Chemistry - A European Journal · 2023 · 14 citations · 44 references
Life SciencesBiochemistryMicrobiologyEnzymologyMicrobial MetabolismNatural Product BiosynthesisCatalytic MechanismsEnzyme-substrate RecognitionMicrobial Metabolite ProductionMicrobial Natural Product BiosynthesisTerpenoid BiosynthesisActive Compound IsolationChemical LabellingDe Novo Structure ElucidationDiterpene BiosynthesisEnzymesMonoterpene BiosynthesisTerpene SynthasesTerpenoid Cyclization Mechanisms
Two homologs of the diterpene synthase CotB2 from Streptomyces collinus (ScCotB2) and Streptomyces iakyrus (SiCotB2) were investigated for their products by in vitro incubations of the recombinant enzymes with geranylgeranyl pyrophosphate, followed by compound isolation and structure elucidation by NMR. ScCotB2 produced the new compound collinodiene, besides the canonical CotB2 product cyclooctat-9-en-7-ol, dolabella-3,7,18-triene and dolabella-3,7,12-triene, while SiCotB2 gave mainly cyclooctat-9-en-7-ol and only traces of dolabella-3,7,18-triene. The cyclisation mechanism towards the ScCotB2 products and their absolute configurations were investigated through isotopic labelling experiments.
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Gregory R. Fulmer, Alexander J. M. Miller, Nathaniel H. Sherden et al. · Organometallics · 2010 · 3.9K citations
Studies on the Biosynthesis of Cholesterol
J. W. Cornforth, Rita H. Cornforth, G. Popják et al. · Journal of Biological Chemistry · 1966 · 228 citations · Full text