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Updated: Jun 17, 2026

Elucidating β-1,3-Glucanase and Peroxidase Physicochemical Properties of Wheat Cell Wall Defense Mechanism Against Diuraphis noxia Infestation
Published on: July 26, 2024
Post-translational processing of beta-d-xylanases and changes in extractability of arabinoxylans during wheat
Evelien De Backer1, Kurt Gebruers, Wim Van den Ende
1Laboratory of Food Chemistry and Biochemistry, and Leuven Food Science and Nutrition Research Centre (LFoRCe), Katholieke Universiteit Leuven, Kasteelpark Arenberg 20 bus 2463, B-3001 Leuven, Belgium.
Abstract:
Endo-1,4-beta-d-xylanase (EC 3.2.1.8, beta-d-xylanase) activity, and arabinoxylan (AX) level and extractability were monitored for the first time simultaneously in wheat kernels (Triticum aestivum cv. Glasgow) up to 24 days post-imbibition (DPI), both in the absence and presence of added gibberellic acid (GA). Roughly three different stages (early, intermediate and late) can be discriminated. Addition of GA resulted in a faster increase of water extractable arabinoxylan (WEAX) level in the early stage (up to 3-4 DPI). This increase was not accompanied by the discernible presence of homologues of the barley X-I beta-d-xylanase as established by immunodetection. This suggests that other, yet unidentified beta-d-xylanases operate in this early time window. The intermediate stage (up to 13 DPI) was characterized by the presence of unprocessed 67 kDa X-I like beta-d-xylanase, which was much more abundant in the presence of GA. The occurrence of higher levels of the unprocessed enzyme was related with higher beta-d-xylanase activities and a further increase in WEAX level, pointing to in vivo activity of the unprocessed 67 kDa beta-d-xylanase. During the late stage (up to 24 DPI) gradual processing of the 67 kDa beta-d-xylanase occurred and was associated with a drastic increase in beta-d-xylanase activity. Up to 120-fold higher activity was recorded at 24 DPI, with approx. 85% thereof originating from the kernel remnants. The WEAX level decreased during the late stage, suggesting that the beta-d-xylanase is processed into more active forms to achieve extensive AX breakdown.
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