Unraveling synergism between various GH family xylanases and deb ranching enzymes during hetero-xylan degradation
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Date
2021
Authors
Malgas, Samkelo
Mafa, Mpho S.
Mathibe, Brian N.
Pletscke, Brett I.
Journal Title
Journal ISSN
Volume Title
Publisher
MDPI
Abstract
Enzymes classified with the same Enzyme Commission (EC) that are allotted in different glycoside hydrolase (GH) families can display different mechanisms of action and substrate specificities. Therefore, the combination of different enzyme classes may not yield synergism during biomass hydrolysis, as the GH family allocation of the enzymes influences their behavior. As a result, it is important to understand which GH family combinations are compatible to gain knowledge on how to efficiently depolymerize biomass into fermentable sugars. We evaluated GH10 (Xyn10D and XT6) and GH11 (XynA and Xyn2A) β-xylanase performance alone and in combination with various GH family α-l-arabinofuranosidases (GH43 AXH-d and GH51 Abf51A) and α-d-glucuronidases (GH4 Agu4B and GH67 AguA) during xylan depolymerization. No synergistic enhancement in reducing sugar, xylose and glucuronic acid released from beechwood xylan was observed when xylanases were supplemented with either one of the glucuronidases, except between Xyn2A and AguA (1.1-fold reducing sugar increase). However, overall sugar release was significantly improved (≥1.1-fold reducing sugar increase) when xylanases were supplemented with either one of the arabinofuranosidases during wheat arabinoxylan degradation. Synergism appeared to result from the xylanases liberating xylo-oligomers, which are the preferred substrates of the terminal arabinofuranosyl-substituent debranching enzyme, Abf51A, allowing the exolytic β-xylosidase, SXA, to have access to the generated unbranched xylo-oligomers. Here, it was shown that arabinofuranosidases are key enzymes in the efficient saccharification of hetero-xylan into xylose. This study demonstrated that consideration of GH family affiliations of the carbohydrate-active enzymes (CAZymes) used to formulate synergistic enzyme cocktails is crucial for achieving efficient biomass saccharification.
Description
Keywords
α-l-arabinofuranosidase, α-d-glucuronidase, β-xylanase, Glycoside hydrolase, Heterosynergy, Xylan degradation
Citation
Malgas, S., Mafa, M.S., Mathibe, B.N., & Platschte, B.I. (2021). Unraveling synergism between various GH family xylanases and deb ranching enzymes during hetero-xylan degradation. Molecules, 26, 6770. https://doi.org/10.3390/molecules26226770