| Literature DB >> 24675224 |
Gustav Rehn1, Patrick Adlercreutz2, Carl Grey3.
Abstract
An attractive option to produce chiral amines of industrial importance is through asymmetric synthesis using ω-transaminase. However, reaching high yields often requires a strategy for shifting the equilibrium position. This paper describes a novel strategy for handling this problem. It involves the use of a supported liquid membrane (SLM) together with a packed bed reactor. The reactor contains Escherichia coli cells with ω-transaminase from Arthrobacter citreus, immobilized by flocculation with chitosan. The SLM consists of a hollow fibre membrane contactor in which the pores contain undecane. The system enables continuous extraction of the amine product and was used to successfully shift the equilibrium in asymmetric synthesis of (S)-α-methylbenzylamine (MBA). A conversion of 98% was reached, compared to 50% without product extraction. Moreover, a selective extraction of the produced MBA was realized. A high product concentration of 55g/l was reached after 80h, and the system showed promising potential for continuous operation.Entities:
Keywords: Asymmetric synthesis; Chiral amines; In situ product removal; Supported liquid membrane; ω-Transaminase
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Year: 2014 PMID: 24675224 DOI: 10.1016/j.jbiotec.2014.03.022
Source DB: PubMed Journal: J Biotechnol ISSN: 0168-1656 Impact factor: 3.307