Use of molecular methods for the identification of yeast associated with table olives

被引:91
作者
Arroyo-Lopez, F. N.
Duran-Quintana, M. C.
Ruiz-Barba, J. L.
Querol, A.
Garrido-Fernandez, A.
机构
[1] CSIC, Inst Grasa, Dept Biotecnol Aliementos, Seville 41012, Spain
[2] CSIC, Inst Agroquim & Tecnol Alimentos, Dept Biotecnol Alimentos, Valencia 46100, Spain
关键词
table olives; yeast; molecular identification;
D O I
10.1016/j.fm.2006.02.008
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 ; 0836 ; 090102 ; 100705 ;
摘要
A molecular approach is used for the identification of yeast isolated from table olives. Our results validate those obtained in the past by the classical biochemical methodology. Yeast were isolated from both aerobically and anacrobically processed black table olives and also from canned seasoned green table olives. Molecular identification methodology used included restriction pattern analysis of both PCR-amplified 5.8S rRNA gene and internal transcribed spacers ITS1 and ITS2. For some species, sequence analysis of the 26S rRNA gene was necessary. These techniques allowed the identification of three yeast species (Issatchenkia occidentalis, Geotrichum candidum and Hanseniaspora guilliermondii) which had not been described previously in table olives. Saccharomyces cerevisiae and Candida boidinii were the most frequent species in green seasoned olives and processed black olives, respectively. The molecular study of total DNA variability among the S. cerevisiae strains isolated indicates a quite heterogeneous population, with at least four different restriction patterns. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:791 / 796
页数:6
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