Bartell P F, Orr T E, Lam G K
J Bacteriol. 1966 Jul;92(1):56-62. doi: 10.1128/jb.92.1.56-62.1966.
Bartell, Pasquale F. (University of Pennsylvania, Philadelphia), Thomas E. Orr, and Grace K. H. Lam. Polysaccharide depolymerase associated with bacteriophage infection. J. Bacteriol. 92:56-62. 1966.-A recently isolated bacteriophage of Pseudomonas aeruginosa was observed, in association with bacteria, to produce a polysaccharide depolymerase. Exposure of slime polysaccharide to the enzyme at the pH optimum of 7.5 for 30 to 60 min resulted in a decreased viscosity of 20 to 25%, and a measurable increase in the levels of hexosamines, hexoses, and reducing substances, distinguishing it from other phage-associated depolymerases. Like egg-white lysozyme, the depolymerase produced a clearing of mature bacterial lawns, but was shown to be devoid of muralytic activity by turbidimetric and paper chromatographic analysis. The depolymerase reacted with polysaccharides of only certain strains of P. aeruginosa, and there appeared to be no correlation with phage susceptibility. The enzyme was not detectable in uninfected cultures, nor was it synthesized when infection was initiated by phages other than phage 2. The available data suggest that the genetic information required for biosynthesis of this enzyme is furnished by the phage 2 genome.
巴特尔,帕斯夸莱·F.(宾夕法尼亚大学,费城),托马斯·E.奥尔,以及格蕾丝·K.H.林。与噬菌体感染相关的多糖解聚酶。《细菌学杂志》92:56 - 62。1966年。——观察到一种最近分离出的铜绿假单胞菌噬菌体,与细菌一起会产生一种多糖解聚酶。在最适pH值7.5下,将黏液多糖暴露于该酶30至60分钟,导致黏度降低20%至25%,并且己糖胺、己糖和还原物质的水平有可测量的增加,这使其有别于其他与噬菌体相关的解聚酶。与蛋清溶菌酶一样,该解聚酶能使成熟的细菌菌苔出现清亮区,但通过比浊法和纸色谱分析表明它没有溶壁活性。该解聚酶仅与某些铜绿假单胞菌菌株的多糖发生反应,并且似乎与噬菌体敏感性无关。在未感染的培养物中检测不到该酶,当由噬菌体2以外的噬菌体引发感染时也不会合成该酶。现有数据表明,这种酶生物合成所需的遗传信息由噬菌体2基因组提供。