Evidence for the Presence of an Alternative Glucose Transport System in Clostridium beijerinckii NCIMB 8052 and the Solvent-Hyperproducing Mutant BA101

ABSTRACT The effects of substrate analogs and energy inhibitors on glucose uptake and phosphorylation by Clostridium beijerinckii provide evidence for the operation of two uptake systems: a previously characterized phosphoenolpyruvate-dependent phosphotransferase system (PTS) and a non-PTS system probably energized by the transmembrane proton gradient. In both wild-type C. beijerinckii NCIMB 8052 and the butanol-hyperproducing mutant BA101, PTS activity declined at the end of exponential growth, while glucokinase activity increased in the later stages of fermentation. The non-PTS uptake system, together with enhanced glucokinase activity, may provide an explanation for the ability of the mutant to utilize glucose more effectively during fermentation despite the fact that it is partially defective in PTS activity.

[1]  W. Mitchell,et al.  Identification of two α‐glucosidase activities in Clostridium acetobutylicum NCIB 8052 , 1995 .

[2]  N. Qureshi,et al.  Soy molasses as fermentation substrate for production of butanol using Clostridium beijerinckii BA101 , 2001, Journal of Industrial Microbiology and Biotechnology.

[3]  Eva R. Kashket,et al.  Intracellular Conditions Required for Initiation of Solvent Production by Clostridium acetobutylicum , 1986, Applied and environmental microbiology.

[4]  H. Blaschek,et al.  Isolation and characterization of Clostridium acetobutylicum mutants with enhanced amylolytic activity , 1991, Applied and environmental microbiology.

[5]  W. Mitchell,et al.  Physiology of carbohydrate to solvent conversion by clostridia. , 1998, Advances in microbial physiology.

[6]  H. Blaschek,et al.  Glucose Uptake in Clostridium beijerinckii NCIMB 8052 and the Solvent-Hyperproducing Mutant BA101 , 2001, Applied and Environmental Microbiology.

[7]  J. Deutscher,et al.  Analysis of the Elements of Catabolite Repression in Clostridium acetobutylicum ATCC 824 , 2003, Journal of Molecular Microbiology and Biotechnology.

[8]  J. Shaw,et al.  Properties of the glucose phosphotransferase system of Clostridium acetobutylicum NCIB 8052 , 1991, Applied and environmental microbiology.

[9]  Philippe Soucaille,et al.  Regulation of metabolic shifts in Clostridium acetobutylicum ATCC 824 , 1995 .

[10]  M. Saier Mechanisms of Carbohydrate Transport , 1985 .

[11]  G. Gottschalk,et al.  The internal pH of Clostridium acetobutylicum and its effect on the shift from acid to solvent formation , 1985, Archives of Microbiology.

[12]  W. Mitchell,et al.  Carbohydrate Uptake and Utilization byClostridium beijerinckiiNCIMB 8052 , 1996 .

[13]  M. Saier,et al.  Mechanisms and Regulation of Carbohydrate Transport in Bacteria , 1985 .

[14]  H. Blaschek,et al.  Acetate enhances solvent production and prevents degeneration in Clostridium beijerinckii BA101 , 1999, Applied Microbiology and Biotechnology.

[15]  H. Blaschek,et al.  Enhanced Butanol Production by Clostridium beijerinckii BA101 Grown in Semidefined P2 Medium Containing 6 Percent Maltodextrin or Glucose , 1997, Applied and environmental microbiology.

[16]  N. Minton,et al.  A Gene System for Glucitol Transport and Metabolism in Clostridium beijerinckii NCIMB 8052 , 1998, Applied and Environmental Microbiology.

[17]  S. Reid,et al.  The genes controlling sucrose utilization in Clostridium beijerinckii NCIMB 8052 constitute an operon. , 1999, Microbiology.