Amplified Expression of Fructose 1,6-Bisphosphatase in Corynebacterium glutamicum Increases In Vivo Flux through the Pentose Phosphate Pathway and Lysine Production on Different Carbon Sources
Author:
Affiliation:
1. Biochemical Engineering, Saarland University, Saarland, Germany
2. Research Fine Chemicals and Biotechnology, BASF AG, Ludwigshafen, Germany
Abstract
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
Link
https://journals.asm.org/doi/pdf/10.1128/AEM.71.12.8587-8596.2005
Reference35 articles.
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2. Babul, J., and V. Guixe. 1983. Fructose bisphosphatase from Escherichia coli. Purification and characterization. Arch. Biochem. Biophys.225:944-949.
3. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding
4. Dominguez, H., C. Rollin, A. Guyonvarch, J. L. Guerquin-Kern, M. Cocaign-Bousquet, and N. D. Lindley. 1998. Carbon-flux distribution in the central metabolic pathways of Corynebacterium glutamicum during growth on fructose. Eur. J. Biochem.254:96-102.
5. Gamo, F. J., M. A. Navas, M. A. Blazquez, C. Gancedo, and J. M. Gancedo. 1994. Catabolite inactivation of heterologous fructose-1,6-bisphosphatases and fructose-1,6-bisphosphatase-beta-galactosidase fusion proteins in Saccharomyces cerevisiae. Eur. J. Biochem.222:879-884.
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