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Understanding enzyme-substrate interactions in Carbohydrate Esterase Family 15

Mazurkewich, Scott, 1982 (author)
Chalmers tekniska högskola,Chalmers University of Technology
Arnling Bååth, Jenny, 1987 (author)
Chalmers tekniska högskola,Chalmers University of Technology
Poulsen, Jens-Christian N (author)
Köpenhamns universitet,University of Copenhagen
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Olsson, Lisbeth, 1963 (author)
Chalmers tekniska högskola,Chalmers University of Technology
Lo Leggio, Leila (author)
Köpenhamns universitet,University of Copenhagen
Larsbrink, Johan, 1982 (author)
Chalmers tekniska högskola,Chalmers University of Technology
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 (creator_code:org_t)
2019
2019
English.
  • Conference paper (other academic/artistic)
Abstract Subject headings
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  • Carbohydrate Esterase Family 15 (CE15) is a rather small family, comprising approximately 200 members, which was established in CAZy (www.cazy.org) in 2006. The family was created following the characterization of a glucuronoyl esterase (GE) from the fungus Schizophyllum commune [1], which was shown to cleave methyl moieties ester-linked to the O6 position of glucuronic acid. CE15 enzymes are proposed to cleave ester linkages between lignin and glucuronoxylan, so-called lignin-carbohydrate complexes (LCCs), which are important features in biomass recalcitrance. We recently characterized ten new GEs from three bacterial species and solved the structures of two of these, essentially doubling both the biochemical and structural data available for the family [2]. An in-depth understanding of how CE15 enzymes interact with their complex substrates is still lacking, as only one structure with a monosaccharide ligand has been solved to date [3]. To address this, we have pursued solving new GE structures and obtaining protein-ligand complex structures. The studies have resulted in a novel structure exhibiting features with prominent inserts surrounding the active site, suggesting different specificities between bacterial and fungal GEs. In addition, we have solved the first structures of a CE15 enzyme with larger ligands, which gives direct evidence of how these enzymes interact with the different parts of its proposed physiological LCC substrates. Combined with kinetic characterizations, these new investigations greatly add to the knowledge of enzyme-substrate interactions in CE15 and enhances how these enzymes may act in natural conditions, which could aid in industrial biomass conversion. ______________ [1]  Španiková S.; Biely P. FEBS Lett. 2006, 580, 4597-4601. [2]  Arnling Bååth J.; Mazurkewich S.; Knudsen R.M.; Poulsen J.N.; Olsson L.; Lo Leggio L.; Larsbrink J. Biotechnol Biofuels. 2018, 11, 213-226. [3]  Charavgi M.D.; Dimarogona M.; Topakas E.; Christakopoulos P.; Chrysina E.D. Acta Crystallogr. D Biol. Crystallogr. 2013, 69, 63-73.

Subject headings

NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)
NATURVETENSKAP  -- Biologi -- Strukturbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Structural Biology (hsv//eng)
TEKNIK OCH TEKNOLOGIER  -- Industriell bioteknik -- Biokatalys och enzymteknik (hsv//swe)
ENGINEERING AND TECHNOLOGY  -- Industrial Biotechnology -- Biocatalysis and Enzyme Technology (hsv//eng)

Keyword

lignin-carbohydrate complexes
glucuronoyl esterase
biochemistry
CE15
crystallography
structural biology
glucuronoxylan

Publication and Content Type

kon (subject category)
vet (subject category)

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