Advanced Laboratory for Plant Genetic Engineering (ALPGE), IIT-Kharagpur, Kharagpur, India.
Department of Biotechnology, IIT Kharagpur, Kharagpur, 721302, India.
Sci Rep. 2021 May 18;11(1):10543. doi: 10.1038/s41598-021-90050-8.
Pigeon pea, a grain legume of the semiarid tropics, is a rich source of high-quality protein. The productivity of this pulse is seriously affected by lepidopteron insect pests. To generate a sustainable insect-resistant plant, synthetically prepared bioactive key constituents of a crystal protein (Syn Cry1Ab) of Bacillus thuringiensis were expressed in pigeon pea under the guidance of a tissue-specific promoter of the RuBP carboxylase/oxygenase small subunit (rbcS) gene. Regenerated transgenic plants with the cry1Ab expression cassette (cry1Ab-lox-bar-lox) showed the optimum insect motility rate (90%) in an in vitro insect bioassay with second instar larvae, signifying the insecticidal potency of Syn Cry1Ab. In parallel, another plant line was also generated with a chimaeric vector harbouring a cre recombinase gene under the control of the CaMV 2 × 35S promoter. Crossing between T plants with a single insertion of cry1Ab-lox-bar-lox T-DNA and T plants with moderate expression of a cre gene with a linked hygromycin resistance (hptII) gene was performed to exclude the bialaphos resistance (bar) marker gene. Excision of the bar gene was achieved in TF hybrids, with up to 35.71% recombination frequency. Insect-resistant pigeon pea plants devoid of selectable marker genes (syn Cry1Ab- bar and cre-hptII) were established in a consecutive generation (TF) through genetic segregation.
兵豆是一种半干旱热带地区的谷物豆科植物,是高质量蛋白质的丰富来源。这种豆类的生产力受到鳞翅目昆虫的严重影响。为了生成可持续的抗虫植物,在 RuBP 羧化酶/加氧酶小亚基(rbcS)基因的组织特异性启动子的指导下,在兵豆中表达了苏云金芽孢杆菌合成的生物活性关键晶体蛋白(SynCry1Ab)的生物活性关键成分。具有 cry1Ab 表达盒(cry1Ab-lox-bar-lox)的再生转基因植物在第二龄幼虫的体外昆虫生物测定中表现出最佳的昆虫运动率(90%),表明 SynCry1Ab 的杀虫效力。同时,还生成了另一个植物株系,其带有 Cre 重组酶基因的嵌合载体在 CaMV2×35S 启动子的控制下表达。具有单个插入 cry1Ab-lox-bar-loxT-DNA 的 T 植物与具有连接的潮霉素抗性(hptII)基因的 Cre 基因中度表达的 T 植物之间进行了杂交,以排除草丁膦抗性(bar)标记基因。在 TF 杂种中,bar 基因的缺失达到了 35.71%的重组频率。通过遗传分离,在连续代(TF)中建立了不含选择标记基因(synCry1Ab-bar 和 cre-hptII)的抗虫兵豆植物。