Molecular cloning, expression and characterization of a bacteriophage JN01 endolysin and its antibacterial activity against E. coli O157:H7. (1st August 2022)
- Record Type:
- Journal Article
- Title:
- Molecular cloning, expression and characterization of a bacteriophage JN01 endolysin and its antibacterial activity against E. coli O157:H7. (1st August 2022)
- Main Title:
- Molecular cloning, expression and characterization of a bacteriophage JN01 endolysin and its antibacterial activity against E. coli O157:H7
- Authors:
- Shen, Kai-Sheng
Shu, Mei
Tang, Meng-Xuan
Yang, Wen-Yu
Wang, Shu-Chao
Zhong, Chan
Wu, Guo-Ping - Abstract:
- Abstract: Endolysins encoded by bacteriophages are considered bacteriostatic agents for the prevention of pathogenic bacteria proliferations. In this study, a possible endolysin from bacteriophage JN01, namely LysJN01, belonging to the lysozyme-like superfamily, was cloned, expressed and characterized. Meanwhile, the bactericidal activity of recombinant LysJN01 (rLysJN01) against E. coli O157:H7 was evaluated in Tris-HCl buffer and on lettuce. Recombinant LysJN01(rLysJN01) consists of a single domain with a molecular weight of about 20 kDa. The yield of rLysJN01 was about 20 mg/L rLysJN01 had a strong lytic activity against chloroform treated E. coli O157:H7. It combined with EDTA could also significantly lyse E. coli O157:H7. Afterward, rlysJN01 showed high enzymatic activity stability at temperature (4–95 O C) and pH (5.0–11.0). Moreover, it also revealed a broad spectrum of antimicrobial activity against Gram-negative pathogens, such as E. coli, Salmonella and Pseudomonas aeruginosa . Furthermore, the counts of E. coli O157:H7 on contaminated lettuce was significantly reduced by 91.6% and 97.8% after treatment with a combination of 60 μg/mL rLysJN01 and 0.5 mmol/L EDTA for 30 min and 60 min, respectively. All these results indicated that rLysJN01 is a potential and efficient bacteriostatic agent for biocontrol of E. coli O157:H7. Highlights: The endolysin LysJN01 of phage JN01 was soluble recombinant expressed and characterized. RLysJN01 had stable lytic activity againstAbstract: Endolysins encoded by bacteriophages are considered bacteriostatic agents for the prevention of pathogenic bacteria proliferations. In this study, a possible endolysin from bacteriophage JN01, namely LysJN01, belonging to the lysozyme-like superfamily, was cloned, expressed and characterized. Meanwhile, the bactericidal activity of recombinant LysJN01 (rLysJN01) against E. coli O157:H7 was evaluated in Tris-HCl buffer and on lettuce. Recombinant LysJN01(rLysJN01) consists of a single domain with a molecular weight of about 20 kDa. The yield of rLysJN01 was about 20 mg/L rLysJN01 had a strong lytic activity against chloroform treated E. coli O157:H7. It combined with EDTA could also significantly lyse E. coli O157:H7. Afterward, rlysJN01 showed high enzymatic activity stability at temperature (4–95 O C) and pH (5.0–11.0). Moreover, it also revealed a broad spectrum of antimicrobial activity against Gram-negative pathogens, such as E. coli, Salmonella and Pseudomonas aeruginosa . Furthermore, the counts of E. coli O157:H7 on contaminated lettuce was significantly reduced by 91.6% and 97.8% after treatment with a combination of 60 μg/mL rLysJN01 and 0.5 mmol/L EDTA for 30 min and 60 min, respectively. All these results indicated that rLysJN01 is a potential and efficient bacteriostatic agent for biocontrol of E. coli O157:H7. Highlights: The endolysin LysJN01 of phage JN01 was soluble recombinant expressed and characterized. RLysJN01 had stable lytic activity against chloroform treated E. coli O157:H7. RlysJN01 had a broad spectrum of antibacterial activity against Gram-negative bacteria. RLysJN01 combined with EDTA reduced E. coli O157:H7 on lettuce by 97.8% in 1 h. … (more)
- Is Part Of:
- Lebensmittel-Wissenschaft + Technologie =. Volume 165(2022)
- Journal:
- Lebensmittel-Wissenschaft + Technologie =
- Issue:
- Volume 165(2022)
- Issue Display:
- Volume 165, Issue 2022 (2022)
- Year:
- 2022
- Volume:
- 165
- Issue:
- 2022
- Issue Sort Value:
- 2022-0165-2022-0000
- Page Start:
- Page End:
- Publication Date:
- 2022-08-01
- Subjects:
- Bacteriophage endolysin -- Expression -- Characterization -- E. coli O157:H7 -- Antibacterial activity
Food industry and trade -- Periodicals
Food -- Composition -- Periodicals
Microbiology -- Periodicals
Nutrition -- Periodicals
664.005 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00236438 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.lwt.2022.113705 ↗
- Languages:
- English
- ISSNs:
- 0023-6438
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3983.070000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 22602.xml