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Journal of Bacteriology, June 2001, p. 3752-3760, Vol. 183, No. 12
Symbiosis Research Group, Max Planck
Institute for Terrestrial Microbiology, D-35043
Marburg,1 and Laboratory of General
Microbiology, Faculty of Biology and Chemistry, University of Bremen,
D-28334 Bremen,2 Germany
Received 16 January 2001/Accepted 27 March 2001
The endophytic diazotroph Azoarcus sp. strain BH72
is capable of infecting rice roots and of expressing the nitrogenase
(nif) genes there. In order to study the genetic
background for nitrogen fixation in strain BH72, the structural genes
of nitrogenase (nifHDK) were cloned and sequenced. The
sequence analysis revealed an unusual gene organization: downstream of
nifHDK, a ferredoxin gene (fdxN; 59%
amino acid sequence identity to R. capsulatus FdxN) and
open reading frames showing 52 and 36% amino acid sequence identity to
nifY of Pseudomonas stutzeri A15 and ORF1
of Azotobacter vinelandii were located. Northern blot
analysis, reverse transcriptase PCR and primer extension analysis
revealed that these six genes are located on one transcript transcribed
from a
0021-9193/01/$04.00+0 DOI: 10.1128/JB.183.12.3752-3760.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Role of a Ferredoxin Gene Cotranscribed with the
nifHDK Operon in N2 Fixation and Nitrogenase
"Switch-Off" of Azoarcus sp. Strain BH72

54-type promoter. Shorter transcripts
sequentially missing genes of the 3' part of the full-length mRNA were
more abundantly detected. Mutational analyses suggested that FdxN is an
important but not the essential electron donor for dinitrogenase
reductase. An in-frame deletion of fdxN resulted in
reduced growth rates (59% ± 9%) and nitrogenase activities (81%) in
nitrogen-fixing pure cultures in comparison to the wild type.
Nitrogenase activity was fully complemented in an fdxN
mutant which carried a nifH promoter-driven fdxN gene in trans. Also, in coculture
with the ascomycete Acremonium alternatum, where strain
BH72 develops intracytoplasmic membrane stacks, the nitrogenase
activity in the fdxN deletion mutant was decreased to
56% of the wild-type level. Surprisingly, the fdxN deletion also had an effect on the rapid "switch-off" of
nitrogenase activity in response to ammonium. Wild-type strain BH72 and
the deletion mutant complemented with fdxN in
trans showed a rapid reversible inactivation of
acetylene reduction, while the deletion mutant did not cease to reduce
acetylene. In concordance with the hypothesis that changes in the redox
state of NifH or electron flux towards nitrogenase may be involved in
the mechanism of physiological nitrogenase switch-off, our results
suggest that the ferredoxin may be a component involved in this process.
*
Corresponding author. Mailing address: University of
Bremen, Faculty of Biology and Chemistry, Laboratory of General
Microbiology, P.O. Box 33 04 40, D-28334 Bremen, Germany. Phone: (49)
421-218-2370. Fax: (49) 421-218-4042. E-mail:
breinhold{at}uni-bremen.de.
Present address: Freiburg University, Plant Biotechnology,
D-79104 Freiburg, Germany.
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