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Research Article

Impact of Yeasts Present during Prefermentation Cold Maceration of Pinot noir Grapes on Wine Volatile Aromas

Harper Hall, Qin Zhou, Michael C. Qian, James P. Osborne
Am J Enol Vitic.  2017  68: 81-90  ; DOI: 10.5344/ajev.2016.16046
Harper Hall
1Oregon State University, Department of Food Science and Technology, 100 Wiegand Hall, Corvallis, OR 97331, United States
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Qin Zhou
1Oregon State University, Department of Food Science and Technology, 100 Wiegand Hall, Corvallis, OR 97331, United States
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Michael C. Qian
1Oregon State University, Department of Food Science and Technology, 100 Wiegand Hall, Corvallis, OR 97331, United States
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James P. Osborne
1Oregon State University, Department of Food Science and Technology, 100 Wiegand Hall, Corvallis, OR 97331, United States
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  • For correspondence: james.osborne{at}oregonstate.edu
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Abstract

Yeasts isolated from a prefermentation cold maceration (at 8 to 9°C) of Vitis vinifera L. cv. Pinot noir grapes were evaluated for β-glucosidase activity. Among the 13 distinct yeast isolates investigated, five had β-glucosidase activity. Sequence analysis of the D1/D2 domain of the 26S rDNA gene confirmed the identity of these yeasts as Metschnikowia pulcherrima, Hanseniaspora uvarum, Lachancea thermotolerans, and two isolates of Saccharomyces cerevisiae. The β-glucosidase activity of these yeast isolates was further investigated at different sugar concentrations and temperatures before the isolates were used in the production of Pinot noir wines. Pinot noir grapes sterilized by high hydrostatic pressure were inoculated with the individual yeast species or a mixture of all yeast species. A seven day prefermentation cold maceration (9°C) was then performed, followed by alcoholic fermentation conducted by S. cerevisiae RC212 at 27°C. Pinot noir grapes were also cold-macerated without the addition of any yeast, while fermentations were also undertaken with no cold maceration. Solid-phase microextraction-gas chromatography-mass spectrometry analysis of the wines indicated that the presence of the different yeast species during the prefermentation cold-maceration altered the volatile aroma composition of the wines. These yeasts altered the concentrations of ethyl esters, branch-chained esters, higher alcohols, and some monoterpenes in the wines.

  • β-glucosidase
  • non-Saccharomyces yeast
  • Pinot noir
  • prefermentation cold maceration
  • SPME-GC-MS
  • wine volatile aromas
  • ©2017 by the American Society for Enology and Viticulture
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Impact of Yeasts Present during Prefermentation Cold Maceration of Pinot noir Grapes on Wine Volatile Aromas
Harper Hall, Qin Zhou, Michael C. Qian, James P. Osborne
Am J Enol Vitic.  2017  68: 81-90  ; DOI: 10.5344/ajev.2016.16046
Harper Hall
1Oregon State University, Department of Food Science and Technology, 100 Wiegand Hall, Corvallis, OR 97331, United States
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Qin Zhou
1Oregon State University, Department of Food Science and Technology, 100 Wiegand Hall, Corvallis, OR 97331, United States
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Michael C. Qian
1Oregon State University, Department of Food Science and Technology, 100 Wiegand Hall, Corvallis, OR 97331, United States
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James P. Osborne
1Oregon State University, Department of Food Science and Technology, 100 Wiegand Hall, Corvallis, OR 97331, United States
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  • For correspondence: james.osborne{at}oregonstate.edu

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Impact of Yeasts Present during Prefermentation Cold Maceration of Pinot noir Grapes on Wine Volatile Aromas
Harper Hall, Qin Zhou, Michael C. Qian, James P. Osborne
Am J Enol Vitic.  2017  68: 81-90  ; DOI: 10.5344/ajev.2016.16046
Harper Hall
1Oregon State University, Department of Food Science and Technology, 100 Wiegand Hall, Corvallis, OR 97331, United States
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Qin Zhou
1Oregon State University, Department of Food Science and Technology, 100 Wiegand Hall, Corvallis, OR 97331, United States
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Michael C. Qian
1Oregon State University, Department of Food Science and Technology, 100 Wiegand Hall, Corvallis, OR 97331, United States
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
James P. Osborne
1Oregon State University, Department of Food Science and Technology, 100 Wiegand Hall, Corvallis, OR 97331, United States
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • For correspondence: james.osborne{at}oregonstate.edu
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