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3. FOOD ChEMISTRy & bIOTEChNOLOGy 3.1. Lectures

3. FOOD ChEMISTRy & bIOTEChNOLOGy 3.1. Lectures

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Chem. Listy, 102, s265–s1311 (2008) Food Chemistry & Biotechnology<br />

At 80 ml of water, 2 ml of the oil and 50 µl enzymatic<br />

preparations was added in to the separatory funnel. One<br />

of the separatory funnel was used as a control. The volume<br />

of the separatory funnel was mixed and within 20 min the<br />

sample of the water phase was taken to determine chemical<br />

oxygen demand (COD).<br />

Results<br />

S p i r i t B l u e A g a r ( D e t e c t i o n o f<br />

L i p o l y t i c A c t i v i t y )<br />

The lipolytic microorganisms metabolized the lipid in<br />

the medium and form colonies with halos indicating lipolysis.<br />

It was found out, that in all tested microorganism preparations<br />

were presented and formed colonies with halos indicated<br />

lipolysis.<br />

Fig. 1. bacterial colonies with halos indicating lipolysis<br />

L i p o l y t i c A c t i v i t y<br />

Cultivation on agar plates. The highest value of the<br />

lipolytic activity was determined at EP 1, the lowest lipolytic<br />

activity was determined at EP <strong>3.</strong><br />

The highest calculated value was found in supernatant<br />

of EP 1 by anaerobic conditions, value of the activity was<br />

a = 9. 16 × 10 –3 mmol min –1 , the lowest value was in sediment<br />

of EP 3 by aerobic conditions, (a = 1 × 10 –4 mmol min –1 ).<br />

Lipolytic activity was detected at all five enzymatic preparations.<br />

Table I<br />

Lipolytic activity in 5 of enzymatic preparations (expression<br />

a × 10 –3 mmol min –1 )<br />

eP aerobe anaerobe<br />

supernatant sediment supernatant sediment<br />

1 7.11 1.96 8.79 2.95<br />

2 6.59 1.40 8.51 2.86<br />

3 5.04 0.10 7.25 1.77<br />

4 5.44 1.19 7.42 2.48<br />

5 8.52 2.32 9.16 <strong>3.</strong>28<br />

s661<br />

Fig. 2. Comparsion values of the lipolytic activity for the individual<br />

enzymatic preparations<br />

Submers cultivation. The highest activity was measured<br />

on the 10 th day of the cultivation. The decrease of activity<br />

was registered on the 10 th day. The highest activity had the<br />

enzymatic preparation 5 and the lowest had the enzymatic<br />

preparation <strong>3.</strong><br />

Table II<br />

Relativic activity a rel [%] in enzymatic preparations during<br />

submers cultivation<br />

eP<br />

[days]<br />

1 2 3 4 5<br />

2 62.97 5<strong>3.</strong>09 46.06 50.32 7<strong>3.</strong>56<br />

6 8<strong>3.</strong>26 74.35 66.98 68.69 85.46<br />

8 84.73 78.74 75.54 77.82 94.15<br />

10 100.00 100.00 100.00 100.00 100.00<br />

14 75.52 68.73 62.23 6<strong>3.</strong>50 90.00<br />

3 . 3 L i p i d D e g r a d a t i o n a n d F a t t y<br />

A c i d s U t i l i z a t i o n<br />

Results of the determination demonstrate at Table III<br />

and at Fig. <strong>3.</strong><br />

Table III<br />

% free fatty acids of EP during submers cultivation<br />

EP1 EP2 EP3 EP4 EP5 days<br />

9.69 10.07 14.87 <strong>3.</strong>68 <strong>3.</strong>72 2<br />

1<strong>3.</strong>04 37.74 19.02 4.75 25.43 6<br />

48.91 48.42 3<strong>3.</strong>28 7.13 39.02 8<br />

66.57 56.5 40.75 37.66 48.04 10<br />

20.1 22.83 26.49 20.38 26.15 14

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