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Updated: Jun 12, 2026

A Platform of Anti-biofilm Assays Suited to the Exploration of Natural Compound Libraries
Published on: December 27, 2016
Microplate-based quantification of poly-γ-glutamic acid levels in biofilm samples
David Stevenson1, Cait E MacPhee2, Nicola Stanley-Wall1
1Division of Molecular Microbiology, School of Life Sciences, University of Dundee, Dundee, DD1 5EH, UK.
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Poly-γ-glutamic acid (PGA) is a commercially useful biopolymer produced by many Bacillus species. PGA has a diverse range of applications across medicine and industry, generating significant interest in optimizing PGA production and enhancing yields. One approach to improve PGA recovery involves identifying high-yield PGA-producing strains and determining optimal production conditions, both of which require an appropriate screening method. Here, we present a sensitive and reproducible assay for quantifying PGA from Bacillus subtilis biofilms, whereby the spectral profile of methylene blue changes when bound to PGA. PGA was purified and lyophilized from NCIB 3610 ΔtasA liquid cultures grown at 50 °C, allowing production of protein-free PGA for use as a standard at known concentrations. Standard curves were generated from methylene blue absorbance readings at 564 and 664 nm, enabling subsequent quantification of PGA from biofilm extracts. We validated the quantification protocol and determined the treatment steps required to minimize interference. The assay has a 96-well plate format, enabling quantification of many samples at low sample volume, while minimizing waste of laboratory consumables. Overall, our method offers a sensitive, reproducible approach for PGA quantification in biofilm research and should facilitate comparative analyses across strains, treatments or environmental conditions.

