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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 />

The material hydrophobicity was determined by contact<br />

angle measurement. The results are summarised in the<br />

Table I. If value of contact angle is less than 90 ° the material<br />

is considered to be hydrophilic, if contact angle is greater<br />

than 90 ° the material is hydrophobic.<br />

The cell hydrophobicity was determined by the BATH<br />

test. It was found that Rhodococcus erythropolis belongs to<br />

microorganisms with hydrophobic cell envelope character;<br />

the determined hydrophobicity is 89.0 ± 6.3 %.<br />

The quantity of proteins and saccharides in EPS is<br />

shown in the Table II. Both proteins and saccharides amount<br />

is approximately two times higher in biofilm EPS from silicon<br />

carriers.<br />

Table II<br />

The concentration of saccharides and proteins in EPS<br />

EPS composition<br />

silicon glass<br />

Saccharides 4.9 2.7<br />

Proteins 4.8 2.5<br />

Rate of adhesion during initial period of cultivation was<br />

determined by the method of image analysis. Results have<br />

shown (Table III) that silicone is colonized more rapidly<br />

and better that glass. Small colonies were visible on silicone<br />

materials immediately after beginning of cultivation. Their<br />

area increased in time.<br />

Table III<br />

Portion of carrier occupied area by biofilm<br />

Image analysis<br />

1h 24h<br />

colonized area [%] 0.0 0.2<br />

glass number of objects in the<br />

measured area<br />

0 46<br />

colonized area [%] 12.5 47.9<br />

silicone number of objects in<br />

measured area<br />

1,394 1,103<br />

The biofilm experiments were carried out in glass<br />

columns (Ø = 5 cm, volume 220 ml). The silicone and glass<br />

tubes (external diameter 0.5 cm, 1.0 cm length) were chosen<br />

as carriers. The biofilm growth was the first stage of<br />

the process. The cells were cultivated in columns in mineral<br />

medium (BSM) with phenol (concentration 0.3 g dm –3 ,<br />

changed at regular intervals) for 3 weeks at 20 °C. After this<br />

period the stabilized biofilm was used for phenol degradation.<br />

The results are summarised in the Fig. 2. The biofilm<br />

concentration on glass (silicone) tubes was 4.1 (8.7) g dm –3 ,<br />

respectively. The concentration of suspended cells in medium<br />

s704<br />

was lower in column with silicon tubes than in column with<br />

glass ones. The phenol was totally degraded in column with<br />

glass/silicone after 65 h/90 h, respectively.<br />

Fig. 2. Phenol biodegradation by biofilm of rhodococcus<br />

erythopolis. The cultivation was carried out in glass columns<br />

with two types of carrier (glass and silicone tubes, external diameter<br />

0.5 cm, length 1 cm). The biomass was measured as total<br />

protein concentration at 595 nm<br />

The comparison of the biodegradation rates of the pollutants<br />

are summarised in the Table IV. Results indicate that<br />

catechol has a lower degradation rate than phenol. The highest<br />

biodegradation rate is reached in biofilm system with<br />

glass carriers.<br />

Table IV<br />

Comparison of biodegradation rate of the pollutants by suspended<br />

and sessile cells<br />

Biodegradation rate<br />

Suspended<br />

cells<br />

Biofilm<br />

Phenol Catechol<br />

0.7 g dm –3 0.7 g dm –3<br />

<strong>3.</strong>89 1.61<br />

glass silicon not tested in<br />

12.01 4.09 glass collums<br />

Conclusions<br />

It was found out that Rhodococcus erythroposlis cells<br />

better colonize silicone carriers to glass ones. Although the<br />

biomass concentration on glass carriers was two times lower<br />

the biodegradation rate was three times higher than in system<br />

with silicone. This indicates that only a part of biofilm is<br />

metabolically active. Results confirmed the hypothesis of higher<br />

biodegradation velocity of pollutants in biofilm system.

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