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汞抗性的遗传学与生物化学

The genetics and biochemistry of mercury resistance.

作者信息

Foster T J

机构信息

Department of Microbiology, Trinity College, Dublin, Ireland.

出版信息

Crit Rev Microbiol. 1987;15(2):117-40. doi: 10.3109/10408418709104455.

Abstract

The ability of bacteria to detoxify mercurial compounds by reduction and volatilization is conferred by mer genes, which are usually plasmid located. The narrow spectrum (Hg2+ detoxifying) Tn501 and R100 determinants have been subjected to molecular genetic and DNA sequence analysis. Biochemical studies on the flavoprotein mercuric reductase have elucidated the mechanism of reduction of Hg2+ to Hg0. The mer genes have been mapped and sequenced and their protein products studied in minicells. Based on the deduced amino acid sequences, these proteins have been assigned a role in a mechanistic scheme for mercury flux in resistant bacteria. The mer genes are inducible, with regulatory control being exerted at the transcriptional level both positively and negatively. Attention is now focusing on broad-spectrum resistance involving detoxification of organomercurials by an additional enzyme, organomercurial lyase. Lyase genes have recently been cloned and sequencing studies are in progress.

摘要

细菌通过还原和挥发作用对汞化合物进行解毒的能力是由mer基因赋予的,这些基因通常位于质粒上。窄谱(Hg2+解毒)转座子Tn501和R100决定簇已进行了分子遗传学和DNA序列分析。对黄素蛋白汞还原酶的生化研究阐明了Hg2+还原为Hg0的机制。mer基因已被定位和测序,并在小细胞中对其蛋白质产物进行了研究。根据推导的氨基酸序列,已确定这些蛋白质在抗性细菌中汞通量的机制中发挥作用。mer基因是可诱导的,在转录水平上受到正调控和负调控。现在的注意力集中在涉及通过另一种酶——有机汞裂解酶对有机汞进行解毒的广谱抗性上。裂解酶基因最近已被克隆,测序研究正在进行中。

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