食品科学 ›› 2017, Vol. 38 ›› Issue (10): 55-60.doi: 10.7506/spkx1002-6630-201710010

• 生物工程 • 上一篇    下一篇

抗荧光假单胞菌Carnobacterium spp. LB1培养 发酵条件的优化

董韩博,谢 晶,钱韻芳,杨胜平,苟 怡   

  1. 上海水产品加工及贮藏工程技术研究中心,上海海洋大学食品学院,上海 201306
  • 出版日期:2017-05-25 发布日期:2017-05-23
  • 基金资助:
    国家自然科学基金面上项目(31571914);上海市科技兴农重点攻关项目(沪农科攻字(2016)第1-1号); 上海市科委平台能力提升项目(16DZ2280300)

Optimization of Culture Conditions of Carnobacterium spp. LB1 for Enhanced Production of Anti-Pseudomonas fluorescens Metabolites

DONG Hanbo, XIE Jing , QIAN Yunfang, YANG Shengping, GOU Yi   

  1. Shanghai Engineering Research Center of Aquatic Product Processing and Preservation, College of Food Science and Technology, Shanghai Ocean University, Shanghai 201306, China
  • Online:2017-05-25 Published:2017-05-23

摘要: 为了改善和优化海产品源肉食杆菌(Carnobacterium)spp. LB1产有效抑菌代谢产物的培养发酵条件,提 高对荧光假单胞菌(Pseudomonas fluorescens)的抑菌效果。基于单因素试验,从对Carnobacterium spp. LB1抑菌 效果有影响的5 个因素中筛选出3 个显著影响因素,运用Design-Expert软件的Box-Behnken试验设计原则研究3 个 显著影响因素的重要水平和交互作用。结果表明:Carnobacterium spp. LB1的最佳培养发酵条件:初始pH 6.22、 温度28.6 ℃、葡萄糖质量分数3%。在最优培养条件下,Carnobacterium spp. LB1的浓缩发酵液在15 h和18 h对 P. fluorescens的抑菌率分别为80.7%、86.3%,其抑菌机理是Carnobacterium spp. LB1破坏了P. fluorescens的细胞壁, 导致其通透性增大,碱性磷酸酶大量溢出,使其代谢紊乱,从而抑制了P. fluorescens的生长。同时,最优发酵条件 下获得的实验结果平均值与模型预测值基本吻合,进而说明所建立回归模型是可靠的。

关键词: 肉食杆菌, 荧光假单胞菌, 抑菌, 响应面

Abstract: This study aimed to optimize the culture conditions for Carnobacterium spp. LB1, isolated from the ribbonfish intestine, to produce anti-Pseudomonas fluorescens metabolites. By using one-factor-at-a-time method, three of the five factors were selected for their significant influences on the antibacterial activity. A Box-Behnken design was applied to evaluate the effects of interaction among the chosen variables and optimize them. The optimum culture conditions obtained were as follows: initial pH, 6.22; temperature, 28.6 ℃; and glucose concentration, 3%, where the percentage inhibition of concentrated fermentation broth harvested after 15 and 18 h against Pseudomonas fluorescens were 80.7% and 86.3%, respectively. The antibacterial mechanism was due to increased cell wall permeability and leakage of a large amount of alkaline phosphatase (AKP) after the destruction of the cell wall of Pseudomonas fluorescens, leading to metabolic disorders. Finally, the experimental results obtained under the optimized fermentation conditions were in good agreement with the model predictions, indicating that the established model in this study was feasible.

Key words: Carnobacterium spp. LB1, Pseudomonas fluorescens, antibacterial activity, response surface methodology

中图分类号: