Yakult Central Institute for Microbiological Research, Kunitachi, Tokyo 186, Japan.
Appl Environ Microbiol. 1983 Feb;45(2):669-74. doi: 10.1128/aem.45.2.669-674.1983.
For protection from the abnormal fermentation of Lactobacillus casei S-1 caused by contamination of a virulent phage, phiFSV, the origin of this phage was studied. Morphologies, viral structural proteins, and DNA structures of three independent isolates of phiFSV were compared with those of phiFSW, which is lysogenized in strain S-1. The results showed (i) that the morphology of phiFSV phages is indistinguishable from that of phiFSW and (ii) that all viral structural components found in phiFSW are present in the particles of phiFSV's. In addition, restriction endonuclease analyses of viral DNA showed that the HindIII-digested fragments of phiFSW DNA, the sum of which covered at least 94.7% of this phage genome, were conserved in the phiFSV DNA digests. Results of Southern filter hybridization of the S-1 and prophage-cured cell (C239) DNAs with phiFSV DNA as a probe revealed that C239 had lost most of the phiFSV DNA sequence, whereas S-1 had about one copy of the phiFSV DNA sequence. These results indicate that virulent phage phiFSV is derived from the lysogenized phage phiFSW. Therefore, the appearance of phiFSV can be eliminated by using the prophage-cured derivative of S-1.
为了防止因污染烈性噬菌体 phiFSV 而导致干酪乳杆菌 S-1 异常发酵,我们对这种噬菌体的起源进行了研究。将三个独立分离的 phiFSV 与在 S-1 中溶原化的 phiFSW 的形态、病毒结构蛋白和 DNA 结构进行了比较。结果表明:(i)phiFSV 噬菌体的形态与 phiFSW 无法区分;(ii)phiFSW 中存在的所有病毒结构成分都存在于 phiFSV 的颗粒中。此外,phiFSV DNA 的限制性内切酶分析表明,phiFSW DNA 的 HindIII 消化片段(其总和至少覆盖了该噬菌体基因组的 94.7%)在 phiFSV DNA 的消化物中得以保留。用 phiFSV DNA 作为探针对 S-1 和前噬菌体失活细胞(C239)DNA 进行 Southern 滤膜杂交的结果表明,C239 丢失了大部分 phiFSV DNA 序列,而 S-1 大约有一个 phiFSV DNA 序列的拷贝。这些结果表明,烈性噬菌体 phiFSV 是从溶原化的噬菌体 phiFSW 衍生而来的。因此,可以通过使用 S-1 的前噬菌体失活衍生物来消除 phiFSV 的出现。