Cyanobacterial $ H_{2} $ production — a comparative analysis
Abstract Several unicellular and filamentous, nitrogen-fixing and non-nitrogen-fixing cyanobacterial strains have been investigated on the molecular and the physiological level in order to find the most efficient organisms for photobiological hydrogen production. These strains were screened for the...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Schütz, Kathrin [verfasserIn] Happe, Thomas [verfasserIn] Troshina, Olga [verfasserIn] Lindblad, Peter [verfasserIn] Leitão, Elsa [verfasserIn] Oliveira, Paulo [verfasserIn] Tamagnini, Paula [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2003 |
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| Schlagwörter: |
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| Übergeordnetes Werk: |
Enthalten in: Planta - Berlin : Springer, 1925, 218(2003), 3 vom: 15. Okt., Seite 350-359 |
|---|---|
| Übergeordnetes Werk: |
volume:218 ; year:2003 ; number:3 ; day:15 ; month:10 ; pages:350-359 |
| Links: |
|---|
| DOI / URN: |
10.1007/s00425-003-1113-5 |
|---|
| Katalog-ID: |
SPR005643465 |
|---|
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| 245 | 1 | 0 | |a Cyanobacterial $ H_{2} $ production — a comparative analysis |
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| 520 | |a Abstract Several unicellular and filamentous, nitrogen-fixing and non-nitrogen-fixing cyanobacterial strains have been investigated on the molecular and the physiological level in order to find the most efficient organisms for photobiological hydrogen production. These strains were screened for the presence or absence of hup and hox genes, and it was shown that they have different sets of genes involved in $ H_{2} $ evolution. The uptake hydrogenase was identified in all $ N_{2} $-fixing cyanobacteria, and some of these strains also contained the bidirectional hydrogenase, whereas the non-nitrogen fixing strains only possessed the bidirectional enzyme. In $ N_{2} $-fixing strains, hydrogen was mainly produced by the nitrogenase as a by-product during the reduction of atmospheric nitrogen to ammonia. Therefore, hydrogen production was investigated both under non-nitrogen-fixing conditions and under nitrogen limitation. It was shown that the hydrogen uptake activity is linked to the nitrogenase activity, whereas the hydrogen evolution activity of the bidirectional hydrogenase is not dependent or even related to diazotrophic growth conditions. With regard to large-scale hydrogen evolution by $ N_{2} $-fixing cyanobacteria, hydrogen uptake-deficient mutants have to be used because of their inability to re-oxidize the hydrogen produced by the nitrogenase. On the other hand, fermentative $ H_{2} $ production by the bidirectional hydrogenase should also be taken into account in further investigations of biological hydrogen production. | ||
| 650 | 4 | |a Cyanobacterium |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Hydrogen |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Hydrogenase |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Nitrogenase |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Photobiological H |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a production |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Screening (H |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a production) |7 (dpeaa)DE-He213 | |
| 700 | 1 | |a Happe, Thomas |e verfasserin |4 aut | |
| 700 | 1 | |a Troshina, Olga |e verfasserin |4 aut | |
| 700 | 1 | |a Lindblad, Peter |e verfasserin |4 aut | |
| 700 | 1 | |a Leitão, Elsa |e verfasserin |4 aut | |
| 700 | 1 | |a Oliveira, Paulo |e verfasserin |4 aut | |
| 700 | 1 | |a Tamagnini, Paula |e verfasserin |4 aut | |
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10.1007/s00425-003-1113-5 doi (DE-627)SPR005643465 (SPR)s00425-003-1113-5-e DE-627 ger DE-627 rakwb eng 580 ASE 42.38 bkl Schütz, Kathrin verfasserin aut Cyanobacterial $ H_{2} $ production — a comparative analysis 2003 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Several unicellular and filamentous, nitrogen-fixing and non-nitrogen-fixing cyanobacterial strains have been investigated on the molecular and the physiological level in order to find the most efficient organisms for photobiological hydrogen production. These strains were screened for the presence or absence of hup and hox genes, and it was shown that they have different sets of genes involved in $ H_{2} $ evolution. The uptake hydrogenase was identified in all $ N_{2} $-fixing cyanobacteria, and some of these strains also contained the bidirectional hydrogenase, whereas the non-nitrogen fixing strains only possessed the bidirectional enzyme. In $ N_{2} $-fixing strains, hydrogen was mainly produced by the nitrogenase as a by-product during the reduction of atmospheric nitrogen to ammonia. Therefore, hydrogen production was investigated both under non-nitrogen-fixing conditions and under nitrogen limitation. It was shown that the hydrogen uptake activity is linked to the nitrogenase activity, whereas the hydrogen evolution activity of the bidirectional hydrogenase is not dependent or even related to diazotrophic growth conditions. With regard to large-scale hydrogen evolution by $ N_{2} $-fixing cyanobacteria, hydrogen uptake-deficient mutants have to be used because of their inability to re-oxidize the hydrogen produced by the nitrogenase. On the other hand, fermentative $ H_{2} $ production by the bidirectional hydrogenase should also be taken into account in further investigations of biological hydrogen production. Cyanobacterium (dpeaa)DE-He213 Hydrogen (dpeaa)DE-He213 Hydrogenase (dpeaa)DE-He213 Nitrogenase (dpeaa)DE-He213 Photobiological H (dpeaa)DE-He213 production (dpeaa)DE-He213 Screening (H (dpeaa)DE-He213 production) (dpeaa)DE-He213 Happe, Thomas verfasserin aut Troshina, Olga verfasserin aut Lindblad, Peter verfasserin aut Leitão, Elsa verfasserin aut Oliveira, Paulo verfasserin aut Tamagnini, Paula verfasserin aut Enthalten in Planta Berlin : Springer, 1925 218(2003), 3 vom: 15. Okt., Seite 350-359 (DE-627)254639100 (DE-600)1463030-8 1432-2048 nnns volume:218 year:2003 number:3 day:15 month:10 pages:350-359 https://dx.doi.org/10.1007/s00425-003-1113-5 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_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 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_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 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_2018 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_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_2946 GBV_ILN_2949 GBV_ILN_2951 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4393 GBV_ILN_4700 42.38 ASE AR 218 2003 3 15 10 350-359 |
| spelling |
10.1007/s00425-003-1113-5 doi (DE-627)SPR005643465 (SPR)s00425-003-1113-5-e DE-627 ger DE-627 rakwb eng 580 ASE 42.38 bkl Schütz, Kathrin verfasserin aut Cyanobacterial $ H_{2} $ production — a comparative analysis 2003 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Several unicellular and filamentous, nitrogen-fixing and non-nitrogen-fixing cyanobacterial strains have been investigated on the molecular and the physiological level in order to find the most efficient organisms for photobiological hydrogen production. These strains were screened for the presence or absence of hup and hox genes, and it was shown that they have different sets of genes involved in $ H_{2} $ evolution. The uptake hydrogenase was identified in all $ N_{2} $-fixing cyanobacteria, and some of these strains also contained the bidirectional hydrogenase, whereas the non-nitrogen fixing strains only possessed the bidirectional enzyme. In $ N_{2} $-fixing strains, hydrogen was mainly produced by the nitrogenase as a by-product during the reduction of atmospheric nitrogen to ammonia. Therefore, hydrogen production was investigated both under non-nitrogen-fixing conditions and under nitrogen limitation. It was shown that the hydrogen uptake activity is linked to the nitrogenase activity, whereas the hydrogen evolution activity of the bidirectional hydrogenase is not dependent or even related to diazotrophic growth conditions. With regard to large-scale hydrogen evolution by $ N_{2} $-fixing cyanobacteria, hydrogen uptake-deficient mutants have to be used because of their inability to re-oxidize the hydrogen produced by the nitrogenase. On the other hand, fermentative $ H_{2} $ production by the bidirectional hydrogenase should also be taken into account in further investigations of biological hydrogen production. Cyanobacterium (dpeaa)DE-He213 Hydrogen (dpeaa)DE-He213 Hydrogenase (dpeaa)DE-He213 Nitrogenase (dpeaa)DE-He213 Photobiological H (dpeaa)DE-He213 production (dpeaa)DE-He213 Screening (H (dpeaa)DE-He213 production) (dpeaa)DE-He213 Happe, Thomas verfasserin aut Troshina, Olga verfasserin aut Lindblad, Peter verfasserin aut Leitão, Elsa verfasserin aut Oliveira, Paulo verfasserin aut Tamagnini, Paula verfasserin aut Enthalten in Planta Berlin : Springer, 1925 218(2003), 3 vom: 15. Okt., Seite 350-359 (DE-627)254639100 (DE-600)1463030-8 1432-2048 nnns volume:218 year:2003 number:3 day:15 month:10 pages:350-359 https://dx.doi.org/10.1007/s00425-003-1113-5 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_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 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_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 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_2018 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_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_2946 GBV_ILN_2949 GBV_ILN_2951 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4393 GBV_ILN_4700 42.38 ASE AR 218 2003 3 15 10 350-359 |
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10.1007/s00425-003-1113-5 doi (DE-627)SPR005643465 (SPR)s00425-003-1113-5-e DE-627 ger DE-627 rakwb eng 580 ASE 42.38 bkl Schütz, Kathrin verfasserin aut Cyanobacterial $ H_{2} $ production — a comparative analysis 2003 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Several unicellular and filamentous, nitrogen-fixing and non-nitrogen-fixing cyanobacterial strains have been investigated on the molecular and the physiological level in order to find the most efficient organisms for photobiological hydrogen production. These strains were screened for the presence or absence of hup and hox genes, and it was shown that they have different sets of genes involved in $ H_{2} $ evolution. The uptake hydrogenase was identified in all $ N_{2} $-fixing cyanobacteria, and some of these strains also contained the bidirectional hydrogenase, whereas the non-nitrogen fixing strains only possessed the bidirectional enzyme. In $ N_{2} $-fixing strains, hydrogen was mainly produced by the nitrogenase as a by-product during the reduction of atmospheric nitrogen to ammonia. Therefore, hydrogen production was investigated both under non-nitrogen-fixing conditions and under nitrogen limitation. It was shown that the hydrogen uptake activity is linked to the nitrogenase activity, whereas the hydrogen evolution activity of the bidirectional hydrogenase is not dependent or even related to diazotrophic growth conditions. With regard to large-scale hydrogen evolution by $ N_{2} $-fixing cyanobacteria, hydrogen uptake-deficient mutants have to be used because of their inability to re-oxidize the hydrogen produced by the nitrogenase. On the other hand, fermentative $ H_{2} $ production by the bidirectional hydrogenase should also be taken into account in further investigations of biological hydrogen production. Cyanobacterium (dpeaa)DE-He213 Hydrogen (dpeaa)DE-He213 Hydrogenase (dpeaa)DE-He213 Nitrogenase (dpeaa)DE-He213 Photobiological H (dpeaa)DE-He213 production (dpeaa)DE-He213 Screening (H (dpeaa)DE-He213 production) (dpeaa)DE-He213 Happe, Thomas verfasserin aut Troshina, Olga verfasserin aut Lindblad, Peter verfasserin aut Leitão, Elsa verfasserin aut Oliveira, Paulo verfasserin aut Tamagnini, Paula verfasserin aut Enthalten in Planta Berlin : Springer, 1925 218(2003), 3 vom: 15. Okt., Seite 350-359 (DE-627)254639100 (DE-600)1463030-8 1432-2048 nnns volume:218 year:2003 number:3 day:15 month:10 pages:350-359 https://dx.doi.org/10.1007/s00425-003-1113-5 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_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 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_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 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_2018 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_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_2946 GBV_ILN_2949 GBV_ILN_2951 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4393 GBV_ILN_4700 42.38 ASE AR 218 2003 3 15 10 350-359 |
| allfieldsGer |
10.1007/s00425-003-1113-5 doi (DE-627)SPR005643465 (SPR)s00425-003-1113-5-e DE-627 ger DE-627 rakwb eng 580 ASE 42.38 bkl Schütz, Kathrin verfasserin aut Cyanobacterial $ H_{2} $ production — a comparative analysis 2003 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Several unicellular and filamentous, nitrogen-fixing and non-nitrogen-fixing cyanobacterial strains have been investigated on the molecular and the physiological level in order to find the most efficient organisms for photobiological hydrogen production. These strains were screened for the presence or absence of hup and hox genes, and it was shown that they have different sets of genes involved in $ H_{2} $ evolution. The uptake hydrogenase was identified in all $ N_{2} $-fixing cyanobacteria, and some of these strains also contained the bidirectional hydrogenase, whereas the non-nitrogen fixing strains only possessed the bidirectional enzyme. In $ N_{2} $-fixing strains, hydrogen was mainly produced by the nitrogenase as a by-product during the reduction of atmospheric nitrogen to ammonia. Therefore, hydrogen production was investigated both under non-nitrogen-fixing conditions and under nitrogen limitation. It was shown that the hydrogen uptake activity is linked to the nitrogenase activity, whereas the hydrogen evolution activity of the bidirectional hydrogenase is not dependent or even related to diazotrophic growth conditions. With regard to large-scale hydrogen evolution by $ N_{2} $-fixing cyanobacteria, hydrogen uptake-deficient mutants have to be used because of their inability to re-oxidize the hydrogen produced by the nitrogenase. On the other hand, fermentative $ H_{2} $ production by the bidirectional hydrogenase should also be taken into account in further investigations of biological hydrogen production. Cyanobacterium (dpeaa)DE-He213 Hydrogen (dpeaa)DE-He213 Hydrogenase (dpeaa)DE-He213 Nitrogenase (dpeaa)DE-He213 Photobiological H (dpeaa)DE-He213 production (dpeaa)DE-He213 Screening (H (dpeaa)DE-He213 production) (dpeaa)DE-He213 Happe, Thomas verfasserin aut Troshina, Olga verfasserin aut Lindblad, Peter verfasserin aut Leitão, Elsa verfasserin aut Oliveira, Paulo verfasserin aut Tamagnini, Paula verfasserin aut Enthalten in Planta Berlin : Springer, 1925 218(2003), 3 vom: 15. Okt., Seite 350-359 (DE-627)254639100 (DE-600)1463030-8 1432-2048 nnns volume:218 year:2003 number:3 day:15 month:10 pages:350-359 https://dx.doi.org/10.1007/s00425-003-1113-5 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_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 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_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 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_2018 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_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_2946 GBV_ILN_2949 GBV_ILN_2951 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4393 GBV_ILN_4700 42.38 ASE AR 218 2003 3 15 10 350-359 |
| allfieldsSound |
10.1007/s00425-003-1113-5 doi (DE-627)SPR005643465 (SPR)s00425-003-1113-5-e DE-627 ger DE-627 rakwb eng 580 ASE 42.38 bkl Schütz, Kathrin verfasserin aut Cyanobacterial $ H_{2} $ production — a comparative analysis 2003 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Several unicellular and filamentous, nitrogen-fixing and non-nitrogen-fixing cyanobacterial strains have been investigated on the molecular and the physiological level in order to find the most efficient organisms for photobiological hydrogen production. These strains were screened for the presence or absence of hup and hox genes, and it was shown that they have different sets of genes involved in $ H_{2} $ evolution. The uptake hydrogenase was identified in all $ N_{2} $-fixing cyanobacteria, and some of these strains also contained the bidirectional hydrogenase, whereas the non-nitrogen fixing strains only possessed the bidirectional enzyme. In $ N_{2} $-fixing strains, hydrogen was mainly produced by the nitrogenase as a by-product during the reduction of atmospheric nitrogen to ammonia. Therefore, hydrogen production was investigated both under non-nitrogen-fixing conditions and under nitrogen limitation. It was shown that the hydrogen uptake activity is linked to the nitrogenase activity, whereas the hydrogen evolution activity of the bidirectional hydrogenase is not dependent or even related to diazotrophic growth conditions. With regard to large-scale hydrogen evolution by $ N_{2} $-fixing cyanobacteria, hydrogen uptake-deficient mutants have to be used because of their inability to re-oxidize the hydrogen produced by the nitrogenase. On the other hand, fermentative $ H_{2} $ production by the bidirectional hydrogenase should also be taken into account in further investigations of biological hydrogen production. Cyanobacterium (dpeaa)DE-He213 Hydrogen (dpeaa)DE-He213 Hydrogenase (dpeaa)DE-He213 Nitrogenase (dpeaa)DE-He213 Photobiological H (dpeaa)DE-He213 production (dpeaa)DE-He213 Screening (H (dpeaa)DE-He213 production) (dpeaa)DE-He213 Happe, Thomas verfasserin aut Troshina, Olga verfasserin aut Lindblad, Peter verfasserin aut Leitão, Elsa verfasserin aut Oliveira, Paulo verfasserin aut Tamagnini, Paula verfasserin aut Enthalten in Planta Berlin : Springer, 1925 218(2003), 3 vom: 15. Okt., Seite 350-359 (DE-627)254639100 (DE-600)1463030-8 1432-2048 nnns volume:218 year:2003 number:3 day:15 month:10 pages:350-359 https://dx.doi.org/10.1007/s00425-003-1113-5 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_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 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_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 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_2018 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_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_2946 GBV_ILN_2949 GBV_ILN_2951 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4393 GBV_ILN_4700 42.38 ASE AR 218 2003 3 15 10 350-359 |
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English |
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Enthalten in Planta 218(2003), 3 vom: 15. Okt., Seite 350-359 volume:218 year:2003 number:3 day:15 month:10 pages:350-359 |
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Enthalten in Planta 218(2003), 3 vom: 15. Okt., Seite 350-359 volume:218 year:2003 number:3 day:15 month:10 pages:350-359 |
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findex.gbv.de |
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Cyanobacterium Hydrogen Hydrogenase Nitrogenase Photobiological H production Screening (H production) |
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Schütz, Kathrin @@aut@@ Happe, Thomas @@aut@@ Troshina, Olga @@aut@@ Lindblad, Peter @@aut@@ Leitão, Elsa @@aut@@ Oliveira, Paulo @@aut@@ Tamagnini, Paula @@aut@@ |
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2003-10-15T00:00:00Z |
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These strains were screened for the presence or absence of hup and hox genes, and it was shown that they have different sets of genes involved in $ H_{2} $ evolution. The uptake hydrogenase was identified in all $ N_{2} $-fixing cyanobacteria, and some of these strains also contained the bidirectional hydrogenase, whereas the non-nitrogen fixing strains only possessed the bidirectional enzyme. In $ N_{2} $-fixing strains, hydrogen was mainly produced by the nitrogenase as a by-product during the reduction of atmospheric nitrogen to ammonia. Therefore, hydrogen production was investigated both under non-nitrogen-fixing conditions and under nitrogen limitation. It was shown that the hydrogen uptake activity is linked to the nitrogenase activity, whereas the hydrogen evolution activity of the bidirectional hydrogenase is not dependent or even related to diazotrophic growth conditions. With regard to large-scale hydrogen evolution by $ N_{2} $-fixing cyanobacteria, hydrogen uptake-deficient mutants have to be used because of their inability to re-oxidize the hydrogen produced by the nitrogenase. 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|
| author |
Schütz, Kathrin |
| spellingShingle |
Schütz, Kathrin ddc 580 bkl 42.38 misc Cyanobacterium misc Hydrogen misc Hydrogenase misc Nitrogenase misc Photobiological H misc production misc Screening (H misc production) Cyanobacterial $ H_{2} $ production — a comparative analysis |
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Schütz, Kathrin |
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@@773@@(DE-627)254639100 |
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electronic Article |
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580 - Plants (Botany) |
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keep |
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aut aut aut aut aut aut aut |
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springer |
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true |
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Not Illustrated |
| issn |
1432-2048 |
| topic_title |
580 ASE 42.38 bkl Cyanobacterial $ H_{2} $ production — a comparative analysis Cyanobacterium (dpeaa)DE-He213 Hydrogen (dpeaa)DE-He213 Hydrogenase (dpeaa)DE-He213 Nitrogenase (dpeaa)DE-He213 Photobiological H (dpeaa)DE-He213 production (dpeaa)DE-He213 Screening (H (dpeaa)DE-He213 production) (dpeaa)DE-He213 |
| topic |
ddc 580 bkl 42.38 misc Cyanobacterium misc Hydrogen misc Hydrogenase misc Nitrogenase misc Photobiological H misc production misc Screening (H misc production) |
| topic_unstemmed |
ddc 580 bkl 42.38 misc Cyanobacterium misc Hydrogen misc Hydrogenase misc Nitrogenase misc Photobiological H misc production misc Screening (H misc production) |
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ddc 580 bkl 42.38 misc Cyanobacterium misc Hydrogen misc Hydrogenase misc Nitrogenase misc Photobiological H misc production misc Screening (H misc production) |
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Elektronische Aufsätze Aufsätze Elektronische Ressource |
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Cyanobacterial $ H_{2} $ production — a comparative analysis |
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Cyanobacterial $ H_{2} $ production — a comparative analysis |
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Schütz, Kathrin |
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Schütz, Kathrin Happe, Thomas Troshina, Olga Lindblad, Peter Leitão, Elsa Oliveira, Paulo Tamagnini, Paula |
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Schütz, Kathrin |
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10.1007/s00425-003-1113-5 |
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cyanobacterial $ h_{2} $ production — a comparative analysis |
| title_auth |
Cyanobacterial $ H_{2} $ production — a comparative analysis |
| abstract |
Abstract Several unicellular and filamentous, nitrogen-fixing and non-nitrogen-fixing cyanobacterial strains have been investigated on the molecular and the physiological level in order to find the most efficient organisms for photobiological hydrogen production. These strains were screened for the presence or absence of hup and hox genes, and it was shown that they have different sets of genes involved in $ H_{2} $ evolution. The uptake hydrogenase was identified in all $ N_{2} $-fixing cyanobacteria, and some of these strains also contained the bidirectional hydrogenase, whereas the non-nitrogen fixing strains only possessed the bidirectional enzyme. In $ N_{2} $-fixing strains, hydrogen was mainly produced by the nitrogenase as a by-product during the reduction of atmospheric nitrogen to ammonia. Therefore, hydrogen production was investigated both under non-nitrogen-fixing conditions and under nitrogen limitation. It was shown that the hydrogen uptake activity is linked to the nitrogenase activity, whereas the hydrogen evolution activity of the bidirectional hydrogenase is not dependent or even related to diazotrophic growth conditions. With regard to large-scale hydrogen evolution by $ N_{2} $-fixing cyanobacteria, hydrogen uptake-deficient mutants have to be used because of their inability to re-oxidize the hydrogen produced by the nitrogenase. On the other hand, fermentative $ H_{2} $ production by the bidirectional hydrogenase should also be taken into account in further investigations of biological hydrogen production. |
| abstractGer |
Abstract Several unicellular and filamentous, nitrogen-fixing and non-nitrogen-fixing cyanobacterial strains have been investigated on the molecular and the physiological level in order to find the most efficient organisms for photobiological hydrogen production. These strains were screened for the presence or absence of hup and hox genes, and it was shown that they have different sets of genes involved in $ H_{2} $ evolution. The uptake hydrogenase was identified in all $ N_{2} $-fixing cyanobacteria, and some of these strains also contained the bidirectional hydrogenase, whereas the non-nitrogen fixing strains only possessed the bidirectional enzyme. In $ N_{2} $-fixing strains, hydrogen was mainly produced by the nitrogenase as a by-product during the reduction of atmospheric nitrogen to ammonia. Therefore, hydrogen production was investigated both under non-nitrogen-fixing conditions and under nitrogen limitation. It was shown that the hydrogen uptake activity is linked to the nitrogenase activity, whereas the hydrogen evolution activity of the bidirectional hydrogenase is not dependent or even related to diazotrophic growth conditions. With regard to large-scale hydrogen evolution by $ N_{2} $-fixing cyanobacteria, hydrogen uptake-deficient mutants have to be used because of their inability to re-oxidize the hydrogen produced by the nitrogenase. On the other hand, fermentative $ H_{2} $ production by the bidirectional hydrogenase should also be taken into account in further investigations of biological hydrogen production. |
| abstract_unstemmed |
Abstract Several unicellular and filamentous, nitrogen-fixing and non-nitrogen-fixing cyanobacterial strains have been investigated on the molecular and the physiological level in order to find the most efficient organisms for photobiological hydrogen production. These strains were screened for the presence or absence of hup and hox genes, and it was shown that they have different sets of genes involved in $ H_{2} $ evolution. The uptake hydrogenase was identified in all $ N_{2} $-fixing cyanobacteria, and some of these strains also contained the bidirectional hydrogenase, whereas the non-nitrogen fixing strains only possessed the bidirectional enzyme. In $ N_{2} $-fixing strains, hydrogen was mainly produced by the nitrogenase as a by-product during the reduction of atmospheric nitrogen to ammonia. Therefore, hydrogen production was investigated both under non-nitrogen-fixing conditions and under nitrogen limitation. It was shown that the hydrogen uptake activity is linked to the nitrogenase activity, whereas the hydrogen evolution activity of the bidirectional hydrogenase is not dependent or even related to diazotrophic growth conditions. With regard to large-scale hydrogen evolution by $ N_{2} $-fixing cyanobacteria, hydrogen uptake-deficient mutants have to be used because of their inability to re-oxidize the hydrogen produced by the nitrogenase. On the other hand, fermentative $ H_{2} $ production by the bidirectional hydrogenase should also be taken into account in further investigations of biological hydrogen production. |
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Cyanobacterial $ H_{2} $ production — a comparative analysis |
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| score |
7.4007196 |