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Recombinant expression and activity analysis of the lyase lysV208 from aphage of Vibrio alginolyticus
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Jinrong NI1, Yingying YE1, Ying MA1, Hongjiao CAI1, Honglian TAN2, Guixiang TONG2, Xinxian WEI2, Wenhong FANG3, Qibiao WENG4, Mao LIN1
Acta Microbiologica Sinica | 2025, 65(10) : 4431 - 4443
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Acta Microbiologica Sinica | 2025, 65(10): 4431-4443
Research Article
Recombinant expression and activity analysis of the lyase lysV208 from aphage of Vibrio alginolyticus
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Jinrong NI1, Yingying YE1, Ying MA1, Hongjiao CAI1, Honglian TAN2, Guixiang TONG2, Xinxian WEI2, Wenhong FANG3, Qibiao WENG4, Mao LIN1
Affiliations
  • 1Engineering Research Center of the Modern Technology for Eel Industry, Ministry of Education, Fisheries College of Jimei University, Xiamen, Fujian, China
  • 2Key Laboratory of Aquaculture Genetic Breeding and Healthy Aquaculture of Guangxi, Guangxi Academy of Fishery Sciences, Nanning, Guangxi, China
  • 3East China Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Shanghai, China
  • 4Key Laboratory of Eel Aquaculture and Processing of Fujian Province, Fuzhou, Fujian, China
Published: 2025-09-04 doi: 10.13343/j.cnki.wsxb.20250170
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[Objective] To identify and develop a phage-derived lyase that can be heterologously expressed with high activity and stability and determine its optimal working conditions. [Methods] We employed the turbidity reduction assay to evaluate the bacteriolytic activity and identify the optimal parameters. [Results] Genome annotation and protein prediction of the Vibrio alginolyticus phage phiV208 showed that ORF30 encoded a lyase, named lysV208. This enzyme demonstrated soluble expression in Escherichia coli BL21(DE3), reaching a purified concentration of 204 μg/mL after 16 h induction with 0.25 mmol/L IPTG. Its bacteriolytic activity (turbidity reduction rate) increased from 24.2% to 68.0% in the presence of 0.5 mmol/L EDTA. Enzymatic characterization revealed that lysV208 exhibited the maximum bacteriolytic activity (75.6%) at 45 ℃ while maintaining high activity (52.8%-71.9%) within the temperature range of 25-37 ℃, which is typical for bacterial disease outbreaks in aquatic and terrestrial animals. The enzyme showed the maximum activity at pH 7.0 and retained substantial bacteriolytic activity (44.0%-63.2%) under alkalescence conditions (pH 7.0-9.0), demonstrating adaptability to marine and freshwater aquaculture environments. Divalent metal ions including Zn2+, Mg2+, Mn2+, and Fe2+ at 0.1-1.0 mmol/L moderately enhanced the bacteriolytic activity of lysV208, whereas those at 10.0 mmol/L reduced the activity (P<0.01). In addition, lysV208 displayed broad-spectrum lytic effects, showing the bacteriolytic activity of 59.7% against V. alginolyticus V039, 68.9% against Vibrio vulnificus H1, 65.8% against Vibrio parahaemolyticus GH32, and 38.0% and 65.6% against Vibrio harveyi TY13 and G1, respectively. [Conclusion] The recombinant lyase lysV208 demonstrates robust and stable in vitro bacteriolytic activity and a broader spectrum than its source phage. These findings highlight its potential for the control of bacterial infections and the development of phage-lyase synergistic agents.

Vibrio alginolyticus  /  phage  /  lyase  /  recombinant expression  /  bacteriolysis
Jinrong NI, Yingying YE, Ying MA, Hongjiao CAI, Honglian TAN, Guixiang TONG, Xinxian WEI, Wenhong FANG, Qibiao WENG, Mao LIN. Recombinant expression and activity analysis of the lyase lysV208 from aphage of Vibrio alginolyticus[J]. Acta Microbiologica Sinica, 2025 , 65 (10) : 4431 -4443 . DOI: 10.13343/j.cnki.wsxb.20250170
  • Key Research and Development Program of Guangxi Zhuang Autonomous Region(GUIKE AB23026030)
  • Natural Science Foundation of Fujian Province(2023J01143)
  • Social Science Foundation of Fujian Province(FJ2024B185)
  • Quanzhou Science and Technology Project(2022N044)
Year 2025 volume 65 Issue 10
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Article Info
doi: 10.13343/j.cnki.wsxb.20250170
  • Receive Date:2025-03-03
  • Online Date:2025-11-03
  • Published:2025-09-04
Article Data
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History
  • Received:2025-03-03
  • Accepted:2025-06-25
Funding
Key Research and Development Program of Guangxi Zhuang Autonomous Region(GUIKE AB23026030)
Natural Science Foundation of Fujian Province(2023J01143)
Social Science Foundation of Fujian Province(FJ2024B185)
Quanzhou Science and Technology Project(2022N044)
Affiliations
    1Engineering Research Center of the Modern Technology for Eel Industry, Ministry of Education, Fisheries College of Jimei University, Xiamen, Fujian, China
    2Key Laboratory of Aquaculture Genetic Breeding and Healthy Aquaculture of Guangxi, Guangxi Academy of Fishery Sciences, Nanning, Guangxi, China
    3East China Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Shanghai, China
    4Key Laboratory of Eel Aquaculture and Processing of Fujian Province, Fuzhou, Fujian, China

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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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