Komoriya K, Shibano N, Higano T, Azuma N, Yamaguchi S, Aizawa S I
Department of Biosciences, Teikyo University, 1-1 Toyosatodai, Utsunomiya 320-8551, Japan. Department of Applied Biochemistry, Utsunomiya University, Utsunomiya 321-8505, Japan.
Mol Microbiol. 1999 Nov;34(4):767-79. doi: 10.1046/j.1365-2958.1999.01639.x.
We analysed all major proteins secreted into culture media from Salmonella typhimurium. Proteins in culture supernatants were collected by trichloroacetic acid precipitation, separated in SDS-polyacrylamide gels and analysed by amino acid sequencing. Wild-type strain SJW1103 cells typically gave rise to nine bands in SDS gels: 89, 67, 58, 52, 50, 42, 40, 35 and (sometimes) 28 kDa. A search of the sequences in the available databases revealed that they were either flagellar proteins or virulence factors. Six of them were flagella specific: FlgK or HAP1 (58 kDa), FliC or flagellin (52 kDa), FliD or HAP2 (50 kDa), FlgE or hook protein (42 kDa), FlgL or HAP3 (35 kDa) and FlgD or hook-cap protein (28 kDa). The other four bands were specific for virulence factors: SipA (89 kDa), SipB (67 kDa), SipC (42 kDa) and InvJ (40 kDa). The 42 kDa band was a mixture of FlgE and SipC. We also analysed secreted proteins from more than 30 flagellar mutants, and they were categorized into four groups according to their band patterns: wild type, mot type, polyhook type and master gene type. Virulence factors were constantly secreted at a higher level in all flagellar mutants except a deltamot (motAB deletion) mutant, in which the amounts were greatly reduced. A new morphological pathway of flagellar biogenesis including protein secretion is presented.
我们分析了鼠伤寒沙门氏菌分泌到培养基中的所有主要蛋白质。通过三氯乙酸沉淀收集培养上清液中的蛋白质,在SDS-聚丙烯酰胺凝胶中进行分离,并通过氨基酸测序进行分析。野生型菌株SJW1103细胞在SDS凝胶中通常产生九条带:89、67、58、52、50、42、40、35 kDa以及(有时)28 kDa。在现有数据库中搜索这些序列发现,它们要么是鞭毛蛋白,要么是毒力因子。其中六条是鞭毛特异性的:FlgK或HAP1(58 kDa)、FliC或鞭毛蛋白(52 kDa)、FliD或HAP2(50 kDa)、FlgE或钩蛋白(42 kDa)、FlgL或HAP3(35 kDa)以及FlgD或钩帽蛋白(28 kDa)。其他四条带是毒力因子特异性的:SipA(89 kDa)、SipB(67 kDa)、SipC(42 kDa)和InvJ(40 kDa)。42 kDa的条带是FlgE和SipC的混合物。我们还分析了30多个鞭毛突变体分泌的蛋白质,根据其条带模式将它们分为四组:野生型、运动型、多钩型和主基因型。除了一个deltamot(motAB缺失)突变体中毒力因子的分泌量大幅减少外,所有鞭毛突变体中毒力因子的分泌水平都持续较高。本文提出了一种包括蛋白质分泌的鞭毛生物合成新形态学途径。