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鳞翅目活性苏云金芽孢杆菌蛋白晶体的非酶糖基化。

Nonenzymatic Glycosylation of Lepidopteran-Active Bacillus thuringiensis Protein Crystals.

机构信息

School of Biological Sciences, University of Nebraska, Lincoln, Nebraska 68588-0343.

出版信息

Appl Environ Microbiol. 1993 Aug;59(8):2666-72. doi: 10.1128/aem.59.8.2666-2672.1993.

Abstract

We used high-pH anion-exchange chromatography with pulsed amperometric detection to quantify the monosaccharides covalently attached to Bacillus thuringiensis HD-1 (Dipel) crystals. The crystals contained 0.54% sugars, including, in decreasing order of prevalence, glucose, fucose, arabinose/rhamnose, galactose, galactosamine, glucosamine, xylose, and mannose. Three lines of evidence indicated that these sugars arose from nonenzymatic glycosylation: (i) the sugars could not be removed by N- or O-glycanases; (ii) the sugars attached were influenced both by the medium in which the bacteria had been grown and by the time at which the crystals were harvested; and (iii) the chemical identity and stoichiometry of the sugars detected did not fit any known glycoprotein models. Thus, the sugars detected were the product of fermentation conditions rather than bacterial genetics. The implications of these findings are discussed in terms of crystal chemistry, fermentation technology, and the efficacy of B. thuringiensis as a microbial insecticide.

摘要

我们使用高 pH 值阴离子交换色谱和脉冲安培检测来定量分析苏云金芽孢杆菌 HD-1(Dipel)晶体上共价结合的单糖。晶体中含有 0.54%的糖,按出现频率递减的顺序依次为:葡萄糖、岩藻糖、阿拉伯糖/鼠李糖、半乳糖、半乳糖胺、葡糖胺、木糖和甘露糖。有三条证据表明这些糖是由非酶糖基化产生的:(i)糖不能被 N-或 O-糖苷酶去除;(ii)附着的糖既受细菌生长的培养基影响,也受晶体收获时间的影响;(iii)检测到的糖的化学性质和化学计量与任何已知的糖蛋白模型都不相符。因此,检测到的糖是发酵条件的产物,而不是细菌遗传学的产物。这些发现的意义从晶体化学、发酵技术和苏云金芽孢杆菌作为微生物杀虫剂的功效等方面进行了讨论。

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