Literature DB >> 2144189

The role of futile cycles in the energetics of bacterial growth.

O M Neijssel1, E T Buurman, M J Teixeira de Mattos.   

Abstract

In this contribution we describe the occurrence of futile cycles in growing bacteria. These cycles are thought to be active when organisms contain two uptake systems for a particular nutrient (one with a high, the other with a low affinity for its substrate). The high-affinity system is responsible for uptake of the nutrient, some of which is subsequently lost to the medium again via leakage through the low-affinity-system. A special futile cycle is caused under some growth conditions by the extremely rapid diffusion of ammonia through bacterial membranes. When the ammonium ion is taken up via active transport, the couple NH3/NH4+ will act as an uncoupler. This is aggravated by the chemical similarity of the potassium and the ammonium ion, which leads to ammonium ion transport via the Kdp potassium transport system when the potassium concentration in the medium is low. Other examples of futile cycles, such as those caused by the production of fatty acids by fermentation, are briefly discussed.

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Year:  1990        PMID: 2144189     DOI: 10.1016/0005-2728(90)90260-b

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  17 in total

1.  Characterization of amino acid substitutions in KdpA, the K+-binding and -translocating subunit of the KdpFABC complex of Escherichia coli.

Authors:  Martin van der Laan; Michael Gassel; Karlheinz Altendorf
Journal:  J Bacteriol       Date:  2002-10       Impact factor: 3.490

2.  Bacillus subtilis metabolism and energetics in carbon-limited and excess-carbon chemostat culture.

Authors:  M Dauner; T Storni; U Sauer
Journal:  J Bacteriol       Date:  2001-12       Impact factor: 3.490

3.  Adenosine diphosphate sugar pyrophosphatase prevents glycogen biosynthesis in Escherichia coli.

Authors:  B Moreno-Bruna; E Baroja-Fernández; F J Muñoz; A Bastarrica-Berasategui; A Zandueta-Criado; M Rodriguez-López; I Lasa; T Akazawa; J Pozueta-Romero
Journal:  Proc Natl Acad Sci U S A       Date:  2001-06-19       Impact factor: 11.205

Review 4.  Bacterial resistance to uncouplers.

Authors:  K Lewis; V Naroditskaya; A Ferrante; I Fokina
Journal:  J Bioenerg Biomembr       Date:  1994-12       Impact factor: 2.945

5.  Energetics and product formation by Saccharomyces cerevisiae grown in anaerobic chemostats under nitrogen limitation.

Authors:  G Lidén; A Persson; L Gustafsson; C Niklasson
Journal:  Appl Microbiol Biotechnol       Date:  1995-11       Impact factor: 4.813

6.  Growth and metabolism of Saccharomyces cerevisiae in chemostat cultures under carbon-, nitrogen-, or carbon- and nitrogen-limiting conditions.

Authors:  C Larsson; U von Stockar; I Marison; L Gustafsson
Journal:  J Bacteriol       Date:  1993-08       Impact factor: 3.490

7.  Glycolytic flux is conditionally correlated with ATP concentration in Saccharomyces cerevisiae: a chemostat study under carbon- or nitrogen-limiting conditions.

Authors:  C Larsson; A Nilsson; A Blomberg; L Gustafsson
Journal:  J Bacteriol       Date:  1997-12       Impact factor: 3.490

8.  Kinetic analysis of Clostridium cellulolyticum carbohydrate metabolism: importance of glucose 1-phosphate and glucose 6-phosphate branch points for distribution of carbon fluxes inside and outside cells as revealed by steady-state continuous culture.

Authors:  E Guedon; M Desvaux; H Petitdemange
Journal:  J Bacteriol       Date:  2000-04       Impact factor: 3.490

9.  Transcriptional occlusion caused by overlapping promoters.

Authors:  M Ammar Zafar; Valerie J Carabetta; Mark J Mandel; Thomas J Silhavy
Journal:  Proc Natl Acad Sci U S A       Date:  2014-01-13       Impact factor: 11.205

10.  Metabolic investigation of host/pathogen interaction using MS2-infected Escherichia coli.

Authors:  Rishi Jain; Ranjan Srivastava
Journal:  BMC Syst Biol       Date:  2009-12-30
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