Literature DB >> 10934439

Tandem mass spectrometry studies of green tea catechins. Identification of three minor components in the polyphenolic extract of green tea.

P Miketova1, K H Schram, J Whitney, M Li, R Huang, E Kerns, S Valcic, B N Timmermann, R Rourick, S Klohr.   

Abstract

Liquid chromatography/electrospray ionization mass and tandem mass spectrometry (MS/MS) techniques were used to identify two minor components and one new compound in the polyphenolic extract of green tea (Camellia sinensis). Identification and structure assignments were based on previously reported sub-structural features in the MS/MS product, precursor and neutral loss scans of reference samples. The structures of two minor components, related to the known green tea components epicatechin gallate (ECG, 5) and epigallocatechin gallate (EGCG, 6), are formed by methylation at the 3"-O-position of the gallic acid moiety. The new compound contained a gallic acid ester group, but had only one phenolic group in either the A- or B-ring, relative to the structure of 5. High-resolution mass measurements supported the empirical formula assigned to the new compounds. An important fragmentation for defining the position of methylation of the ester function involves ionization of the phenolic group at the 4"-position of the gallic acid, followed by elimination of the ester function as a neutral with concomitant formation of the m/z 169 ion. If the 4"-position is blocked by methylation, the formation of m/z 169 incorporating the gallic acid group would be blocked. Thus, the presence of an ion representing the ester group indicates a free 4"-phenol and the absence of this ion would signify the 4"-position as a site of methylation. The operation of this mechanism should be general and useful in assigning the site of methylation of any polyphenolic ester group in natural products. A similar conclusion can be drawn concerning alkylation or esterification of the 4'-position of the catechins, i. e. blocking the 4'-phenol would prevent formation of the m/z 125 ion common to all of the catechin compounds thus far examined. Therefore, mass spectral data are of considerable importance in deducing the sites of alkylation or esterification in the structures of the components of green tea. Copyright 2000 John Wiley & Sons, Ltd.

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Year:  2000        PMID: 10934439     DOI: 10.1002/1096-9888(200007)35:7<860::AID-JMS10>3.0.CO;2-J

Source DB:  PubMed          Journal:  J Mass Spectrom        ISSN: 1076-5174            Impact factor:   1.982


  14 in total

1.  Determination of flavone, flavonol, and flavanone aglycones by negative ion liquid chromatography electrospray ion trap mass spectrometry.

Authors:  N Fabre; I Rustan; E de Hoffmann; J Quetin-Leclercq
Journal:  J Am Soc Mass Spectrom       Date:  2001-06       Impact factor: 3.109

2.  Plasma pharmacokinetics of catechin metabolite 4'-O-Me-EGC in healthy humans.

Authors:  Mathieu Renouf; Karine Redeuil; Karin Longet; Cynthia Marmet; Fabiola Dionisi; Martin Kussmann; Gary Williamson; Kornél Nagy
Journal:  Eur J Nutr       Date:  2011-01-07       Impact factor: 5.614

3.  Tentative identification, quantitation, and principal component analysis of green pu-erh, green, and white teas using UPLC/DAD/MS.

Authors:  Yang Zhao; Pei Chen; Longze Lin; J M Harnly; Liangli Lucy Yu; Zhangwan Li
Journal:  Food Chem       Date:  2011-06-01       Impact factor: 7.514

4.  Structural identification of novel glucoside and glucuronide metabolites of (-)-epigallocatechin-3-gallate in mouse urine using liquid chromatography/electrospray ionization tandem mass spectrometry.

Authors:  Shengmin Sang; Chung S Yang
Journal:  Rapid Commun Mass Spectrom       Date:  2008-11       Impact factor: 2.419

5.  New phenolic components and chromatographic profiles of green and fermented teas.

Authors:  Long-Ze Lin; Pei Chen; James M Harnly
Journal:  J Agric Food Chem       Date:  2008-08-08       Impact factor: 5.279

6.  Screening non-colored phenolics in red wines using liquid chromatography/ultraviolet and mass spectrometry/mass spectrometry libraries.

Authors:  Jianping Sun; Feng Liang; Yan Bin; Ping Li; Changqing Duan
Journal:  Molecules       Date:  2007-03-30       Impact factor: 4.411

7.  Phenolic antioxidants identified by ESI-MS from Yerba maté (Ilex paraguariensis) and green tea (Camelia sinensis) extracts.

Authors:  Deborah H Markowicz Bastos; Luciane A Saldanha; Rodrigo R Catharino; Alexandra C H F Sawaya; Ildenize B S Cunha; Patricia O Carvalho; Marcos N Eberlin
Journal:  Molecules       Date:  2007-03-12       Impact factor: 4.411

8.  Isomeric differentiation of green tea catechins using gas-phase hydrogen/deuterium exchange reactions.

Authors:  Emily D Niemeyer; Jennifer S Brodbelt
Journal:  J Am Soc Mass Spectrom       Date:  2007-07-17       Impact factor: 3.109

9.  Green Tea Extract Induces the Resistance of Caenorhabditis elegans against Oxidative Stress.

Authors:  Sami Abbas; Michael Wink
Journal:  Antioxidants (Basel)       Date:  2014-03-04

Review 10.  Food-grade Encapsulation Systems for (-)-Epigallocatechin Gallate.

Authors:  Meng Shi; Yun-Long Shi; Xu-Min Li; Rui Yang; Zhuo-Yu Cai; Qing-Sheng Li; Shi-Cheng Ma; Jian-Hui Ye; Jian-Liang Lu; Yue-Rong Liang; Xin-Qiang Zheng
Journal:  Molecules       Date:  2018-02-17       Impact factor: 4.411

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