http://researchbank.swinburne.edu.au/vital/access/manager/Index ${session.getAttribute("locale")} 5 Identification of polyphosphate-accumulating organisms and design of 16S rRNA-directed probes for their detection and quantitation http://researchbank.swinburne.edu.au/vital/access/manager/Repository/swin:29582 80 percent of the A sludge bacteria were β-2 Proteobacteria arranged in clusters of coccobacilli, strongly suggesting that this group contains a PAO responsible for EBPR. The second dominant group in the A sludge was the Actinobacteria. Clone libraries of PCR-amplified bacterial 16S rRNA genes from three high-performance P-removing sludges were prepared, and clones belonging to the β-2 Proteobacteria were fully sequenced. A distinctive group of clones (sharing ≥ 98 percent sequence identity) related to Rhodocyclus spp. (94 to 97 percent identity) and Propionibacter pelophilus (95 to 96 percent identity) was identified as the most likely candidate PAOs. Three probes specific for the highly related candidate PAO group were designed from the sequence data. All three probes specifically bound to the morphologically distinctive clusters of PAOs in the A sludge, exactly coinciding with the β-2 Proteobacteria probe. Sequential FISH and polyphosphate staining of EBPR sludges clearly demonstrated that PAO probe-binding cells contained polyphosphate. Subsequent PAO probe analyses of a number of sludges with various P removal capacities indicated a strong positive correlation between P removal from the wastewater as determined by sludge P content and number of PAO probe-binding cells. We conclude therefore that an important group of PAOs in EBPR sludges are bacteria closely related to Rhodocyclus and Propionibacter.]]> Mon 15 Dec 2014 02:43:55 EST ]]>