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苏云金芽孢杆菌暗黑变种突变毒素基因的异源表达。

Heterologous expression of a mutated toxin gene from Bacillus thuringiensis subsp. tenebrionis.

作者信息

Rhim S L, Jahn N, Schnetter W, Geider K

机构信息

Max-Planck-Institut für medizinische Forschung, Abteilung Molekulare Biologie, Heidelberg, F.R.G.

出版信息

FEMS Microbiol Lett. 1990 Jan 1;54(1-3):95-9. doi: 10.1016/0378-1097(90)90264-q.

Abstract

Using oligonucleotide probes we have isolated a DNA fragment encoding an insecticidal toxin of the coleopteran specific Bacillus thuringiensis subsp. tenebrionis. The gene was altered by site directed mutagenesis at its 5'-end and adapted for general cloning and expression purposes with a linker including a start codon and new restriction sites. The constructs were inserted into several vector plasmids and expressed in Escherichia coli. Expression E. coli was strongly enhanced by the lac-promoter. A fusion protein with phage MS2-polymerase was produced together with a 67 kDa protein also found for normal expression of the toxin gene. Synthesis of the latter protein indicated a second ribosome binding site at the 5'-terminus of the toxin encoding sequence. Toxin-containing proteins were identified by Western blot analysis. The positive cell extracts from E. coli had insecticidal activity on larvae of the Colorado potato beetle. The cloned gene is not homologous to a gene previously cloned by us whose gene products were also toxic to coleopteran larvae.

摘要

我们使用寡核苷酸探针分离出了一段DNA片段,该片段编码鞘翅目特异性苏云金芽孢杆菌亚种tenebrionis的一种杀虫毒素。通过定点诱变改变了该基因的5′端,并通过包含起始密码子和新限制酶切位点的接头使其适用于一般的克隆和表达目的。构建体被插入到几种载体质粒中并在大肠杆菌中表达。lac启动子强烈增强了在大肠杆菌中的表达。产生了一种与噬菌体MS2聚合酶的融合蛋白,同时还产生了一种67 kDa的蛋白,该蛋白在毒素基因正常表达时也能被发现。后一种蛋白的合成表明在毒素编码序列的5′端存在第二个核糖体结合位点。通过蛋白质免疫印迹分析鉴定了含毒素的蛋白。来自大肠杆菌的阳性细胞提取物对科罗拉多马铃薯甲虫幼虫具有杀虫活性。克隆的基因与我们之前克隆的一个基因不同源,我们之前克隆的那个基因的产物对鞘翅目幼虫也有毒性。

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