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嗜甲基菌AM1中参与甲醇氧化的基因的启动子和转录本。

Promoters and transcripts for genes involved in methanol oxidation in Methylobacterium extorquens AM1.

作者信息

Zhang Meng, Lidstrom Mary E

机构信息

Departments of Chemical Engineering, University of Washington, Seattle, WA 98195-1750, USA.

Departments of Microbiology, University of Washington, Seattle, WA 98195-1750, USA.

出版信息

Microbiology (Reading). 2003 Apr;149(Pt 4):1033-1040. doi: 10.1099/mic.0.26105-0.

Abstract

Twenty-five genes are involved in methanol oxidation to formaldehyde by the methanol dehydrogenase system in the facultative methylotroph Methylobacterium extorquens AM1 organized in five gene clusters. RT-PCR was used to assess the transcripts for the main gene clusters that encode methanol dehydrogenase and proteins required for its activity (mxaFGJIRSACKLDEHB), and the enzymes that are required for the synthesis of the methanol dehydrogenase prosthetic group, pyrroloquinoline quinone (pqqABC/DE and the pqqFG cluster). In both cases, positive bands were obtained corresponding to mRNA spanning each of the genes in the cluster, but not across the first and last genes and the gene immediately upstream or downstream of the cluster, respectively. These results suggest that these three gene clusters are each transcribed as a single operon. Confirmation was obtained by cloning a number of intergenic regions into a promoter probe vector. None of these regions showed significant promoter activity. Promoter regions were analysed for mxaF, pqqA, orf181 upstream of pqqFG, and mxaW, a gene located upstream of mxaF and divergently transcribed. The promoter regions for these genes were defined to within 100, 46, 124 and 146 bp, respectively, and the two unknown transcriptional start sites were determined, for mxaW and orf181. Alignment of these promoter regions suggests that they all may be transcribed by the sigma(70) orthologue in M. extorquens AM1.

摘要

在兼性甲基营养菌嗜甲基甲基杆菌AM1中,甲醇脱氢酶系统将甲醇氧化为甲醛的过程涉及25个基因,这些基因组成了5个基因簇。采用逆转录聚合酶链反应(RT-PCR)来评估主要基因簇的转录本,这些基因簇编码甲醇脱氢酶及其活性所需的蛋白质(mxaFGJIRSACKLDEHB),以及甲醇脱氢酶辅基吡咯喹啉醌(PQQ)合成所需的酶(pqqABC/DE和pqqFG簇)。在这两种情况下,均获得了与跨越基因簇中每个基因的mRNA相对应的阳性条带,但分别未跨越基因簇的第一个和最后一个基因以及基因簇紧邻的上游或下游基因。这些结果表明,这三个基因簇各自作为一个单一操纵子进行转录。通过将多个基因间区域克隆到启动子探针载体中获得了证实。这些区域均未显示出显著的启动子活性。对mxaF、pqqA、pqqFG上游的orf181以及位于mxaF上游且转录方向相反的mxaW的启动子区域进行了分析。这些基因的启动子区域分别被确定在100、46、124和146 bp范围内,并确定了mxaW和orf181这两个未知的转录起始位点。这些启动子区域的比对表明,它们可能均由嗜甲基甲基杆菌AM1中的σ⁷⁰同源物进行转录。

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