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将溶藻弧菌中Na⁺依赖的K⁺摄取系统KtrAB的四个选择性过滤器甘氨酸中的一个替换为丙氨酸,会导致该系统对K⁺和Na⁺的亲和力降低两个数量级。

Change to alanine of one out of four selectivity filter glycines in KtrB causes a two orders of magnitude decrease in the affinities for both K+ and Na+ of the Na+ dependent K+ uptake system KtrAB from Vibrio alginolyticus.

作者信息

Tholema N, Bakker E P, Suzuki A, Nakamura T

机构信息

Abteilung Mikrobiologie, Universität Osnabrück, Germany.

出版信息

FEBS Lett. 1999 May 7;450(3):217-20. doi: 10.1016/s0014-5793(99)00504-9.

Abstract

KtrAB from Vibrio alginolyticus is a recently described new type of high affinity bacterial K+ uptake system. Its activity assayed in an Escherichia coli K+ uptake negative mutant depended on Na+ ions (Km of 40 microM). Subunit KtrB contains four putative P-loops. The selectivity filter from each P-loop contains a conserved glycine residue. Residue Gly-290 from the third P-loop selectivity filter in KtrB was exchanged for Ala, Ser or Asp. KtrB variants Ser-290 and Asp-290 were without activity. In contrast, KtrB variant Ala-290 was still active. This variant transported K+ with a two orders of magnitude decrease in apparent affinity for both K+ and Na+ with little effect on Vmax.

摘要

溶藻弧菌的KtrAB是最近描述的一种新型高亲和力细菌钾离子摄取系统。在大肠杆菌钾离子摄取阴性突变体中测定其活性时,该活性依赖于钠离子(Km为40微摩尔)。亚基KtrB包含四个假定的P环。每个P环的选择性过滤器都含有一个保守的甘氨酸残基。KtrB中第三个P环选择性过滤器的甘氨酸-290残基被替换为丙氨酸、丝氨酸或天冬氨酸。KtrB变体丝氨酸-290和天冬氨酸-290没有活性。相比之下,KtrB变体丙氨酸-290仍然具有活性。该变体转运钾离子时,对钾离子和钠离子的表观亲和力下降了两个数量级,而对最大反应速度影响很小。

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