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1.
J Exp Bot ; 62(3): 1325-36, 2011 Jan.
Article in English | MEDLINE | ID: mdl-21115666

ABSTRACT

The biosynthesis of S-(3-hexan-1-ol)-glutathione (3MH-S-glut) and S-(3-hexan-l-ol)-L-cysteine (3MH-S-cys), which act as flavour precursors in wines, in Vitis vinifera grapes exposed to various environmental stress conditions is reported here. Ultraviolet (UV-C) irradiation, water deficit, and biological stimulation up-regulated 3MH-S-glut and 3MH-S-cys biosynthesis in grape leaves. 3MH-S-glut and 3MH-S-cys contents in grape berries were increased by cold shock, heat shock, UV-C irradiation, and biological stimulation. The results suggest that environmental stress enhances the biosynthesis of both flavour precursors in grapevine. The transcription of VvGST1, VvGST3, VvGST4, and GGT in grapevine exposed to the stress conditions was increased markedly compared with that in control grapevine. Also, UV irradiation increased GST (glutathione S-transferase) and GGT (γ-glutamyl transferase) enzyme activities in grape berries. Recombinant VvGST3 and VvGST4, but not VvGST1, mediated the synthesis of 3MH-S-glut from reduced glutathione and trans-2-hexenal in vitro. The enzymatic mediation of flavour precursor production is a novel function of plant GSTs and may result in the detoxification of damaged grape cells under stress conditions.


Subject(s)
Cysteine/analogs & derivatives , Flavoring Agents/metabolism , Glutathione Transferase/metabolism , Glutathione/analogs & derivatives , Plant Proteins/metabolism , Vitis/enzymology , Vitis/physiology , Cold Temperature , Cysteine/biosynthesis , Droughts , Enzyme Activation , Gene Expression Regulation, Enzymologic , Glutathione/biosynthesis , Glutathione Transferase/genetics , Hot Temperature , Plant Proteins/genetics , Stress, Physiological , Ultraviolet Rays , Vitis/genetics , Vitis/radiation effects , Wine/analysis
2.
J Agric Food Chem ; 57(18): 8550-6, 2009 Sep 23.
Article in English | MEDLINE | ID: mdl-19708656

ABSTRACT

Fishy aftertaste is sometimes perceived in wine with fish and seafood pairing. However, what component of wine clashes with seafood or what compound contributes to the unpleasant fishy aftertaste in the mouth remains an open problem. First, intensities of unpleasant fishy aftertaste of wine and dried scallop pairings were rated by sensory analysis. Second, components of the wines were analyzed. Strong positive correlations were found between the intensity of fishy aftertaste and the concentration of both total iron and ferrous ion. Moreover, the intensity of fishy aftertaste was increased by the addition of ferrous ion in model wine and suppressed by the chelation of ferrous ion in red wine. Third, potent volatile compounds of fishy aftertaste, such as hexanal, heptanal, 1-octen-3-one, (E,Z)-2,4-heptadienal, nonanal, and decanal, were determined by gas chromatography-olfactometry and gas chromatography-mass spectrometry in dried scallop soaked in red wine. The formations of these compounds depended on the dose of ferrous ion in the model wine. These results suggest that ferrous ion is a key compound of the formation of fishy aftertaste in wine and seafood pairing within the concentration range commonly found in wine.


Subject(s)
Iron/analysis , Pectinidae , Seafood , Taste , Wine/analysis , Adult , Animals , Chromatography, Gas/methods , Female , Ferrous Compounds/analysis , Food, Preserved , Gas Chromatography-Mass Spectrometry , Humans , Iron Chelating Agents/analysis , Male , Middle Aged , Volatile Organic Compounds/analysis
3.
Biosci Biotechnol Biochem ; 71(5): 1342-4, 2007 May.
Article in English | MEDLINE | ID: mdl-17485844

ABSTRACT

A polysaccharide-rich substance isolated from black currant, named cassis polysaccharide (CAPS), was partially digested with beta-galactosidase from Aspergillus oryzae and its immunostimulatory activity was investigated. The in vitro cytokine-inducing effect of CAPS on RAW264 cells was gradually decreased along with lowering of the average MW of CAPS. In vivo, partially digested CAPS with a mean MW of approximately 20,000 showed the most potent antitumor activity against Ehrlich carcinoma in mice.


Subject(s)
Antineoplastic Agents/pharmacology , Carcinoma, Ehrlich Tumor/drug therapy , Polysaccharides/metabolism , Polysaccharides/pharmacology , Ribes/chemistry , beta-Galactosidase/pharmacology , Animals , Antineoplastic Agents/chemistry , Aspergillus oryzae/enzymology , Buffers , Cell Line , Chromatography, High Pressure Liquid , Dose-Response Relationship, Drug , Hydrogen-Ion Concentration , Macrophage Activation/drug effects , Macrophages, Peritoneal/drug effects , Mice , Mice, Inbred ICR , Molecular Weight , Neoplasm Transplantation , Phosphates/chemistry , Polysaccharides/chemistry , Reference Standards , Temperature , Time Factors , Transplantation, Homologous
4.
Biosci Biotechnol Biochem ; 69(11): 2042-50, 2005 Nov.
Article in English | MEDLINE | ID: mdl-16306683

ABSTRACT

The fruit juice of black currant was found to contain a polysaccharide-rich substance, which was designated cassis polysaccharide (CAPS), with macrophage-stimulating activity. Especially, its interleukin (IL)-1beta-inducing activity was remarkably high, compared with other fruit juice preparations. CAPS was found to consist of rhamnose, mannose, arabinose, galactose, xylose, and glucose in a molar ratio of 11.3:0.9:54.1:29.8:2.0:1.9. CAPS turned out to be partitioned into a soluble component (CAPS-l.m.) and a precipitable component (CAPS-h.m.) with mean MWs of 80,000 and 600,000 respectively in 45% (v/v) ethanol solution. At least in vitro, CAPS-l.m. rather than CAPS-h.m. appeared to play an important role in macrophage activation. Oral administration of black currant juice and CAPS to Ehrlich carcinoma-bearing mice retarded the growth of the solid tumor by 45% and 51% respectively. CAPS administration had a stimulatory effect on the release of IL-2, IL-10, interferon-gamma, and IL-4 from splenocytes in comparison with PBS treatment in tumor-bearing mice. The IL-4 level was, however, still lower than that exhibited by a group of normal mice. CAPS showed a certain cytotoxicity directly against tumor cells.


Subject(s)
Antineoplastic Agents/pharmacology , Immunity/drug effects , Polysaccharides/pharmacology , Ribes/chemistry , Animals , Antineoplastic Agents/isolation & purification , Carbohydrates/analysis , Carcinoma, Ehrlich Tumor/drug therapy , Female , Interferon-gamma/metabolism , Interleukins/metabolism , Macrophages/drug effects , Mice , Mice, Inbred ICR , Plant Extracts , Polysaccharides/chemistry , Polysaccharides/isolation & purification , Solubility , Spleen/cytology , Spleen/metabolism , Tumor Burden/drug effects
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