Literature DB >> 227860

Changes in the EPR signal of dinitrogenase from Azotobacter vinelandii during the lag period before hydrogen evolution begins.

R V Hageman, R H Burris.   

Abstract

During the lag period before H2 is evolved by the nitrogenase system, the EPR signal of dinitrogenase decreases steadily, indicating transfer of electrons into dinitrogenase. The rate constant for the decrease in amplitude of the EPR signal, the steady state rate of H2 evolution from nitrogenase, and the length of the lag period have been measured. The data suggest that H2 is evolved only after dinitrogenase has been reduced by 2 electrons/molybdenum. The electrons that have been transfered into dinitrogenase during the lag period are not evolved as H2 upon denaturation of dinitrogenase. The existence of a lag indicates that the two nitrogenase proteins dissociate after every electron transfer. The lag occurs and the nitrogenase proteins dissociate under a variety of conditions of pH and temperature.

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Year:  1979        PMID: 227860

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  6 in total

1.  Products of the iron-molybdenum cofactor-specific biosynthetic genes, nifE and nifN, are structurally homologous to the products of the nitrogenase molybdenum-iron protein genes, nifD and nifK.

Authors:  K E Brigle; M C Weiss; W E Newton; D R Dean
Journal:  J Bacteriol       Date:  1987-04       Impact factor: 3.490

2.  Klebsiella pneumoniae nitrogenase. The pre-steady-state kinetics of MoFe-protein reduction and hydrogen evolution under conditions of limiting electron flux show that the rates of association with the Fe-protein and electron transfer are independent of the oxidation level of the MoFe-protein.

Authors:  K Fisher; D J Lowe; R N Thorneley
Journal:  Biochem J       Date:  1991-10-01       Impact factor: 3.857

3.  Nitrogenase of Klebsiella pneumoniae. Kinetics of the dissociation of oxidized iron protein from molybdenum-iron protein: identification of the rate-limiting step for substrate reduction.

Authors:  R N Thorneley; D J Lowe
Journal:  Biochem J       Date:  1983-11-01       Impact factor: 3.857

4.  Activity, reconstitution, and accumulation of nitrogenase components in Azotobacter vinelandii mutant strains containing defined deletions within the nitrogenase structural gene cluster.

Authors:  A C Robinson; B K Burgess; D R Dean
Journal:  J Bacteriol       Date:  1986-04       Impact factor: 3.490

5.  Evidence for an alternative nitrogen fixation system in Azotobacter vinelandii.

Authors:  P E Bishop; D M Jarlenski; D R Hetherington
Journal:  Proc Natl Acad Sci U S A       Date:  1980-12       Impact factor: 11.205

6.  Hydrogen burst associated with nitrogenase-catalyzed reactions.

Authors:  J Liang; R H Burris
Journal:  Proc Natl Acad Sci U S A       Date:  1988-12       Impact factor: 11.205

  6 in total

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