Bartell P F, Orr T E
J Virol. 1969 Nov;4(5):580-4. doi: 10.1128/JVI.4.5.580-584.1969.
Five new polysaccharide depolymerases were isolated from cultures of Pseudomonas aeruginosa infected with phages 6, 7, 8, 9, and 10. The production of enzyme paralleled the release of phage. Depolymerase associated with phage 8 was active on slime polysaccharide A, whereas depolymerases associated with phages 6, 7, 9, and 10, like pseudomonas phage 2, hydrolyzed slime polysaccharide B. None of the depolymerases was active on slime polysaccharide C. Despite exhaustive purification, depolymerase activity was found to band with the phage particles at a density of 1.49 to 1.51 g/ml in a density gradient composed to cesium chloride. These results suggest that the depolymerases are firmly bound to the phage particles.
从感染噬菌体6、7、8、9和10的铜绿假单胞菌培养物中分离出5种新的多糖解聚酶。酶的产生与噬菌体的释放同步。与噬菌体8相关的解聚酶对黏液多糖A有活性,而与噬菌体6、7、9和10相关的解聚酶,像假单胞菌噬菌体2一样,水解黏液多糖B。没有一种解聚酶对黏液多糖C有活性。尽管进行了彻底的纯化,但在由氯化铯组成的密度梯度中,发现解聚酶活性与密度为1.49至1.51 g/ml的噬菌体颗粒一起形成条带。这些结果表明解聚酶与噬菌体颗粒紧密结合。