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海洋来源酵母Williopsis saturnus WC91-2 所产杀伤毒素的纯化、特性分析与基因克隆。

Purification, characterization and gene cloning of the killer toxin produced by the marine-derived yeast Williopsis saturnus WC91-2.

机构信息

UNESCO Chinese Center of Marine Biotechnology and Institute of Marine Biodiversity and Evolution, Ocean University of China, Yushan Road, No. 5, Qingdao, China.

出版信息

Microbiol Res. 2012 Oct 12;167(9):558-63. doi: 10.1016/j.micres.2011.12.001. Epub 2011 Dec 29.

Abstract

As the killer toxin produced by Williopsis saturnus WC91-2 could kill many sensitive yeast strains, including the pathogenic ones, the extracellular killer toxin in the supernatant of cell culture of the marine yeast strain was purified and characterized. The molecular mass of the purified killer toxin was estimated to be 11.0 kDa according to the data from SDS-PAGE. The purified killer toxin had killing activity, but could not hydrolyze laminarin. The optimal conditions for action of the purified killer toxin against the pathogenic yeast Metschnikowia bicuspidate WCY were the assay medium with 10% NaCl, pH 3-3.5 and temperature 16 °C. The gene encoding the killer toxin from the marine killer yeast WC91-2 was cloned and the ORF of the gene was 378 bp. The deduced protein from the cloned gene encoding the killer toxin had 125 amino acids with calculated molecular weight of 11.6 kDa. It was also found that the N-terminal amino acid sequence of the purified killer toxin had the same corresponding sequence deduced from the cloned killer toxin gene in this marine yeast, confirming that the purified killer toxin was indeed encoded by the cloned gene.

摘要

由于威氏被孢霉 WC91-2 产生的杀伤毒素能够杀死许多敏感酵母菌株,包括致病性酵母,因此对海洋酵母菌株细胞培养上清液中的细胞外杀伤毒素进行了纯化和特性分析。根据 SDS-PAGE 的数据,纯化的杀伤毒素的分子量估计为 11.0 kDa。纯化的杀伤毒素具有杀伤活性,但不能水解昆布多糖。对致病性酵母双尾酵母 WCY 起作用的最佳条件是含 10%NaCl、pH 值为 3-3.5 和温度为 16°C 的测定培养基。从海洋杀伤酵母 WC91-2 克隆了编码杀伤毒素的基因,该基因的 ORF 为 378 bp。从克隆的杀伤毒素基因编码的推导蛋白具有 125 个氨基酸,计算分子量为 11.6 kDa。还发现,纯化的杀伤毒素的 N 端氨基酸序列与该海洋酵母中克隆的杀伤毒素基因推导的相应序列相同,这证实了纯化的杀伤毒素确实是由克隆的基因编码的。

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