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戈登链球菌中的DNA结合活性:一种受体切口酶和一种组蛋白样蛋白的鉴定

DNA-binding activities in Streptococcus gordonii: identification of a receptor-nickase and a histonelike protein.

作者信息

Lunsford R D, Nguyen N, London J

机构信息

Laboratory of Microbial Ecology, National Institute for Dental Research, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

Curr Microbiol. 1996 Feb;32(2):95-100. doi: 10.1007/s002849900017.

Abstract

Extraction of Streptococcus gordonii cells with the mild chaotropic agent, LiCl, drastically decreased DNA transforming ability, had little effect on viability, and released both DNA nicking and binding activities. Both activities were Mg2+ and Ca2+ independent and were not competence specific. Southwestern blot analysis of the extract identified putative surface proteins of 56 kDa and 68 kDa in strain Challis and Wicky, respectively. Extracts also contained a 10-kDa DNA-binding protein, designated HSgo, that belongs to the eubacterial histonelike class of proteins.

摘要

用温和的离液剂氯化锂提取戈登氏链球菌细胞,会大幅降低DNA转化能力,对活力影响不大,并释放出DNA切口和结合活性。这两种活性都不依赖镁离子和钙离子,也不是感受态特异性的。对提取物进行的蛋白质印迹分析分别在Challis菌株和Wicky菌株中鉴定出推定的56 kDa和68 kDa表面蛋白。提取物中还含有一种10 kDa的DNA结合蛋白,命名为HSgo,它属于真细菌类组蛋白。

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