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将溶菌酶通过共价键固定在乙烯-乙烯醇薄膜上,用于非迁移性抗菌包装应用。

Covalent immobilization of lysozyme on ethylene vinyl alcohol films for nonmigrating antimicrobial packaging applications.

机构信息

Packaging Lab, Instituo de Agroquímica y Tecnología de los Alimentos, CSIC, Avenida Agustín Escardino 7, 46980 Paterna, Spain.

出版信息

J Agric Food Chem. 2013 Jul 10;61(27):6720-7. doi: 10.1021/jf401818u. Epub 2013 Jul 1.

Abstract

The objective of this study was to develop a new antimicrobial film, in which lysozyme was covalently attached onto two different ethylene vinyl alcohol copolymers (EVOH 29 and EVOH 44). The EVOH surface was modified with UV irradiation treatment to generate carboxylic acid groups, and lysozyme was covalently attached to the functionalized polymer surface. Surface characterization of control and modified films was performed using attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR) and dye assay. The value of protein loading after attachment on the surface was 8.49 μg protein/cm(2) and 5.74 μg protein/cm(2) for EVOH 29 and EVOH 44, respectively, after 10 min UV irradiation and bioconjugation. The efficacy of the EVOH-lysozyme films was assessed using Micrococcus lysodeikticus. The antimicrobial activity of the films was tested against Listeria monocytogenes and was similar to an equivalent amount of free enzyme. The reduction was 1.08 log for EVOH 29-lysozyme, 0.95 log for EVOH 44-lysozyme, and 1.34 log for free lysozyme. This work confirmed the successful use of lysozyme immobilization on the EVOH surface for antimicrobial packaging.

摘要

本研究旨在开发一种新型抗菌膜,即将溶菌酶共价连接到两种不同的乙烯-乙烯醇共聚物(EVOH29 和 EVOH44)上。通过 UV 辐射处理对 EVOH 表面进行改性,生成羧酸基团,并将溶菌酶共价连接到功能化聚合物表面。使用衰减全反射傅里叶变换红外光谱(ATR-FTIR)和染料测定法对对照和改性膜的表面特性进行了表征。经 10 分钟 UV 辐射和生物偶联后,在表面附着的蛋白质负载量分别为 8.49μg 蛋白质/cm²和 5.74μg 蛋白质/cm²,用于 EVOH29 和 EVOH44。采用微球菌溶菌酶评估了 EVOH-溶菌酶膜的功效。测试了膜对单核细胞增生李斯特菌的抗菌活性,其效果与等量的游离酶相当。EVOH29-溶菌酶的减少量为 1.08 对数,EVOH44-溶菌酶为 0.95 对数,游离溶菌酶为 1.34 对数。这项工作证实了成功地将溶菌酶固定在 EVOH 表面上用于抗菌包装。

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