Moreno-Cortez Iván E, Romero-García Jorge, González-González Virgilio, García-Gutierrez Domingo I, Garza-Navarro Marco A, Cruz-Silva Rodolfo
Centro de Investigación en Química Aplicada (CIQA), Blvd. Enrique Reyna # 140, San José de los Cerritos, Saltillo, Coahuila 25100, México; Universidad Autónoma de Nuevo León (UANL), Fac. de Ingeniería Mecánica y Eléctrica (FIME), Av. Universidad S/N, Cd. Universitaria, San Nicolás de los Garza, Nuevo León C.P. 66450, México; Universidad Autónoma de Nuevo León (UANL), Centro de Innovación, Investigación y Desarrollo en Ingeniería y Tecnología (CIIDIT), Apodaca, Nuevo León, México.
Centro de Investigación en Química Aplicada (CIQA), Blvd. Enrique Reyna # 140, San José de los Cerritos, Saltillo, Coahuila 25100, México.
Mater Sci Eng C Mater Biol Appl. 2015;52:306-14. doi: 10.1016/j.msec.2015.03.049. Epub 2015 Mar 25.
In this paper, papain enzyme (E.C. 3.4.22.2, 1.6 U/mg) was successfully immobilized in poly(vinyl alcohol) (PVA) nanofibers prepared by electrospinning. The morphology of the electrospun nanofibers was characterized by scanning electron microscopy (SEM) and the diameter distribution was in the range of 80 to 170 nm. The presence of the enzyme within the PVA nanofibers was confirmed by infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS) and energy dispersive X-ray spectroscopy (EDXS) analyses. The maximum catalytic activity was reached when the enzyme loading was 13%. The immobilization of papain in the nanofiber membrane was achieved by chemical crosslinking with a glutaraldehyde vapor treatment (GAvt). The catalytic activity of the immobilized papain was 88% with respect to the free enzyme. The crosslinking time by GAvt to immobilize the enzyme onto the nanofiber mat was 24h, and the enzyme retained its catalytic activity after six cycles. The crosslinked samples maintained 40% of their initial activity after being stored for 14 days. PVA electrospun nanofibers are excellent matrices for the immobilization of enzymes due to their high surface area and their nanoporous structure.
在本文中,木瓜蛋白酶(E.C. 3.4.22.2,1.6 U/mg)成功固定在通过静电纺丝制备的聚乙烯醇(PVA)纳米纤维中。通过扫描电子显微镜(SEM)对静电纺纳米纤维的形态进行了表征,其直径分布在80至170 nm范围内。通过红外光谱(FTIR)、X射线光电子能谱(XPS)和能量色散X射线光谱(EDXS)分析证实了PVA纳米纤维中酶的存在。当酶负载量为13%时达到最大催化活性。通过戊二醛蒸汽处理(GAvt)进行化学交联实现了木瓜蛋白酶在纳米纤维膜中的固定化。固定化木瓜蛋白酶相对于游离酶的催化活性为88%。通过GAvt将酶固定在纳米纤维垫上的交联时间为24小时,并且酶在六个循环后仍保留其催化活性。交联样品在储存14天后保持其初始活性的40%。由于其高表面积和纳米多孔结构,PVA静电纺纳米纤维是固定化酶的优良基质。