A rheostat mechanism governs the bifurcation of carbon flux in mycobacteria

10.1038/ncomms12527

محفوظ في:

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Murima, P, Zimmermann, M, Chopra, T, Pojer, F, Fonti, G, Dal Peraro, M, Alonso, S, Sauer, U, Pethe, K, McKinney, J.D
مؤلفون آخرون:	MICROBIOLOGY AND IMMUNOLOGY
التنسيق:	مقال
منشور في:	Nature Publishing Group 2020
الموضوعات:	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
الوصول للمادة أونلاين:	https://scholarbank.nus.edu.sg/handle/10635/182436
الوسوم:	إضافة وسم لا توجد وسوم, كن أول من يضع وسما على هذه التسجيلة!
المؤسسة:	National University of Singapore

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