Station de Recherches Laitières, Institut National de la Recherche Agronomique, 78350 Jouy-en-Josas, France.
Appl Environ Microbiol. 1990 Nov;56(11):3412-9. doi: 10.1128/aem.56.11.3412-3419.1990.
The presence of a restriction-modification (R/M) system against two bacteriophages, 328-B1 and hv, was demonstrated in three Lactobacillus helveticus strains, CNRZ 1094, CNRZ 1095, and CNRZ 1096. In addition, the burst size of phage 328-B1 in the three restrictive strains CNRZ 1094, CNRZ 1095, and CNRZ 1096 was reduced with respect to the values obtained in its propagating strain, CNRZ 328. Heating at 60 degrees C did not inactivate the R/M system. Nonrestrictive variants from CNRZ 1094 were easily obtained under several culture conditions, but treatment with novobiocin at 42 degrees C followed by storage at -20 degrees C resulted in drastic elimination of the R/M phenotype from all clones tested. Electrophoretic analysis of CNRZ 1094 nonrestrictive variants revealed the concomitant loss of a 34-kb plasmid. Four EcoRI fragments from the 34-kb plasmid were cloned in the Escherichia coli vector pACYC184. The use of one or several of these fragments as probes confirmed the plasmidic location of the genes responsible for the R/M system. These probes also showed the presence of R/M plasmids in the two other restrictive strains, CNRZ 1095 and CNRZ 1096. Lactose-fermenting ability and/or proteolytic capacity was not linked to the 34-kb plasmid.
三个瑞士乳杆菌(Lactobacillus helveticus)菌株 CNRZ 1094、CNRZ 1095 和 CNRZ 1096 中存在针对两种噬菌体(328-B1 和 hv)的限制-修饰(R/M)系统。此外,噬菌体 328-B1 在三个限制菌株 CNRZ 1094、CNRZ 1095 和 CNRZ 1096 中的爆发规模相对于其繁殖菌株 CNRZ 328 的值有所降低。在 60°C 加热不会使 R/M 系统失活。在几种培养条件下,很容易从 CNRZ 1094 中获得非限制变体,但在 42°C 下用新霉素处理,然后在-20°C 下储存,会导致所有测试克隆的 R/M 表型急剧消除。CNRZ 1094 非限制变体的电泳分析显示,同时丢失了一个 34-kb 质粒。该 34-kb 质粒的四个 EcoRI 片段被克隆到大肠杆菌载体 pACYC184 中。使用这些片段中的一个或几个作为探针,证实了负责 R/M 系统的基因位于质粒上。这些探针还显示出其他两个限制菌株 CNRZ 1095 和 CNRZ 1096 中存在 R/M 质粒。乳糖发酵能力和/或蛋白水解能力与 34-kb 质粒无关。