
To achieve an efficient production of geraniol and its derivatives in Escherichia coli, we aimed to improve the activity of geraniol synthase (GES) through a single round of mutagenesis and screening for higher substrate consumption. We isolated GES variants that outperform their parent in geraniol production. The analysis of GES variants indicated that the expression level of GES was the bottleneck for geraniol synthesis. Over-expression of the mutant GESM53 with a 5'-untranslated sequence designed for high translational efficiency, along with the additional expression of mevalonate pathway enzymes, isopentenyl pyrophosphate isomerase, and geranyl pyrophosphate synthase, yielded 300 mg/L/12 h geraniol and its derivatives (>1000 mg/L/42 h in total) in a shaking flask.
Terpenes, Acyclic Monoterpenes, Escherichia coli Proteins, Recombinant Fusion Proteins, Geranyltranstransferase, Carbon-Carbon Double Bond Isomerases, Carotenoids, High-Throughput Screening Assays, Substrate Specificity, Hemiterpenes, Metabolic Engineering, Polyisoprenyl Phosphates, Mutagenesis, Escherichia coli, Directed Molecular Evolution, Peptide Chain Initiation, Translational, Plant Proteins
Terpenes, Acyclic Monoterpenes, Escherichia coli Proteins, Recombinant Fusion Proteins, Geranyltranstransferase, Carbon-Carbon Double Bond Isomerases, Carotenoids, High-Throughput Screening Assays, Substrate Specificity, Hemiterpenes, Metabolic Engineering, Polyisoprenyl Phosphates, Mutagenesis, Escherichia coli, Directed Molecular Evolution, Peptide Chain Initiation, Translational, Plant Proteins
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