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Inhibitory Effect of DMSO on Halohydrin Dehalogenase: Experimental and Computational Insights into the Influence of an Organic Co-solvent on the Structural and Catalytic Properties of a Biocatalyst
Authors:Nevena Mil?i?  Dr Vi?nja Stepani?  Dr Ivo Crnolatac  Prof Zvjezdana Findrik Bla?evi?  Dr Zlatko Brklja?a  Dr Maja Majeri? Elenkov
Institution:1. Faculty of Chemical Engineering and Technology, University of Zagreb, Savska c. 16, 10000 Zagreb, Croatia;2. Laboratory for Machine Learning and Knowledge Representation, Ru?er Bo?kovi? Institute, Bijeni?ka c. 54, 10000 Zagreb, Croatia;3. Division of Organic Chemistry and Biochemistry, Ru?er Bo?kovi? Institute, Bijeni?ka c. 54, 10000 Zagreb, Croatia
Abstract:Although the application of organic solvents in biocatalysis is well explored, in-depth understanding of the interactions of solvent with proteins, in particular oligomeric ones, is still scant. Understanding these interactions is essential in tailoring enzymes for industrially relevant catalysis in nonaqueous media. In our study, the homotetrameric enzyme halohydrin dehalogenase (HHDH) from Agrobacterium radiobacter AD1 (HheC) was investigated, as a model system, in DMSO/water solvent mixtures. DMSO, the most commonly used co-solvent for biocatalytic transformations, was found to act as a mixed-type inhibitor with a prevalent competitive contribution. Even 5 % (v/v) DMSO inhibits the activity of HheC by half. Molecular dynamics (MD) simulations showed that DMSO keeps close to Ser-Tyr catalytic residues forming alternate H-bonds with them. Stability measurements paired with differential scanning calorimetry, dynamic light scattering methods and MD studies revealed that HheC maintains its structural integrity with as much as 30 % (v/v) DMSO.
Keywords:activity  biocatalysis  DMSO  halohydrin dehalogenase  molecular dynamics
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