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来自不动杆菌属菌株ADP1的烷烃羟化酶的表达可被多种正构烷烃诱导,并且需要转录激活因子AlkR。

Expression of alkane hydroxylase from Acinetobacter sp. Strain ADP1 is induced by a broad range of n-alkanes and requires the transcriptional activator AlkR.

作者信息

Ratajczak A, Geissdörfer W, Hillen W

机构信息

Lehrstuhl für Mikrobiologie, Institut für Mikrobiologie, Biochemie und Genetik der Friedrich-Alexander-Universität Erlangen-Nürnberg, 91058 Erlangen, Federal Republic of Germany.

出版信息

J Bacteriol. 1998 Nov;180(22):5822-7. doi: 10.1128/JB.180.22.5822-5827.1998.

Abstract

In Acinetobacter sp. strain ADP1, alkane degradation depends on at least five essential genes. rubAB and xcpR are constitutively transcribed. Here we describe inducible transcription of alkM, which strictly depends on the presence of the transcriptional activator AlkR. alkR itself is expressed at a low level, while a chromosomally located alkM::lacZ fusion is inducible by middle-chain-length alkanes from heptane to undecane, which do not support growth of ADP1, and by long-chain-length alkanes from dodecane to octadecane, which are used as sources of carbon and energy. The putative AlkM substrate 1-dodecene is also an effective inducer. Products of alkane hydroxylase activity like 1-dodecanol prevent induction of alkM expression. alkM is expressed only in stationary phase, suggesting its dependence on at least one other regulatory mechanism.

摘要

在不动杆菌属菌株ADP1中,烷烃降解至少依赖于五个必需基因。rubAB和xcpR组成型转录。在此,我们描述了alkM的诱导型转录,其严格依赖于转录激活因子AlkR的存在。alkR本身表达水平较低,而染色体定位的alkM::lacZ融合体可被庚烷至十一烷的中链长度烷烃(这些烷烃不支持ADP1生长)以及十二烷至十八烷的长链长度烷烃(用作碳源和能源)诱导。推测的AlkM底物1-十二碳烯也是一种有效的诱导剂。烷烃羟化酶活性产物如1-十二醇可阻止alkM表达的诱导。alkM仅在稳定期表达,表明其依赖于至少一种其他调控机制。

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