Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/151959
Title: Pyruvate kinase regulates the pentose-phosphate pathway in response to hypoxia in mycobacterium tuberculosis
Authors: Zhong, Wenhe
Guo, Jingjing
Cui, Liang
Chionh, Yok Hian
Li, Kuohan
El Sahili, Abbas
Cai, Qixu
Yuan, Meng
Michels, Paul A. M.
Fothergill-Gilmore, Linda A.
Walkinshaw, Malcolm D.
Mu, Yuguang
Lescar, Julien
Dedon, Peter C.
Keywords: Science::Biological sciences
Issue Date: 2019
Source: Zhong, W., Guo, J., Cui, L., Chionh, Y. H., Li, K., El Sahili, A., Cai, Q., Yuan, M., Michels, P. A. M., Fothergill-Gilmore, L. A., Walkinshaw, M. D., Mu, Y., Lescar, J. & Dedon, P. C. (2019). Pyruvate kinase regulates the pentose-phosphate pathway in response to hypoxia in mycobacterium tuberculosis. Journal of Molecular Biology, 431(19), 3690-3705. https://dx.doi.org/10.1016/j.jmb.2019.07.033
Project: NMRC/CBRG/ 0073/2014 
RG146/17 
Journal: Journal of Molecular Biology 
Abstract: In response to the stress of infection, Mycobacterium tuberculosis (Mtb) reprograms its metabolism to accommodate nutrient and energetic demands in a changing environment. Pyruvate kinase (PYK) is an essential glycolytic enzyme in the phosphoenolpyruvate-pyruvate-oxaloacetate node that is a central switch point for carbon flux distribution. Here we show that the competitive binding of pentose monophosphate inhibitors or the activator glucose 6-phosphate (G6P) to MtbPYK tightly regulates the metabolic flux. Intriguingly, pentose monophosphates were found to share the same binding site with G6P. The determination of a crystal structure of MtbPYK with bound ribose 5-phosphate (R5P), combined with biochemical analyses and molecular dynamic simulations, revealed that the allosteric inhibitor pentose monophosphate increases PYK structural dynamics, weakens the structural network communication, and impairs substrate binding. G6P, on the other hand, primes and activates the tetramer by decreasing protein flexibility and strengthening allosteric coupling. Therefore, we propose that MtbPYK uses these differences in conformational dynamics to up- and down-regulate enzymic activity. Importantly, metabolome profiling in mycobacteria reveals a significant increase in the levels of pentose monophosphate during hypoxia, which provides insights into how PYK uses dynamics of the tetramer as a competitive allosteric mechanism to retard glycolysis and facilitate metabolic reprogramming toward the pentose-phosphate pathway for achieving redox balance and an anticipatory metabolic response in Mtb.
URI: https://hdl.handle.net/10356/151959
ISSN: 0022-2836
DOI: 10.1016/j.jmb.2019.07.033
Rights: © 2019 Elsevier Ltd. All rights reserved. This paper was published in Journal of Molecular Biology and is made available with permission of Elsevier Ltd.
Fulltext Permission: open
Fulltext Availability: With Fulltext
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