Slettan A, Gebhardt K, Kristiansen E, Birkeland N K, Lindqvist B H
Department of Biology, University of Oslo, Norway.
J Bacteriol. 1992 Jun;174(12):4094-100. doi: 10.1128/jb.174.12.4094-4100.1992.
The bacteriophage P2 ogr gene encodes an essential 72-amino-acid protein which acts as a positive regulator of P2 late transcription. A P2 ogr deletion phage, which depends on the supply of Ogr protein in trans for lytic growth on Escherichia coli C, has previously been constructed. E. coli B and K-12 were found to support the growth of the ogr-defective P2 phage because of the presence of functional ogr genes located in cryptic P2-like prophages in these strains. The cryptic ogr genes were cloned and sequenced. Compared with the P2 wild-type ogr gene, the ogr genes in the B and K-12 strains are conserved, containing mostly silent base substitutions. One of the base substitutions in the K-12 ogr gene results in replacement of an alanine with valine at position 57 in the Ogr protein but does not seem to affect the function of Ogr as a transcriptional activator. The cryptic ogr genes are constitutively transcribed, apparently at a higher level than the wild-type ogr gene in a P2 lysogen.
噬菌体P2 ogr基因编码一种由72个氨基酸组成的必需蛋白,该蛋白作为P2晚期转录的正调控因子发挥作用。先前已构建出一种P2 ogr缺失噬菌体,其在大肠杆菌C上进行裂解生长依赖于反式提供的Ogr蛋白。由于在大肠杆菌B和K-12菌株中存在位于隐蔽的P2样原噬菌体中的功能性ogr基因,发现它们能支持ogr缺陷型P2噬菌体的生长。对这些隐蔽的ogr基因进行了克隆和测序。与P2野生型ogr基因相比,B和K-12菌株中的ogr基因是保守的,大多含有沉默碱基替换。K-12 ogr基因中的一个碱基替换导致Ogr蛋白第57位的丙氨酸被缬氨酸取代,但似乎不影响Ogr作为转录激活因子的功能。这些隐蔽的ogr基因组成型转录,显然其转录水平高于P2溶原菌中的野生型ogr基因。