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酿酒酵母细胞壁内层中一种甘露糖蛋白的鉴定。

Identification of a mannoprotein present in the inner layer of the cell wall of Saccharomyces cerevisiae.

作者信息

Moukadiri I, Armero J, Abad A, Sentandreu R, Zueco J

机构信息

Sección Departamental de Microbiología, Facultad de Farmacia, Universidad de Valencia, Burjassot, Spain.

出版信息

J Bacteriol. 1997 Apr;179(7):2154-62. doi: 10.1128/jb.179.7.2154-2162.1997.

DOI:10.1128/jb.179.7.2154-2162.1997
PMID:9079899
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC178950/
Abstract

Cell wall extracts from the double-mutant mnn1 mnn9 strain were used as the immunogen to obtain a monoclonal antibody (MAb), SAC A6, that recognizes a specific mannoprotein--which we have named Icwp--in the walls of cells of Saccharomyces cerevisiae. Icwp runs as a polydisperse band of over 180 kDa in sodium dodecyl sulfate-polyacrylamide gel electrophoresis analysis of Zymolyase extracts of cell walls, although an analysis of the secretory pattern of the mannoprotein shows that at the level of secretory vesicles, it behaves like a discrete band of 140 kDa. Immunofluorescence analysis with the MAb showed that Icwp lies at the inner layer of the cell wall, being accessible to the antibody only after the outer layer of mannoproteins is disturbed by treatment with tunicamycin. The screening of a lambda gt11 expression library enabled us to identify the open reading frame (ORF) coding for Icwp. ICWP (EMBL accession number YLR391w, frame +3) codes for 238 amino acids, of which over 40% are serine or threonine, and contains a putative N-glycosylation site and a putative glycosylphosphatidylinositol attachment signal. Both disruption and overexpression of the ORF caused increased sensitivities to calcofluor white and Congo red, while the disruption caused an increased sensitivity to Zymolyase digestion, suggesting for Icwp a structural role in association with glucan.

摘要

来自双突变体mnn1 mnn9菌株的细胞壁提取物被用作免疫原,以获得一种单克隆抗体(MAb)SAC A6,该抗体可识别酿酒酵母细胞壁中一种特定的甘露糖蛋白——我们将其命名为Icwp。在对细胞壁的溶菌酶提取物进行十二烷基硫酸钠-聚丙烯酰胺凝胶电泳分析时,Icwp呈现为一条超过180 kDa的多分散条带,尽管对该甘露糖蛋白分泌模式的分析表明,在分泌小泡水平上,它表现为一条140 kDa的离散条带。用该单克隆抗体进行的免疫荧光分析表明,Icwp位于细胞壁的内层,只有在用衣霉素处理使外层甘露糖蛋白受到干扰后,抗体才能接触到它。对λgt11表达文库的筛选使我们能够鉴定出编码Icwp的开放阅读框(ORF)。ICWP(EMBL登录号YLR391w,读码框+3)编码238个氨基酸,其中超过40%是丝氨酸或苏氨酸,并含有一个推定的N-糖基化位点和一个推定的糖基磷脂酰肌醇附着信号。该开放阅读框的破坏和过表达均导致对荧光增白剂和刚果红的敏感性增加,而破坏则导致对溶菌酶消化的敏感性增加,这表明Icwp在与葡聚糖结合中起结构作用。

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本文引用的文献

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Cell surface anchorage and ligand-binding domains of the Saccharomyces cerevisiae cell adhesion protein alpha-agglutinin, a member of the immunoglobulin superfamily.酿酒酵母细胞粘附蛋白α-凝集素的细胞表面锚定域和配体结合域,免疫球蛋白超家族的成员。
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