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The molecular basis of polysaccharide cleavage by lytic polysaccharide monooxygenases
- Source :
- Nature Chemical Biology, Nature Chemical Biology, Nature Publishing Group, 2016, 12 (4), pp.298+. ⟨10.1038/NCHEMBIO.2029⟩, Nature Chemical Biology, 2016, 12 (4), pp.298+. ⟨10.1038/NCHEMBIO.2029⟩
- Publication Year :
- 2016
- Publisher :
- HAL CCSD, 2016.
-
Abstract
- Lytic polysaccharide monooxygenases (LPMOs) are copper-containing enzymes which oxidatively break down recalcitrant polysaccharides such as cellulose and chitin. Since their discovery LPMOs have become integral factors in the industrial utilization of biomass, especially in the sustainable generation of cellulosic bioethanol. We report here the first structural determination of an LPMO–oligosaccharide complex, yielding detailed insights into the mechanism of action of these enzymes. Using a combination of structure and electron paramagnetic resonance spectroscopy, we reveal the means by which LPMOs interact with saccharide substrates. We further uncover electronic and structural features of the enzyme active site, showing how LPMOs orchestrate the reaction of oxygen with polysaccharide chains.
- Subjects :
- 0301 basic medicine
Models, Molecular
conformation
coordination
oxygenases
Aspergillus oryzae
Oligosaccharides
Chitin
Lentinula
Crystallography, X-Ray
Mixed Function Oxygenases
Substrate Specificity
chemistry.chemical_compound
Catalytic Domain
Fluorescence Resonance Energy Transfer
ComputingMilieux_MISCELLANEOUS
chemistry.chemical_classification
biology
[SDV.BBM.BS]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Structural Biology [q-bio.BM]
[SDV.BIBS]Life Sciences [q-bio]/Quantitative Methods [q-bio.QM]
[SDV.BBM.BS]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Biomolecules [q-bio.BM]
Biochemistry
Oxidation-Reduction
Molecular Sequence Data
mechanism
Polysaccharide
chemistry
Article
03 medical and health sciences
cellulose degradation
Oxidoreductase
Amino Acid Sequence
Cellulose
Molecular Biology
Binding Sites
Active site
Cell Biology
Monooxygenase
enzyme
030104 developmental biology
Enzyme
substrate-specificity
biology.protein
activation
Copper
discovery
Subjects
Details
- Language :
- English
- ISSN :
- 15524450 and 15524469
- Database :
- OpenAIRE
- Journal :
- Nature Chemical Biology, Nature Chemical Biology, Nature Publishing Group, 2016, 12 (4), pp.298+. ⟨10.1038/NCHEMBIO.2029⟩, Nature Chemical Biology, 2016, 12 (4), pp.298+. ⟨10.1038/NCHEMBIO.2029⟩
- Accession number :
- edsair.doi.dedup.....e7340da79c7e1faff6724ce001812232