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Destruction of biological particles using non-thermal plasma

机译:使用非热等离子体破坏生物颗粒

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摘要

Mechanism of inactivation of bio-particles exposed to non-thermal plasma (NTP), namely, dielectric barrier discharge (DBD), and plasma jet (PJ), has been studied using E. coli, B. subtilis spore, S. cerevisiae and bacteriophages. States of different biological components were monitored during the course of inactivation. Analysis of green fluorescent protein, GFP, introduced into E. coli. or B. subtiles spore cells proved that radicals generated by NTP penetrate into microbes, destroying the cell membrane and finally damage the genes. We have evaluated the damage of the bacteriophages. Bacteriophage λ having double stranded DNA was exposed to DBD, then DNA was purified and subjected to in vitro DNA packaging reactions. The re-packaged phages consist of the DNA from discharged phages and brand-new coat proteins were proved to be active, indicating that the damage of coat proteins is responsible for inactivation. M13 phages having single stranded DNA were also examined with the same manner. In this case, damage to the DNA was as severe as that of the coat proteins. For practical applications, DBD showed very intense sterilization ability for B. Subtilis spore with the D-value of less than 10 s. This result indicates a possibility of application of NTP for quick sterilization.
机译:已使用大肠杆菌,枯草芽孢杆菌孢子,酿酒酵母和大肠杆菌研究了暴露于非热等离子体(NTP)的生物粒子失活的机制,即介电势垒放电(DBD)和等离子体射流(PJ)。噬菌体。在灭活过程中监测不同生物成分的状态。分析引入大肠杆菌的绿色荧光蛋白GFP。或B. subtiles孢子细胞证明NTP产生的自由基渗透到微生物中,破坏细胞膜并最终破坏基因。我们已经评估了噬菌体的损害。将具有双链DNA的噬菌体λ暴露于DBD,然后纯化DNA并进行体外DNA包装反应。重新包装的噬菌体由排出噬菌体的DNA组成,全新的外壳蛋白被证明具有活性,表明外壳蛋白的损坏是导致失活的原因。还以相同的方式检查了具有单链DNA的M13噬菌体。在这种情况下,对DNA的破坏与外壳蛋白一样严重。在实际应用中,DBD对枯草芽孢杆菌的孢子表现出非常强的杀菌能力,D值小于10秒。该结果表明将NTP用于快速灭菌的可能性。

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