Tucker S D, Murgola E J
DNA. 1986 Apr;5(2):123-8. doi: 10.1089/dna.1986.5.123.
Over the past 30 years, a variety of mutations have been characterized in trpA, the gene for the alpha-subunit of tryptophan synthetase in Escherichia coli. On the basis of amino acid sequence analyses, reversion studies, or suppressibility by codon-specific translational suppressors, base substitutions were deduced and codons assigned for each mutation. In the present study, three of the trpA mutants obtained over 25 years ago and a series of codon position 234 trpA mutants isolated more recently by specific selection methods have been cloned and characterized by DNA sequence analysis. Our results establish the reliability of the mutant codon assignments, confirm the validity of the selection and detection procedures used to obtain missense and nonsense mutations in trpA, and demonstrate that the trpA sequence has been stably maintained throughout 30 years of laboratory culturing and mutagenic treatments.
在过去30年里,已对大肠杆菌中色氨酸合成酶α亚基的基因trpA中的多种突变进行了表征。基于氨基酸序列分析、回复突变研究或密码子特异性翻译抑制因子的抑制作用,推断出碱基替换并为每个突变指定了密码子。在本研究中,25年前获得的三个trpA突变体以及最近通过特定选择方法分离的一系列密码子位置234的trpA突变体已被克隆,并通过DNA序列分析进行了表征。我们的结果确立了突变密码子指定的可靠性,证实了用于获得trpA错义突变和无义突变的选择和检测程序的有效性,并表明trpA序列在30年的实验室培养和诱变处理过程中一直得到稳定维持。