Full Text Available

Note: Clicking the button above will open the full text document at the original institutional repository in a new window.

PCR detection, denaturing gradient gel electrophoresis (DGGE) fingerprinting and identification of the microbial consortium in different types of UASB granules

Thesis (PhD (Food Science))--University of Stellenbosch, 2006.

Saved in:
Bibliographic Details
Main Author: Keyser, Maricel
Other Authors: Witthuhn, R. C.
Format: Thesis
Language:English
Published: Stellenbosch: University of Stellenbosch 2008
Subjects:
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1867613918914936833
access_status_str Open Access
author Keyser, Maricel
author2 Witthuhn, R. C.
author_browse Keyser, Maricel
Witthuhn, R. C.
author_facet Witthuhn, R. C.
Keyser, Maricel
author_sort Keyser, Maricel
collection Thesis
dc_rights_str_mv University of Stellenbosch
description Thesis (PhD (Food Science))--University of Stellenbosch, 2006.
format Thesis
id oai:scholar.sun.ac.za:10019.1/1297
institution Stellenbosch University (South Africa)
language English
last_indexed 2026-06-10T12:43:47.401Z
license_str Other — see source repository
provenance_str_mv Harvested via OAI-PMH from SUNScholar — Stellenbosch University Repository
publishDate 2008
publishDateRange 2008
publishDateSort 2008
publisher Stellenbosch: University of Stellenbosch
publisherStr Stellenbosch: University of Stellenbosch
record_format dspace
source_str SUNScholar — Stellenbosch University Repository
spelling oai:scholar.sun.ac.za:10019.1/1297 PCR detection, denaturing gradient gel electrophoresis (DGGE) fingerprinting and identification of the microbial consortium in different types of UASB granules Keyser, Maricel Witthuhn, R. C. Britz, T. J. University of Stellenbosch. Faculty of Agrisciences. Dept. of Food Science. Theses -- Food science Dissertations -- Food science Polymerase chain reaction Sewage -- Purification -- Anaerobic treatment Bioreactors Food Science Thesis (PhD (Food Science))--University of Stellenbosch, 2006. High-rate anaerobic bioreactors are used for the treatment of various wastewaters, of which the upflow anaerobic sludge blanket (UASB) bioreactor has the widest application, especially in the food and beverage industries. In an UASB bioreactor sludge develops in a particular granular or flocculent form and the success of the anaerobic process relies on the formation of active and settable granules. These granules are formed by self-aggregation of bacteria that can be divided into different trophic groups that are responsible for the metabolic breakdown of organic substrates. The successful performance of a bioreactor is influenced by the composition of the substrate which subsequently may have an impact on the microbial consortium present in the UASB granules. In order to determine if a change in the structure of the non-methanogenic microbial community takes place, UASB brewery granules were subjected to the sudden addition of different carbon sources at different concentrations. A shift in the microbial community did occur when the granules were subjected to lactate medium (5 g.l-1). No changes in the microbial community were observed when the granules were stressed with glucose medium as carbon source, regardless of an increase in the glucose concentration. In order to better understand the effect that different wastewaters may have on the microbial consortium present in different UASB granules, the polymerase chain reaction (PCR) based denaturing gradient gel electrophoresis (DGGE) technique and sequence analysis were used to fingerprint and identify the Bacteria and Archaea present in either, winery, brewery, distillery or peach-lye canning UASB granules. Each granule type showed distinct PCR-based DGGE fingerprints with unique bands, while other bands were found to be present in all the granules regardless of the wastewater being treated. Bacillus, Pseudomonas, Bacteroides, Enterococcus, Alcaligenes, Clostridium, Shewanella, Microbacterium, Leuconostoc, Sulfurospirillum, Acidaminococcus, Vibrio, Aeromonas, Nitrospira, Synergistes, Rhodococcus, Rhodocyclus, Syntrophobacter and uncultured bacteria were identified, representing different acidogenic, acetogenic and homoacetogenic Bacteria.Different methanogenic bacteria such as Methanosaeta, Methanosarcina, Methanobacterium and uncultured bacteria belonging to the group Archaea were also fingerprinted and identified from different UASB granules. In both these studies a DGGE marker was constructed that may be used to assist in the identification of bacteria. The DGGE marker can also be used to monitor the presence of bacteria over a time period during anaerobic digestion. Bioaugmentation or the enrichment of granules results in tailor-made granules that may be used for the treatment of specific wastewaters. One of the most important contributions to the maintenance and enhancement of UASB granule formation is the inclusion of suitable microbes in the granule structure. Enterobacter sakazakii was isolated from raw winery wastewater and was found to produce sufficient amounts of desired fatty acids. This bacteria was, therefore, incorporated into batch cultured granular sludge. In order to identify and monitor the presence of the incorporated E. sakazakii in the tailor-made granules, 16S rRNA gene sequence primers and PCR conditions were developed. The use of molecular techniques such as PCR-based DGGE and sequence analysis proved to be successful methods to fingerprint and identify the microbial consortium present in the different UASB granules. Doctoral 2008-02-04T10:26:25Z 2010-06-01T08:17:56Z 2008-02-04T10:26:25Z 2010-06-01T08:17:56Z 2006-12 Thesis http://hdl.handle.net/10019.1/1297 en University of Stellenbosch 2335827 bytes application/pdf application/pdf Stellenbosch: University of Stellenbosch
spellingShingle Theses -- Food science
Dissertations -- Food science
Polymerase chain reaction
Sewage -- Purification -- Anaerobic treatment
Bioreactors
Food Science
Keyser, Maricel
PCR detection, denaturing gradient gel electrophoresis (DGGE) fingerprinting and identification of the microbial consortium in different types of UASB granules
title PCR detection, denaturing gradient gel electrophoresis (DGGE) fingerprinting and identification of the microbial consortium in different types of UASB granules
title_full PCR detection, denaturing gradient gel electrophoresis (DGGE) fingerprinting and identification of the microbial consortium in different types of UASB granules
title_fullStr PCR detection, denaturing gradient gel electrophoresis (DGGE) fingerprinting and identification of the microbial consortium in different types of UASB granules
title_full_unstemmed PCR detection, denaturing gradient gel electrophoresis (DGGE) fingerprinting and identification of the microbial consortium in different types of UASB granules
title_short PCR detection, denaturing gradient gel electrophoresis (DGGE) fingerprinting and identification of the microbial consortium in different types of UASB granules
title_sort pcr detection denaturing gradient gel electrophoresis dgge fingerprinting and identification of the microbial consortium in different types of uasb granules
topic Theses -- Food science
Dissertations -- Food science
Polymerase chain reaction
Sewage -- Purification -- Anaerobic treatment
Bioreactors
Food Science
url http://hdl.handle.net/10019.1/1297
work_keys_str_mv AT keysermaricel pcrdetectiondenaturinggradientgelelectrophoresisdggefingerprintingandidentificationofthemicrobialconsortiumindifferenttypesofuasbgranules