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• W2562613841 abstract "β-Methyltryptophans (β-mTrp) are precursors in the biosynthesis of bioactive natural products and are used in the synthesis of peptidomimetic-based therapeutics. Currently β-mTrp is produced by inefficient multistep synthetic methods. Here we demonstrate how an engineered variant of tryptophan synthase from Salmonella (StTrpS) can catalyse the efficient condensation of l-threonine and various indoles to generate β-mTrp and derivatives in a single step. Although l-serine is the natural substrate for TrpS, targeted mutagenesis of the StTrpS active site provided a variant (βL166V) that can better accommodate l-Thr as a substrate. The condensation of l-Thr and indole proceeds with retention of configuration at both α- and β-positions to give (2S,3S)-β-mTrp. The integration of StTrpS (βL166V) with l-amino acid oxidase, halogenase enzymes and palladium chemocatalysts provides access to further d-configured and regioselectively halogenated or arylated β-mTrp derivatives." @default.
• W2562613841 created "2017-01-06" @default.
• W2562613841 creator A5040446294 @default.
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• W2562613841 date "2017-01-20" @default.
• W2562613841 modified "2023-09-25" @default.
• W2562613841 title "An Engineered Tryptophan Synthase Opens New Enzymatic Pathways to β-Methyltryptophan and Derivatives" @default.
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• W2562613841 doi "https://doi.org/10.1002/cbic.201600471" @default.
• W2562613841 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/28005309" @default.
• W2562613841 hasPublicationYear "2017" @default.
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