Chemoenzymatic synthesis of aroma active 5,6-dihydro- and tetrahydropyrazines from aliphatic acyloins produced by baker's yeast

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

  • Toshinari Kurniadi
  • Rachid Bel Rhlid
  • Laurent Bernard Fay
  • Marcel Alexandre Juillerat
  • Ralf Günter Berger

Organisationseinheiten

Externe Organisationen

  • Nestlé SA
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Details

OriginalspracheEnglisch
Seiten (von - bis)3103-3107
Seitenumfang5
FachzeitschriftJournal of Agricultural and Food Chemistry
Jahrgang51
Ausgabenummer10
PublikationsstatusVeröffentlicht - 15 Apr. 2003

Abstract

Twenty-five acyloins were generated by biotransformation of aliphatic aldehydes and 2-ketocarboxylic acids using whole cells of baker's yeast as catalyst. Six of these acyloins were synthesized and tentatively characterized for the first time. Subsequent chemical reaction with 1,2-propanediamine under mild conditions resulted in the formation of thirteen 5,6-dihydropyrazines and six tetrahydropyrazines. Their odor qualities were evaluated, and their odor thresholds were estimated. Among these pyrazine derivatives, 2-ethyl-3,5-dimethyl-5,6-dihydropyrazine (roasted, nutty, 0.002 ng/L air), 2,3-diethyl-5-methyl-5,6-dihydropyrazine (roasted, 0.004 ng/L air), and 2-ethyl-3,5-dimethyltetrahy-dropyrazine (bread crustlike, 1.9 ng/L air) were the most intensive-smelling aroma active compounds.

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Chemoenzymatic synthesis of aroma active 5,6-dihydro- and tetrahydropyrazines from aliphatic acyloins produced by baker's yeast. / Kurniadi, Toshinari; Bel Rhlid, Rachid; Fay, Laurent Bernard et al.
in: Journal of Agricultural and Food Chemistry, Jahrgang 51, Nr. 10, 15.04.2003, S. 3103-3107.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Kurniadi T, Bel Rhlid R, Fay LB, Juillerat MA, Berger RG. Chemoenzymatic synthesis of aroma active 5,6-dihydro- and tetrahydropyrazines from aliphatic acyloins produced by baker's yeast. Journal of Agricultural and Food Chemistry. 2003 Apr 15;51(10):3103-3107. doi: 10.1021/jf0261809
Kurniadi, Toshinari ; Bel Rhlid, Rachid ; Fay, Laurent Bernard et al. / Chemoenzymatic synthesis of aroma active 5,6-dihydro- and tetrahydropyrazines from aliphatic acyloins produced by baker's yeast. in: Journal of Agricultural and Food Chemistry. 2003 ; Jahrgang 51, Nr. 10. S. 3103-3107.
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abstract = "Twenty-five acyloins were generated by biotransformation of aliphatic aldehydes and 2-ketocarboxylic acids using whole cells of baker's yeast as catalyst. Six of these acyloins were synthesized and tentatively characterized for the first time. Subsequent chemical reaction with 1,2-propanediamine under mild conditions resulted in the formation of thirteen 5,6-dihydropyrazines and six tetrahydropyrazines. Their odor qualities were evaluated, and their odor thresholds were estimated. Among these pyrazine derivatives, 2-ethyl-3,5-dimethyl-5,6-dihydropyrazine (roasted, nutty, 0.002 ng/L air), 2,3-diethyl-5-methyl-5,6-dihydropyrazine (roasted, 0.004 ng/L air), and 2-ethyl-3,5-dimethyltetrahy-dropyrazine (bread crustlike, 1.9 ng/L air) were the most intensive-smelling aroma active compounds.",
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T1 - Chemoenzymatic synthesis of aroma active 5,6-dihydro- and tetrahydropyrazines from aliphatic acyloins produced by baker's yeast

AU - Kurniadi, Toshinari

AU - Bel Rhlid, Rachid

AU - Fay, Laurent Bernard

AU - Juillerat, Marcel Alexandre

AU - Berger, Ralf Günter

PY - 2003/4/15

Y1 - 2003/4/15

N2 - Twenty-five acyloins were generated by biotransformation of aliphatic aldehydes and 2-ketocarboxylic acids using whole cells of baker's yeast as catalyst. Six of these acyloins were synthesized and tentatively characterized for the first time. Subsequent chemical reaction with 1,2-propanediamine under mild conditions resulted in the formation of thirteen 5,6-dihydropyrazines and six tetrahydropyrazines. Their odor qualities were evaluated, and their odor thresholds were estimated. Among these pyrazine derivatives, 2-ethyl-3,5-dimethyl-5,6-dihydropyrazine (roasted, nutty, 0.002 ng/L air), 2,3-diethyl-5-methyl-5,6-dihydropyrazine (roasted, 0.004 ng/L air), and 2-ethyl-3,5-dimethyltetrahy-dropyrazine (bread crustlike, 1.9 ng/L air) were the most intensive-smelling aroma active compounds.

AB - Twenty-five acyloins were generated by biotransformation of aliphatic aldehydes and 2-ketocarboxylic acids using whole cells of baker's yeast as catalyst. Six of these acyloins were synthesized and tentatively characterized for the first time. Subsequent chemical reaction with 1,2-propanediamine under mild conditions resulted in the formation of thirteen 5,6-dihydropyrazines and six tetrahydropyrazines. Their odor qualities were evaluated, and their odor thresholds were estimated. Among these pyrazine derivatives, 2-ethyl-3,5-dimethyl-5,6-dihydropyrazine (roasted, nutty, 0.002 ng/L air), 2,3-diethyl-5-methyl-5,6-dihydropyrazine (roasted, 0.004 ng/L air), and 2-ethyl-3,5-dimethyltetrahy-dropyrazine (bread crustlike, 1.9 ng/L air) were the most intensive-smelling aroma active compounds.

KW - Acyloins

KW - Baker's yeast

KW - Carboligation

KW - Flavor

KW - Pyrazine derivatives

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