Hall B G, Xu L
Biology Department, University of Rochester, New York 14627.
Mol Biol Evol. 1992 Jul;9(4):688-706. doi: 10.1093/oxfordjournals.molbev.a040753.
The cryptic asc (previous called "SAC") operon of Escherichia coli K12 has been completely sequenced. It encodes a repressor (ascG); a PTS enzyme IIasc for the transport of arbutin, salicin, and cellobiose (ascF); and a phospho-beta-glucosidase that hydrolyzes the sugars which are phosphorylated during transport (ascB). ascG and ascFB are transcribed from divergent promoters. The cryptic operon is activated by the insertion of IS186 into the ascG (repressor) gene. The ascFB genes are paralogous to the cryptic bglFB genes, and ascG is paralogous to galR. The duplications that gave rise to these paralogous genes are estimated to have occurred approximately 320 Mya, a time that predates the divergence of E. coli and Salmonella typhimurium.
大肠杆菌K12的隐秘asc(以前称为“SAC”)操纵子已被完全测序。它编码一种阻遏物(ascG);一种用于转运熊果苷、水杨苷和纤维二糖的磷酸转移酶系统(PTS)酶IIasc(ascF);以及一种磷酸β-葡萄糖苷酶,可水解在转运过程中被磷酸化的糖类(ascB)。ascG和ascFB由不同的启动子转录。隐秘操纵子通过IS186插入ascG(阻遏物)基因而被激活。ascFB基因与隐秘的bglFB基因是旁系同源的,而ascG与galR是旁系同源的。导致这些旁系同源基因产生的重复事件估计发生在大约3.2亿年前,这一时期早于大肠杆菌和鼠伤寒沙门氏菌的分化时间。