Zago Miriam, Rossetti Lia, Reinheimer Jorge, Carminati Domenico, Giraffa Giorgio
CRA-FLC Centro di Ricerca per le Produzioni Foraggere e Lattiero Casearie, Lodi (Italy).
J Dairy Res. 2008 May;75(2):196-201. doi: 10.1017/S0022029908003208.
A PCR protocol for detection of Lactobacillus helveticus bacteriophages was optimized. PCR was designed taking into account the sequence of the lys gene of temperate bacteriophage Phi-0303 and optimized to obtain a fragment of 222 bp using different Lb. helveticus phages from our collection. PCR was applied to total phage DNA extracted from 53 natural whey starters used for the production of Grana cheese and all gave the expected fragment. The presence of actively growing phages in the cultures was verified by traditional tests. Several PCR products of the lys gene were sequenced and aligned. The resulting sequences showed variable heterogeneity between the phages.
优化了用于检测瑞士乳杆菌噬菌体的PCR方案。设计PCR时考虑了温和噬菌体Phi-0303的lys基因序列,并进行了优化,以便使用我们收集的不同瑞士乳杆菌噬菌体获得222 bp的片段。将PCR应用于从53种用于生产格拉纳奶酪的天然乳清发酵剂中提取的总噬菌体DNA,所有样本均得到了预期的片段。通过传统测试验证了培养物中活跃生长的噬菌体的存在。对lys基因的几个PCR产物进行了测序和比对。结果序列显示噬菌体之间存在可变的异质性。