Interfacing Phylogenetic Oligonucleotide Probe Hybridizations with Representations of Microbial Populations and Specific Growth Rates in Mathematical Models of Activated Sludge Processes
Accurate estimates of microbial population concentrations and the direct, in situ determination of kinetic parameters could improve the calibration and validation of existing mechanistic mathematical models of biological nutrient removal activated sludge systems. Oligonucleotide probe hybridizations show promise for measuring concentrations and in situ specific growth rates of microbial populations. The most common targets for oligonucleotide probes are the phylogenetically conserved ribosomal RNA molecules. Recent advances in hybridization techniques have improved the quantitative nature of ribosomal RNA based assays. However, correlations between concentrations of 'theoretical' microbial populations predicted by mechanistic models and quantitative information obtained with oligonucleotide probe hybridizations are not yet developed. Future work should develop such correlations, while addressing the limitations of the molecular assays.
D. B. Oerther et al., "Interfacing Phylogenetic Oligonucleotide Probe Hybridizations with Representations of Microbial Populations and Specific Growth Rates in Mathematical Models of Activated Sludge Processes," Water Science and Technology, vol. 39, no. 1, pp. 11-20, IWA Publishing, Mar 1999.
The definitive version is available at https://doi.org/10.1016/S0273-1223(98)00771-9
4th IAWQ Seminar on Modelling and Microbiology of Activated Sludge Processes (1998, Mar. 16-18, Kollekolle, Denmark)
Civil, Architectural and Environmental Engineering
Keywords and Phrases
ribosome RNA; activated sludge; mathematical method; activated sludge; growth rate; microbial growth; oligonucleotide probe; phylogeny; waste water management; Biological nutrient removal; Mechanistic mathematical models
International Standard Serial Number (ISSN)
Article - Conference proceedings
© 1999 IWA Publishing, All rights reserved.
01 Mar 1999