Trapping and structural characterisation of a covalent intermediate in vitamin B6biosynthesis catalysed by the Pdx1 PLP synthase

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Abstract

The Pdx1 enzyme catalyses condensation of two carbohydrates and ammonia to form pyridoxal 5-phosphate (PLP) via an imine relay mechanism of carbonyl intermediates. The I333 intermediate characterised here using structural, UV-vis absorption spectroscopy and mass spectrometry analyses rationalises stereoselective deprotonation and subsequent substrate assisted phosphate elimination, central to PLP biosynthesis.

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Rodrigues, M. J., Giri, N., Royant, A., Zhang, Y., Bolton, R., Evans, G., … Tews, I. (2022). Trapping and structural characterisation of a covalent intermediate in vitamin B6biosynthesis catalysed by the Pdx1 PLP synthase. RSC Chemical Biology, 3(2), 227–230. https://doi.org/10.1039/d1cb00160d

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