食品科学 ›› 2023, Vol. 44 ›› Issue (15): 19-27.doi: 10.7506/spkx1002-6630-20220628-316

• 基础研究 • 上一篇    

爱媛类芽孢杆菌抗菌肽对扩展青霉孢子的抑制作用机制

王志新,刘丹丹,贾紫伟,黄玉清,宁亚维,贾英民   

  1. (1.河北科技大学食品与生物学院,河北 石家庄 050018;2.北京工商大学食品与健康学院,北京 100048)
  • 发布日期:2023-09-01
  • 基金资助:
    河北省自然科学基金资助项目(C2020208014);河北省省级科技计划资助项目(22327107D)

Antimicrobial Mechanism of Antimicrobial Peptide from Paenibacillus ehimensis against Penicillium expansum Spores

WANG Zhixin, LIU Dandan, JIA Ziwei, HUANG Yuqing, NING Yawei, JIA Yingmin   

  1. (1. College of Food Science and Biology, Hebei University of Science and Technology, Shijiazhuang 050018, China; 2. School of Food and Health, Beijing Technology and Business University, Beijing 100048, China)
  • Published:2023-09-01

摘要: 扩展青霉(Penicillium expansum)会导致水果腐烂变质,危害消费者身体健康,是采后水果常见的腐败菌,研究爱媛类芽孢杆菌(Paenibacillus ehimensis)抗菌肽对扩展青霉孢子的抑制作用机制具有重要意义。本实验采用微量二倍稀释法和时间-杀菌曲线测定抗菌肽对扩展青霉孢子的抑菌活性,采用扫描电子显微镜和透射电子显微镜观察抗菌肽对扩展青霉孢子超微结构的影响,采用荧光探针分析抗菌肽对扩展青霉细胞膜和活性氧累积的影响,以探究爱媛类芽孢杆菌抗菌肽对扩展青霉孢子的抑制作用机制。结果显示,抗菌肽对扩展青霉孢子的最小抑菌浓度(minimum inhibitory concentration,MIC)为3.5 AU/mL。经0.5、1 MIC和2 MIC抗菌肽处理的扩展青霉孢子萌发率降低显著(P<0.05),与空白对照组相比,分别降低了28.30%、84.57%和100%。抗菌肽作用后,导致扩展青霉孢子凹陷严重、内容物泄漏、形态和结构发生改变,且抗菌肽使扩展青霉的细胞壁受到损伤,导致碱性磷酸酶外泄。抗菌肽作用扩展青霉后,消散了细胞膜电势,且消散程度呈浓度依赖性;增加了细胞膜渗透性,导致K+外泄;增加了细胞膜的流动性,使DPH荧光强度显著降低(P<0.05);破坏了细胞膜完整性,使SYTOX-Green荧光强度和PI沾染率升高。同时,经1、2 MIC抗菌肽处理的扩展青霉孢子DCFH-DA荧光强度显著增大(P<0.05),细胞内出现活性氧累积,影响了扩展青霉孢子正常的生理代谢。综上,抗菌肽对扩展青霉孢子抑制作用的靶位点主要为细胞膜和活性氧代谢。

关键词: 爱媛类芽孢杆菌;抗菌肽;扩展青霉;孢子;抑菌机制

Abstract: Penicillium expansum, a common spoilage organism in postharvest fruits, can cause fruit decay and deterioration and endanger human health. It is of great significance to investigate the antimicrobial mechanism of the antimicrobial peptide from Paenibacillus ehimensis on P. expansum spores. The antimicrobial activity of the antimicrobial peptide against P. expansum spores was determined by using the two-fold dilution method as well as measuring the time-killing curve. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) were used to evaluate the effect of the antimicrobial peptide on the ultrastructure of P. expansum spores. The effects of the antimicrobial peptide on the cell membrane and reactive oxygen species (ROS) accumulation of P. expansum were analyzed by fluorescence probes. The results showed that the minimum inhibitory concentration (MIC) of the antimicrobial peptide against P. expansum spores was 3.5 AU/mL. The spore germination rate was significantly decreased by 28.30%, 84.57% and 100% by the antimicrobial peptide at concentrations of 0.5 MIC, 1 MIC and 2 MIC compared with the blank control (P < 0.05). After treatment with the antimicrobial peptide, the spores appeared seriously sunken, the intracellular contents were leaked out, and the morphology and structure were changed. The antimicrobial peptide damaged the cell wall of P. expansum, resulting in the leakage of alkaline phosphatase. The antimicrobial peptide depolarized the cell membrane potential in a dose-dependent manner, and increased the cell membrane permeability, leading to K+ leakage. The fluidity of the cell membrane was increased, which in turn resulted in a significant decrease in DPH fluorescence intensity (P < 0.05). The integrity of the cell membrane was damaged by the antimicrobial peptide, so the fluorescence intensity of SYTOX-Green and the contamination rate of PI were increased. Moreover, the antimicrobial peptide at 1 MIC and 2 MIC increased the fluorescence intensity of DCFH-DA significantly (P < 0.05) and resulted in ROS accumulation, which affected the physiology and metabolism of P. expansum spores. This study indicated that the target sites of the antimicrobial peptide against P. expansum spores were mainly the cell membrane and ROS metabolism.

Key words: Paenibacillus ehimensis; antimicrobial peptide; Penicillium expansum; spore; antimicrobial mechanism

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