Metabolic engineering for microbial production of aromatic amino acids and derived compounds.

No abstract is available for this paper.

• Publication year

  2001

• Venue

  Metabolic Engineering

• Publication date

  2001-10-01

• Fields of study

  Biology, Medicine, Chemistry, Engineering

• Identifiers
  DOI 10.1006/MBEN.2001.0196PMID 11676565
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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• Benzene-Free Synthesis of Phenol This research was supported by a grant awarded by the U.S. Department of Agriculture.

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• Disruption of a Global Regulatory Gene to Enhance Central Carbon Flux into Phenylalanine Biosynthesis in Escherichia coli

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• The influence of ATP on the binding of aromatic amino acids to the ligand response domain of the tyrosine repressor of Haemophilus influenzae

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• Analysis of interaction of regulatory protein TyrR with DNA.

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• Control of L‐phenylalanine production by dual feeding of glucose and L‐tyrosine

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• Distances between DNA and ATP binding sites in the TyrR-DNA complex.

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• Effects of tktA, $aroF^{FBR}$and aroL Expression in the Tryptophan-Producing Escherichia coli

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• The ς70 Transcription Factor TyrR Has Zinc-Stimulated Phosphatase Activity That Is Inhibited by ATP and Tyrosine

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• A direct comparison of approaches for increasing carbon flow to aromatic biosynthesis inEscherichia coli

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• Improving production of aromatic compounds in Escherichia coli by metabolic engineering.

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