Regioselective C4 and C6 Double Oxidation of Cellulose by Lytic Polysaccharide Monooxygenases

Lytic polysaccharide monooxygenases (LPMOs) play a key role in enzymatic degradation of hard‐to‐convert polysaccharides, such as chitin and cellulose. It is widely accepted that LPMOs catalyze a single regioselective oxidation of the C1 or C4 carbon of a glycosidic linkage, after which the destabili...

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Bibliographic Details
Published in:ChemSusChem 2022-01, Vol.15 (2), p.e202102203-n/a
Main Authors: Sun, Peicheng, Laurent, Christophe V. F. P., Boerkamp, Vincent J. P., Erven, Gijs, Ludwig, Roland, Berkel, Willem J. H., Kabel, Mirjam A.
Format: Article
Language:English
Subjects:
Aldehydes
Cellulose
Cellulose - metabolism
Chitin
isotopic labeling
lytic polysaccharide monooxygenase
mass spectrometry
Mixed Function Oxygenases - metabolism
Oligosaccharides
Oxidation
Oxidation-Reduction
Oxygenation
Polysaccharides
Reduction
Regioselectivity
Spectrometry
Substrates
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Summary:Lytic polysaccharide monooxygenases (LPMOs) play a key role in enzymatic degradation of hard‐to‐convert polysaccharides, such as chitin and cellulose. It is widely accepted that LPMOs catalyze a single regioselective oxidation of the C1 or C4 carbon of a glycosidic linkage, after which the destabilized linkage breaks. Here, a series of novel C4/C6 double oxidized cello‐oligosaccharides was discovered. Products were characterized, aided by sodium borodeuteride reduction and hydrophilic interaction chromatography coupled to mass spectrometric analysis. The C4/C6 double oxidized products were generated by C4 and C1/C4 oxidizing LPMOs, but not by C1 oxidizing ones. By performing incubation and reduction in H218O, it was confirmed that the C6 gem‐diol structure resulted from oxygenation, although oxidation to a C6 aldehyde, followed by hydration to the C6 gem‐diol, could not be excluded. These findings can be extended to how the reactive LPMO‐cosubstrate complex is positioned towards the substrate. Single and double? Lytic polysaccharide monooxygenases (LPMOs) were reported to form C1/C4 double oxidized cello‐oligosaccharides in addition to C1 or C4 single oxidized ones. Using NaBD4 reduction and HILIC‐ESI‐CID‐MS/MS2 approach, it is found that C4/C6 double oxidized cello‐oligosaccharides are generated, and not C1/C4 double oxidized products. Experiments in H218O further show that C6 gem‐diol is formed by an LPMO‐catalyzed reaction.
ISSN:1864-5631
1864-564X
DOI:10.1002/cssc.202102203