| Literature DB >> 29051046 |
Adiphol Dilokpimol1, Miia R Mäkelä2, Gabriella Cerullo3, Miaomiao Zhou1, Simona Varriale3, Loknath Gidijala4, Joana L A Brás5, Peter Jütten6, Alexander Piechot6, Raymond Verhaert4, Vincenza Faraco7, Kristiina S Hilden8, Ronald P de Vries9.
Abstract
4-O-Methyl-d-glucuronic acid (MeGlcA) is a side-residue of glucuronoarabinoxylan and can form ester linkages to lignin, contributing significantly to the strength and rigidity of the plant cell wall. Glucuronoyl esterases (4-O-methyl-glucuronoyl methylesterases, GEs) can cleave this ester bond, and therefore may play a significant role as auxiliary enzymes in biomass saccharification for the production of biofuels and biochemicals. GEs belong to a relatively new family of carbohydrate esterases (CE15) in the CAZy database (www.cazy.org), and so far around ten fungal GEs have been characterized. To explore additional GE enzymes, we used a genome mining strategy. BLAST analysis with characterized GEs against approximately 250 publicly accessible fungal genomes identified more than 150 putative fungal GEs, which were classified into eight phylogenetic sub-groups. To validate the genome mining strategy, 21 selected GEs from both ascomycete and basidiomycete fungi were heterologously produced in Pichia pastoris. Of these enzymes, 18 were active against benzyl d-glucuronate demonstrating the suitability of our genome mining strategy for enzyme discovery.Entities:
Keywords: Fungi; Genome mining; Glucuronic acid; Glucuronoyl esterase; Plant cell wall
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Year: 2017 PMID: 29051046 DOI: 10.1016/j.nbt.2017.10.003
Source DB: PubMed Journal: N Biotechnol ISSN: 1871-6784 Impact factor: 5.079