Peptiligase, an Enzyme for Efficient Chemoenzymatic Peptide Synthesis and Cyclization in Water
We describe a novel, organic cosolvent‐stable and cation‐independent engineered enzyme for peptide coupling reactions. The enzyme is a variant of a stable calcium‐independent mutant of subtilisin BPN′, with the catalytic Ser212 mutated to Cys and Pro216 converted to Ala. The enzyme, called peptiliga...
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Published in | Advanced synthesis & catalysis Vol. 358; no. 13; pp. 2140 - 2147 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Weinheim
WILEY-VCH Verlag
30.06.2016
WILEY‐VCH Verlag Wiley |
Subjects | |
Online Access | Get full text |
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Summary: | We describe a novel, organic cosolvent‐stable and cation‐independent engineered enzyme for peptide coupling reactions. The enzyme is a variant of a stable calcium‐independent mutant of subtilisin BPN′, with the catalytic Ser212 mutated to Cys and Pro216 converted to Ala. The enzyme, called peptiligase, catalyzes exceptionally efficient peptide coupling in water with a surprisingly high synthesis over hydrolysis (S/H) ratio. The S/H ratio of the peptide ligation reaction is correlated to the length of the peptide substrate and proved to be >100 for the synthesis of a 13‐mer peptide, which corresponds to >99% conversion to the ligated peptide product and <1% hydrolytic side‐reaction. Furthermore, peptiligase does not require a particular recognition motif resulting in a broadly applicable and traceless peptide ligation technology. Peptiligase is very robust, easy to produce in Bacillus subtilis, and its purification is straightforward. It shows good activity and stability in the presence of organic cosolvents and chelating or denaturing agents, enabling the ligation of poorly soluble (hydrophobic) or folded peptides. This enzyme could be useful for the (industrial) synthesis of diverse (pharmaceutical) peptides. In addition, peptiligase is able to efficiently catalyze head‐to‐tail peptide cyclization reactions. |
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Bibliography: | Advanced Chemical Technologies for Sustainability (ACTS) ArticleID:ADSC201600017 The Netherlands Organisation for Scientific Research (NWO) ark:/67375/WNG-N546D01Z-7 istex:6A344B00EA0FAE7ABB78E6C133882130B23BA56C Integration of Biosynthesis and Organic Synthesis program - No. IBOS-2; program number: 053.63.014 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1615-4150 1615-4169 |
DOI: | 10.1002/adsc.201600017 |