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A rheostat mechanism governs the bifurcation of carbon flux in mycobacteria

A rheostat mechanism governs the bifurcation of carbon flux in mycobacteria

10.1038/ncomms12527

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書目詳細資料
Main Authors: Murima, P, Zimmermann, M, Chopra, T, Pojer, F, Fonti, G, Dal Peraro, M, Alonso, S, Sauer, U, Pethe, K, McKinney, J.D
其他作者: MICROBIOLOGY AND IMMUNOLOGY
格式: Article
出版: Nature Publishing Group 2020
主題:
carbon
glyoxylic acid
isocitrate lyase
bacterial protein
fatty acid
glyoxylic acid derivative
isocitrate dehydrogenase
bifurcation
carbon flux
chemotherapy
coliform bacterium
enzyme activity
infectivity
metabolism
partitioning
pathogenicity
steady-state equilibrium
tuberculosis
allosterism
Article
bacterial growth
bacterial strain
biosynthesis
carbon source
citric acid cycle
controlled study
energy metabolism
energy yield
enzyme phosphorylation
Escherichia coli
fatty acid metabolism
Mycobacterium tuberculosis
nonhuman
regulatory mechanism
biological model
carbon cycle
classification
kinetics
Mycobacterium
species difference
Corynebacterineae
Bacterial Proteins
Carbon
Carbon Cycle
Citric Acid Cycle
Fatty Acids
Glyoxylates
Isocitrate Dehydrogenase
Isocitrate Lyase
Kinetics
Models, Biological
Species Specificity
在線閱讀:https://scholarbank.nus.edu.sg/handle/10635/182436
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機構: National University of Singapore
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因特網

https://scholarbank.nus.edu.sg/handle/10635/182436

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