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Received October 1, 2018
Accepted March 1, 2019
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Enhancement of catalytic activity of lipase-immobilized Fe3O4-chitosan microsphere for enantioselective acetylation of racemic 1-phenylethylamine
College of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou, Zhejiang, China 1The Third Affiliated Hospital of Qiqihar Medical College, Qiqihar, Heilongjiang, China
oozzmm@163.com
Korean Journal of Chemical Engineering, May 2019, 36(5), 729-739(11), 10.1007/s11814-019-0249-3
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Abstract
Racemic 1-phenylethylamine was resolved by enantiomer selective acetylation using Fe3O4-chitosan microsphere (CTS)-glutaraldehyde-lipase in a solvent-free system under an alternating magnetic field. Magnetic chitosan microspheres (Fe3O4-CTS) were prepared via chemical co-precipitation and cross-linked with lipase using glutaraldehyde to form Fe3O4-CTS-glutaraldehyde-lipase particles. The magnetic, physicochemical, and textural characteristics of Fe3O4-CTS-glutaraldehyde-lipase particles were assessed by Fourier transform infrared spectroscopy, X-ray diffraction, and scanning electron microscopy. The optimal immobilization conditions were 2.4mg/mL lipase, 10mg/mL Fe3O4- CTS-glutaraldehyde, pH 8.5, 35 oC, 3 h. The loading amount of lipase and the specific activity got to 132mg/g carrier and 48U/g. The optimal reaction conditions of the acylation reaction using Fe3O4-CTS-glutaraldehyde-lipase were 300mmol/L 1-phenylethylamine, 150mg immobilized lipase, 2mL vinyl acetate, 12.6 ⊥g rotating speed, 40 oC, 8 h. The activity of the Fe3O4-CTS-glutaraldehyde-lipase particles and conversion were improved when they were exposed to an external alternating magnetic field. The optimum magnetic field was 12 Gs (500 Hz). The conversion, enantiomeric excess of (R)-N-(1-phenylethyl)acetamide, and E value reached 41.8%, 98.4%, and 264, respectively. Fe3O4-CTS-glutaraldehyde- lipase could be reused seven times. A kinetic model of the immobilized lipase-catalyzed resolution of 1- phenylethylamine was set up based on the ping-pong bi좻bi mechanism. The kinetic constants were Vmax=1.62⊥10?2 mM/min, KA=2.84⊥10?4mM, and KB=5.8⊥10?1mM. The model data fit well with the experimental data.
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References
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Qu ZY, Hu FL, Chen KM, Duan ZQ, Gu HC, Xu H, J. Colloid Interface Sci., 398, 82 (2013)
Hwang ET, Gu MB, Eng. Life Sci., 13(1), 49 (2013)
Ye P, Xu ZK, Che AF, Wu J, Seta P, Biomaterials, 26(25), 6394 (2005)
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Gros F, Baup S, Aurousseau M, Powder Technol., 183(2), 152 (2008)
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Chen CS, Fujimoto Y, Girdaukas G, Sih CJ, J. Am. Chem. Soc., 104(25), 7294 (1982)
Bradford MM, Anal. Biochem., 72(s1-2), 248 (1976)
Baghban A, Heidarizadeh M, Doustkhah E, Rostamnia S, Rezaei PF, Int. J. Biol. Macromol., 103, 1194 (2017)
Pan CL, Hu B, Li W, Sun Y, Ye H, Zeng XX, J. Mol. Catal. B-Enzym., 61(3-4), 208 (2009)
Zhang QK, Kang JQ, Yang B, Zhao LZ, Hou ZS, Tang B, Chinese. J. Catal., 37(3), 389 (2016)
Yadav GD, Trivedi AH, Enzyme Microb. Technol., 32(7), 783 (2003)
Paivio M, Perkio P, Kanerva LT, Tetrahedron: Asymmetry, 23(3-4), 230 (2012)