College of Pharmaceutical Science, Hebei University, Baoding, 071002, China.
Affiliated Hospital of Hebei University, Baoding, China.
Colloids Surf B Biointerfaces. 2020 May;189:110874. doi: 10.1016/j.colsurfb.2020.110874. Epub 2020 Feb 15.
Here, PEI@PMMA microspheres were prepared by grafting polyethyleneimine (PEI) on poly(methyl methacrylate) (PMMA) magnetic microspheres and successfully used to immobilize lipase. The results showed that PEI@PMMA microspheres had strongly adsorbed lipase (49.1 mg/g microsphere) via electrostatic attraction. To prevent lipase shedding, the adsorbed lipase was further crosslinked with PEI on microspheres using glutaraldehyde as crosslinker. Consequently, PEI-crosslinked lipase (2.14 U/mg) exhibited 2.6 times and 1.4 times higher activity respectively than the directly covalent lipase (0.82 U/mg) and the crosslinked lipase aggregates (1.57 U/mg), which was close to the activity of adsorbed lipase (2.20 U/mg). Conformational analysis from FTIR spectroscopy showed that PEI-crosslinked lipase retained its natural structure well. And the α-helix structure seemed to play a key role in enhancing lipase activity. Furthermore, the effects of various parameters on crosslinking reaction were investigated. Also, PEI-crosslinked lipase revealed higher pH and thermal stability. The Michaelis constant (K) was increased and the optimum temperature of lipase was widened observably after crosslinking with PEI on PEI@PMMA magnetic microspheres.
在这里,通过在聚甲基丙烯酸甲酯(PMMA)磁性微球上接枝聚乙烯亚胺(PEI)制备了 PEI@PMMA 微球,并成功将其用于固定脂肪酶。结果表明,PEI@PMMA 微球通过静电吸引强烈吸附脂肪酶(49.1mg/g 微球)。为了防止脂肪酶脱落,用戊二醛作为交联剂将吸附的脂肪酶进一步交联到微球上的 PEI 上。结果,PEI 交联的脂肪酶(2.14 U/mg)的活性分别比直接共价脂肪酶(0.82 U/mg)和交联的脂肪酶聚集体(1.57 U/mg)高 2.6 倍和 1.4 倍,接近于吸附脂肪酶(2.20 U/mg)的活性。傅里叶变换红外光谱的构象分析表明,PEI 交联的脂肪酶很好地保留了其天然结构。α-螺旋结构似乎在提高脂肪酶活性方面起着关键作用。此外,还研究了各种参数对交联反应的影响。此外,PEI 交联的脂肪酶具有更高的 pH 和热稳定性。在 PEI@PMMA 磁性微球上用 PEI 交联后,Michaelis 常数(K)显著增加,脂肪酶的最适温度变宽。