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鼠伤寒沙门氏菌flhB操纵子及其蛋白质产物的分子特征

Molecular characterization of the Salmonella typhimurium flhB operon and its protein products.

作者信息

Minamino T, Iino T, Kutuskake K

机构信息

Faculty of Applied Biological Science, Hiroshima University, Japan.

出版信息

J Bacteriol. 1994 Dec;176(24):7630-7. doi: 10.1128/jb.176.24.7630-7637.1994.

Abstract

The flhB and flhA genes constitute an operon called flhB operon on the Salmonella typhimurium chromosome. Their gene products are required for formation of the rod structure of flagellar apparatus. Furthermore, several lines of evidence suggest that they, together with FliI and FliH, may constitute the export apparatus of flagellin, the component protein of flagellar filament. In this study, we determined the nucleotide sequence of the entire flhB operon from S. typhimurium. It was shown that the flhB and flhA genes encode highly hydrophobic polypeptides with calculated molecular masses of 42,322 and 74,848 Da, respectively. Both proteins have several potential membrane-spanning segments, suggesting that they may be integral membrane proteins. The flhB operon was found to contain an additional open reading frame capable of encoding a polypeptide with a calculated molecular mass of 14,073 Da. We designated this open reading frame flhE. The N-terminal 16 amino acids of FlhE displays a feature of a typical signal sequence. A maxicell labeling experiment enabled us to identify the precursor and mature forms of the flhE gene products. Insertion of a kanamycin-resistant gene cartridge into the chromosomal flhE gene did not affect the motility of the cells, indicating that the flhE gene is not essential for flagellar formation and function. We have overproduced and purified N-terminally truncated FlhB and FlhA proteins and raised antibodies against them. By use of these antibodies, localization of the FlhB and FlhA proteins was analyzed by Western blotting (immunoblotting) with the fractionated cell extracts. The results obtained indicated that both proteins are localized in the cytoplasmic membrane.

摘要

flhB和flhA基因在鼠伤寒沙门氏菌染色体上构成一个名为flhB操纵子的操纵子。鞭毛装置杆状结构的形成需要它们的基因产物。此外,多项证据表明,它们与FliI和FliH一起,可能构成鞭毛丝组成蛋白鞭毛蛋白的输出装置。在本研究中,我们测定了鼠伤寒沙门氏菌整个flhB操纵子的核苷酸序列。结果表明,flhB和flhA基因分别编码计算分子量为42,322和74,848 Da的高度疏水多肽。这两种蛋白质都有几个潜在的跨膜区段,表明它们可能是整合膜蛋白。发现flhB操纵子包含一个额外的开放阅读框,能够编码一个计算分子量为14,073 Da的多肽。我们将这个开放阅读框命名为flhE。FlhE的N端16个氨基酸显示出典型信号序列的特征。一项大细胞标记实验使我们能够鉴定flhE基因产物的前体和成熟形式。将卡那霉素抗性基因盒插入染色体flhE基因中并不影响细胞的运动性,这表明flhE基因对于鞭毛的形成和功能不是必需的。我们过量表达并纯化了N端截短的FlhB和FlhA蛋白,并制备了针对它们的抗体。通过使用这些抗体,利用分级分离的细胞提取物进行蛋白质印迹法(免疫印迹法)分析了FlhB和FlhA蛋白的定位。所得结果表明这两种蛋白都定位于细胞质膜中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f51/197220/6f187d5009e0/jbacter00042-0237-a.jpg

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