食品科学 ›› 2026, Vol. 47 ›› Issue (9): 138-146.doi: 10.7506/spkx1002-6630-20251024-181

• 生物工程 • 上一篇    下一篇

鼠李糖乳酪杆菌高分子质量代谢产物的抑菌作用

陈昊暄,刘一平,刘雪,周炜,杨仁琴,陈大卫,张臣臣,关成冉   

  1. (1.扬州大学食品科学与工程学院,江苏 扬州 225009;2.扬州市扬大康源乳业有限公司,江苏 扬州 225009)
  • 出版日期:2026-05-15 发布日期:2026-06-03
  • 基金资助:
    国家自然科学基金青年科学基金项目(31700079)

Antibacterial Effects of High-Molecular-Mass Metabolites from Lacticaseibacillus rhamnosus

CHEN Haoxuan, LIU Yiping, LIU Xue, ZHOU Wei, YANG Renqin, CHEN Dawei, ZHANG Chenchen, GUAN Chengran   

  1. (1. College of Food Science and Engineering, Yangzhou University, Yangzhou 225009, China;2. Yangzhou Yangda Kangyuan Dairy Co. Ltd., Yangzhou 225009, China)
  • Online:2026-05-15 Published:2026-06-03

摘要: 探究鼠李糖乳酪杆菌(Lacticaseibacillus rhamnosus)YT 3 种高分子质量的代谢产物(表面活性剂、脂磷壁酸、胞外多糖)的抑菌、抑生物被膜能力,并从生牛乳中分离菌株,进一步研究3 种代谢产物对乳源微生物的抑制作用。结果表明,通过测定抑菌圈和生长曲线,3 种代谢产物在质量浓度为50 mg/mL和100 mg/mL时对6 种常见的食源腐败菌具有不同抑菌效果。3 种代谢产物对沙门氏菌(Salmonella enterica)的最低抑菌浓度(minimal inhibitory concentration,MIC)在60~100 mg/mL范围内,对铜绿假单胞菌(Pseudomonas aeruginosa)的MIC在80~150 mg/mL范围内。在1/4 MIC时,表面活性剂对S. enterica及P. aeruginosa生物被膜抑制率分别为43.33%、36.26%,脂磷壁酸为29.72%、24.19%,胞外多糖的生物被膜抑制能力则明显弱于表面活性剂、脂磷壁酸。当质量浓度提升至MIC时,3 种代谢成分对成熟生物被膜的破坏率均明显提高。对生牛乳中的微生物进行分离并开展16S rDNA测序,共分离出8 株菌,质量浓度60 mg/mL的表面活性剂对8 株菌的抑菌圈直径范围为9.00~14.00 mm,质量浓度120 mg/mL的脂磷壁酸抑菌圈直径范围为9.00~10.00 mm,质量浓度120 mg/mL的胞外多糖暂未表现明显的抑菌效果。本研究可用于开发以L. rhamnosus YT代谢产物为核心的天然抑菌剂,降低食品污染风险,满足消费者对绿色、安全食品的需求。

关键词: 鼠李糖乳酪杆菌;表面活性剂;脂磷壁酸;胞外多糖;食源腐败菌

Abstract: This study investigates the antibacterial and anti-biofilm activities of three high-molecular-mass metabolites (biosurfactant, lipoteichoic acid, and exopolysaccharide) from Lacticaseibacillus rhamnosus YT. Additionally, the bacteriostatic effects of these three metabolites on different strains isolated from raw milk were examined. The results showed that based on inhibition zone and growth curve assays, these metabolites exhibited varying degrees of antibacterial activity against six common food spoilage microorganisms at concentrations of 50 and 100 mg/mL. The minimum inhibitory concentration (MIC) against Salmonella enterica ranged from 60 to 100 mg/mL, while those against Pseudomonas aeruginosa ranged from 80 to 150 mg/mL. At 1/4 MIC concentration, the biosurfactant inhibited the biofilms of S. enterica and P. aeruginosa by 43.33% and 36.26%, respectively, compared with 29.72% and 24.19% for lipoteichoic acid. The anti-biofilm capacity of the exopolysaccharide was significantly weaker than those of the biosurfactant and lipoteichoic acid. When the concentration increased to the MIC, the disruption rates of mature biofilms by the three metabolites significantly increased. Eight strains from raw milk were isolated and identified by 16S rDNA sequencing. The diameters of the inhibition zones of the biosurfactant against these strains ranged from 9.00 to 14.00 mm, while those of the lipoteichoic acid ranged from 9.00 to 10.00 mm. At 120 mg/mL concentration, the exopolysaccharide showed no significant antibacterial effects. These findings support the development of natural antibacterial agents based on the metabolites of L. rhamnosus YT, thereby reducing the risk of food contamination and meeting consumer demand for green and safe food products.

Key words: Lacticaseibacillus rhamnosus; biosurfactant; lipoteichoic acid; exopolysaccharide; food spoilage microorganisms

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