Structural and Functional Characterization of a Lytic Polysaccharide Monooxygenase with Broad Substrate Specificity

The recently discovered lytic polysaccharide monooxygenases (LPMOs) carry out oxidative cleavage of polysaccharides and are of major importance for efficient processing of biomass. NcLPMO9C from Neurospora crassa acts both on cellulose and on non-cellulose β-glucans, including cellodextrins and xylo...

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Veröffentlicht in:The Journal of biological chemistry 2015-09, Vol.290 (38), p.22955-22969
Hauptverfasser: Borisova, Anna S., Isaksen, Trine, Dimarogona, Maria, Kognole, Abhishek A., Mathiesen, Geir, Várnai, Anikó, Røhr, Åsmund K., Payne, Christina M., Sørlie, Morten, Sandgren, Mats, Eijsink, Vincent G.H.
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container_end_page 22969
container_issue 38
container_start_page 22955
container_title The Journal of biological chemistry
container_volume 290
creator Borisova, Anna S.
Isaksen, Trine
Dimarogona, Maria
Kognole, Abhishek A.
Mathiesen, Geir
Várnai, Anikó
Røhr, Åsmund K.
Payne, Christina M.
Sørlie, Morten
Sandgren, Mats
Eijsink, Vincent G.H.
description The recently discovered lytic polysaccharide monooxygenases (LPMOs) carry out oxidative cleavage of polysaccharides and are of major importance for efficient processing of biomass. NcLPMO9C from Neurospora crassa acts both on cellulose and on non-cellulose β-glucans, including cellodextrins and xyloglucan. The crystal structure of the catalytic domain of NcLPMO9C revealed an extended, highly polar substrate-binding surface well suited to interact with a variety of sugar substrates. The ability of NcLPMO9C to act on soluble substrates was exploited to study enzyme-substrate interactions. EPR studies demonstrated that the Cu2+ center environment is altered upon substrate binding, whereas isothermal titration calorimetry studies revealed binding affinities in the low micromolar range for polymeric substrates that are due in part to the presence of a carbohydrate-binding module (CBM1). Importantly, the novel structure of NcLPMO9C enabled a comparative study, revealing that the oxidative regioselectivity of LPMO9s (C1, C4, or both) correlates with distinct structural features of the copper coordination sphere. In strictly C1-oxidizing LPMO9s, access to the solvent-facing axial coordination position is restricted by a conserved tyrosine residue, whereas access to this same position seems unrestricted in C4-oxidizing LPMO9s. LPMO9s known to produce a mixture of C1- and C4-oxidized products show an intermediate situation. Background: The recently discovered lytic polysaccharide monooxygenases (LPMOs) are important in enzymatic conversion of lignocellulosic biomass. Results: We describe structural and functional studies of NcLPMO9C, which cleaves both cellulose and certain hemicelluloses. Conclusion:NcLPMO9C has structural and functional features that correlate with the enzyme's catalytic capabilities. Significance: This study shows how LPMO active sites are tailored to varying functionalities and adds to a growing LPMO knowledge base.
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NcLPMO9C from Neurospora crassa acts both on cellulose and on non-cellulose β-glucans, including cellodextrins and xyloglucan. The crystal structure of the catalytic domain of NcLPMO9C revealed an extended, highly polar substrate-binding surface well suited to interact with a variety of sugar substrates. The ability of NcLPMO9C to act on soluble substrates was exploited to study enzyme-substrate interactions. EPR studies demonstrated that the Cu2+ center environment is altered upon substrate binding, whereas isothermal titration calorimetry studies revealed binding affinities in the low micromolar range for polymeric substrates that are due in part to the presence of a carbohydrate-binding module (CBM1). Importantly, the novel structure of NcLPMO9C enabled a comparative study, revealing that the oxidative regioselectivity of LPMO9s (C1, C4, or both) correlates with distinct structural features of the copper coordination sphere. In strictly C1-oxidizing LPMO9s, access to the solvent-facing axial coordination position is restricted by a conserved tyrosine residue, whereas access to this same position seems unrestricted in C4-oxidizing LPMO9s. LPMO9s known to produce a mixture of C1- and C4-oxidized products show an intermediate situation. Background: The recently discovered lytic polysaccharide monooxygenases (LPMOs) are important in enzymatic conversion of lignocellulosic biomass. Results: We describe structural and functional studies of NcLPMO9C, which cleaves both cellulose and certain hemicelluloses. Conclusion:NcLPMO9C has structural and functional features that correlate with the enzyme's catalytic capabilities. 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subjects biodegradation
bioenergy
Biofysik
Biophysics
Calcium - chemistry
copper monooxygenase
crystal structure
electron paramagnetic resonance (EPR)
Enzymology
Fungal Proteins - chemistry
isothermal titration calorimetry (ITC)
Microbiology
Mikrobiologi
Mixed Function Oxygenases - chemistry
Neurospora crassa - enzymology
Polysaccharides - chemistry
Structural Biology
Strukturbiologi
Substrate Specificity
title Structural and Functional Characterization of a Lytic Polysaccharide Monooxygenase with Broad Substrate Specificity
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