Antibacterial activity and mechanism of three isomeric terpineols of Cinnamomum longepaniculatum leaf oil

福氏志贺氏菌 松油醇 抗菌活性 抗菌剂 最小抑制浓度 最低杀菌浓度 化学 生物 食品科学 细菌 生物化学 色谱法 有机化学 大肠杆菌 遗传学 基因
作者
Jinfeng Huang,Liyan Yang,Yue Zou,Sican Luo,Xin Wang,Yujuan Liang,Yonghua Du,Ruizhang Feng,Wei Qin
出处
期刊:Folia Microbiologica [Springer Science+Business Media]
卷期号:66 (1): 59-67 被引量:68
标识
DOI:10.1007/s12223-020-00818-0
摘要

α-Terpineol, terpinen-4-ol, and δ-terpineol, isomers of terpineol, are among the compounds that give Cinnamomum longepaniculatum leaf oil its distinguished pleasant smell. The objective of this study was to evaluate the antimicrobial activity of these three isomeric terpineols. The determination of antibacterial activity was based on the minimum inhibition concentration (MIC) and minimum bactericide concentration (MBC). Changes in time-kill curve, alkaline phosphatase (AKP), UV-absorbing material, membrane potential, and scanning electron microscopy (SEM) were measured to elucidate the possible antimicrobial mechanism. α-Terpineol, terpinen-4-ol, and δ-terpineol demonstrated good inhibitory effects against several gram-negative bacteria, particularly Shigella flexneri. MIC and MBC of α-terpineol and terpinen-4-ol were similar (0.766 mg/mL and 1.531 mg/mL, respectively) for S. flexneri, while the MIC and MBC values of δ-terpineol were 0.780 mg/mL and 3.125 mg/mL, respectively. Time-kill curves showed that the antibacterial activities of the tested compounds were in a concentration-dependent manner. Release of nucleic acids and proteins along with a decrease in membrane potential proved that α-terpineol, terpinen-4-ol, and δ-terpineol could increase the membrane permeability of Shigella flexneri. Additionally, the release of AKP suggested that the cell wall was destroyed. SEM analysis further confirmed that S. flexneri cell membranes were damaged by α-terpineol, terpinen-4-ol, and δ-terpineol. Our research suggests that these three isomeric terpineols have the potential of being used as natural antibacterial agents by destroying the cell membrane and wall, resulting in cell death. However, the specific antibacterial activity differences need further investigation.
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