Scherkus, ChristianChristianScherkusSchmidt, SandySandySchmidtBornscheuer, Uwe TheoUwe TheoBornscheuerGröger, HaraldHaraldGrögerKara, SelinSelinKaraLiese, AndreasAndreasLiese2020-02-112020-02-112016-11-22ChemCatChem 22 (8): 3446-3452 (2016-11-22)http://hdl.handle.net/11420/4880A three-step enzymatic reaction sequence for the synthesis of poly-ϵ-caprolactone (PCL) was designed running in a fed-batch operation. The first part of the cascade consisted of two oxidation steps starting with alcohol dehydrogenase catalyzed oxidation from cyclohexanol to cyclohexanone and further oxidation to ϵ-caprolactone (ECL) by means of a Baeyer–Villiger monooxygenase. As a third step, lipase-catalyzed hydrolysis of the lactone to 6-hydroxyhexanoic acid (6-HHA) was designed. With this biocatalytic multistep process reported herein, severe substrate surplus and product inhibition could be circumvented by the fed-batch operation by adding the cyclohexanol substrate and by in situ product removal of ECL by hydrolysis, respectively. Up to 283 mm product concentration of 6-HHA was reached in the fed-batch operated process without loss in productivity within 20 h. After extraction and subsequent polymerization catalyzed by Candida antarctica lipase B, analysis of the unfractionated polymer revealed a bimodal distribution of the polymer population, which reached a mass average molar mass (Mw) value of approximately 63 000 g mol−1 and a dispersity (Mw/Mn) of 1.1 for the higher molecular weight population, which thus revealed an alternative route to the conventional synthesis of PCL.en1867-388020162234463452enzymatic cascadeenzymesoxidoreductasespolymerizationϵ-caprolactoneJournal Article10.1002/cctc.201600806Other