Stirling C J, Colloms S D, Collins J F, Szatmari G, Sherratt D J
Institute of Genetics, University of Glasgow, UK.
EMBO J. 1989 May;8(5):1623-7. doi: 10.1002/j.1460-2075.1989.tb03547.x.
The heritable stability of ColE1 is dependent on a site-specific recombination system which acts to resolve plasmid multimers into monomers. This plasmid stabilizing recombination system requires the presence in cis of the ColE1 cer region, plus at least two trans-acting factors encoded by the xerA and xerB genes of Escherichia coli. The xerB gene has been cloned and sequenced and found to encode a polypeptide with a calculated mol. wt of 55.3 kd. The predicted amino acid sequence of this protein exhibits striking similarity to that of bovine lens leucine aminopeptidase (53 kd). The biological significance of this similarity is corroborated by genetic and biochemical evidence which suggests that xerB is identical to the E.coli and S.typhimurium pepA genes that encode aminopeptidase A.
ColE1的遗传稳定性依赖于一个位点特异性重组系统,该系统作用是将质粒多聚体分解为单体。这个质粒稳定重组系统需要ColE1 cer区域顺式存在,以及至少两个由大肠杆菌xerA和xerB基因编码的反式作用因子。xerB基因已被克隆和测序,发现它编码一种计算分子量为55.3 kd的多肽。该蛋白的预测氨基酸序列与牛晶状体亮氨酸氨肽酶(53 kd)的序列具有显著相似性。遗传和生化证据证实了这种相似性的生物学意义,这些证据表明xerB与编码氨肽酶A的大肠杆菌和鼠伤寒沙门氏菌pepA基因相同。