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Characterization of the gene encoding the protective paracrystalline-surface-layer protein of Rickettsia prowazekii: presence of a truncated identical homolog in Rickettsia typhi.

机译:编码立克次体立克次体的保护性晶体旁表面层蛋白的基因的特征:伤寒立克次体中存在一个截短的相同同源物。

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摘要

The DNA sequence of the gene encoding the protective surface protein antigen (SPA) of Rickettsia prowazekii has been determined. The open reading frame of 4836 nucleotides with promoter and ribosome-binding site is present on a 10.1-kilobase EcoRI fragment. The encoded carboxyl terminus of the 169-kDa protein contains a potential transmembrane region and hydrophilic regions with many lysine and arginine residues potentially accessible to proteolytic cleavage. Because the rickettsia-derived SPA has an estimated molecular mass of only 120 kDa and does not contain several predicted large carboxyl-region CNBr fragments, the SPA product appears to be processed by the rickettsiae. Eight other CNBr fragments were identical in sequence to those predicted from the encoded gene. A complementary 8.7-kilobase EcoRI fragment of Rickettsia typhi DNA was cloned. This fragment lacked a 1433-base-pair region that included the promoter, ribosome-binding site, and the initial 1162 base pairs of the open reading frame encoding the R. prowazekii SPA but had a 3674-base-pair region identical with the remainder of the R. prowazekii SPA gene sequence.
机译:已经确定了编码立氏立克次体的保护性表面蛋白抗原(SPA)的基因的DNA序列。具有启动子和核糖体结合位点的4836个核苷酸的开放阅读框存在于10.1-碱基碱基的EcoRI片段上。 169-kDa蛋白的编码羧基末端包含一个潜在的跨膜区域和亲水区域,其中许多赖氨酸和精氨酸残基可能被蛋白水解切割。由于立克次体来源的SPA的估计分子量仅为120 kDa,并且不包含几个预测的大羧基区域CNBr片段,因此SPA产物似乎由立克次体加工。其他八个CNBr片段的序列与从编码基因预测的序列相同。克隆了伤寒立克次体DNA的8.7碱基互补的EcoRI片段。该片段缺少一个1433个碱基对的区域,该区域包括启动子,核糖体结合位点和编码R. prowazekii SPA的开放阅读框的最初的1162个碱基对,但与其余的3674个碱基对区域相同prowazekii SPA基因序列的序列。

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