TY - JOUR
T1 - Effect of water activity control on the catalytic performance of surfactant - Arthromyces ramosus peroxidase complex in toluene
AU - Kamiya, Noriho
AU - Nagamune, Teruyuki
N1 - Funding Information:
We are grateful to Suntry for providing ARP sample. We also thank Prof. Sakayu Shimizu of Kyoto University for his useful comments on the characteristics of ARP. Mr. Masahito Inoue and Prof. Masahiro Goto of Kyushu University are appreciated for providing a synthetic surfactant. This work was supported by the Proposal-based New Industry Creative Type Technology R&D Promotion Program from the New Energy and Industrial Technology Development Organization (NEDO) of Japan.
PY - 2002
Y1 - 2002
N2 - Arthromyces ramosus peroxidase (ARP) was successfully modified with a synthetic surfactant for one-electron oxidation reaction of a hydrophobic substrate in toluene. Although UV-visible absorption spectrum of surfactant-ARP complex in toluene showed slight red shift of Soret band compared to that in water, the complex can catalyze oxidation reaction of o-phenylenediamine (o-PDA) with hydrogen peroxide. It appeared that thermodynamic water activity in the reaction system has dominant effect on either the catalytic activity or the stability in the catalytic cycle. Steady-state kinetics under the optimal condition revealed that the specific constant (kcat/Km) of ARP complex for o-PDA was 2 orders of magnitude lower than that in aqueous media, while only 13-fold lower for hydrogen peroxide. The reduction of catalytic activity caused by altering the reaction media from water to toluene was found to be mainly due to the low specific constant of ARP complex for o-PDA rather than hydrogen peroxide.
AB - Arthromyces ramosus peroxidase (ARP) was successfully modified with a synthetic surfactant for one-electron oxidation reaction of a hydrophobic substrate in toluene. Although UV-visible absorption spectrum of surfactant-ARP complex in toluene showed slight red shift of Soret band compared to that in water, the complex can catalyze oxidation reaction of o-phenylenediamine (o-PDA) with hydrogen peroxide. It appeared that thermodynamic water activity in the reaction system has dominant effect on either the catalytic activity or the stability in the catalytic cycle. Steady-state kinetics under the optimal condition revealed that the specific constant (kcat/Km) of ARP complex for o-PDA was 2 orders of magnitude lower than that in aqueous media, while only 13-fold lower for hydrogen peroxide. The reduction of catalytic activity caused by altering the reaction media from water to toluene was found to be mainly due to the low specific constant of ARP complex for o-PDA rather than hydrogen peroxide.
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U2 - 10.1016/S1369-703X(01)00162-0
DO - 10.1016/S1369-703X(01)00162-0
M3 - Article
AN - SCOPUS:0036159141
SN - 1369-703X
VL - 10
SP - 55
EP - 59
JO - Biochemical Engineering Journal
JF - Biochemical Engineering Journal
IS - 1
ER -