Real-time PCR quantification of nitrifying bacteria in a municipal wastewater treatment plant
- Autores
- Harms, Gerda; Layton, Alice C.; Dionisi, Hebe Monica; Gregory, Igrid R.; Garrett, Victoria M.; Hawkins, Shawn A.; Robinson, Kevin G.; Sayler, Gary S.
- Año de publicación
- 2003
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Real-time PCR assays using TaqMan or Molecular Beacon probes were developed and optimized for the quantification of total bacteria, the nitrite-oxidizing bacteria Nitrospira, and Nitrosomonas oligotropha-like ammonia oxidizing bacteria (AOB) in mixed liquor suspended solids (MLSS) from a municipal wastewater treatment plant (WWTP) using a single-sludge nitrification process. The targets for the real-time PCR assays were the 16S rRNA genes (16S rDNA) for bacteria and Nitrospira spp. and the amoA gene for N. oligotropha. A previously reported assay for AOB 16S rDNA was also tested for its application to activated sludge. The Nitrospira 16S rDNA, AOB 16S rDNA, and N. oligotropha-like amoA assays were log-linear over 6 orders of magnitude and the bacterial 16S rDNA real-time PCR assay was log-linear over 4 orders of magnitude with DNA standards. When these real-time PCR assays were applied to DNA extracted from MLSS, dilution of the DNA extracts was necessary to prevent PCR inhibition. The optimal DNA dilution range was broad for the bacterial 16S rDNA (1000-fold) and Nitrospira 16S rDNA assays (2500-fold) but narrow for the AOB 16S rDNA assay (10-fold) and N. oligotropha-like amoA real-time PCR assay (5-fold). In twelve MLSS samples collected over one year, mean cell per L values were 4.3 ± 2.0 × 1011 for bacteria, 3.7 ± 3.2 × 1010 for Nitrospira, 1.2 ± 0.9 × 1010 for all AOB, and 7.5 ± 6.0 × 109 for N. oligotropha-like AOB. The percent of the nitrifying population was 1.7% N. oligotropha-like AOB based on the N. oligotropha amoA assay, 2.9% total AOB based on the AOB 16S rDNA assay, and 8.6% nitrite-oxidizing bacteria based on the Nitrospira 16S rDNA assay. Ammonia-oxidizing bacteria in the wastewater treatment plant were estimated to oxidize 7.7 ± 6.8 fmol/hr/cell based on the AOB 16S rDNA assay and 12.4 ± 7.3 fmol/hr/cell based on the N. oligotropha amoA assay.
Fil: Harms, Gerda. University of Tennessee; Estados Unidos
Fil: Layton, Alice C.. University of Tennessee; Estados Unidos
Fil: Dionisi, Hebe Monica. University of Tennessee; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Gregory, Igrid R.. University of Tennessee; Estados Unidos
Fil: Garrett, Victoria M.. University of Tennessee; Estados Unidos
Fil: Hawkins, Shawn A.. University of Tennessee; Estados Unidos
Fil: Robinson, Kevin G.. University of Tennessee; Estados Unidos
Fil: Sayler, Gary S.. University of Tennessee; Estados Unidos - Materia
-
NITRIFYING BACTERIA
REAL-TIME PCR
MUNICIPAL WASTEWATER TREATMENT PLANT - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
.jpg)
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/98939
Ver los metadatos del registro completo
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Real-time PCR quantification of nitrifying bacteria in a municipal wastewater treatment plantHarms, GerdaLayton, Alice C.Dionisi, Hebe MonicaGregory, Igrid R.Garrett, Victoria M.Hawkins, Shawn A.Robinson, Kevin G.Sayler, Gary S.NITRIFYING BACTERIAREAL-TIME PCRMUNICIPAL WASTEWATER TREATMENT PLANThttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Real-time PCR assays using TaqMan or Molecular Beacon probes were developed and optimized for the quantification of total bacteria, the nitrite-oxidizing bacteria Nitrospira, and Nitrosomonas oligotropha-like ammonia oxidizing bacteria (AOB) in mixed liquor suspended solids (MLSS) from a municipal wastewater treatment plant (WWTP) using a single-sludge nitrification process. The targets for the real-time PCR assays were the 16S rRNA genes (16S rDNA) for bacteria and Nitrospira spp. and the amoA gene for N. oligotropha. A previously reported assay for AOB 16S rDNA was also tested for its application to activated sludge. The Nitrospira 16S rDNA, AOB 16S rDNA, and N. oligotropha-like amoA assays were log-linear over 6 orders of magnitude and the bacterial 16S rDNA real-time PCR assay was log-linear over 4 orders of magnitude with DNA standards. When these real-time PCR assays were applied to DNA extracted from MLSS, dilution of the DNA extracts was necessary to prevent PCR inhibition. The optimal DNA dilution range was broad for the bacterial 16S rDNA (1000-fold) and Nitrospira 16S rDNA assays (2500-fold) but narrow for the AOB 16S rDNA assay (10-fold) and N. oligotropha-like amoA real-time PCR assay (5-fold). In twelve MLSS samples collected over one year, mean cell per L values were 4.3 ± 2.0 × 1011 for bacteria, 3.7 ± 3.2 × 1010 for Nitrospira, 1.2 ± 0.9 × 1010 for all AOB, and 7.5 ± 6.0 × 109 for N. oligotropha-like AOB. The percent of the nitrifying population was 1.7% N. oligotropha-like AOB based on the N. oligotropha amoA assay, 2.9% total AOB based on the AOB 16S rDNA assay, and 8.6% nitrite-oxidizing bacteria based on the Nitrospira 16S rDNA assay. Ammonia-oxidizing bacteria in the wastewater treatment plant were estimated to oxidize 7.7 ± 6.8 fmol/hr/cell based on the AOB 16S rDNA assay and 12.4 ± 7.3 fmol/hr/cell based on the N. oligotropha amoA assay.Fil: Harms, Gerda. University of Tennessee; Estados UnidosFil: Layton, Alice C.. University of Tennessee; Estados UnidosFil: Dionisi, Hebe Monica. University of Tennessee; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Gregory, Igrid R.. University of Tennessee; Estados UnidosFil: Garrett, Victoria M.. University of Tennessee; Estados UnidosFil: Hawkins, Shawn A.. University of Tennessee; Estados UnidosFil: Robinson, Kevin G.. University of Tennessee; Estados UnidosFil: Sayler, Gary S.. University of Tennessee; Estados UnidosAmerican Chemical Society2003-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/98939Harms, Gerda; Layton, Alice C.; Dionisi, Hebe Monica; Gregory, Igrid R.; Garrett, Victoria M.; et al.; Real-time PCR quantification of nitrifying bacteria in a municipal wastewater treatment plant; American Chemical Society; Environmental Science & Technology; 37; 2; 1-2003; 343-3510013-936XCONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1021/es0257164info:eu-repo/semantics/altIdentifier/url/https://pubs.acs.org/doi/10.1021/es0257164info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-11-05T09:50:28Zoai:ri.conicet.gov.ar:11336/98939instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-11-05 09:50:28.344CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
| dc.title.none.fl_str_mv |
Real-time PCR quantification of nitrifying bacteria in a municipal wastewater treatment plant |
| title |
Real-time PCR quantification of nitrifying bacteria in a municipal wastewater treatment plant |
| spellingShingle |
Real-time PCR quantification of nitrifying bacteria in a municipal wastewater treatment plant Harms, Gerda NITRIFYING BACTERIA REAL-TIME PCR MUNICIPAL WASTEWATER TREATMENT PLANT |
| title_short |
Real-time PCR quantification of nitrifying bacteria in a municipal wastewater treatment plant |
| title_full |
Real-time PCR quantification of nitrifying bacteria in a municipal wastewater treatment plant |
| title_fullStr |
Real-time PCR quantification of nitrifying bacteria in a municipal wastewater treatment plant |
| title_full_unstemmed |
Real-time PCR quantification of nitrifying bacteria in a municipal wastewater treatment plant |
| title_sort |
Real-time PCR quantification of nitrifying bacteria in a municipal wastewater treatment plant |
| dc.creator.none.fl_str_mv |
Harms, Gerda Layton, Alice C. Dionisi, Hebe Monica Gregory, Igrid R. Garrett, Victoria M. Hawkins, Shawn A. Robinson, Kevin G. Sayler, Gary S. |
| author |
Harms, Gerda |
| author_facet |
Harms, Gerda Layton, Alice C. Dionisi, Hebe Monica Gregory, Igrid R. Garrett, Victoria M. Hawkins, Shawn A. Robinson, Kevin G. Sayler, Gary S. |
| author_role |
author |
| author2 |
Layton, Alice C. Dionisi, Hebe Monica Gregory, Igrid R. Garrett, Victoria M. Hawkins, Shawn A. Robinson, Kevin G. Sayler, Gary S. |
| author2_role |
author author author author author author author |
| dc.subject.none.fl_str_mv |
NITRIFYING BACTERIA REAL-TIME PCR MUNICIPAL WASTEWATER TREATMENT PLANT |
| topic |
NITRIFYING BACTERIA REAL-TIME PCR MUNICIPAL WASTEWATER TREATMENT PLANT |
| purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.6 https://purl.org/becyt/ford/1 |
| dc.description.none.fl_txt_mv |
Real-time PCR assays using TaqMan or Molecular Beacon probes were developed and optimized for the quantification of total bacteria, the nitrite-oxidizing bacteria Nitrospira, and Nitrosomonas oligotropha-like ammonia oxidizing bacteria (AOB) in mixed liquor suspended solids (MLSS) from a municipal wastewater treatment plant (WWTP) using a single-sludge nitrification process. The targets for the real-time PCR assays were the 16S rRNA genes (16S rDNA) for bacteria and Nitrospira spp. and the amoA gene for N. oligotropha. A previously reported assay for AOB 16S rDNA was also tested for its application to activated sludge. The Nitrospira 16S rDNA, AOB 16S rDNA, and N. oligotropha-like amoA assays were log-linear over 6 orders of magnitude and the bacterial 16S rDNA real-time PCR assay was log-linear over 4 orders of magnitude with DNA standards. When these real-time PCR assays were applied to DNA extracted from MLSS, dilution of the DNA extracts was necessary to prevent PCR inhibition. The optimal DNA dilution range was broad for the bacterial 16S rDNA (1000-fold) and Nitrospira 16S rDNA assays (2500-fold) but narrow for the AOB 16S rDNA assay (10-fold) and N. oligotropha-like amoA real-time PCR assay (5-fold). In twelve MLSS samples collected over one year, mean cell per L values were 4.3 ± 2.0 × 1011 for bacteria, 3.7 ± 3.2 × 1010 for Nitrospira, 1.2 ± 0.9 × 1010 for all AOB, and 7.5 ± 6.0 × 109 for N. oligotropha-like AOB. The percent of the nitrifying population was 1.7% N. oligotropha-like AOB based on the N. oligotropha amoA assay, 2.9% total AOB based on the AOB 16S rDNA assay, and 8.6% nitrite-oxidizing bacteria based on the Nitrospira 16S rDNA assay. Ammonia-oxidizing bacteria in the wastewater treatment plant were estimated to oxidize 7.7 ± 6.8 fmol/hr/cell based on the AOB 16S rDNA assay and 12.4 ± 7.3 fmol/hr/cell based on the N. oligotropha amoA assay. Fil: Harms, Gerda. University of Tennessee; Estados Unidos Fil: Layton, Alice C.. University of Tennessee; Estados Unidos Fil: Dionisi, Hebe Monica. University of Tennessee; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Gregory, Igrid R.. University of Tennessee; Estados Unidos Fil: Garrett, Victoria M.. University of Tennessee; Estados Unidos Fil: Hawkins, Shawn A.. University of Tennessee; Estados Unidos Fil: Robinson, Kevin G.. University of Tennessee; Estados Unidos Fil: Sayler, Gary S.. University of Tennessee; Estados Unidos |
| description |
Real-time PCR assays using TaqMan or Molecular Beacon probes were developed and optimized for the quantification of total bacteria, the nitrite-oxidizing bacteria Nitrospira, and Nitrosomonas oligotropha-like ammonia oxidizing bacteria (AOB) in mixed liquor suspended solids (MLSS) from a municipal wastewater treatment plant (WWTP) using a single-sludge nitrification process. The targets for the real-time PCR assays were the 16S rRNA genes (16S rDNA) for bacteria and Nitrospira spp. and the amoA gene for N. oligotropha. A previously reported assay for AOB 16S rDNA was also tested for its application to activated sludge. The Nitrospira 16S rDNA, AOB 16S rDNA, and N. oligotropha-like amoA assays were log-linear over 6 orders of magnitude and the bacterial 16S rDNA real-time PCR assay was log-linear over 4 orders of magnitude with DNA standards. When these real-time PCR assays were applied to DNA extracted from MLSS, dilution of the DNA extracts was necessary to prevent PCR inhibition. The optimal DNA dilution range was broad for the bacterial 16S rDNA (1000-fold) and Nitrospira 16S rDNA assays (2500-fold) but narrow for the AOB 16S rDNA assay (10-fold) and N. oligotropha-like amoA real-time PCR assay (5-fold). In twelve MLSS samples collected over one year, mean cell per L values were 4.3 ± 2.0 × 1011 for bacteria, 3.7 ± 3.2 × 1010 for Nitrospira, 1.2 ± 0.9 × 1010 for all AOB, and 7.5 ± 6.0 × 109 for N. oligotropha-like AOB. The percent of the nitrifying population was 1.7% N. oligotropha-like AOB based on the N. oligotropha amoA assay, 2.9% total AOB based on the AOB 16S rDNA assay, and 8.6% nitrite-oxidizing bacteria based on the Nitrospira 16S rDNA assay. Ammonia-oxidizing bacteria in the wastewater treatment plant were estimated to oxidize 7.7 ± 6.8 fmol/hr/cell based on the AOB 16S rDNA assay and 12.4 ± 7.3 fmol/hr/cell based on the N. oligotropha amoA assay. |
| publishDate |
2003 |
| dc.date.none.fl_str_mv |
2003-01 |
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info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
| format |
article |
| status_str |
publishedVersion |
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http://hdl.handle.net/11336/98939 Harms, Gerda; Layton, Alice C.; Dionisi, Hebe Monica; Gregory, Igrid R.; Garrett, Victoria M.; et al.; Real-time PCR quantification of nitrifying bacteria in a municipal wastewater treatment plant; American Chemical Society; Environmental Science & Technology; 37; 2; 1-2003; 343-351 0013-936X CONICET Digital CONICET |
| url |
http://hdl.handle.net/11336/98939 |
| identifier_str_mv |
Harms, Gerda; Layton, Alice C.; Dionisi, Hebe Monica; Gregory, Igrid R.; Garrett, Victoria M.; et al.; Real-time PCR quantification of nitrifying bacteria in a municipal wastewater treatment plant; American Chemical Society; Environmental Science & Technology; 37; 2; 1-2003; 343-351 0013-936X CONICET Digital CONICET |
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eng |
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American Chemical Society |
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American Chemical Society |
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CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
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dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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