Biotechnology Institute, Shanghai Academy of Agricultural Sciences, Shanghai, China.
College of Chemistry, Chemical Engineering and Biotechnology of Donghua University, Shanghai, China.
Microbiologyopen. 2020 Nov;9(11):e1125. doi: 10.1002/mbo3.1125. Epub 2020 Oct 15.
Synthetic Cry1Ab/Ac proteins expressed by genetically modified (GM) crops have a high potential to control insect pests without utilizing large amounts of chemical insecticides. Before these crops are used in agriculture, the environmental fate and interactions in the soil must be understood. Stable isotope-labeled Cry1Ab/Ac protein is a highly useful tool for collecting such data. We developed a protocol to produce C/ N single-labeled Cry proteins. The artificially synthesized gene Cry1Ab/Ac of Bt rice Huahui No. 1, which has been certified by the Chinese government to be safe for human consumption, was subcloned into pUC57, and the expression vector pET-28a-CryAb/Ac was constructed and transformed into Escherichia coli BL21 (DE3) competent cells. Next, 0.2 mM isopropyl thiogalactoside (IPTG) was added to these cells and cultured at 37°C for 4 h to induce the synthesis and formation of inclusion bodies in M9 growth media containing either [U- C] glucose (5% C-enriched) or [ N] ammonium chloride (5% N-enriched). Then, Cry inclusion bodies were dissolved in urea and purified by affinity chromatography under denaturing conditions, renatured by dialysis, and further detected by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and Western blotting. The purities of C/ N-labeled Cry proteins reached 99% with amounts of 12.6 mg/L and 8.8 mg/L, respectively. The δ C and ä N values of C-labeled Cry protein and N-labeled Cry protein were 3,269‰ and 2,854‰, respectively. A bioassay test revealed that the labeled Cry1Ab/Ac proteins had strong insecticidal activity. The stable isotope-labeled insecticidal Cry proteins produced for the first time in this study will provide an experimental basis for future metabolic studies on Cry proteins in soil and the characteristics of nitrogen (N) and carbon (C) transformations. Our findings may also be employed as a reference for elucidating the environmental behavior and ecological effects of BT plants and expressed products.
由基因改良(GM)作物表达的合成 Cry1Ab/Ac 蛋白具有在不使用大量化学杀虫剂的情况下控制害虫的巨大潜力。在这些作物用于农业之前,必须了解其在土壤中的环境命运和相互作用。稳定同位素标记的 Cry1Ab/Ac 蛋白是收集此类数据的非常有用的工具。我们开发了一种生产 C/N 单标记 Cry 蛋白的方案。人工合成的经中国政府认证可安全食用的转 Bt 水稻华恢 1 号的 Cry1Ab/Ac 基因被亚克隆到 pUC57 中,并构建了表达载体 pET-28a-CryAb/Ac,然后转化到大肠杆菌 BL21(DE3)感受态细胞中。接下来,向这些细胞中加入 0.2 mM 的异丙基硫代半乳糖苷(IPTG),并在含有 [U- C] 葡萄糖(5% C 富集)或 [ N] 氯化铵(5% N 富集)的 M9 生长培养基中于 37°C 培养 4 小时,以诱导包含体在 M9 生长培养基中的合成和形成。然后,将 Cry 包含体溶解在脲中,并在变性条件下通过亲和层析进行纯化,通过透析复性,并进一步通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)和 Western 印迹进行检测。C/N 标记的 Cry 蛋白的纯度分别达到 99%,产量分别为 12.6mg/L 和 8.8mg/L。C 标记的 Cry 蛋白和 N 标记的 Cry 蛋白的 δ C 和 ä N 值分别为 3,269‰和 2,854‰。生物测定试验表明,标记的 Cry1Ab/Ac 蛋白具有很强的杀虫活性。本研究首次制备的稳定同位素标记杀虫 Cry 蛋白将为未来 Cry 蛋白在土壤中的代谢研究以及氮(N)和碳(C)转化的特性提供实验基础。我们的研究结果也可以作为阐明 BT 植物及其表达产物的环境行为和生态效应的参考。