A new PCR-based method for monitoring inoculated wine fermentations

被引:45
作者
López, V
Fernández-Espinar, MT
Barrio, E
Ramón, D
Querol, A
机构
[1] Inst Agroquim & Tecnol Alimentos CSIC, Dept Biotecnol, Valencia 46100, Spain
[2] Univ Valencia, Unitat Genet Evolut, Inst Cavanilles Biodiversitat & Biol Eviluat, Edificio Inst, Valencia 46071, Spain
关键词
identification; characterization; yeast; PCR; COXl; GROUP-II INTRON; MITOCHONDRIAL-DNA; YEAST STRAINS; SACCHAROMYCES-CEREVISIAE; KLUYVEROMYCES-LACTIS; NUCLEOTIDE-SEQUENCE; NEUROSPORA-CRASSA; IDENTIFICATION; GENE; DIFFERENTIATION;
D O I
10.1016/S0168-1605(02)00194-0
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
A new PCR-based method has been developed to monitor inoculated wine fermentations. The method is based on the variation in the number and position of introns in the mitochondrial gene COX1. Oligonucleotide primers homologous to the regions flanking the Saccharomyces cerevisiae COX1 introns have been designed and tested for S. cerevisiae wine yeast strain differentiation. Four primers were selected for their subsequent use in a multiplex PCR reaction and have proved to be very effective in uncovering polymorphism in natural and commercial yeast strains. An important point is that the speed and simplicity of the technique, which does not require the isolation of DNA, allows early detection of the starter yeast strain throughout the fermentation process. The main advantage for the wineries is that the must sample can be used directly for the PCR reaction obtaining very fast results (in approximately 8 h). This allows the wine industries to intervene quickly if necessary. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:63 / 71
页数:9
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