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从深海嗜压细菌紫色希瓦氏菌中分离编码RNA聚合酶α亚基的rpoA基因并进行压阻响应研究

Isolation and piezoresponse of the rpoA gene encoding the RNA polymerase alpha subunit from the deep-sea piezophilic bacterium Shewanella violacea.

作者信息

Nakasone K, Ikegami A, Fujii S, Kato C, Horikoshi K

机构信息

The DEEP STAR Group, Japan Marine Science and Technology Center, Yokosuka, Kanagawa, Japan.

出版信息

FEMS Microbiol Lett. 2000 Dec 15;193(2):261-8. doi: 10.1111/j.1574-6968.2000.tb09434.x.

Abstract

The rpoA gene encoding the alpha subunit of RNA polymerase from the deep-sea piezophilic bacterium Shewanella violacea DSS12 was cloned and sequenced. The rpoA gene was found to encode a polypeptide consisting of 329 amino acids with a molecular mass of 36238 Da. S. violacea alpha protein was expressed in a ts Escherichia coli mutant, to confirm whether the rpoA gene is functional. It complemented this mutation, indicating a chimeric RNA polymerase is assembled at the non-permissive temperature. Recombinant alpha protein was overexpressed using an expression plasmid harboring the rpoA gene and purified to near homogeneity. Primer extension analysis revealed that two transcriptional initiation sites are recognized by sigma(70) RNA polymerase. It also indicated that pressure response (piezoresponse) in the alpha operon occurred at the transcriptional level, suggesting some positive regulators may interact with the transcriptional apparatus and regulate the expression of the operon at different pressure conditions.

摘要

对来自深海嗜压细菌紫色希瓦氏菌DSS12的编码RNA聚合酶α亚基的rpoA基因进行了克隆和测序。发现rpoA基因编码一个由329个氨基酸组成、分子量为36238道尔顿的多肽。在一个温度敏感型大肠杆菌突变体中表达了紫色希瓦氏菌α蛋白,以确认rpoA基因是否具有功能。它弥补了这种突变,表明在非允许温度下组装了嵌合RNA聚合酶。使用携带rpoA基因的表达质粒对重组α蛋白进行了过量表达,并纯化至近乎同质。引物延伸分析表明,σ(70)RNA聚合酶识别两个转录起始位点。这也表明α操纵子中的压力响应(压力应答)发生在转录水平,提示一些正调控因子可能与转录装置相互作用,并在不同压力条件下调节操纵子的表达。

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