不同降解方法得到的壳聚糖的抗微生物活性
首发时间:2009-01-31
摘要:考察了用不同的降解方法(过氧化氢降解法与胃蛋白酶降解法)制备得到的壳聚糖对大肠杆菌(E. coli, 革兰氏阴性菌)、金黄色葡萄球菌(S. aureus, 革兰氏阳性菌)及白色念珠菌(C. albicans, 酵母)的抑菌性能。结果表明壳聚糖对微生物的抑制作用存在多种机理,其抗微生物作用受浓度、重均分子量、降解方法,以及所作用微生物的细胞壁或细胞膜结构等因素的影响。当壳聚糖的浓度≥0.5 g/L时,其对三种试验菌种均有较好的抑制作用(抑菌率≥99.78%)。一般而言,过氧化氢降解产物对E. coli和C. albican的抑制作用优于胃蛋白酶降解产物。相对分子质量对壳聚糖抗细菌性能具有双重影响:一方面,高相对分子质量的壳聚糖不但可以在细菌外围形成更厚的外囊,而且还可以赋予体系更高的粘度,从而有效地阻碍营养物质进入细菌;另一方面,低相对分子质量的壳聚糖则可以暴露更多的活性—NH2,使之和体系中的营养物质以及金属离子反应,从而有效地提高壳聚糖对细菌的抑制作用。壳聚糖对真菌的抑制作用可能与其对寄主防御系统的诱发有关。
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Antimicrobial Activity of Chitosans Degraded by Different Methods
Abstract:Antimicrobial activities of chitosans degraded by different methods (hydrogen peroxide/pepsin degradation) were examined against Escherichia coli (E. coli, gram-negative bacterium), Staphylococcus aureus (S. aureus, gram-positive bacterium) and Candida albicans (C. albicans, yeast). The results indicated that the antimicrobial activity of chitosan is determined by the degradation method, molecular weight (Mw) and concentration of chitosan, and the characteristic of the microorganism tested. All chitosans exhibit high inhibitory rates (≥99.78%) against three tested microbes at a concentration of ≥0.5 g/L. Antimicrobial activities of chitosan against E. coli and C. albicans are greatly depended on the concentration of the sample when the value of it is in the range of 0.25~0.125 g/L. Chitosan shows high inhibitory rate against bacteria at either high or low Mw when the mass average Mw of it is in the range of 1460~285 kDa, which indicating that Mw might have dual effects on its antibacterial activity. The antifungal activity of chitosan might have greater concerned to the activation of defense processes. Degradation method has great influence on the antimicrobial activity, especially antifungal activity, of chitosan by changing the Mw and acetyl groups’ distribution of the polymer, which might be one of the reasons that why there are inconsistent conclusions obtained concerning the antimicrobial activity of chitosan.
Keywords: chitosan antimicrobial activity hydrogen peroxide pepsin degradation
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