Suppr超能文献

苏云金芽孢杆菌苏云金变种产生的鳞翅目毒素在大肠杆菌中的克隆与表达。

Cloning and expression of the lepidopteran toxin produced by Bacillus thuringiensis var. thuringiensis in Escherichia coli.

作者信息

Honigman A, Nedjar-Pazerini G, Yawetz A, Oron U, Schuster S, Broza M, Sneh B

出版信息

Gene. 1986;42(1):69-77. doi: 10.1016/0378-1119(86)90151-4.

Abstract

The Bacillus thuringiensis var. thuringiensis strain 3A produces a proteinaceous parasporal crystal toxic to larvae of a variety of lepidopteran pests including Spodoptera littoralis (Egyptian cotton leaf worm), Heliothis zeae, H. virescens and Boarmia selenaria. By cloning of individual plasmids of B. thuringiensis in Escherichia coli, we localized a gene coding for the delta-endotoxin on the B. thuringiensis plasmid of about 17 kb designated pTN4. Following partial digestion of the B. thuringiensis plasmid pTN4 and cloning into the E. coli pACYC184 plasmid three clones were isolated in which toxin production was detected. One of these hybrid plasmids pTNG43 carried a 1.7-kb insert that hybridized to the 14-kb BamHI DNA fragments of B. thuringiensis var. thuringiensis strains 3A and berliner 1715. This BamHI DNA fragment of strain berliner 1715 has been shown to contain the gene that codes for the toxic protein of the crystal (Klier et al., 1982). No homologous sequences have been found between pTNG33 and the DNA of B. thuringiensis var. entomocidus strain 24, which exhibited insecticidal activity against S. littoralis similar to that of strain 3A.

摘要

苏云金芽孢杆菌苏云金变种菌株3A产生一种蛋白质伴孢晶体,对多种鳞翅目害虫的幼虫有毒,这些害虫包括滨海夜蛾(埃及棉叶虫)、玉米螟、绿铃虫和苜蓿尺蛾。通过将苏云金芽孢杆菌的单个质粒克隆到大肠杆菌中,我们在约17 kb的苏云金芽孢杆菌质粒pTN4上定位了一个编码δ-内毒素的基因。对苏云金芽孢杆菌质粒pTN4进行部分酶切并克隆到大肠杆菌pACYC184质粒后,分离出三个检测到毒素产生的克隆。其中一个杂交质粒pTNG43携带一个1.7 kb的插入片段,它与苏云金芽孢杆菌苏云金变种菌株3A和柏林1715的14 kb BamHI DNA片段杂交。已证明柏林1715菌株的这个BamHI DNA片段含有编码晶体毒性蛋白的基因(Klier等人,1982年)。在pTNG33与对滨海夜蛾表现出与3A菌株类似杀虫活性的苏云金芽孢杆菌杀昆虫变种菌株24的DNA之间未发现同源序列。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验