The Usefulness of Transglutaminase for Food ... - ACS Publications

Chapter 3

The Usefulness of Transglutaminase for Food Processing 1

Chiya Kuraishi, Jiro Sakamoto, and Takahiko Soeda

Downloaded by UNIV OF ROCHESTER on June 24, 2013 | http://pubs.acs.org Publication Date: August 13, 1996 | doi: 10.1021/bk-1996-0637.ch003

Food Research and Development Laboratories, Ajinomoto Co., Inc., 1-1 Suzuki-cho, Kawasaki-ku, Kawasaki-shi, 210 Japan

Transglutaminase (TG) is an enzyme that catalyzes the crosslinking reaction between glutamine residues and lysine residues in protein molecules. This crosslinking results in many unique effects on protein properties through the Є-(γ-glutamyl)lysyl peptide bonds. Ajinomoto Co., Inc., and Amano Pharmaceutical Co., Ltd., have found a new transglutaminase in a microorganism (MTG) and are the first in mass production and commercialization of this enzyme. This transglutaminase has various effects on the physical properties of food proteins, gelation capability, thermal stability, water -holdingcapacity, etc.

Transglutaminase (E.C. 2.3.2.13) (TG) is an enzyme that catalyzes an acyltransfer reaction between the 7-carboxyamide group of peptide- or protein bound glutaminyl residues and primary amines (1) (Fig. 1-a). When transglutaminase acts on protein molecules, they are cross-linked and polymerized through e-(7-glutamyl)lysyl peptide bonds [e-(7-Glu)Lys bond] (Fig. 1-b). In the absence of suitable primary amines or in the case that the e-amine of lysine is blocked by certain chemical reagents, e.g., citraconic anhydride, it is possible to make water act as the acceptor, and the glutamyl residue changes to a glutaminyl residue by deamidation through transglutaminase reaction (2) (Fig. 1-c). There is no appropriate blocking reagent that is safe and edible, and this deamidation reaction is not utilized in food industry. Transglutaminase is widely distributed in the nature and has been found in various animal tissues, fish, plants, and micro organisms (3-6). For example, transglutaminase in human blood is known as factor XIII. It takes part in a human blood clotting system that forms crosslinks 1

Current address: Ajinomoto Europe Sales GMBH, Stubbenhuk 3, 20459 Hamburg, Germany

0097-6156/%/0637-0029$15.00/0 © 1996 American Chemical Society

In Biotechnology for Improved Foods and Flavors; Takeoka, G., et al.; ACS Symposium Series; American Chemical Society: Washington, DC, 1996.

30

BIOTECHNOLOGY FOR IMPROVED FOODS AND FLAVORS


of fibrin molecules and stabilizes fibrin polymer. The transglutaminase-mediated crosslinking of protein units cause drastic physical changes not only in biological systems but also in protein-rich foods. Many studies are being carried out to use the enzyme for food industry as a protein modifier having unique effects. But most of these studies have been done by using mammal transglutaminase which was too expensive to utilize on an industrial scale. Recently, for the first time by anyone in the world, we have succeeded in mass production and commercialization of transglutaminase by a fermentation method in association with Amano Pharma ceutical. This new transglutaminase from microorganism (MTG) is generally very useful in the food industry. Properties of Microorganism Transglutaminase Measuring Transglutaminase Activity. Enzymic activity of transglutaminase is measured by the hydroxamate procedure with N-carbobenzoxy-L-glutaminylglycine (Z-Gln-Gly) (Fig. 2). The enzymic activity unit is defined as the amount causing the formation of 1 /zmole of hydroxamic acid in one minute at 37°C (7). Enzymological Properties of MTG. MTG is active over a wide range of temperature and the optimal temperature is 50°C. It is stable between pH 5-9, which is the pH range for most food processing (4). As contrasted with mammal transglutaminase (guinea pig liver transglutaminase), MTG is characterized by its calcium independent activity (4) (Table I). MTG is able to react without adding calcium ion so that it is easier to handle and more practical to use in food processing. The €-(7-Glutamyl)lysyl peptide bonds The Effect on Physical Properties. The most effective reaction of MTG is the crosslinking through e-(7-Glu)Lys bonds (Fig. 1-b). When e-amino groups of lysine residues act as acyl acceptors, e-(7-Glu)Lys crosslinks are formed. The crosslinking reaction may be both intermolecular and intramolecular and causes significant physical property changes in protein-rich foods. The e-(7-Glu)Lys bonds are covalent bonds which are stable unlike ionic bonds and hydrophobic bonds. Therefore, even the few e-(7-Glu)Lys bonds in foods have a profound effect on the physical properties. Nutritional Values. There are some chemicals, e.g., glutaraldehyde, known to be able to act as crosslinking reagents, but these are not allowed in foods because of food safety considerations. Polymerization by enzymes is much more mild because biological transformations are considered safer than chemical reactions. Moreover, with respect to nutritional values, the bioavailability of e-(7-Glu)Lys crosslinks has been reported by several researchers (8-10). The nutritional value of MTG-treated casein has been examined, and it has been confirmed that the crosslinked proteins have no adverse effect and can be absorbed in the body (77). The analytical method for estimating e-(7-Glu)Lys bonds in foods was investigated and it has been confirmed that e-(7-Glu)Lys bonds exist in a number of general



3.

Usefulness of Transglutaminase for Food Processing

KURAISHIET AL.

i

i

(a)

Gln-C-NH + ' 0

RNH

(b)

Gln-C-NH +NH -Lys

2

>• G l n - C - N H R ' O

2

I I

I

H

?

0

2

I

I

C=0 NH

>•

II

O

Figure 1.

Z-Gln-Gly

I

J

I

3

I

G l n - C - N H ? + HOH

I

3

>• G l n - C - N H - L y s + N H

I (c)

I

+ NH

G i n - C ~ OH

I

II

+ NH3

*

O

General reactions catalyzed by transglutaminases. (a) acyl-transfer reaction (b) crosslinking reaction (c) deamidation

Transglutaminase

9

'

^

NH2OH

Figure 2.

V NH3

z

_ ln-Gly G

C=0 NH ^

F e

ci

Ferric complex 3

(measure absorbance at 525nm

Hydroxamate procedure.


31

32



Table I. Calcium Independent Activity of MTG MTG

GTG 0%

OmM CaCl

2

100%

ImM CaCl

2

100%

39%

5mM CaCl2

99%

100%

a

Guinea pig liver transglutaminase

MTG conc.(U/g protein) Figure 3. Effect of MTG treatment on gel strength of soy protein and amount of e-(7-Glu)Lys bonds of soy protein incubated at pH 7.0 at 37°C for 1 hr. Protein concentration: 10 (w/w%).


3. KURAISHIET AL. foods (12). consumed.


Thus, foods containing €-(?-Glu)Lys bonds are already being


Changes through e-(7-Glu)Lys bond formed by Transglutaminase. e-(7-Glu)Lys bonds cause unique effects on proteins. Those effects are very useful for many kinds of foods containing proteins and help to increase their commercial value. Gelation Capability. Even a protein solution that can not form a gel by itself usually will turn into a gel if transglutaminase is used to form crosslinks in such proteins. In the case of protein that has gelation capabilities, the protein gel becomes firmer through the transglutaminase treatment. A caseinate solution will not form a gel by itself. When MTG is added to a caseinate solution at 5 units/g protein, a gel is formed from the liquid phase after 1 hr incubation at pH 7 at 37°C. It is known that soy protein and myosin will gel with heat treatment. If transglutaminase is added, such protein solutions will form gels without heat treatment (13). These changes in gelation capabilities are due to e-(7-Glu)Lys bond formation. The firmness of the gel from soy protein isolate (SPI), prepared by the MTG treatment at pH 7 at 37°C, is related to the number of e-(7-Glu)Lys bonds (Fig. 3). The breaking strength of the gel is increased as the number of e-(7-Glu)Lys bonds increase. It is interesting to note that if too much MTG is added, the firmness of the gel is decreased, an unexpected result. A gel formed with a ten percent caseinate solution treated with MTG 20 units/g protein at 37 °C at pH 6.5 is weaker than a gel formed with MTG 15 units/g protein (Fig. 4). There may be a limit to the ability of €-(7-Glu)Lys bonds to improve gel strength, and perhaps an excess of e-(7-Glu)Lys bonds may weaken the gel structure. Such a gel formed with an excess of e-(7-Glu)Lys bonds by use of transglutaminase becomes weak and has less water-holding capacity. Sometimes syneresis, a separation of liquid from a gel, is observed. We hypothesized that excess €-(7Glu)Lys bonds would inhibit uniform develpment of the protein network for entraining sufficient water. Viscosity. When a protein is polymerized and increases in molecular weight, a solution of it usually increases in viscosity. Therefore, a protein solution treated with MTG increases in viscosity. Caseinate solutions treated with various concentrations of MTG at pH 6.5 at 55°C for 30 minutes were heated to deactivate the enzyme and to stop the crosslinking reaction. After freeze-drying, the MTG-treated caseinate powder was rehydrated, and the viscosity of caseinate solution was determined. The caseinate gel gets more viscous at higher enzyme concentrations (Fig. 5). Formation of cross-linked caseinate was confirmed by SDS-PAGE (data not shown). The monomer fractions of caseinate diminished or disappeared, and polymer fractions (dimers and trimers) increased. Polymer fractions which did not enter the running gels were formed by MTG treatment at above 3 units/g protein. With more reaction (longer time, more enzyme added, higher temperature, etc.) a caseinate solution can be transformed to a gel. Sols of various viscosities, not gels, can be prepared by controlling the enzyme reaction conditions, i.e. reaction time, temperature, concentration of enzyme added, etc.


33


34


0

10 20 MTG conc.(U/g protein)

Figure 4. Effect of MTG on gel strength of caseinate solution incubated at pH 6.5 at 37°C for 1 hr. Protein concentration: 10 (w/w%).

100000

10000 CJ

•~ o o

1000

0

1

2

3

4

5

6

MTG conc.(U/g protein) Figure 5.

Viscosity of MTG-treated sodium caseinate.



3.

KURAISHIET AL.


Thermal Stability. As described above, e-(7-Glu)Lys bonds formed by transglu taminase reaction are covalent bonds and stable even with temperature changes. The thermal stability of protein gel structure transglutaminase-treated is improved by e-(7-Glu)Lys bonds formed inter/intra protein molecules. Gelation of gelatin is a phenomenon dependent on thermal changes, and the gels are thermoreversible. The gelatin gel is stabilized by hydrophobic bonds, so if it is heated to certain temperatures, it turns to a sol or solution state. If a gelatin gel is treated with MTG, a few c-(7-Glu)Lys bonds are introduced into its structure, and its thermostability is significantly improved. Jelly products stable to high temperatures can be produced. Table II shows the thermal stability data by MTG treatment. A gelatin gel difficult to melt even at 120°C can be prepared depending on the gelatin concentration and enzyme reaction conditions. Water-holding Capacity. A gel formed with e-(7-Glu)Lys bonds with MTG has improved water-holding capacities. Gelatin gel holds water molecules in its protein matrix structure, and it is possible to form stable aqueous gel even at 2% protein concentration. Gelatin gel is a good representative of a water-holding protein gel. Food gels, such as sausages and yogurts, often have problems of syneresis, separation of a solution from the gel, so that gelatin is usually added to such food gels to improve water-holding capacities. Food gels treated with transglutaminase, which forms more stable covalent bonds, e-(7-Glu)Lys bonds, are able to hold more water in spite of temperature changes or physical shocks. For example, yogurt, which is an acid milk gel formed by gradual acidification with a lactic starter, has some problems of serum separation with a change of temperature or physical impact. As shown in Fig. 6, yogurt which is made from MTG-treated milk has a larger capacity for holding water, and the whey syneresis is prevented. With use of transglutaminase, food gel products with good water-holding capacities can be produced without adding gelatin. Applications in the Food Industry Binding Food Pieces (Restructured Meat). The function of transglutaminase, which is capable of crosslinking protein molecules, is to bind pieces of food together. In order to bind pieces of meat, it has been necessary to restructure meat. These restructured products have been developed to utilize low-value, small meat pieces and to enhance their market value. The conventional way is to bind meat pieces to each other with salt-extracted (cured) muscle protein, with heat treatment if necessary. Recently, a new useful binding system was developed by utilizing MTG. Meat or fish pieces can be bound together using only the enzyme. Binding can be improved by using transglutaminase and caseinate (Fig.7). Caseinate treated with transglutaminase becomes more viscous, and viscous caseinate acts as a stable glue which can be used to hold together different foodstuffs. It is possible to bind meat cubes or thin fish fillets and to make larger beef steaks or larger fish fillets. Heating and/or freezing is not needed to get good binding with transglutaminase. Reformed meat/fish products can be prepared for distribution in the chilled state. Uniform products from various sized or shaped meats and fish portion by using MTG leads to effective utilization and added-value enhancement of food resources. In Biotechnology for Improved Foods and Flavors; Takeoka, G., et al.; ACS Symposium Series; American Chemical Society: Washington, DC, 1996.

35

36


Table II. Thermostability of MTG-treated Gelatin Gel

20 minute

Gel appearance after incubation for 20 minute at 100 °C Fluid

30 minute

Weak gel

60 minute

Gel


MTG reaction time

0

1 3 5 MTG cone. (U/g protein)

10

Figure 6. Effect of MTG treatment on water-holding capacity of the acid milk gel (set-type yogurt). MTG was added to reconstituted milk solution and incubated at 25°C for 2 hr. After enzyme reaction, the lactic starter was added, and the acid milk gel, set-type yogurt, was prepared after 4-6 hr fermentation.



3.

KURAISHIET AL.


Figure 7. Effect of MTG and caseinate on binding strength of restructured meat. Raw pork meat cubes that had MTG and caseinate added were put into a mold and incubated at 5°C for 2 hr. Reformed meat was sliced and the binding strength was measured.

Health Demands. In processing of prepared foods, especially meat products, salt and/or some phosphates is/are usually added to increase water-holding capacity, binding, consistency, and to improve texture. Recently, as health demands increase, prepared foods with reduced salts or phosphates are distributed widely and have glutted the food industry. However, these healthy foods with reduced salts or phosphates have undesirable texture and physical properties. With the use of transglutaminase for preparing these "healthy" meat products, binding capacity, water-holding capacity, and viscosity are improved through e-(7-Glu)Lys crosslinks. For example, the breaking strength of the low-salt sausage, in which the salt content was reduced from 1.7% to 0.4%, decreased by 20% as compared with the control sausage containing 1.7% salt. But the addition of MTG 2 units/g protein recovered the decreased quality of the texture of the low-salt sausage and enhanced the breaking strength equal to that of the control sausage. Healthy prepared foods can be enjoyed which have higher qualities than those previously prepared. Improvement of Yogurt Quality. Milk proteins are also good substrates for transglutaminase. As previously stated, die problems of serum separation of yogurt can be solved by adding transglutaminase, which improved the waterholding capacity of the gel (Fig. 6). MTG treatment improves qualitites other than syneresis. Gel strength of set-type yogurt and viscosity of stirred yogurt are much more acceptable sensorially. Because transglutaminase treatment improves gel strength and increases the viscosity of protein solutions (sols), MTG gives good physical qualities and sensory properties to set-and stirred yogurt. When the yogurt was treated with MTG 3 units/g protein at 25°C for 2 hr, the breaking strength of the set-type yogurt was increased from 15 g/cm to 32 g/cm . Excess 3

3


37


38


enzyme treatment, however, does not produce the same effect. The set-type yogurt treated with MTG 10 units/g protein was weaker than the gel treated with 5 units/gram protein. This result suggests that the excessive formation of €-(7Glu)Lys bonds in intra/intermolecular proteins may inhibit the network formation of the yogurt gel. The optimal reaction conditions are at 25°C for 2 hr, 1-5 unit/g protein of MTG. Stabilizers are often used during the manufacture of yogurt to enhance and maintain the desirable characteristics in yogurt. Their mode of action in yogurt includes two basic functions: the binding of water and increase in viscosity. The effect of MTG, preventing syneresis and improving viscosity, is that of a stabilizer. Many unique characteristics in protein properties are obtained by introducing e-(7-Glu)Lys bonds into proteins by the use of transglutaminase. In the research of protein gel structure and conformation, the formation of e-(7-Glu)Lys bonds provides many interesting topics to be discussed. In Japan, the use of our microbial transglutaminase, MTG, is dramatically increasing as an innovative ingredient for food processing because of the recognition of its unique characteristics. We are expanding the applications of transglutaminase and hope that the use of MTG will contribute to the global food industry. Literature Cited 1. Folk, J.E. Adv. Enzymol. 1983, 54, 1-56. 2. Motoki, M . ; Seguro,K.; Nio, N.; Takanami, K. Agric. Biol. Chem. 1986, 50, 3025-3030. 3. Folk, J.E. Ann. Rev. Biochem. 1980, 49, 517-531. 4. Ando, H.; Adachi, M.; Umeda, K.; Matsuura, A.; Nonaka, M.; Uchio, R.; Tanaka, H.; Motoki, M. Agric. Biol. Chem. 1989, 53, 2613-2617. 5. Yasueda, H.; Kumazawa, Y.; Motoki, M. Biosci. Biotech. Biochem. 1994, 58, 2041-2045. 6. Icekson, I.; Apelbaum, A. Plant Physiology, 1987, 84, 972-974. 7. Folk, J.E.; Cole, P.W. J. Biol. Chem. 1966, 241, 5518-5525. 8. Raczynski, G.; Snochowski, M . ; Buraczewski, S. Br. J. Nutr. 1975, 34, 291-296. 9. Finot, P.-A.; Mottu, F.; Bujard, E . ; Mauron, J.; In Nutritional Improvement of Food and Feeds Proteins; Friedman, M . , Ed.; Plenum: London, 1978; pp 549-570. 10. Friedman, M . ; Finot, P.-A. J. Agric. Food. Chem. 1990, 38, 2011-2020. 11. Seguro, K. et. al., J. of Nutr. submitted for publication. 12. Sakamoto, H.; Kumazawa, Y; Kawajiri, H.; Motoki, M . J. Food. Sci. 1965, 60, 416-419. 13. Nonaka, M . ; Tanaka, H.; Okiyama, A.; Motoki, M . ; Ando, H.; Umeda, K.; Matsuura, A. Agric. Biol. Chem. 1989, 53, 2619-2623.


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