Molecular self-assembly mediates the flocculation activity of benzimidazole derivatives against E. coli

I Isalyne Drewek A Aurélie Pietka T Thi Quynh Tran M Marharyta Blazhynska A Adéla Jeništova C Christophe Chipot (Laboratoire International Associé CNRS and University of Illinois at Urbana−Champaign, LPCT, UMR CNRS 7019) A Andreas Barth M Mathieu Surin P Philippe Leclère R Ruddy Wattiez R Robert N. Muller D Dimitri Stanicki S Sophie Laurent

Abstract

Abstract Bacterial flocculation is a process in which bacteria aggregate to form cloudy, flake-like clusters known as flocs. While this phenomenon is commonly associated with water treatment, it also has interesting industrial applications, particularly as a method for cell immobilisation. Escherichia coli, extensively employed in industrial processes, typically does not possess inherent flocculation ability. In this study, we found that certain bisbenzimidazole derivatives can rapidly induce flocculation in E. coli (K-12 MG1655) in a structure-dependent manner. Among others, high-resolution microscopy (SEM, fluid AFM) revealed a dense fibrillar network within the flocs, initially suggestive of an extracellular matrix. Mechanistic investigations demonstrated that this phenomenon cannot be linked to the secretion of extracellular polymeric substances (EPS). Our findings suggest that flocculation arises from the self-assembly of bisbenzimidazole derivatives into supramolecular fibres that anchor to bacterial membranes. These results uncover an atypical flocculation process distinct from charge neutralisation or EPS-mediated pathways, broadening the potential applications of bisbenzimidazole derivatives in bacterial immobilisation.

Article Details

Volume / Issue Vol. 15, Issue 1
Published August 05, 2025
ISSN 2045-2322
Publisher Nature Portfolio

Journal Info

Scientific Reports

Nature Portfolio

ISSN: 2045-2322 Open Access Life Sciences

Authors (13)

I

Isalyne Drewek

A

Aurélie Pietka

T

Thi Quynh Tran

M

Marharyta Blazhynska

A

Adéla Jeništova

C

Christophe Chipot

Laboratoire International Associé CNRS and University of Illinois at Urbana−Champaign, LPCT, UMR CNRS 7019

A

Andreas Barth

M

Mathieu Surin

P

Philippe Leclère

R

Ruddy Wattiez

R

Robert N. Muller

D

Dimitri Stanicki

S

Sophie Laurent