Effects of cyclodextrins on the antimicrobial activity of plant-derived essential oil compounds

被引:54
|
作者
Liang, Hao [1 ]
Yuan, Qipeng [1 ]
Vriesekoop, Frank [2 ]
Lv, Fei [1 ]
机构
[1] Beijing Univ Chem Technol, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
[2] Harper Adams Univ Coll, Dept Food Sci, Newport TF10 8NB, Shrops, England
基金
中国国家自然科学基金;
关键词
Essential oils; Antimicrobial activity; Cyclodextrins; Carvacrol; Membrane toxicity; SPOILAGE BACTERIA; BETA-CYCLODEXTRIN; COMBINATIONS; FOODS; STABILITY; MECHANISM; PRODUCTS; EXTRACTS; GROWTH;
D O I
10.1016/j.foodchem.2012.05.054
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Essential oils (EOs) from plants are considered to be a safer alternative when compared to synthetic antimicrobial food additives. However, a major drawback of many EOs is their hydrophobic nature, which makes them insoluble in water based media and matrices. Although cyclodextrins (CDs) can increase the solubility of EO compounds, the effects of CDs on the antimicrobial activity of EOs have not been reported. In this paper, four different EO compounds (carvacrol, eugenol, linalool and 2-pentanoylfuran) were chosen to study the influence of CDs on the solubility and antimicrobial activity on bacteria and yeast. The greatest enhancement with regards to solubility of the four test compounds was achieved by hydroxypropyl-beta-CD. In most instances, not only were the minimal antimicrobial concentrations of EO compounds decreased, but the interactivity of two combined EO compounds could be strengthened by the co-addition of CDs. Furthermore, the combination of carvacrol with hydroxypropyl-beta-CD caused a marked change in the major membrane lipid composition of all microorganisms investigated; while scanning electron microscopy revealed that cellular integrity was significantly affected by 2 x MIC, ultimately resulting in cell lysis. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1020 / 1027
页数:8
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