Salama M, Sandine W, Giovannoni S
Department of Microbiology, Oregon State University, Corvallis 97331-3804.
Appl Environ Microbiol. 1991 May;57(5):1313-8. doi: 10.1128/aem.57.5.1313-1318.1991.
Lactococcus lactis subsp. cremoris is of considerable interest to the dairy industry, which relies upon the few available strains for the manufacture of cheddar cheese free of fermented and fruity flavors. The subspecies cremoris differs from related subspecies by the lack of a few phenotypic traits. Our purpose was to identify unique rRNA sequences that could be used to discriminate L. lactis subsp. cremoris from related subspecies. The 16S rRNAs from 13 Lactococcus strains were partially sequenced by using reverse transcriptase to identify domains unique to L. lactis subsp. cremoris. All five strains of the subspecies cremoris had a unique base sequence in a hypervariable region located 70 to 100 bases from the 5' terminus. In this region, all L. lactis subsp. lactis biovar diacetylactis strains examined had a sequence identical to that of L. lactis subsp. lactis 7962, which was different from other strains of the subspecies lactis by only one nucleotide at position 90 (Escherichia coli 16S rRNA structural model) (J. Brosius, J. L. Palmer, J. P. Kennedy, and H. F. Noller, Proc. Natl. Acad. Sci. USA 75:4801-4805, 1978). Oligonucleotide probes specific for the genus Lactococcus (212RLa) and for the subspecies cremoris (68RCa) were synthesized and evaluated by hybridization to known rRNAs as well as fixed whole cells. Efficient and specific hybridization to the genus-specific probe was observed for the 13 Lactococcus strains tested. No hybridization was seen with the control species. All five strains of the subspecies cremoris hybridized to the subspecies-specific probe.
乳酸乳球菌乳脂亚种对乳制品行业具有重要意义,该行业依赖于少数可用菌株来生产无发酵和果味的切达干酪。乳脂亚种与相关亚种的区别在于缺乏一些表型特征。我们的目的是鉴定可用于区分乳酸乳球菌乳脂亚种与相关亚种的独特rRNA序列。通过使用逆转录酶对13株乳球菌菌株的16S rRNA进行部分测序,以鉴定乳酸乳球菌乳脂亚种特有的结构域。乳脂亚种的所有五株菌株在距5'末端70至100个碱基的高变区具有独特的碱基序列。在该区域,所有检测的乳酸乳球菌乳酸亚种双乙酰变种菌株的序列与乳酸乳球菌乳酸亚种7962相同,该序列与乳酸亚种的其他菌株仅在第90位核苷酸处有一个差异(大肠杆菌16S rRNA结构模型)(J. Brosius、J. L. Palmer、J. P. Kennedy和H. F. Noller,《美国国家科学院院刊》75:4801 - 4805,1978年)。合成了针对乳球菌属(212RLa)和乳脂亚种(68RCa)的寡核苷酸探针,并通过与已知rRNA以及固定的全细胞杂交进行评估。在所测试的13株乳球菌菌株中观察到与属特异性探针的高效且特异性杂交。对照物种未出现杂交。乳脂亚种的所有五株菌株均与亚种特异性探针杂交。