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Oxygen sensitivity of NifA protein of Azospirillum lipoferum FS as suggested by gene cloning and expression in Escherichia coli.

作者信息

Shigematsu T, Inoue A, Hidaka M, Masaki H, Uozumi T

机构信息

Department of Biotechnology, Graduate School of Agricultural and Life Sciences, University of Tokyo, Japan.

出版信息

Biosci Biotechnol Biochem. 1997 May;61(5):768-71. doi: 10.1271/bbb.61.768.

DOI:10.1271/bbb.61.768
PMID:9178550
Abstract

We cloned and sequenced a 2.8-kb SalI fragment of Azospirillum lipoferum FS as a homologue of the Klebsiella oxytoca nifA gene. The amino acid sequence deduced from an open reading frame of 1872 bases showed 91% identity to that of the A. brasilense NifA, and the putative central sigma54 interaction domain was conserved as well as the C-terminal DNA-binding domain. The NifA function on the nifH promoter was examined in Escherichia coli using a combination of a nifA driver plasmid and a nifH-lacZ reporter plasmid, in which the transcriptional activation of the nifH promoter by the NifA was evaluated with the beta-galactosidase activity. The A. lipoferum NifA activated the nifH promoter solely under microaerobic conditions, while the K. oxytoca NifA activated it irrespective of the oxygen condition. These observations suggest that oxygen sensitivity is an intrinsic property of the A. lipoferum NifA.

摘要

相似文献

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Oxygen sensitivity of NifA protein of Azospirillum lipoferum FS as suggested by gene cloning and expression in Escherichia coli.
Biosci Biotechnol Biochem. 1997 May;61(5):768-71. doi: 10.1271/bbb.61.768.
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