Guo Tingting, Xin YongPing, Zhang Chenchen, Ouyang Xudong, Kong Jian
State Key Laboratory of Microbial Technology, Shandong University, 27 Shanda Nanlu, Jinan, 250100, People's Republic of China.
School of Environmental Science and Engineering, Shandong University, Jinan, 250100, People's Republic of China.
Appl Microbiol Biotechnol. 2016 Apr;100(8):3545-54. doi: 10.1007/s00253-015-7185-x. Epub 2015 Dec 1.
Phage endolysins have received increased attention in recent times as potential antibacterial agents and the biopreservatives in food production processes. Staphylococcus aureus is one of the most common pathogens in bacterial food poisoning outbreaks. In this study, the endolysin Lysdb, one of the two-component cell lysis cassette of Lactobacillus delbrueckii phage phiLdb, was shown to possess a muramidase domain and catalytic sites with homology to Chalaropsis-type lysozymes. Peptidoglycan hydrolytic bond specificity determination revealed that Lysdb was able to cleave the 6-O-acetylated peptidoglycans present in the cell walls of S. aureus. Turbidity reduction assays demonstrated that Lysdb could effectively lyse the S. aureus live cells under acidic and mesothermal conditions. To further evaluate the ability of Lysdb as a potential antibacterial agent against S. aureus in cheese manufacture, Lactobacillus casei BL23 was engineered to constitutively deliver active Lysdb to challenge S. aureus in lab-scale cheese making from raw milk. Compared with the raw milk, the viable counts of S. aureus were reduced by 10(5)-fold in the cheese inoculated with the engineered L. casei strain during the fermentation process, and the pathogenic bacterial numbers remained at a low level (10(4) CFU/g) after 6 weeks of ripening at 10 °C. Taken together, all results indicated that the Lysdb has the function as an effective tool for combating S. aureus during cheese manufacture from raw milk.
近年来,噬菌体溶菌酶作为潜在的抗菌剂和食品生产过程中的生物防腐剂受到了越来越多的关注。金黄色葡萄球菌是细菌性食物中毒爆发中最常见的病原体之一。在本研究中,德氏乳杆菌噬菌体phiLdb的双组分细胞裂解盒之一的溶菌酶Lysdb被证明具有一个胞壁质酶结构域和与Chalaropsis型溶菌酶具有同源性的催化位点。肽聚糖水解键特异性测定表明,Lysdb能够裂解金黄色葡萄球菌细胞壁中存在的6-O-乙酰化肽聚糖。浊度降低试验表明,Lysdb在酸性和中温条件下能够有效裂解金黄色葡萄球菌活细胞。为了进一步评估Lysdb作为一种潜在抗菌剂在奶酪制造中对抗金黄色葡萄球菌的能力,干酪乳杆菌BL23被改造为组成型表达活性Lysdb,以在实验室规模的生牛奶奶酪制作中挑战金黄色葡萄球菌。与生牛奶相比,在发酵过程中,接种了工程化干酪乳杆菌菌株的奶酪中金黄色葡萄球菌的活菌数减少了10^5倍,并且在10℃成熟6周后,病原菌数量保持在较低水平(10^4 CFU/g)。综上所述,所有结果表明,Lysdb在生牛奶奶酪制造过程中具有作为对抗金黄色葡萄球菌的有效工具的功能。