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Heterologous expression of two novel bacteriocins produced by Lactobacillus crustorum MN047 and application of BM1157 in control of Listeria monocytogenes

机译:乳酸杆菌MN047产生的两种新菌菌素的异源表达及BM1157在李斯特菌单核细胞增生中的应用中的应用

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Foodbome pathogens cause diseases by food chain transmission, therefore preservatives or antimicrobials are essential for food products, among which bacteriocins are considered as promising alternatives of chemical preservatives. Moreover, bacteriocins can potentially be used as antibiotic alternatives. In this study, two genes of novel bacteriocins (BM1157 and BM1300) from probiotic Lactobacillus crustorum MN047 were identified, cloned, and then expressed in Escherichia coli expression system. The genes were inserted into expression vector pET-28a and transformed into competent E. coli BL21 (DE3) pLysS, after which the two bacteriocins were successfully heterologously expressed. Further, it showed that the BM1157 and the BM1300 had broad spectrum activity against gram-positive and gram-negative bacteria, including multidrug-resistant strains. The characteristics and action mode of the BM1157 were further investigated because of its higher antimicrobial activity. It was found that the BM1157 had MIC value of 5.2 mu g/mL against both S. aureus and E. coli. Moreover, it was stable at high temperature and resistant to proteinases. The BM1157 had bactericidal action mode according to time-kill curve. The results of scanning electron microscope and transmission electron microscope demonstrated that the BM1157 killed Listeria monocytogenes by biofilm destruction and pore formation. The antibiofilm activity and pore formation were further verified by crystal violet dye and lactic dehydrogenase release. In addition, the BM1157 inhibited the growth of L monocytogenes in milk. (C) 2017 Elsevier Ltd. All rights reserved.
机译:食品组群病原体引起食物链传输的疾病,因此防腐剂或抗微生物剂对食品至关重要,其中细菌科被认为是化学防腐剂的有前途的替代品。此外,细菌偶联可能用作抗生素替代品。在该研究中,鉴定了来自益生菌乳酸杆菌MN047的两种新型菌丝(BM1157和BM1300),克隆,然后在大肠杆菌表达系统中表达。将该基因插入表达载体PET-28a中并转化为竞争力的大肠杆菌BL21(DE3)帘布层,之后成功地表达了两种菌丝。此外,它表明,BM1157和BM1300对革兰氏阳性和革兰氏阴性细菌具有广泛的光谱活性,包括多药抗性菌株。由于其抗微生物活性较高,进一步研究了BM1157的特征和动作模式。发现BM1157的MIC值为5.2μg/ mL,对氏菌氏菌和大肠杆菌具有5.2μg/ ml。此外,它在高温下稳定,抗蛋白酶。根据时间杀死曲线,BM1157具有杀菌作用模式。扫描电子显微镜和透射电子显微镜的结果表明,BM1157通过生物膜破坏和孔形成杀死了李斯特菌单核细胞增生。通过晶体紫染料和乳酸脱氢酶释放进一步验证抗血丝活性和孔形成。此外,BM1157抑制牛奶中L单核细胞增生的生长。 (c)2017 Elsevier Ltd.保留所有权利。

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