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beta-1,3-Glucanase Inhibits Activity of the Killer Toxin Produced by the Marine-Derived Yeast Williopsis saturnus WC91-2

机译:β-1,3-葡聚糖酶抑制海洋衍生的酵母Williopsis saturnus WC91-2产生的杀手毒素活性

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The marine-derived Williopsis saturnus WC91-2 was found to produce very high killer toxin activity against the pathogenic yeast Metschnikowia bicuspidata WCY isolated from the diseased crab. It is interesting to observe that the purified beta-1,3-glucanase from W. saturnus WC91-2 had no killer toxin activity but could inhibit activity of the WC91-2 toxin produced by the same yeast. In contrast, the WC91-2 toxin produced had no beta-1,3-glucanase activity. We found that the mechanisms of the inhibition may be that the beta-1,3-glucanase competed for binding to beta-1,3-glucan on the sensitive yeast cell wall with the WC91-2 toxin, causing decrease in the amount of the WC91-2 toxin bound to beta-1,3-glucan on the sensitive yeast cell wall and the activity of the WC91-2 toxin against the sensitive yeast cells. In order to make W. saturnus WC91-2 produce high activity of the WC91-2 toxin against the yeast disease in crab, it is necessary to delete the gene encoding beta-1,3-glucanase.
机译:发现海洋来源的Williopiss saturnus WC91-2对分离自患病蟹的致病性酵母Metschnikowia bicuspidata WCY产生很高的杀伤毒素活性。有趣的是,从土蜂WC91-2纯化的β-1,3-葡聚糖酶没有杀手毒素活性,但可以抑制同一酵母产​​生的WC91-2毒素的活性。相反,产生的WC91-2毒素没有β-1,3-葡聚糖酶活性。我们发现抑制的机制可能是β-1,3-葡聚糖酶与WC91-2毒素竞争结合敏感酵母细胞壁上的β-1,3-葡聚糖,从而导致其减少。 WC91-2毒素与敏感酵母细胞壁上的β-1,3-葡聚糖结合,并且WC91-2毒素针对敏感酵母细胞的活性。为了使W.saturnus WC91-2产生高活性的WC91-2毒素抵抗蟹中的酵母菌病,有必要删除编码β-1,3-葡聚糖酶的基因。

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