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大肠杆菌的torR基因编码一种参与三甲胺N-氧化物还原酶基因表达的应答调节蛋白。

The torR gene of Escherichia coli encodes a response regulator protein involved in the expression of the trimethylamine N-oxide reductase genes.

作者信息

Simon G, Méjean V, Jourlin C, Chippaux M, Pascal M C

机构信息

Laboratoire de Chimie Bactérienne, Centre National de la Recherche Scientifique, Marseille, France.

出版信息

J Bacteriol. 1994 Sep;176(18):5601-6. doi: 10.1128/jb.176.18.5601-5606.1994.

Abstract

Expression of the Escherichia coli torCAD operon encoding the trimethylamine N-oxide (TMAO) reductase system is induced by both TMAO and anaerobiosis. A torR insertion mutant unable to express the torA gene had previously been isolated. The torR gene was cloned and sequenced. It encodes a 25,000-Da protein which shares homology with response regulators of two-component systems and belongs to the OmpR-PhoB subclass. Overproduction of TorR mimics the presence of the inducer TMAO while the anaerobic control is unchanged, suggesting that TorR mediates only the TMAO induction. The overproduced TorR protein was purified to more than 90%. The torR gene is located just upstream of the torCAD operon, with an opposite transcription direction. The torR-torCAD intergenic region is unusual in that it contains four direct repeats of a 10-nucleotide motif. Part or all of these motifs could be involved in the binding of TorR. The gene encoding the sensor partner does not seem to be adjacent to torR, since the divergent open reading frame found immediately downstream of torR exhibits none of the features of a protein histidine kinase.

摘要

编码三甲胺 N-氧化物(TMAO)还原酶系统的大肠杆菌 torCAD 操纵子的表达受 TMAO 和厌氧环境的诱导。之前已分离出一个无法表达 torA 基因的 torR 插入突变体。torR 基因被克隆并测序。它编码一种 25,000 道尔顿的蛋白质,该蛋白质与双组分系统的应答调节因子具有同源性,属于 OmpR-PhoB 亚类。TorR 的过量表达模拟了诱导剂 TMAO 的存在,而厌氧控制不受影响,这表明 TorR 仅介导 TMAO 诱导。过量产生的 TorR 蛋白的纯度达到了 90%以上。torR 基因位于 torCAD 操纵子的上游,转录方向相反。torR-torCAD 基因间区域不同寻常之处在于它包含一个 10 个核苷酸基序的四个直接重复序列。这些基序的部分或全部可能参与 TorR 的结合。由于在 torR 下游紧邻发现的发散性开放阅读框不具备蛋白质组氨酸激酶的任何特征,所以编码传感器伴侣的基因似乎不与 torR 相邻。

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