Xu H H, Janka J J, Viebahn M, Hanson R S
Department of Microbiology, Gray Freshwater Biological Institute, University of Minnesota, Navarre 55392, USA.
Microbiology (Reading). 1995 Oct;141 ( Pt 10):2543-51. doi: 10.1099/13500872-141-10-2543.
Nucleotide sequence analysis of the mxcQ and mxcE loci, required for the synthesis of methanol dehydrogenase in Methylobacterium organophilum XX, has revealed two open reading frames that show significant similarity to sequences of prokaryotic two-component systems, especially MxaY and MxaX proteins of another methylotrophic bacterium, Paracoccus denitrificans. Cell-free extracts and DNA-column-fractionated proteins from wild-type M. organophilum XX cells grown on methanol or succinate contained protein(s) that were able to bind specifically to the upstream region of methanol dehydrogenase large subunit gene (mxaF). In contrast, cell-free extracts from mxcQ and mxcE mutant strains of M. organophilum XX had zero or reduced binding activity towards the promoter fragments of the mxaF gene. This is consistent with the involvement of the mxcQ and mxcE genes in transcriptional regulation of methanol dehydrogenase synthesis. Analyses of sequential deletions of the mxaF upstream region have defined the functional boundary of the promoter/operator region of this gene and identified one nucleotide segment as essential to the activation of mxaF.
嗜有机甲基杆菌XX中甲醇脱氢酶合成所需的mxcQ和mxcE基因座的核苷酸序列分析,揭示了两个开放阅读框,它们与原核双组分系统的序列具有显著相似性,特别是与另一种甲基营养细菌反硝化副球菌的MxaY和MxaX蛋白的序列相似。在甲醇或琥珀酸盐上生长的野生型嗜有机甲基杆菌XX细胞的无细胞提取物和DNA柱分级分离蛋白中含有能够特异性结合甲醇脱氢酶大亚基基因(mxaF)上游区域的蛋白质。相比之下,嗜有机甲基杆菌XX的mxcQ和mxcE突变株的无细胞提取物对mxaF基因的启动子片段的结合活性为零或降低。这与mxcQ和mxcE基因参与甲醇脱氢酶合成的转录调控是一致的。对mxaF上游区域的连续缺失分析确定了该基因启动子/操纵子区域的功能边界,并确定了一个核苷酸片段对mxaF的激活至关重要。