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A Tandem Enzymatic sp2 -C-Methylation Process: Coupling in Situ S-Adenosyl-l-Methionine Formation with Methyl Transfer.
Sadler, Joanna C; Humphreys, Luke D; Snajdrova, Radka; Burley, Glenn A.
Afiliação
  • Sadler JC; GlaxoSmithKline Medicines Research Centre, Gunnels Wood Road, Stevenage, SG1 2NY, UK.
  • Humphreys LD; WestCHEM, Department of Pure and Applied Chemistry, University of Strathclyde, 295 Cathedral Street, Glasgow, G1 1XL, UK.
  • Snajdrova R; GlaxoSmithKline Medicines Research Centre, Gunnels Wood Road, Stevenage, SG1 2NY, UK.
  • Burley GA; Present address: Gilead Alberta ULC, 1021 Hayter Road NW, Edmonton, AB, T6S 1A1, Canada.
Chembiochem ; 18(11): 992-995, 2017 06 01.
Article em En | MEDLINE | ID: mdl-28371017
A one-pot, two-step biocatalytic platform for the regiospecfic C-methylation and C-ethylation of aromatic substrates is described. The tandem process utilises SalL (Salinospora tropica) for in situ synthesis of S-adenosyl-l-methionine (SAM), followed by alkylation of aromatic substrates by the C-methyltransferase NovO (Streptomyces spheroides). The application of this methodology is demonstrated for the regiospecific labelling of aromatic substrates by the transfer of methyl, ethyl and isotopically labelled 13 CH3,13 CD3 and CD3 groups from their corresponding SAM analogues formed in situ.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: S-Adenosilmetionina / Metiltransferases Idioma: En Revista: Chembiochem Assunto da revista: BIOQUIMICA Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: S-Adenosilmetionina / Metiltransferases Idioma: En Revista: Chembiochem Assunto da revista: BIOQUIMICA Ano de publicação: 2017 Tipo de documento: Article