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  • 1
    Electronic Resource
    Electronic Resource
    A reappraisal of antigenic determinants for nitrogenase from Azotobacter and nitrate reductase from Escherichia coli (1982)
    Springer
    Archives of microbiology 132 (1982), S. 304-307 
    Details
    ISSN: 1432-072X
    Keywords: Azotobacter ; E. coli ; Nitrate reductase ; Nitrogenase ; Antigenic Determinants
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Previous work based on double immunodiffusion assays had shown that there are common antigenic determinants for nitrate reductase from Escherichia coli and component I of nitrogenase from Azotobacter vinelandii. Further work reported herein using a variety of immunoelectrophoretic techniques indicates that the cross-reaction between nitrate reductase and antiserum to component I of nitrogenase results from a contaminant antigen co-purified with nitrate reductase.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00413379
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  • 2
    Electronic Resource
    Electronic Resource
    Denitrification in Rhodopseudomonas sphaeroides f. denitrificans (1985)
    Springer
    Archives of microbiology 141 (1985), S. 57-62 
    Details
    ISSN: 1432-072X
    Keywords: Rhodopseudomonas sphaeroides f. denitrificans ; Photodenitrifier ; Denitrification ; Nitrate reductase ; Nitrite reductase ; Nitrous oxide reductase
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Rhodopseudomonas sphaeroides f. denitrificans grown photosynthetically with NO 3 - under anaerobic conditions accumulated NO 2 - in the culture medium. In washed cells succinate, lactate, fumarate, citrate and malate, were effective electron donors for the reduction of NO 3 - , NO 2 - and N2O to N2 gas. Nitrate reductase was inhibited by amytal and potassium thocyanate. Nitrite reductase activity was severely restricted by potassium cyanide, sodium diethyldithiocarbamate, Amytal and 2-n-heptyl-4-hydroxyquinoline-N-oxide whereas N2O reductase was inhibited by NaN3, C2H2 and KCNS. Cells incubated with either K15NO3 or K15NO2 produced 15N2O and 15N2. A stoichiometry of 2:1 was recorded for the reduction of either NO 3 - or NO 2 - to N2O and N2 and for N2O to N2 it was 1:1.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00446740
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  • 3
    Electronic Resource
    Electronic Resource
    Derepression of nitrate reductase from Derxia gummosa and some properties of the purified enzyme (1986)
    Springer
    Archives of microbiology 145 (1986), S. 20-26 
    Details
    ISSN: 1432-072X
    Keywords: Nitrate reductase ; Derxia gummosa ; Ammonia ; Glutamine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The assimilatory NADH-nitrate reductase has been purified to electrophoretic homogeneity from the N2-fixing bacterium Derxia gummosa. This enzyme has a molecular weight of ∼ 175 kdaltons and is composed of two dissimilar subunits (88 and 80 kdaltons, respectively). Typical cytochrome b 557 spectra were observed for the purified enzyme, reduced with sodium dithionite. Both ammonia and glutamine inhibited the induction of nitrate reductase in washed cells from cultures grown with NH4Cl. The inhibition by ammonia, but not that by glutamine was relieved by methionine sulphoximine. The induction of nitrate reductase was also inhibited by azaserine. In cells treated with methionine sulphoximine, glutamine content was decreased whereas it increased in those treated with azaserine. The synthesis of RNA during the derepression of nitrate reductase was also inhibited by glutamine. Thus glutamine is involved in regulating the derepression of nitrate reductase at the transcription level.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00413022
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  • 4
    Electronic Resource
    Electronic Resource
    Utilization of nitrate by bacteroids of Bradyrhizobium japonicum in the soybean root nodule (1988)
    Springer
    Planta 174 (1988), S. 51-58 
    Details
    ISSN: 1432-2048
    Keywords: Bacteroid ; Bradyrhizobium ; Glycine (N2 fixation) ; Nitrate reductase ; Nitrite reductase ; Nitrogen fixation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Bacteroids of Bradyrhizobium japonicum strain CB1809, unlike CC705, do not have a high level of constitutive nitrate reductase (NR; EC 1.7.99.4) in the soybean (Glycine max. Merr.) nodule. Ex planta both strains have a high activity of NR when cultured on 5 mM nitrate at 2% O2 (v/v). Nitrite reductase (NiR) was active in cultured cells of bradyrhizobia, but activity with succinate as electron donor was not detected in freshly-isolated bacteroids. A low activity was measured with reduced methyl viologen. When bacteroids of CC705 were incubated with nitrate there was a rapid production of nitrite which resulted in repression of NR. Subsequently when NiR was induced, nitrite was utilized and NR activity recovered. Nitrate reductase was induced in bacteroids of strain CB1809 when they were incubated in-vitro with nitrate or nitrite. Increase in NR activity was prevented by rifampicin (10 μg· ml-1) or chloramphenicol (50 μg·ml-1). Nitrite-reductase activity in bacteroids of strain CB1809 was induced in parallel with NR. When nitrate was supplied to soybeans nodulated with strain CC705, nitrite was detected in nodule extracts prepared in aqueous media and it accumulated during storage (1°C) and on further incubation at 25°C. Nitrite was not detected in nodule extracts prepared in ethanol. Thus nitrite accumulation in nodule tissue appears to occur only after maceration and although bacteroids of some strains of B. japonicum have a high level of a constitutive NR, they do not appear to reduce nitrate in the nodule because this anion does not gain access to the bacteroid zone. Soybeans nodulated with strains CC705 and CB1809 were equally sensitive to nitrate inhibition of N2 fixation.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00394873
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