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一株酿酒酵母的抗木霉菌素突变体,其天然核糖体亚基分布异常。

A trichodermin-resistant mutant of Saccharomyces cerevisiae with an abnormal distribution of native ribosomal subunits.

作者信息

Carter C J, Cannon M, Jiménez A

出版信息

Eur J Biochem. 1980;107(1):173-83. doi: 10.1111/j.1432-1033.1980.tb04638.x.

Abstract
  1. A yeast mutant (CLP-8), resistant at the ribosome level to the trichothecene antibiotic trichodermin, differs from its parent in having an unusual distribution of native ribosomal subunits. Sucrose gradient analysis of cytoplasmic extracts from this mutant revealed a large excess of material sedimenting at 60 S with little or no material sedimenting at 40 S. 2. The excess 609-S material consists predominantly of functionally active 60-S ribosomal subunits, as indicated by both analysis of ribosomal RNA and studies in vitro using a poly(U)-directed protein-synthesizing system. 3. Using the poly(U) system it was found that high-salt-washed particles derived from either the excess 60-S peak or 80-S ribosomes of CLP-8 exhibited very similar levels of resistance to the antibiotic fusarenon-X, a drug closely related chemically to trichodermin. The same level of resistance to fusarenon-X was also shown by high-salt-washed 60-S ribosomal particles obtained from a further trichodermin-resistant yeast strain (TR-1), although this strain has a normal distribution of native ribosomal subunits. In addition, both CLP-8 and TR-1 are equally resistant to inhibition of protein synthesis by trichothecene antibiotics, as assayed in vivo. 4. Genetic analysis of CLP-8 indicates that the trichodermin-resistant trait can be segregated from the lesion responsible for the inbalance of native ribosomal subunits. However, the latter defect is only expressed phenotypically in cells that retain the trichodermin-resistant character. 5. CLP-8 has a further defect in that both in vivo and in vitro it fails to generate native 40-S ribosomal subunits from 80-S particles. There may be a lesion in the protein factor normally required for this process.
摘要
  1. 一种酵母突变体(CLP - 8),在核糖体水平对单端孢霉烯族抗生素木霉烯素具有抗性,与其亲本的不同之处在于天然核糖体亚基的分布异常。对该突变体细胞质提取物进行蔗糖梯度分析,结果显示在60S处有大量物质沉降,而在40S处只有少量或没有物质沉降。2. 过量的60S物质主要由功能活性的60S核糖体亚基组成,核糖体RNA分析以及使用聚(U)指导的蛋白质合成系统进行的体外研究均表明了这一点。3. 使用聚(U)系统发现,源自CLP - 8过量60S峰或80S核糖体的高盐洗涤颗粒,对与木霉烯素化学结构密切相关的抗生素镰刀菌烯醇 - X表现出非常相似的抗性水平。从另一株对木霉烯素具有抗性的酵母菌株(TR - 1)获得的高盐洗涤60S核糖体颗粒,对镰刀菌烯醇 - X也表现出相同水平的抗性,尽管该菌株天然核糖体亚基分布正常。此外,如体内测定所示,CLP - 8和TR - 1对单端孢霉烯族抗生素抑制蛋白质合成的抗性相同。4. 对CLP - 8的遗传分析表明,对木霉烯素的抗性性状可以与导致天然核糖体亚基失衡的损伤分离。然而,后一种缺陷仅在保留木霉烯素抗性特征的细胞中表现出表型。\n5. CLP - 8还有另一个缺陷,即无论在体内还是体外,它都无法从80S颗粒生成天然40S核糖体亚基。在这个过程中正常所需的蛋白质因子可能存在损伤。

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