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Volumn 56, Issue 9, 2008, Pages 2883-2887

Quantification of cysteine S-conjugate of 3-sulfanylhexan-1-ol in must and wine of petite arvine vine by stable isotope dilution analysis

Author keywords

3 mercaptohexan 1 ol; 3 sulfanylhexan 1 ol; Cysteine S conjugate; Deuterated analogue; Petite arvine vine; S 3 (hexan 1 ol) cysteine; Stable isotope dilution assay

Indexed keywords

3 MERCAPTOHEXANOL; 3-MERCAPTOHEXANOL; CYSTEINE; DEUTERIUM; DRUG DERIVATIVE; HEXANOL; S (3 HEXAN 1 OL)CYSTEINE; S-(3-HEXAN-1-OL)CYSTEINE; THIOL DERIVATIVE;

EID: 44349084975     PISSN: 00218561     EISSN: None     Source Type: Journal    
DOI: 10.1021/jf072963o     Document Type: Article
Times cited : (30)

References (25)
  • 1
    • 0029193852 scopus 로고
    • Identification of a powerful aromatic of Vitis vinefera L. var. Sauvignon wines: 4-mercapto-4-methylpentan-2-one
    • Darriet, P.; Tominaga, T.; Lavigne, V.; Boidron, J. N.; Dubourdieu, D. Identification of a powerful aromatic of Vitis vinefera L. var. Sauvignon wines: 4-mercapto-4-methylpentan-2-one. Flavour Fragrance J. 1995, 10, 385-392.
    • (1995) Flavour Fragrance J , vol.10 , pp. 385-392
    • Darriet, P.1    Tominaga, T.2    Lavigne, V.3    Boidron, J.N.4    Dubourdieu, D.5
  • 2
    • 0031825535 scopus 로고    scopus 로고
    • Identification of new volatile thiols in the aroma of Vitis vinifera L. var. Sauvignon wines
    • Tominaga, T.; Furrer, A.; Henry, R.; Duboudieu, D. Identification of new volatile thiols in the aroma of Vitis vinifera L. var. Sauvignon wines. Flavour Fragrance J. 1998, 13, 159-162.
    • (1998) Flavour Fragrance J , vol.13 , pp. 159-162
    • Tominaga, T.1    Furrer, A.2    Henry, R.3    Duboudieu, D.4
  • 3
    • 0035187837 scopus 로고    scopus 로고
    • Assessing the aromatic potential of Cabernet Sauvignon and Merlot musts used to produce rose wine by assaying the cysteinylated precursor of 3-mercaptohexan-1-ol
    • Murat, M.-L.; Tominaga, T.; Dubourdieu, D. Assessing the aromatic potential of Cabernet Sauvignon and Merlot musts used to produce rose wine by assaying the cysteinylated precursor of 3-mercaptohexan-1-ol. J. Agric. Food Chem. 2001, 49, 5412-5417.
    • (2001) J. Agric. Food Chem , vol.49 , pp. 5412-5417
    • Murat, M.-L.1    Tominaga, T.2    Dubourdieu, D.3
  • 4
    • 29544436906 scopus 로고    scopus 로고
    • 3-Mercaptohexanol: An aroma impact compound of petite arvine wine
    • Fretz, C. B.; Luisier, J.-L.; Tominaga, T.; Amado, R. 3-Mercaptohexanol: an aroma impact compound of petite arvine wine. Am. J. Enol. Vitic. 2005, 56, 407-410.
    • (2005) Am. J. Enol. Vitic , vol.56 , pp. 407-410
    • Fretz, C.B.1    Luisier, J.-L.2    Tominaga, T.3    Amado, R.4
  • 6
    • 29544450635 scopus 로고    scopus 로고
    • Sensory characterisation of Petite Arvine wines
    • Fretz, C. B.; Luisier, J.-L.; Amado, R. Sensory characterisation of Petite Arvine wines. Mitt. Lebensm. Hyg. 2006, 96, 189-198.
    • (2006) Mitt. Lebensm. Hyg , vol.96 , pp. 189-198
    • Fretz, C.B.1    Luisier, J.-L.2    Amado, R.3
  • 7
    • 0001389623 scopus 로고    scopus 로고
    • A new type of flavor precursor in Vitis vinifera L. cv. Sauvignon Blanc S-cysteine conjugates
    • Tominaga, T.; Peyrot des Gachons, C.; Dubourdieu, D. A new type of flavor precursor in Vitis vinifera L. cv. Sauvignon Blanc S-cysteine conjugates. J. Agric. Food Chem. 1998, 46, 5215-5219.
    • (1998) J. Agric. Food Chem , vol.46 , pp. 5215-5219
    • Tominaga, T.1    Peyrot des Gachons, C.2    Dubourdieu, D.3
  • 8
    • 0037014370 scopus 로고    scopus 로고
    • Suflur aroma precursor present in S-giutathione conjugate form: Identification of 5-3-(hexan-1-ol)-glutathione in must from Vitis vinifera L. cv. Sauvignon Blanc
    • Peyrot des Gachons, C.; Tominaga, T.; Dubourdieu, D. Suflur aroma precursor present in S-giutathione conjugate form: identification of 5-3-(hexan-1-ol)-glutathione in must from Vitis vinifera L. cv. Sauvignon Blanc. J. Agric. Food Chem. 2002, 50, 4076-4079.
    • (2002) J. Agric. Food Chem , vol.50 , pp. 4076-4079
    • Peyrot des Gachons, C.1    Tominaga, T.2    Dubourdieu, D.3
  • 9
    • 0347355024 scopus 로고    scopus 로고
    • Stereochemical course of the generation of 3-mercaptohexanal and 3-mercaptohexanol by β-lyase-catalyzed cleavage of cysteine conjugates
    • Wakabayashi, H.; Wakabayashi, M.; Eisenreich, W.; Engel, K.-H. Stereochemical course of the generation of 3-mercaptohexanal and 3-mercaptohexanol by β-lyase-catalyzed cleavage of cysteine conjugates. J. Agric. Food Chem. 2004, 52, 110-116.
    • (2004) J. Agric. Food Chem , vol.52 , pp. 110-116
    • Wakabayashi, H.1    Wakabayashi, M.2    Eisenreich, W.3    Engel, K.-H.4
  • 10
    • 33947265676 scopus 로고    scopus 로고
    • Modulation of volatile sulfur compounds by wine yeast
    • Swiegers, J. H.; Pretorius, I. S. Modulation of volatile sulfur compounds by wine yeast. Appl. Microbiol. Biotechnol. 2007, 74, 954-960.
    • (2007) Appl. Microbiol. Biotechnol , vol.74 , pp. 954-960
    • Swiegers, J.H.1    Pretorius, I.S.2
  • 11
    • 34250646720 scopus 로고    scopus 로고
    • Volatile organic sulfur-containing constituents in Poncirus trifoliata (L.) Raf. (Rutaceae)
    • Starkenmann, C.; Niclass, Y.; Escher, S. Volatile organic sulfur-containing constituents in Poncirus trifoliata (L.) Raf. (Rutaceae). J. Agric. Food Chem. 2007, 55, 4511-4517.
    • (2007) J. Agric. Food Chem , vol.55 , pp. 4511-4517
    • Starkenmann, C.1    Niclass, Y.2    Escher, S.3
  • 12
    • 0001380611 scopus 로고
    • Quantitative determination of β-damascenone in foods using a stable isotope dilution assay
    • Sen, A.; Laskawy, G.; Schieberle, P.; Grosch, W. Quantitative determination of β-damascenone in foods using a stable isotope dilution assay. J. Agric. Food Chem. 1991, 39, 757-759.
    • (1991) J. Agric. Food Chem , vol.39 , pp. 757-759
    • Sen, A.1    Laskawy, G.2    Schieberle, P.3    Grosch, W.4
  • 13
    • 0032840419 scopus 로고    scopus 로고
    • Development of a stable isotope dilution assay for the quantification of 5-methyl-(E)-2-hepten-4-one: Application to hazelnut oils and hazelnuts
    • Pfnuer, P.; Matsui, T.; Grosch, W.; Guth, H.; Hofmann, T.; Schieberle, P. Development of a stable isotope dilution assay for the quantification of 5-methyl-(E)-2-hepten-4-one: application to hazelnut oils and hazelnuts. J. Agric. Food Chem. 1999, 47, 2044-2047.
    • (1999) J. Agric. Food Chem , vol.47 , pp. 2044-2047
    • Pfnuer, P.1    Matsui, T.2    Grosch, W.3    Guth, H.4    Hofmann, T.5    Schieberle, P.6
  • 14
    • 0038624011 scopus 로고    scopus 로고
    • Quantitative determination of sulfur-containing wine odorants at sub parts per billion levels. 2. Development and application of a stable isotope dilution assay
    • Schneider, R.; Kotseridis, Y.; Ray, J.-L.; Augier, C.; Baumes, R. Quantitative determination of sulfur-containing wine odorants at sub parts per billion levels. 2. Development and application of a stable isotope dilution assay. J. Agric. Food Chem. 2003, 51, 3242-3248.
    • (2003) J. Agric. Food Chem , vol.51 , pp. 3242-3248
    • Schneider, R.1    Kotseridis, Y.2    Ray, J.-L.3    Augier, C.4    Baumes, R.5
  • 15
    • 34248682133 scopus 로고    scopus 로고
    • Synthesis of isotopically labelled thiol volatiles and cysteine conjugates for quantification of Sauvignon Blanc wine
    • Katherine, R.; Hebditch, R.; Nicolau, L.; Brimble, M. A. Synthesis of isotopically labelled thiol volatiles and cysteine conjugates for quantification of Sauvignon Blanc wine. J. Labelled Compd. Radiopharm. 2007, 50, 237-243.
    • (2007) J. Labelled Compd. Radiopharm , vol.50 , pp. 237-243
    • Katherine, R.1    Hebditch, R.2    Nicolau, L.3    Brimble, M.A.4
  • 16
    • 34547742001 scopus 로고    scopus 로고
    • Characterisation and simple synthesis of S-[3-hydroxy-1-propylpropyl]-L-cysteine
    • Luisier, J.-L.; Veyrand, J.; Piantini, U. Characterisation and simple synthesis of S-[3-hydroxy-1-propylpropyl]-L-cysteine. Chimia 2007, 61, 533-535.
    • (2007) Chimia , vol.61 , pp. 533-535
    • Luisier, J.-L.1    Veyrand, J.2    Piantini, U.3
  • 17
    • 0007154614 scopus 로고
    • New method for synthesis of α,β-unsaturated carboxylic esters from carbonyl compounds using monoanions of dithiocarbonates, and dianions of ethyl mercaptoacetate and ethyl 2-mercaptopropionate
    • Tanaka, K.; Yamagishi, N.; Tanikaga, R.; Kaji, A. New method for synthesis of α,β-unsaturated carboxylic esters from carbonyl compounds using monoanions of dithiocarbonates, and dianions of ethyl mercaptoacetate and ethyl 2-mercaptopropionate. Bull. Chem. Soc. Jpn. 1979, 52, 3619-3625.
    • (1979) Bull. Chem. Soc. Jpn , vol.52 , pp. 3619-3625
    • Tanaka, K.1    Yamagishi, N.2    Tanikaga, R.3    Kaji, A.4
  • 18
    • 44349115563 scopus 로고
    • Addition reaction of copper(I) methyltrialkylborates with ethyl propiolate. Stereospecific synthesis of (E)-α,β-unsaturated acid esters
    • Yamada, K.; Miyaura, N.; Itoh, M.; Suzuki, A. Addition reaction of copper(I) methyltrialkylborates with ethyl propiolate. Stereospecific synthesis of (E)-α,β-unsaturated acid esters. Bull. Chem. Soc. Jpn. 1977, 50, 3431-3432.
    • (1977) Bull. Chem. Soc. Jpn , vol.50 , pp. 3431-3432
    • Yamada, K.1    Miyaura, N.2    Itoh, M.3    Suzuki, A.4
  • 19
    • 0033851483 scopus 로고    scopus 로고
    • Measuring the aromatic potential of Vitis vinifera L. Cv. Sauvignon Blanc grapes by assaying S-cysteine conjugates, precursors of the volatile thiols responsible of their varietal aroma
    • Peyrot des Gachons, C.; Tominaga, T.; Dubourdieu, D. Measuring the aromatic potential of Vitis vinifera L. Cv. Sauvignon Blanc grapes by assaying S-cysteine conjugates, precursors of the volatile thiols responsible of their varietal aroma. J. Agric. Food Chem. 2000, 48, 3387-3391.
    • (2000) J. Agric. Food Chem , vol.48 , pp. 3387-3391
    • Peyrot des Gachons, C.1    Tominaga, T.2    Dubourdieu, D.3
  • 21
    • 2342667939 scopus 로고
    • Linolenic acid and its 13-hydroperoxide inhibit hexanal formation from linoleic acid in plant tissues
    • Hatanaka, A.; Sekiya, J.; Kajiwara, T. Linolenic acid and its 13-hydroperoxide inhibit hexanal formation from linoleic acid in plant tissues. J. Agric. Food Chem. 1983, 31, 176-178.
    • (1983) J. Agric. Food Chem , vol.31 , pp. 176-178
    • Hatanaka, A.1    Sekiya, J.2    Kajiwara, T.3
  • 22
    • 33745454758 scopus 로고    scopus 로고
    • Adducts of oxylipin electrophiles to glutathione reflect a 13 specificity of the downstream lipoxygenase pathway in the tobacco hypersensitive response
    • Davoine, C.; Falletti, O.; Douki, T.; Iacazio, G.; Ennar, N.; Montillet, J.-L.; Triantaphylidès, C. Adducts of oxylipin electrophiles to glutathione reflect a 13 specificity of the downstream lipoxygenase pathway in the tobacco hypersensitive response. Plant Physiol. 2006, 140, 1484-1493.
    • (2006) Plant Physiol , vol.140 , pp. 1484-1493
    • Davoine, C.1    Falletti, O.2    Douki, T.3    Iacazio, G.4    Ennar, N.5    Montillet, J.-L.6    Triantaphylidès, C.7
  • 23
    • 0347624953 scopus 로고    scopus 로고
    • Recherches sur le potentiel aromatique des raisins de Vitis vinifera L cv
    • Ph.D. Thesis, Université Victor Segalen Bordeaux II
    • Peyrot des Gachons, C. Recherches sur le potentiel aromatique des raisins de Vitis vinifera L cv. Sauvignon blanc. Ph.D. Thesis 799, Université Victor Segalen Bordeaux II, 2000.
    • (2000) Sauvignon blanc , pp. 799
    • Peyrot des Gachons, C.1
  • 25
    • 33749674486 scopus 로고    scopus 로고
    • Stereoisomeric distribution of 3-mercaptohexan-1-ol and 3-mercaptohexylacetate in dry and sweet white wines made from Vitis vinifera (var. Sauvignon Blanc and Semillon)
    • Tominaga, T.; Niclass, Y.; Frerot, E.; Dubourdieu, D. J. Stereoisomeric distribution of 3-mercaptohexan-1-ol and 3-mercaptohexylacetate in dry and sweet white wines made from Vitis vinifera (var. Sauvignon Blanc and Semillon). J. Agric. Food Chem. 2006, 54, 7251-7255.
    • (2006) J. Agric. Food Chem , vol.54 , pp. 7251-7255
    • Tominaga, T.1    Niclass, Y.2    Frerot, E.3    Dubourdieu, D.J.4


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