Previous Article | Next Article 
Journal of Bacteriology, April 2000, p. 2010-2017, Vol. 182, No. 7
0021-9193/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
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
Emmanuel
Guedon,
Mickaël
Desvaux, and
Henri
Petitdemange*
Laboratoire de Biochimie des Bactéries
Gram+, Domaine Scientifique Victor Grignard, Université Henri
Poincare, Faculté des Sciences, 54506 Vandoeuvre-lès-Nancy Cédex, France
Received 3 August 1999/Accepted 7 January 2000
During the growth of Clostridium cellulolyticum in
chemostat cultures with ammonia as the growth-limiting nutrient, as
much as 30% of the original cellobiose consumed by C. cellulolyticum was converted to cellotriose, glycogen, and
polysaccharides regardless of the specific growth rates. Whereas the
specific consumption rate of cellobiose and of the carbon flux through
glycolysis increased, the carbon flux through the
phosphoglucomutase slowed. The limitation of the path through the
phosphoglucomutase had a great effect on the accumulation of glucose
1-phosphate (G1P), the precursor of cellotriose, exopolysaccharides,
and glycogen. The specific rates of biosynthesis of these compounds are
important since as much as 16.7, 16.0, and 21.4% of the specific rate
of cellobiose consumed by the cells could be converted to cellotriose,
exopolysaccharides, and glycogen, respectively. With the increase of
the carbon flux through glycolysis, the glucose 6-phosphate (G6P) pool
decreased, whereas the G1P pool increased. Continuous culture
experiments showed that glycogen biosynthesis was associated
with rapid growth. The same result was obtained in batch culture, where
glycogen biosynthesis reached a maximum during the exponential
growth phase. Glycogen synthesis in C. cellulolyticum was
also not subject to stimulation by nutrient limitation. Flux analyses
demonstrate that G1P and G6P, connected by the phosphoglucomutase
reaction, constitute important branch points for the distribution of
carbon fluxes inside and outside cells. From this study it appears that the properties of the G1P-G6P branch points have been selected to
control excretion of carbon surplus and to dissipate excess energy,
whereas the pyruvate-acetyl coenzyme A branch points chiefly regulate
the redox balance of the carbon catabolism as was shown previously (E. Guedon et al., J. Bacteriol. 181:3262-3269, 1999).
*
Corresponding author. Mailing address: Laboratoire de
Biochimie des Bactéries Gram+, Domaine Scientifique Victor
Grignard, Université Henri Poincaré, Faculté des
Sciences, 54506 Vandoeuvre-lès- Nancy Cédex, France. Phone:
33-3-83-91-20-53. Fax: 33-3-83-91-25-50. E-mail:
hpetitde{at}lcb.u-nancy.fr.
Journal of Bacteriology, April 2000, p. 2010-2017, Vol. 182, No. 7
0021-9193/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
This article has been cited by other articles:
-
Baroja-Fernandez, E., Munoz, F. J., Montero, M., Etxeberria, E., Sesma, M. T., Ovecka, M., Bahaji, A., Ezquer, I., Li, J., Prat, S., Pozueta-Romero, J.
(2009). Enhancing Sucrose Synthase Activity in Transgenic Potato (Solanum tuberosum L.) Tubers Results in Increased Levels of Starch, ADPglucose and UDPglucose and Total Yield. Plant Cell Physiol
50: 1651-1662
[Abstract]
[Full Text]
-
Alonso-Casajus, N., Dauvillee, D., Viale, A. M., Munoz, F. J., Baroja-Fernandez, E., Moran-Zorzano, M. T., Eydallin, G., Ball, S., Pozueta-Romero, J.
(2006). Glycogen Phosphorylase, the Product of the glgP Gene, Catalyzes Glycogen Breakdown by Removing Glucose Units from the Nonreducing Ends in Escherichia coli.. J. Bacteriol.
188: 5266-5272
[Abstract]
[Full Text]
-
Munoz, F. J., Baroja-Fernandez, E., Moran-Zorzano, M. T., Viale, A. M., Etxeberria, E., Alonso-Casajus, N., Pozueta-Romero, J.
(2005). Sucrose Synthase Controls Both Intracellular ADP Glucose Levels and Transitory Starch Biosynthesis in Source Leaves. Plant Cell Physiol
46: 1366-1376
[Abstract]
[Full Text]
-
Baroja-Fernandez, E., Munoz, F. J., Zandueta-Criado, A., Moran-Zorzano, M. T., Viale, A. M., Alonso-Casajus, N., Pozueta-Romero, J.
(2004). Most of ADP{middle dot}glucose linked to starch biosynthesis occurs outside the chloroplast in source leaves. Proc. Natl. Acad. Sci. USA
101: 13080-13085
[Abstract]
[Full Text]
-
Baroja-Fernandez, E., Munoz, F. J., Saikusa, T., Rodriguez-Lopez, M., Akazawa, T., Pozueta-Romero, J.
(2003). Sucrose Synthase Catalyzes the de novo Production of ADPglucose Linked to Starch Biosynthesis in Heterotrophic Tissues of Plants. Plant Cell Physiol
44: 500-509
[Abstract]
[Full Text]
-
Lynd, L. R., Weimer, P. J., van Zyl, W. H., Pretorius, I. S.
(2002). Microbial Cellulose Utilization: Fundamentals and Biotechnology. Microbiol. Mol. Biol. Rev.
66: 506-577
[Abstract]
[Full Text]
-
Guedon, E., Desvaux, M., Petitdemange, H.
(2002). Improvement of Cellulolytic Properties of Clostridium cellulolyticum by Metabolic Engineering. Appl. Environ. Microbiol.
68: 53-58
[Abstract]
[Full Text]
-
Baroja-Fernandez, E., Munoz, F. J., Akazawa, T., Pozueta-Romero, J.
(2001). Reappraisal of the Currently Prevailing Model of Starch Biosynthesis in Photosynthetic Tissues: A Proposal Involving the Cytosolic Production of ADP-Glucose by Sucrose Synthase and Occurrence of Cyclic Turnover of Starch in the Chloroplast. Plant Cell Physiol
42: 1311-1320
[Abstract]
[Full Text]
-
Desvaux, M., Guedon, E., Petitdemange, H.
(2001). Kinetics and Metabolism of Cellulose Degradation at High Substrate Concentrations in Steady-State Continuous Cultures of Clostridium cellulolyticum on a Chemically Defined Medium. Appl. Environ. Microbiol.
67: 3837-3845
[Abstract]
[Full Text]
-
Desvaux, M., Petitdemange, H.
(2001). Flux Analysis of the Metabolism of Clostridium cellulolyticum Grown in Cellulose-Fed Continuous Culture on a Chemically Defined Medium under Ammonium-Limited Conditions. Appl. Environ. Microbiol.
67: 3846-3851
[Abstract]
[Full Text]
-
Verrelli, B. C., Eanes, W. F.
(2001). The Functional Impact of Pgm Amino Acid Polymorphism on Glycogen Content in Drosophila melanogaster. Genetics
159: 201-210
[Abstract]
[Full Text]
-
Moreno-Bruna, B., Baroja-Fernandez, E., Munoz, F. J., Bastarrica-Berasategui, A., Zandueta-Criado, A., Rodriguez-Lopez, M., Lasa, I., Akazawa, T., Pozueta-Romero, J.
(2001). Adenosine diphosphate sugar pyrophosphatase prevents glycogen biosynthesis in Escherichia coli. Proc. Natl. Acad. Sci. USA
10.1073/pnas.131214098v1
[Abstract]
[Full Text]
-
Desvaux, M., Guedon, E., Petitdemange, H.
(2001). Metabolic flux in cellulose batch and cellulose-fed continuous cultures of Clostridium cellulolyticum in response to acidic environment. Microbiology
147: 1461-1471
[Abstract]
[Full Text]
-
Desvaux, M., Guedon, E., Petitdemange, H.
(2001). Carbon Flux Distribution and Kinetics of Cellulose Fermentation in Steady-State Continuous Cultures of Clostridium cellulolyticum on a Chemically Defined Medium. J. Bacteriol.
183: 119-130
[Abstract]
[Full Text]
-
Moreno-Bruna, B., Baroja-Fernandez, E., Munoz, F. J., Bastarrica-Berasategui, A., Zandueta-Criado, A., Rodriguez-Lopez, M., Lasa, I., Akazawa, T., Pozueta-Romero, J.
(2001). Adenosine diphosphate sugar pyrophosphatase prevents glycogen biosynthesis in Escherichia coli. Proc. Natl. Acad. Sci. USA
98: 8128-8132
[Abstract]
[Full Text]