Parsot C, Cossart P, Saint-Girons I, Cohen G N
Nucleic Acids Res. 1983 Nov 11;11(21):7331-45. doi: 10.1093/nar/11.21.7331.
The entire threonine operon (thrABC) of Escherichia coli K12 was cloned, and the nucleotide sequence of the thrC gene and its 3' flanking region was determined. The translation initiation codon was identified by sequencing the N-terminal part of threonine synthase, the thrC gene product. Analysis of the deduced protein sequence (428 amino acid residues) revealed a region of homology, 35 amino acids long, between the three enzymes encoded by the threonine operon. During examination of the nucleotide sequence of the 1045 base pair fragments following the thrC gene, we detected some potential rho-independent and rho-dependent transcription termination signals.
克隆了大肠杆菌K12的整个苏氨酸操纵子(thrABC),并测定了thrC基因及其3'侧翼区域的核苷酸序列。通过对苏氨酸合酶(thrC基因产物)N端部分进行测序,确定了翻译起始密码子。对推导的蛋白质序列(428个氨基酸残基)进行分析,发现苏氨酸操纵子编码的三种酶之间存在一个35个氨基酸长的同源区域。在检查thrC基因之后的1045个碱基对片段的核苷酸序列时,我们检测到了一些潜在的不依赖于rho和依赖于rho的转录终止信号。