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全长 Cry1Ac 原毒素未经蛋白水解激活对昆虫细胞系 CF-203 具有毒性。

The full-length Cry1Ac protoxin without proteolytic activation exhibits toxicity against insect cell line CF-203.

机构信息

College of Life Science, State Key Laboratory of Developmental Biology of Freshwater Fish, Hunan Normal University, Changsha 410081, PR China.

College of Life Science, State Key Laboratory of Developmental Biology of Freshwater Fish, Hunan Normal University, Changsha 410081, PR China.

出版信息

J Invertebr Pathol. 2018 Feb;152:25-29. doi: 10.1016/j.jip.2018.01.004. Epub 2018 Feb 3.

Abstract

The new dual model for Bacillus thuringiensis insecticidal mechanism proposed that Cry1A protoxins without proteolytic activation could bind to insect midgut receptors to exert toxicity. To evaluate insecticidal potency of Cry1Ac protoxin at precluding interference of midgut proteases, the cytotoxicity of Cry1Ac protoxin against midgut cell line CF-203 derived from Choristoneura fumiferana was analyzed. It was revealed that Cry1Ac protoxin was toxic to CF-203 cells and there existed certain differences in the cytological changes when treated with protoxin and toxin. Our cell-based study provided direct evidence for the proposed dual model and shed light on exploring the difference between two toxic pathways elicited by intact protoxin and activated toxin.

摘要

新的苏云金芽孢杆菌杀虫机制双模理论提出,Cry1A 原毒素未经蛋白水解激活也能与昆虫中肠受体结合而发挥毒性。为了评估 Cry1Ac 原毒素在排除中肠蛋白酶干扰时的杀虫效力,分析了 Cry1Ac 原毒素对源自舞毒蛾的中肠细胞系 CF-203 的细胞毒性。结果表明,Cry1Ac 原毒素对 CF-203 细胞有毒性,原毒素和毒素处理时存在细胞形态变化的差异。我们的基于细胞的研究为提出的双模理论提供了直接证据,并为探索完整原毒素和激活毒素引发的两种毒性途径之间的差异提供了线索。

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