Tejal Barkhade, Kushagra Nigam, G. Ravi, Seema Rawat, S. K. Nema
{"title":"血浆灭菌灭活细菌:可能的机制和生化作用的研究","authors":"Tejal Barkhade, Kushagra Nigam, G. Ravi, Seema Rawat, S. K. Nema","doi":"10.1007/s11090-023-10429-5","DOIUrl":null,"url":null,"abstract":"<div><p>The underlying mechanisms and biochemical actions responsible for inactivation of pathogenic gram-positive <i>Staphylococcus aureus</i> (<i>S. aureus</i>) and gram-negative <i>Salmonella abony</i> (<i>S. abony</i>) bacteria upon exposure to sub-atmospheric plasma has been investigated. Reduction in colony forming units of the bacteria is established in 60 min and 40 min for <i>S. aureus </i>and <i>S. abony</i> respectively via 6-log reduction curves. The percentage change in reactive oxygen species, such as <sup>•</sup>OH and H<sub>2</sub>O<sub>2</sub> formed on bacterial membrane during plasma exposure are analysed using spectroflurometer. <i>S. aureus</i> exhibited a significant increase of 324.23% and 1554.84% in <sup>•</sup>OH and H<sub>2</sub>O<sub>2</sub> radicals respectively. Whereas, 98.14% and 54.49% increase in <sup>•</sup>OH and H<sub>2</sub>O<sub>2</sub> radicals respectively was observed in <i>S. abony</i>. The oxidation and degradation of DNA is analysed using an ultra violet visible spectrophotometer. The leakage of proteins, lipids, and nucleic acid molecules due to plasma exposure is studied by Attenuated Total Reflectance Fourier-transform infrared spectroscopy (ATR-FTIR). The alteration of secondary protein structure on the cell membrane is observed using Circular Dichroism. Upon exposure to plasma, <i>S. aureus </i>shows a secondary protein structural transition from α-helix (2.4%), β-sheet (78.3%) mixture to modified β-sheet structure (0% α-helix, 79.1% β-sheet). Whereas, <i>S.abony</i> shows a transition from α-helix (1%), β-sheet (64.9%) mixture to modified β-sheet structure (0% α-helix, 74.5% β-sheet). The bacterial morphological study (swelling/shrinking) done using Field Emission Scanning Electron Microscopy (FE-SEM) reveals the deformation of cell membrane. Above findings pave the way for a better understanding of the processes of antimicrobial inactivation strategies when the plasma sterilization process is employed.</p></div>","PeriodicalId":734,"journal":{"name":"Plasma Chemistry and Plasma Processing","volume":null,"pages":null},"PeriodicalIF":2.6000,"publicationDate":"2023-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Plasma Sterilization for Bacterial Inactivation: Studies on Probable Mechanisms and Biochemical Actions\",\"authors\":\"Tejal Barkhade, Kushagra Nigam, G. Ravi, Seema Rawat, S. K. Nema\",\"doi\":\"10.1007/s11090-023-10429-5\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The underlying mechanisms and biochemical actions responsible for inactivation of pathogenic gram-positive <i>Staphylococcus aureus</i> (<i>S. aureus</i>) and gram-negative <i>Salmonella abony</i> (<i>S. abony</i>) bacteria upon exposure to sub-atmospheric plasma has been investigated. Reduction in colony forming units of the bacteria is established in 60 min and 40 min for <i>S. aureus </i>and <i>S. abony</i> respectively via 6-log reduction curves. The percentage change in reactive oxygen species, such as <sup>•</sup>OH and H<sub>2</sub>O<sub>2</sub> formed on bacterial membrane during plasma exposure are analysed using spectroflurometer. <i>S. aureus</i> exhibited a significant increase of 324.23% and 1554.84% in <sup>•</sup>OH and H<sub>2</sub>O<sub>2</sub> radicals respectively. Whereas, 98.14% and 54.49% increase in <sup>•</sup>OH and H<sub>2</sub>O<sub>2</sub> radicals respectively was observed in <i>S. abony</i>. The oxidation and degradation of DNA is analysed using an ultra violet visible spectrophotometer. The leakage of proteins, lipids, and nucleic acid molecules due to plasma exposure is studied by Attenuated Total Reflectance Fourier-transform infrared spectroscopy (ATR-FTIR). The alteration of secondary protein structure on the cell membrane is observed using Circular Dichroism. Upon exposure to plasma, <i>S. aureus </i>shows a secondary protein structural transition from α-helix (2.4%), β-sheet (78.3%) mixture to modified β-sheet structure (0% α-helix, 79.1% β-sheet). Whereas, <i>S.abony</i> shows a transition from α-helix (1%), β-sheet (64.9%) mixture to modified β-sheet structure (0% α-helix, 74.5% β-sheet). The bacterial morphological study (swelling/shrinking) done using Field Emission Scanning Electron Microscopy (FE-SEM) reveals the deformation of cell membrane. Above findings pave the way for a better understanding of the processes of antimicrobial inactivation strategies when the plasma sterilization process is employed.</p></div>\",\"PeriodicalId\":734,\"journal\":{\"name\":\"Plasma Chemistry and Plasma Processing\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.6000,\"publicationDate\":\"2023-11-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Plasma Chemistry and Plasma Processing\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s11090-023-10429-5\",\"RegionNum\":3,\"RegionCategory\":\"物理与天体物理\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"ENGINEERING, CHEMICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plasma Chemistry and Plasma Processing","FirstCategoryId":"5","ListUrlMain":"https://link.springer.com/article/10.1007/s11090-023-10429-5","RegionNum":3,"RegionCategory":"物理与天体物理","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
Plasma Sterilization for Bacterial Inactivation: Studies on Probable Mechanisms and Biochemical Actions
The underlying mechanisms and biochemical actions responsible for inactivation of pathogenic gram-positive Staphylococcus aureus (S. aureus) and gram-negative Salmonella abony (S. abony) bacteria upon exposure to sub-atmospheric plasma has been investigated. Reduction in colony forming units of the bacteria is established in 60 min and 40 min for S. aureus and S. abony respectively via 6-log reduction curves. The percentage change in reactive oxygen species, such as •OH and H2O2 formed on bacterial membrane during plasma exposure are analysed using spectroflurometer. S. aureus exhibited a significant increase of 324.23% and 1554.84% in •OH and H2O2 radicals respectively. Whereas, 98.14% and 54.49% increase in •OH and H2O2 radicals respectively was observed in S. abony. The oxidation and degradation of DNA is analysed using an ultra violet visible spectrophotometer. The leakage of proteins, lipids, and nucleic acid molecules due to plasma exposure is studied by Attenuated Total Reflectance Fourier-transform infrared spectroscopy (ATR-FTIR). The alteration of secondary protein structure on the cell membrane is observed using Circular Dichroism. Upon exposure to plasma, S. aureus shows a secondary protein structural transition from α-helix (2.4%), β-sheet (78.3%) mixture to modified β-sheet structure (0% α-helix, 79.1% β-sheet). Whereas, S.abony shows a transition from α-helix (1%), β-sheet (64.9%) mixture to modified β-sheet structure (0% α-helix, 74.5% β-sheet). The bacterial morphological study (swelling/shrinking) done using Field Emission Scanning Electron Microscopy (FE-SEM) reveals the deformation of cell membrane. Above findings pave the way for a better understanding of the processes of antimicrobial inactivation strategies when the plasma sterilization process is employed.
期刊介绍:
Publishing original papers on fundamental and applied research in plasma chemistry and plasma processing, the scope of this journal includes processing plasmas ranging from non-thermal plasmas to thermal plasmas, and fundamental plasma studies as well as studies of specific plasma applications. Such applications include but are not limited to plasma catalysis, environmental processing including treatment of liquids and gases, biological applications of plasmas including plasma medicine and agriculture, surface modification and deposition, powder and nanostructure synthesis, energy applications including plasma combustion and reforming, resource recovery, coupling of plasmas and electrochemistry, and plasma etching. Studies of chemical kinetics in plasmas, and the interactions of plasmas with surfaces are also solicited. It is essential that submissions include substantial consideration of the role of the plasma, for example, the relevant plasma chemistry, plasma physics or plasma–surface interactions; manuscripts that consider solely the properties of materials or substances processed using a plasma are not within the journal’s scope.