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Molecular Fingerprinting by PCR-denaturing Gradient Gel Electrophoresis Reveals Differences in the Levels of Microbial Diversity for Musty-earthy Tainted Corks

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Date 2009 Feb 10
PMID 19201983
Citations 3
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Abstract

The microbial community structure of cork with marked musty-earthy aromas was analyzed using denaturing gradient gel electrophoresis of amplified ribosomal DNA. Cork stoppers and discs were used for DNA extraction and were analyzed by using selective primers for bacteria and fungi. Stoppers clearly differed from discs harboring a different fungal community. Moreover, musty-earthy samples of both types were shown to have a specific microbiota. The fungi Penicillium glabrum and Neurospora spp. were present in all samples and were assumed to make only a small contribution to off-odor development. In contrast, Penicillium islandicum and Penicillium variabile were found almost exclusively in 2,4,6-trichloroanisole (TCA) tainted discs. Conversely, Rhodotorula minuta and Rhodotorula sloofiae were most common in cork stoppers, where only small amounts of TCA were detected. Alpha- and gammaproteobacteria were the most commonly found bacteria in either control or tainted cork stoppers. Specific Pseudomonas and Actinobacteria were detected in stoppers with low amounts of TCA and 2-methoxy-3,5-dimethylpyrazine. These results are discussed in terms of biological degradation of taint compounds by specific microorganisms. Reliable and straightforward microbial identification methods based on a molecular approach provided useful data to determine and evaluate the risk of taint formation in cork.

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References
1.
Doare-Lebrun E, El Arbi A, Charlet M, Guerin L, Pernelle J, Ogier J . Analysis of fungal diversity of grapes by application of temporal temperature gradient gel electrophoresis - potentialities and limits of the method. J Appl Microbiol. 2006; 101(6):1340-50. DOI: 10.1111/j.1365-2672.2006.03030.x. View

2.
Cocolin L, Bisson L, Mills D . Direct profiling of the yeast dynamics in wine fermentations. FEMS Microbiol Lett. 2000; 189(1):81-7. DOI: 10.1111/j.1574-6968.2000.tb09210.x. View

3.
Gardes M, Bruns T . ITS primers with enhanced specificity for basidiomycetes--application to the identification of mycorrhizae and rusts. Mol Ecol. 1993; 2(2):113-8. DOI: 10.1111/j.1365-294x.1993.tb00005.x. View

4.
Gallois A, Grimont P . Pyrazines responsible for the potatolike odor produced by some serratia and cedecea strains. Appl Environ Microbiol. 1985; 50(4):1048-51. PMC: 291791. DOI: 10.1128/aem.50.4.1048-1051.1985. View

5.
Mills D, Johannsen E, Cocolin L . Yeast diversity and persistence in botrytis-affected wine fermentations. Appl Environ Microbiol. 2002; 68(10):4884-93. PMC: 126389. DOI: 10.1128/AEM.68.10.4884-4893.2002. View