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β-1,3-葡聚糖酶抑制了海洋来源酵母威克汉姆酵母 WC91-2 产生的杀伤毒素的活性。

beta-1,3-glucanase inhibits activity of the killer toxin produced by the marine-derived yeast Williopsis saturnus WC91-2.

机构信息

Key Laboratory of Marine Genetics and Gene Resource Exploitation (Ministry of Education), Ocean University of China, Yushan Road, No.5, Qingdao, China.

出版信息

Mar Biotechnol (NY). 2010 Aug;12(4):479-85. doi: 10.1007/s10126-009-9243-9. Epub 2009 Nov 26.

Abstract

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.

摘要

从患病螃蟹中分离到的病原酵母 Metschnikowia bicuspidata WCY 对海洋来源的Williopsis saturnus WC91-2 产生了很高的杀伤毒素活性。有趣的是,观察到从 W. saturnus WC91-2 中纯化的β-1,3-葡聚糖酶没有杀伤毒素活性,但可以抑制同一酵母产生的 WC91-2 毒素的活性。相比之下,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-葡聚糖酶与敏感酵母细胞壁上的β-1,3-葡聚糖竞争结合,导致与敏感酵母细胞壁上的β-1,3-葡聚糖结合的 WC91-2 毒素减少,以及对敏感酵母细胞的 WC91-2 毒素活性降低。为了使 W. saturnus WC91-2 对螃蟹中的酵母病产生高活性的 WC91-2 毒素,有必要删除编码β-1,3-葡聚糖酶的基因。

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