L-malate production by metabolically engineered Escherichia coli

X. Zhang, Xuan Wang, K. T. Shanmugam, L. O. Ingram

Research output: Contribution to journalArticle

101 Citations (Scopus)

Abstract

Escherichia coli strains (KJ060 and KJ073) that were previously developed for succinate production have now been modified for malate production. Many unexpected changes were observed during this investigation. The initial strategy of deleting fumarase isoenzymes was ineffective, and succinate continued to accumulate. Surprisingly, a mutation in fumarate reductase alone was sufficient to redirect carbon flow into malate even in the presence of fumarase. Further deletions were needed to inactivate malic enzymes (typically gluconeogenic) and prevent conversion to pyruvate. However, deletion of these genes (sfcA and maeB) resulted in the unexpected accumulation of D-lactate despite the prior deletion of mgsA and ldhA and the absence of apparent lactate dehydrogenase activity. Although the metabolic source of this D-lactate was not identified, lactate accumulation was increased by supplementation with pyruvate and decreased by the deletion of either pyruvate kinase gene (pykA or pykF) to reduce the supply of pyruvate. Many of the gene deletions adversely affected growth and cell yield in minimal medium under anaerobic conditions, and volumetric rates of malate production remained low. The final strain (XZ658) produced 163mMmalate, with a yield of 1.0 mol (mol glucose-1), half of the theoretical maximum. Using a two-stage process (aerobic cell growth and anaerobic malate production), this engineered strain produced 253 mM malate (34 g liter-1) within 72 h, with a higher yield (1.42 mol mol-1) and productivity (0.47 g liter-1 h-1). This malate yield and productivity are equal to or better than those of other known biocatalysts.

Original languageEnglish (US)
Pages (from-to)427-434
Number of pages8
JournalApplied and Environmental Microbiology
Volume77
Issue number2
DOIs
StatePublished - Jan 2011
Externally publishedYes

Fingerprint

malates
Escherichia coli
Pyruvic Acid
Fumarate Hydratase
lactates
gene
Lactic Acid
gene deletion
Gene Deletion
Succinic Acid
succinic acid
productivity
succinate dehydrogenase (quinone)
Cell Growth Processes
anoxic conditions
mutation
glucose
pyruvate kinase
Pyruvate Kinase
Succinate Dehydrogenase

ASJC Scopus subject areas

  • Applied Microbiology and Biotechnology
  • Food Science
  • Biotechnology
  • Ecology

Cite this

L-malate production by metabolically engineered Escherichia coli. / Zhang, X.; Wang, Xuan; Shanmugam, K. T.; Ingram, L. O.

In: Applied and Environmental Microbiology, Vol. 77, No. 2, 01.2011, p. 427-434.

Research output: Contribution to journalArticle

Zhang, X. ; Wang, Xuan ; Shanmugam, K. T. ; Ingram, L. O. / L-malate production by metabolically engineered Escherichia coli. In: Applied and Environmental Microbiology. 2011 ; Vol. 77, No. 2. pp. 427-434.
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