Lawther R P, Calhoun D H, Gray J, Adams C W, Hauser C A, Hatfield G W
J Bacteriol. 1982 Jan;149(1):294-8. doi: 10.1128/jb.149.1.294-298.1982.
Six ilvG (IlvG+) mutations of Escherichia coli K-12 were transferred to recombinant plasmids, and the DNA sequence of each mutation was determined. This analysis confirmed that expression of the ilvG gene product (acetohydroxy acid synthase II) requires the deletion of a single base pair or the addition of two base pairs within ilvG to displace a frameshift site present in wild-type E. coli K-12. This system should be useful in the analysis of potential frameshift mutagens.
将大肠杆菌K-12的6个ilvG(IlvG+)突变转移至重组质粒,并测定每个突变的DNA序列。该分析证实,ilvG基因产物(乙酰羟酸合酶II)的表达需要在ilvG内缺失一个碱基对或添加两个碱基对,以取代野生型大肠杆菌K-12中存在的移码位点。该系统应有助于分析潜在的移码诱变剂。