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. 2004 Jul;186(14):4596–4604. doi: 10.1128/JB.186.14.4596-4604.2004

FIG. 3.

FIG. 3.

Kinetics of pyruvate degradation and product formation by resting cells of P. aeruginosa in 100 mM phosphate buffer (pH 7.4). The cells were grown for 21 h in OS minimal medium with 50 mM nitrate as electron acceptor and 10 mM gluconate-20 mM pyruvate as carbon source under oxygen limitation and then were harvested and washed in phosphate buffer. Finally, the cell suspensions (OD578 between 8 and 9) of bacteria were incubated under anoxic conditions with the addition of 50 mM arginine (A), 50 mM nitrate (B), or without further additions (C). Pyruvate (•), lactate (□), acetate (▿), and succinate (▵) were detected by HPLC analysis of the supernatant as described in Materials and Methods. Graphs represent the results of three independent experiments; standard deviations were below 7% for the determined pyruvate, lactate, and acetate concentrations and below 15% for the already low succinate concentrations.