Taylor T Matthew, Davidson P Michael, Zhong Qixin
Department of Food Science and Technology, University of Tennessee, 2509 River Road, Knoxville, Tennessee 37996-4539, USA.
J Food Prot. 2007 May;70(5):1272-6. doi: 10.4315/0362-028x-70.5.1272.
Nisin is a class Ia bacteriocin used widely in the food industry to inhibit a number of gram-positive pathogens. Although this peptide exhibits activity against many gram-positive bacteria, its effectiveness can vary significantly depending upon the food application. Encapsulation is one method that has been investigated for improving the activity of nisin. Improvement of the encapsulation efficiency of nisin requires purification of the compound, which can be accomplished utilizing organic solvents. The objective of this study was to use methanol and ethanol solutions to extract and concentrate nisin from a commercial preparation containing 2.5% nisin. Commercial nisin was extracted with different concentrations of ethanol or methanol in sterile water for up to 8 h. Approximately 75% of the nisin activity was recovered with 10 or 50% ethanol compared with less than 1% recovery with an ethanol concentration higher than 90%. Extraction with 10 or 50% methanol was approximately as effective as that with lower concentrations of ethanol. However, yields were significantly greater for extraction with methanol at concentrations greater than 90%. The solubility of the nisin likely influenced the extraction profiles for the conditions used. Purification for an 8-h extraction using 10 and 50% ethanol was 1.36 and 1.93 times, respectively. Purification was less than 0.1 at higher ethanol concentrations due to poor extraction. For methanol treatments, purification factors were all 1.09 to 5.98, and they increased as methanol concentration increased. This method for extracting and purifying nisin from dairy proteins using organic solvents may provide an alternative means for preparing and concentrating nisin for encapsulation and other applications.
乳酸链球菌素是一种I a类细菌素,在食品工业中广泛用于抑制多种革兰氏阳性病原体。尽管这种肽对许多革兰氏阳性细菌都有活性,但其有效性会因食品应用的不同而有显著差异。包封是一种已被研究用于提高乳酸链球菌素活性的方法。提高乳酸链球菌素的包封效率需要对该化合物进行纯化,这可以通过使用有机溶剂来实现。本研究的目的是使用甲醇和乙醇溶液从含2.5%乳酸链球菌素的商业制剂中提取并浓缩乳酸链球菌素。将商业乳酸链球菌素用不同浓度的乙醇或甲醇在无菌水中提取长达8小时。与乙醇浓度高于90%时回收率低于1%相比,用10%或50%乙醇提取时约75%的乳酸链球菌素活性得以回收。用10%或50%甲醇提取的效果与较低浓度乙醇提取的效果大致相同。然而,甲醇浓度大于90%时提取的产量显著更高。乳酸链球菌素的溶解度可能影响了所用条件下的提取情况。用10%和50%乙醇进行8小时提取的纯化倍数分别为1.36倍和1.93倍。由于提取效果不佳,乙醇浓度较高时纯化倍数小于0.1。对于甲醇处理,纯化因子均为1.09至5.98,且随着甲醇浓度的增加而增加。这种使用有机溶剂从乳蛋白中提取和纯化乳酸链球菌素的方法可能为制备和浓缩乳酸链球菌素以用于包封及其他应用提供一种替代方法。