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8ID7

Crystal structure of YbiW in complex with 1,5-anhydroglucitol-6-phosphate in Escherichia coli

Summary for 8ID7
Entry DOI10.2210/pdb8id7/pdb
DescriptorProbable dehydratase YbiW, 1,5-anhydro-6-O-phosphono-D-glucitol (3 entities in total)
Functional Keywordsglycyl radical enzyme, ybiw, 1, 5-anhydroglucitol-6-phosphate, lyase
Biological sourceEscherichia coli str. K-12 substr. MG1655
Total number of polymer chains1
Total formula weight90301.11
Authors
Ma, K.L.,Zhang, Y. (deposition date: 2023-02-12, release date: 2024-10-02, Last modification date: 2024-10-09)
Primary citationMa, K.,Xue, B.,Chu, R.,Zheng, Y.,Sharma, S.,Jiang, L.,Hu, M.,Xie, Y.,Hu, Y.,Tao, T.,Zhou, Y.,Liu, D.,Li, Z.,Yang, Q.,Chen, Y.,Wu, S.,Tong, Y.,Robinson, R.C.,Yew, W.S.,Jin, X.,Liu, Y.,Zhao, H.,Ang, E.L.,Wei, Y.,Zhang, Y.
A Widespread Radical-Mediated Glycolysis Pathway.
J.Am.Chem.Soc., 146:26187-26197, 2024
Cited by
PubMed Abstract: Glycyl radical enzymes (GREs) catalyze mechanistically diverse radical-mediated reactions, playing important roles in the metabolism of anaerobic bacteria. The model bacterium MG1655 contains two GREs of unknown function, YbiW and PflD, which are widespread among human intestinal bacteria. Here, we report that YbiW and PflD catalyze ring-opening C-O cleavage of 1,5-anhydroglucitol-6-phosphate (AG6P) and 1,5-anhydromannitol-6-phosphate (AM6P), respectively. The product of both enzymes, 1-deoxy-fructose-6-phosphate (DF6P), is then cleaved by the aldolases FsaA or FsaB to form glyceraldehyde-3-phosphate (G3P) and hydroxyacetone (HA), which are then reduced by the NADH-dependent dehydrogenase GldA to form 1,2-propanediol (1,2-PDO). Crystal structures of YbiW and PflD in complex with their substrates provided insights into the mechanism of radical-mediated C-O cleavage. This "anhydroglycolysis" pathway enables anaerobic growth of on 1,5-anhydroglucitol (AG) and 1,5-anhydromannitol (AM), and we probe the feasibility of harnessing this pathway for the production of 1,2-PDO, a highly demanded chiral chemical feedstock, from inexpensive starch. Discovery of the anhydroglycolysis pathway expands the known catalytic repertoire of GREs, clarifies the hitherto unknown physiological functions of the well-studied enzymes FsaA, FsaB, and GldA, and demonstrates how enzyme discovery efforts can cast light on prevalent yet overlooked metabolites in the microbiome.
PubMed: 39283600
DOI: 10.1021/jacs.4c07718
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.65 Å)
Structure validation

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