Anaerobic central metabolic pathways active during polyhydroxyalkanoate production in uncultured cluster 1 Defluviicoccus enriched in activated sludge communities

• Published in: FEMS microbiology letters 2009-09, Vol.298 (1), p.79-84
• Main Authors: Burow, Luke C., Mabbett, Amanda N., Borrás, Luis, Blackall, Linda L.
• Format: Article
• Language: English
• Subjects: 3-Nitropropionic acid; Acetates - metabolism; Acetic acid; Aconitate Hydratase - metabolism; Activated sludge; Anaerobic conditions; Anaerobiosis; Bacterial Proteins - metabolism; Bioaccumulation; Biological activity; Carbon sequestration; Clusters; Dehydrogenase; Dehydrogenases; enhanced biological phosphorus removal; Enrichment; FISH; Fluorescence; Glycogen; glycogen (nonpolyphosphate)‐accumulating organisms; Glycolysis; Glyoxylate cycle; Isocitrate lyase; Metabolic Networks and Pathways; Metabolic pathways; Metabolism; microautoradiography; Microbiology; Microorganisms; Models, Biological; Organic chemistry; Phosphorus; Phosphorus removal; Polyhydroxyalkanoates; Polyhydroxyalkanoates - biosynthesis; Polyhydroxyalkanoic acid; Polyhydroxyvalerate; Polymers; Reductase; Reductases; Rhodospirillaceae - metabolism; Sewage - microbiology; Succinate dehydrogenase; Succinate Dehydrogenase - metabolism; Tricarboxylic acid cycle; wastewater
• ISSN: 0378-1097; 1574-6968
• DOI: 10.1111/j.1574-6968.2009.01695.x

Abstract A glycogen nonpolyphosphate-accumulating organism (GAO) enrichment culture dominated by the Alphaproteobacteria cluster 1 Defluviicoccus was investigated to determine the metabolic pathways involved in the anaerobic formation of polyhydroxyalkanoates, carbon storage polymers important for the proliferation of microorganisms in enhanced biological phosphorus removal processes. FISH–microautoradiography and post-FISH fluorescent chemical staining confirmed acetate assimilation as polyhydroxyalkanoates in cluster 1 Defluviicoccus under anaerobic conditions. Chemical inhibition of glycolysis using iodoacetate, and of isocitrate lyase by 3-nitropropionate and itaconate, indicated that carbon is likely to be channelled through both glycolysis and the glyoxylate cycle in cluster 1 Defluviicoccus. The effect of metabolic inhibitors of aconitase (monofluoroacetate) and succinate dehydrogenase (malonate) suggested that aconitase, but not succinate dehydrogenase, was active, providing further support for the role of the glyoxylate cycle in these GAOs. Metabolic inhibition of fumarate reductase using oxantel decreased polyhydroxyalkanoate production. This indicated reduction of fumarate to succinate and the operation of the reductive branch of the tricarboxylic acid cycle, which is possibly important in the production of the polyhydroxyvalerate component of polyhydroxyalkanoates observed in cluster 1 Defluviicoccus enrichment cultures. These findings were integrated with previous metabolic models for GAOs and enabled an anaerobic central metabolic pathway model for polyhydroxyalkanoate formation in cluster 1 Defluviicoccus to be proposed.