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Engineered biosynthesis of novel spinosyns bearing altered deoxyhexose substituentsElectronic supplementary information (ESI) available: 1H and 13C NMR data for compounds 5–8. See http://www.rsc.org/suppdata/cc/b2/b200536k/
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References
2002
Year
Bioorganic ChemistryEngineeringGlycobiologyMolecular BiologyNovel Spinosyns BearingBeta-d-forosamine MoietyChemical BiologyRedox BiologyNovel SpinosynsBiosynthesisMetabolic EngineeringNatural Product BiosynthesisCompounds 5–8GlycosylationBiotransformationBiochemistryHydroxy GroupBiocatalysisBiomolecular EngineeringNmr DataNatural SciencesBiotechnologySynthetic BiologyDeoxygenation
Novel spinosyns have been prepared by biotransformation, using a genetically engineered strain of Saccharopolyspora erythraea, in which the beta-D-forosamine moiety in glycosidic linkage to the hydroxy group at C17 is replaced by alpha-L-mycarose.
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