DocumentCode
2678429
Title
Asymmetric Synthesis of Ethyl (R)-2-hydroxy-4-phenylbutyrate with Catalytic Antibody NB5 as Catalyst
Author
Zhimin, Ou ; Gensheng, Yang
Author_Institution
Pharmaceuticals Coll., Zhejiang Univ. of Technol. Hang Zhou, HangZhou, China
fYear
2012
fDate
28-30 May 2012
Firstpage
74
Lastpage
77
Abstract
Ethyl (R)-2-hydroxy-4-phenylbutanoate ((R)-HPBE) was synthesized by asymmetric reduction of ethyl 2-oxo-4-phenylbutyrate with catalytic antibody NB5. Catalytic antibodies were generated by hybridoma technology. The hapten and holoantigen were synthesized. A lot of monoclonal antibodies were obtained. Catalytic antibody NB5 showed good reduction activity in synthesis of ethyl (R)-2-hydroxy-4-phenylbutanoate ((R)-HPBE). The biotransformation process was optimized with catalytic antibody NB5. The optimum reduction conditions were 30 0C, pH 6.0 and 210 min. NaBH4 in excess was added in reduction. Conversion was decreased with addition more amount of substrate. Conversion can reach 100% when initial substrate concentration was 30 umol/L. The enantiometric excess of ethyl (R)-2-hydroxy-4-phenylbutyrate was <;99.9%.
Keywords
biochemistry; catalysis; catalysts; enzymes; molecular biophysics; pH; reduction (chemical); asymmetric reduction; asymmetric synthesis; biotransformation process; catalyst; catalytic antibody NB5; enzyme; ethyl 2-oxo-4-phenylbutyrate; ethyl(R)-2-hydroxy-4-phenylbutanoate; ethyl(R)-2-hydroxy-4-phenylbutyrate; hapten; holoantigen; hybridoma technology; initial substrate concentration; monoclonal antibodies; pH; temperature 30 degC; time 210 min; Biochemistry; Chemicals; Educational institutions; Immune system; Inhibitors; Mice; Substrates; Asymmetric reduction; Catalytic antibody NB5; Ethyl (R)-2-hydroxy-4-phenylbutanoate;
fLanguage
English
Publisher
ieee
Conference_Titel
Biomedical Engineering and Biotechnology (iCBEB), 2012 International Conference on
Conference_Location
Macau, Macao
Print_ISBN
978-1-4577-1987-5
Type
conf
DOI
10.1109/iCBEB.2012.85
Filename
6245060
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