Gregory Crocetti
University of Queensland
20 Papers
239 Citations
Gregory Crocetti is an academic researcher from University of Queensland. The author has contributed to research in topics: Polyphosphate-accumulating organisms & Enhanced biological phosphorus removal. The author has an hindex of 14, co-authored 19 publications. Previous affiliations of Gregory Crocetti include Lund University & University of New South Wales.
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Papers
Identification of polyphosphate-accumulating organisms and design of 16S rRNA-directed probes for their detection and quantitation.
Gregory Crocetti,Philip Hugenholtz,Philip L. Bond,Andrew J. Schuler,Jurg Keller,David Jenkins,Linda L. Blackall +6 more
TL;DR: An important group of PAOs in EBPR sludges are bacteria closely related to Rhodocyclus and Propionibacter, identified as the most likely candidate PAOs.
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Glycogen-accumulating organisms in laboratory-scale and full-scale wastewater treatment processes
TL;DR: FISH and post-FISH chemical staining for PHA were used to determine that bacteria from a novel gamma-Proteobacteria cluster were phenotypically GAOs in one laboratory-scale SBR and two full-scale wastewater treatment plants.
A review and update of the microbiology of enhanced biological phosphorus removal in wastewater treatment plants.
TL;DR: To preclude making the mistakes of previous researchers, it is recommended that the sludge ‘biography’ be well understood – i.e. details of phenotype (process performance and biochemistry) and microbial community structure should be linked.
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Identifying causes for N2O accumulation in a lab-scale sequencing batch reactor performing simultaneous nitrification, denitrification and phosphorus removal.
Romain Lemaire,Rikke Louise Meyer,Annelies Taske,Gregory Crocetti,Gregory Crocetti,Jurg Keller,Zhiguo Yuan +6 more
TL;DR: It is suggested that the N(2)O accumulation observed in the SNDPR reactor is an artefact of the low microbial diversity facilitated by the use of synthetic wastewater with only a single carbon source.
170
An update and optimisation of oligonucleotide probes targeting methanogenic Archaea for use in fluorescence in situ hybridisation (FISH).
TL;DR: The updated set of probes was optimised for use in FISH for a more accurate detection of methanogenic Archaea.
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