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Regulation of cadmium uptake by Saccharomyces cerevisiae

机译:酿酒酵母对镉吸收的调节

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In this work, we verified that yeast cells deleted in ZRT1 were not capable of transporting cadmium, suggesting that the transport of this metal into the cell would be carried out through this zinc transporter. On the other hand, cadmium absorption shown by a Δgsh1 strain (a mutant not able of synthesizing glutathione) was twofold higher than in the control strain. Moreover, the deletion of YCF1 (which encodes a vacuolar glutathione S-conjugate pump) impaired the transport of this metal significantly. Using a mutant strain deficient in YAP1, which codifies a transcription factor that controls the expression of both GSH1 and YCF1, we also observed a twofold increase in cadmium uptake, the same behavior shown by Δgsh1 cells. Cadmium is compartmentalized in vacuoles through the Ycf1 transporter, in the form of a bis-glutathionato-cadmium complex. We propose that gsh1 cells are unable to form the Cd-GS_2 complex, while ycf1 cells would accumulate high levels of this complex in the cytoplasm. In face of these results we raised the hypothesis that Cd-GS_2 complex controls cadmium uptake through the Zrt1 protein.
机译:在这项工作中,我们验证了ZRT1中缺失的酵母细胞不能够转运镉,这表明这种金属向细胞的转运将通过该锌转运蛋白进行。另一方面,Δgsh1菌株(不能合成谷胱甘肽的突变体)显示的镉吸收比对照菌株高两倍。此外,YCF1(编码液泡谷胱甘肽S-共轭泵)的缺失大大损害了这种金属的运输。使用缺乏YAP1的突变株,该株编码控制GSH1和YCF1两者表达的转录因子,我们还观察到镉吸收增加了两倍,与Δgsh1细胞显示的行为相同。镉以双谷胱甘肽-镉复合物的形式通过Ycf1转运蛋白在液泡中分隔。我们提出gsh1细胞无法形成Cd-GS_2复合物,而ycf1细胞将在细胞质中积累高水平的这种复合物。面对这些结果,我们提出了Cd-GS_2复合物控制通过Zrt1蛋白吸收镉的假设。

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