| Literature DB >> 20083145 |
Kyoungseon Min1, Don-Hee Park, Young Je Yoo.
Abstract
Parkinson's disease is caused by a deficiency of the neurotransmitter dopamine. Since l-DOPA (l-3,4-dihydroxyphenylalanine) is a precursor of dopamine and can pass across the blood-brain barrier, it has been used as a treatment for Parkinson's disease. Hundreds tons of l-DOPA are produced per year, and most of the current supply is produced by a chemical method of asymmetric synthesis. However, the chemical process for l-DOPA synthesis requires an expensive metal catalyst and shows low conversion rates and low enantioselectivity. In this study, we developed a novel technology for the production of l-DOPA, an electroenzymatic synthesis with a tyrosinase-immobilized cathode under the reduction potential of DOPAquinone, which is -530 mV. Compared to other approaches for l-DOPA synthesis reported previously, this electroenzymatic system showed the highest conversion rate and a highly enhanced productivity of up to 95.9% and 47.27 mg l(-1)h(-1), respectively. Copyright 2010 Elsevier B.V. All rights reserved.Entities:
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Year: 2010 PMID: 20083145 DOI: 10.1016/j.jbiotec.2010.01.002
Source DB: PubMed Journal: J Biotechnol ISSN: 0168-1656 Impact factor: 3.307