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2.7 Enzyme Utilization in the Food Industry 149

2.7.2 Individual Enzymes

2.7.2.1 Oxidoreductases

Broader applications for the processing industry,

besides the familiar use of glucose oxidase, are

found primarily for catalase and lipoxygenase,

among the many enzymes of this group. A number

of oxidoreductases have been suggested or

are in the experimental stage of utilization, particularly

for aroma improvement (examples under

2.7.2.1.4 and 2.7.2.1.5).

2.7.2.1.1 Glucose Oxidase

The enzyme produced by fungi such as Aspergillus

niger and Penicillium notatum catalyzes

glucose oxidation by consuming oxygen from

the air. Hence, it is used for the removal of

either glucose or oxygen (Table 2.20). The H 2 O 2

formed in the reaction is occasionally used as an

oxidizing agent (cf. 10.1.2.7.2), but it is usually

degraded by catalase.

Removal of glucose during the production of egg

powder using glucose oxidase (cf. 11.4.3) prevents

the Maillard reaction responsible for discoloration

of the product and deterioration of its

whippability. Similar use of glucose oxidase for

some meat and protein products would enhance

the golden-yellow color rather than the brown

color of potato chips or French fries which is obtained

in the presence of excess glucose.

Removal of oxygen from a sealed package system

results in suppression of fat oxidation and oxidative

degradation of natural pigments. For example,

the color change of crabs and shrimp from

pink to yellow is hindered by dipping them into

a glucose oxidase/catalase solution. The shelf life

of citrus fruit juices, beer and wine can be prolonged

with such enzyme combinations since the

oxidative reactions which lead to aroma deterioration

are retarded.

2.7.2.1.2 Catalase

The enzyme isolated from microorganisms is important

as an auxiliary enzyme for the decomposition

of H 2 O 2 :

(2.108)

Hydrogen peroxide is a by-product in the treatment

of food with glucose oxidase. It is added to

food in some specific canning procedures. An example

is the pasteurization of milk with H 2 O 2 ,

which is important when the thermal process is

shut down by technical problems. Milk thus stabilized

is also suitable for cheesemaking since the

sensitive casein system is spared from heat damage.

The excess H 2 O 2 is then eliminated by catalase.

2.7.2.1.3 Lipoxygenase

The properties of this enzyme are described under

section 3.7.2.2 and its utilization in the bleaching

of flour and the improvement of the rheological

properties of dough is covered under section

15.4.1.4.3.

2.7.2.1.4 Aldehyde Dehydrogenase

During soya processing, volatile degradation

compounds (hexanal, etc.) with a “bean-like”

aroma defect are formed because of the enzymatic

oxidation of unsaturated fatty acids. These

defects can be eliminated by the enzymatic

oxidation of the resultant aldehydes to carboxylic

acids. Since the flavor threshold values of

these acids are high, the acids generated do not

interfere with the aroma improvement process.

(2.109)

Of the various aldehyde dehydrogenases, the

enzyme from beef liver mitochondria has

a particularly high affinity for n-hexanal (Table

2.21). Hence its utilization in the production

of soya milk is recommended.

2.7.2.1.5 Butanediol Dehydrogenase

Diacetyl formed during the fermentation of beer

can be a cause of a flavor defect. The enzyme

from Aerobacter aerogenes, for example, is able

to correct this defect by reducing the diketone to

the flavorless 2,3-butanediol:

(2.110)

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