首页> 外文OA文献 >Cloning, sequencing, and expression in Escherichia coli of the gene encoding a 45-kilodalton protein, elongation factor Tu, from Chlamydia trachomatis serovar F.
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Cloning, sequencing, and expression in Escherichia coli of the gene encoding a 45-kilodalton protein, elongation factor Tu, from Chlamydia trachomatis serovar F.

机译:沙眼衣原体沙眼衣原体F编码45千达尔顿蛋白,延伸因子Tu的基因的克隆,测序和在大肠杆菌中的表达。

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摘要

The gene encoding a 45-kDa protein (45K) of Chlamydia trachomatis serovar F was cloned, sequenced, and overexpressed in Escherichia coli. Alignment of the deduced peptide sequence with E. coli elongation factor Tu (EF-Tu) demonstrated 69% identity. The 45K was recognized by a Chlamydia genus-specific monoclonal antibody GP-45 and cross-reacted with a monospecific polyclonal antibody to E. coli EF-Tu. Purified recombinant 45K has the capability to bind GDP, and the binding was enhanced in the presence of E. coli elongation factor Ts (EF-Ts). The GDP binding was specifically inhibited by the monoclonal antibody GP-45. These data suggest that the 45K is a chlamydial EF-Tu, and it forms a functional complex with E. coli EF-Ts protein.
机译:克隆,编码并在大肠杆菌中过表达沙眼衣原体血清型F的45 kDa蛋白(45K)的基因。推导的肽序列与大肠杆菌延伸因子Tu(EF-Tu)的比对显示69%的同一性。 45K被衣原体属特异性单克隆抗体GP-45识别,并与针对大肠杆菌EF-Tu的单特异性多克隆抗体交叉反应。纯化的重组45K具有结合GDP的能力,并且在存在大肠杆菌延伸因子Ts(EF-Ts)的情况下增强了结合。 GDP结合被单克隆抗体GP-45特异性抑制。这些数据表明45K是衣原体EF-Tu,并且与大肠杆菌EF-Ts蛋白形成功能复合物。

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