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Development of a New Method for Detection and Identification of Oenococcus oeni Bacteriophages Based on Endolysin Gene Sequence and Randomly Amplified Polymorphic DNA

机译:基于溶血素基因序列和随机扩增多态性DNA的新发现和鉴定大肠球菌噬菌体的方法

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Malolactic fermentation (MLF) is a biochemical transformation conducted by lactic acid bacteria (LAB) that occurs in wine at the end of alcoholic fermentation. Oenococcus oeni is the main species responsible for MLF in most wines. As in other fermented foods, where bacteriophages represent a potential risk for the fermentative process, O. oeni bacteriophages have been reported to be a possible cause of unsuccessful MLF in wine. Thus, preparation of commercial starters that take into account the different sensitivities of O. oeni strains to different phages would be advisable. However, currently, no methods have been described to identify phages infecting O. oeni . In this study, two factors are addressed: detection and typing of bacteriophages. First, a simple PCR method was devised targeting a conserved region of the endolysin ( lys ) gene to detect temperate O. oeni bacteriophages. For this purpose, 37 O. oeni strains isolated from Italian wines during different phases of the vinification process were analyzed by PCR for the presence of the lys gene, and 25 strains gave a band of the expected size (1,160 bp). This is the first method to be developed that allows identification of lysogenic O. oeni strains without the need for time-consuming phage bacterial-lysis induction methods. Moreover, a phylogenetic analysis was conducted to type bacteriophages. After the treatment of bacteria with UV light, lysis was obtained for 15 strains, and the 15 phage DNAs isolated were subjected to two randomly amplified polymorphic DNA (RAPD)-PCRs. By combining the RAPD profiles and lys sequences, 12 different O. oeni phages were clearly distinguished.
机译:苹果乳酸发酵(MLF)是由乳酸菌(LAB)进行的生化转化,在酒精发酵结束时会在葡萄酒中发生。 Oenococcus oeni是大多数葡萄酒中造成MLF的主要物种。与其他发酵食品一样,噬菌体是发酵过程的潜在风险,据报道,O。oeni噬菌体可能是导致葡萄酒中MLF失败的可能原因。因此,考虑到O. oeni菌株对不同噬菌体的不同敏感性,准备商业发酵剂是明智的。但是,目前还没有描述鉴定感染O. oeni的噬菌体的方法。在这项研究中,解决了两个因素:噬菌体的检测和分型。首先,设计了一种针对内溶素(lys)基因保守区域的简单PCR方法,以检测温和的O. oeni噬菌体。为此目的,通过PCR分析了在葡萄酒酿造过程的不同阶段从意大利葡萄酒中分离的37种O. oeni菌株,其中lys基因的存在,而25种菌株给出了预期大小的条带(1,160 bp)。这是第一个开发的方法,它无需耗时的噬菌体细菌裂解诱导方法就可以鉴定溶原性大肠弯曲杆菌O. oeni菌株。此外,对种类的噬菌体进行了系统发育分析。用紫外线处理细菌后,裂解了15个菌株,并对分离出的15个噬菌体DNA进行了两次随机扩增的多态性DNA(RAPD)-PCR。通过结合RAPD图谱和lys序列,可以清楚地区分12种不同的O. oeni噬菌体。

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