Bacteria immobilised in Gels: Improved methodologies for antifouling and biocontrol applications

Abstract

A range of bacteria, including the marine bacterium Pseudoalteromonas tunicata which produces antifouling compounds, and Escherichia coli were used to investigate methods for immobilising bacteria in gels. Different types of matrices were screened using the survival of barnacle nauplii as a bioassay. A Dupont® polyvinylalcohol (PVOH) 10% gel was found to be the optimal matrix. This non‐toxic gel remained stable in seawater while allowing for an outflux of active biological compounds from the bacterial cells. The presence of active bacterial cells in the matrix was tested by CTC‐staining, green fluorescent protein (GFP) expressing bacteria and a barnacle larvae bioassay. The Dupont® PVOH 10% gels containing P. tunicata cells were inhibitory against larvae for a period of up to 2 weeks. In further studies using gels containing immobilised bacteria, the E. coli strain C600 was employed based on its cell size, stress resistance and the fact that a plasmid for the expression of GFP could be transferred and maintained in the cells. Immobilised E. Coli cells maintained their viability in the Dupont® PVOH 10% gels for as long as 2 months, and the life‐span of these “biologically active”; gels was increased to more than 2 months by the incorporation of small beads into the gels. The results indicate that bacteria can be immobilised in coatings for periods of time consistent with the needs of some antifouling and antibacterial applications.

Key words:

• immobilised bacteria
• green fluorescent protein (GFP)
• Pseudoalteromonas
• coatings
• antifouling activity

Notes

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