Pavelka M S, Wright L F, Silver R P
Department of Microbiology and Immunology, University of Rochester Medical Center, New York 14642.
J Bacteriol. 1991 Aug;173(15):4603-10. doi: 10.1128/jb.173.15.4603-4610.1991.
The polysialic acid capsule of Escherichia coli K1, a causative agent of neonatal septicemia and meningitis, is an essential virulence determinant. The 17-kb kps gene cluster, which is divided into three functionally distinct regions, encodes proteins necessary for polymer synthesis and expression at the cell surface. The central region, 2, encodes products required for synthesis, activation, and polymerization of sialic acid, while flanking regions, 1 and 3, are thought to be involved in polymer assembly and transport. In this study, we identified two genes in region 3, kpsM and kpsT, which encode proteins with predicted sizes of 29.6 and 24.9 kDa, respectively. The hydrophobicity profile of KpsM suggests that it is an integral membrane protein, while KpsT contains a consensus ATP-binding domain. KpsM and KpsT belong to a family of prokaryotic and eukaryotic proteins involved with a variety of biological processes, including membrane transport. A previously described kpsT chromosomal mutant that accumulates intracellular polysialic acid was characterized and could be complemented in trans. Results of site-directed mutagenesis of the putative ATP-binding domain of KpsT are consistent with the view that KpsT is a nucleotide-binding protein. KpsM and KpsT have significant similarity to BexB and BexA, two proteins that are essential for polysaccharide capsule expression in Haemophilus influenzae type b. We propose that KpsM and KpsT constitute a system for transport of polysialic acid across the cytoplasmic membrane.
大肠杆菌K1的多聚唾液酸荚膜是新生儿败血症和脑膜炎的病原体,是一种重要的毒力决定因素。17kb的kps基因簇分为三个功能不同的区域,编码细胞表面聚合物合成和表达所需的蛋白质。中心区域2编码唾液酸合成、激活和聚合所需的产物,而侧翼区域1和3被认为参与聚合物的组装和运输。在本研究中,我们在区域3中鉴定出两个基因,kpsM和kpsT,它们分别编码预测大小为29.6 kDa和24.9 kDa的蛋白质。KpsM的疏水性图谱表明它是一种整合膜蛋白,而KpsT含有一个共有ATP结合结构域。KpsM和KpsT属于原核和真核蛋白质家族,参与包括膜运输在内的多种生物过程。一个先前描述的积累细胞内多聚唾液酸的kpsT染色体突变体被鉴定出来,并且可以通过反式互补。KpsT推定的ATP结合结构域的定点诱变结果与KpsT是一种核苷酸结合蛋白的观点一致。KpsM和KpsT与BexB和BexA有显著相似性,这两种蛋白对b型流感嗜血杆菌多糖荚膜的表达至关重要。我们提出KpsM和KpsT构成了一个多聚唾液酸跨细胞质膜运输的系统。