首页> 美国卫生研究院文献>Journal of Bacteriology >Identification of dcmR the regulatory gene governing expression of dichloromethane dehalogenase in Methylobacterium sp. strain DM4.
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Identification of dcmR the regulatory gene governing expression of dichloromethane dehalogenase in Methylobacterium sp. strain DM4.

机译:dcmR的鉴定dcmR是控制甲烷脱氢酶在甲基杆菌属中表达的调控基因。菌株DM4。

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摘要

The genes for dichloromethane utilization by Methylobacterium sp. strain DM4 are encoded on a 2.8-kb sequenced DNA fragment, the dcm region. This fragment contains dcmA, the structural gene of dichloromethane dehalogenase and, upstream of dcmA, a 1.5-kb region responsible for inducibility of dichloromethane dehalogenase by dichloromethane. A fragment of the dcm region covering dcmA and 230 bp of its upstream region was integrated into the chromosome of a Methylobacterium sp. strain DM4 mutant deleted for the dcm region. This yielded a strain expressin dichloromethane dehalogenase constitutively at the induced level. Plasmids carrying various segments of the 1.5-kb regulatory region were tested for their ability to restore regulation. The data obtained led to the identification of dcmR, the structural gene of a putative dcm-specific repressor. Transcription of dcmR was divergent from dcmA. dcmR encoded a 30-kDa protein with a helix-turn-helix motif near the amino terminus. The transcription start sites of dcmA and dcmR were identified by nuclease S1 mapping. The promoter regions of these genes contained nearly identical 12-bp sequences covering positions -14 to -25 relative to the mRNA start sites. Experiments with dcmR'-'lacZ fusions demonstrated that dcmR expression was markedly autoregulated at the level of transcription and less so at the protein level. These findings are compatible with both dcmA and dcmR expression being negatively controlled at the transcriptional level by the DcmR protein.
机译:甲基杆菌利用二氯甲烷的基因。 DM4菌株在2.8kb测序的DNA片段dcm区编码。该片段包含dcmA,它是二氯甲烷脱卤酶的结构基因,在dcmA的上游,有一个1.5 kb的区域,负责由二氯甲烷诱导二氯甲烷脱卤酶。覆盖dcmA和其上游区域230 bp的dcm区域片段被整合到甲基杆菌属的染色体中。在dcm区域缺失了DM4菌株。这在诱导水平上组成性地产生了一种表达素二氯甲烷脱卤酶。测试了携带1.5kb调节区的各个区段的质粒恢复调节的能力。获得的数据导致鉴定了dcmR,推定的dcm特异性阻遏物的结构基因。 dcmR的转录与dcmA不同。 dcmR编码一个30-kDa的蛋白质,在氨基末端附近有一个螺旋-转-螺旋基序。通过核酸酶S1作图鉴定了dcmA和dcmR的转录起始位点。这些基因的启动子区域包含几乎相同的12 bp序列,覆盖相对于mRNA起始位点的位置-14至-25。 dcmR'-'lacZ融合蛋白的实验表明,dcmR表达在转录水平上显着自动调节,而在蛋白质水平上则较少。这些发现与由DcmR蛋白在转录水平上负调控的dcmA和dcmR表达均兼容。

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