TY - JOUR
T1 - A study on the electrochemical synthesis of L-DOPA using oxidoreductase enzymes
T2 - Optimization of an electrochemical process
AU - Rahman, Siti Fauziyah
AU - Gobikrishnan, Sriramulu
AU - Indrawan, Natarianto
AU - Park, Seok Hwan
AU - Park, Jae Hee
AU - Min, Kyoungseon
AU - Yoo, Young Je
AU - Park, Don Hee
PY - 2012/10
Y1 - 2012/10
N2 - Levodopa or L-3,4-dihydroxyphenylalanine (L-DOPA) is the precursor of the neurotransmitter dopamine. L-DOPA is a famous treatment for Parkinson's disease symptoms. In this study, electroenzymatic synthesis of L-DOPA was performed in a three-electrode cell, comprising a Ag/AgCl reference electrode, a platinum wire auxiliary electrode, and a glassy carbon working electrode. L-DOPA had an oxidation peak at 376 mV and a reduction peak at-550 mV. The optimum conditions of pH, temperature, and amount of free tyrosinase enzyme were pH 7, 30°C, and 250 IU, respectively. The kinetic constant of the free tyrosinase enzyme was found for both cresolase and catacholase activity to be 0.25 and 0.4 mM, respectively. A cyclic voltammogram was used to investigate the electron transfer rate constant. The mean heterogeneous electron transfer rate (ke) was 5.8 × 10-4cm/s. The results suggest that the electroenzymatic method could be an alternative way to produce L-DOPA without the use of a reducing agent such as ascorbic acid.
AB - Levodopa or L-3,4-dihydroxyphenylalanine (L-DOPA) is the precursor of the neurotransmitter dopamine. L-DOPA is a famous treatment for Parkinson's disease symptoms. In this study, electroenzymatic synthesis of L-DOPA was performed in a three-electrode cell, comprising a Ag/AgCl reference electrode, a platinum wire auxiliary electrode, and a glassy carbon working electrode. L-DOPA had an oxidation peak at 376 mV and a reduction peak at-550 mV. The optimum conditions of pH, temperature, and amount of free tyrosinase enzyme were pH 7, 30°C, and 250 IU, respectively. The kinetic constant of the free tyrosinase enzyme was found for both cresolase and catacholase activity to be 0.25 and 0.4 mM, respectively. A cyclic voltammogram was used to investigate the electron transfer rate constant. The mean heterogeneous electron transfer rate (ke) was 5.8 × 10-4cm/s. The results suggest that the electroenzymatic method could be an alternative way to produce L-DOPA without the use of a reducing agent such as ascorbic acid.
KW - Electrochemical synthesis
KW - L-DOPA
KW - Parkinson's disease
KW - Tyrosinase
UR - http://www.scopus.com/inward/record.url?scp=84930482656&partnerID=8YFLogxK
U2 - 10.4014/jmb.1206.06043
DO - 10.4014/jmb.1206.06043
M3 - Article
C2 - 23075798
AN - SCOPUS:84930482656
SN - 1017-7825
VL - 22
SP - 1446
EP - 1451
JO - Journal of Microbiology and Biotechnology
JF - Journal of Microbiology and Biotechnology
IS - 10
ER -