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首页> 外文期刊>EMBO Journal >Tolerance to toxic metals by a gene family of phytochelatin synthases from plants and yeast.
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Tolerance to toxic metals by a gene family of phytochelatin synthases from plants and yeast.

机译:宽容有毒金属的基因家族决定液泡植物螯合肽合成酶从植物和酵母。

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摘要

Phytochelatins play major roles in metal detoxification in plants and fungi. However, genes encoding phytochelatin synthases have not yet been identified. By screening for plant genes mediating metal tolerance we identified a wheat cDNA, TaPCS1, whose expression in Saccharomyces cerevisiae results in a dramatic increase in cadmium tolerance. TaPCS1 encodes a protein of approximately 55 kDa with no similarity to proteins of known function. We identified homologs of this new gene family from Arabidopsis thaliana, Schizosaccharomyces pombe, and interestingly also Caenorhabditis elegans. The Arabidopsis and S.pombe genes were also demonstrated to confer substantial increases in metal tolerance in yeast. PCS-expressing cells accumulate more Cd2+ than controls. PCS expression mediates Cd2+ tolerance even in yeast mutants that are either deficient in vacuolar acidification or impaired in vacuolar biogenesis. PCS-induced metal resistance is lost upon exposure to an inhibitor of glutathione biosynthesis, a process necessary for phytochelatin formation. Schizosaccharomyces pombe cells disrupted in the PCS gene exhibit hypersensitivity to Cd2+ and Cu2+ and are unable to synthesize phytochelatins upon Cd2+ exposure as determined by HPLC analysis. Saccharomyces cerevisiae cells expressing PCS produce phytochelatins. Moreover, the recombinant purified S.pombe PCS protein displays phytochelatin synthase activity. These data demonstrate that PCS genes encode phytochelatin synthases and mediate metal detoxification in eukaryotes.
机译:金属转移中扮演主要的角色解毒的植物和真菌。决定液泡植物螯合肽合成酶基因编码没有未被确认。调节金属宽容我们确定了小麦在酿酒cDNA、TaPCS1的表达式酵母导致戏剧性的增加镉宽容。大约55 kDa没有相似性蛋白质的功能。从拟南芥同源染色体的基因家族芥、粟酒裂殖酵母有趣的是秀丽隐杆线虫。拟南芥和S.pombe基因也证明带来大幅增加金属耐受酵母。积累更多Cd2 +比控制。即使在酵母表达介导Cd2 +公差突变体,在空泡的不足酸化或受损的空泡的生物转化。PCS-induced金属电阻丢失谷胱甘肽的抑制剂生物合成,一个必要的过程决定液泡植物螯合肽的形成。非洲酒细胞破坏电脑基因的展览过敏症Cd2 +和Cu2 +和不能合成对Cd2 +风险转移由高效液相色谱分析。酵母细胞表达个人电脑生产转移。蛋白质纯化S.pombe电脑显示器决定液泡植物螯合肽合成酶活性。证明电脑基因编码决定液泡植物螯合肽合成酶和调解金属解毒真核生物。

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