CalA, a Cyanobacterial AbrB Protein, Interacts with the Upstream Region of hypC and Acts as a Repressor of Its Transcription in the Cyanobacterium Nostoc sp Strain PCC 7120

被引:22
作者
Agervald, Asa [1 ]
Zhang, Xiaohui [1 ,2 ]
Stensjo, Karin [1 ]
Devine, Ellenor [1 ]
Lindblad, Peter [1 ]
机构
[1] Uppsala Univ, Dept Photochem & Mol Sci, Angstrom Labs, SE-75120 Uppsala, Sweden
[2] Purdue Univ, Dept Biol Sci, W Lafayette, IN 47907 USA
关键词
PUNCTIFORME ATCC 29133; BIDIRECTIONAL HYDROGENASE; DNA-BINDING; REGULATOR; METABOLISM; PROMOTER; SEQUENCE; PHYCOBILIPROTEINS; SUPERFAMILY; SPECIFICITY;
D O I
10.1128/AEM.02521-09
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
The filamentous, heterocystous, nitrogen-fixing cyanobacterium Nostoc sp. strain PCC 7120 may contain, depending on growth conditions, up to two hydrogenases directly involved in hydrogen metabolism. HypC is one out of at least seven auxiliary gene products required for synthesis of a functional hydrogenase, specifically involved in the maturation of the large subunit. In this study we present a protein, CalA (Alr0946 in the genome), belonging to the transcription regulator family AbrB, which in protein-DNA assays was found to interact with the upstream region of hypC. Transcriptional investigations showed that calA is cotranscribed with the downstream gene alr0947, which encodes a putative protease from the abortive infection superfamily, Abi. CalA was shown to interact specifically not only with the upstream region of hypC but also with its own upstream region, acting as a repressor on hypC. The bidirectional hydrogenase activity was significantly downregulated when CalA was overexpressed, demonstrating a correlation with the transcription factor, either direct or indirect. In silico studies showed that homologues to both CalA and Alr0947 are highly conserved proteins within cyanobacteria with very similar physical organizations of the corresponding structural genes. Possible functions of the cotranscribed downstream protein Alr0947 are presented. In addition, we present a three-dimensional (3D) model of the DNA binding domain of CalA and putative DNA binding mechanisms are discussed.
引用
收藏
页码:880 / 890
页数:11
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