immobilization of enzymes that have greater efficiency and wider usage. During the period of last two decades, this area has rapidly expanded into a multidisciplinary field.
This study is a comprehensive review of a variety of literature produced on the different enzymes that have been immobilized on various supporting materials and of the immobilized enzymes having a wide range of applications. These include applications in the sugar, fish, and wine industries, where they are used for removing organic compounds from waste water. This study also reviews their use in sophisticated biosensors for metabolite control and in situ measurement of environmental pollutants. Immobilized enzymes also find significant application in drug metabolism, biodiesel and antibiotic production, bioremediation, and the food industry. The widespread usage of immobilized enzyme technology is largely due to the fact that they are cheaper, environment friendly, and much easier to use when compared to other technologies.
Altikaynak et al. (2016) have reported that “many different micro and nano-sized materials can be used for enzyme immobilization in order to increase their catalytic activity and stability. Generally, immobilized enzymes with conventional immobilization techniques exhibit improved stability, while their activity is lowered compared to free enzymes”. Recently, an excellent immobilization approach was discovered in synthesis of flower-like organic–inorganic hybrid nanostructures with extraordinary catalytic activity and stability. In this novel immobilization strategy, “proteins (enzymes) and metal ions act as organic and inorganic components, respectively, to form hybrid nanoflowers (hNFs). It is demonstrated that the hNFs highly enhanced catalytic activities and stability in a wide range of experimental conditions: pHs, temperatures and salt concentration, etc. compared to free and conventionally immobilized enzymes”. This review mainly discussed the synthesis, characterization, development and applications of organic–inorganic hybrid nanoflowers formed from different enzymes and metal ions and explained potential mechanism underlying enhanced catalytic activity and stability.
Medical applications of immobilized enzymes
The medical applications of immobilized enzymes have been extensively studied and developed and have been reviewed thoroughly by the author of the current review Khan (2021) and it may be fruitful for the seekers of detailed information about the medical applications to refer to his exercise. In his opinion, the enzymes immobilized by entrapping method particularly offer their therapeutic use in case of enzyme deficiency or metabolic disorders. He has outlined the attempts of major contributors in this context: Liang et al. (2000a) description of the medical applications of immobilized proteins, enzymes and cells. Examples are given below.
- Microencapsulated catalase for enzyme replacement in acatalasemic mice
- Use of liposomes for the microencapsulation of enzyme asparaginase and other enzymes in chemotherapy with reference to their use associated with problems related to toxicity.
- Immunogenicity and duration of action
- Lymphoma as the third most common cancer diagnosed in dogs.
Because of the importance of cancer treatment, many studies have been carried out using all available immobilization approaches. The immobilized enzymes are used in detoxification, because many of the detoxifying functions in the body are carried out by enzymatic reactions. Chang et al. (Online), for instance, investigated the application of enzymes microcapsules entrapped inside a semi-permeable poly membrane. Later workers prepared asparaginase microcapsule and attempted to use them for the treatment of leukemia (Lang et al. 2005; Harrer et al. 2007)”. They also studied the changes of asparaginase level in blood after administration of asparaginase microcapsule.
Utilization of immobilized enzymes for the treatment of blood outside the body, i.e., “Extra Corporeal Shunt System” was attempted. Mori et al. (1972) investigated the application of immobilized asparaginase prepared by entrapping in poly acryl amide gel that is mechanistically stronger than the enzyme microcapsule for the therapy of leukemia by means of an extra corporeal shunt system. “This preparation was very stable towards the proteolytic enzymes and L-asparagin in blood was completely decomposed when blood was passed through a column packed with immobilized enzyme”.
An extra corporeal shunt system is known to have great potential and may be applied for emergency cases. The time required for such a therapy can be controlled easily, and specific detoxicating material used for the system can be prepared readily.
An extra corporeal shunt system is known to have great potential and may be applied for emergency cases. The time required for such a therapy can be controlled easily, and specific detoxicating material used for the system can be prepared readily.
Liang et al. (2000a) presented a brief review of developments in use of immobilized enzyme in medicine. The panel divided the use of immobilized enzyme in medicine into two major categories: Biosensors and Bioreactors. A brief overview of the evolution of the biosensor and bioreactor technology pertaining to existing applications of immobilized enzymes at that time, of problems that researchers encountered, and of possible future developments were also highlighted.
Medical applications of immobilized proteins, enzymes and cells are also extensively encountered in the literature of Science Direct (Online).
The current research is mostly focused on the medical applications of immobilized microfluidic enzymatic reactors and biosensors for which the readers and reviewers may have the flashback to Khan’s review article (2021) with many quotes in this context (Matosevic et al. 2011a, b; Khan and Talib 1986; Zhong 2007; Tischer and Wedekind 1999; Kawamura et al.; Kilbanov 1983; Science Direct, Rao Online, and others).
Different types of biosensors are in the market:
- 1. Electrochemical Biosensors. …
- 2. Immunosensors
- 3. Magnetic Biosensors
- 4. Thermometric Biosensors
- 5. Acoustic Biosensors
- 6. Optical Biosensors
All these types are widely used. Reference list may be consulted for mechanics and uses of different types of biosensors.
As the focus is mainly on the use of immobilized enzymes as biosensors in bioreactors in pharmaceutical industry that manufactures drugs for the medical treatments, let us try to understand what these are? The bioreactor as defined in a Mini-Review on website (https://deepblue.lib.umich.edu/bitstream/handle/2027.42/34503/2_ftp.pdf?sequence=1) as under:
Bioreactor is defined as a vessel that carries out a biological reaction and is used to culture aerobic cells for conducting cellular or enzymatic immobilization.
The cell culturing is the most commonly applied process in biopharmaceutical development, bioprocessing and bio-manufacturing in the pharmaceutical industry. Most biopharmaceutical products are developed from large, complex protein molecules grown in well-defined and highly controlled liquid environment, inside the bioreactors.
The performance of a bioreactor depends largely on biosensors that are defined as under:
“Biosensors are devices used to detect the presence or concentration of a biological analyte, such as a biomolecule, a biological structure or a micro-organism” (Nature Online). A biosensor consists of three parts: a component that recognizes the analyte and produces a signal, a signal transducer, and a reading device. A biosensor is an analytical device, applied for the detection of a chemical substance, that combines a biological component with a physicochemical detector. The research related to biosensors is extensive and documented (Allen 1994; Bergamasco et al. 2000; Cabral et al. 2017; DeLoach and Droleskey 1993; Garin et al. 1995; Glaxier and McCurley 1995; Guerrieri et al. 1997; Hill et al. 1997; Horiuchi et al. 1997; Korpan et al. 1999; Lee et al. 2015; Li and Rosenzweig 1997; Liang et al. 2000b, 2011; Liu et al. 1997; Magnani et al. 1993; Marazuela et al. 1997; Marazuela and Moreno-Bondi 1998; Marzouk et al. 1999; Sirisha et al. 2016; Vidal et al. 1999).
Conclusion
From the points made in different sections, it may be concluded as under:
- 1. The chemistry and biology of immobilized enzymes are an important field in applied context, and thus, it will continue growing opening new vistas due to their future applications as biosensors and bioreactors, pharmaceuticals and industry in general.
- 2. The classification of immobilized enzymes may be revised to divide them into two major classes: naturally immobilized enzymes and artificially immobilized enzymes, while artificially immobilized enzymes may be sub-classified as done in 1971.
- 3. The naturally immobilized enzymes can be used to hydrolyze proteins to prepare amino acids that can be used to prepare drips for instantaneous supply of nutrients to nutritionally deficient patients.
- 4. The immobilized enzymes can be filled in the dialyzers to remove poisons from the human blood particularly of the kidney patients.
