TY - JOUR
T1 - Molecular characterization of mesophilic and thermophilic sulfate reducing microbial communities in expanded granular sludge bed (EGSB) reactors
AU - Freeman, Stephanie A.
AU - Sierra-Alvarez, Reyes
AU - Altinbas, Mahmut
AU - Hollingsworth, Jeremy
AU - Stams, Alfons J.M.
AU - Smidt, Hauke
N1 - Funding Information:
Acknowledgments Financial support from the National Institute of Health (NIH grant TW00036) and the NSF/SRC Engineering Research Center for Environmentally Benign Semiconductor Manufacturing is acknowledged. M.A. was supported by fellowships from the Scientific and Technical Research Council of Turkey, and the Wageningen Institute for Environment and Climate Research. R.S.A. was supported by the National Science Foundation (NSF-0137368). We are thankful to Hans G.H.J. Heilig for his excellent assistance with DGGE analyses.
PY - 2008/4
Y1 - 2008/4
N2 - The microbial communities established in mesophilic and thermophilic expanded granular sludge bed reactors operated with sulfate as the electron acceptor were analyzed using 16S rRNA targeted molecular methods, including denaturing gradient gel electrophoresis, cloning, and phylogenetic analysis. Bacterial and archaeal communities were examined over 450 days of operation treating ethanol (thermophilic reactor) or ethanol and later a simulated semiconductor manufacturing wastewater containing citrate, isopropanol, and polyethylene glycol 300 (mesophilic reactor), with and without the addition of copper(II). Analysis, of PCR-amplified 16S rRNA gene fragments using denaturing gradient gel electrophoresis revealed a defined shift in microbial diversity in both reactors following a change in substrate composition (mesophilic reactor) and in temperature of operation from 30°C to 55°C (thermophilic reactor). The addition of copper(II) to the influent of both reactors did not noticeably affect the composition of the bacterial or archaeal communities, which is in agreement with the very low soluble copper concentrations (3-310 μg l-1) present in the reactor contents as a consequence of extensive precipitation of copper with biogenic sulfides. Furthermore, clone library analysis confirmed the phylogenetic diversity of sulfate-reducing consortia in mesophilic and thermophilic sulfidogenic reactors operated with simple substrates.
AB - The microbial communities established in mesophilic and thermophilic expanded granular sludge bed reactors operated with sulfate as the electron acceptor were analyzed using 16S rRNA targeted molecular methods, including denaturing gradient gel electrophoresis, cloning, and phylogenetic analysis. Bacterial and archaeal communities were examined over 450 days of operation treating ethanol (thermophilic reactor) or ethanol and later a simulated semiconductor manufacturing wastewater containing citrate, isopropanol, and polyethylene glycol 300 (mesophilic reactor), with and without the addition of copper(II). Analysis, of PCR-amplified 16S rRNA gene fragments using denaturing gradient gel electrophoresis revealed a defined shift in microbial diversity in both reactors following a change in substrate composition (mesophilic reactor) and in temperature of operation from 30°C to 55°C (thermophilic reactor). The addition of copper(II) to the influent of both reactors did not noticeably affect the composition of the bacterial or archaeal communities, which is in agreement with the very low soluble copper concentrations (3-310 μg l-1) present in the reactor contents as a consequence of extensive precipitation of copper with biogenic sulfides. Furthermore, clone library analysis confirmed the phylogenetic diversity of sulfate-reducing consortia in mesophilic and thermophilic sulfidogenic reactors operated with simple substrates.
KW - 16S rRNA gene clone library
KW - Anaerobic wastewater treatment
KW - Copper
KW - DGGE
KW - Ethanol
KW - Methanogens
KW - Sulfate reducing bacteria
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U2 - 10.1007/s10532-007-9123-9
DO - 10.1007/s10532-007-9123-9
M3 - Article
C2 - 17479349
AN - SCOPUS:39749187249
SN - 0923-9820
VL - 19
SP - 161
EP - 177
JO - Biodegradation
JF - Biodegradation
IS - 2
ER -