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Immunological Detection of Nitrogenase

  • G. Sarath
  • F. W. Wagner
Part of the Modern Methods of Plant Analysis book series (MOLMETHPLANT, volume 9)

Abstract

Biological nitrogen fixation involves the catalytic reduction of atmospheric nitrogen to ammonia by the enzyme complex nitrogenase, which is normally detected by monitoring the reduction of the synthetic substrate acetylene (Hardy et al. 1968). Nitrogenase proteins are exceedingly oxygen-labile, and in vivo are protected from free oxygen by several mechanisms (Gallon 1981). Consequently, strict anaerobic conditions are required to assay nitrogenase in extracts. Other means of detecting nitrogenase are required when experimental treatments result in the destruction or modification of enzyme activity without affecting its synthesis or turnover. Immunochemical methods allow the estimation of nitrogenase proteins under ambient oxygen concentrations, and are frequently used.

Keywords

Nitrogen Fixation Symbiotic Nitrogen Fixation Double Diffusion Immunological Detection Nitrocellulose Sheet 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Springer-Verlag Berlin Heidelberg 1989

Authors and Affiliations

  • G. Sarath
  • F. W. Wagner

There are no affiliations available

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