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Chem Commun (Camb) ; 53(91): 12274-12277, 2017 Nov 14.
Article in English | 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.


Subject(s)
Ligases/metabolism , Proline/metabolism , Thiazoles/metabolism , Biocatalysis , Proline/chemistry , Substrate Specificity , Thiazoles/chemistry
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