Electrochemical regeneration of NADH using conductive vanadia-silica xerogels

被引:37
作者
Siu, Eulalia
Won, Keehoon
Park, Chan Beum
机构
[1] Korea Adv Inst Sci & Technol, Dept Mat Sci & Engn, Taejon 305701, South Korea
[2] Korea Res Inst Chem Technol, Taejon 305343, South Korea
[3] Arizona State Univ, Dept Chem & Mat Engn, Tempe, AZ 85287 USA
关键词
D O I
10.1021/bp060247l
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Electrically conductive sol-gel matrices have been first introduced in order to enhance the efficiency of electrochemical NADH regeneration systems for biocatalysis. Vanadia-silica mixed gels as conductive sol-gels were synthesized using vanadium (V) oxytripropoxide (VOTP) and tetramethyl orthosilicate (TMOS) as precursors. Direct electrochemical reductions of NAD(+) were carried out in the presence of vanadia-silica xerogels using unmodified platinum electrodes. Vanadia-silica gels from higher ratios of VOTP to TMOS could effectively improve electrochemical generations of NADH from NAD(+). Direct electrochemical regenerations of NADH were coupled to the synthesis of L-glutamate from alpha-ketoglutarate catalyzed by glutamate dehydrogenases (GDH). In this case, vanadia-silica gels were used as matrices for enzyme encapsulation, as opposed to serving as additives. When GDH were entrapped in "nonconductive" silica gels, synthesized using only TMOS, in the control experiment, the initial supply of NADH exhausted quickly and a final conversion of 30% was obtained. However, the use of conductive vanadia-silica gels with encapsulated GDH resulted in complete conversion of alpha-ketoglutarate to L-glutamate. A turnover number of a cofactor was also enhanced 3-fold by the application of conductive vanadia-silica gels.
引用
收藏
页码:293 / 296
页数:4
相关论文
共 21 条
[1]   Direct regeneration of NADH on a ruthenium modified glassy carbon electrode [J].
Azem, A ;
Man, F ;
Omanovic, S .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2004, 219 (02) :283-299
[2]   Direct electrochemical regeneration of NADH from NAD+ using cholesterol-modified gold amalgam electrode [J].
Baik, SH ;
Kang, C ;
Jeon, IC ;
Yun, SE .
BIOTECHNOLOGY TECHNIQUES, 1999, 13 (01) :1-5
[3]   Oxidizing enzymes as biocatalysts [J].
Burton, SG .
TRENDS IN BIOTECHNOLOGY, 2003, 21 (12) :543-549
[4]   Potential applications of NAD(P)-dependent oxidoreductases in synthesis: A survey [J].
DevauxBasseguy, R ;
Bergel, A ;
Comtat, M .
ENZYME AND MICROBIAL TECHNOLOGY, 1997, 20 (04) :248-258
[5]   ENZYME-CATALYZED ORGANIC-SYNTHESIS - ELECTROCHEMICAL REGENERATION OF NAD(P)H FROM NAD(P) USING METHYL VIOLOGEN AND FLAVOENZYMES [J].
DICOSIMO, R ;
WONG, CH ;
DANIELS, L ;
WHITESIDES, GM .
JOURNAL OF ORGANIC CHEMISTRY, 1981, 46 (22) :4622-4623
[6]  
FABER K, 1997, BIOTRANSFORMATIONS O, P160
[7]   Bio-doped nanocomposite polymers: Sol-gel bioencapsulates [J].
Gill, I .
CHEMISTRY OF MATERIALS, 2001, 13 (10) :3404-3421
[8]   Non-enzymatic regeneration of nicotinamide and flavin cofactors for monooxygenase catalysis [J].
Hollmann, F ;
Hofstetter, K ;
Schmid, A .
TRENDS IN BIOTECHNOLOGY, 2006, 24 (04) :163-171
[9]   Direct electrochemical regeneration of monooxygenase subunits for biocatalytic asymmetric epoxidation [J].
Hollmann, F ;
Hofstetter, K ;
Habicher, T ;
Hauer, B ;
Schmid, A .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (18) :6540-6541
[10]   Electrochemical regeneration of oxidoreductases for cell-free biocatalytic redox reactions [J].
Hollmann, F ;
Schmid, A .
BIOCATALYSIS AND BIOTRANSFORMATION, 2004, 22 (02) :63-88