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在光滑球拟酵母中,唯一的钾特异性转运蛋白 Trk1 有助于各种细胞过程的正常运作。

Trk1, the sole potassium-specific transporter in Candida glabrata, contributes to the proper functioning of various cell processes.

机构信息

Department of Microbiology, University of Córdoba, 14071, Córdoba, Spain.

Department of Membrane Transport, Institute of Physiology, Czech Academy of Sciences, 142 20, Prague 4, Czech Republic.

出版信息

World J Microbiol Biotechnol. 2019 Jul 26;35(8):124. doi: 10.1007/s11274-019-2698-6.

Abstract

Candida glabrata is a haploid yeast that is considered to be an emergent pathogen since it is the second most prevalent cause of candidiasis. Contrary to most yeasts, this species carries only one plasma membrane potassium transporter named CgTrk1. We show in this work that the activity of this transporter is regulated at the posttranslational level, and thus Trk1 contributes to potassium uptake under very different external cation concentrations. In addition to its function in potassium uptake, we report a diversity of physiological effects related to this transporter. CgTRK1 contributes to proper cell size, intracellular pH and membrane-potential homeostasis when expressed in Saccharomyces cerevisiae. Moreover, lithium influx experiments performed both in C. glabrata and S. cerevisiae indicate that the salt tolerance phenotype linked to CgTrk1 can be related to a high capacity to discriminate between potassium and lithium (or sodium) during the transport process. In summary, we show that CgTRK1 exerts a diversity of pleiotropic physiological roles and we propose that the corresponding protein may be an attractive pharmacological target for the development of new antifungal drugs.

摘要

光滑念珠菌是一种单倍体酵母,被认为是一种新兴的病原体,因为它是导致念珠菌病的第二大常见原因。与大多数酵母不同,该物种只携带一种名为 CgTrk1 的质膜钾转运蛋白。在这项工作中,我们表明该转运蛋白的活性在翻译后水平受到调节,因此 Trk1 在非常不同的外部阳离子浓度下有助于钾的摄取。除了其在钾摄取中的功能外,我们还报告了与该转运蛋白相关的多种生理效应。当在酿酒酵母中表达时,CgTRK1 有助于适当的细胞大小、细胞内 pH 和膜电位的动态平衡。此外,在 C. glabrata 和 S. cerevisiae 中进行的锂流入实验表明,与 CgTrk1 相关的耐盐表型可能与在运输过程中对钾和锂(或钠)进行高区分能力有关。总之,我们表明 CgTRK1 发挥了多种多效的生理作用,我们提出相应的蛋白可能是开发新型抗真菌药物的有吸引力的药理学靶标。

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