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A multistep (semi)-continuous biocatalytic setup for the production of polycaprolactone.
Valotta, Alessia; Stelzer, Daniela; Reiter, Tamara; Kroutil, Wolfgang; Gruber-Woelfler, Heidrun.
Afiliación
  • Valotta A; Institute of Process and Particle Engineering, Graz University of Technology Inffeldgasse 13 8010 Graz Austria valotta@tugraz.at woelfler@tugraz.at.
  • Stelzer D; Institute of Process and Particle Engineering, Graz University of Technology Inffeldgasse 13 8010 Graz Austria valotta@tugraz.at woelfler@tugraz.at.
  • Reiter T; Department of Chemistry, NAWI Graz, BioTechMed Graz, Field of Excellence BioHealth, University of Graz Heinrichstrasse 28 8010 Graz Austria.
  • Kroutil W; Department of Chemistry, NAWI Graz, BioTechMed Graz, Field of Excellence BioHealth, University of Graz Heinrichstrasse 28 8010 Graz Austria.
  • Gruber-Woelfler H; Institute of Process and Particle Engineering, Graz University of Technology Inffeldgasse 13 8010 Graz Austria valotta@tugraz.at woelfler@tugraz.at.
React Chem Eng ; 9(3): 713-727, 2024 Feb 29.
Article en En | MEDLINE | ID: mdl-38433980
ABSTRACT
Biocatalysis has gained increasing importance as an eco-friendly alternative for the production of bulk and fine chemicals. Within this paradigm, Baeyer Villiger monoxygenases (BVMOs) serve as enzymatic catalysts that provide a safe and sustainable route to the conventional synthesis of lactones, such as caprolactone, which is employed for the production of polycaprolactone (PCL), a biocompatible polymer for medicinal applications. In this work, we present a three-step, semi-continuous production of PCL using an entirely biocatalytic process, highlighting the merits of continuous manufacturing for enhancing biocatalysis. First, caprolactone is produced in batch from cyclohexanol using a coenzymatic cascade involving an alcohol dehydrogenase (ADH) and BVMO. Different process parameters and aeration modes were explored to optimize the cascade's productivity. Secondly, the continuous extraction of caprolactone into an organic solvent, needed for the polymerization step, was optimized. 3D-printed mixers were applied to enhance the mass transfer between the organic and the aqueous phases. Lastly, we investigated the ring-opening polymerization of caprolactone to PCL catalyzed by Candida antarctica lipase B (CAL-B), with a focus on eco-friendly solvents like cyclopentyl-methyl-ether (CPME). Space-time-yields up to 58.5 g L-1 h-1 were achieved with our overall setup. By optimizing the individual process steps, we present an efficient and sustainable pathway for PCL production.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: React Chem Eng Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: React Chem Eng Año: 2024 Tipo del documento: Article