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Degree of blockiness of amide groups as indicator for difference in physical behavior of amidated pectins

✍ Scribed by Stéphanie E. Guillotin; Janine Van Kampen; Patrick Boulenguer; Henk A. Schols; Alphons G. J. Voragen


Publisher
Wiley (John Wiley & Sons)
Year
2006
Tongue
English
Weight
266 KB
Volume
82
Category
Article
ISSN
0006-3525

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✦ Synopsis


Abstract

Thickening and gelling properties of commercial amidated pectins depend on the degree of amidation and methyl‐esterification, but also the distribution of these groups is of great importance. Methods have been developed during the last few years to determine the distribution of methyl esters over the pectic backbone. We applied the strategies developed for the analysis of high methyl‐esterified pectins for studying the distribution of amide groups in amidated pectins. Low methyl‐esterified amidated (LMA) pectins were digested before and after removal of methyl esters by an endo‐polygalacturonase to determine the degree of blockiness of the substituents. The nature of the substituents (amide groups compared to methyl esters) did not modify the behavior of the enzyme. Oligomers released were separated by using high‐performance anion exchange chromatography and pulsed amperometric detection (HPAEC–PAD) at pH 5. Fractions collected after on‐line desalting were identified by using MALDI–TOF mass spectrometry. Oligomers were found to elute from the column as a function of their total charge. For the same overall charge and size, oligomers with methyl esters eluted before oligomers with amide groups. Both amide groups and methyl esters of the LMA pectins studied were found to be semirandomly distributed over the pectic backbone, but this may vary according to the amidation process used. © 2006 Wiley Periodicals, Inc. Biopolymers 82: 29–37, 2006

This article was originally published online as an accepted preprint. The “Published Online” date corresponds to the preprint version. You can request a copy of the preprint by emailing the Biopolymers editorial office at [email protected]


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