Work

Functionally Diverse Peroxygenases by AlphaFold2, Design, and Signal Peptide Shuffling

Year: 2024
Type: article
Abstract: High Resolution Image Download MS PowerPoint Slide Unspecific peroxygenases (UPOs) are fungal enzymes that attract significant attention for their ability to perform versatile oxyfunctionalization reactions using H 2 O 2 . Unlike other oxygenases, UPOs do not require additional reductive equivalents or electron transfer chains that complicate basic and applied research. Nevertheless, UPOs generally exhibit low to no heterologous production levels and only four UPO structures have been determined to date by crystallography limiting their usefulness and obstructing research. To overcome this bottleneck, we implemented a workflow that applies PROSS stability design to AlphaFold2 model structures of 10 unique and diverse UPOs followed by a signal peptide shuffling to enable heterologous production. Nine UPOs were functionally produced in Pichia pastoris, including the recalcitrant Cci UPO and three UPOs derived from oomycetes─the first nonfungal UPOs to be experimentally characterized. We conclude that the high accuracy and reliability of new modeling and design workflows dramatically expand the pool of enzymes for basic and applied research.
Language: English
Open Access status: hybrid
Estimated APC paid: $4,500
OpenAlex ID: W4392744707
FWCI: 3.136
Cites: 69
Cited by: 23
Related to: 10