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一种肠杆菌对苯酚的降解作用:一株克雷伯氏菌携带一种类TOL质粒和一个编码新型苯酚羟化酶的基因。

Phenol degradation by an enterobacterium: a Klebsiella strain carries a TOL-like plasmid and a gene encoding a novel phenol hydroxylase.

作者信息

Heesche-Wagner K, Schwarz T, Kaufmann M

机构信息

Thgymoorgan GmbH, Vienenburg, Germany.

出版信息

Can J Microbiol. 1999 Feb;45(2):162-71.

Abstract

Although phenol catabolism is described for many different microorganisms, there is no example for such a pathway in an enterobacterial strain. Here we characterize a Klebsiella oxytoca strain that grows on phenol as the only source of carbon and energy. As the key enzyme of phenol degradation, phenol hydroxylase was purified to apparent homogeneity. Compared with other phenol hydroxylases, the Klebsiella enzyme differs with respect to several properties: (i) SDS-PAGE and gel-filtration analysis of the purified protein revealed that the enzyme is a monomer with a molecular mass of 156 kDa; (ii) steady-state kinetic measurements resulted in a K(m) value of 0.22 mM for phenol; and (iii) the enzyme is both dependent on NADPH/FAD and sensitive to EDTA. Further degradation of catechol, the reaction product of phenol hydroxylase, may occur via the effective meta-fission pathway often located on TOL or TOL-like plasmids. Such a plasmid was prepared from the Klebsiella strain and further characterized. The given data demonstrate that the isolated strain exhibits all characteristics of an efficient phenol-degrading microorganism.

摘要

尽管许多不同的微生物都存在苯酚分解代谢现象,但在肠杆菌菌株中尚未发现这样的代谢途径实例。在此,我们对一株产酸克雷伯菌进行了特性描述,该菌株能够以苯酚作为唯一碳源和能源生长。作为苯酚降解的关键酶,苯酚羟化酶被纯化至表观均一性。与其他苯酚羟化酶相比,克雷伯菌的这种酶在几个特性方面存在差异:(i)对纯化蛋白进行SDS-PAGE和凝胶过滤分析表明,该酶是一种分子量为156 kDa的单体;(ii)稳态动力学测量得出苯酚的K(m)值为0.22 mM;(iii)该酶既依赖于NADPH/FAD,又对EDTA敏感。苯酚羟化酶的反应产物儿茶酚的进一步降解可能通过有效的间位裂解途径发生,该途径通常存在于TOL或类TOL质粒上。我们从克雷伯菌菌株中制备了这样一种质粒并对其进行了进一步特性分析。所给出的数据表明,分离出的菌株具备高效苯酚降解微生物的所有特征。

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