Basu D, Das S, Bandyopadhyay D, Sen S K
Plant Molecular and Cellular Genetics, Bose Institute, Calcutta, India.
Indian J Exp Biol. 1991 Nov;29(11):1002-9.
Necessity for the production of transgenic crop plants of India, capable of expression of insecticidal Bt protein in plant to combat lepidopteran pest damage has been strongly felt. Bacillus thuringiensis Kurstaki HD73 crystal protein coded by CryIA(c)73 gene has been found to be sufficiently effective against the major pests of jute and chickpea. An attempt to isolate the gene and make its use in a chimaeric gene construct for expression in plant was carried out. The plasmid CryIA(c)73 gene was cloned and tailored at the 3' end. The expression of the truncated gene was monitored in the minicell systems of E. coli. The entomocidal property was found to be fully retained by the gene product. Deletion of the nucleotides at the 5' end was carried out and chimaeric gene construct of cryIA(c)73 was made in such a way that it was fused in frame with GUS gene under the control of the caMV 35S promoter with Nos polyadenylated terminus. Such a chimaeric gene construct was used as the passenger of a Ti plasmid derived plant vector with kanamycin gene (NPTII) as the additional plant marker. Transformation through infection of tobacco and mustard plant cells in culture was carried out. Plants regenerated from the transformed cells showed the presence of GUS gene indicating the expression of the cloned fused gene. Also, Northern analysis established the presence of cryIA(c)73 gene transcripts in the transgenic plants.
印度迫切需要培育能够在植物中表达杀虫Bt蛋白以对抗鳞翅目害虫危害的转基因作物。已发现由CryIA(c)73基因编码的苏云金芽孢杆菌库尔斯塔克HD73晶体蛋白对黄麻和鹰嘴豆的主要害虫具有足够的防治效果。开展了分离该基因并将其用于嵌合基因构建体以在植物中表达的尝试。对质粒CryIA(c)73基因进行了克隆并在3'端进行了改造。在大肠杆菌的小细胞系统中监测了截短基因的表达。发现该基因产物完全保留了杀虫特性。对5'端的核苷酸进行了缺失操作,并构建了cryIA(c)73的嵌合基因构建体,使其与受caMV 35S启动子控制且带有Nos多聚腺苷酸化末端的GUS基因读框融合。这样的嵌合基因构建体被用作携带卡那霉素基因(NPTII)作为附加植物标记的Ti质粒衍生植物载体的外源基因。通过感染培养中的烟草和芥菜植物细胞进行了转化。从转化细胞再生的植物显示出GUS基因的存在,表明克隆的融合基因得到了表达。此外,Northern分析证实了转基因植物中存在cryIA(c)73基因转录本。