Affiliation:
1. Gene Regulation Laboratory, Centre for Biotechnology, Jawaharlal Nehru University, New Delhi 110067, India
Abstract
ABSTRACT
Nitrogen fixation in
Azotobacter vinelandii
is regulated by the
nifLA
operon. NifA activates the transcription of
nif
genes, while NifL antagonizes the transcriptional activator NifA in response to fixed nitrogen and molecular oxygen levels. However, transcriptional regulation of the
nifLA
operon of
A. vinelandii
itself is not fully understood. Using the S1 nuclease assay, we mapped the transcription start site of the
nifLA
operon, showing it to be similar to the σ
54
-dependent promoters. We also identified a positive
cis-
acting regulatory element (+134 to +790) of the
nifLA
operon within the coding region of the
nifL
gene of
A. vinelandii
. Deletion of this element results in complete loss of promoter activity. Several protein factors bind to this region, and the specific binding sites have been mapped by DNase I foot printing. Two of these sites, namely dR1 (+134 to +204) and dR2 (+745 to +765), are involved in regulating the
nifLA
promoter activity. The absence of NtrC-like binding sites in the upstream region of the
nifLA
operon in
A. vinelandii
makes the identification of these downstream elements a highly significant finding. The interaction of the promoter with the proteins binding to the dR2 region spanning +745 to +765 appears to be dependent on the face of the helix as introduction of 4 bases just before this region completely disrupts promoter activity. Thus, the positive regulatory element present within the BglII-BglII fragment may play, in part; an important role in
nifLA
regulation in
A. vinelandii
.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
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