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The phenolic fraction of maize bran: evidence for lignin-heteroxylan association

Authors :
Brigitte Pollet
Marie-Christine Ralet
Luc Saulnier
Catherine Lapierre
Chimie Biologique (UCB)
Institut National de la Recherche Agronomique (INRA)-Institut National Agronomique Paris-Grignon (INA P-G)
Laboratoire de biochimie et technologie des glucides
Institut National de la Recherche Agronomique (INRA)
ProdInra, Migration
Source :
Phytochemistry, Phytochemistry, Elsevier, 2001, 57, pp.765-772
Publication Year :
2001

Abstract

Maize bran heteroxylan samples were extracted in various conditions of severity. Their ferulate and diferulate content was investigated by GC-MS of methyl ester-TMSi derivatives. When extracted by 0.5 M NaOH in mild conditions, the heteroxylan sample contained a low level of ferulic acid (0.032% by wt.) and the main diferulate surviving alkaline extraction was found to be the 8-8' diferulate. On peroxidase treatment, this sample nevertheless produced a firm and brittle gel without any change in the diferulate profile. Typical lignin structures, mainly comprising syringyl units interconnected through beta-O-4, beta-1 and beta-beta interunit bonds, were evidenced in the maize bran sample. More importantly, these lignin structures were found to be tightly associated with the alkali-extracted heteroxylans. Thioacidolysis revealed the occurrence of 0.1-0.5% (by wt.) lignin structures in heteroxylan fractions extracted in mild or severe conditions, before and after purification of the polysaccharides. The gelling potential of the heteroxylan fractions was not only dependent on their ferulate level, but also influenced by associated lignin structures. These results argue for the occurrence of covalent linkages between heteroxylan chains and lignin structures which could participate in the peroxidase-driven gelation of feruloylated polysaccharides. They demonstrate the role of low lignin levels in the organization of native or reconstructed polysaccharide networks.

Details

ISSN :
00319422
Volume :
57
Issue :
5
Database :
OpenAIRE
Journal :
Phytochemistry
Accession number :
edsair.doi.dedup.....7dc434de64c73a5d36368d444de5b676