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Open AccessJournal ArticleDOI

Altered End-Product Patterns and Catabolite Repression in Escherichia coli

Walter J. Dobrogosz
- 01 Jun 1966 - 
- Vol. 91, Iss: 6, pp 2263-2269
TLDR
The results presented in this report indicate that oxidative decarboxylation of pyruvate may markedly affect the amount of energy that can be derived from glucose catabolism, which may play a key role in the mechanism of catabolite repression.
Abstract
Dobrogosz, Walter J. (North Carolina State University, Raleigh). Altered end-product patterns and catabolite repression in Escherichia coli. J. Bacteriol. 91:2263–2269. 1966.—End products formed during growth of Escherichia coli ML30 on glucose were examined under various conditions known to promote or prevent catabolite repression of the inducible β-galactosidase system in this organism. Cultures were grown under these conditions in the presence of C14-glucose or C14-pyruvate. The products formed were assayed isotopically after separation on columns of silicic acid. Under conditions known to promote catabolite repression, glucose was degraded primarily to acetate and CO2. When repression was turned off by anaerobic shock, glucose metabolism was characterized by the accumulation of ethyl alcohol in addition to acetate and CO2. The results presented in this report indicate that oxidative decarboxylation of pyruvate may markedly affect the amount of energy that can be derived from glucose catabolism. In turn, the amount of energy derived from catabolic processes may play a key role in the mechanism of catabolite repression.

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Citations
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Journal ArticleDOI

Enzyme pattern and aerobic growth of Saccharomyces cerevisiae under various degrees of glucose limitation.

TL;DR: The enzyme pattern of Saccharomyces cerevisiae was followed during batch growth and in continuous culture in a synthetic medium limited for glucose under aerobic conditions and showed to depend on the rate of substrate consumption as well as on the type of metabolism and to be correlated with the budding cycle.
Book ChapterDOI

Catabolite Repression and other Control Mechanisms in Carbohydrate Utilization

TL;DR: This chapter focuses on three devices: catabolite repression, transient repression, and catabolites inhibition, which regulate the utilization of many carbohydrates, which influences many aspects of microbial growth and metabolism.
Journal ArticleDOI

Regulation of inducible enzyme synthesis in Escherichia coli by cyclic adenosine 3', 5'-monophosphate.

TL;DR: It is proposed that the intracellular level of cyclic AMP regulates the rate of synthesis of many inducible enzymes in E. coli and other microorganisms and that glucose lowers the rate
References
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Journal ArticleDOI

[The kinetics of the biosynthesis of beta-galactosidase in Escherichia coli as a function of growth].

TL;DR: Le rapport de the quantite d'enzyme synthetisea la quantite de substance vivante formee dans le meme temps (taux differentiel de synthese) est constant dans des conditions donnees d'induction.
Journal ArticleDOI

Comparative study of glucose catabolism by the radiorespirometric method.

TL;DR: A method is presented which provides information by means of the time-course study of the utilization of C'4 specifically labeled carbohydrates by growing microorganisms which will aid in recognizing the nature, estimating the extent of participation, and evaluating the function of the various carbohydrate catabolic pathways.
Journal ArticleDOI

PHYSIOLOGY OF THE INHIBITION BY GLUCOSE OF THE INDUCED SYNTHESIS OF THE β-GALACTOSIDE-ENZYME SYSTEM OF ESCHERICHIA COLI

TL;DR: The experiments described here are best understood in terms of the hypothesis that induced enzymes are those whose synthesis can be repressed by some derivative of the carbon source and the inducer relieves the repression.
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