New biochemical methods for production of N-benzyloxycarbonyl-d,l-aminoadipic- delta -semialdehyde and N-benzyloxycarbonyl-d,l-aminoadipic acid

New biochemical methods for the production of N alpha -benzyloxycarbonyl-l-aminoadipate delta -semialdehyde (N alpha -Z-l-AASA), N alpha -Z-d-AASA, N alpha -Z-l-aminoadipic acid (N alpha -Z-l-AAA), N alpha -Z-d-AAA were developed using cells of Rhodococcus sp. AIU Z-35-1. When the cells harvested af...

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Veröffentlicht in:Enzyme and microbial technology 2007-02, Vol.40 (3), p.433-436
Hauptverfasser: Isobe, Kimiyasu, Tokuta, Keigo, Nagasawa, Shouko, Matsuura, Akira, Sakaguchi, Takehiko, Wakao, Norio
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Sprache:eng
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Zusammenfassung:New biochemical methods for the production of N alpha -benzyloxycarbonyl-l-aminoadipate delta -semialdehyde (N alpha -Z-l-AASA), N alpha -Z-d-AASA, N alpha -Z-l-aminoadipic acid (N alpha -Z-l-AAA), N alpha -Z-d-AAA were developed using cells of Rhodococcus sp. AIU Z-35-1. When the cells harvested after 1 day of cultivation were incubated with 100mM N alpha -Z-l-lysine at pH 5.0 for 1 day at 30°C or at pH 7.0 for 2 days at 10°C, more than 95mM N alpha -Z-l-AASA was produced. Using the cells harvested after 3 days of cultivation, N alpha -Z-l-AAA was efficiently produced by incubating at pH 7.0 for 4 days at 30°C. Similar conversion yields of N alpha -Z-d-AASA and N alpha -Z-d-AAA were also obtained under the same conditions. Thus, the microbial methods proposed here were superior to the chemical and other biochemical methods in simplicity, reaction rate, and yield.
ISSN:0141-0229
DOI:10.1016/j.enzmictec.2006.07.016