Koyasu S
J Biochem. 1984 Nov;96(5):1351-64. doi: 10.1093/oxfordjournals.jbchem.a134963.
Defective flagellar organella, stubs, and flagellin synthesis by L-[35S]methionine labeling of two non-motile mutants of C. crescentus CB15 were studied. CB15 wild type synthesized two flagellin species, flagellin A of molecular weight 26,000 and flagellin B of molecular weight 28,000. A DNA phage phi0CbK-resistant non-motile mutant, CB15 pdr-816 [Fukuda et al. (1981) J. Bacteriol. 145, 559-572] did not synthesize flagellin B but synthesized large amounts of flagellin A and a novel flagellin of smaller molecular weight 22,000 (22K flagellin), and formed stubs composed of both flagellin A and 22K flagellin. The other mutant, CB15 fla-801 synthesized only 22K flagellin and formed very short stubs composed of 22K flagellin. Motile revertants were isolated from these mutants. Full revertants were isolated from CB15 fla-801 at a frequency of ca. 10(-7). However, only partial revertants swimming slowly were obtained from CB15 pdr-816 at a similar frequency. Such partial revertants synthesized only flagellin A and formed short flagella in spite of the fact that flagellin A was still synthesized at a higher level than in the wild type. Given the previous finding that flagellin B first polymerizes onto the hook followed by addition of flagellin A onto flagellin B filament [Koyasu et al. (1981) J. Mol. Biol. 153, 471-475], flagellin B seems very important in the formation of normal flagella in C. crescentus. A small amount of 22K flagellin was detected even in wild type cell. Neither conversion nor alteration was observed in flagellin A or B or 22K flagellin by short-pulse and pulse-chase experiments. It was thus suggested that 22K flagellin was not a degradation product formed from other flagellins but was of different origin from flagellins A and B. C. crescentus flagellins consist of several subspecies of different isoelectric points. 22K flagellin consisted of at least three subspecies, in two-dimensional gel, with more basic isoelectric points than other flagellins. Heterogeneity in isoelectric point of polymerized and nascent flagellins was similar, indicating that each subspecies of different isoelectric point can polymerize into filament, and that conversion between subspecies is not needed to form flagellar filament.
通过用L-[35S]甲硫氨酸标记新月柄杆菌CB15的两个非运动型突变体,研究了有缺陷的鞭毛细胞器、残端以及鞭毛蛋白的合成。CB15野生型合成了两种鞭毛蛋白,分子量为26,000的鞭毛蛋白A和分子量为28,000的鞭毛蛋白B。一个对DNA噬菌体phi0CbK有抗性的非运动型突变体,CB15 pdr-816 [福田等人(1981年)《细菌学杂志》145卷,559 - 572页]不合成鞭毛蛋白B,但合成大量的鞭毛蛋白A和一种分子量较小的新型鞭毛蛋白22,000(22K鞭毛蛋白),并形成了由鞭毛蛋白A和22K鞭毛蛋白组成的残端。另一个突变体CB15 fla-801只合成22K鞭毛蛋白,并形成了由22K鞭毛蛋白组成的非常短的残端。从这些突变体中分离出了运动型回复体。从CB15 fla-801中以约10^(-7)的频率分离出了完全回复体。然而,从CB15 pdr-816中仅以类似频率获得了游动缓慢的部分回复体。尽管鞭毛蛋白A的合成水平仍高于野生型,但这些部分回复体只合成鞭毛蛋白A并形成短鞭毛。鉴于先前的发现,即鞭毛蛋白B首先在钩上聚合,随后鞭毛蛋白A添加到鞭毛蛋白B丝上[小安素等人(1981年)《分子生物学杂志》153卷,471 - 475页],鞭毛蛋白B在新月柄杆菌正常鞭毛的形成中似乎非常重要。即使在野生型细胞中也检测到少量的22K鞭毛蛋白。通过短脉冲和脉冲追踪实验未观察到鞭毛蛋白A、B或22K鞭毛蛋白的转化或改变。因此表明22K鞭毛蛋白不是由其他鞭毛蛋白形成的降解产物,而是与鞭毛蛋白A和B来源不同。新月柄杆菌鞭毛蛋白由几个不同等电点的亚种组成。在二维凝胶中,22K鞭毛蛋白至少由三个亚种组成,其等电点比其他鞭毛蛋白更碱性。聚合的和新生的鞭毛蛋白在等电点上的异质性相似,表明不同等电点的每个亚种都可以聚合成丝,并且在形成鞭毛丝时不需要亚种之间的转化。