New PCR-based methods for yeast identification

被引:48
作者
Hierro, N [1 ]
González, A [1 ]
Mas, A [1 ]
Guillamón, JM [1 ]
机构
[1] Univ Rovira & Virgili, CeRTA, Unitat Enol, Fac Enol,Dept Bioquim & Biotecnol, Tarragona 43005, Spain
关键词
5 center dot 8S-ITS; ERIC-PCR; PCR-intron splice sites; REP-PCR; RFLP-PCR; yeast identification;
D O I
10.1111/j.1365-2672.2004.02369.x
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 0836 [生物工程]; 090102 [作物遗传育种]; 100705 [微生物与生化药学];
摘要
Aims: To characterize reference yeast strains and identify indigenous strains isolated from wine fermentations by PCR methods. Methods and Results: We compared several PCR techniques for yeast identification. We used oligonucleotide primers that are complementary to (i) intron splice sites, (ii) REP and (iii) ERIC elements to produce PCR fingerprints that display specific patterns between the different yeast species. These three techniques were used to characterize 41 reference yeast strains belonging to 15 different species and to identify 40 indigenous strains isolated from grape must and wine fermentations. Species-specific banding patterns were obtained with the three PCR-techniques with different degrees of intraspecific differentiation depending on the method. By comparing the PCR fingerprints of unknown isolates with those produced by reference strains, we identified yeast strains isolated from an industrial wine fermentation. Conclusions: All three PCR techniques are rapid, reliable and simple methods of yeast identification. As far as we know, this is the first time that the primers designed for amplifying repetitive elements in bacteria have been successfully used in yeast. Significance and Impact of the Study: Industry needs rapid, reliable and simple methods of yeast identification. The proposed PCR techniques will allow to achive this objective.
引用
收藏
页码:792 / 801
页数:10
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