Abstract
To enhance the isomerization rate of galactose into tagatose, a thermostable galactose isomerase, which was isolated from bacteria growing in a hot spring, was genetically improved using the error-prone PCR method. From 500 mutant clones, a clone showing improved conversion activity was selected. The sequence of the selected clone had five amino acid changes: His228 → Asp, Gly384 → Asp, Ser393 → Thr, Lys428 → Asn and Asp475 → Lys. The improved galactose isomerase had an II-fold higher reaction rate than the original.
| Original language | English |
|---|---|
| Pages (from-to) | 99-102 |
| Number of pages | 4 |
| Journal | Biotechnology and Applied Biochemistry |
| Volume | 34 |
| Issue number | 2 |
| DOIs | |
| State | Published - 2001 |
Keywords
- Activity enhancement
- Error-prone PCR
- Isomerization
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