کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
69969 | 48804 | 2013 | 4 صفحه PDF | دانلود رایگان |

Although l-DOPA (l-3,4-dihydroxyphenylalanine) is widely used as a drug for Parkinson's disease, there are critical drawbacks in the commercial synthetic method such as low conversion rate, poor productivity, and long operational time. In order to overcome these limitations, a novel electroenzymatic system using tyrosinase/carbon nanopowder/polypyrrole composite as a working cathode was reported with the outstanding conversion rate up to 95.9%. However, the productivity was still limited due to a low solubility of the substrate l-tyrosine in aqueous phase. Herein, we demonstrated a novel strategy for enhancing the productivity by employing well-dispersed l-tyrosine as the substrate. When using well-dispersed l-tyrosine, not only the concentration of the substrate was increased to 90.6 gL−1 in aqueous phase but also the productivity was enhanced up to 15.3 gL−1 h−1. We also determined kinetic parameters in the electroenzymatic system and the kinetic results revealed that the outstanding conversion rate was based on the fast electrical reduction of the by-product to l-DOPA. Thus the electroenzymatic synthesis using well-dispersed l-tyrosine can be a potential candidate as a novel process for l-DOPA synthesis.
Figure optionsDownload as PowerPoint slideHighlights
► Well-dispersed l-tyrosine was prepared by wet-milling method and used as the substrate for l-DOPA synthesis in electroenzymatic system.
► Using well-dispersed l-tyrosine, we overcame solubility limitation in aqueous phase and the concentration was increased up to 500 mM.
► Consequently, the productivity was increased from 0.39 gL−1 h−1to 15.3 gL−1 h−1 in the electroenzymatic system for l-DOPA synthesis.
► Kinetic study and current response during the reaction revealed the reason for the outstanding conversion rate in the electroenzymatic system.
Journal: Journal of Molecular Catalysis B: Enzymatic - Volume 90, June 2013, Pages 87–90