Department of Biochemistry, University of Otago, Dunedin, New Zealand.
Appl Environ Microbiol. 1984 Jul;48(1):242-4. doi: 10.1128/aem.48.1.242-244.1984.
The yield of bacteriophage 643 was increased by infecting cultures of Streptococcus lactis ML3 in late-log phase growth, harvesting the infected cells, and suspending them in fresh, phosphate-buffered minimal medium. The cells lysed after this treatment and produced high titers of bacteriophage. The phage particles were dissociated from debris by 2 M NaCl and purified by differential and CsCl band centrifugation.
通过感染处于对数末期生长的乳链球菌 ML3 培养物,收获感染的细胞,并将其悬浮在新鲜的磷酸盐缓冲的最小培养基中,可以提高噬菌体 643 的产量。经过这种处理后,细胞裂解并产生高滴度的噬菌体。噬菌体颗粒通过 2 M NaCl 从碎片中解离出来,并通过差速和 CsCl 带离心进行纯化。