Using Molecular Signature Methods to Measure the in Situ Physiology of Acinetobacter Spp. In Enhanced Biological Phosphorus Removal Activated Sludge Wastewater Treatment
Oerther, Daniel Barton
This item is only available for download by members of the University of Illinois community. Students, faculty, and staff at the U of I may log in with your NetID and password to view the item. If you are trying to access an Illinois-restricted dissertation or thesis, you can request a copy through your library's Inter-Library Loan office or purchase a copy directly from ProQuest.
Permalink
https://hdl.handle.net/2142/83199
Description
Title
Using Molecular Signature Methods to Measure the in Situ Physiology of Acinetobacter Spp. In Enhanced Biological Phosphorus Removal Activated Sludge Wastewater Treatment
Author(s)
Oerther, Daniel Barton
Issue Date
2002
Doctoral Committee Chair(s)
Raskin, Lutgarde
Department of Study
Civl and Environmental Engineering
Discipline
Civl and Environmental Engineering
Degree Granting Institution
University of Illinois at Urbana-Champaign
Degree Name
Ph.D.
Degree Level
Dissertation
Keyword(s)
Engineering, Sanitary and Municipal
Language
eng
Abstract
Herein, we have adapted, developed, and implemented novel technologies from molecular microbial ecology to understand the role of Acinetobacter spp. as a model phosphorus accumulating organisms in biological phosphorus removal. Oligonucleotide hybridization probes targeting the 16S ribosomal ribonucleic acid of various phylogenetic groups of microorganisms including the beta-subclass Proteobacteria, gamma-subclass Proteobacteria, the genus Acinetobacter, Acinetobacter johnsonii, Acinetobacter lwoffii , and Acinetobacter strain ED were designed and experimentally characterized for radiolabeled oligonucleotide hybridizations of membrane immobilized cellular extracts as well as whole cell fluorescence in situ hybridizations. In addition, a novel class of oligonucleotide probes targeting the precursor 16S ribosomal ribonucleic acid of the genus Acinetobacter were developed. Subsequently, these molecular tools were used to identify, enumerate, quantify long-term (with a characteristic time-frame of hours to days) growth activity, and monitor short-term (with a characteristic time-frame of minutes to hours) changes in growth activity of Acinetobacter spp. in laboratory- and full-scale activated sludge wastewater treatment systems. Our results suggest that Acinetobacter spp. are a high ribosome containing, low abundance microbial population in activated sludge systems. Furthermore, the addition of idle stages at the end of the decant phase of fill-and-draw reactor operation stimulated transient increases in both the abundance and growth activity of Acinetobacter spp. Precursor 16S ribosomal ribonucleic acid levels were a sensitive indicator of rapid changes in the in situ growth activity of Acinetobacter spp, and Acinetobacter spp. responded to dynamic changes in the operation of activated sludge systems including the rapid addition of fresh influent. Although we failed to find any correlation between the abundance and growth activity of Acinetobacter spp. and biological phosphorus removal, the results of our work have demonstrated a proposed role for Acinetobacter spp. in activated sludge wastewater treatment systems. We propose that Acinetobacter spp. occupy an ecological niche that includes dynamic operating conditions in activated sludge systems. We hypothesize that Acinetobacter spp. have an ecological advantage in wastewater treatment systems that are not at steady-state. Thus, the role of Acinetobacter spp. in activated sludge systems could include transient removal of organic pollution during fluctuations in the operation of bioreactors.
Use this login method if you
don't
have an
@illinois.edu
email address.
(Oops, I do have one)
IDEALS migrated to a new platform on June 23, 2022. If you created
your account prior to this date, you will have to reset your password
using the forgot-password link below.