Abstract
Rapid and reliable detection of pathogenic bacteria requires support materials relying on functional polymeric materials that can immobilize bacteria. Herein, a straightforward approach for the fabrication of surfaces for bacterial immobilization. The surfaces were designed to be conjugated with Concanavalin A (Con A), a lectin that recognizes mannosyl and glucosyl groups of lipopolysaccharides, the protective outer cell membrane of Gram-negative bacteria such as Escherichia coli. Two distinct surfaces, glass and polymeric microparticles, were chosen and modified for the Con A conjugation. Both surfaces were grafted with the same constituting monomers: poly(ethylene glycol) methyl ether methacrylate (PEGMA) and N-(methacryloxy)succinimide (NMAS) through a surface-initiated atom transfer radical polymerization. Subsequently, Con A was conjugated to the surfaces via succinimidyl functionalities of the P(PEGMA-co-NMAS)grafted to the surfaces. A green fluorescent protein (GFP)-expressing E. coli strain was utilized to monitor the bacterial attachment. Fluorescent microscopy results revealed that the Con A-conjugated surfaces captured GFP E. coli.
| Original language | English |
|---|---|
| Pages (from-to) | 1382-1392 |
| Number of pages | 11 |
| Journal | Journal of Macromolecular Science, Part A: Pure and Applied Chemistry |
| Volume | 62 |
| Issue number | 12 |
| DOIs | |
| Publication status | Published - 2025 |
Bibliographical note
Publisher Copyright:© 2025 Taylor & Francis Group, LLC.
Keywords
- Concanavalin A
- Functional surface
- SI-ATRP
- bacterial immobilization
- succinimide
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