Lindström P H, Stüber D, Björk G R
J Bacteriol. 1985 Dec;164(3):1117-23. doi: 10.1128/jb.164.3.1117-1123.1985.
The enzyme catalyzing the formation of 5-methyluridine (ribothymidine) in tRNA of Escherichia coli is tRNA (uracil-5)-methyltransferase (EC 2.1.1.35). A 2.8-kilobase EcoRI chromosomal DNA fragment contains trmA, the structural gene for this enzyme. Subcloning, transcription in vitro, Tn5 insertion mutagenesis, and transcriptional fusion experiments were performed to establish the gene organization of the trmA region on the E. coli chromosome. trmA is a monocistronic operon. The trmA promoter was localized by in vitro experiments, and the direction of transcription was shown to be counterclockwise on the standard E. coli K-12 chromosomal map. The level of transcription of trmA in vitro and the expression of protein in minicells equal those of the bla gene of plasmid pBR322.
催化大肠杆菌转运RNA中5-甲基尿苷(核糖胸腺嘧啶核苷)形成的酶是转运RNA(尿嘧啶-5)-甲基转移酶(EC 2.1.1.35)。一个2.8千碱基的EcoRI染色体DNA片段包含trmA,即该酶的结构基因。进行了亚克隆、体外转录、Tn5插入诱变和转录融合实验,以确定大肠杆菌染色体上trmA区域的基因组织。trmA是一个单顺反子操纵子。通过体外实验确定了trmA启动子的位置,并且在标准的大肠杆菌K-12染色体图谱上显示转录方向是逆时针的。trmA在体外的转录水平以及在微小细胞中的蛋白质表达水平与质粒pBR322的bla基因相当。