克隆嗜树杆菌DNA在大肠杆菌多肽合成中的应用

Claus Bollschweiler, Albrecht Klein
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引用次数: 13

摘要

在含蔗糖的培养基中,用杆菌肽处理嗜树嗜甲烷杆菌,分离出嗜树嗜甲烷杆菌的DNA。将Hind III限制性内切片段插入表达载体质粒。当将新构建的质粒引入大肠杆菌时,产生由产甲烷菌DNA编码的多肽合成。通过与质粒上携带的甲烷预防菌DNA的长度相比所发现的多肽的总分子量来判断,大肠杆菌中甲烷预防菌DNA的遗传信息的表达是有效的。
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Polypeptide Synthesis in Escherichia coli Directed by Cloned Methanobrevibacter arboriphilus DNA

Methanobrevibacter arboriphilus DNA was isolated after treatment of the cells with bacitracin in a sucrose containing growth medium. Hind III restriction fragments of the DNA were inserted into an expression vector plasmid. The newly constructed plasmids when introduced into E. coli gave rise to the synthesis of polypeptides coded for by the methanogen DNA. The expression of genetic information from the Methanobrevibacter DNA in E. coli is efficient as judged by the total molecular weight of the polypeptides found as compared to the length of the Methanobrevibacter DNA carried on the plasmids.

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