2017
DOI: 10.1094/asbcj-2017-3276-01
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Investigation of 2-Sulfanylethyl Acetate Cysteine-S-Conjugate as a Potential Precursor of Free Thiols in Beer

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Cited by 5 publications
(3 citation statements)
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“…[21] 2MEA S-conjugate of cysteine (2-thioglycolate; Cys-2MEA) was identified as a potential precursor of 2MEA. [22] The main precursor of 2M3MB formed by yeast during beer fermentation has been identified as 2, 3-epoxy-3-methylbutyraldehyde (EMB), with a conversion rate of about 3%, and the sulfur source can react with EMB and then reduce the terminal aldehyde. [23] Several new mercaptan precursors have been shown to exist in hops: Amarillo-glutathione S-conjugate,3-mercapto-4-methylpentane-1-ol(G3M4MP );Citra-glutathione-S-conjugate-3-mercaptoamyl-alcohol( G-3MP);Hallertau,Blanc-cysteine-S-conjugate,3-mercapt o-4-methylpentane-1-ol(Cys3M4MP);Polaris-cysteine-sconjugate 3-thio-amyl alcohol (Cys-3MP).…”
Section: Hopsmentioning
confidence: 99%
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“…[21] 2MEA S-conjugate of cysteine (2-thioglycolate; Cys-2MEA) was identified as a potential precursor of 2MEA. [22] The main precursor of 2M3MB formed by yeast during beer fermentation has been identified as 2, 3-epoxy-3-methylbutyraldehyde (EMB), with a conversion rate of about 3%, and the sulfur source can react with EMB and then reduce the terminal aldehyde. [23] Several new mercaptan precursors have been shown to exist in hops: Amarillo-glutathione S-conjugate,3-mercapto-4-methylpentane-1-ol(G3M4MP );Citra-glutathione-S-conjugate-3-mercaptoamyl-alcohol( G-3MP);Hallertau,Blanc-cysteine-S-conjugate,3-mercapt o-4-methylpentane-1-ol(Cys3M4MP);Polaris-cysteine-sconjugate 3-thio-amyl alcohol (Cys-3MP).…”
Section: Hopsmentioning
confidence: 99%
“…This suggested that hops may not be the only source of mercaptan and mercaptan precursors in beer, and malt was hypothesized as another source. [32] However, further verification is still needed in combination with other precursors identified in grape (CysGly-3Mh, γGluCys-3Mh, G-3Mh-Al).…”
Section: Maltmentioning
confidence: 99%
“…This is particularly evident in the neutral grapes most often used for producing dry wines. In these grapes most aroma compounds are present as nonvolatile precursors, including polyolic forms (Williams et al, 1980), cysteinylated, glutathionylated, cysteinyl-glycine conjugated and glutamyl-cysteine conjugated precursors (Bonnaffoux et al, 2018;Cibaka et al, 2017;Tominaga et al, 1998), dimethyl sulfide (DMS) precursors (Segurel et al, 2005) and glycosidic precursors (Hjelmeland & Ebeler, 2015).…”
Section: Introductionmentioning
confidence: 99%