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1.
Molecules ; 27(15)2022 Jul 26.
Article in English | MEDLINE | ID: mdl-35897960

ABSTRACT

Although ginseng leaf is a good source of health-beneficial phytochemicals, such as polyphenols and ginsenosides, few studies have focused on the variation in compounds and bioactivities during leaf thermal processing. The efficiency of far-infrared irradiation (FIR) between 160 °C and 200 °C on the deglycosylation of bioactive compounds in ginseng leaves was analyzed. FIR treatment significantly increased the total polyphenol content (TPC) and kaempferol production from panasenoside conversion. The highest content or conversion ratio was observed at 180 °C (FIR-180). Major ginsenoside contents gradually decreased as the FIR temperature increased, while minor ginsenoside contents significantly increased. FIR exhibited high efficiency to produce dehydrated minor ginsenosides, of which F4, Rg6, Rh4, Rk3, Rk1, and Rg5 increased to their highest levels at FIR-190, by 278-, 149-, 176-, 275-, 64-, and 81-fold, respectively. Moreover, significantly increased antioxidant activities were also observed in FIR-treated leaves, particularly FIR-180, mainly due to the breakage of phenolic polymers to release antioxidants. These results suggest that FIR treatment is a rapid and efficient processing method for producing various health-beneficial bioactive compounds from ginseng leaves. After 30 min of treatment without leaf burning, FIR-190 was the optimum temperature for producing minor ginsenosides, whereas FIR-180 was the optimum temperature for producing polyphenols and kaempferol. In addition, the results suggested that the antioxidant benefits of ginseng leaves are mainly due to polyphenols rather than ginsenosides.


Subject(s)
Panax , Plant Leaves , Temperature , Antioxidants , Ginsenosides , Infrared Rays , Kaempferols , Panax/chemistry , Panax/radiation effects , Plant Leaves/chemistry , Plant Leaves/radiation effects , Polyphenols
2.
Food Microbiol ; 55: 16-24, 2016 May.
Article in English | MEDLINE | ID: mdl-26742612

ABSTRACT

Lactic acid bacteria (LAB) used for malolactic fermentation (MLF) has a great effect on the production and quality of cherry wines. The present study used an autochthonous Lb. plantarum strain of SGJ-24 which was isolated from spontaneous MLF cherry wines and selected by its best MLF performance and tolerance, to investigate its effect on the kinetic of vinification and on chemical and volatile characteristics of Rainer and May Duck cherry wines, in comparison with a commercial Oenococcus oeni strain of 31 MBR. Monitoring of MLF was carried out by measuring cell viability and malic acid metabolism, and results showed that for both cherry varieties, SGJ-24 can significantly minimize MLF duration. After fermentation, wine samples were chemically characterized and analyzed for volatile profiles. Results demonstrated that no negative impact on the analytical parameters has been found, and a general increase of volatile esters and terpenes was observed when SGJ-24 was involved. Sensory analysis revealed that the global aromatic intensity was enhanced by the introduction of SGJ-24. All these data suggested that the application of Lb. plantarum strain of SGJ-24 as a worthwhile alternative LAB species for Rainer and May Duck cherry winemaking.


Subject(s)
Flavoring Agents/metabolism , Lactobacillus plantarum/metabolism , Malates/metabolism , Prunus avium/microbiology , Volatile Organic Compounds/metabolism , Wine/microbiology , Adult , Female , Fermentation , Humans , Male , Middle Aged , Oenococcus/metabolism , Taste , Wine/analysis , Young Adult
3.
J Sci Food Agric ; 96(6): 1880-7, 2016 Apr.
Article in English | MEDLINE | ID: mdl-26041620

ABSTRACT

BACKGROUND: There has been limited research on the use of non-Saccharomyces yeasts for the production of cherry wines. This work used an autochthonous Torulaspora delbrueckii strain 49 (TD49) in association with a commercial S. cerevisiae RC212 yeast, to investigate the effect of multi-starter culture (sequential inoculation and simultaneous inoculation) and fermentation temperature on the quality of cherry wines. RESULTS: Both TD49 and RC212 proliferated during alcoholic fermentation (AF) under sequential inoculation conditions, whereas in the case of simultaneous inoculation, TD49 increased slowly at first and then declined sharply near the fermentation end. The analytical profile showed that both mixed fermentations produced lower levels of volatile acidy and higher levels of aromatic compounds than those from RC212 mono-culture. During sensory analysis, wines from sequential fermentation obtained the highest score, mainly due to the higher intensity in 'fruity' and 'floral' characters. As for the influence of temperature, a low temperature (20 °C) enhanced TD49 persistence during AF, but the sensory quality decreased anyway; 30 °C resulted in decreases in most measured descriptors. Therefore, 25 °C was selected as the best culture temperature. CONCLUSION: TD49/RC212 sequential inoculation and fermentation at 25 °C significantly enhanced the cherry wine quality.


Subject(s)
Saccharomyces cerevisiae/physiology , Temperature , Torulaspora/physiology , Wine/standards , Fermentation , Food Quality , Fruit , Prunus avium , Time Factors
4.
Food Microbiol ; 44: 15-23, 2014 Dec.
Article in English | MEDLINE | ID: mdl-25084640

ABSTRACT

This study examined the effect of mixed fermentation of non-Saccharomyces (Torulaspora delbrueckii ZYMAFLORE Alpha(TD n. Sacch) and Metschnikowia pulcherrima JS22) and Saccharomyces cerevisiae yeasts (D254 and EC1118) on the production of cherry wines, in comparison with commonly used mono-culture. Results obtained during AF demonstrated that negligible inhibitory effect was observed in S. cerevisiae/Alpha pair, whereas a strong antagonistic effect was detected between MJS22 and S. cerevisiae strain, resulting in an early death of MJS22. For volatile components determined, S. cerevisiae/MJS22 couple was found to significantly boost the production of most detected compounds, more particularly in higher alcohols, esters, acids and terpenes; while the characteristic of S. cerevisiae/Alpha pair is an increase in fruity esters, higher alcohols and decrease in acid production. Sensory evaluation revealed that S. cerevisiae/MJS22 pair reinforced sweet, green and fatty notes to the cherry wines, and S. cerevisiae/Alpha trial enhanced the fruity odour and reduced green note.


Subject(s)
Ethanol/metabolism , Prunus/microbiology , Saccharomyces/metabolism , Volatile Organic Compounds/metabolism , Wine/microbiology , Yeasts/metabolism , Adult , Female , Fermentation , Flavoring Agents/chemistry , Flavoring Agents/metabolism , Humans , Male , Middle Aged , Prunus/chemistry , Taste , Volatile Organic Compounds/chemistry , Wine/analysis , Young Adult
5.
J Basic Microbiol ; 50 Suppl 1: S37-45, 2010 Dec.
Article in English | MEDLINE | ID: mdl-20967788

ABSTRACT

Plantaricin MG is a 2,180-Da bacteriocin produced by Lactobacillus plantarum KLDS1.0391, which was isolated from Chinese traditional fermented cream. Plantaricin MG showed a broad inhibitory activity against not only Gram-positive bacteria but also Gram-negative bacteria including Listeria monocytogenes and Salmonella typhimurium. The mode of action of plantaricin MG on S. typhimurium was reported in this article. The addition of plantaricin MG to energized cells of S. typhimurium dissipated both, the transmembrane potential (Δψ) and the pH gradient (ΔpH). Energized membrane, obtained after the addition of glucose, was more susceptible to plantaricin MG action, leading to the release of intracellular K(+)ions, inorganic phosphate, ATP and UV-absorbing materials. These data suggest that the presence of a proton motive force promotes the interaction of plantaricin MG with the cytoplasmic membrane of energized cells, leading to pores formation which allows the efflux of ions, thereby ensuring efficient killing of target bacteria.


Subject(s)
Bacteriocins/pharmacology , Lactobacillus plantarum/metabolism , Membrane Potentials/drug effects , Proton-Motive Force , Salmonella typhimurium/drug effects , Adenosine Triphosphate/analysis , Cell Membrane/drug effects , Phosphates/analysis , Potassium/analysis , Salmonella typhimurium/ultrastructure
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