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苏云金芽孢杆菌δ-内毒素片段的基因组扩增与表达

Genomic amplification and expression of delta-endotoxin fragment of Bacillus thuringiensis.

作者信息

Roy P

机构信息

Hindustan Lever Research Centre, Bombay, India.

出版信息

Biochem Biophys Res Commun. 1992 Sep 16;187(2):641-7. doi: 10.1016/0006-291x(92)91243-j.

Abstract

delta-Endotoxin gene of Bacillus thuringiensis HD-1 var kurstaki codes for the insecticidal crystal protein (ICP) specific for lepidopteran insects. Since the N-terminal half of the toxin is sufficient both for insect specificity and toxicity, the coding sequence of this part of the gene CryIA(b) was amplified by PCR and cloned in pUC19. As there was no expression of immunologically detectable delta-endotoxin in this clone in E. coli, the amplified ICP gene was transferred to an expression vector pGEx2T. Restriction mapping and immunoblotting confirmed the presence and expression of the CryIA(b) gene. This insert should be suitable for expression in plant system if it is mobilized into a plant binary vector.

摘要

苏云金芽孢杆菌HD-1库斯塔克变种的δ-内毒素基因编码对鳞翅目昆虫具有特异性的杀虫晶体蛋白(ICP)。由于毒素的N端一半对于昆虫特异性和毒性而言已足够,因此通过PCR扩增该基因CryIA(b)这部分的编码序列,并克隆到pUC19中。由于该克隆在大肠杆菌中未表达出可免疫检测的δ-内毒素,因此将扩增的ICP基因转移到表达载体pGEx2T中。限制性图谱分析和免疫印迹证实了CryIA(b)基因的存在和表达。如果将该插入片段导入植物双元载体,它应该适合在植物系统中表达。

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