Oliver G, Gosset G, Sanchez-Pescador R, Lozoya E, Ku L M, Flores N, Becerril B, Valle F, Bolivar F
Departamento de Biología Molecular, U.N.A.M., Morelos.
Gene. 1987;60(1):1-11. doi: 10.1016/0378-1119(87)90207-1.
We have determined the complete nucleotide sequence of a 6.3-kb chromosomal HpaI-EcoRI fragment, that contains the structural genes for both the large and small subunits of the Escherichia coli K-12 glutamate synthase (GOGAT) enzyme, as well as the 5'- and 3'-flanking and intercistronic DNA regions. The Mrs of the two subunits, as deduced from the nucleotide (nt) sequence, were estimated as 166,208 and 52,246. Partial amino acid sequence of the GOGAT enzyme revealed that the large subunit starts with a cysteine residue that is probably generated by a proteolytic cleavage. Northern blotting experiments revealed a transcript of approximately 7300 nt, that at least contains the cistrons for both subunits. A transcriptional start point and a functional promoter were identified in the 5' DNA flanking region of the large subunit gene. The messenger RNA nontranslated leader region has 120 nt and shares identity with the leader regions of E. coli ribosomal operons, in particular around the so-called boxA sequence implicated in antitermination. Other possible regulatory sequences are described.
我们已经确定了一个6.3kb染色体HpaI - EcoRI片段的完整核苷酸序列,该片段包含大肠杆菌K - 12谷氨酸合酶(GOGAT)酶的大亚基和小亚基的结构基因,以及5'和3'侧翼及基因间DNA区域。根据核苷酸(nt)序列推导,两个亚基的相对分子质量估计分别为166,208和52,246。GOGAT酶的部分氨基酸序列显示,大亚基起始于一个半胱氨酸残基,可能是由蛋白水解切割产生的。Northern印迹实验显示有一个约7300nt的转录本,其至少包含两个亚基的顺反子。在大亚基基因的5'侧翼DNA区域鉴定出一个转录起始点和一个功能性启动子。信使RNA的非翻译前导区有120nt,与大肠杆菌核糖体操纵子的前导区具有同源性,特别是在涉及抗终止的所谓boxA序列周围。还描述了其他可能的调控序列。