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中国精品科技期刊2020
王伟宇, 林洪, 王静雪. 副溶血弧菌噬菌体qdvp001重组内溶素诱导表达以及理化性质初步研究[J]. 食品工业科技, 2016, (16): 205-209. DOI: 10.13386/j.issn1002-0306.2016.16.032
引用本文: 王伟宇, 林洪, 王静雪. 副溶血弧菌噬菌体qdvp001重组内溶素诱导表达以及理化性质初步研究[J]. 食品工业科技, 2016, (16): 205-209. DOI: 10.13386/j.issn1002-0306.2016.16.032
WANG Wei-yu, LIN Hong, WANG Jing-xue. Characterization of recombinant endolysin from Vibrio parahaemolytics-infecting bacteriophage qdvp001[J]. Science and Technology of Food Industry, 2016, (16): 205-209. DOI: 10.13386/j.issn1002-0306.2016.16.032
Citation: WANG Wei-yu, LIN Hong, WANG Jing-xue. Characterization of recombinant endolysin from Vibrio parahaemolytics-infecting bacteriophage qdvp001[J]. Science and Technology of Food Industry, 2016, (16): 205-209. DOI: 10.13386/j.issn1002-0306.2016.16.032

副溶血弧菌噬菌体qdvp001重组内溶素诱导表达以及理化性质初步研究

Characterization of recombinant endolysin from Vibrio parahaemolytics-infecting bacteriophage qdvp001

  • 摘要: 对重组内溶素Lysqdvp001诱导表达条件进行探讨,发现适当降低诱导温度,可以避免包涵体的形成。最终确定诱导表达条件为25℃、IPTG浓度为1 mmol/L、诱导4 h,此时不仅蛋白表达量大并且不形成包涵体。为研究Lyqdvp001抑菌以及理化性能,采用浊度法对p H、温度、离子强度对裂解活性的影响进行探讨。结果表明,Lysqdvp001具有宽p H适应性,p H310均能很好发挥作用;耐高温,在75℃处理30 min仍能维持70%活性;低浓度(0.1 mmol/L)的Zn2+、Fe2+以及各浓度(10、1、0.1 mmol/L)的Ca2+可以明显提高重组内溶素Lysqdvp001活性。结果显示重组内溶素有作为抑菌剂的潜力。 

     

    Abstract: The inducible expression conditions of the recombinant endolysin Lysqdvp001 were discussed,founding that lowering temperature properly could avoid forming inclusion bodies. It was concluded that the recombinant endolysin Lysqdvp001 was induced by the addition of 1 mmol / L IPTG at 25 ℃ for 4 h. Under this condition,the Lysqdvp001 was soluble and was expressed in a high level.Then the Lysqdvp001 was characterized its lytic activity and biochemical properties such as p H,temperature and iron concentration by turbidity assay.The results showed that the Lysqdvp001 was stable over broad p H,maintaining good activities in p H3 ~ 10,and temperature ranges,maintaining 70% activity after 30 min at 75 ℃.Low iron concentration( 0.1 mmol / L) of Zn2+and Fe2+and different iron concentration( 10,1,0.1 mmol / L) of Ca2+could increase lytic activity of Lysqdvp001. In conclusion,the Lysqdvp001 had the potential to be antibacterial agents.

     

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