Department of Microbiology, University of Manitoba, Winnipeg, Manitoba, Canada.
J Bacteriol. 2013 Aug;195(15):3424-32. doi: 10.1128/JB.00289-13. Epub 2013 May 24.
In Rhizobium leguminosarum the ABC transporter responsible for rhamnose transport is dependent on RhaK, a sugar kinase that is necessary for the catabolism of rhamnose. This has led to a working hypothesis that RhaK has two biochemical functions: phosphorylation of its substrate and affecting the activity of the rhamnose ABC transporter. To address this hypothesis, a linker-scanning random mutagenesis of rhaK was carried out. Thirty-nine linker-scanning mutations were generated and mapped. Alleles were then systematically tested for their ability to physiologically complement kinase and transport activity in a strain carrying an rhaK mutation. The rhaK alleles generated could be divided into three classes: mutations that did not affect either kinase or transport activity, mutations that eliminated both transport and kinase activity, and mutations that affected transport activity but not kinase activity. Two genes of the last class (rhaK72 and rhaK73) were found to have similar biochemical phenotypes but manifested different physiological phenotypes. Whereas rhaK72 conferred a slow-growth phenotype when used to complement rhaK mutants, the rhaK73 allele did not complement the inability to use rhamnose as a sole carbon source. To provide insight to how these insertional variants might be affecting rhamnose transport and catabolism, structural models of RhaK were generated based on the crystal structure of related sugar kinases. Structural modeling suggests that both rhaK72 and rhaK73 affect surface-exposed residues in two distinct regions that are found on one face of the protein, suggesting that this protein's face may play a role in protein-protein interaction that affects rhamnose transport.
在根瘤菌属中,负责鼠李糖运输的 ABC 转运蛋白依赖于 RhaK,这是一种糖激酶,对于鼠李糖的分解代谢是必需的。这导致了一个工作假设,即 RhaK 具有两种生化功能:其底物的磷酸化和影响鼠李糖 ABC 转运蛋白的活性。为了解决这个假设,对 rhaK 进行了连接扫描随机诱变。生成并映射了 39 个连接扫描突变。然后系统地测试等位基因在携带 rhaK 突变的菌株中补充激酶和运输活性的能力。生成的 rhaK 等位基因可分为三类:不影响激酶或运输活性的突变、消除运输和激酶活性的突变以及影响运输活性但不影响激酶活性的突变。最后一类的两个基因(rhaK72 和 rhaK73)具有相似的生化表型,但表现出不同的生理表型。虽然 rhaK72 用于补充 rhaK 突变体时赋予了缓慢生长表型,但 rhaK73 等位基因不能补充不能将鼠李糖作为唯一碳源的能力。为了深入了解这些插入变体如何影响鼠李糖的运输和分解代谢,根据相关糖激酶的晶体结构生成了 RhaK 的结构模型。结构建模表明,rhaK72 和 rhaK73 都影响位于蛋白质一个面上的两个不同区域的表面暴露残基,这表明该蛋白质的表面可能在影响鼠李糖运输的蛋白质-蛋白质相互作用中起作用。