Biodegradation of different molecular-mass polyphenols derived from olive mill wastewaters by Geotrichum candidum

被引:33
作者
Asses, Nedra [1 ]
Ayed, Lamia [1 ]
Bouallagui, Hassib [1 ]
Sayadi, Sami [2 ]
Hamdi, Moktar [1 ]
机构
[1] INSAT, Lab Ecol & Technol Microbienne, Tunis 1080, Tunisia
[2] Ctr Biotechnol Sfax, Lab Bioprocedes, Sfax 3038, Tunisia
关键词
Geotrichum candidum; Olive mill wastewater; Polyphenols; Decolourisation; Lignin peroxidase; Manganese peroxidase; AEROBIC BIOLOGICAL TREATMENT; WASTE-WATER; PHANEROCHAETE-CHRYSOSPORIUM; PLEUROTUS-OSTREATUS; MANGANESE PEROXIDASE; LIGNIN PEROXIDASE; ASPERGILLUS-NIGER; DECOLORIZATION; DECOLOURIZATION; PURIFICATION;
D O I
10.1016/j.ibiod.2008.11.005
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The decolourisation of fresh and stored olive mill wastewaters (OMW) and the biodegradation of three groups (F1, F2 and F3) of phenolic compounds by Geotrichum candidum were investigated. Separated phenolic compounds derived from natural OMW ultrafiltration using membranes with a cutoff 2 and 100 kDa. G. candidum growth on fresh OMW decreased pH and reduced COD and colour of 75% and 65%, respectively. However, on the stored-black OMW a failure of COD and colour removal were observed. G. candidum activity on this later substrate was enhanced by the addition of a carbon source easily metabolised, misleading an improvement of the COD reduction and decolourization that reached 58% and 48%, respectively. Growth of G. candidum in the presence of F2 or F3 polyphenolic fractions induced high decolourisation and depolymerisation of phenolic compounds. Whereas, very week decolourisation and biodegradation were observed with F1 fraction. Moreover, the highest levels of lignin peroxidase (UP) and manganese peroxidase (MnP) activities were obtained in the presence of F2 fraction. These results showed that increasing of molecular-mass of aromatics led to an increase in levels of depolymerisation, decolourisation and COD removal by G. candidum culture. (C) 2008 Published by Elsevier Ltd.
引用
收藏
页码:407 / 413
页数:7
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