The proposal applies for extented storage space for 2024/5-346 to be able to install protein design tools locally (including AlphaFold2). This extended storage would be needed for 2024/5-346 This project is funded by VR individual grant to Per-Olof Syrén, SSF, MISTRA and FORMAS. Published papers using NAISS 2023/5-232 3, and 1 paper under review. 1 patent The PI has been selected for interview for ERC consolidator grant and will now work full time during the summer to prepare for the interview in October 2024 using the resources applied for herein. The low use of allocated resources at KTH PDC from the previous round was due to parental leave of Per-Olof Syrén. The PI is back since mid April and ready to lead and perform work in this project. He will work the whole summer. The main goal of this research project is to construct novel green biocatalytic pathways for expedient generation of sustainable monomers and biomaterials from CO2. This will be achieved by retrofitting existing metalloenzymes - driven by computations - for new-to-nature chemistries for mild CO2 upcycling. CO2 is the most oxidized form of carbon and is inert towards further chemical transformations. Thus, harsh reaction conditions and high pressure has up to now been needed to activate CO2 and to enable its use as a chemical feedstock (Beller et al. Nat. Commun. 2015). This project will instead use enzymes as green catalysts to upcycle CO2 under mild conditions into platform chemicals with applications in polymers and additives to Lithium-ion battery electrolytes. Existing enzymes for CO2 upcycling are limited to (de)carboxylation and reduction chemistries, whereas applications in material science require formation of carbonates; a new type of transformation that is hitherto unknown in biology. Using computational methods, we will fill current gaps in available biocatalytic transformations to enable biosynthesis of carbonates from CO2. This will be achieved by implementing new reactions and mechanisms in existing metalloenzymes, such as carbonic anhydrase and decarboxylases so that they instead enable formation of carbonates. The proposed project utilizes quantum mechanical (QM) calculations to explore the chemistry that governs the new biological activity: high-level QM calculations will be used to elucidate the reaction mechanism and the resulted knowledge will be used to guide enzyme engineering efforts. Together, the project’s pipeline allows for generation of enzyme variants with improved catalytic properties in CO2 upcycling. Great progress was made in previous PDC-supported projects, as we unraveled how tertiary amide bonds undergo hydrolysis in nature by metallopeptidases. This demonstrates necessary expertise of the main applicant in performing state of the art quantum mechanical calculations on metalloenzymes (see e.g. Syrén et al. J. Org. Chem. 2018; J. Am. Chem. Soc. 2021 and Nat. Commun. 2023). It is envisaged that the present investigation centered on generating novel enzymatic reactions for CO2 upcycling will be of high value in industrial biotechnology and chemistry. .