Control of inoculated fermentations in wine cellars by mitochondrial DNA analysis of starter yeast

被引:12
作者
Capece, Angela [1 ]
Romaniello, Rossana [1 ]
Poeta, Cinzia [1 ]
Siesto, Gabriella [1 ]
Massari, Carmela [1 ]
Pietrafesa, Rocchina [1 ]
Romano, Patrizia [1 ]
机构
[1] Univ Basilicata, Dipartimento Biol Dif & Biotecnol Agroforestali, I-85100 Potenza, Italy
关键词
Yeast starter; Saccharomyces cerevisiae; Non-Saccharomyces yeasts; RFLP-mtDNA; Wine flavour; MOLECULAR CHARACTERIZATION; SACCHAROMYCES-CEREVISIAE; ALCOHOLIC FERMENTATION; STRAINS; BIODIVERSITY; REGION; GRAPE; POPULATIONS; DIVERSITY; ACETATE;
D O I
10.1007/s13213-010-0087-3
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
The main purpose of this work was to test the effective dominance of the inoculated strain during the fermentation process. During this research activity, two Saccharomyces cerevisiae selected strains, isolated from Aglianico del Vulture grapes, were tested during inoculated fermentations at pilot scale in three wine cellars producing Aglianico del Vulture wine and characterized by different typologies. Yeast colonies sampled during the processes of fermentation were identified by restriction analysis of the internal transcribed spacer (ITS) region, and S. cerevisiae strains were differentiated by restriction fragment length polymorphism of mitochondrial DNA (RFLP-mtDNA). Analysis of the yeast population during the inoculated fermentations evidenced a significant presence of non-Saccharomyces, which varied with the cellar. The presence of non-Saccharomyces yeasts at different levels affected the aromatic composition of the experimental wines, as determined by gas-chromatographic analysis. The RFLP-mtDNA of S. cerevisiae isolates revealed the differing dominance of inoculated strains as a function of the wine cellar. In two cellars, all the isolates showed the same restriction profile, which was identical to that of the starter pattern. In contrast, in the third cellar, a significant percentage of S. cerevisiae isolates exhibited mtDNA-RFLP patterns different from the yeast starter profile, showing that, in this case, the starter exhibited low dominance in the fermentation. Our results demonstrate that, although the inoculated strains were found with high frequency, other yeasts (S. cerevisiae and non-Saccharomyces) developed, contributing to the fermentative process and to organoleptic quality of the final wine.
引用
收藏
页码:49 / 56
页数:8
相关论文
共 33 条
[1]   Ecological study of wine yeast in inoculated vats from La Mancha region [J].
Barrajon, N. ;
Arevalo-Villena, M. ;
Rodriguez-Aragon, L. J. ;
Briones, A. .
FOOD CONTROL, 2009, 20 (09) :778-783
[2]   Molecular and technological approaches to evaluate strain biodiversity in Hanseniaspora uvarum of wine origin [J].
Capece, A ;
Fiore, C ;
Maraz, A ;
Romano, P .
JOURNAL OF APPLIED MICROBIOLOGY, 2005, 98 (01) :136-144
[3]  
Capece A, 2009, J ENG TECHNOL RES, V1, P68
[4]   Molecular characterization and oenological properties of wine yeasts isolated during spontaneous fermentation of six varieties of grape must [J].
Clemente-Jimenez, JM ;
Mingorance-Cazorla, L ;
Martínez-Rodríguez, S ;
Heras-Vázquez, FJL ;
Rodríguez-Vico, F .
FOOD MICROBIOLOGY, 2004, 21 (02) :149-155
[5]  
Constanti M, 1997, AM J ENOL VITICULT, V48, P339
[6]   Dynamics of indigenous and inoculated yeast populations and their effect on the sensory character of Riesling and Chardonnay wines [J].
Egli, CM ;
Edinger, WD ;
Mitrakul, CM ;
Henick-Kling, T .
JOURNAL OF APPLIED MICROBIOLOGY, 1998, 85 (05) :779-789
[7]   Selection and molecular characterization of wine yeasts isolated from the 'El Penedes' area (Spain) [J].
Esteve-Zarzoso, B ;
Gostíncar, A ;
Bobet, R ;
Uruburu, F ;
Querol, A .
FOOD MICROBIOLOGY, 2000, 17 (05) :553-562
[8]  
Fleet G., 1993, WINE MICROBIOLOGY BI, P27
[9]   Wine yeasts for the future [J].
Fleet, Graham H. .
FEMS YEAST RESEARCH, 2008, 8 (07) :979-995
[10]   Effect of wine yeast monoculture practice on the biodiversity of non-Saccharomyces yeasts [J].
Ganga, MA ;
Martínez, C .
JOURNAL OF APPLIED MICROBIOLOGY, 2004, 96 (01) :76-83