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Use of 16S rRNA Gene Terminal Restriction Fragment Analysis To Assess the Impact of Solids Retention Time on the Bacterial Diversity of Activated Sludge
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Zeitschriftentitel: | Applied and Environmental Microbiology |
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Personen und Körperschaften: | , , |
In: | Applied and Environmental Microbiology, 71, 2005, 10, S. 5814-5822 |
Format: | E-Article |
Sprache: | Englisch |
veröffentlicht: |
American Society for Microbiology
|
Schlagwörter: |
author_facet |
Saikaly, Pascal E. Stroot, Peter G. Oerther, Daniel B. Saikaly, Pascal E. Stroot, Peter G. Oerther, Daniel B. |
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author |
Saikaly, Pascal E. Stroot, Peter G. Oerther, Daniel B. |
spellingShingle |
Saikaly, Pascal E. Stroot, Peter G. Oerther, Daniel B. Applied and Environmental Microbiology Use of 16S rRNA Gene Terminal Restriction Fragment Analysis To Assess the Impact of Solids Retention Time on the Bacterial Diversity of Activated Sludge Ecology Applied Microbiology and Biotechnology Food Science Biotechnology |
author_sort |
saikaly, pascal e. |
spelling |
Saikaly, Pascal E. Stroot, Peter G. Oerther, Daniel B. 0099-2240 1098-5336 American Society for Microbiology Ecology Applied Microbiology and Biotechnology Food Science Biotechnology http://dx.doi.org/10.1128/aem.71.10.5814-5822.2005 <jats:title>ABSTRACT</jats:title> <jats:p> Terminal restriction fragment length polymorphism (T-RFLP) analysis of 16S rRNA genes was used to investigate the reproducibility and stability in the bacterial community structure of laboratory-scale sequencing batch bioreactors (SBR) and to assess the impact of solids retention time (SRT) on bacterial diversity. Two experiments were performed. In each experiment two sets of replicate SBRs were operated for a periods of three times the SRT. One set was operated at an SRT of 2 days and another set was operated at an SRT of 8 days. Samples for T-RFLP analysis were collected from the two sets of replicate reactors. HhaI, MspI, and RsaI T-RFLP profiles were analyzed using cluster analysis and diversity statistics. Cluster analysis with Ward's method using Jaccard distance and Hellinger distance showed that the bacterial community structure in both sets of reactors from both experimental runs was dynamic and that replicate reactors were clustered together and evolved similarly from startup. Richness ( <jats:italic>S</jats:italic> ), evenness ( <jats:italic>E</jats:italic> ), the Shannon-Weaver index ( <jats:italic>H</jats:italic> ), and the reciprocal of Simpson's index (1/ <jats:italic>D</jats:italic> ) were calculated, and the values were compared between the two sets of reactors. Evenness values were higher for reactors operated at an SRT of 2 days. Statistically significant differences in diversity ( <jats:italic>H</jats:italic> and <jats:italic>D</jats:italic> ) between the two sets of reactors were tested using a randomization procedure, and the results showed that reactors from both experimental runs that were operated at an SRT of 2 days had higher diversity ( <jats:italic>H</jats:italic> and <jats:italic>D</jats:italic> ) at the 5% level. T-RFLP analysis with diversity indices proved to be a powerful tool to analyze changes in the bacterial community diversity in response to changes in the operational parameters of activated-sludge systems. </jats:p> Use of 16S rRNA Gene Terminal Restriction Fragment Analysis To Assess the Impact of Solids Retention Time on the Bacterial Diversity of Activated Sludge Applied and Environmental Microbiology |
doi_str_mv |
10.1128/aem.71.10.5814-5822.2005 |
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Online Free |
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Land- und Forstwirtschaft, Gartenbau, Fischereiwirtschaft, Hauswirtschaft Geographie Biologie Technik |
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American Society for Microbiology, 2005 |
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American Society for Microbiology, 2005 |
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2005 |
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American Society for Microbiology |
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Applied and Environmental Microbiology |
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49 |
title |
Use of 16S rRNA Gene Terminal Restriction Fragment Analysis To Assess the Impact of Solids Retention Time on the Bacterial Diversity of Activated Sludge |
title_unstemmed |
Use of 16S rRNA Gene Terminal Restriction Fragment Analysis To Assess the Impact of Solids Retention Time on the Bacterial Diversity of Activated Sludge |
title_full |
Use of 16S rRNA Gene Terminal Restriction Fragment Analysis To Assess the Impact of Solids Retention Time on the Bacterial Diversity of Activated Sludge |
title_fullStr |
Use of 16S rRNA Gene Terminal Restriction Fragment Analysis To Assess the Impact of Solids Retention Time on the Bacterial Diversity of Activated Sludge |
title_full_unstemmed |
Use of 16S rRNA Gene Terminal Restriction Fragment Analysis To Assess the Impact of Solids Retention Time on the Bacterial Diversity of Activated Sludge |
title_short |
Use of 16S rRNA Gene Terminal Restriction Fragment Analysis To Assess the Impact of Solids Retention Time on the Bacterial Diversity of Activated Sludge |
title_sort |
use of 16s rrna gene terminal restriction fragment analysis to assess the impact of solids retention time on the bacterial diversity of activated sludge |
topic |
Ecology Applied Microbiology and Biotechnology Food Science Biotechnology |
url |
http://dx.doi.org/10.1128/aem.71.10.5814-5822.2005 |
publishDate |
2005 |
physical |
5814-5822 |
description |
<jats:title>ABSTRACT</jats:title>
<jats:p>
Terminal restriction fragment length polymorphism (T-RFLP) analysis of 16S rRNA genes was used to investigate the reproducibility and stability in the bacterial community structure of laboratory-scale sequencing batch bioreactors (SBR) and to assess the impact of solids retention time (SRT) on bacterial diversity. Two experiments were performed. In each experiment two sets of replicate SBRs were operated for a periods of three times the SRT. One set was operated at an SRT of 2 days and another set was operated at an SRT of 8 days. Samples for T-RFLP analysis were collected from the two sets of replicate reactors. HhaI, MspI, and RsaI T-RFLP profiles were analyzed using cluster analysis and diversity statistics. Cluster analysis with Ward's method using Jaccard distance and Hellinger distance showed that the bacterial community structure in both sets of reactors from both experimental runs was dynamic and that replicate reactors were clustered together and evolved similarly from startup. Richness (
<jats:italic>S</jats:italic>
), evenness (
<jats:italic>E</jats:italic>
), the Shannon-Weaver index (
<jats:italic>H</jats:italic>
), and the reciprocal of Simpson's index (1/
<jats:italic>D</jats:italic>
) were calculated, and the values were compared between the two sets of reactors. Evenness values were higher for reactors operated at an SRT of 2 days. Statistically significant differences in diversity (
<jats:italic>H</jats:italic>
and
<jats:italic>D</jats:italic>
) between the two sets of reactors were tested using a randomization procedure, and the results showed that reactors from both experimental runs that were operated at an SRT of 2 days had higher diversity (
<jats:italic>H</jats:italic>
and
<jats:italic>D</jats:italic>
) at the 5% level. T-RFLP analysis with diversity indices proved to be a powerful tool to analyze changes in the bacterial community diversity in response to changes in the operational parameters of activated-sludge systems.
</jats:p> |
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author | Saikaly, Pascal E., Stroot, Peter G., Oerther, Daniel B. |
author_facet | Saikaly, Pascal E., Stroot, Peter G., Oerther, Daniel B., Saikaly, Pascal E., Stroot, Peter G., Oerther, Daniel B. |
author_sort | saikaly, pascal e. |
container_issue | 10 |
container_start_page | 5814 |
container_title | Applied and Environmental Microbiology |
container_volume | 71 |
description | <jats:title>ABSTRACT</jats:title> <jats:p> Terminal restriction fragment length polymorphism (T-RFLP) analysis of 16S rRNA genes was used to investigate the reproducibility and stability in the bacterial community structure of laboratory-scale sequencing batch bioreactors (SBR) and to assess the impact of solids retention time (SRT) on bacterial diversity. Two experiments were performed. In each experiment two sets of replicate SBRs were operated for a periods of three times the SRT. One set was operated at an SRT of 2 days and another set was operated at an SRT of 8 days. Samples for T-RFLP analysis were collected from the two sets of replicate reactors. HhaI, MspI, and RsaI T-RFLP profiles were analyzed using cluster analysis and diversity statistics. Cluster analysis with Ward's method using Jaccard distance and Hellinger distance showed that the bacterial community structure in both sets of reactors from both experimental runs was dynamic and that replicate reactors were clustered together and evolved similarly from startup. Richness ( <jats:italic>S</jats:italic> ), evenness ( <jats:italic>E</jats:italic> ), the Shannon-Weaver index ( <jats:italic>H</jats:italic> ), and the reciprocal of Simpson's index (1/ <jats:italic>D</jats:italic> ) were calculated, and the values were compared between the two sets of reactors. Evenness values were higher for reactors operated at an SRT of 2 days. Statistically significant differences in diversity ( <jats:italic>H</jats:italic> and <jats:italic>D</jats:italic> ) between the two sets of reactors were tested using a randomization procedure, and the results showed that reactors from both experimental runs that were operated at an SRT of 2 days had higher diversity ( <jats:italic>H</jats:italic> and <jats:italic>D</jats:italic> ) at the 5% level. T-RFLP analysis with diversity indices proved to be a powerful tool to analyze changes in the bacterial community diversity in response to changes in the operational parameters of activated-sludge systems. </jats:p> |
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spelling | Saikaly, Pascal E. Stroot, Peter G. Oerther, Daniel B. 0099-2240 1098-5336 American Society for Microbiology Ecology Applied Microbiology and Biotechnology Food Science Biotechnology http://dx.doi.org/10.1128/aem.71.10.5814-5822.2005 <jats:title>ABSTRACT</jats:title> <jats:p> Terminal restriction fragment length polymorphism (T-RFLP) analysis of 16S rRNA genes was used to investigate the reproducibility and stability in the bacterial community structure of laboratory-scale sequencing batch bioreactors (SBR) and to assess the impact of solids retention time (SRT) on bacterial diversity. Two experiments were performed. In each experiment two sets of replicate SBRs were operated for a periods of three times the SRT. One set was operated at an SRT of 2 days and another set was operated at an SRT of 8 days. Samples for T-RFLP analysis were collected from the two sets of replicate reactors. HhaI, MspI, and RsaI T-RFLP profiles were analyzed using cluster analysis and diversity statistics. Cluster analysis with Ward's method using Jaccard distance and Hellinger distance showed that the bacterial community structure in both sets of reactors from both experimental runs was dynamic and that replicate reactors were clustered together and evolved similarly from startup. Richness ( <jats:italic>S</jats:italic> ), evenness ( <jats:italic>E</jats:italic> ), the Shannon-Weaver index ( <jats:italic>H</jats:italic> ), and the reciprocal of Simpson's index (1/ <jats:italic>D</jats:italic> ) were calculated, and the values were compared between the two sets of reactors. Evenness values were higher for reactors operated at an SRT of 2 days. Statistically significant differences in diversity ( <jats:italic>H</jats:italic> and <jats:italic>D</jats:italic> ) between the two sets of reactors were tested using a randomization procedure, and the results showed that reactors from both experimental runs that were operated at an SRT of 2 days had higher diversity ( <jats:italic>H</jats:italic> and <jats:italic>D</jats:italic> ) at the 5% level. T-RFLP analysis with diversity indices proved to be a powerful tool to analyze changes in the bacterial community diversity in response to changes in the operational parameters of activated-sludge systems. </jats:p> Use of 16S rRNA Gene Terminal Restriction Fragment Analysis To Assess the Impact of Solids Retention Time on the Bacterial Diversity of Activated Sludge Applied and Environmental Microbiology |
spellingShingle | Saikaly, Pascal E., Stroot, Peter G., Oerther, Daniel B., Applied and Environmental Microbiology, Use of 16S rRNA Gene Terminal Restriction Fragment Analysis To Assess the Impact of Solids Retention Time on the Bacterial Diversity of Activated Sludge, Ecology, Applied Microbiology and Biotechnology, Food Science, Biotechnology |
title | Use of 16S rRNA Gene Terminal Restriction Fragment Analysis To Assess the Impact of Solids Retention Time on the Bacterial Diversity of Activated Sludge |
title_full | Use of 16S rRNA Gene Terminal Restriction Fragment Analysis To Assess the Impact of Solids Retention Time on the Bacterial Diversity of Activated Sludge |
title_fullStr | Use of 16S rRNA Gene Terminal Restriction Fragment Analysis To Assess the Impact of Solids Retention Time on the Bacterial Diversity of Activated Sludge |
title_full_unstemmed | Use of 16S rRNA Gene Terminal Restriction Fragment Analysis To Assess the Impact of Solids Retention Time on the Bacterial Diversity of Activated Sludge |
title_short | Use of 16S rRNA Gene Terminal Restriction Fragment Analysis To Assess the Impact of Solids Retention Time on the Bacterial Diversity of Activated Sludge |
title_sort | use of 16s rrna gene terminal restriction fragment analysis to assess the impact of solids retention time on the bacterial diversity of activated sludge |
title_unstemmed | Use of 16S rRNA Gene Terminal Restriction Fragment Analysis To Assess the Impact of Solids Retention Time on the Bacterial Diversity of Activated Sludge |
topic | Ecology, Applied Microbiology and Biotechnology, Food Science, Biotechnology |
url | http://dx.doi.org/10.1128/aem.71.10.5814-5822.2005 |