Comparative study of the enzymatic synthesis of cephalexin at high substrate concentration in aqueous and organic media using statistical model

Synthesis of cephalexin with immobilized penicillin acylase at high substrates concentration at an acyl donor to nucleophile molar ratio of 3 was comparatively evaluated in aqueous and ethylene glycol media using a statistical model. Variables under study were temperature, pH and enzyme to substrate...

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Published inBiotechnology and bioprocess engineering Vol. 17; no. 4; pp. 711 - 721
Main Authors Bahamondes, Carola, Pontificia Universidad Catolica de Valparaiso, Valparaiso, Chile, Wilson, Lorena, Pontificia Universidad Catolica de Valparaiso, Valparaiso, Chile, Aguirre, Carolina, Universidad Catolica de la Ssma. Concepcion Avenida Brasil 2147, Valparaiso, Chile, Illanes, Andres, Pontificia Universidad Catolica de Valparaiso, Valparaiso, Chile
Format Journal Article
LanguageEnglish
Published Heidelberg The Korean Society for Biotechnology and Bioengineering 01.08.2012
Springer Nature B.V
한국생물공학회
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Summary:Synthesis of cephalexin with immobilized penicillin acylase at high substrates concentration at an acyl donor to nucleophile molar ratio of 3 was comparatively evaluated in aqueous and ethylene glycol media using a statistical model. Variables under study were temperature, pH and enzyme to substrate ratio and their effects were evaluated on cephalexin yield, ratio of initial rates of cephalexin synthesis to phenylglycine methyl ester hydrolysis, volumetric and specific productivity of cephalexin synthesis, that were used as response parameters. Results obtained in both reaction media were modeled using surface of response methodology and optimal operation conditions were determined in terms of an objective function based on the above parameters. At very high substrates concentrations the use of organic co-solvents was not required to attain high yields and actually almost stoichiometric yields were obtained in a fully aqueous media with the advantages of higher productivities than in an organic co-solvent media and compliance with the principles of green chemistry.
Bibliography:E21
2013001213
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G704-000785.2012.17.4.006
ISSN:1226-8372
1976-3816
DOI:10.1007/s12257-011-0674-6