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葡聚糖共轭溶菌酶对凝乳中大肠杆菌和金黄色葡萄球菌的抗菌活性。

Antibacterial activity of dextran-conjugated lysozyme against Escherichia coli and Staphylococcus aureus in cheese curd.

作者信息

Amiri S, Ramezani R, Aminlari M

机构信息

Department of Food Science and Technology, School of Agriculture, Shiraz University, Shiraz, 71345, Iran.

出版信息

J Food Prot. 2008 Feb;71(2):411-5. doi: 10.4315/0362-028x-71.2.411.

Abstract

The purposes of this research were to glycosylate lysozyme with dextran under Maillard reaction conditions and assess the antimicrobial characteristics of the lysozyme-dextran conjugate in a culture medium and cheese curd. Solutions containing lysozyme and dextran were incubated at 60 degrees C and at 79% relative humidity. Gel permeation chromatography and sodium dodecyl sulfate-polyacrylamide gel electrophoresis were used to follow the glycosylation process. Under optimum conditions 3.7 mol of dextran were coupled to 1 mol of lysozyme. Lytic activity of the conjugate against the cell wall of Micrococcus luteus was about 62% of that of native lysozyme. Evaluation of the lysozyme-dextran conjugate against test microorganisms (Staphylococcus aureus and Escherichia coli) in culture media indicated a progressive increase in antimicrobial activity, with an increase in enzyme-conjugate concentration. The lysozyme-dextran conjugate was also effective against E. coli in a natural food system, as it reduced the bacterial count by 3 log in cheese curd after 40 days of storage. Unlike E. coli, the antimicrobial action of lysozyme against S. aureus was not improved by conjugation with dextran in both in vitro and in vivo tests. Antimicrobial activity of the lysozyme-dextran conjugate against gram-negative bacteria is probably related to the remaining lytic activity as well as the excellent surfactant properties of the lysozyme-dextran conjugate. These results might increase the applicability of lysozyme as a natural antimicrobial ingredient in different food products.

摘要

本研究的目的是在美拉德反应条件下用葡聚糖对溶菌酶进行糖基化,并评估溶菌酶 - 葡聚糖缀合物在培养基和凝乳中的抗菌特性。将含有溶菌酶和葡聚糖的溶液在60℃和79%相对湿度下孵育。使用凝胶渗透色谱法和十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳来跟踪糖基化过程。在最佳条件下,3.7摩尔葡聚糖与1摩尔溶菌酶偶联。缀合物对藤黄微球菌细胞壁的裂解活性约为天然溶菌酶的62%。在培养基中对溶菌酶 - 葡聚糖缀合物针对测试微生物(金黄色葡萄球菌和大肠杆菌)的评估表明,随着酶 - 缀合物浓度的增加,抗菌活性逐渐增强。溶菌酶 - 葡聚糖缀合物在天然食品体系中对大肠杆菌也有效,因为在储存40天后,它使凝乳中的细菌数量减少了3个对数。与大肠杆菌不同,在体外和体内试验中,溶菌酶与葡聚糖缀合后对金黄色葡萄球菌的抗菌作用并未得到改善。溶菌酶 - 葡聚糖缀合物对革兰氏阴性菌的抗菌活性可能与剩余的裂解活性以及溶菌酶 - 葡聚糖缀合物优异的表面活性剂特性有关。这些结果可能会增加溶菌酶作为天然抗菌成分在不同食品中的适用性。

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