Biotransformation of D-Methionine into L-methionine in the cascade of four enzymes

被引:49
作者
Findrik, Z. [1 ]
Vasic-Racki, D. [1 ]
机构
[1] Univ Zagreb, Fac Chem Engn & Technol, HR-10000 Zagreb, Croatia
关键词
enzyme kinetics; L-phenylatanine dehydrogenase; D-amino acid oxidase; formate dehydrogenase;
D O I
10.1002/bit.21501
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
D-Methionine was converted to L-methionine in a reaction system where four enzymes were used. D-amino acid oudase (D-AAO) from Arthrobacter protophormiae was used for the complete conversion of D-methionine to 2-oxo-4-methylthiobutyric acid. Catalase was added to prevent 2-oxo-4-methylthiobutyric acid decarboxylation. In the second reaction step, L-phenylalanine dehydrogenase (L-PheDH) from Rhodococcus sp. was used to convert 2- oxo-4-methylthiobutyric acid to L-methionine, and formate dehydrogenase (FDH) from Candida boidinii was added for NADH regeneration. Enzyme kinetics of all enzymes was analyzed in detail. Mathematical models for separate reactions steps, as well as for the complete system were developed and validated in the batch reactor experiments. Complete conversion Of D-methionine to L-methionine was achieved. Considering that both enzymes act on different substrates, such a system could be easily employed for the synthesis of other amino acids from D-isomer, as well as from the racemate of a certain amino acid (DL-amino acid).
引用
收藏
页码:956 / 967
页数:12
相关论文
共 34 条
[1]   Production of aromatic D-amino acids from α-keto acids and ammonia by coupling of four enzyme reactions [J].
Bae, HS ;
Lee, SG ;
Hong, SP ;
Kwak, MS ;
Esaki, N ;
Soda, K ;
Sung, MH .
JOURNAL OF MOLECULAR CATALYSIS B-ENZYMATIC, 1999, 6 (03) :241-247
[2]  
*BIOCH INF, 1973, BOGHR MANH GMBH, P36
[3]  
*BIOCH INF, 1973, BOEHR MANH GMBH, P41
[4]   Synthesis and use of enantiomerically pure tert-leucine [J].
Bommarius, AS ;
Schwarm, M ;
Stingl, K ;
Kottenhahn, M ;
Huthmacher, K ;
Drauz, K .
TETRAHEDRON-ASYMMETRY, 1995, 6 (12) :2851-2888
[5]   Concepts of nature in organic synthesis: Cascade catalysis and multistep conversions in concert [J].
Bruggink, A ;
Schoevaart, R ;
Kieboom, T .
ORGANIC PROCESS RESEARCH & DEVELOPMENT, 2003, 7 (05) :622-640
[6]   Simultaneous synthesis of enantiomerically pure (S)-amino acids and (R)-amines using coupled transaminase reactions [J].
Cho, BK ;
Cho, HJ ;
Park, SH ;
Yun, H ;
Kim, BG .
BIOTECHNOLOGY AND BIOENGINEERING, 2003, 81 (07) :783-789
[7]   Engineering aromatic L-amino acid transaminase for the asymmetric synthesis of constrained analogs of L-phenylalanine [J].
Cho, Byung-Kwan ;
Seo, Joo-Hyun ;
Kang, Taek-Jin ;
Kim, Juhan ;
Park, Hyung-Yeon ;
Lee, Bon-Su ;
Kim, Byung-Gee .
BIOTECHNOLOGY AND BIOENGINEERING, 2006, 94 (05) :842-850
[8]   Kinetic modeling of amino acid oxidation catalyzed by a new D-amino acid oxidase from Arthrobacter protophormiae [J].
Findrik, Z ;
Vasic-Racki, D ;
Geueke, B ;
Kuzu, M ;
Hummel, W .
ENGINEERING IN LIFE SCIENCES, 2005, 5 (06) :550-555
[9]   Modelling Of L-DOPA enzymatic oxidation catalyzed by L-amino acid oxidases from Crotalus adamanteus and Rhodococcus opacus [J].
Findrik, Z ;
Geueke, B ;
Hummel, W ;
Vasic-Racki, D .
BIOCHEMICAL ENGINEERING JOURNAL, 2006, 27 (03) :275-286
[10]   Kinetic modeling of acetophenone reduction catalyzed by alcohol dehydrogenase from Thermoanaerobacter sp. [J].
Findrik, Z ;
Vasic-Racki, D ;
Lütz, S ;
Daussmann, T ;
Wandrey, C .
BIOTECHNOLOGY LETTERS, 2005, 27 (15) :1087-1095