ArticleFrontiers in microbiology2026
Classification of tungsten-containing oxidoreductases provides insights into their biochemical and physiological diversity.
Article in Frontiers in microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Tungsten-containing oxidoreductases (WORs) are a diverse family of enzymes with over 4,000 known members that can be subdivided into 92 clades based on the phylogeny of the large pyranopterin cofactor-containing large subunit (WorL). Despite being widespread in Bacteria and Archaea, particularly in members of the human microbiome, only five of the 92 WOR clades contain a WOR with a defined physiological role in cellular metabolism, primarily-but not exclusively-involved in oxidation of various aldehydes. However, this phylogenetic-based organizational system lacks a perspective on the diversity and complexity of WOR enzymes. Herein, we propose a non-phylogenetic classification system for WORs based on predicted subunit composition and electron carrier specificity that provides insight into potential physiological roles. WORs can be divided into five classes that range in complexity and predicted function. The simpler cytoplasmic Class I-III WORs are involved in aldehyde detoxification, a modified glycolysis pathway and cold adaptation. More complex multimeric WORs are proposed to use multiple electron carriers in bifurcating reactions (Class IV) or interact with various respiratory systems via associations with the cell membrane (Class V). We characterized two new WORs, one Class I and one Class V, from the human gut bacterium
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