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鼠伤寒沙门氏菌中鞭毛钩和基体基因产物(FlaFV、FlaFVI、FlaFVII和FlaFVIII)的鉴定

Identification of flagellar hook and basal body gene products (FlaFV, FlaFVI, FlaFVII and FlaFVIII) in Salmonella typhimurium.

作者信息

Homma M, Ohnishi K, Iino T, Macnab R M

出版信息

J Bacteriol. 1987 Aug;169(8):3617-24. doi: 10.1128/jb.169.8.3617-3624.1987.

Abstract

The flagellar genes flaFV, flaFVII, and flaFVIII of Salmonella typhimurium were cloned, and their presence on a given plasmid was verified by complementation of Escherichia coli mutants defective in the homologous genes. The gene products were identified by radiolabeling in a minicell system as being proteins of the following molecular masses: FlaFV, 42 kilodaltons (kDa); FlaFVI, 32 kDa; FlaFVII, 30 kDA; and FlaFVIII, 27 kDa. These data, together with isoelectric focusing data, confirm gene product assignments of flagellar components made indirectly from mutant studies. Flagellar components are transported by either a signal peptide-dependent or a flagellar-specific pathway. Consistent with its location in the outer membrane ring of the basal body, protein FlaFVIII seems to use the signal peptide-dependent pathway, since it was synthesized in a precursor form and processed, presumably by peptide cleavage, to a mature form; the maturation process was inhibited by addition of a proton ionophore. Proteins synthesized in minicells were localized as follows: FlaFVI was localized to the soluble fraction (cytoplasm); pre-FlaFVIII and FlaFVIII were localized to the particulate fraction (membrane or high-molecular-weight aggregate); FlaFV and FlaFVII were localized to both fractions. The significance of these locations in terms of known or suspected roles in the flagellar apparatus is discussed.

摘要

鼠伤寒沙门氏菌的鞭毛基因flaFV、flaFVII和flaFVIII被克隆出来,通过对同源基因有缺陷的大肠杆菌突变体进行互补,验证了它们在特定质粒上的存在。通过在小细胞系统中进行放射性标记,确定基因产物为以下分子量的蛋白质:FlaFV,42千道尔顿(kDa);FlaFVI,32 kDa;FlaFVII,30 kDa;FlaFVIII,27 kDa。这些数据与等电聚焦数据一起,证实了从突变体研究中间接得出的鞭毛成分的基因产物归属。鞭毛成分通过信号肽依赖性途径或鞭毛特异性途径进行转运。与它在基体的外膜环中的位置一致,蛋白质FlaFVIII似乎使用信号肽依赖性途径,因为它以前体形式合成并加工,大概是通过肽裂解加工成成熟形式;加入质子离子载体可抑制成熟过程。在小细胞中合成的蛋白质定位如下:FlaFVI定位于可溶性部分(细胞质);前体FlaFVIII和FlaFVIII定位于颗粒部分(膜或高分子量聚集体);FlaFV和FlaFVII定位于两个部分。讨论了这些位置在鞭毛装置中已知或疑似作用方面的意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/991d/212441/3e5b5948b762/jbacter00198-0235-a.jpg

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