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甲烷营养菌-异养菌混合培养物对直链烷基苯磺酸盐(LAS)的生物降解

Biodegradation of linear alkylbenzenesulphonates (LAS) by mixed methanotrophic-heterotrophic cultures.

作者信息

Hrsak D, Grbić-Galić D

机构信息

Center for Marine Research Zagreb, Rudjer Bosković Institute, Croatia.

出版信息

J Appl Bacteriol. 1995 May;78(5):487-94. doi: 10.1111/j.1365-2672.1995.tb03090.x.

DOI:10.1111/j.1365-2672.1995.tb03090.x
PMID:7759381
Abstract

The biodegradation of undecylbenzenesulphonate (C11LAS) was studied in shake flasks at 21 degrees C using two mixed bacterial cultures. The first culture, MM1, contained a type II methanotroph and four heterotrophs, and was enriched from a groundwater aquifer. The second culture, MC, consisted of five heterotrophic strains, most of them belonging to the genus Pseudomonas, and was isolated from the wastewater of a detergent plant. Methane, carbon dioxide and oxygen concentrations were determined by gas chromatography. Concentrations of C11LAS and the aromatic intermediates were determined by reversed-phase HPLC. In spite of faster transformation of the alkyl side-chain by the culture MC, the culture MM1 containing type II methanotroph was capable of further degradation of C11LAS aromatic intermediates (sulphophenylalkanoates). The most probable mechanism for the degradation of the alkyl part of the C11LAS molecule by both cultures was omega-oxidation of the terminal methyl group followed by beta-oxidation. Studies of methane utilization demonstrated an approximately three times higher second-order rate coefficient for methane consumption (kmax/Ks) in the absence of C11LAS. This indicates a possible metabolic activity of methanotrophs in the transformation of the complex LAS molecule due to the methane monooxygenase enzyme system.

摘要

在21摄氏度的摇瓶中,使用两种混合细菌培养物研究了十一烷基苯磺酸盐(C11LAS)的生物降解。第一种培养物MM1包含一种II型甲烷氧化菌和四种异养菌,是从地下水含水层中富集得到的。第二种培养物MC由五种异养菌株组成,其中大多数属于假单胞菌属,是从一家洗涤剂厂的废水中分离出来的。通过气相色谱法测定甲烷、二氧化碳和氧气的浓度。通过反相高效液相色谱法测定C11LAS和芳香族中间体的浓度。尽管培养物MC对烷基侧链的转化速度更快,但含有II型甲烷氧化菌的培养物MM1能够进一步降解C11LAS芳香族中间体(磺基苯基链烷酸酯)。两种培养物对C11LAS分子烷基部分进行降解的最可能机制是末端甲基的ω-氧化,随后是β-氧化。甲烷利用研究表明,在不存在C11LAS的情况下,甲烷消耗的二级速率系数(kmax/Ks)大约高出三倍。这表明由于甲烷单加氧酶酶系统,甲烷氧化菌在复杂LAS分子转化过程中可能具有代谢活性。

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