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Biodegradation of variable-chain-length n-alkanes in Rhodococcus opacus R7 and the involvement of an alkane hydroxylase system in the metabolism

机译:不透明红球菌R7中可变链长正构烷烃的生物降解及烷烃羟化酶系统参与代谢

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摘要

Rhodococcus opacus R7 is a Gram-positive bacterium isolated from a polycyclic aromatic hydrocarbon contaminated soil for its versatile metabolism; indeed the strain is able to grow on naphthalene, o-xylene, and several long- and medium-chain n-alkanes. In this work we determined the degradation of n-alkanes in Rhodococcus opacus R7 in presence of n-dodecane (C12), n-hexadecane (C16), n-eicosane (C20), n-tetracosane (C24) and the metabolic pathway in presence of C12. The consumption rate of C12 was 88%, of C16 was 69%, of C20 was 51% and of C24 it was 78%. The decrement of the degradation rate seems to be correlated to the length of the aliphatic chain of these hydrocarbons. On the basis of the metabolic intermediates determined by the R7 growth on C12, our data indicated that R. opacus R7 metabolizes medium-chain n-alkanes by the primary alcohol formation. This represents a difference in comparison with other Rhodococcus strains, in which a mixture of the two alcohols was observed. By GC-MSD analysis we also identified the monocarboxylic acid, confirming the terminal oxidation.Moreover, the alkB gene cluster from R. opacus R7 was isolated and its involvement in the n-alkane degradation system was investigated by the cloning of this genomic region into a shuttle-vector E. coli-Rhodococcus to evaluate the alkane hydroxylase activity. Our results showed an increased biodegradation of C12 in the recombinant strain R. erythropolis AP (pTipQT1-alkR7) in comparison with the wild type strain R. erythropolis AP. These data supported the involvement of the alkB gene cluster in the n-alkane degradation in the R7 strain.
机译:不透明红球菌R7是革兰氏阳性细菌,其从多环芳香烃污染的土壤中分离,具有多种代谢功能。确实,该菌株能够在萘,邻二甲苯以及几种长链和中链正构烷烃上生长。在这项工作中,我们确定了在存在正十二烷(C12),正十六烷(C16),正二十烷(C20),正十四烷(C24)的情况下,不透明红球菌R7中正构烷烃的降解及其代谢途径。存在C12。 C12的消耗率为88%,C16的消耗率为69%,C20的消耗率为51%,C24的消耗率为78%。降解速率的降低似乎与这些烃的脂族链的长度有关。根据R7在C12上生长所确定的代谢中间体,我们的数据表明,不透明芽孢杆菌R7通过伯醇的形成代谢中链正构烷烃。与观察到两种醇的混合物的其他红球菌菌株相比,这代表了差异。通过GC-MSD分析,我们还鉴定出了单羧酸,确认了末端氧化作用。此外,从不透明红球菌R7中分离出alkB基因簇,并通过将该基因组区域克隆到正链烷烃降解系统中来研究其参与正构烷烃降解系统的过程穿梭载体大肠杆菌 Rhodococcus 评估烷烃羟化酶活性。我们的结果表明重组菌株 R中C12的生物降解增加。与野生型菌株 R相比,赤字型AP(pTipQT1- alk R7)。 erythropolis AP。这些数据支持 alkB 基因簇参与R7菌株的 n -烷烃降解。

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