4.7 Article

Two Fusarium copper radical oxidases with high activity on aryl alcohols

期刊

BIOTECHNOLOGY FOR BIOFUELS
卷 14, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s13068-021-01984-0

关键词

Copper radical oxidase; Aryl alcohol oxidase; Galactose oxidase; Biocatalysis; Metalloenzyme

资金

  1. Natural Sciences and Engineering Research Council of Canada (NSERC) [RGPIN 435223-13, RGPIN-2018-03892]
  2. NSERC [STPGP 493781-16, NETGP 451431-13]
  3. Agence Nationale de la Recherche grant [ANR-17-CE07-0047]
  4. FUNTASTIC-Fungal copper radical oxidases as new biocatalysts for the valorization of biomass carbohydrates and alcohols
  5. Genome Canada/Genome BC/Ontario Genomics/Genome Quebec for the Large-Scale Applied Research Project (LSARP) [10405]
  6. Agence Nationale de la Recherche (ANR) [ANR-17-CE07-0047] Funding Source: Agence Nationale de la Recherche (ANR)

向作者/读者索取更多资源

This work identifies two homologues from Fusarium species as aryl alcohol oxidases (AAOs) with unique catalytic diversity within the Auxiliary Activity Family 5/Subfamily 2 (AA5_2). Detailed enzymological analysis reveals the potential biotechnological applications of these orthologs in the production of renewable plastic polymer precursors and other chemicals. The study highlights the broader substrate scope of native CROs for applications beyond traditional galactose 6-oxidase activity.
Background Biomass valorization has been suggested as a sustainable alternative to petroleum-based energy and commodities. In this context, the copper radical oxidases (CROs) from Auxiliary Activity Family 5/Subfamily 2 (AA5_2) are attractive biocatalysts for the selective oxidation of primary alcohols to aldehydes. Originally defined by the archetypal galactose 6-oxidase from Fusarium graminearum, fungal AA5_2 members have recently been shown to comprise a wide range of specificities for aromatic, aliphatic and furan-based alcohols. This suggests a broader substrate scope of native CROs for applications. However, only 10% of the annotated AA5_2 members have been characterized to date. Results Here, we define two homologues from the filamentous fungi Fusarium graminearum and F. oxysporum as predominant aryl alcohol oxidases (AAOs) through recombinant production in Pichia pastoris, detailed kinetic characterization, and enzyme product analysis. Despite possessing generally similar active-site architectures to the archetypal FgrGalOx, FgrAAO and FoxAAO have weak activity on carbohydrates, but instead efficiently oxidize specific aryl alcohols. Notably, both FgrAAO and FoxAAO oxidize hydroxymethyl furfural (HMF) directly to 5-formyl-2-furoic acid (FFCA), and desymmetrize the bioproduct glycerol to the uncommon L-isomer of glyceraldehyde. Conclusions This work expands understanding of the catalytic diversity of CRO from AA5_2 to include unique representatives from Fusarium species that depart from the well-known galactose 6-oxidase activity of this family. Detailed enzymological analysis highlights the potential biotechnological applications of these orthologs in the production of renewable plastic polymer precursors and other chemicals.

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