首页> 外文OA文献 >CSD2, CSD3, and CSD4, genes required for chitin synthesis in Saccharomyces cerevisiae: the CSD2 gene product is related to chitin synthases and to developmentally regulated proteins in Rhizobium species and Xenopus laevis.
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CSD2, CSD3, and CSD4, genes required for chitin synthesis in Saccharomyces cerevisiae: the CSD2 gene product is related to chitin synthases and to developmentally regulated proteins in Rhizobium species and Xenopus laevis.

机译:CSD2,CSD3和CSD4是酿酒酵母中几丁质合成所需的基因:CSD2基因产物与几丁质合酶以及根瘤菌属和非洲爪蟾中发育受调节的蛋白质有关。

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摘要

In Saccharomyces cerevisiae, chitin forms the primary division septum and the bud scar in the walls of vegetative cells. Three chitin synthetic activities have been detected. Two of them, chitin synthase I and chitin synthase II, are not required for synthesis of most of the chitin present in vivo. Using a novel screen, I have identified three mutations, designated csd2, csd3, and csd4, that reduce levels of chitin in vivo by as much as 10-fold without causing any obvious perturbation of cell division. The csd2 and csd4 mutants lack chitin synthase III activity in vitro, while csd3 mutants have wild-type levels of this enzyme. In certain genetic backgrounds, these mutations cause temperature-sensitive growth on rich medium; inclusion of salts or sorbitol bypasses this phenotype. Gene disruption experiments show that CSD2 is nonessential; a small amount of chitin, about 5% of the wild-type level, is detected in the disruptants. DNA sequencing indicates that the CSD2 protein has limited, but statistically significant, similarity to chitin synthase I and chitin synthase II. Other significant similarities are to two developmental proteins: the nodC protein from Rhizobium species and the DG42 protein of Xenopus laevis. The relationship between the nodC and CSD2 proteins suggests that nodC may encode an N-acetylglucosaminyltransferase that synthesizes the oligosaccharide backbone of the nodulation factor NodRm-1.
机译:在酿酒酵母中,几丁质在营养细胞壁上形成初次分裂的隔膜和芽疤。已检测到三种甲壳素合成活性。它们中的两个,几丁质合酶I和几丁质合酶II,对于体内存在的大多数几丁质的合成而言并不需要。使用新颖的屏幕,我确定了三个突变,分别命名为csd2,csd3和csd4,这些突变可将体内几丁质水平降低多达10倍,而不会引起细胞分裂的任何明显干扰。 csd2和csd4突变体在体外缺乏几丁质合酶III活性,而csd3突变体具有这种酶的野生型水平。在某些遗传背景下,这些突变会导致对温度敏感的培养基在富营养培养基上生长。包含盐或山梨糖醇可绕过该表型。基因破坏实验表明,CSD2是非必需的。在干扰物中检测到少量的几丁质,约占野生型水平的几丁质。 DNA测序表明,CSD2蛋白与几丁质合酶I和几丁质合酶II具有有限的相似性,但在统计学上具有显着意义。其他重要的相似之处是与两个发育蛋白:根瘤菌属的nodC蛋白和非洲爪蟾的DG42蛋白。 nodC和CSD2蛋白之间的关系表明,nodC可能编码N-乙酰氨基葡萄糖氨基转移酶,该酶合成结瘤因子NodRm-1的寡糖骨架。

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    Bulawa, C E;

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  • 年度 1992
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  • 正文语种 en
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