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- W41984430 abstract "Steady-state assays of nitrogenases share at least five requirements: an anaerobic environment, a consistent source of magnesium adenosine triphosphate (MgATP), a suitable source of reductant, a buffer system compatible with the product-quantification protocol to be used, and the desired substrate. The assay is initiated by injection of the component protein(s) of the enzyme or MgATP and terminated by injection of either acid or a solution of Na(2)EDTA. The various nitrogenases catalyze the reduction of a wide variety of substrates. This chapter outlines the methods used to analyze the products of nitrogenase-catalyzed reactions involving nitrogen-nitrogen bonds, nitrogen-oxygen bonds, carbon-nitrogen bonds, carbon-carbon bonds, carbon-oxygen bonds, carbon-sulfur bonds, and hydrogen only. The usefulness of measurements of residual amounts of other components of nitrogenase assays is also discussed." @default.
- W41984430 created "2016-06-24" @default.
- W41984430 creator A5011735129 @default.
- W41984430 creator A5061559316 @default.
- W41984430 date "2011-01-01" @default.
- W41984430 modified "2023-10-14" @default.
- W41984430 title "Assays of Nitrogenase Reaction Products" @default.
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- W41984430 doi "https://doi.org/10.1007/978-1-61779-194-9_8" @default.
- W41984430 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/21833864" @default.
- W41984430 hasPublicationYear "2011" @default.
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