首页> 外文期刊>Biological trace element research >Promotion of Zn(2+) uptake by Al (3+) in a Saccharomyces Cerevisiae mutant that lacks the ZRT1 gene encoding a high-affinity Zn transporter.
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Promotion of Zn(2+) uptake by Al (3+) in a Saccharomyces Cerevisiae mutant that lacks the ZRT1 gene encoding a high-affinity Zn transporter.

机译:铝(3+)在酿酒酵母突变体中缺少编码高亲和力锌转运蛋白的ZRT1基因的锌(2+)吸收的促进。

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摘要

A Saccharomyces cerevisiae mutant (zrt1Delta) lacking the ZRT1 gene, which encodes a high-affinity Zn(2+) transporter, scarcely thrived in a low-pH, low-phosphate medium because of Zn(2+) deficiency. Supplementation of the medium with Al(3+) restored growth to a level comparable to that of a wild-type strain. A metal determination study clearly demonstrated that Al(3+) induced the incorporation of Zn(2+) into zrt1Delta cells, probably through the low-affinity Zn(2+) transporter Zrt2p, given that the zrt1Deltazrt2Delta double mutant did not show Al-induced growth enhancement. Al(3+) may have altered the speciation of Zn(2+) in the medium, resulting in enhanced levels of free Zn(2+). Alternatively, it might be that Zrt2p was degraded by endocytosis in the absence of Al(3+) and Al(3+) interfered with this process, resulting in enhanced Zn(2+) accumulation.
机译:一个酿酒酵母突变体(zrt1Delta)缺乏ZRT1基因,该基因编码一种高亲和力的Zn(2+)转运蛋白,由于Zn(2+)缺乏,在低pH值,低磷酸盐的培养基中几乎不旺盛。用Al(3+)补充培养基可使生长恢复到与野生型菌株相当的水平。一项金属测定研究清楚地表明,假设zrt1Deltazrt2Delta双突变体未显示Al-,Al(3+)可能通过低亲和力Zn(2+)转运蛋白Zrt2p诱导了Zn(2+)掺入zrt1Delta细胞。促进生长。 Al(3+)可能已经改变了培养基中Zn(2+)的形态,导致游离Zn(2+)含量提高。或者,可能是Zrt2p在不存在Al(3+)的情况下被胞吞作用降解了,Al(3+)干扰了此过程,导致增强的Zn(2+)积累。

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