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在嗜甲基甲基杆菌AM1中鉴定介导mox基因转录的上游调控序列。

Identification of an upstream regulatory sequence that mediates the transcription of mox genes in Methylobacterium extorquens AM1.

作者信息

Zhang Meng, FitzGerald Kelly A, Lidstrom Mary E

机构信息

Department of Chemical Engineering, University of Washington, Seattle, WA 98195-2125, USA.

Department of Microbiology, University of Washington, Seattle, WA 98195-2125, USA.

出版信息

Microbiology (Reading). 2005 Nov;151(Pt 11):3723-3728. doi: 10.1099/mic.0.28243-0.

Abstract

A multiple A-tract sequence has been identified in the promoter regions for the mxaF, pqqA, mxaW, mxbD and mxcQ genes involved in methanol oxidation in Methylobacterium extorquens AM1, a facultative methylotroph. Site-directed mutagenesis was exploited to delete or change this conserved sequence. Promoter-xylE transcriptional fusions were used to assess promoter activity in these mutants. A fiftyfold drop in the XylE activity was observed for the mxaF and pqqA promoters without this sequence, and a five- to sixfold drop in the XylE activity was observed for the mxbD and mxcQ promoters without this sequence. Mutants were generated in the chromosomal copies in which this sequence was either deleted or altered, and these mutants were unable to grow on methanol. When one of these sequences was added to Plac of Escherichia coli, which is a weak constitutive promoter in M. extorquens AM1, the activity increased two- to threefold. These results suggest that this sequence is essential for normal expression of these genes in M. extorquens AM1, and may serve as a general enhancer element for genetic constructs in this bacterium.

摘要

在兼性甲基营养菌嗜甲基甲基杆菌AM1中,已在参与甲醇氧化的mxaF、pqqA、mxaW、mxbD和mxcQ基因的启动子区域鉴定出一个多聚A序列。利用定点诱变删除或改变这个保守序列。使用启动子-xylE转录融合来评估这些突变体中的启动子活性。对于没有该序列的mxaF和pqqA启动子,观察到XylE活性下降了50倍,对于没有该序列的mxbD和mxcQ启动子,观察到XylE活性下降了5至6倍。在该序列被删除或改变的染色体拷贝中产生了突变体,这些突变体无法在甲醇上生长。当将这些序列之一添加到大肠杆菌的Plac(在嗜甲基甲基杆菌AM1中是一个弱组成型启动子)时,活性增加了2至3倍。这些结果表明,该序列对于嗜甲基甲基杆菌AM1中这些基因的正常表达至关重要,并且可能作为该细菌中基因构建体的一般增强子元件。

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