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鸡毒支原体HU蛋白的鉴定与特性分析

Identification and characterization of HU protein from Mycoplasma gallisepticum.

作者信息

Kenri T, Sasaki T, Kano Y

机构信息

Department of Safety Research on Biologics, National Institute of Infectious Diseases, Tokyo, Japan.

出版信息

Biochem Biophys Res Commun. 1998 Aug 10;249(1):48-52. doi: 10.1006/bbrc.1998.9090.

Abstract

A hypothetical ORF of Mycoplasma gallisepticum with a putative 99-amino-acid product (ORF99) was noted previously in the upstream region from the type II topoisomerase gene. The amino acid sequence shows weak homology with the Escherichia coli histone-like protein HU. To identify and characterize the protein product of ORF99, we prepared mouse antiserum against recombinant GST-ORF99 fusion protein. The antiserum reacted with an 11-kDa peptide in the crude cell extract of M. gallisepticum, indicating that this protein is an ORF99 product. ORF99 protein binds to DNA, although its binding affinity is weaker than that of E. coli HU. When ORF99 was cloned in a plasmid and expressed in E. coli cells depleted of HU, Mu phage growth was strongly promoted in the cells, showing the presence of HU activity. The effect of IHF mutation was suppressed when a high level of ORF99 protein was expressed in an E. coli mutant deficient in IHF.

摘要

先前在鸡毒支原体II型拓扑异构酶基因上游区域发现了一个假定的开放阅读框(ORF),其推测产物为一种含99个氨基酸的蛋白质(ORF99)。该氨基酸序列与大肠杆菌组蛋白样蛋白HU具有弱同源性。为了鉴定和表征ORF99的蛋白质产物,我们制备了针对重组GST-ORF99融合蛋白的小鼠抗血清。该抗血清与鸡毒支原体粗细胞提取物中的一种11 kDa肽发生反应,表明该蛋白是ORF99的产物。ORF99蛋白能与DNA结合,尽管其结合亲和力比大肠杆菌HU的弱。当ORF99克隆到质粒中并在缺乏HU的大肠杆菌细胞中表达时,Mu噬菌体在这些细胞中的生长受到强烈促进,表明存在HU活性。当在缺乏整合宿主因子(IHF)的大肠杆菌突变体中高水平表达ORF99蛋白时,IHF突变的影响受到抑制。

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