Journalartikel
Autorenliste: Lee, HM; Flores, E; Forchhammer, K; Herrero, A; de Marsac, NT
Jahr der Veröffentlichung: 2000
Seiten: 591-600
Zeitschrift: European Journal of Biochemistry
Bandnummer: 267
Heftnummer: 2
ISSN: 0014-2956
Open Access Status: Bronze
DOI Link: https://doi.org/10.1046/j.1432-1327.2000.01043.x
Verlag: Wiley: No OnlineOpen
Abstract:
In the cyanobacterium Synechococcus sp. strain PCC 7942, the phosphorylation states of the signal transducer P-II protein (GlnB) can change rapidly depending on the nitrogen and carbon supply. A P-II-null mutant (MP2) shows no ammonium-dependent inhibition of the nitrate and nitrite uptake, in contrast to the wild-type. New mutants with different types of P-II, which may mimic either the phosphorylated (GlnB(S49E) or GlnB(S49D)) or unphosphorylated (GlnB(S49A)) form of the protein, were constructed using site-directed in vitro mutagenesis. Mutant MP2-A (GlnB(S49A)) grew poorly using nitrate as a nitrogen source and was unable to take up nitrate supplied at 100 mu M, even in the absence of externally added ammonium. Mutants MP2-D and MP2-E (GlnB(S49D) and GlnB(S49E), respectively), however, showed nitrate-dependent growth and regulation of nitrate uptake by ammonium, as in the wild-type. Characterization of the mutants also included an analysis of nitrite uptake and of the levels of the nir (nitrate/nitrite assimilation) operon transcripts, the presence of NrtA (nitrate/nitrite transport binding protein), and nitrate and nitrite reductase activities. In vitro, no significant difference was observed in the cooperative binding of ATP and 2-oxoglutarate between the wild-type and the unphosphorylated or phosphorylated-like forms of the mutant P-II proteins. The results obtained indicate that both unphosphorylated and phosphorylated-like forms of P-II are able to inhibit nitrate uptake in the presence of ammonium, but the unphosphorylated form also has a negative effect in the absence of this nitrogen source. Therefore, an additional effector, possibly 2-oxoglutarate, is required for the P-II protein to relieve inhibition of nitrate uptake in the absence of ammonium.
Zitierstile
Harvard-Zitierstil: Lee, H., Flores, E., Forchhammer, K., Herrero, A. and de Marsac, N. (2000) Phosphorylation of the signal transducer PII protein and an additional effector are required for the PII-mediated regulation of nitrate and nitrite uptake in the cyanobacterium Synechococcus sp PCC 7942, European Journal of Biochemistry, 267(2), pp. 591-600. https://doi.org/10.1046/j.1432-1327.2000.01043.x
APA-Zitierstil: Lee, H., Flores, E., Forchhammer, K., Herrero, A., & de Marsac, N. (2000). Phosphorylation of the signal transducer PII protein and an additional effector are required for the PII-mediated regulation of nitrate and nitrite uptake in the cyanobacterium Synechococcus sp PCC 7942. European Journal of Biochemistry. 267(2), 591-600. https://doi.org/10.1046/j.1432-1327.2000.01043.x
Schlagwörter
ammonium inhibition; ANACYSTIS-NIDULANS; glnB gene product; GLNB GENE-PRODUCT; nitrate/nitrite uptake; NITROGEN ASSIMILATION; PHORMIDIUM-LAMINOSUM; SP STRAIN PCC-7942; Synechococcus sp strain PCC 7942