Falero Alina, Caballero Andy, Ferrán Beatriz, Izquierdo Yovanny, Fando Rafael, Campos Javier
Department of Molecular Biology, National Center for Scientific Research, P.O. Box 6414, Ave. 25 y 158, Cubanacán, Playa, Ciudad de la Habana, Cuba.
J Bacteriol. 2009 Sep;191(18):5873-6. doi: 10.1128/JB.01206-08. Epub 2009 Jul 17.
The native product of open reading frame 112 (orf112) and a recombinant variant of the RstB protein, encoded by Vibrio cholerae pathogen-specific bacteriophages VGJphi and CTXphi, respectively, were purified to more than 90% homogeneity. Orf112 protein was shown to specifically bind single-stranded genomic DNA of VGJphi; however, RstB protein unexpectedly bound double-stranded DNA in addition to the single-stranded genomic DNA. The DNA binding properties of these proteins may explain their requirement for the rolling circle replication of the respective phages and RstB's requirement for single-stranded-DNA chromosomal integration of CTXphi phage dependent on XerCD recombinases.
霍乱弧菌病原体特异性噬菌体VGJphi和CTXphi分别编码的开放阅读框112(orf112)的天然产物和RstB蛋白的重组变体被纯化至均一性超过90%。已证明Orf112蛋白能特异性结合VGJphi的单链基因组DNA;然而,RstB蛋白除了能结合单链基因组DNA外,还意外地能结合双链DNA。这些蛋白质的DNA结合特性可能解释了它们对于各自噬菌体滚环复制的需求,以及RstB对于依赖XerCD重组酶的CTXphi噬菌体单链DNA染色体整合的需求。