Oliveira Paulo, Leitão Elsa, Tamagnini Paula, Moradas-Ferreira Pedro, Oxelfelt Fredrik
Department of Botany, Faculty of Sciences, University of Porto, Rua do Campo Alegre 1191, 4150-181 Porto, Portugal.
Institute for Molecular and Cell Biology - Cellular and Applied Microbiology Unit, University of Porto, Rua do Campo Alegre 823, 4150-180 Porto, Portugal.
Microbiology (Reading). 2004 Nov;150(Pt 11):3647-3655. doi: 10.1099/mic.0.27248-0.
The structural genes (hupSL) encoding an uptake hydrogenase in the unicellular cyanobacterium Gloeothece sp. ATCC 27152, a strain capable of aerobic N(2) fixation, were identified and sequenced. 3'-RACE experiments uncovered the presence of an additional ORF 184 bp downstream of hupL, showing a high degree of sequence identity with a gene encoding an uptake-hydrogenase-specific endopeptidase (hupW) in other cyanobacteria. In addition, the transcription start point was identified 238 bp upstream of the hupS translational start. RT-PCR experiments revealed that hupW is co-transcribed with the uptake hydrogenase structural genes in Gloeothece sp. ATCC 27152. In addition, Northern hybridizations clearly showed that hupSLW are transcribed under nitrogen fixing conditions, but not in the presence of combined nitrogen. A putative NtcA binding site was identified in the promoter region upstream of hupS, centred at -41.5 bp with respect to the transcription start point. Electrophoretic retardation of a labelled DNA fragment (harbouring the putative NtcA-binding motif) was significantly affected by an Escherichia coli cell-free extract containing overexpressed NtcA, suggesting that NtcA is involved in the transcriptional regulation of hupSLW.
在能够进行好氧固氮的单细胞蓝细菌Gloeothece sp. ATCC 27152中,编码摄取型氢化酶的结构基因(hupSL)被鉴定并测序。3'-RACE实验发现在hupL下游184 bp处存在一个额外的开放阅读框(ORF),其与其他蓝细菌中一个编码摄取型氢化酶特异性内肽酶(hupW)的基因具有高度的序列同一性。此外,在hupS翻译起始位点上游238 bp处鉴定到转录起始点。RT-PCR实验表明,在Gloeothece sp. ATCC 27152中hupW与摄取型氢化酶结构基因共转录。此外,Northern杂交清楚地表明,hupSLW在固氮条件下转录,但在有化合态氮存在时不转录。在hupS上游的启动子区域鉴定到一个假定的NtcA结合位点,相对于转录起始点位于-41.5 bp处。含有过表达NtcA的大肠杆菌无细胞提取物显著影响了一个标记DNA片段(含有假定的NtcA结合基序)的电泳阻滞,这表明NtcA参与hupSLW的转录调控。