Łoś J M, Łoś M, Wegrzyn A, Wegrzyn G
Department of Molecular Biology, University of Gdańsk, 80-822, Gdańsk, Poland.
Folia Microbiol (Praha). 2008;53(5):443-50. doi: 10.1007/s12223-008-0068-0. Epub 2008 Dec 16.
Various processes of bacteriophage lambda development in Escherichia coli cells bearing either the whole lambda exo-xis region (with truncated, thus nonfunctional, exo and xis genes) or particular genes from this region were investigated. The presence of either the exo-xis region or the ea8.5 gene on a plasmid resulted in formation of fuzzy plaques by infecting phage. Both efficiency of plating and efficiency of lysogenization were decreased in such hosts. On the other hand, neither the efficiency of adsorption nor intracellular lytic development of the infecting phage (measured in one-step-growth experiments) was affected while significantly more host cells survived the infection, when containing the exo-xis region. Although no effects of the exo-xis region on the activity of the p (L) promoter was detected, this region contributed to a decreased transcription from the cII-stimulated promoters p (I), p (aQ) and p (E). These results, together with the results of measurement of efficiency of plating of phages bearing mutations in cI, cII and cIII genes on hosts containing the exo-xis region, strongly suggest that genes from this region (especially ea8.5) are involved in the regulation of bacteriophage lambda development at the stage of the lysis-vs.-lysogenization decision.
对带有整个λ外切核酸酶 - 整合酶识别位点(xis)区域(外切核酸酶和xis基因被截断,因此无功能)或该区域特定基因的大肠杆菌细胞中λ噬菌体的各种发育过程进行了研究。质粒上存在外切核酸酶 - xis区域或ea8.5基因会导致感染噬菌体形成模糊噬菌斑。在这样的宿主中,平板接种效率和溶原化效率均降低。另一方面,感染噬菌体的吸附效率和细胞内裂解发育(在一步生长实验中测量)均未受影响,而当含有外切核酸酶 - xis区域时,明显更多的宿主细胞在感染后存活下来。尽管未检测到外切核酸酶 - xis区域对p(L)启动子活性的影响,但该区域导致cII刺激的启动子p(I)、p(aQ)和p(E)的转录减少。这些结果,连同对在含有外切核酸酶 - xis区域的宿主上携带cI、cII和cIII基因突变的噬菌体的平板接种效率测量结果,强烈表明该区域的基因(尤其是ea8.5)在噬菌体λ发育的裂解与溶原化决定阶段参与调控。