| Keyword search (4,163 papers available) | ![]() |
"galactose" Keyword-tagged Publications:
| Title | Authors | PubMed ID | |
|---|---|---|---|
| 1 | Expansion of Auxiliary Activity Family 5 sequence space via biochemical characterization of six new copper radical oxidases | Fong JK; Mathieu Y; Vo MT; Bellemare A; Tsang A; Brumer H; | 38953370 CSFG |
| 2 | Discovery and characterization of family 39 glycoside hydrolases from rumen anaerobic fungi with polyspecific activity on rare arabinosyl substrates. | Jones DR, Uddin MS, Gruninger RJ, Pham TTM, Thomas D, Boraston AB, Briggs J, Pluvinage B, McAllister TA, Forster RJ, Tsang A, Selinger LB, Abbott DW | 28588026 CSFG |
| Title: | Expansion of Auxiliary Activity Family 5 sequence space via biochemical characterization of six new copper radical oxidases | ||||
| Authors: | Fong JK, Mathieu Y, Vo MT, Bellemare A, Tsang A, Brumer H | ||||
| Link: | https://pubmed.ncbi.nlm.nih.gov/38953370/ | ||||
| DOI: | 10.1128/aem.01014-24 | ||||
| Publication: | Applied and environmental microbiology | ||||
| Keywords: | Auxiliary Activity Family 5; HMF oxidase; alcohol oxidase; carbohydrate-active enzyme; copper radical oxidase; galactose oxidase; | ||||
| PMID: | 38953370 | Category: | Date Added: | 2024-07-02 | |
| Dept Affiliation: |
CSFG
1 Michael Smith Laboratories, University of British Columbia, Vancouver, British Columbia, Canada. 2 Department of Chemistry, University of British Columbia, Vancouver, British Columbia, Canada. 3 Centre for Structural and Functional Genomics, Concordia University, Montreal, Quebec, Canada. 4 Department of Biochemistry and Molecular Biology, University of British Columbia, Vancouver, British Columbia, Canada. 5 Department of Botany, University of British Columbia, Vancouver, British Columbia, Canada. |
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Description: |
Bacterial and fungal copper radical oxidases (CROs) from Auxiliary Activity Family 5 (AA5) are implicated in morphogenesis and pathogenesis. The unique catalytic properties of CROs also make these enzymes attractive biocatalysts for the transformation of small molecules and biopolymers. Despite a recent increase in the number of characterized AA5 members, especially from subfamily 2 (AA5_2), the catalytic diversity of the family as a whole remains underexplored. In the present study, phylogenetic analysis guided the selection of six AA5_2 members from diverse fungi for recombinant expression in Komagataella pfaffii (syn. Pichia pastoris) and biochemical characterization in vitro. Five of the targets displayed predominant galactose 6-oxidase activity (EC 1.1.3.9), and one was a broad-specificity aryl alcohol oxidase (EC 1.1.3.7) with maximum activity on the platform chemical 5-hydroxymethyl furfural (EC 1.1.3.47). Sequence alignment comparing previously characterized AA5_2 members to those from this study indicated various amino acid substitutions at active site positions implicated in the modulation of specificity.IMPORTANCEEnzyme discovery and characterization underpin advances in microbial biology and the application of biocatalysts in industrial processes. On one hand, oxidative processes are central to fungal saprotrophy and pathogenesis. On the other hand, controlled oxidation of small molecules and (bio)polymers valorizes these compounds and introduces versatile functional groups for further modification. The biochemical characterization of six new copper radical oxidases further illuminates the catalytic diversity of these enzymes, which will inform future biological studies and biotechnological applications. |



