Publication | Closed Access
Engineered biosynthesis of hybrid macrolide polyketides containing d-angolosamine and d-mycaminose moieties
29
Citations
39
References
2008
Year
Bioorganic ChemistryEngineeringD-mycaminose MoietiesGlycobiologyMolecular BiologyCarbohydrate-protein InteractionEnzymatic ModificationHybrid Macrolide PolyketidesBiosynthesisNatural Product BiosynthesisGlycosylationSynthetic MacromoleculeActivated DeoxysugarsBiochemistryBioconjugationNatural Product ScaffoldsNatural Product SynthesisBiomolecular EngineeringNatural SciencesBiotechnologySynthetic BiologyBroad Substrate ToleranceSynthetic Chemistry
The glycosylation of natural product scaffolds with highly modified deoxysugars is often essential for their biological activity, being responsible for specific contacts to molecular targets and significantly affecting their pharmacokinetic properties. In order to provide tools for the targeted alteration of natural product glycosylation patterns, significant strides have been made to understand the biosynthesis of activated deoxysugars and their transfer. We report here efforts towards the production of plasmid-borne biosynthetic gene cassettes capable of producing TDP-activated forms of D-mycaminose, D-angolosamine and D-desosamine. We additionally describe the transfer of these deoxysugars to macrolide aglycones using the glycosyl transferases EryCIII, TylMII and AngMII, which display usefully broad substrate tolerance.
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