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Genes involved in novel adaptive aluminum resistance in Rhodotorula glutinis

机译:参与新型适应性铝抗性的基因

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Rhodotorula glutinis IFO1125 acquired increased aluminum (Al) resistance from 50 μM to more than 5 mM by repetitive culturing with stepwise increases in Al concentration at pH 4.0. In our previous study we performed differential display to find that three genes (RgFET3, RgCET3, and RgCMK) encoding proteins homologous to Saccharomyces cerevisiae FET3p, GET3p, and CMK1p and CMK2p, respectively, were up-regulated in the Al-resistant cells. In this study we cloned these genes and found they were indeed up-regulated in Al-resistant strains. The cloned genes were introduced into 5. cerevisiae and corresponding mutants to test their relevance to Al resistance. The introduction of RgFET3 and RgGET3 conferred Al resistance to the host, but that of RgCMK did not. Green fluorescent protein (GFP)-tagged RgFet3p was localized at the cell periphery in the host. GFP-tagged RgGet3p formed more punctate bodies in the host under Al stress than in the absence of Al. Different growth responses to Fe (III), Cu (II), Ca ions, and cyclosporin A in the wild type and resistant cells of R. glutinis suggested the involvement and possible links of the three genes in Al resistance.
机译:通过在pH 4.0下逐步培养,通过在pH 4.0下逐步培养,rhodotorula Glutinis IFO1125获得从50μm的铝(Al)电阻从50μm到大于5mm。在我们之前的研究中,我们进行了差异显示,以发现将蛋白质的三种基因(RGFET3,RGCET3和RGCMK)分别在抗抗体细胞中调节与酿酒酵母FET3P,GET3P和CMK1P和CMK2P同源的蛋白质。在这项研究中,我们克隆了这些基因,发现它们在抗性菌株中确实调节了。将克隆基因引入5.酿酒酵母和相应的突变体,以测试它们与Al抗性的相关性。 RGFET3和RGGET3的引入赋予了抗议者的抗性,但RGCMK没有。绿色荧光蛋白(GFP)-GGFET3P在主体的细胞周边定位。 GFP标记的RGGET3P在宿主中形成了更多的点状物,而不是在缺乏A1的情况下。在野生型和抗菌细胞中对Fe(III),Cu(II),Ca离子和环孢菌素A不同的生长反应表明了三种基因在Al抗性中的参与和可能的链接。

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