- Select a language for the TTS:
- UK English Female
- UK English Male
- US English Female
- US English Male
- Australian Female
- Australian Male
- Language selected: (auto detect) - EN
Play all audios:
Access through your institution Buy or subscribe Enzymes efficiently catalyze numerous reactions, but re-engineering them to speed up reactions that are not known in nature is challenging.
Lanthanides, particularly cerium complexes, have previously been used in photocatalytic transformations that proceed via radical species. However, these radical reactions are rarely
stereoselective. In an effort to address this, Klein, Leiss-Maier et al. developed a lanthanide-binding enzyme by adding four glutamates in the center of a computationally designed protein
scaffold. The resulting enzyme — which they called PhotoLanZyme 1.0 (PLZ1.0) — catalyzes radical C-C bond cleavage of 1,2-diols in the presence of cerium(III) chloride and visible light. To
improve the photostability and metal binding kinetics, the team further engineered the photoenzyme by mutating tryptophans near the lanthanide binding site and introducing mutations to the
protein surface to minimize unspecific cerium binding. The final variant, PLZ1.4, could catalyze cleavage of several aromatic substituted diols in a diastereoselective manner, as well as
cleavage of aromatic lignin model compounds. Using a fusion construct of PLZ1.1 with a Lpp–OmpA sequence (previously used for surface display of artificial metalloenzymes), the team
established a whole-cell biocatalytic system for degradation of lignin model compounds in _Escherichia coli_. Finally, they demonstrated the applicability of natural lanthanide-dependent
enzymes for cerium photoredox catalysis using alcohol dehydrogenase PedH from _Pseudomonas putida_ KT2440, which requires the redox cofactor pyrroloquinoline quinone (PQQ) and a lanthanide
ion for the reaction. The enzyme was expressed and reconstituted without PQQ. In the presence of cerium(III) chloride and light, PedH could catalyze diol cleavage. This study opens new
avenues for engineering of artificial enzymes that can catalyze lanthanide-mediated photoredox reactions. This is a preview of subscription content, access via your institution ACCESS
OPTIONS Access through your institution Access Nature and 54 other Nature Portfolio journals Get Nature+, our best-value online-access subscription $29.99 / 30 days cancel any time Learn
more Subscribe to this journal Receive 12 print issues and online access $259.00 per year only $21.58 per issue Learn more Buy this article * Purchase on SpringerLink * Instant access to
full article PDF Buy now Prices may be subject to local taxes which are calculated during checkout ADDITIONAL ACCESS OPTIONS: * Log in * Learn about institutional subscriptions * Read our
FAQs * Contact customer support AUTHOR INFORMATION AUTHORS AND AFFILIATIONS * Nature Communications https://www.nature.com/ncomms/ Majda Bratovič Authors * Majda Bratovič View author
publications You can also search for this author inPubMed Google Scholar CORRESPONDING AUTHOR Correspondence to Majda Bratovič. RIGHTS AND PERMISSIONS Reprints and permissions ABOUT THIS
ARTICLE CITE THIS ARTICLE Bratovič, M. A cerium-dependent photoenzyme. _Nat Chem Biol_ 20, 1387 (2024). https://doi.org/10.1038/s41589-024-01767-2 Download citation * Published: 22 October
2024 * Issue Date: November 2024 * DOI: https://doi.org/10.1038/s41589-024-01767-2 SHARE THIS ARTICLE Anyone you share the following link with will be able to read this content: Get
shareable link Sorry, a shareable link is not currently available for this article. Copy to clipboard Provided by the Springer Nature SharedIt content-sharing initiative