Trans-membrane Trafficking Unit, Okinawa Institute of Science and Technology, Onna, Kunigami, Okinawa, Japan.
PLoS One. 2012;7(8):e44030. doi: 10.1371/journal.pone.0044030. Epub 2012 Aug 29.
The bacterial type III export apparatus is found in the flagellum and in the needle complex of some pathogenic Gram-negative bacteria. In the needle complex its function is to secrete effector proteins for infection into Eukaryotic cells. In the bacterial flagellum it exports specific proteins for the building of the flagellum during its assembly. The export apparatus is composed of about five membrane proteins and three soluble proteins. The mechanism of the export apparatus is not fully understood. The five membrane proteins are well conserved and essential. Here a cross-complementation assay was performed: substituting in the flagellar system of Salmonella one of these membrane proteins, FlhB, by the FlhB ortholog from Aquifex aeolicus (an evolutionary distant hyperthermophilic bacteria) or a chimeric protein (AquSalFlhB) made by the combination of the trans-membrane domain of A. aeolicus FlhB with the cytoplasmic domain of Salmonella FlhB dramatically reduced numbers of flagella and motility. From cells expressing the chimeric AquSalFlhB protein, suppressor mutants with enhanced motility were isolated and the mutations were identified using whole genome sequencing. Gain-of-function mutations were found in the gene encoding FlhA, another membrane protein of the type III export apparatus. Also, mutations were identified in genes encoding 4-hydroxybenzoate octaprenyltransferase, ubiquinone/menaquinone biosynthesis methyltransferase, and 4-hydroxy-3-methylbut-2-en-1-yl diphosphate synthase, which are required for ubiquinone biosynthesis. The mutations were shown by reversed-phase high performance liquid chromatography to reduce the quinone pool of the cytoplasmic membrane. Ubiquinone biosynthesis could be restored for the strain bearing a mutated gene for 4-hydroxybenzoate octaprenyltransferase by the addition of excess exogenous 4-hydroxybenzoate. Restoring the level of ubiquinone reduced flagella biogenesis with the AquSalFlhB chimera demonstrating that the respiratory chain quinone pool is responsible for this phenomenon.
III 型细菌分泌装置存在于某些致病性革兰氏阴性菌的鞭毛和针状复合物中。在针状复合物中,它的功能是将效应蛋白分泌到真核细胞中以进行感染。在细菌鞭毛中,它在组装过程中输出特定的鞭毛构建蛋白。分泌装置由大约 5 种膜蛋白和 3 种可溶性蛋白组成。分泌装置的机制尚未完全了解。这 5 种膜蛋白高度保守且必不可少。在这里进行了交叉互补测定:在沙门氏菌的鞭毛系统中,用来自水生栖热菌(一种进化上较远的嗜热菌)的 FlhB 同源物或嵌合蛋白(由 A.aeolicus FlhB 的跨膜结构域与沙门氏菌 FlhB 的细胞质结构域组合而成)替代一种膜蛋白 FlhB,可显著降低鞭毛数量和运动性。从表达嵌合蛋白 AquSalFlhB 的细胞中,分离出具有增强运动性的抑制突变体,并使用全基因组测序鉴定突变。发现编码 FlhA 的基因发生了功能获得性突变,FlhA 是 III 型分泌装置的另一种膜蛋白。此外,还鉴定了编码 4-羟基苯甲酸八异戊烯基转移酶、泛醌/menaquinone 生物合成甲基转移酶和 4-羟基-3-甲基-2-丁烯-1-二磷酸合酶的基因突变,这些基因是泛醌生物合成所必需的。反向高效液相色谱法显示,突变导致质膜醌库减少。通过添加过量的外源 4-羟基苯甲酸,可以恢复 4-羟基苯甲酸八异戊烯基转移酶突变菌株的泛醌生物合成。恢复泛醌水平可减少携带 AquSalFlhB 嵌合体的菌毛生物发生,表明呼吸链醌库对此现象负责。