Daines D A, Wright L F, Chaffin D O, Rubens C E, Silver R P
Department of Microbiology and Immunolgy, University of Rochester Medical Center, Rochester, NY 14642, USA.
FEMS Microbiol Lett. 2000 Aug 15;189(2):281-4. doi: 10.1111/j.1574-6968.2000.tb09244.x.
The polysialic acid capsule of Escherichia coli K1 is an essential virulence determinant. The kps gene cluster, which encodes the proteins necessary for polymer synthesis and transport, is divided into three functional regions. In this report, we present evidence that the neuD gene from region 2 is involved in sialic acid synthesis. A non-polar chromosomal deletion in neuD was constructed. The defect was complemented by neuD in trans or by the addition of exogenous sialic acid. A NeuD homologue, Neu(III)D, from serotype III Streptococcus agalactiae (GBS) also restored capsule expression to the neuD deletion strain. These data confirm the role of neuD in E. coli sialic acid capsule synthesis and demonstrate that the neu(III)D homologue from GBS shares a similar enzymatic function.
大肠杆菌K1的多聚唾液酸荚膜是一种重要的毒力决定因素。编码聚合物合成和运输所需蛋白质的kps基因簇分为三个功能区域。在本报告中,我们提供证据表明来自区域2的neuD基因参与唾液酸合成。构建了neuD中的非极性染色体缺失。该缺陷通过反式的neuD或添加外源性唾液酸得到互补。来自III型无乳链球菌(GBS)的NeuD同源物Neu(III)D也使neuD缺失菌株恢复了荚膜表达。这些数据证实了neuD在大肠杆菌唾液酸荚膜合成中的作用,并表明来自GBS的neu(III)D同源物具有相似的酶功能。