Gerl L, Sumper M
Institut für Biochemie, Genetik und Mikrobiologie, Universität Regensburg, Federal Republic of Germany.
J Biol Chem. 1988 Sep 15;263(26):13246-51.
Purified flagellar filaments of Halobacterium halobium contain three different protein species based on sodium dodecyl sulfate-polyacrylamide gel electrophoresis. These proteins were designated as flagellins Fla I, Fla II, and Fla III and were characterized as sulfated glycoproteins with N-glycosidically linked oligosaccharides of the type GlcA-(1----4)-GlcA-(1----4)-GlcA-(1----4)-Glc. All halobacterial flagellin polypeptides are immunologically cross-reactive. A gene fragment of one flagellin was isolated in an expression vector using antibody probes. Using this gene fragment as probe, we identified, subcloned, and determined the nucleotide sequences of five different but highly homologous flagellin genes. Two flagellin (flg) genes are arranged tandemly at one locus (flg A1 and -2), and the other three in a tandem arrangement at a different locus (flg B1, -2, and -3), Two flg mRNAs were detected, one from the A genes and the other from the B genes. Based on immunological analysis, the products of the flg A1 and A2 are Fla II and Fla I, respectively.
基于十二烷基硫酸钠-聚丙烯酰胺凝胶电泳分析,嗜盐栖热菌纯化的鞭毛丝含有三种不同的蛋白质。这些蛋白质被命名为鞭毛蛋白Fla I、Fla II和Fla III,其特征为硫酸化糖蛋白,带有N-糖苷键连接的GlcA-(1→4)-GlcA-(1→4)-GlcA-(1→4)-Glc型寡糖。所有嗜盐菌鞭毛蛋白多肽都具有免疫交叉反应性。利用抗体探针在表达载体中分离出一种鞭毛蛋白的基因片段。以该基因片段为探针,我们鉴定、亚克隆并测定了五个不同但高度同源的鞭毛蛋白基因的核苷酸序列。两个鞭毛蛋白(flg)基因在一个位点串联排列(flg A1和-2),另外三个在另一个不同位点串联排列(flg B1、-2和-3)。检测到两种flg mRNA,一种来自A基因,另一种来自B基因。基于免疫分析,flg A1和A2的产物分别为Fla II和Fla I。