Research Article
Influence of pH on the expression of a recombinant epoxide hydrolase in Aspergillus niger
Article first published online: 18 MAY 2009
DOI: 10.1002/biot.200900034
Copyright © 2009 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Issue
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Biotechnology Journal
Special Issue: Biochemical Engineering Science
Volume 4, Issue 5, pages 756–765, May 2009
Additional Information
How to Cite
Naundorf, A., Melzer, G., Archelas, A., Furstoss, R. and Wohlgemuth, R. (2009), Influence of pH on the expression of a recombinant epoxide hydrolase in Aspergillus niger. Biotechnology Journal, 4: 756–765. doi: 10.1002/biot.200900034
Publication History
- Issue published online: 18 MAY 2009
- Article first published online: 18 MAY 2009
- Manuscript Accepted: 8 APR 2009
- Manuscript Revised: 6 APR 2009
- Manuscript Received: 10 FEB 2009
Funded by
- European Community Fifth Framework Programme. Grant Number: QLK3-CT2000-00426 EPOX
- State Secretariat of Education and Research SER, Switzerland
- Abstract
- References
- Cited By
Keywords:
- Aspergillus niger;
- Biocatalysis;
- Epoxide hydrolase;
- Protein stability;
- Recombinant protein expression
Abstract
The filamentous fungus Aspergillus niger was investigated in relation to its ability to produce a soluble epoxide hydrolase (EH) (E.C. 3.3.2.3) belonging to the microsomal EH family. This EH is a highly useful biocatalyst for kinetic resolution of racemic epoxides to give enantiopure building blocks. The production of EH on an industrial scale is still a major challenge and is linked to various optimization processes. In this work, production of protein and organic acids as a function of pH and cultivation time was investigated. The production of EH was highest (1000 U/L for p-nitrostyrene oxide) under acidic fermentation conditions (pH value of about 3). The metabolic flux toward production of organic acids and thereby acidification of the environment increased with an increasing pH value. At pH 7, nearly 50% of total carbon of the substrate was incorporated into organic acids, mainly gluconic and oxalic acid. Finally, the addition of protease inhibitors, antioxidants and cryoprotectants was investigated in relation to the stability of the EH during the downstream process. The determination of the pH dependence during fermentation and understanding of the parameters influencing the stability of the enzyme has allowed us to optimize intracellular expression. The EH has been easily isolated from the biomass with high activity (1.67 U/mg lyophilisate) in a robust process.

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