Affiliation:
1. Laboratory of Molecular Plant Physiology, Graduate School of Bioagricultural Sciences, Nagoya University, Nagoya, 464-8601 Japan
Abstract
ABSTRACT
In
Synechocystis
sp. strain PCC 6803, the genes encoding the proteins involved in nitrate assimilation are organized into two transcription units,
nrtABCD
-
narB
and
nirA
, the expression of which was repressed by ammonium and induced by inhibition of ammonium assimilation, suggesting involvement of NtcA in the transcriptional regulation. Under inducing conditions, expression of the two transcription units was enhanced by nitrite, suggesting regulation by NtcB, the nitrite-responsive transcriptional enhancer we previously identified in
Synechococcus
sp. strain PCC 7942. The
slr0395
gene, which encodes a protein 47% identical to
Synechococcus
NtcB, was identified as the
Synechocystis ntcB
gene, on the basis of the inability of an
slr0395
mutant to rapidly accumulate the transcripts of the nitrate assimilation genes upon induction and to respond to nitrite. While
Synechococcus
NtcB strictly requires nitrite for its action,
Synechocystis
NtcB enhanced transcription significantly even in the absence of nitrite. Whereas the
Synechococcus ntcB
mutant expresses the nitrate assimilation genes to a significant level in an NtcA-dependent manner, the
Synechocystis ntcB
mutant showed only low-level expression of the nitrate assimilation genes, indicating that NtcA by itself cannot efficiently promote expression of these genes in
Synechocystis
. Activities of the nitrate assimilation enzymes in the
Synechocystis ntcB
mutant were consequently low, being 40 to 50% of the wild-type level, and the cells grew on nitrate at a rate approximately threefold lower than that of the wild-type strain. These results showed that the contribution of NtcB to the expression of nitrate assimilation capability varies considerably among different strains of cyanobacteria.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
68 articles.
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