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bioRxiv · 10.1101/841569

Allosteric Regulation of Vitamin K2 Biosynthesis in a Human Pathogen

Bashiri, G.·Nigon, L. V.·Jirgis, E. N. M.·Ho, N. A. T.·Stanborough, T.·Dawes, S. S.·Baker, E. N.·Bulloch, E. M. M.·Johnston, J. M.
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Abstract

Menaquinone (Vitamin K2) plays a vital role in energy generation and environmental adaptation in many bacteria, including Mycobacterium tuberculosis (Mtb). Although menaquinone levels are known to be tightly linked to the redox/energy status of the cell, the regulatory mechanisms underpinning this phenomenon are unclear. The first committed step in menaquinone biosynthesis is catalyzed by MenD, a thiamine diphosphate-dependent enzyme comprising three domains. Domains I and III form the MenD active site, but no function has yet been ascribed to domain II. Here we show the last cytosolicmetabolite in the menaquinone biosynthesis pathway (1,4-dihydroxy-2-napthoic acid, DHNA) binds to domain II of Mtb-MenD and inhibits enzyme activity. We identified three arginine residues (Arg97, Arg277 and Arg303) that are important for both enzyme activity and the feedback inhibition by DHNA: Arg277 appears to be particularly important for signal propagation from the allosteric site to the active site. This is the first evidence of feedback regulation of the menaquinone biosynthesis pathway in bacteria, unravelling a protein level regulatory mechanism for control of menaquinone levels within the cell.

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Bashiri, G., Nigon, L. V., Jirgis, E. N. M., Ho, N. A. T., Stanborough, T., Dawes, S. S., Baker, E. N., Bulloch, E. M. M., Johnston, J. M.. 2019-11-14. Allosteric Regulation of Vitamin K2 Biosynthesis in a Human Pathogen. https://doi.org/10.1101/841569

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