Literature DB >> 9514788

Analysis of partially methyl-esterified galacturonic acid oligomers by high-performance anion-exchange chromatography and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.

P J Daas1, P W Arisz, H A Schols, G A De Ruiter, A G Voragen.   

Abstract

Two methods were developed to detect partially methyl-esterified galacturonic acid oligomers, generated by endopolygalacturonase treatment of a 30% methyl-esterified pectin. The enzyme digest was shown, by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry, to contain sodiated galacturonic acid oligomers with a degree of polymerization of 2-12, containing 0-6 methyl esters. Galacturonic acid (monomer) could not be detected because of matrix ions interference in the low mass region. Using high-performance anion-exchange chromatography, with a sodium acetate gradient at pH 5.0 and postcolumn sodium hydroxide addition to allow pulsed amplified detection, a complex elution profile was obtained with the endopolygalacturonase-treated 30% methyl-esterified pectin. All the components eluted before nonesterified tetragalacturonic acid. The partially methyl-esterified oligogalacturonic acids eluted in a discernible series of oligomers with an identical number of nonesterified carboxylic acid groups; the large, more esterified oligomers eluted before small, less esterified oligomers. The methyl esters may hinder the interaction of the neighboring carboxylic acid groups with the anion-exchange resin, thereby giving the components an apparent lower overall negative charge.

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Year:  1998        PMID: 9514788     DOI: 10.1006/abio.1997.2554

Source DB:  PubMed          Journal:  Anal Biochem        ISSN: 0003-2697            Impact factor:   3.365


  7 in total

1.  Overexpression of pectin methylesterase inhibitors in Arabidopsis restricts fungal infection by Botrytis cinerea.

Authors:  Vincenzo Lionetti; Alessandro Raiola; Laura Camardella; Alfonso Giovane; Nicolai Obel; Markus Pauly; Francesco Favaron; Felice Cervone; Daniela Bellincampi
Journal:  Plant Physiol       Date:  2007-02-02       Impact factor: 8.340

2.  Endo-xylogalacturonan hydrolase, a novel pectinolytic enzyme.

Authors:  C J van der Vlugt-Bergmans; P J Meeuwsen; A G Voragen; A J van Ooyen
Journal:  Appl Environ Microbiol       Date:  2000-01       Impact factor: 4.792

3.  Pectate lyase 10A from Pseudomonas cellulosa is a modular enzyme containing a family 2a carbohydrate-binding module.

Authors:  I E Brown; M H Mallen; S J Charnock; G J Davies; G W Black
Journal:  Biochem J       Date:  2001-04-01       Impact factor: 3.857

4.  Tandem mass spectrometric analysis of aspergillus niger pectin methylesterase: mode of action on fully methyl-esterified oligogalacturonates.

Authors:  H C Kester; J A Benen; J Visser; M E Warren; R Orlando; C Bergmann; D Magaud; D Anker; A Doutheau
Journal:  Biochem J       Date:  2000-03-01       Impact factor: 3.857

5.  Partially esterified oligogalacturonides are the preferred substrates for pectin methylesterase of Aspergillus niger.

Authors:  Gert-Jan W M van Alebeek; Katrien van Scherpenzeel; Gerrit Beldman; Henk A Schols; Alphons G J Voragen
Journal:  Biochem J       Date:  2003-05-15       Impact factor: 3.857

6.  De-Oiled Citrus Peels as Feedstock for the Production of Pectin Oligosaccharides and Its Effect on Lactobacillus fermentum, Probiotic Source.

Authors:  Rohan Sarkar; Lata Nain; Aditi Kundu; Anirban Dutta; Debarup Das; Shruti Sethi; Supradip Saha
Journal:  Front Nutr       Date:  2022-05-17

7.  A novel enzyme activity involving the demethylation of specific partially methylated oligogalacturonides.

Authors:  Martin A K Williams; Jacques A E Benen
Journal:  Biochem J       Date:  2002-10-15       Impact factor: 3.857

  7 in total

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