Vakulenko S B, Fomina I P, Navashin S M
Antibiot Khimioter. 1989 May;34(5):370-4.
To investigate the evolutionary relationships between the aph(3') genes from different plasmids, the nucleotide sequence of the aph(3') gene from the E. coli R plasmid was determined and compared with the known aph(3') genes of Tn903 and Tn4352. Three point mutations in the structural part of the cloned aph(3') gene caused amino acid changes in the enzyme molecule at positions 19, 27 and 48 beginning from the start codon. The structural part of the gene was followed by two stop codons and a long DNA region containing no nucleotide sequences homologous to the sequences of Tn903 or Tn4352. Both the cloned aph(3') gene and Tn4352 were limited on the left by the spacer sequence and the insertion sequence IS176. Twenty one base pairs deletion abolished the -35 sequence of the promoter suggested for the aph(3') gene of Tn4352 and resulted in formation of a fusion promoter utilizing the -35 box of IS176 and the -10 box of the aph(3') gene. The distance between the -35 and -10 sequences changed from 18 to 17 bp. Changes in the cloned aph(3') gene and the flanking DNA regions resulted in formation of a new promoter and loss of the right IS176 element.
为了研究来自不同质粒的aph(3')基因之间的进化关系,测定了大肠杆菌R质粒中aph(3')基因的核苷酸序列,并与已知的Tn903和Tn4352的aph(3')基因进行了比较。克隆的aph(3')基因结构部分的三个点突变导致酶分子中从起始密码子开始第19、27和48位的氨基酸发生变化。该基因的结构部分后面跟着两个终止密码子和一个长的DNA区域,该区域不包含与Tn903或Tn4352序列同源的核苷酸序列。克隆的aph(3')基因和Tn4352在左侧都受到间隔序列和插入序列IS176的限制。21个碱基对的缺失消除了为Tn4352的aph(3')基因所建议的启动子的-35序列,并导致形成一个利用IS176的-35框和aph(3')基因的-10框的融合启动子。-35和-10序列之间的距离从18 bp变为17 bp。克隆的aph(3')基因和侧翼DNA区域的变化导致形成一个新的启动子并丢失右侧的IS176元件。