Applied and Environmental Microbiology · 2010 · 21 citations · 23 references
Life SciencesMicrobiologyMolecular BiologyMetabolic EngineeringMetabolismMicrobial MetabolismBacterial MetabolismCatalytic MechanismsMetabolic Pathway EngineeringMicrobial Metabolic EngineeringMicrobial Metabolite ProductionBacterial Glycan BiosynthesisBioconversion PathwaysEscherichia ColiHeterologous Expression SystemsHeterologous Gene ExpressionHexosamine Biosynthesis PathwayHydroxylationMicrobial Synthesis Pathways
In vivo reconstitution of the TDP-l-megosamine pathway from the megalomicin gene cluster of Micromonospora megalomicea was accomplished by the heterologous expression of its biosynthetic genes in Escherichia coli. Mass spectrometric analysis of the TDP-sugar intermediates produced from operons containing different sets of genes showed that the production of TDP-l-megosamine from TDP-4-keto-6-deoxy-d-glucose requires only five biosynthetic steps, catalyzed by MegBVI, MegDII, MegDIII, MegDIV, and MegDV. Bioconversion studies demonstrated that the sugar transferase MegDI, along with the helper protein MegDVI, catalyzes the transfer of l-megosamine to either erythromycin C or erythromycin D, suggesting two possible routes for the production of megalomicin A. Analysis in vivo of the hydroxylation step by MegK indicated that erythromycin C is the intermediate of megalomicin A biosynthesis.
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Molecular Cloning. A Laboratory Manual
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