Wallace R G, Lee N, Fowler A V
Gene. 1980 Dec;12(3-4):179-90. doi: 10.1016/0378-1119(80)90100-6.
The nucleotide sequence of the Escherichia coli araC gene and flanking regions have been determined from a series of overlapping fragments using the technique of base-specific chemical cleavage of Maxam and Gilbert (1980). The nucleotide sequence of araC gene was confirmed by the partial amino acid sequences of araC protein and its methionine peptides. The primary structure of araC polypeptide consists of 291 amino acid residues, giving it a chemical molecular weight of 33 314 daltons. The transcriptional start-point has been deduced from the sequence of araC mRNA synthesized in vitro and in vivo, and it is located 148 bp away from the transcriptional start-point of the araBAD operon. The translational start-point for the araC gene was deduced from the N-terminal amino acid sequence of the protein, and is located 165 bp from the 5'-end of araC mRNA. There is, therefore, a leader sequence of 164 bp preceding the araC gene.
利用马克萨姆和吉尔伯特(1980年)的碱基特异性化学切割技术,从一系列重叠片段中确定了大肠杆菌araC基因及其侧翼区域的核苷酸序列。通过araC蛋白及其甲硫氨酸肽段的部分氨基酸序列,证实了araC基因的核苷酸序列。araC多肽的一级结构由291个氨基酸残基组成,其化学分子量为33314道尔顿。转录起始点已根据体外和体内合成的araC mRNA序列推导得出,它位于距araBAD操纵子转录起始点148 bp处。araC基因的翻译起始点是根据该蛋白的N端氨基酸序列推导得出的,位于距araC mRNA 5'端165 bp处。因此,在araC基因之前有一个164 bp的前导序列。