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FgLPMO9A from Fusarium graminearum cleaves xyloglucan independently of the backbone substitution pattern.

FEBS Lett. 2016; 
Nekiunaite L, Petrovi? DM, Westereng B, Vaaje-Kolstad G, Hachem MA, Várnai A, Eijsink VG.
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Codon Optimization graminearum LPMO The gene encoding FgLPMO9A [UniProt: I1REU9], including its native signal sequence, was codon optimized for Pichia pastoris (GenScript, NJ, USA). Get A Quote

摘要

Lytic polysaccharide monooxygenases (LPMOs) are important for the enzymatic conversion of biomass and seem to play a key role in degradation of the plant cell wall. In this study, we characterize an LPMO from the fungal plant pathogen Fusarium graminearum (FgLPMO9A) that catalyzes the mixed C1/C4 oxidative cleavage of cellulose and xyloglucan, but is inactive toward other (1,4)-linked β-glucans. Our findings indicate that FgLPMO9A has unprecedented broad specificity on xyloglucan, cleaving any glycosidic bond in the β-glucan main chain, regardless of xylosyl substitutions. Interestingly, we found that when incubated with a mixture of xyloglucan and cellulose, FgLPMO9A efficiently attacks the xyloglucan, where... More

關鍵詞

Fusarium graminearum ; AA9; cellulose; lytic polysaccharide monooxygenase; xyloglucan
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