Perez Gerardo L, Huynh Bao, Slater Miranda, Maloy Stanley
Center for Microbial Sciences, Department of Biology, College of Sciences, San Diego State University, San Diego, California 92182-1010, USA.
J Bacteriol. 2009 Jan;191(1):135-40. doi: 10.1128/JB.00778-08. Epub 2008 Oct 31.
Although a great deal is known about the life cycle of bacteriophage P22, the mechanism of phage DNA transport into Salmonella is poorly understood. P22 DNA is initially ejected into the periplasmic space and subsequently transported into the host cytoplasm. Three phage-encoded proteins (gp16, gp20, and gp7) are coejected with the DNA. To test the hypothesis that one or more of these proteins mediate transport of the DNA across the cytoplasmic membrane, we purified gp16, gp20, and gp7 and analyzed their ability to associate with membranes and to facilitate DNA uptake into membrane vesicles in vitro. Membrane association experiments revealed that gp16 partitioned into the membrane fraction, while gp20 and gp7 remained in the soluble fraction. Moreover, the addition of gp16, but not gp7 or gp20, to liposomes preloaded with a fluorescent dye promoted release of the dye. Transport of (32)P-labeled DNA into liposomes occurred only in the presence of gp16 and an artificially created membrane potential. Taken together, these results suggest that gp16 partitions into the cytoplasmic membrane and mediates the active transport of P22 DNA across the cytoplasmic membrane of Salmonella.
尽管人们对噬菌体P22的生命周期已经了解很多,但噬菌体DNA转运到沙门氏菌中的机制却知之甚少。P22 DNA最初被注入到周质空间,随后被转运到宿主细胞质中。三种噬菌体编码蛋白(gp16、gp20和gp7)与DNA一起被注入。为了验证这些蛋白中的一种或多种介导DNA穿过细胞质膜转运的假说,我们纯化了gp16、gp20和gp7,并分析了它们与膜结合以及在体外促进DNA摄取到膜泡中的能力。膜结合实验表明,gp16分配到膜组分中,而gp20和gp7保留在可溶组分中。此外,向预先装载荧光染料的脂质体中添加gp16可促进染料释放,但添加gp7或gp20则不然。只有在gp16和人工创建的膜电位存在的情况下,(32)P标记的DNA才能转运到脂质体中。综上所述,这些结果表明gp16分配到细胞质膜中,并介导P22 DNA穿过沙门氏菌细胞质膜的主动转运。