The combination of enzymatic and chemical reaction steps is one important area of research in organic synthesis, preferentially as cascade reactions in one-pot to improve total conversion and achieve high operational stability. Here, the combination of the Suzuki-Miyaura reaction is described to synthesize biaryl compounds followed by a transamination reaction. Careful optimization of the reaction conditions required for the chemo- and biocatalysis reaction enabled an efficient two-step-one-pot reaction yielding the final chiral amines with excellent optical purity (>99 % ee) in up to 84 % total conversion. Key to the success was the protein engineering of the amine transaminases from Asperguillus fumigatus (4CHI-TA) where single alanine mutations increased the conversion up to 2.3-fold. Finally, the transfer to a continuous flow system after immobilization of the best 4CHI-TA variant is demonstrated.
Sustainability in chemistry heavily relies on heterogeneous catalysis. Enzymes, the main catalyst for biochemical reactions in nature, are an elegant choice to catalyze reactions due to their high activity and selectivity, although they usually suffer from lack of robustness. To overcome this drawback, enzyme‐decorated nanoporous heterogeneous catalysts were developed. Three different approaches for Candida antarctica lipase B (CAL‐B) immobilization on a covalent organic framework (PPF‐2) were employed: physical adsorption on the surface, covalent attachment of the enzyme in functional groups on the surface and covalent attachment into a linker added post‐synthesis. The influence of the immobilization strategy on the enzyme uptake, specific activity, thermal stability, and the possibility of its use through multiple cycles was explored. High specific activities were observed for PPF‐2‐supported CAL‐B in the esterification of oleic acid with ethanol, ranging from 58 to 283 U mg−1, which was 2.6 to 12.7 times greater than the observed for the commercial Novozyme 435.
BACKGROUND: In this work, lipase B from Candida antarctica (CaLB) was immobilized on Purolite ® ECR8205F, Purolite ® ECR8214F and Immobead ® IB150 P epoxy resins with no modification to their surfaces. Biocatalysts were evaluated for thermal stability and applied in reactions of hydrolysis, esterification and the synthesis of glyceryl carbonate by transesterification with dimethyl-carbonate both with glycerol and Macauba oil as well as dynamic kinetic resolution of -methylbenzylamine, all of them compared with commercial Novozyme 435 ® .
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