Vallari D S, Rock C O
J Bacteriol. 1985 Jun;162(3):1156-61. doi: 10.1128/jb.162.3.1156-1161.1985.
The transport system for pantothenic acid uptake in Escherichia coli was characterized. This transport system was specific for pantothenate, had a Kt of 0.4 microM, and had a maximum velocity of 1.6 pmol/min per 10(8) cells (45 pmol/min per mg [dry weight]). Pantothenate uptake was not reduced in osmotically shocked cells or by ATP depletion with arsenate, but was reduced greater than 90% by the dissipation of the membrane electrochemical gradient with 2,4-dinitrophenol. Sodium ions stimulated pantothenate uptake (Kt, 0.8 mM) by reducing the Kt for pantothenate by an order of magnitude. Intracellular pantothenate was rapidly phosphorylated, but phosphorylation of pantothenate was not required for uptake since pantothenate was the only labeled intracellular compound concentrated by ATP-depleted, glucose-energized cells. The data were consistent with the presence of a high-affinity pantothenate permease that concentrates the vitamin by sodium cotransport.
对大肠杆菌中泛酸摄取的转运系统进行了表征。该转运系统对泛酸盐具有特异性,其米氏常数(Kt)为0.4微摩尔,最大转运速度为每10⁸个细胞1.6皮摩尔/分钟(每毫克[干重]45皮摩尔/分钟)。在经渗透压休克的细胞中或用砷酸盐耗尽ATP后,泛酸盐的摄取并未减少,但用2,4-二硝基苯酚耗散膜电化学梯度后,摄取减少超过90%。钠离子通过将泛酸盐的Kt降低一个数量级来刺激泛酸盐的摄取(Kt为0.8毫摩尔)。细胞内的泛酸盐迅速被磷酸化,但摄取并不需要泛酸盐的磷酸化,因为泛酸盐是ATP耗尽、葡萄糖供能的细胞中唯一被浓缩的标记细胞内化合物。这些数据与存在一种通过钠共转运来浓缩维生素的高亲和力泛酸盐通透酶相一致。