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首页> 外文期刊>Photodiagnosis and Photodynamic Therapy >Inactivation of specific spoilage organism (Pseudomonas) of sturgeon by curcumin-mediated photodynamic inactivation
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Inactivation of specific spoilage organism (Pseudomonas) of sturgeon by curcumin-mediated photodynamic inactivation

机译:通过姜黄介导的光动力灭活使鲟鱼特异性腐败生物(假鼠)的灭活

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摘要

The present study aimed to measure the inactivation effect and mechanism of curcumin-mediated photodynamic inactivation (PDI) on the specific spoilage organism (Pseudomonas) of the sturgeon. The conditions of PDI used were as follows: 30 mu M curcumin, 15 W LED light (470 nm) power and 90 s irradiation time. Under these conditions, the high-throughput sequencing was used to study the microbiota of sturgeon. The method of aerobic plate colony count (APC) was used to determine the viability of Pseudomonas after PDI. Sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE), the propidium iodide (PI) single staining method, and agarose gel electrophoresis were used to study the inactivation mechanism of PDI on Pseudomonas. The results showed that Pseudomonas was the specific spoilage organism of sturgeon, and PDI significantly inhibited the growth of Pseudomonas. The in-vitro inactivation rate of Pseudomonas was 99.9% with counts decreased by 3.19 +/- 0.15 log(10) CFU/mL. The mechanism of PDI to inactivate Pseudomonas is as follows. Firstly, the high-level structure of membrane protein was destroyed, and the cell membrane permeability was increased, which caused leakage of cellular content. Then the nucleic acid inside the cell was destroyed, which eventually caused the death of bacteria. These findings demonstrate that curcumin-mediated PDI can be utilized as an effective way to inactivate the specific spoilage organism (Pseudomonas) of the sturgeon.
机译:本研究旨在测量姜黄素介导的光动力灭活(PDI)对鲟鱼的特定腐败生物(Pseudomonas)的灭活效应和机制。使用的PDI条件如下:30μm姜黄素,15W LED光(470nm)功率和90秒照射时间。在这些条件下,使用高通量测序来研究鲟鱼的微生物群。使用有氧板菌落计数(APC)的方法来确定PDI后假单胞菌的活力。二甲基硫酸钠聚丙烯酰胺凝胶电泳(SDS-PAGE),碘化钛(PI)单染色方法和琼脂糖凝胶电泳研究PDI对假单胞菌的灭活机制。结果表明,假单胞菌是鲟鱼的特异性腐败生物,PDI显着抑制了假单胞菌的生长。假单胞菌的体外灭活率为99.9%,计数下降3.19 +/- 0.15对数(10)CFU / mL。 PDI对失活伪蛋白酶的机制如下。首先,破坏了膜蛋白的高级结构,并且升高了细胞膜渗透性,这导致细胞含量泄漏。然后破坏细胞内的核酸,最终导致细菌死亡。这些发现表明,姜黄素介导的PDI可以用作灭活鲟鱼的特定腐败生物(假单胞菌)的有效方法。

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  • 来源
    《Photodiagnosis and Photodynamic Therapy》 |2020年第9期|101827.1-101827.7|共7页
  • 作者单位

    Ocean Univ China Coll Food Sci & Engn 5 Yushan Rd Qingdao 266003 Peoples R China;

    Ocean Univ China Coll Food Sci & Engn 5 Yushan Rd Qingdao 266003 Peoples R China;

    Jiangsu Univ Sch Food & Bioengn Zhenjiang 212013 Jiangsu Peoples R China;

    Henan Univ Sci & Technol Coll Food & Bioengn Luoyang 471023 Peoples R China;

    Hisense Shandong Refrigerator Co Ltd Qingdao 266100 Peoples R China;

    Hisense Shandong Refrigerator Co Ltd Qingdao 266100 Peoples R China;

    Jiangsu Baoyuan Biotechnol Co Ltd Lianyungang 222100 Peoples R China;

    Ocean Univ China Coll Food Sci & Engn 5 Yushan Rd Qingdao 266003 Peoples R China;

    Ocean Univ China Coll Food Sci & Engn 5 Yushan Rd Qingdao 266003 Peoples R China;

    Ocean Univ China Coll Food Sci & Engn 5 Yushan Rd Qingdao 266003 Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Sturgeon; Pseudomonas; Photodynamic; Curcumin; Microbiota; Inactivation mechanism;

    机译:鲟鱼;假动力学;姜黄素;微生物蛋白;灭活机制;

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