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中肠液成分影响苏云金芽孢杆菌杀虫毒素 Cry9Ca 的孔形成。

Midgut juice components affect pore formation by the Bacillus thuringiensis insecticidal toxin Cry9Ca.

机构信息

Groupe d'étude des protéines membranaires, Université de Montréal, Montreal, Quebec, Canada.

出版信息

J Invertebr Pathol. 2010 Jul;104(3):203-8. doi: 10.1016/j.jip.2010.04.007. Epub 2010 Apr 24.

Abstract

The pore-forming ability of the Bacillus thuringiensis toxin Cry9Ca, its two single-site mutants R164A and R164K, and the 55-kDa fragment resulting from its proteolytic cleavage at R164 was evaluated under a variety of experimental conditions using an electrophysiological assay. All four toxin preparations depolarized the apical membrane of freshly isolated third-instar Manduca sexta midguts bathing in a solution containing 122 mM KCl at pH 10.5, but the 55-kDa fragment was considerably more active than Cry9Ca and its mutants. The activity of the latter toxins was greatly enhanced, however, when the experiments were conducted in the presence of fifth-instar M. sexta midgut juice. This effect was also observed after midgut juice proteins had been denatured by heating at 95 degrees C or after inorganic ions and small molecules had been removed from the midgut juice by extensive dialysis. A similar stimulation of toxin activity was also observed when the experiments were carried out in the presence of the lipids extracted from an equivalent volume of midgut juice. Depolarization of the cell membrane was also greatly enhanced, in the absence of midgut juice, by the addition of a cocktail of water-soluble protease inhibitors. These results indicate that, depending on the cleavage site and on the experimental conditions used, further proteolysis of the activated Cry9Ca toxin can either stimulate or be detrimental to its activity and that M. sexta midgut juice probably contains protease inhibitors that could play a major role in the activity of B. thuringiensis toxins in the insect midgut.

摘要

采用电生理学检测方法,在各种实验条件下,评价了苏云金芽孢杆菌毒素 Cry9Ca 及其两个单点突变体 R164A 和 R164K 的成孔能力,以及在 R164 位点发生蛋白水解切割后产生的 55kDa 片段。这四种毒素制剂均能使 pH 值为 10.5、含 122mM KCl 的溶液中浸泡的刚分离的三龄烟蚜马氏管顶端膜去极化,但 55kDa 片段的活性明显高于 Cry9Ca 及其突变体。然而,当实验在五龄烟蚜马氏管消化液存在的情况下进行时,后两种毒素的活性大大增强。当用 95°C 加热使中肠液蛋白变性,或用大量透析去除中肠液中的无机离子和小分子后,也观察到这种效应。在用相当于中肠液体积的脂质提取物存在的情况下进行实验时,也观察到类似的毒素活性刺激作用。在没有中肠液的情况下,添加水溶性蛋白酶抑制剂混合物也大大增强了细胞膜的去极化作用。这些结果表明,根据裂解部位和实验条件的不同,激活的 Cry9Ca 毒素的进一步蛋白水解可能会刺激或损害其活性,并且烟蚜马氏管消化液可能含有蛋白酶抑制剂,这些抑制剂可能在昆虫中肠中苏云金芽孢杆菌毒素的活性中发挥重要作用。

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