Microbial Biofilm Inhibition Using Magnetic Cross-Linked Polyphenol Oxidase Aggregates

ACS Appl Bio Mater. 2024 May 20;7(5):3164-3178. doi: 10.1021/acsabm.4c00175. Epub 2024 May 9.

Abstract

Microbial biofilm accumulation poses a serious threat to the environment, presents significant challenges to different industries, and exhibits a large impact on public health. Since there has not been a conclusive answer found despite various efforts, the potential green and economical methods are being focused on, particularly the innovative approaches that employ biochemical agents. In the present study, we propose a bio-nanotechnological method using magnetic cross-linked polyphenol oxidase aggregates (PPO m-CLEA) for inhibition of microbial biofilm including multidrug resistant bacteria. Free PPO solution showed only 55-60% biofilm inhibition, whereas m-CLEA showed 70-75% inhibition, as confirmed through microscopic techniques. The carbohydrate and protein contents in biofilm extracellular polymeric substances (EPSs) were reduced significantly. The m-CLEA demonstrated reusability up to 5 cycles with consistent efficiency in biofilm inhibition. Computational work was also done where molecular docking of PPO with microbial proteins associated with biofilm formation was conducted, resulting in favorable binding scores and inter-residual interactions. Overall, both in vitro and in silico results suggest that PPO interferes with microbial cell attachment and EPS formation, thereby preventing biofilm colonization.

Keywords: Polyphenol oxidase; biofilm inhibition; interaction analysis; magnetic cross-linked enzyme aggregates; molecular docking; multidrug resistance bacteria.

MeSH terms

  • Anti-Bacterial Agents* / chemistry
  • Anti-Bacterial Agents* / pharmacology
  • Biocompatible Materials / chemistry
  • Biocompatible Materials / pharmacology
  • Biofilms* / drug effects
  • Catechol Oxidase* / antagonists & inhibitors
  • Catechol Oxidase* / chemistry
  • Catechol Oxidase* / metabolism
  • Cross-Linking Reagents / chemistry
  • Cross-Linking Reagents / pharmacology
  • Escherichia coli / drug effects
  • Materials Testing
  • Microbial Sensitivity Tests
  • Molecular Docking Simulation
  • Particle Size*