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720 15 Cereals and Cereal Products

Fig. 15.37. The effect of a proteinase preparation on resistance

to extension (in extensogram units) of a wheat

flour dough (according to Sproessler, 1980). Proteinase

preparation: 1 fungal, 2 papain, and 3 bacterial. U Hb

proteinase activity units determined with hemoglobin

as a substrate

Fig. 15.36. Farinograms. Effect of L-cysteine hydrochloride

on a flour with strong gluten (according to

Finney et al., 1971). A control (no addition), B cysteine

added (120 ppm)

of the dough decreases and the extensibility

increases (cf. Table 15.42). Decreases in dough

development time and dough stability, as shown

in farinograms (Fig. 15.36), clearly reveal the

addition of cysteine. Flours with strong gluten

and with optimum levels of cysteine also show

a favorable increase in baking volume since,

prior to baking, the gas trapped within the dough

can develop a more spongy dough. The action of

sodium sulfite is similar to that of cysteine.

15.4.1.4.5 Proteinases (Peptidases)

Proteinase preparations of microbial or plant origin

are used for dough softening (cf. 2.7.2.2.1).

Their action involves protein hydrolysis, i. e.,

gluten-protein endo-hydrolysis. Their effect on

dough rheology, therefore, depends on the nature

of the enzymes and the activity of the preparations

towards gluten proteins. This is shown

in Fig. 15.37. Despite equal hydrolase activities

with hemoglobin as a test substrate, a fungal

proteinase degrades gluten to a lesser extent

and consequently causes a smaller decrease in

dough resistance to extension in comparison to

a bacterial enzyme preparation. Also, the latter is

more effective than papain.

Fungal proteinases, because of their low enzyme

activity and, therefore, high dosage tolerance,

are suitable for optimization of flours containing

strong gluten, used for bread and buns. However,

bacterial enzymes are preferred in production of

biscuits and wafers since they degrade gluten

to a greater extent, providing accurate flat

dough pieces with high form stability. Bacterial

enzymes are also preferred for the desirable

end product qualities of porosity and breaking

strength.

Data are shown in Table 15.45 for white bread

prepared with and without papain. There is

a rise in the content of both free amino acids

in the crumb and volatile carbonyl compounds

in the crust when proteinase is used. As long

as proteinases are active in a baking process,

they release amino acids from flour proteins,

which are then changed via Strecker degradation

Table 15.45. Effects of papain addition in white bread

making (values in µmole/g dry matter)

Constituent Without With

papain papain

Free amino acids Dough 183 186

Crumb 182 272

Crust 10 15

Volatile carbonyl

compounds Crust 158 217

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