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Journal of Bacteriology, January 2005, p. 498-506, Vol. 187, No. 2
0021-9193/05/$08.00+0     doi:10.1128/JB.187.2.498-506.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

Posttranslational Regulation of Nitrate Assimilation in the Cyanobacterium Synechocystis sp. Strain PCC 6803

Masaki Kobayashi ,{dagger},{ddagger} Nobuyuki Takatani,{dagger} Mari Tanigawa, and Tatsuo Omata*

Laboratory of Molecular Plant Physiology, Graduate School of Bioagricultural Sciences, Nagoya University, Nagoya, Japan

Received 18 June 2004/ Accepted 19 October 2004


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ABSTRACT
 
Posttranslational regulation of nitrate assimilation was studied in the cyanobacterium Synechocystis sp. strain PCC 6803. The ABC-type nitrate and nitrite bispecific transporter encoded by the nrtABCD genes was completely inhibited by ammonium as in Synechococcus elongatus strain PCC 7942. Nitrate reductase was insensitive to ammonium, while it is inhibited in the Synechococcus strain. Nitrite reductase was also insensitive to ammonium. The inhibition of nitrate and nitrite transport required the PII protein (glnB gene product) and the C-terminal domain of NrtC, one of the two ATP-binding subunits of the transporter, as in the Synechococcus strain. Mutants expressing the PII derivatives in which Ala or Glu is substituted for the conserved Ser49, which has been shown to be the phosphorylation site in the Synechococcus strain, showed ammonium-promoted inhibition of nitrate uptake like that of the wild-type strain. The S49A and S49E substitutions in GlnB did not affect the regulation of the nitrate and nitrite transporter in Synechococcus either. These results indicated that the presence or absence of negative electric charge at the 49th position does not affect the activity of the PII protein to regulate the cyanobacterial ABC-type nitrate and nitrite transporter according to the cellular nitrogen status. This finding suggested that the permanent inhibition of nitrate assimilation by an S49A derivative of PII, as was previously reported for Synechococcus elongatus strain PCC 7942, is likely to have resulted from inhibition of nitrate reductase rather than the nitrate and nitrite transporter.


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INTRODUCTION
 
Assimilation of nitrate by cyanobacteria is regulated by ammonium at both transcriptional and posttranslational levels (5, 11, 30); addition of ammonium to medium promptly inhibits transcription of the relevant genes and uptake of nitrate. The inhibition of transcription of the nitrate assimilation genes is a part of global nitrogen regulation in cyanobacteria, which involves NtcA, a Crp family protein, as the transcriptional activator (40, 41). Recent in vitro experiments showed that 2-oxoglutarate (2-OG), which serves as the acceptor of the newly fixed nitrogen in the glutamine synthetase-glutamate synthase cycle, activates transcription from NtcA-dependent promoters in a concentration-dependent manner (38). Since the intracellular 2-OG concentration is low in the presence of ammonium and is increased by nitrogen deprivation (28), 2-OG is supposed to act as a coinducer of transcription of the NtcA-dependent genes, conferring ammonium sensitivity to their expression in vivo.

There are three biochemical steps essential to nitrate assimilation, i.e., transport of nitrate into the cell, reduction of nitrate to nitrite, and reduction of nitrite to ammonium (11). These are mediated by an active nitrate and nitrite transporter (NRT), ferredoxin-dependent nitrate reductase (NR), and ferredoxin-dependent nitrite reductase (NiR), respectively, in cyanobacteria (5, 30). Studies using Synechococcus elongatus strain PCC 7942 have shown that activities of NRT and NR are inhibited upon addition of ammonium to medium (18), whereas NiR activity is not (25). The inhibition is reversible, and assimilation of nitrate is resumed after consumption of ammonium in medium. The PII protein and an NRT subunit (NrtC) are involved in the regulation (18, 23). NrtC is an ATP-binding subunit of the ABC-type nitrate and nitrite bispecific transporter (18, 31). It is unique among the ATP-binding subunits of bacterial ABC transporters in having a large C-terminal extension (31), which is involved in the ammonium-promoted regulation of the transport activity (18). The PII protein (homotrimer of the glnB gene product) has the ability to bind 2-OG, suggesting that it senses the cellular nitrogen status by binding 2-OG (6). Similar to its counterparts in proteobacteria, the cyanobacterial PII protein is modified when nitrogen is limited, but the modification is by phosphorylation at Ser49 rather than by uridylylation at the Tyr51 residue (9); the phosphorylation state of the GlnB trimer changes from a fully dephosphorylated state in ammonium-grown cells to a highly phosphorylated state in the cells subjected to nitrogen starvation. Since PII-deficient mutants show ammonium-insensitive nitrate assimilation (23), it is clear that PII negatively regulates both NRT and NR in the presence of ammonium. However, it remains unclear how PII transduces the nitrogen signal to the nitrate assimilation enzymes. In some phosphoproteins, the presence of negative electric charge at the phosphorylation site plays a role in regulating the activity of the protein (20, 27, 39, 43). Studies using site-specific mutant forms of PII, however, revealed a complex relationship between the electric charge at the phosphorylation site and the regulation of nitrate assimilation; a Synechococcus mutant expressing an unphosphorylatable derivative of PII with an S49A substitution shows negligible nitrate assimilation activity irrespective of the cellular nitrogen status, whereas a mutant expressing an S49E derivative of PII, having a negative charge on the 49th amino acid, shows ammonium-responsive regulation of nitrate assimilation like that of the wild-type strain (22). Taking into account these observations, it was hypothesized that a factor other than the electric charge at the 49th amino acid position plays a role in controlling the activity of PII(S49E), whereas PII(S49A) is fixed in a state that is inhibitory to nitrate assimilation (22).

Studies of posttranslational regulation of nitrate assimilation by cyanobacterial cells have so far focused mainly on Synechococcus elongatus strain PCC 7942. Synechocystis sp. strain PCC 6803 is potentially useful for molecular genetic analysis of the regulatory mechanisms, because its genome is the best characterized among the cyanobacterial genomes (Cyanobase, http://www.kazusa.or.jp/cyano/cyano.html; CYORF, http://cyano.genome.jp/), but information about the regulation of nitrate and nitrite uptake at the posttranslational level is limited (14, 16). To expand our knowledge on the regulation of nitrate assimilation in this cyanobacterium, we characterized the mutants expressing modified NRT and PII in the present study. The C-terminal portion of NrtC is shown to act as the regulatory domain of NRT, as in Synechococcus elongatus strain PCC 7942. It is shown that NR is not regulated in Synechocystis sp. strain PCC 6803. Characterization of the Synechocystis mutants having amino acid substitutions at the 49th amino acid position of GlnB suggested that regulation of NRT is independent of the phosphorylation of PII. This finding led us to investigate the specific effects of GlnB modification on the regulation of NRT in Synechococcus elongatus strain PCC 7942.


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MATERIALS AND METHODS
 
Strains and growth conditions. The glucose-tolerant derivative of Synechocystis sp. strain PCC 6803 isolated by Williams (44) and commonly used for photosynthesis research (designated GT or referred to simply as the wild-type strain herein) and a derivative of Synechococcus elongatus strain PCC 7942 which is cured of the resident small plasmid pUH24 (R2-SPc [19]; hereafter designated strain PCC 7942) were the parental strains of all of the cyanobacterial strains used in this study (Table 1). The cyanobacterial cells were grown photoautotrophically at 30°C under continuous illumination provided by fluorescent lamps (70 microeinsteins m–2 s–1). The basal medium used was a nitrogen-free medium obtained by modification of BG11 medium (36) as described previously (37). Ammonium- and nitrate-containing media were prepared by addition of 3.75 mM (NH4)2SO4 and 15 mM KNO3, respectively, to the basal medium. Both media were buffered with 20 mM HEPES-KOH (pH 8.2). The cultures were aerated with 2% (vol/vol) CO2 in air. When appropriate, kanamycin, spectinomycin, and gentamicin were added to the media at 15, 15, and 5 µg/ml, respectively. Escherichia coli strains NM522, HB101, and SL906 were grown on Luria-Bertani medium supplemented with ampicillin (50 µg/ml), spectinomycin (25 µg/ml), streptomycin (30 µg/ml), gentamicin (30 µg/ml), or kanamycin (15 µg/ml) when appropriate.


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  		TABLE 1. Cyanobacterial strains and plasmids used

Isolation and analysis of DNA. Chromosomal DNA was extracted and purified from the cyanobacterial cells as described by Williams (44). Manipulations and analyses of DNA were performed according to standard protocols (35). All the cloned DNA fragments that had been generated by PCR amplification were sequenced to verify the nucleotide sequence. For Southern hybridization analysis of the genomic DNA digests of Synechocystis and Synechococcus, the following DNA fragments were amplified from the cyanobacterial DNA samples by PCR, labeled with 32P, and used as probes: a 443-bp Synechocystis DNA fragment carrying the glnB coding region and 107 bases of its 3' flanking sequence (Fig. 1), a 487-bp Synechocystis DNA fragment carrying the nrtC-nrtD intergenic region and 430 bases of the nrtD coding region (Fig. 1), and a 343-bp Synechococcus DNA fragment carrying the glnB coding region (see Fig. 6).



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  		FIG. 1. Construction of the Synechocystis sp. strain PCC 6803 nrtC and glnB mutants. (A and B) Physical maps of the nrtA-to-narB region and the glnB region, respectively, of the genomes of the wild-type strain (GT) and the mutants. Bars above the maps in panels A and B, probes used for Southern hybridization analysis in panels C and D, respectively; inverted triangle (A), site of insertion of the nptI-sacB gene cassette in the nrtC insertional mutant SNC1. Restriction endonuclease sites are abbreviated as follows: Sp, SpeI; Nh, NheI; Af, AflII. (C and D) Southern hybridization analysis of genomic DNA from wild-type and mutant strains, with nrtD and glnB, respectively, as probes. DNA samples (2 µg/lane) were digested with SpeI (C) or AflII (D), fractionated on a 1% agarose gel, transferred to a positively charged nylon membrane (Hybond N+; Amersham), and hybridized with the 32P-labeled probes.



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  		FIG. 6. Construction of a Synechococcus elongatus strain PCC 7942 glnB mutant and overexpression of the glnB derivatives. (A) Physical map of the glnB region of the genome of the wild-type strain and the glnB-deficient mutant PD1. Bar, probe used for Southern hybridization analysis in panel B. Restriction endonuclease sites are abbreviated as follows: Ps, PstI; Xh, XhoI. (B) Southern hybridization analysis of PstI-digested genomic DNA samples (2 µg per lane) from the wild-type strain and the PD1 mutant, with glnB as a probe. (C) Polypeptide compositions of the soluble fraction extracted from the wild-type (lane 1), PD1 (lane 2), PD1S (lane 3), PD1A (lane 4), and PD1E (lane 5) strains. Samples (30 µg of protein per lane) were fractionated by electrophoresis in an SDS-10 to 20% polyacrylamide gradient gel, and the polypeptides were stained with Coomassie blue. (D) Autoradiogram showing the 32P-labeled proteins extracted from cells of the wild-type (lanes 1 and 2), PD1 (lanes 3 and 4), PD1S (lanes 5 and 6), PD1A (lanes 7 and 8), and PD1E (lanes 9 and 10) cells. Labeling with H332PO4 was performed for 1.5 h in nitrate (17.5 mM)-containing medium (lanes 1, 3, 5, 7, and 9) or for 1.5 h in the nitrate-containing medium and then for an additional 1 h after addition of ammonium (0.5 mM) to the medium (lanes 2, 4, 6, 8, and 10). Total cellular protein (70 µg of protein per lane) was pelleted with trichloroacetic acid, solubilized with SDS, and fractionated on an SDS-10 to 20% polyacrylamide gradient gel. For panels C and D, PD1S, PD1A, and PD1E cells were treated with 1 mM IPTG for 16 h prior to the experiment. Dots, positions of the weakly labeled bands.

Insertional and deletional mutagenesis. For targeted mutagenesis of Synechocystis sp. strain PCC 6803 and Synechococcus elongatus strain PCC 7942, the genes with insertions and/or deletions were constructed with vectors that do not replicate in the cyanobacteria. The resulting plasmids were used to transform the cyanobacterial cells by replacing the wild-type gene with the mutated gene through homologous recombination. Transformation of the cyanobacteria and isolation of homozygous mutants were performed as described by Williams (44).

SNC1, an nrtC insertional mutant derivative of Synechocystis sp. strain PCC 6803, was constructed by inserting a 3.8-kbp nptI-sacB cartridge from pRL250 (3) into the NheI site located in the 3' portion of the coding region. A mutant lacking the C-terminal domain of NrtC (SNC2) was obtained from SNC1 by deleting the 3' portion of nrtC corresponding to the C-terminal domain by the eviction mutagenesis method using sacB as a negative selection marker (33). In SNC2, a 1,188-bp internal segment of nrtC, corresponding to nucleotides 823 to 2010 of the 2,010-nucleotide coding region (Fig. 1A), had been deleted from the genome and, as a consequence of the in-frame deletion of nucleotides, the modified nrtC encoded a protein of 274 amino acid residues, consisting of the N-terminal ATP-binding domain (amino acids 1 to 254) and a part of the linker sequence connecting the N-terminal and C-terminal domains (amino acids 255 to 274) of NrtC.

The plasmid used for inactivation of glnB in Synechocystis sp. strain PCC 6803, which was provided by T. Ogawa (Nagoya University), carried a disrupted glnB and 437 and 304 bp of its 5' and 3' flanking sequences, respectively. In this construct, the 208-bp internal fragment of glnB, extending from nucleotide +109 to +316 with respect to the translation start site, had been replaced by an nptI kanamycin resistance gene cartridge originating from pUC4K (42).

For construction of a glnB-deficient Synechococcus elongatus strain PCC 7942 mutant, a 1.3-kbp XbaI-PstI fragment of Synechococcus DNA carrying glnB was cloned as follows. A HindIII digest of chromosomal DNA was fractionated on an agarose gel. DNA fragments of 4 to 5 kbp were recovered from the gel and ligated with a 167-bp HindIII-PvuII fragment of pT7Blue (Novagen), carrying the multiple cloning region of the plasmid. With primers specific to internal sequences of glnB and the fragment of pT7Blue, the 5' and 3' halves of glnB were amplified by PCR with 1.1 and 2.9 kb of the respective flanking sequences and separately cloned into pT7Blue T-Vector (Novagen). The DNA fragments carrying the 5' and 3' halves of glnB were excised from the resulting plasmids and joined on the pUC19 vector. From this plasmid, a 1.3-kbp XbaI-PstI fragment, carrying the glnB coding region and 330 and 640 bases of its 5' and 3' flanking sequences, respectively, was excised and cloned between the XbaI and PstI sites of pT7Blue. In the glnB sequence thus cloned, a 5-base sequence 5'-TAATT-3', which was derived from the primer sequences used for PCR, replaced the A at position 152 of the coding region, resulting in a frameshift mutation. A spectinomycin and streptomycin resistance gene cassette ({Omega} cassette) excised from plasmid pRL463 (4) was subsequently inserted into the XhoI site located at nucleotide 182 of the glnB coding region. The resulting plasmid was used to inactivate glnB in wild-type Synechococcus elongatus strain PCC 7942 to yield the PD1 mutant.

For inactivation of narB in Synechococcus elongatus strain PCC 7942, a 1.7-kbp fragment of Synechococcus DNA, carrying the 3' half of the gene, was cloned into pUC18 and the 605-bp internal fragment of narB, extending from nucleotide +1071 to +1674 with respect to the translation start site, was removed by digestion with MscI and replaced with the {Omega} cassette excised from pRL463 (4). The plasmid carrying disrupted narB was used to inactivate narB in the Synechococcus elongatus strain PCC 7942 NC2 mutant to yield the NC41 mutant.

Expression of plasmid-borne glnB in Synechocystis. A 853-bp fragment of Synechocystis DNA, carrying the glnB coding region and 410 and 107 bp of its 5' and 3' flanking sequences, respectively, was amplified by PCR and cloned into pT7Blue T-Vector. The cloned fragment contained the entire promoter region of glnB (10). Two derivatives of this plasmid, encoding the S49A and S49E derivatives of GlnB, were obtained by changing the 49th codon of glnB from TCT to GCT and GAA, respectively, with the QuikChange site-directed mutagenesis kit (Stratagene). After verification of the nucleotide sequence, the 853-bp inserts carrying the wild-type and the modified glnB genes were excised from the plasmids with BamHI and XbaI and cloned between the BamHI and XbaI sites of the shuttle vector pSL1211 (29) to construct pSGLNBS (encoding wild-type GlnB) and pSGLNBA and pSGLNBE (encoding the S49A and S49E derivatives, respectively). The plasmids were transferred from E. coli HB101 carrying the helper plasmid to the Synechocystis sp. strain PCC 6803 glnB deletion mutant (SPD1) by conjugation to yield the SPD1S, SPD1A, and SPD1E strains, respectively.

Expression of plasmid-borne narB in Synechococcus. For heterologous expression of NR of Synechocystis sp. strain PCC 6803 in cells of Synechococcus elongatus strain PCC 7942, a 2,147-bp fragment of Synechocystis DNA carrying the entire sll1454 open reading frame was amplified by PCR. The second and the sixth bases of the sense primer used, corresponding to bases –1 and +4 with respect to the translation start site, had been changed from A and G in the original sequence to C and A, respectively, to create a BspHI recognition site at the translation start site. The PCR-amplified sll1454 gene was cloned into pT7Blue T-Vector and, after verification of the nucleotide sequence, excised from the plasmid with BspHI and XbaI and cloned between the NcoI and XbaI sites of the Synechococcus shuttle expression vector pSE1 (26). Due to the G4A replacement in the nucleotide sequence, the protein encoded by sll1454 in the resulting plasmid (pSNARB) carried a D2N mutation.

For expression of the narB gene of Synechococcus elongatus strain PCC 7942 from the shuttle vector pSE1, a 2,210-bp Synechococcus DNA fragment carrying the entire narB open reading frame was amplified by PCR. The sixth to eighth bases of the sense primer used, corresponding to the ATG initiation codon, had been changed to GAA to create an EcoRI recognition site. The antisense primer used had an XbaI recognition sequence downstream of the stop codon. The PCR-amplified Synechococcus narB gene was digested with EcoRI and XbaI and cloned between the EcoRI and XbaI sites of pSE1. The protein encoded by the resulting plasmid (pNARB) had an additional glutamic acid inserted next to the initiator methionine residue.

The pSE1 derivatives pSNARB and pNARB were transformed into the Synechococcus elongatus strain PCC 7942 NC41 mutant (nrtC{Delta}C {Delta}narB::{Omega}) to yield the spectinomycin-resistant transformants NC51 and NC52, respectively. Expression of plasmid-borne narB was induced by treatment of the cells of the transformants with 1 mM isopropyl-1-thio-ß-D-galactopyranoside (IPTG) for 16 h in nitrate-containing medium.

Expression of plasmid-borne glnB in Synechococcus. A fragment of Synechococcus DNA carrying the entire glnB coding region (from nucleotide –2 to +341 with respect to the translation start site) was amplified by PCR. The third and sixth bases of the sense primer used, corresponding to the first and fourth bases of the coding region, had been changed from T and A in the original glnB sequence to A and G, respectively, to create an NcoI recognition site at the translation start site. The protein encoded by the amplified sequence hence carried a K2E mutation. Two other derivatives of glnB, carrying additional base replacements to create S49A and S49E mutations, were generated by overlap extension PCR (15) with oligonucleotide primers carrying mismatches with the wild-type sequence. The PCR-amplified DNA fragments were cloned into pT7Blue T-Vector, and, after verification of the nucleotide sequences, the modified glnB genes were excised from the plasmids with NcoI and XbaI and cloned between the NcoI and XbaI sites of pSE1 (26) to place the glnB coding sequence under the control of the Ptrc promoter. The resulting plasmids were transformed into the glnB-deficient mutant PD1 to yield the strains PD1S, PD1A, and PD1E, and expression of the modified glnB genes was induced by 16-h treatment with 1 mM IPTG. The GlnB derivatives thus expressed had the following amino acid substitutions: K2E in PD1S, K2E and S49A in PD1A, and K2E and S49E in PD1E.

In vivo labeling of PII in Synechococcus. Nitrate-grown Synechococcus cells were collected by centrifugation at 5,000 x g for 5 min at 25°C, washed by resuspension and recentrifugation in phosphate- and nitrogen-free medium prepared by omitting K2HPO4 from the basal medium, and resuspended in the medium supplemented with 2 mM KNO3 at a chlorophyll (Chl) concentration of 5 µg per ml. A 2-ml aliquot of the cell suspension, to which carrier-free H332PO4 (Amersham) at 5.5 x 107 dpm was added, was placed under illumination at 30°C. After incubation for 1.5 h, a 0.5-ml aliquot of the cell suspension was removed from the test tube, mixed with 0.5 ml of 10% trichloroacetic acid in a 1.5-ml centrifuge tube, and placed on ice for 30 min. To the remainder of the cell suspension, (NH4)2SO4 was added to a final concentration of 0.25 mM and the cells were incubated for additional 1 h under illumination, after which another aliquot of 0.5 ml was removed from the cell suspension and processed as described above. From the cell samples treated with trichloroacetic acid, total protein was pelleted by centrifugation at 14,000 x g for 5 min. The pelleted protein was washed twice with acetone, dried, suspended in 40 µl of the sample buffer for sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) (21), and lysed by heat treatment at 100°C for 5 min. Twenty microliters of the protein solution, containing approximately 70 µg of protein, was electrophoresed in an SDS-10 to 20% polyacrylamide gradient gel in the buffer system of Laemmli (21). The fractionated polypeptides were electrotransferred to a Hybond C Extra membrane (Amersham), and the 32P-labeled polypeptides were detected by autoradiography on X-ray film. Soluble fractions from unlabeled Synechococcus cells were prepared as described previously (32), and their polypeptide compositions were analyzed by SDS-PAGE as described above.

Measurements of nitrate and nitrite uptake. Uptake of nitrate and nitrite by the cyanobacterial cells was measured at pH 9.6 by monitoring the decrease in the extracellular concentration of nitrate and nitrite, respectively, in cell suspensions containing 5 µg of Chl per ml, as previously described (18). When the effects of ammonium on the uptake of nitrate and nitrite were examined, 250 µM (NH4)2SO4 was added to the cell suspensions immediately after the addition of nitrate or nitrite. Nitrate and nitrite were determined with a flow injection analyzer (NOX-1000W; Tokyo Chemical Industry Co., Ltd.). Chl was determined as described by Mackinney (24).

Other methods. In vitro activities of NR in toluene-permeabilized cells were determined at 30°C with dithionite-reduced methylviologen as the electron donor (13).


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RESULTS
 
Construction of the nrtC and glnB Synechocystis mutants. To study the roles of the C-terminal domain of NrtC and the PII protein in the regulation of NRT in Synechocystis sp. strain PCC 6803, a mutant having truncated nrtC (SNC2) and a PII-deficient mutant (SPD1) were constructed (Table 1 and Fig. 1). The absence of the 3' portion of nrtC, encoding the putative regulatory domain of NRT, and the wild-type glnB gene was confirmed by Southern hybridization analysis of the genomic DNA samples from SNC2 and SPD1, respectively (Fig. 1). Both mutants grew normally on nitrate as well as on ammonium (data not shown), indicating that PII and the C-terminal domain of NrtC are not essential for nitrate assimilation.

Unlike the SNC2 mutant, the nrtC insertional mutant SNC1 (the parental strain of SNC2) showed negligible NR activity (data not shown) and failed to utilize nitrate as the nitrogen source even when the nitrate concentration in the medium was as high as 60 mM (Fig. 2A), suggesting that insertional interruption of nrtC had caused polar inhibition of expression of the putative NR structural gene sll1454. SNC1 grew normally in a medium containing 5 mM nitrite or 7.5 mM ammonium (Fig. 2A) but failed to take up <100 µM nitrite in a medium at pH 9.6 (Fig. 2B). Under the conditions of low nitrite concentration and high pH, passive entrance of nitrous acid (HNO2, the protonated form of nitrite) into the cell is negligible and uptake of nitrite requires the operation of an active transport system (25). The results therefore indicated that SNC1 is defective in active transport of nitrite. Because eviction of the 3' region of nrtC and the nptI-sacB gene cartridge from the genome of SNC1 to construct SNC2 restored the ability to grow on nitrate (see above) and to take up low concentrations of nitrate and nitrite (see below), we concluded that the truncation of nrtC had no inhibitory effect on expression of the genes located downstream.



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  		FIG. 2. (A) Growth of the insertional nrtC (sll1452) mutant (SNC1) on 3.75 mM (NH4)2SO4 (circles), 5 mM NaNO2 (triangles), and 60 mM KNO3 (squares). (B) Nitrite uptake capability of the wild-type stain (GT) and the SNC1 mutant. Nitrite was added at time zero to the cell suspensions containing 5 µg of Chl per ml. Changes in the concentrations of nitrite are shown. OD730, optical density at 730 nm.

Ammonium-insensitive NRT activity in the Synechocystis mutant having truncated nrtC. The cell suspensions of the wild-type Synechocystis strain efficiently used 100 µM nitrate and nitrite until its exhaustion in the medium at pH 9.6 (Fig. 3A), indicating operation of a high-affinity active transport system for nitrite as well as nitrate. During nitrate assimilation, there was no accumulation of nitrite (Fig. 3A, a) or ammonium (not shown) in medium, indicating that the rate of net nitrate uptake was equal to the rate of nitrate assimilation. As in Synechococcus elongatus strain PCC 7942 (18), nitrate and nitrite uptake by the wild-type cells was completely inhibited by addition of ammonium to the medium (Fig. 3A). The inhibition was reversible, and nitrate and nitrite uptake was resumed after consumption of the ammonium in the medium (data not shown). The SNC2 mutant, having a truncated nrtC, also exhibited high-affinity nitrate and nitrite uptake activity (Fig. 3B), but the uptake was not inhibited by ammonium (Fig. 3B). This indicated that, as in Synechococcus elongatus strain PCC 7942, NrtC is involved in the transport of both nitrate and nitrite, with its C-terminal domain being required for regulation of the transport activity (18). During the nitrate uptake measurements, transient accumulation of low concentrations of nitrite was observed in the cultures of SNC2 (Fig. 3B, a), indicating that there was an imbalance between the rate of nitrite production by NR and that of nitrite consumption by NiR, with the former being faster than the latter. Since no nitrite was detected in the cultures of the wild-type cells assimilating nitrate (Fig. 3A, a), it was deduced that the C-terminal domain of NrtC modulates NRT activity in the absence of exogenously added ammonium as well, presumably responding to the ammonium generated intracellularly by nitrate reduction.



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  		FIG. 3. Effects of ammonium on the uptake of nitrate and nitrite by the wild-type strain (A) and the mutants having truncated nrtC (SNC2) (B) and disrupted glnB (SPD1) (C). Nitrate (a) or nitrite (b) was added at time zero to the cell suspensions containing 5 µg of Chl per ml, and ammonium (500 µM) was added immediately after the addition of nitrate and nitrite. Changes in the nitrate and nitrite concentrations in the medium are shown. Circles, control; triangles, suspensions with added ammonium.

Insensitivity of Synechocystis NR to ammonium. Because modification of an NRT subunit abolished the inhibition of nitrate and nitrite assimilation by ammonium (Fig. 3B), it was deduced that NR and NiR are not inhibited by ammonium in Synechocystis sp. strain PCC 6803. This was in contrast with the results obtained previously with Synechococcus elongatus strain PCC 7942; the Synechococcus NC2 mutant, which lacks the C-terminal domain of NrtC and which has ammonium-resistant NRT activity, could not assimilate nitrate in the presence of ammonium, because its NR was inhibited by ammonium (18). To gain insight into the mechanism of inhibition of NR by ammonium, the Synechocystis NR enzyme was expressed in Synechococcus elongatus strain PCC 7942 and the effect of ammonium was examined (Fig. 4). Expression of the sll1454 gene of Synechocystis (Fig. 1A) in an NR-null derivative of the Synechococcus NC2 mutant (NC41 nrtC{Delta}C narB::{Omega}) restored the ability of the cells to assimilate nitrate (Fig. 4a) as the Synechococcus narB gene did (Fig. 4b), verifying that sll1454 is the NR gene (narB) of Synechocystis sp. strain PCC 6803. In the presence of ammonium, the NC41 derivative expressing Synechocystis narB (NC51) continued nitrate assimilation (Fig. 4a), whereas nitrate assimilation by the NC41 derivative expressing Synechococcus narB (NC52) was inhibited (Fig. 4b). These results showed that NR of Synechocystis sp. strain PCC 6803 has ammonium-resistant activity not only in Synechocystis cells but also in Synechococcus cells.



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  		FIG. 4. Ammonium-resistant activity of Synechocystis NR in the cells of Synechococcus elongatus strain PCC 7942. The NR structural genes of Synechocystis sp. strain PCC 6803 (sll1454) and Synechococcus elongatus strain PCC 7942 (narB) were introduced into the Synechococcus elongatus mutant that lacks NR and has ammonium-resistant NRT (NC41) to construct NC51 (a) and NC52 (b), respectively. Nitrate was added at time zero to the cell suspensions containing 5 µg of Chl per ml, and ammonium (500 µM) was added immediately after the addition of nitrate. Changes in the nitrate concentration in the medium are shown. Circles, control; triangles, suspensions with added ammonium.

Regulation of NRT by nonmodifiable derivatives of PII in Synechocystis. Nitrate assimilation has been shown to be unaffected by ammonium in PII-deficient Synechococcus elongatus strain PCC 7942 (23) and Synechocystis sp. strain PCC 6803 (14) mutants. In accordance with the previous observations, nitrate assimilation by the Synechocystis glnB mutant constructed in the present study (SPD1) was not affected by ammonium (Fig. 3C, a). Since NRT is the regulatory step of the nitrate assimilation pathway in the Synechocystis strain (see above), the results indicated that the PII protein is required for regulation of NRT. Similar to the SNC2 mutant having truncated NrtC, SPD1 excreted nitrite into medium during nitrate assimilation (Fig. 3C, a), indicating the imbalance between the rates of nitrate reduction and nitrite reduction. In accordance with the involvement of NRT in transport of nitrite as well as nitrate (see above), nitrite assimilation by the mutant, measured under high-pH and low-nitrite conditions, was also insensitive to ammonium (Fig. 3C, b). An SPD1 derivative (SPD1S) carrying a plasmid-borne wild-type glnB gene showed ammonium-promoted inhibition of nitrate uptake like that of the wild-type strain (Fig. 5a). The SPD1A and SPD1E strains, expressing the S49A and S49E derivatives of PII, respectively, also showed ammonium-responsive inhibition of nitrate uptake (Fig. 5b and c). These findings demonstrated that the presence or absence of a negative charge at amino acid position 49 does not affect the ability of PII to regulate the NRT activity in an ammonium-responsive manner.



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  		FIG. 5. Effects of ammonium on nitrate uptake by the cells of the SPD1S (a), SPD1A (b), and SPD1E (c) strains, which have the wild-type PII, the S49A derivative of PII, and the S49E derivative of PII, respectively. Nitrate was added at time zero to the cell suspensions containing 5 µg of Chl per ml, and ammonium (500 µM) was added immediately after the addition of nitrate. Changes in the nitrate and nitrite concentrations in the medium are shown.

Regulation of NRT by nonmodifiable derivatives of PII in Synechococcus. To see whether or not the responsiveness of NRT to ammonium is independent of the presence or absence of a negative charge at the 49th amino acid position in Synechococcus elongatus strain PCC 7942 as well, we examined nitrite uptake activity and its regulation in the Synechococcus mutants expressing modified glnB. A glnB-deficient Synechococcus mutant (PD1) was constructed by insertion of a spectinomycin and streptomycin resistance gene cassette (Fig. 6A), and segregation of the homozygous mutant was confirmed by Southern hybridization analysis (Fig. 6B). For overexpression of PII, the glnB derivatives were cloned in the shuttle expression vector pSE1 to make a transcriptional fusion with the Ptrc promoter, and the resulting plasmids were introduced into the PD1 mutant to yield the PD1S, PD1A, and PD1E strains (Table 1). Unlike the plasmid-encoded GlnB expressed in Synechocystis (see above), the plasmid-encoded Synechococcus GlnB carried a K2E mutation introduced for the purpose of cloning into pSE1. Figure 6C compares the polypeptide compositions of the soluble proteins extracted from the wild-type and the mutant strains. The three PD1 derivatives carrying plasmid-borne glnB accumulated large amounts of a polypeptide with apparent molecular mass of 13 kDa, which was close to the calculated molecular mass of GlnB (12.4 kDa) (Fig. 6C, lanes 3 to 5). Incubation of the wild-type cells with H332PO4 in nitrate-containing medium resulted in phosphorylation of a 13-kDa polypeptide (Fig. 6D, lane 1). Addition of ammonium to the medium prevented the labeling of the 13-kDa polypeptide (Fig. 6D, lane 2), indicating that the polypeptide is GlnB. The 13-kDa polypeptide that accumulated in the PD1S cells (Fig. 6C, lane 3) was also labeled with 32P in a nitrogen-responsive manner (Fig. 6D, lanes 5 and 6), verifying that the overexpressed 13-kDa protein is GlnB. The results also showed that the K2E mutation did not affect the nitrogen-responsive modification of the PII protein. Though PD1 lacked the wild-type copy of glnB, a weak 32P signal was often detected in the 13-kDa region (e.g., Fig. 6D, lane 4). Since glnB is a single-copy gene in Synechococcus, this signal was ascribed to a polypeptide other than GlnB. There were also several other weakly labeled polypeptides (Fig. 6D), the nature of which is currently unknown. In agreement with the previous report that Ser49 is the only site for PII phosphorylation in Synechococcus elongatus strain PCC 7942 (8), no significant incorporation of 32P into the 13-kDa polypeptide that accumulated in the PD1A and PD1E strains was observed (Fig. 6C, lanes 4 and 5, and D, lanes 7 to 10).

Figure 7 compares the effects of ammonium on nitrite uptake by the wild-type and the mutant strains of Synechococcus at pH 9.6 and nitrite concentrations of <100 µM. Nitrite uptake by the wild-type cells was inhibited by ammonium, as previously shown (Fig. 7a) (18). Since ammonium does not affect in vivo NiR activity of Synechococcus (25), the results indicate inhibition of NRT activity by ammonium. In the glnB-deficient mutant PD1, ammonium reduced the rate of nitrite uptake but the cells exhibited ammonium-resistant NRT activity and continued nitrite uptake in the presence of ammonium (Fig. 7b), confirming that PII is required for the ammonium-promoted inhibition of NRT. The PD1S strain, expressing the K2E derivative of GlnB, showed ammonium-responsive inhibition of NRT like that of the wild-type strain (Fig. 7c), indicating that the substitution of the second amino acid residue did not affect the activity of PII to regulate NRT. The PD1A and PD1E strains, expressing nonmodifiable forms of PII, also showed nitrite uptake activity similar to that in the wild-type strain, and the activity was inhibited by ammonium as in the wild-type strain (Fig. 7d and e). These results showed that changes in the electric charge at the 49th amino acid position do not affect the ability of PII to respond to cellular nitrogen status and to regulate the NRT activity accordingly in Synechococcus elongatus strain PCC 7942 as well as in Synechocystis sp. strain PCC 6803.



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  		FIG. 7. Effects of ammonium on nitrite uptake by the cells of the wild-type Synechococcus elongatus strain PCC 7942 (a), the PII-deficient strain PD1 (b), and the PD1S (c), PD1A (d), and PD1E (e) strains expressing the plasmid-encoded GlnB derivatives. Nitrite was added at time zero to the cell suspensions containing 5 µg of Chl per ml, and ammonium (500 µM) was added immediately after the addition of nitrite. Changes in the nitrite concentrations in the medium are shown. PD1S, PD1A, and PD1E cells were treated with 1 mM IPTG for 16 h prior to the experiment.


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DISCUSSION
 
In Synechocystis sp. strain PCC 6803, the sll1450-sll1451-sll1452-sll1453 gene cluster has been believed to encode an NRT, because (i) it is strongly similar to the Synechococcus elongatus nrtABCD gene cluster, which codes for an ABC-type NRT; (ii) its expression is regulated by the nitrogen conditions of the cell (1); and (iii) it forms an operon with the NR gene narB (sll1454) (1). The defect of the sll1452 insertional mutant SNC1 in active uptake of nitrite (Fig. 2B) and the ammonium-insensitive uptake of nitrate and nitrite in the SNC2 mutant, which has a truncated sll1452 gene (Fig. 3B), verify the involvement of this gene cluster in transport of nitrate and nitrite, providing the first experimental evidence for the identification of sll1450, sll1451, sll1452, and sll1453 as nrtA, nrtB, nrtC, and nrtD, respectively, of Synechocystis sp. strain PCC 6803.

Since the extent of PII phosphorylation reflects the nitrogen status of the cell, it has been presumed to act as the major biochemical signal for regulation of nitrate assimilation (7). However, the ammonium-responsive regulation of NRT by the S49A and S49E derivatives of PII (Fig. 5 and 7) indicates that PII can sense the cellular nitrogen status and control the NRT activity accordingly, irrespective of the presence or absence of negative charge or of a change in the size of the side chain at the 49th amino acid position. It is therefore unlikely that changes in the phosphorylation state of PII play a role in regulation of NRT. The binding of ATP and 2-OG to phospho-PII, on the other hand, has been shown to inhibit dephosphorylation of the protein by PII phosphatase, verifying that the effectors provoke a conformational change in PII (34). Since the intracellular 2-OG concentration is high in cells grown with nitrate and is decreased by ammonium (28), we hypothesize that the conformational change of PII, provoked by the binding of 2-OG, controls the activity of the protein to inhibit NRT. It remains to be elucidated how PII and the C-terminal domain of NrtC regulate the NRT activity.

Recent studies of Synechococcus elongatus strain PCC 7942 revealed the binding of PII to N-acetyl-L-glutamate (NAG) kinase, the key enzyme of the arginine biosynthetic pathway (2, 12). Detailed in vitro and in vivo analyses have shown that PII strongly enhances NAG kinase activity by binding to the enzyme (12). This interaction requires the nonphosphorylated Ser49 residue of PII, indicating that NAG kinase activity is regulated by phosphorylation and dephosphorylation of PII (12). The independence of NRT regulation from modification of Ser49 indicates that PII has two distinct modes of action for regulation of different targets: one involving modification of the Ser49 residue and the other depending on the binding of the effector molecules.

In a previous study of Synechococcus elongatus strain PCC 7942 (22), the mutant having an S49A derivative of PII was shown to express negligible activity of nitrate assimilation irrespective of the nitrogen status of the cell, whereas the mutant having an S49E derivative of PII showed ammonium-sensitive nitrate assimilation activity like that of the wild-type strain. These observations suggest that PII(S49A) permanently inhibits either NRT or NR. The present results show that PII(S49A) of Synechocystis inhibits NRT only in the presence of ammonium (Fig. 5b). Also, PII(K2E, S49A) of Synechococcus was shown to require the presence of ammonium for inhibition of NRT even when overexpressed from the Ptrc promoter (Fig. 7d). These findings suggest that it is the NR that is permanently inhibited by PII(S49A) in Synechococcus. On the other hand, the ammonium-sensitive assimilation of nitrate in the Synechococcus mutant expressing PII(S49E) (22) can be accounted for by regulation of NRT; PII(S49E) clearly does not inhibit NR in the absence of ammonium in the medium and may not inhibit NR in the presence of ammonium either. Thus the presence or absence of a negative charge at the 49th position of GlnB, and hence the changes in the phosphorylation state of PII, seem to have a role in the regulation of NR activity in Synechococcus.

Whereas NR of Synechococcus elongatus strain PCC 7942 is inhibited by ammonium (18), the present results show that NR of Synechocystis sp. strain PCC 6803 is resistant to ammonium in the Synechococcus cells as well as in the Synechocystis cells (Fig. 4A). Thus Synechocystis NR does not respond to the NR regulatory mechanism of the Synechococcus cell. This is presumably due to a structural difference(s) between Synechocystis NR and Synechococcus NR. Although the deduced Synechococcus NR protein (X74597 in the EMBL, GenBank, and DDBJ databases) is 61% identical in amino acid sequence to the Synechocystis enzyme (17), there are several regions of poor similarity (not shown), which might be involved in the posttranslational regulation of the enzyme activity. The Synechocystis NR can be thus regarded as a naturally occurring mutant enzyme insensitive to ammonium, which will be useful for further molecular genetic analysis of the mechanism of NR regulation in Synechococcus elongatus strain PCC 7942.


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ACKNOWLEDGMENTS
 
This work was supported in part by a Grant-in-Aid for Scientific Research in Priority Areas (13206027) and in part by a Grant-in-Aid for Specially Promoted Research (13CE2005) and The 21st Century COE Program from the Ministry of Education, Culture, Sports, Science and Technology of Japan.


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FOOTNOTES
 
* Corresponding author. Mailing address: Laboratory of Molecular Plant Physiology, Graduate School of Bioagricultural Sciences, Nagoya University, Nagoya 464-8601, Japan. Phone: 81-52-789-4106. Fax: 81-52-789-4107. E-mail: omata{at}agr.nagoya-u.ac.jp. Back

{dagger} M.K. and N.T. contributed equally to this work. Back

{ddagger} Present address: Biological Research Laboratories, Nissan Chemical Industries, Saitama 349-0294, Japan. Back


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Journal of Bacteriology, January 2005, p. 498-506, Vol. 187, No. 2
0021-9193/05/$08.00+0     doi:10.1128/JB.187.2.498-506.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.



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