Aluminium(III) Oxide-The Silent Killer of Bacteria

Molecules. 2023 Jan 3;28(1):401. doi: 10.3390/molecules28010401.

Abstract

In this article, we describe the antimicrobial properties of pristine anodised aluminium oxide matrices-the material many consider biologically inert. During a typical anodisation process, chromium and chlorine compounds are used for electropolishing and the removal of the first-step aluminium oxide. Matrices without the use of those harmful compounds were also fabricated and tested for comparison. The antibacterial tests were conducted on four strains of Escherichia coli: K12, R2, R3 and R4. The properties of the matrices were also compared to the three types of antibiotics: ciprofloxacin, bleomycin and cloxacillin using the Minimal Inhibitory Concentration (MIC) and Minimum Bactericidal Concentration (MBC) tests. Moreover, DNA was isolated from the analysed bacteria which was additionally digested with formamidopyrimidine-DNA glycosylase (Fpg) protein from the group of repair glycosases. These enzymes are markers of modified oxidised bases in nucleic acids produced during oxidative stress in cells. Preliminary cellular studies, MIC and MBC tests and digestion with Fpg protein after modification of bacterial DNA suggest that these compounds may have greater potential as antibacterial agents than the aforementioned antibiotics. The described composites are highly specific for the analysed model Escherichia coli strains and may be used in the future as new substitutes for commonly used antibiotics in clinical and nosocomial infections in the progressing pandemic era. The results show much stronger antibacterial properties of the functionalised membranes on the action of bacterial membranes in comparison to the antibiotics in the Fpg digestion experiment. This is most likely due to the strong induction of oxidative stress in the cell through the breakdown of the analysed bacterial DNA.

Keywords: Fpg glycosylase; anodic aluminium oxide; antibiotics; bacterial E. coli strains; oxidative stress.

MeSH terms

  • Aluminum / pharmacology
  • Aluminum Oxide
  • Anti-Bacterial Agents / pharmacology
  • DNA Repair*
  • DNA, Bacterial
  • DNA-Formamidopyrimidine Glycosylase / genetics
  • DNA-Formamidopyrimidine Glycosylase / metabolism
  • Escherichia coli / metabolism
  • Escherichia coli Proteins* / genetics
  • Oxides

Substances

  • Escherichia coli Proteins
  • Aluminum
  • DNA, Bacterial
  • Oxides
  • DNA-Formamidopyrimidine Glycosylase
  • Anti-Bacterial Agents
  • Aluminum Oxide

Grants and funding

This work was supported by the National Science Centre, Poland, grants 2017/26/E/ST5/00162, 2020/04/X/ST5/00127, and by the grant of the Medical University of Białystok, Poland, SUB/2/DN/22/001/2201.