Cold atmospheric plasma shows a satisfactory ability to inactivate bacterial biofilms that are difficult to remove using conventional methods in some cases. However, the researches on the inactivation mechanism are not quite sufficient. Poly-beta-1-6-N-acetylglucosamine (PNAG), which is one of the important components in some biofilms, was used as the research subject, and the related mechanism of action triggered by different concentrations of the OH in plasma was studied using reactive molecular dynamics simulations. The results showed that OH radicals could not only trigger the hydrogen abstraction reaction leading to cleavage of the PNAG molecular structure, but undergo an OH addition reaction with PNAG molecules. New reaction pathways appeared in the simulations as the OH concentration increased, but the reaction efficiency first increased and then decreased. The simulation study in this paper could, to some extent, help elucidate the microscopic mechanism of the interaction between OH radicals in plasma and bacterial biofilms at the atomic level.
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The Department of Chemistry and Biochemistry, University of Maryland, College Park, MDThe Department of Chemistry and Biochemistry, University of Maryland, College Park, MD
Breslawec A.P.
Wang S.
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The Department of Chemistry and Biochemistry, University of Maryland, College Park, MDThe Department of Chemistry and Biochemistry, University of Maryland, College Park, MD
Wang S.
Li C.
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The Department of Chemistry and Biochemistry, University of Maryland, College Park, MDThe Department of Chemistry and Biochemistry, University of Maryland, College Park, MD
Li C.
Poulin M.B.
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The Department of Chemistry and Biochemistry, University of Maryland, College Park, MDThe Department of Chemistry and Biochemistry, University of Maryland, College Park, MD
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Hosp Sick Children, Program Mol Med, Toronto, ON, Canada
Univ Toronto, Dept Biochem, Toronto, ON, CanadaHosp Sick Children, Program Mol Med, Toronto, ON, Canada
Bamford, Natalie C.
Notte, Christina
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Hosp Sick Children, Program Mol Med, Toronto, ON, CanadaHosp Sick Children, Program Mol Med, Toronto, ON, Canada
Notte, Christina
Baker, Perrin
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Hosp Sick Children, Program Mol Med, Toronto, ON, CanadaHosp Sick Children, Program Mol Med, Toronto, ON, Canada
Baker, Perrin
Guragain, Manita
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Wake Forest Sch Med, Dept Microbiol & Immunol, Winston Salem, NC USA
Ohio State Univ, Wexner Med Ctr, Dept Microbial Infect & Immun, Columbus, OH 43210 USAHosp Sick Children, Program Mol Med, Toronto, ON, Canada
Guragain, Manita
Robinson, Howard
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Brookhaven Natl Lab, Photon Sci Div, Upton, NY 11973 USAHosp Sick Children, Program Mol Med, Toronto, ON, Canada
Robinson, Howard
Pier, Gerald B.
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Harvard Med Sch, Brigham & Womens Hosp, Dept Med, Div Infect Dis, Boston, MA USAHosp Sick Children, Program Mol Med, Toronto, ON, Canada
Pier, Gerald B.
Nitz, Mark
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Univ Toronto, Dept Chem, Toronto, ON, CanadaHosp Sick Children, Program Mol Med, Toronto, ON, Canada
Nitz, Mark
Deora, Rajendar
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Wake Forest Sch Med, Dept Microbiol & Immunol, Winston Salem, NC USA
Ohio State Univ, Wexner Med Ctr, Dept Microbial Infect & Immun, Columbus, OH 43210 USAHosp Sick Children, Program Mol Med, Toronto, ON, Canada
机构:
Hosp Sick Children, Program Mol Med, Toronto, ON, Canada
Univ Toronto, Dept Biochem, Toronto, ON, CanadaHosp Sick Children, Program Mol Med, Toronto, ON, Canada