2010
DOI: 10.1016/j.foodres.2009.11.014
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Effect of fermentation temperature on microbial population evolution using culture-independent and dependent techniques

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Cited by 66 publications
(49 citation statements)
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“…Total yeast, C. zemplinina, H. uvarum and S. cerevisiae were quantified and standard curves made according to Andorrà, Landi et al (2010). All the reagents were from Applied Biosystems and the primers used were from Invitrogen (Warrington, UK).…”
Section: Quantification By Real-time Pcrmentioning
confidence: 99%
See 1 more Smart Citation
“…Total yeast, C. zemplinina, H. uvarum and S. cerevisiae were quantified and standard curves made according to Andorrà, Landi et al (2010). All the reagents were from Applied Biosystems and the primers used were from Invitrogen (Warrington, UK).…”
Section: Quantification By Real-time Pcrmentioning
confidence: 99%
“…Because of its specificity and sensitivity, one of the most promising PCR techniques in food control is the real-time quantitative PCR (QPCR) (Bleve, Rizzotti, Dellaglio, & Torriani, 2003). In the past we developed several protocols to detect microorganisms in wine (Andorrà et al, 2008;Andorrà, Landi, Mas, Esteve-Zarzoso, & Guillamón, 2010;González, Hierro, Poblet, Mas, & Guillamón, 2006;Hierro, Esteve-Zarzoso, Gonzalez, Mas, & Guillamón, 2006). We now aim to study the interactions among the three main yeast species (S. cerevisiae, H. uvarum and Candida zemplinina) by monitoring pure and mixed cultures inoculated in a synthetic grape must by QPCR.…”
Section: Introductionmentioning
confidence: 99%
“…The former technique is more appropriate for detection and monitoring of a desired microorganism, whereas the latter for microbial community profiling. Although both techniques are supplemented with culture-dependent methods, however PCR-DGEE fails to detect species in low abudance, and qPCR suffers from scalability problems when many strains should be targeted [10,11].…”
Section: Introductionmentioning
confidence: 99%
“…This observation supports the hypothesis of the presence of viable but not culturable cells, that are not able to form colonies on agar medium, but are metabolically active during the fermentation. More recently, Andorrà et al (2008Andorrà et al ( , 2009) also studied the effect of SO 2 and temperature on microbial dynamics during wine fermentations. In both cases they demonstrated a good applicability of PCR-DGGE when yeast populations were present with similar counts.…”
Section: Yeast Ecologymentioning
confidence: 99%