Synthesis of ethyl (R)-4-chloro-3-hydroxybutyrate by immobilized cells using amino acid-modified magnetic nanoparticles
[Display omitted] •Ethyl (R)-4-chloro-3-hydroxybutyrate was synthesized by Fe3O4-Arg-Cells.•Arginine is a desirable chemical as ligand anchored with magnetic nanoparticles.•Fe3O4-Arg-Cells like microscopic stirrers in an alternating magnetic field.•Continuous reaction in magnetic fluidized bed react...
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Veröffentlicht in: | Process biochemistry (1991) 2020-12, Vol.99, p.9-20 |
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Sprache: | eng |
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•Ethyl (R)-4-chloro-3-hydroxybutyrate was synthesized by Fe3O4-Arg-Cells.•Arginine is a desirable chemical as ligand anchored with magnetic nanoparticles.•Fe3O4-Arg-Cells like microscopic stirrers in an alternating magnetic field.•Continuous reaction in magnetic fluidized bed reactor improved catalyst efficiency.
Fe3O4-Arg was selected as the optimal carrier due to its high activity recovery of immobilized cells in the preparation of Fe3O4-Arg-Cells. The optimal immobilization conditions for the preparation of Fe3O4-Arg-Cells were 30 °C, 4 h, pH 7, and 3 g dry yeast. The activity recovery of immobilized cells reached 76.8 %. For a batch reduction in a shaker in an alternating magnetic field, Fe3O4-Arg-Cells were used as a catalyst to gain ethyl (R)-4-chloro-3-hydroxybutyrate ((R)-CHBE). For further improvement in reduction productivity, a continuous reduction in the magnetic fluidized bed reactor system (MFBRS) was completed. Under their optimal transformation conditions, it took 24 h for Fe3O4-Arg-Cells to complete the conversion of ethyl 4-chloro-3-oxobutanoate (COBE) (0.8553 mol/L) in the shaker and only 8 h for the batch reduction in an alternating magnetic field. Continuous reduction in MFBRS provided new ideas for the efficient production of (R)-CHBE; 1.5882 mol/L (10 mL) of COBE can be completely converted in 6 h. The conversion and enantiomeric excess (e.e.) of (R)-CHBE were 100 % and above 99.9 % respectively, in the three reaction systems mentioned above. |
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ISSN: | 1359-5113 1873-3298 |
DOI: | 10.1016/j.procbio.2020.07.027 |