Abstract
L-Ornithine could serve as an intermediate in the biobased production of 1,4-diaminobutane from L-arginine. Using the concept of biorefinery, L-arginine could become widely available from biomass waste streams via the nitrogen storage polypeptide cyanophycin. Selective hydrolysis of L-arginine to L-ornithine is difficult to perform chemically, therefore the stabilization and immobilization of Bacillus subtilis arginase (EC 3.5.3.1) was studied in a continuously stirred membrane reactor system. Initial pH of the substrate solution, addition of L-aspartic acid and reducing agents all appeared to have an effect on the operational stability of B. subtilis arginase. A remarkably good operational stability (total turnover number, TTN=1.13108) at the pH of arginine free base (pH 11.0) was observed, which was further improved with the addition of sodium dithionite to the substrate solution (TTN>1109). B. subtilis arginase was successfully immobilized on three commercially available epoxy-activated supports. Immobilization on Sepabeads EC-EP was most promising, resulting in a recovered activity of 75% and enhanced thermostability. In conclusion, the stabilization and immobilization of B. subtilis arginase has opened up possibilities for its application in the biobased production of nitrogen-containing chemicals as an alternative to the petrochemical production
Original language | English |
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Pages (from-to) | 1493-1502 |
Journal | Advanced Synthesis and Catalysis |
Volume | 352 |
Issue number | 9 |
DOIs | |
Publication status | Published - 2010 |
Keywords
- multipoint covalent attachment
- ralstonia-eutropha
- amino-acids
- saccharomyces-cerevisiae
- enzyme immobilization
- pseudomonas-putida
- industrial biocatalyst
- cyanophycin synthetase
- recombinant strains
- epoxy sepabeads