Production of Flavours and Fragrances via Bioreduction of (4R)-(-)-Carvone and (1R)-(-)-Myrtenal by Non-Conventional Yeast Whole-Cells
Articolo
Data di Pubblicazione:
2013
Citazione:
Production of Flavours and Fragrances via Bioreduction of (4R)-(-)-Carvone and (1R)-(-)-Myrtenal by Non-Conventional Yeast Whole-Cells / M., G., B., T., Cramarossa, M.R., Forti, L., P., B.. - In: MOLECULES. - ISSN 1420-3049. - ELETTRONICO. - 18:5(2013), pp. 5736-5748. [10.3390/molecules18055736]
Abstract:
As part of a program aiming at the selection of yeast strains which might be of
interest as sources of natural flavours and fragrances, the bioreduction of (4R)-(−)-carvone
and (1R)-(−)-myrtenal by whole-cells of non-conventional yeasts (NCYs) belonging to the
genera Candida, Cryptococcus, Debaryomyces, Hanseniaspora, Kazachstania, Kluyveromyces,
Lindnera, Nakaseomyces, Vanderwaltozyma and Wickerhamomyces was studied. Volatiles
produced were sampled by means of headspace solid-phase microextraction (SPME) and the
compounds were analysed and identified by gas chromatography–mass spectroscopy
(GC-MS). Yields (expressed as % of biotransformation) varied in dependence of the strain.
The reduction of both (4R)-(−)-carvone and (1R)-(−)-myrtenal were catalyzed by some
ene-reductases (ERs) and/or carbonyl reductases (CRs), which determined the formation of
(1R,4R)-dihydrocarvone and (1R)-myrtenol respectively, as main flavouring products. The
potential of NCYs as novel whole-cell biocatalysts for selective biotransformation of electron-poor
alkenes for producing flavours and fragrances of industrial interest is discussed.
interest as sources of natural flavours and fragrances, the bioreduction of (4R)-(−)-carvone
and (1R)-(−)-myrtenal by whole-cells of non-conventional yeasts (NCYs) belonging to the
genera Candida, Cryptococcus, Debaryomyces, Hanseniaspora, Kazachstania, Kluyveromyces,
Lindnera, Nakaseomyces, Vanderwaltozyma and Wickerhamomyces was studied. Volatiles
produced were sampled by means of headspace solid-phase microextraction (SPME) and the
compounds were analysed and identified by gas chromatography–mass spectroscopy
(GC-MS). Yields (expressed as % of biotransformation) varied in dependence of the strain.
The reduction of both (4R)-(−)-carvone and (1R)-(−)-myrtenal were catalyzed by some
ene-reductases (ERs) and/or carbonyl reductases (CRs), which determined the formation of
(1R,4R)-dihydrocarvone and (1R)-myrtenol respectively, as main flavouring products. The
potential of NCYs as novel whole-cell biocatalysts for selective biotransformation of electron-poor
alkenes for producing flavours and fragrances of industrial interest is discussed.
Tipologia CRIS:
Articolo su rivista
Keywords:
biocatalysis; non-conventional yeasts; ene-reductases; carbonyl reductases; monoterpenoids
Elenco autori:
M., Goretti; B., Turchetti; Cramarossa, Maria Rita; Forti, Luca; P., Buzzini
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