Previous Article | Next Article ![]()
J. Bacteriol., 01 1995, 290-296, Vol 177, No. 2
I Suzuki, N Horie, T Sugiyama and T Omata
Two nitrogen-regulated genes were found in the genomic DNA region upstream
of the nirA operon involved in uptake and utilization of nitrate in
Synechococcus sp. strain PCC7942. The two genes (nirB and ntcB) are
transcribed divergently from nirA and encode proteins of 349 and 309 amino
acid residues, respectively. The levels of nirB and ntcB transcripts were
low in cells growing on ammonium and increased upon transfer of
ammonium-grown cells to nitrate-containing medium. The deduced NirB protein
sequence has no similarities to other known proteins, whereas the deduced
NtcB protein sequence is homologous to bacterial transcriptional activators
of the LysR family. Defined mutants constructed by interrupting nirB or
ntcB with a drug resistance marker grew as fast as the wild-type strain on
ammonium but grew slower than the wild-type strain on nitrate or nitrite.
The nirB mutant had higher activities of nitrate reductase, glutamine
synthetase, and glutamate synthase than the wild-type strain, but its
nitrite reductase activity was 40% of the wild-type levels. The mutant
excreted nitrite into the medium during growth on nitrate, showing that
nitrite reductase limits nitrate assimilation. These findings suggested
that nirB is required for expression of maximum nitrite reductase activity.
When grown on ammonium, the nirB mutant grew normally but cultures of the
ntcB mutant still showed a yellowish-green color typical of
nitrogen-limited cells. NtcB seems to regulate utilization of fixed
nitrogen by controlling the expression of a certain gene(s) involved in
nitrogen metabolism.
Copyright © 1995, American Society for Microbiology
Identification and characterization of two nitrogen-regulated genes of the cyanobacterium Synechococcus sp. strain PCC7942 required for maximum efficiency of nitrogen assimilation
Department of Applied Biological Sciences, School of Agricultural Sciences, Nagoya University, Japan.
This article has been cited by other articles:
Copyright © 2009 by the American Society for Microbiology. For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»