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CheZ Phosphatase Localizes to Chemoreceptor Patches via CheA-Short

机译:CheZ磷酸酶通过CheA-Short定位到化学受体补丁

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摘要

We have investigated the conditions required for polar localization of the CheZ phosphatase by using a CheZ-green fluorescent protein fusion protein that, when expressed from a single gene in the chromosome, restored chemotaxis to a ΔcheZ strain. Localization was observed in wild-type, ΔcheZ, ΔcheYZ, and ΔcheRB cells but not in cells with cheA, cheW, or all chemoreceptor genes except aer deleted. Cells making only CheA-short (CheAS) or CheA lacking the P2 domain also retained normal localization, whereas cells producing only CheA-long or CheA missing the P1 and P2 domains did not. We conclude that CheZ localization requires the truncated C-terminal portion of the P1 domain present in CheAS. Missense mutations targeting residues 83 through 120 of CheZ also abolished localization. Two of these mutations do not disrupt chemotaxis, indicating that they specifically prevent interaction with CheAS while leaving other activities of CheZ intact.
机译:我们已经研究了通过使用CheZ-绿色荧光蛋白融合蛋白对CheZ磷酸酶进行极性定位所需的条件,该蛋白从染色体中的单个基因表达时,将趋化性恢复为ΔcheZ菌株。在野生型,ΔcheZ,ΔcheYZ和ΔcheRB细胞中观察到定位,但在缺失aer或cheA,cheW或所有化学感受器基因的细胞中未观察到定位。仅产生CheA短(CheAS)或CheA缺乏P2域的细胞也保留正常定位,而仅产生CheA短或CheA缺失P1和P2域的细胞则没有。我们得出结论,CheZ定位需要CheAS中存在的P1域的截短的C端部分。针对CheZ的83至120位残基的错义突变也消除了定位。这些突变中的两个不会破坏趋化性,这表明它们在阻止CheZ的其他活性的同时特异性阻止了与CheAS的相互作用。

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