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与RadA共表达以及嗜热泉古菌硫磺矿硫化叶菌中RadA旁系同源物stRad55B的特性分析。

Co-expression with RadA and the characterization of stRad55B, a RadA paralog from the hyperthermophilic crenarchaea Sulfolobus tokodaii.

作者信息

Sheng DuoHong, Li MingFeng, Jiao JianDong, Ni JinFeng, Shen YuLong

机构信息

State Key Laboratory of Microbial Technology, Shandong University, Jinan 250100, China.

出版信息

Sci China C Life Sci. 2008 Jan;51(1):60-5. doi: 10.1007/s11427-008-0008-x.

Abstract

ST0838 (designed stRad55B) is one of the four RadA paralogs (or Rad55 homologues) in the genome of the hyperthermophilic crenarchaeon Sulfolobus tokodaii. The gene is induced by UV irradiation, suggesting that it is involved in DNA recombinational repair in this organism. However, this protein could not be expressed normally in vitro. In this study, thermostable and soluble stRad55B was obtained by co-expression with S. tokodaii RadA (stRadA) in E. coli, and the enzymatic properties were examined. It was found that stRad55B bound ssDNA preferentially and had a very weak ATPase activity that was not stimulated by DNA. The recombinant protein inhibited the strand exchange activity promoted by stRadA, indicating that stRad55B might be an inhibitor to the homologous recombination in this archaeon. The results will be helpful for further functional and interaction analysis of RadA paralogs and for the understanding of the mechanism of recombinational repair in archaea.

摘要

ST0838(设计的stRad55B)是嗜热泉古菌硫磺矿硫化叶菌基因组中四个RadA旁系同源物(或Rad55同源物)之一。该基因受紫外线照射诱导,表明它参与了该生物体的DNA重组修复。然而,这种蛋白质在体外不能正常表达。在本研究中,通过与硫磺矿硫化叶菌RadA(stRadA)在大肠杆菌中共表达获得了耐热且可溶的stRad55B,并对其酶学性质进行了检测。发现stRad55B优先结合单链DNA,并且具有非常弱的ATP酶活性,该活性不受DNA刺激。重组蛋白抑制了stRadA促进的链交换活性,表明stRad55B可能是该古菌同源重组的抑制剂。这些结果将有助于对RadA旁系同源物进行进一步的功能和相互作用分析,并有助于理解古菌中的重组修复机制。

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