Ditty J L, Harwood C S
Department of Microbiology, The University of Iowa, Iowa City, Iowa 52242, USA.
J Bacteriol. 1999 Aug;181(16):5068-74. doi: 10.1128/JB.181.16.5068-5074.1999.
Chemotaxis to the aromatic acid 4-hydroxybenzoate (4-HBA) by Pseudomonas putida is mediated by PcaK, a membrane-bound protein that also functions as a 4-HBA transporter. PcaK belongs to the major facilitator superfamily (MFS) of transport proteins, none of which have so far been implicated in chemotaxis. Work with two well-studied MFS transporters, LacY (the lactose permease) and TetA (a tetracycline efflux protein), has revealed two stretches of amino acids located between the second and third (2-3 loop) and the eighth and ninth (8-9 loop) transmembrane regions that are required for substrate transport. These sequences are conserved among most MFS transporters, including PcaK. To determine if PcaK has functional requirements similar to those of other MFS transport proteins and to analyze the relationship between the transport and chemotaxis functions of PcaK, we generated strains with mutations in amino acid residues located in the 2-3 and 8-9 loops of PcaK. The mutant proteins were analyzed in 4-HBA transport and chemotaxis assays. Cells expressing mutant PcaK proteins had a range of phenotypes. Some transported at wild-type levels, while others were partially or completely defective in 4-HBA transport. An aspartate residue in the 8-9 loop that has no counterpart in LacY and TetA, but is conserved among members of the aromatic acid/H(+) symporter family of the MFS, was found to be critical for 4-HBA transport. These results indicate that conserved amino acids in the 2-3 and 8-9 loops of PcaK are required for 4-HBA transport. Amino acid changes that decreased 4-HBA transport also caused a decrease in 4-HBA chemotaxis, but the effect on chemotaxis was sometimes slightly more severe. The requirement of PcaK for both 4-HBA transport and chemotaxis demonstrates that P. putida has a chemoreceptor that differs from the classical chemoreceptors described for Escherichia coli and Salmonella typhimurium.
恶臭假单胞菌对芳香酸4-羟基苯甲酸(4-HBA)的趋化作用由PcaK介导,PcaK是一种膜结合蛋白,同时也作为4-HBA转运蛋白发挥作用。PcaK属于转运蛋白的主要易化子超家族(MFS),迄今为止,该家族中尚无成员与趋化作用有关。对两个经过充分研究的MFS转运蛋白LacY(乳糖通透酶)和TetA(四环素外排蛋白)的研究表明,在第二和第三跨膜区之间(2-3环)以及第八和第九跨膜区之间(8-9环)存在两段氨基酸序列,它们是底物运输所必需的。这些序列在包括PcaK在内的大多数MFS转运蛋白中是保守的。为了确定PcaK是否具有与其他MFS转运蛋白类似的功能要求,并分析PcaK的转运功能与趋化功能之间的关系,我们构建了PcaK的2-3环和8-9环中氨基酸残基发生突变的菌株。对突变蛋白进行了4-HBA转运和趋化分析。表达突变型PcaK蛋白的细胞具有一系列表型。一些细胞的转运水平与野生型相同,而另一些细胞在4-HBA转运方面部分或完全存在缺陷。在8-9环中发现了一个天冬氨酸残基,它在LacY和TetA中没有对应物,但在MFS的芳香酸/H(+)同向转运蛋白家族成员中是保守的,该残基对4-HBA转运至关重要。这些结果表明,PcaK的2-3环和8-9环中的保守氨基酸是4-HBA转运所必需的。降低4-HBA转运的氨基酸变化也导致4-HBA趋化作用降低,但对趋化作用的影响有时略为严重。PcaK对4-HBA转运和趋化作用都有要求,这表明恶臭假单胞菌有一种不同于大肠杆菌和鼠伤寒沙门氏菌中描述的经典化学感受器的化学感受器。