Biofilm plays an important role in the pathogenicity of the bacterium Stenotrophomonas maltophilia. When sodium phosphate buffer (SPB) supplemented the Luria-Bertani media of 11 clinical isolates of this bacterium, mean growth at 30 h was little changed compared to non-supplemented controls in 45% of the isolates, decreasing by 4%. Increase in mean biofilm formation in that low growth change sub-sample was statistically significant (t = 5.0, df 4, p < 0.008). For a further 36% of isolates, growth at 30 h with SPB supplementation was decreased by 8.5% of controls. Decrease in biofilm formation was seen in that sub-sample compared to controls (t = 4.0, df 3, p < 0.03). The significant phenotypical variety of the clinical presentation of this pathogen may allow population adaptability to varying metabolic provision, improving its pathogenicity.Stenotrophomonas maltophilia is a significant world-wide emerging opportunistic pathogen that forms biofilm on patient implants and equipment (Vo et al., 2005), is associated with a broad range of human infections and disorders (Denton and Kerr, 1998) and has a significant casefatality ratio (Denton and Kerr, 1998;Wang et al., 2004). For bacterial biofilm production, phosphorus is an important nutrient (Keinänen et al., 2002;Lehtola et al., 2004). We tested the hypothesis that sodium phosphate added to media increases cell growth and biofilm formation in this pathogen.In the first experimental series that had triplicate replications we added 0.1 M sodium phosphate buffer (SPB, pH 7.0) to Luria-Bertani (LB) medium. This was expected to increase the buffering of the modified media, as occurs with MOPS (Neidhardt et al., 1974), and provide additional phosphate for bacterial metabolism. In a further experiment, we added 0.1 M sodium phosphate buffer (pH 7.0) to the bacterial isolates without the LB medium.Eleven Stenotrophomonas maltophilia clinical isolates obtained from human upper respiratory tract, peritoneal fluid, and blood were maintained on LB Lennox agar plates/broth medium at 37 °C. Isolate identity was confirmed using an API 20 NE identification kit (Biomerieux).In the first experiment, three independent biofilm determinations were made on each of the 11 isolates. Polyvinyl chloride (PVC) Falcon plastic 96-well plates (Becton Dickinson) were used to detect biofilm production (Watnick and Kolter, 1999). Twenty microliters of each 16-18 h culture were inoculated into microtiter plate wells containing 180 µl of LB medium or LB medium supplemented with 0.1 M SPB (pH 7.0). Control wells in the assay contained LB medium only (or LB medium supplemented with SPB, but no bacterial culture) and no cells. In the second experiment, 20 µl of each culture were inoculated into the microtiter plate wells containing 0.1 M SPB alone. Plates were covered with parafilm and incubated stationary at 37°C for 27 h. Non-adherent cells in the wells were removed and the remaining adhered cells were stained with 1% (w/v) crystal violet for 10 min at room temperature. The wells were rinsed four tim...