A tandem enzymatic sp2-C-methylation process : coupling in situ S-adenosyl-L-methionine formation with methyl transfer
Sadler, Joanna C and Humphreys, Luke D and Burley, Glenn and Snajdrova, Radka (2017) A tandem enzymatic sp2-C-methylation process : coupling in situ S-adenosyl-L-methionine formation with methyl transfer. Chembiochem. ISSN 1439-4227 (https://doi.org/10.1002/cbic.201700115)
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Abstract
A one-pot, two-step biocatalytic platform for the regiospecfic C-methylation and C-ethylation of aromatic substrates is described. The tandem process utilizes SalL (Salinospora tropica) for in situ synthesis of S-adenosyl-L-methionine (SAM), followed by alkylation of aromatic substrates using the C-methyltransferase NovO (Streptomyces spheroides). Application of this methodology is demonstrated by the regiospecific labelling of aromatic substrates via the transfer of methyl, ethyl and isotopically-labelled 13CH3, 13CD3 and CD3 groups from their corresponding SAM analogues formed in situ.
ORCID iDs
Sadler, Joanna C
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Item type: Article ID code: 60384 Dates: DateEvent31 March 2017Published31 March 2017Published Online31 March 2017AcceptedNotes: This is the peer reviewed version of the following article: Sadler, J. C., Humphreys, L. D., Burley, G., & Snajdrova, R. (2017). A tandem enzymatic sp2-C-methylation process: coupling in situ S-adenosyl-L-methionine formation with methyl transfer. Chembiochem, which has been published in final form at https://doi.org/10.1002/cbic.201700115. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving. Subjects: Science > Chemistry Department: Faculty of Science > Pure and Applied Chemistry
Technology and Innovation Centre > BionanotechnologyDepositing user: Pure Administrator Date deposited: 03 Apr 2017 11:04 Last modified: 02 Feb 2025 12:23 URI: https://strathprints.strath.ac.uk/id/eprint/60384