Affiliation:
1. 0000 0004 1936 8278 grid.21940.3e Department of Bioengineering Rice University 6500 Main Street 77030 Houston TX USA
2. 0000 0001 1537 5962 grid.8170.e Escuela de Ingeniería Bioquímica Pontificia Universidad Católica de Valparaíso Valparaiso Chile
3. 0000 0004 1936 8278 grid.21940.3e Department of BioSciences Rice University Houston TX USA
4. 0000 0004 1936 8278 grid.21940.3e Department of Chemical and Biomolecular Engineering Rice University Houston TX USA
Abstract
Abstract
Several metabolic engineered Escherichia coli strains were constructed and evaluated for four-carbon dicarboxylic acid production. Fumarase A, fumarase B and fumarase C single, double and triple mutants were constructed in a ldhA adhE mutant background overexpressing the pyruvate carboxylase from Lactococcus lactis. All the mutants produced succinate as the main four-carbon (C4) dicarboxylic acid product when glucose was used as carbon source with the exception of the fumAC and the triple fumB fumAC deletion strains, where malate was the main C4-product with a yield of 0.61–0.67 mol (mole glucose)−1. Additionally, a mdh mutant strain and a previously engineered high-succinate-producing strain (SBS550MG-Cms pHL413-Km) were investigated for aerobic malate production from succinate. These strains produced 40.38 mM (5.41 g/L) and 50.34 mM (6.75 g/L) malate with a molar yield of 0.53 and 0.55 mol (mole succinate)−1, respectively. Finally, by exploiting the high-succinate production capability, the strain SBS550MG-Cms243 pHL413-Km showed significant malate production in a two-stage process from glucose. This strain produced 133 mM (17.83 g/L) malate in 47 h, with a high yield of 1.3 mol (mole glucose)−1 and productivity of 0.38 g L−1 h−1.
Funder
National Institutes of Health
National Science Foundation
Publisher
Oxford University Press (OUP)
Subject
Applied Microbiology and Biotechnology,Biotechnology,Bioengineering
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