Polar Substitutions on the Surface of a Lipase Substantially Improve Tolerance in Organic Solvents
Year: 2022
Type: article
Abstract: Biocatalysis in organic solvents (OSs) enables more efficient routes to the synthesis of various valuable chemicals. However, OSs often reduce enzymatic activity, which limits the use of enzymes in OSs. Herein, we report a comprehensive understanding of interactions between surface polar substitutions and DMSO by integrating molecular dynamics (MD) simulations of 45 variants from Bacillus subtilis lipase A (BSLA) and substitution landscape into a "BSLA-SSM" library. By systematically analyzing 39 structural-, solvation-, and interaction energy-based observables, we discovered that hydration shell maintenance, DMSO reduction, and decreased local flexibility simultaneously govern the stability of polar variants in OS. Moreover, the fingerprints of 1631 polar-related variants in three OSs demonstrated that substituting aromatic to polar amino acid(s) hold great potential to highly improve OSs resistance. Hence, surface polar engineering is a powerful strategy to generate OS-tolerant lipases and other enzymes, thereby adapting the catalyst to the desired reaction and process with OSs.
Source: ChemSusChem
Institutions: University of Illinois Urbana-Champaign, DWI – Leibniz Institute for Interactive Materials, Carl R. Woese Institute for Genomic Biology, RWTH Aachen University, Chinese Academy of Sciences, Tianjin Institute of Industrial Biotechnology, Forschungszentrum Jülich, Heinrich Heine University Düsseldorf, Leibniz Institute of Plant Biochemistry
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: hybrid
Estimated APC paid: $4,000
Funder: RWTH Aachen University
Awards: G2697667961, G4279169786
OpenAlex ID: W4205429358
