Biological and Medicinal Chemistry

Active site remodelling of a cyclodipeptide synthase redefines substrate scope

Authors

Abstract

Cyclodipeptide synthases (CDPSs) generate a wide range of cyclic dipeptides using aminoacylated tRNAs as substrates. Histidine-containing cyclic dipeptides have important biological activities as anticancer and neuroprotective molecules. Out of the 120 experimentally validated CDPS members, only two are known to accept histidine as a substrate yielding cyclo(His-Phe) and cyclo(His-Pro) as products. It is not fully understood how CDPSs select their substrates, and we must rely on bioprospecting to find new enzymes and novel bioactive cyclic dipeptides. Here, we generated an extensive library of molecules using canonical and non-canonical amino acids as substrates, expanding the chemical space of histidine-containing cyclic dipeptide analogues. To investigate substrate selection we determined the structure of a cyclo(His-Pro)-producing CDPS. Three consecutive generations harbouring single, double and triple residue substitutions elucidated the histidine selection mechanism. Moreover, substrate selection was redefined, yielding enzyme variants that became capable of utilising phenylalanine and leucine. Our work pioneers the successful engineering a CDPS to yield different products, paving the way to direct the promiscuity of these enzymes to produce molecules of our choosing.

Version notes

new data on more mutants added

Content

Thumbnail image of 040322-Sutherland_et-al-Manuscript-Final.pdf

Supplementary material

Thumbnail image of 04032022-Sutherland_et_al-SI-Final.pdf
SI for "Active site remodelling of a cyclodipeptide synthase redefines substrate scope"
Supplementary information includes materials and methods.