Kalmokoff M L, Jarrell K F
Department of Microbiology and Immunology, Queen's University, Kingston, Ontario, Canada.
J Bacteriol. 1991 Nov;173(22):7113-25. doi: 10.1128/jb.173.22.7113-7125.1991.
The flagellins of Methanococcus voltae are encoded by a multigene family of four related genes (flaA, flaB1, flaB2, and flaB3). All four genes map within the same region of the genome, with the last three arranged in a direct tandem. Northern (RNA) blot and primer extension analyses of total cellular RNA indicate that all four genes are transcribed. The flaB1, flaB2, and flaB3 flagellins are transcribed as part of a large polycistronic message which encodes at least one more protein which is not a flagellin. An intercistronic stem-loop followed by a poly(T) tract located between the flaB2 and flaB3 genes appears to increase the resistance of the flaB1/flaB2 portion of this polycistronic message to digestion by endogenous RNases. The flaA gene, located approximately 600 bp upstream from the tandem, is transcribed as a separate message at very low levels. The four open reading frames encode proteins of molecular weights 23,900, 22,400, 22,800, and 25,500, much less than the Mr values of 33,000 and 31,000 for the flagellins calculated from sodium dodecyl sulfate-polyacrylamide gel electrophoresis of isolated flagellar filaments. Each flagellin contains multiple eukaryotic glycosylation signals (Arg-X-Ser/Thr), although they do not appear to be glycoproteins, and each has an 11- or 12-amino-acid leader peptide. The N termini of all four flagellins (amino acids 1 through 47 of the mature protein) are very hydrophobic, and this region shows a high degree of homology with the flagellins from Halobacterium halobium.
沃氏甲烷球菌的鞭毛蛋白由一个包含四个相关基因(flaA、flaB1、flaB2和flaB3)的多基因家族编码。这四个基因都定位在基因组的同一区域内,后三个基因呈直接串联排列。对总细胞RNA进行的Northern(RNA)印迹和引物延伸分析表明,这四个基因都能转录。flaB1、flaB2和flaB3鞭毛蛋白作为一个大的多顺反子信息的一部分进行转录,该多顺反子信息至少还编码一种非鞭毛蛋白的蛋白质。位于flaB2和flaB3基因之间的一个顺反子间茎环结构,后面跟着一个聚(T)序列,似乎增加了这个多顺反子信息中flaB1/flaB2部分对内源核糖核酸酶消化的抗性。位于串联序列上游约600 bp处的flaA基因以极低水平作为一个单独的信息进行转录。这四个开放阅读框编码分子量分别为23,900、22,400、22,800和25,500的蛋白质,远低于根据分离的鞭毛丝进行十二烷基硫酸钠-聚丙烯酰胺凝胶电泳计算出的鞭毛蛋白33,000和31,000的分子量值。每个鞭毛蛋白都含有多个真核糖基化信号(精氨酸- X - 丝氨酸/苏氨酸),尽管它们似乎不是糖蛋白,并且每个都有一个11或12个氨基酸的前导肽。所有四种鞭毛蛋白的N端(成熟蛋白的第1至47个氨基酸)都非常疏水,并且该区域与嗜盐嗜盐杆菌的鞭毛蛋白具有高度同源性。