Abstract
A novel extraction method was developed aiming at increasing the stability of enzymes in organic solvent media. Horseradish peroxidase (HRP), inactivated in a tetrahydrofuran (THF)/water (1:1, v/v), regained and maintained its activity when HRP was extracted by adding a THF/benzene mixture to the original solution. However, the HRP activity was drastically lowered in the enzyme-free blank solution that had been formed by employing the same extraction procedure. As a result, the reactivation after the extraction is believed to depend on enzyme history, and might be arisen from an irreversible structural change of the enzyme.
Original language | English (US) |
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Pages (from-to) | 485-489 |
Number of pages | 5 |
Journal | Biotechnology Letters |
Volume | 22 |
Issue number | 6 |
DOIs | |
State | Published - 2000 |
Keywords
- Enzyme
- Extraction
- Horseradish peroxidase
- Organic solvent
- Reactivation
ASJC Scopus subject areas
- Biotechnology
- Bioengineering
- Applied Microbiology and Biotechnology