Corynebacterium glutamicum was engineered for the production of L-valine from glucose by deletion of the aceE gene encoding the E1p enzyme of the pyruvate dehydrogenase complex and additional overexpression of the ilvBNCE genes encoding the L-valine biosynthetic enzymes acetohydroxyacid synthase, isomeroreductase, and transaminase B. In the absence of cellular growth, C. glutamicum DeltaaceE showed a relatively high intracellular concentration of pyruvate (25.9 mM) and produced significant amounts of pyruvate, L-alanine, and L-valine from glucose as the sole carbon source. Lactate or acetate was not formed. Plasmid-bound overexpression of ilvBNCE in C. glutamicum DeltaaceE resulted in an approximately 10-fold-lower intracellular pyruvate concentration (2.3 mM) and a shift of the extracellular product pattern from pyruvate and L-alanine towards L-valine. In fed-batch fermentations at high cell densities and an excess of glucose, C. glutamicum DeltaaceE(pJC4ilvBNCE) produced up to 210 mM L-valine with a volumetric productivity of 10.0 mM h(-1) (1.17 g l(-1) h(-1)) and a maximum yield of about 0.6 mol per mol (0.4 g per g) of glucose.
%0 Journal Article
%1 blombach_l-valine_2007
%A Blombach, Bastian
%A Schreiner, Mark E.
%A Holátko, Jirí
%A Bartek, Tobias
%A Oldiges, Marco
%A Eikmanns, Bernhard J.
%D 2007
%J Appl. Environ. Microbiol.
%K Acid, Alanine Complex, Corynebacterium Dehydrogenase Fermentation, Isoleucine, Lysine, Pyruvate Pyruvic Valine, glutamicum, myown
%N 7
%P 2079--2084
%R 10.1128/AEM.02826-06
%T L-valine production with pyruvate dehydrogenase complex-deficient Corynebacterium glutamicum
%V 73
%X Corynebacterium glutamicum was engineered for the production of L-valine from glucose by deletion of the aceE gene encoding the E1p enzyme of the pyruvate dehydrogenase complex and additional overexpression of the ilvBNCE genes encoding the L-valine biosynthetic enzymes acetohydroxyacid synthase, isomeroreductase, and transaminase B. In the absence of cellular growth, C. glutamicum DeltaaceE showed a relatively high intracellular concentration of pyruvate (25.9 mM) and produced significant amounts of pyruvate, L-alanine, and L-valine from glucose as the sole carbon source. Lactate or acetate was not formed. Plasmid-bound overexpression of ilvBNCE in C. glutamicum DeltaaceE resulted in an approximately 10-fold-lower intracellular pyruvate concentration (2.3 mM) and a shift of the extracellular product pattern from pyruvate and L-alanine towards L-valine. In fed-batch fermentations at high cell densities and an excess of glucose, C. glutamicum DeltaaceE(pJC4ilvBNCE) produced up to 210 mM L-valine with a volumetric productivity of 10.0 mM h(-1) (1.17 g l(-1) h(-1)) and a maximum yield of about 0.6 mol per mol (0.4 g per g) of glucose.
@article{blombach_l-valine_2007,
abstract = {Corynebacterium glutamicum was engineered for the production of L-valine from glucose by deletion of the aceE gene encoding the E1p enzyme of the pyruvate dehydrogenase complex and additional overexpression of the ilvBNCE genes encoding the L-valine biosynthetic enzymes acetohydroxyacid synthase, isomeroreductase, and transaminase B. In the absence of cellular growth, C. glutamicum DeltaaceE showed a relatively high intracellular concentration of pyruvate (25.9 mM) and produced significant amounts of pyruvate, L-alanine, and L-valine from glucose as the sole carbon source. Lactate or acetate was not formed. Plasmid-bound overexpression of ilvBNCE in C. glutamicum DeltaaceE resulted in an approximately 10-fold-lower intracellular pyruvate concentration (2.3 mM) and a shift of the extracellular product pattern from pyruvate and L-alanine towards L-valine. In fed-batch fermentations at high cell densities and an excess of glucose, C. glutamicum DeltaaceE(pJC4ilvBNCE) produced up to 210 mM L-valine with a volumetric productivity of 10.0 mM h(-1) (1.17 g l(-1) h(-1)) and a maximum yield of about 0.6 mol per mol (0.4 g per g) of glucose.},
added-at = {2018-02-09T13:18:17.000+0100},
author = {Blombach, Bastian and Schreiner, Mark E. and Holátko, Jirí and Bartek, Tobias and Oldiges, Marco and Eikmanns, Bernhard J.},
biburl = {https://puma.ub.uni-stuttgart.de/bibtex/25bac540150e10acba07b2f8205f6f070/bastian},
doi = {10.1128/AEM.02826-06},
interhash = {d744d92c5af8f45409137c58d022ef1c},
intrahash = {5bac540150e10acba07b2f8205f6f070},
issn = {0099-2240},
journal = {Appl. Environ. Microbiol.},
keywords = {Acid, Alanine Complex, Corynebacterium Dehydrogenase Fermentation, Isoleucine, Lysine, Pyruvate Pyruvic Valine, glutamicum, myown},
language = {eng},
month = apr,
number = 7,
pages = {2079--2084},
pmcid = {PMC1855657},
pmid = {17293513},
timestamp = {2018-02-09T12:18:56.000+0100},
title = {L-valine production with pyruvate dehydrogenase complex-deficient {Corynebacterium} glutamicum},
volume = 73,
year = 2007
}