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Bypassing the proline/thiazoline requirement of the macrocyclase PatG.
Oueis, E; Stevenson, H; Jaspars, M; Westwood, N J; Naismith, J H.
Afiliación
  • Oueis E; Biomedical Science Research Complex & School of Chemistry, University of St Andrews, BSRC, North Haugh, St Andrews, KY16 9ST, UK. naismith@strubi.ox.ac.uk.
Chem Commun (Camb) ; 53(91): 12274-12277, 2017 Nov 14.
Article en En | MEDLINE | ID: mdl-29090689
ABSTRACT
Biocatalysis is a fast developing field in which an enzyme's natural capabilities are harnessed or engineered for synthetic chemistry. The enzyme PatG is an extremely promiscuous macrocyclase enzyme tolerating both non-natural amino acids and non-amino acids within the substrate. It does, however, require a proline or thiazoline at the C-terminal position of the core peptide which means the final product must contain this group. Here, we show guided by structural insight we have identified two synthetic routes, triazole and a double cysteine, that circumvent this requirement. With the triazole, we show PatGmac can macrocyclise substrates that do not contain any amino acids in the final product.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Tiazoles / Prolina / Ligasas Idioma: En Revista: Chem Commun (Camb) Asunto de la revista: QUIMICA Año: 2017 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Tiazoles / Prolina / Ligasas Idioma: En Revista: Chem Commun (Camb) Asunto de la revista: QUIMICA Año: 2017 Tipo del documento: Article País de afiliación: Reino Unido