Potential for aerobic $ NO_{2} $− reduction and corresponding key enzyme genes involved in Alcaligenes faecalis strain NR
Abstract The potential for aerobic $ NO_{2} $− removal by Alcaligenes faecalis strain NR was investigated. 35 mg/L of $ NO_{2} $−-N was removed by strain NR under aerobic conditions in the presence of $ NH_{4} $+. 15N-labeling experiment demonstrated that $ N_{2} $O and $ N_{2} $ were possible produ...
Ausführliche Beschreibung
Autor*in: |
Huang, Yuan Sheng [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2017 |
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Schlagwörter: |
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Anmerkung: |
© Springer-Verlag GmbH Germany 2017 |
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Übergeordnetes Werk: |
Enthalten in: Archives of microbiology - Berlin : Springer, 1930, 200(2017), 1 vom: 06. Sept., Seite 147-158 |
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Übergeordnetes Werk: |
volume:200 ; year:2017 ; number:1 ; day:06 ; month:09 ; pages:147-158 |
Links: |
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DOI / URN: |
10.1007/s00203-017-1428-4 |
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Katalog-ID: |
SPR001806203 |
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245 | 1 | 0 | |a Potential for aerobic $ NO_{2} $− reduction and corresponding key enzyme genes involved in Alcaligenes faecalis strain NR |
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520 | |a Abstract The potential for aerobic $ NO_{2} $− removal by Alcaligenes faecalis strain NR was investigated. 35 mg/L of $ NO_{2} $−-N was removed by strain NR under aerobic conditions in the presence of $ NH_{4} $+. 15N-labeling experiment demonstrated that $ N_{2} $O and $ N_{2} $ were possible products during the aerobic nitrite removal process by strain NR. The key enzyme genes of nirK, norB and nosZ, which regulate the aerobic nitrite denitrification process, were successfully amplified from strain NR. The gene sequence analysis indicates that copper-containing nitrite reductase (NIRK) and periplasmic nitrous oxide reductase (NOSZ) were both hydrophilic protein and the transmembrane structures were absent, while nitric oxide reductase large subunit (NORB) was a hydrophobic and transmembrane protein. According to the three-dimensional structure and binding site analysis, the bulky and hydrophobic methionine residue proximity to the nitrite binding sites of NIRK was speculated to be related to the oxygen tolerance of NIRK from strain NR. | ||
650 | 4 | |a Nitrite removal |7 (dpeaa)DE-He213 | |
650 | 4 | |a Aerobic denitrification |7 (dpeaa)DE-He213 | |
650 | 4 | |a Denitrification genes |7 (dpeaa)DE-He213 | |
650 | 4 | |a Nitrite reductase |7 (dpeaa)DE-He213 | |
700 | 1 | |a An, Qiang |4 aut | |
700 | 1 | |a Zhao, Bin |0 (orcid)0000-0001-9080-9361 |4 aut | |
700 | 1 | |a Lv, Qing Hao |4 aut | |
700 | 1 | |a Guo, Jing Song |4 aut | |
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912 | |a GBV_ILN_2021 | ||
912 | |a GBV_ILN_2025 | ||
912 | |a GBV_ILN_2026 | ||
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912 | |a GBV_ILN_2031 | ||
912 | |a GBV_ILN_2034 | ||
912 | |a GBV_ILN_2037 | ||
912 | |a GBV_ILN_2038 | ||
912 | |a GBV_ILN_2039 | ||
912 | |a GBV_ILN_2044 | ||
912 | |a GBV_ILN_2048 | ||
912 | |a GBV_ILN_2049 | ||
912 | |a GBV_ILN_2050 | ||
912 | |a GBV_ILN_2055 | ||
912 | |a GBV_ILN_2057 | ||
912 | |a GBV_ILN_2059 | ||
912 | |a GBV_ILN_2061 | ||
912 | |a GBV_ILN_2064 | ||
912 | |a GBV_ILN_2065 | ||
912 | |a GBV_ILN_2068 | ||
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912 | |a GBV_ILN_2129 | ||
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912 | |a GBV_ILN_2148 | ||
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10.1007/s00203-017-1428-4 doi (DE-627)SPR001806203 (SPR)s00203-017-1428-4-e DE-627 ger DE-627 rakwb eng Huang, Yuan Sheng verfasserin aut Potential for aerobic $ NO_{2} $− reduction and corresponding key enzyme genes involved in Alcaligenes faecalis strain NR 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag GmbH Germany 2017 Abstract The potential for aerobic $ NO_{2} $− removal by Alcaligenes faecalis strain NR was investigated. 35 mg/L of $ NO_{2} $−-N was removed by strain NR under aerobic conditions in the presence of $ NH_{4} $+. 15N-labeling experiment demonstrated that $ N_{2} $O and $ N_{2} $ were possible products during the aerobic nitrite removal process by strain NR. The key enzyme genes of nirK, norB and nosZ, which regulate the aerobic nitrite denitrification process, were successfully amplified from strain NR. The gene sequence analysis indicates that copper-containing nitrite reductase (NIRK) and periplasmic nitrous oxide reductase (NOSZ) were both hydrophilic protein and the transmembrane structures were absent, while nitric oxide reductase large subunit (NORB) was a hydrophobic and transmembrane protein. According to the three-dimensional structure and binding site analysis, the bulky and hydrophobic methionine residue proximity to the nitrite binding sites of NIRK was speculated to be related to the oxygen tolerance of NIRK from strain NR. Nitrite removal (dpeaa)DE-He213 Aerobic denitrification (dpeaa)DE-He213 Denitrification genes (dpeaa)DE-He213 Nitrite reductase (dpeaa)DE-He213 An, Qiang aut Zhao, Bin (orcid)0000-0001-9080-9361 aut Lv, Qing Hao aut Guo, Jing Song aut Enthalten in Archives of microbiology Berlin : Springer, 1930 200(2017), 1 vom: 06. Sept., Seite 147-158 (DE-627)253390079 (DE-600)1458451-7 1432-072X nnns volume:200 year:2017 number:1 day:06 month:09 pages:147-158 https://dx.doi.org/10.1007/s00203-017-1428-4 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_252 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_381 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2360 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 200 2017 1 06 09 147-158 |
spelling |
10.1007/s00203-017-1428-4 doi (DE-627)SPR001806203 (SPR)s00203-017-1428-4-e DE-627 ger DE-627 rakwb eng Huang, Yuan Sheng verfasserin aut Potential for aerobic $ NO_{2} $− reduction and corresponding key enzyme genes involved in Alcaligenes faecalis strain NR 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag GmbH Germany 2017 Abstract The potential for aerobic $ NO_{2} $− removal by Alcaligenes faecalis strain NR was investigated. 35 mg/L of $ NO_{2} $−-N was removed by strain NR under aerobic conditions in the presence of $ NH_{4} $+. 15N-labeling experiment demonstrated that $ N_{2} $O and $ N_{2} $ were possible products during the aerobic nitrite removal process by strain NR. The key enzyme genes of nirK, norB and nosZ, which regulate the aerobic nitrite denitrification process, were successfully amplified from strain NR. The gene sequence analysis indicates that copper-containing nitrite reductase (NIRK) and periplasmic nitrous oxide reductase (NOSZ) were both hydrophilic protein and the transmembrane structures were absent, while nitric oxide reductase large subunit (NORB) was a hydrophobic and transmembrane protein. According to the three-dimensional structure and binding site analysis, the bulky and hydrophobic methionine residue proximity to the nitrite binding sites of NIRK was speculated to be related to the oxygen tolerance of NIRK from strain NR. Nitrite removal (dpeaa)DE-He213 Aerobic denitrification (dpeaa)DE-He213 Denitrification genes (dpeaa)DE-He213 Nitrite reductase (dpeaa)DE-He213 An, Qiang aut Zhao, Bin (orcid)0000-0001-9080-9361 aut Lv, Qing Hao aut Guo, Jing Song aut Enthalten in Archives of microbiology Berlin : Springer, 1930 200(2017), 1 vom: 06. Sept., Seite 147-158 (DE-627)253390079 (DE-600)1458451-7 1432-072X nnns volume:200 year:2017 number:1 day:06 month:09 pages:147-158 https://dx.doi.org/10.1007/s00203-017-1428-4 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_252 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_381 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2360 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 200 2017 1 06 09 147-158 |
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10.1007/s00203-017-1428-4 doi (DE-627)SPR001806203 (SPR)s00203-017-1428-4-e DE-627 ger DE-627 rakwb eng Huang, Yuan Sheng verfasserin aut Potential for aerobic $ NO_{2} $− reduction and corresponding key enzyme genes involved in Alcaligenes faecalis strain NR 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag GmbH Germany 2017 Abstract The potential for aerobic $ NO_{2} $− removal by Alcaligenes faecalis strain NR was investigated. 35 mg/L of $ NO_{2} $−-N was removed by strain NR under aerobic conditions in the presence of $ NH_{4} $+. 15N-labeling experiment demonstrated that $ N_{2} $O and $ N_{2} $ were possible products during the aerobic nitrite removal process by strain NR. The key enzyme genes of nirK, norB and nosZ, which regulate the aerobic nitrite denitrification process, were successfully amplified from strain NR. The gene sequence analysis indicates that copper-containing nitrite reductase (NIRK) and periplasmic nitrous oxide reductase (NOSZ) were both hydrophilic protein and the transmembrane structures were absent, while nitric oxide reductase large subunit (NORB) was a hydrophobic and transmembrane protein. According to the three-dimensional structure and binding site analysis, the bulky and hydrophobic methionine residue proximity to the nitrite binding sites of NIRK was speculated to be related to the oxygen tolerance of NIRK from strain NR. Nitrite removal (dpeaa)DE-He213 Aerobic denitrification (dpeaa)DE-He213 Denitrification genes (dpeaa)DE-He213 Nitrite reductase (dpeaa)DE-He213 An, Qiang aut Zhao, Bin (orcid)0000-0001-9080-9361 aut Lv, Qing Hao aut Guo, Jing Song aut Enthalten in Archives of microbiology Berlin : Springer, 1930 200(2017), 1 vom: 06. Sept., Seite 147-158 (DE-627)253390079 (DE-600)1458451-7 1432-072X nnns volume:200 year:2017 number:1 day:06 month:09 pages:147-158 https://dx.doi.org/10.1007/s00203-017-1428-4 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_252 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_381 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2360 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 200 2017 1 06 09 147-158 |
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10.1007/s00203-017-1428-4 doi (DE-627)SPR001806203 (SPR)s00203-017-1428-4-e DE-627 ger DE-627 rakwb eng Huang, Yuan Sheng verfasserin aut Potential for aerobic $ NO_{2} $− reduction and corresponding key enzyme genes involved in Alcaligenes faecalis strain NR 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag GmbH Germany 2017 Abstract The potential for aerobic $ NO_{2} $− removal by Alcaligenes faecalis strain NR was investigated. 35 mg/L of $ NO_{2} $−-N was removed by strain NR under aerobic conditions in the presence of $ NH_{4} $+. 15N-labeling experiment demonstrated that $ N_{2} $O and $ N_{2} $ were possible products during the aerobic nitrite removal process by strain NR. The key enzyme genes of nirK, norB and nosZ, which regulate the aerobic nitrite denitrification process, were successfully amplified from strain NR. The gene sequence analysis indicates that copper-containing nitrite reductase (NIRK) and periplasmic nitrous oxide reductase (NOSZ) were both hydrophilic protein and the transmembrane structures were absent, while nitric oxide reductase large subunit (NORB) was a hydrophobic and transmembrane protein. According to the three-dimensional structure and binding site analysis, the bulky and hydrophobic methionine residue proximity to the nitrite binding sites of NIRK was speculated to be related to the oxygen tolerance of NIRK from strain NR. Nitrite removal (dpeaa)DE-He213 Aerobic denitrification (dpeaa)DE-He213 Denitrification genes (dpeaa)DE-He213 Nitrite reductase (dpeaa)DE-He213 An, Qiang aut Zhao, Bin (orcid)0000-0001-9080-9361 aut Lv, Qing Hao aut Guo, Jing Song aut Enthalten in Archives of microbiology Berlin : Springer, 1930 200(2017), 1 vom: 06. Sept., Seite 147-158 (DE-627)253390079 (DE-600)1458451-7 1432-072X nnns volume:200 year:2017 number:1 day:06 month:09 pages:147-158 https://dx.doi.org/10.1007/s00203-017-1428-4 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_252 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_381 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2360 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 200 2017 1 06 09 147-158 |
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10.1007/s00203-017-1428-4 doi (DE-627)SPR001806203 (SPR)s00203-017-1428-4-e DE-627 ger DE-627 rakwb eng Huang, Yuan Sheng verfasserin aut Potential for aerobic $ NO_{2} $− reduction and corresponding key enzyme genes involved in Alcaligenes faecalis strain NR 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag GmbH Germany 2017 Abstract The potential for aerobic $ NO_{2} $− removal by Alcaligenes faecalis strain NR was investigated. 35 mg/L of $ NO_{2} $−-N was removed by strain NR under aerobic conditions in the presence of $ NH_{4} $+. 15N-labeling experiment demonstrated that $ N_{2} $O and $ N_{2} $ were possible products during the aerobic nitrite removal process by strain NR. The key enzyme genes of nirK, norB and nosZ, which regulate the aerobic nitrite denitrification process, were successfully amplified from strain NR. The gene sequence analysis indicates that copper-containing nitrite reductase (NIRK) and periplasmic nitrous oxide reductase (NOSZ) were both hydrophilic protein and the transmembrane structures were absent, while nitric oxide reductase large subunit (NORB) was a hydrophobic and transmembrane protein. According to the three-dimensional structure and binding site analysis, the bulky and hydrophobic methionine residue proximity to the nitrite binding sites of NIRK was speculated to be related to the oxygen tolerance of NIRK from strain NR. Nitrite removal (dpeaa)DE-He213 Aerobic denitrification (dpeaa)DE-He213 Denitrification genes (dpeaa)DE-He213 Nitrite reductase (dpeaa)DE-He213 An, Qiang aut Zhao, Bin (orcid)0000-0001-9080-9361 aut Lv, Qing Hao aut Guo, Jing Song aut Enthalten in Archives of microbiology Berlin : Springer, 1930 200(2017), 1 vom: 06. Sept., Seite 147-158 (DE-627)253390079 (DE-600)1458451-7 1432-072X nnns volume:200 year:2017 number:1 day:06 month:09 pages:147-158 https://dx.doi.org/10.1007/s00203-017-1428-4 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_252 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_381 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2360 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 200 2017 1 06 09 147-158 |
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Enthalten in Archives of microbiology 200(2017), 1 vom: 06. Sept., Seite 147-158 volume:200 year:2017 number:1 day:06 month:09 pages:147-158 |
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Enthalten in Archives of microbiology 200(2017), 1 vom: 06. Sept., Seite 147-158 volume:200 year:2017 number:1 day:06 month:09 pages:147-158 |
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Nitrite removal Aerobic denitrification Denitrification genes Nitrite reductase |
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Huang, Yuan Sheng @@aut@@ An, Qiang @@aut@@ Zhao, Bin @@aut@@ Lv, Qing Hao @@aut@@ Guo, Jing Song @@aut@@ |
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2017-09-06T00:00:00Z |
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<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">SPR001806203</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230519093206.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">201001s2017 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1007/s00203-017-1428-4</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)SPR001806203</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(SPR)s00203-017-1428-4-e</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Huang, Yuan Sheng</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Potential for aerobic $ NO_{2} $− reduction and corresponding key enzyme genes involved in Alcaligenes faecalis strain NR</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2017</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="500" ind1=" " ind2=" "><subfield code="a">© Springer-Verlag GmbH Germany 2017</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract The potential for aerobic $ NO_{2} $− removal by Alcaligenes faecalis strain NR was investigated. 35 mg/L of $ NO_{2} $−-N was removed by strain NR under aerobic conditions in the presence of $ NH_{4} $+. 15N-labeling experiment demonstrated that $ N_{2} $O and $ N_{2} $ were possible products during the aerobic nitrite removal process by strain NR. The key enzyme genes of nirK, norB and nosZ, which regulate the aerobic nitrite denitrification process, were successfully amplified from strain NR. The gene sequence analysis indicates that copper-containing nitrite reductase (NIRK) and periplasmic nitrous oxide reductase (NOSZ) were both hydrophilic protein and the transmembrane structures were absent, while nitric oxide reductase large subunit (NORB) was a hydrophobic and transmembrane protein. 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Huang, Yuan Sheng |
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Huang, Yuan Sheng misc Nitrite removal misc Aerobic denitrification misc Denitrification genes misc Nitrite reductase Potential for aerobic $ NO_{2} $− reduction and corresponding key enzyme genes involved in Alcaligenes faecalis strain NR |
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Potential for aerobic $ NO_{2} $− reduction and corresponding key enzyme genes involved in Alcaligenes faecalis strain NR Nitrite removal (dpeaa)DE-He213 Aerobic denitrification (dpeaa)DE-He213 Denitrification genes (dpeaa)DE-He213 Nitrite reductase (dpeaa)DE-He213 |
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Potential for aerobic $ NO_{2} $− reduction and corresponding key enzyme genes involved in Alcaligenes faecalis strain NR |
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Potential for aerobic $ NO_{2} $− reduction and corresponding key enzyme genes involved in Alcaligenes faecalis strain NR |
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Huang, Yuan Sheng An, Qiang Zhao, Bin Lv, Qing Hao Guo, Jing Song |
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title_sort |
potential for aerobic $ no_{2} $− reduction and corresponding key enzyme genes involved in alcaligenes faecalis strain nr |
title_auth |
Potential for aerobic $ NO_{2} $− reduction and corresponding key enzyme genes involved in Alcaligenes faecalis strain NR |
abstract |
Abstract The potential for aerobic $ NO_{2} $− removal by Alcaligenes faecalis strain NR was investigated. 35 mg/L of $ NO_{2} $−-N was removed by strain NR under aerobic conditions in the presence of $ NH_{4} $+. 15N-labeling experiment demonstrated that $ N_{2} $O and $ N_{2} $ were possible products during the aerobic nitrite removal process by strain NR. The key enzyme genes of nirK, norB and nosZ, which regulate the aerobic nitrite denitrification process, were successfully amplified from strain NR. The gene sequence analysis indicates that copper-containing nitrite reductase (NIRK) and periplasmic nitrous oxide reductase (NOSZ) were both hydrophilic protein and the transmembrane structures were absent, while nitric oxide reductase large subunit (NORB) was a hydrophobic and transmembrane protein. According to the three-dimensional structure and binding site analysis, the bulky and hydrophobic methionine residue proximity to the nitrite binding sites of NIRK was speculated to be related to the oxygen tolerance of NIRK from strain NR. © Springer-Verlag GmbH Germany 2017 |
abstractGer |
Abstract The potential for aerobic $ NO_{2} $− removal by Alcaligenes faecalis strain NR was investigated. 35 mg/L of $ NO_{2} $−-N was removed by strain NR under aerobic conditions in the presence of $ NH_{4} $+. 15N-labeling experiment demonstrated that $ N_{2} $O and $ N_{2} $ were possible products during the aerobic nitrite removal process by strain NR. The key enzyme genes of nirK, norB and nosZ, which regulate the aerobic nitrite denitrification process, were successfully amplified from strain NR. The gene sequence analysis indicates that copper-containing nitrite reductase (NIRK) and periplasmic nitrous oxide reductase (NOSZ) were both hydrophilic protein and the transmembrane structures were absent, while nitric oxide reductase large subunit (NORB) was a hydrophobic and transmembrane protein. According to the three-dimensional structure and binding site analysis, the bulky and hydrophobic methionine residue proximity to the nitrite binding sites of NIRK was speculated to be related to the oxygen tolerance of NIRK from strain NR. © Springer-Verlag GmbH Germany 2017 |
abstract_unstemmed |
Abstract The potential for aerobic $ NO_{2} $− removal by Alcaligenes faecalis strain NR was investigated. 35 mg/L of $ NO_{2} $−-N was removed by strain NR under aerobic conditions in the presence of $ NH_{4} $+. 15N-labeling experiment demonstrated that $ N_{2} $O and $ N_{2} $ were possible products during the aerobic nitrite removal process by strain NR. The key enzyme genes of nirK, norB and nosZ, which regulate the aerobic nitrite denitrification process, were successfully amplified from strain NR. The gene sequence analysis indicates that copper-containing nitrite reductase (NIRK) and periplasmic nitrous oxide reductase (NOSZ) were both hydrophilic protein and the transmembrane structures were absent, while nitric oxide reductase large subunit (NORB) was a hydrophobic and transmembrane protein. According to the three-dimensional structure and binding site analysis, the bulky and hydrophobic methionine residue proximity to the nitrite binding sites of NIRK was speculated to be related to the oxygen tolerance of NIRK from strain NR. © Springer-Verlag GmbH Germany 2017 |
collection_details |
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container_issue |
1 |
title_short |
Potential for aerobic $ NO_{2} $− reduction and corresponding key enzyme genes involved in Alcaligenes faecalis strain NR |
url |
https://dx.doi.org/10.1007/s00203-017-1428-4 |
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author2 |
An, Qiang Zhao, Bin Lv, Qing Hao Guo, Jing Song |
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doi_str |
10.1007/s00203-017-1428-4 |
up_date |
2024-07-04T00:29:53.360Z |
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|
score |
7.399349 |