Synthesis of (S)-4-fluorophenylglycine by using immobilized amidase based on metal-organic framework.
- Author:
Chaoping LIN
1
;
Jiangtao TANG
1
;
Renchao ZHENG
1
;
Yuguo ZHENG
1
Author Information
- Publication Type:Journal Article
- Keywords: (S)-4-fluorophenylglycine; amidase; immobilization; metal-organic framework
- MeSH: Amidohydrolases; Enzyme Stability; Enzymes, Immobilized/metabolism*; Glycine/analogs & derivatives*; Hydrogen-Ion Concentration; Metal-Organic Frameworks; Temperature
- From: Chinese Journal of Biotechnology 2021;37(8):2936-2946
- CountryChina
- Language:Chinese
- Abstract: A stable Zr-based metal-organic framework (MOF, UiO-66-NH2) synthesized via micro-water solvothermal method was used to immobilize amidase by using the glutaraldehyde crosslinking method. The effect of immoblization conditions on enzyme immoblization efficiency was studied. An activity recovery rate of 86.4% and an enzyme loading of 115.3 mg/g were achieved under the optimal conditions: glutaraldehyde concentration of 1.0%, cross-linking time of 180 min, and the weight ratio of MOF to enzyme of 8:1. The optimal temperature and optimal pH of the immobilized amidase were determined to be 40 °C and 9.0, respectively, and the Km, Vmax and kcat of the immoblized amidase were 58.32 mmol/L, 16.23 μmol/(min·mg), and 1 670 s⁻¹, respectively. The immobilized enzyme was used for (S)-4-fluorophenylglycine synthesis and the optimal reaction conditions were 300 mmol/L of N-phenylacetyl-4-fluorophenylglycine, 10 g/L of immobilized enzyme loading, and reacting for 180 min at pH 9.0 and 40 °C. A conversion rate of 49.9% was achieved under the optimal conditions, and the conversion rate can be increased to 99.9% under the conditions of enantiomeric excess. The immobilized enzyme can be repeatedly used, 95.8% of its original activity can be retained after 20 cycles.
