Elucidation of metabolic pathways in glycogen-accumulating organisms with in vivo13C nuclear magnetic resonance
Article first published online: 26 JUL 2007
Volume 9, Issue 11, pages 2694–2706, November 2007
How to Cite
Lemos, P. C., Dai, Y., Yuan, Z., Keller, J., Santos, H. and Reis, M. A. M. (2007), Elucidation of metabolic pathways in glycogen-accumulating organisms with in vivo13C nuclear magnetic resonance. Environmental Microbiology, 9: 2694–2706. doi: 10.1111/j.1462-2920.2007.01382.x
- Issue published online: 26 JUL 2007
- Article first published online: 26 JUL 2007
- Received 6 March, 2007; accepted 2 June, 2007.
Glycogen-accumulating organisms (GAOs) are found in enhanced biological phosphorus removal systems where they compete with polyphosphate-accumulating organisms for external carbon substrates. 13C nuclear magnetic resonance (13C-NMR) was used to elucidate the metabolic pathways operating in an enriched GAO culture dominated by two known GAOs (81.2%). The experiments consisted of adding 13C-acetate (labelled on position 1 or 2) to the culture under anaerobic conditions, and operating the culture through a cycle consisting of an anaerobic, an aerobic and a further anaerobic phase. The carbon transformations over the cycle were monitored using in vivo13C-NMR. The two-carbon moieties in hydroxybutyrate and hydroxyvalerate were derived from acetate, while the propionyl precursor of hydroxyvalerate was primarily derived from glycogen, with only a small fraction originating from acetate. Comparison of the labelling patterns in hydroxyvalerate at the end of the first and the second anaerobic periods in pulse experiments with 2-13C-acetate showed that the Entner–Doudoroff (ED) pathway was used for the breakdown of glycogen. This conclusion was further supported by the labelling pattern on glycogen observed in the pulse experiments with 1-13C-acetate, which can only be explained by the operation of ED with recycling of pyruvate and glyceraldehyde 3-phosphate via gluconeogenesis. The activity of the ED pathway for glycogen degradation by GAOs is demonstrated here for the first time. In addition, the decarboxylating part of the tricarboxylic acid cycle was confirmed to operate also under anaerobic conditions.