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Synergy between xylanases from glycoside hydrolase family 10 and family 11 and feruloyl esterase in the release of phenolic acids from cereal arabinoxylan
Institute of Food Research, Norwich.
Institute of Food Research, Norwich.
University of Messina.
University of Messina.
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2006 (English)In: Applied Microbiology and Biotechnology, ISSN 0175-7598, E-ISSN 1432-0614, Vol. 71, no 5, p. 622-629Article in journal (Refereed) Published
Abstract [en]

The bioconversion of waste residues (by-products) from cereal processing industries requires the cooperation of enzymes able to degrade xylanolytic and cellulosic material. The type A feruloyl esterase from Aspergillus niger, AnFaeA, works synergistically with (1→4)-β-d-xylopyranosidases (xylanases) to release monomeric and dimeric ferulic acid (FA) from cereal cell wall-derived material. The esterase was more effective with a family 11 xylanase from Trichoderma viride in releasing FA and with a family 10 xylanase from Thermoascus aurantiacus in releasing the 5,5′ form of diferulic acid from arabinoxylan (AX) derived from brewers’ spent grain. The converse was found for the release of the phenolic acids from wheat bran-derived AXs. This may be indicative of compositional differences in AXs in cereals.

Place, publisher, year, edition, pages
2006. Vol. 71, no 5, p. 622-629
Identifiers
URN: urn:nbn:se:ltu:diva-3601DOI: 10.1007/s00253-005-0184-6ISI: 000239171400006PubMedID: 16292533Scopus ID: 2-s2.0-33746382568Local ID: 16cfc922-e730-4ae7-9172-26d9bbd8ca2fOAI: oai:DiVA.org:ltu-3601DiVA, id: diva2:976459
Note
Upprättat; 2006; 20130215 (ysko)Available from: 2016-09-29 Created: 2016-09-29 Last updated: 2023-09-05Bibliographically approved

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