Molecular Cloning, Expression and Transport Activity of SaNPF6.3/SaNRT1.1, a Novel Protein of the Low-Affinity Nitrate Transporter Family from the Euhalophyte Suaeda altissima (L.) Pall.

The SaNPF6.3 gene, a putative ortholog of the dual-affinity nitrate (NO3−) transporter gene AtNPF6.3/AtNRT1.1 from Arabidopsis thaliana, was cloned from the euhalophyte Suaeda altissima. The nitrate transporting activity of SaNPF6.3 was studied by heterologous expression of the gene in the yeast Hansenula (Ogataea) polymorpha mutant strain Δynt1 lacking the original nitrate transporter. Expression of SaNPF6.3 in Δynt1 cells rescued their ability to grow on the selective medium in the presence of nitrate and absorb nitrate from this medium. Confocal laser microscopy of the yeast cells expressing the fused protein GFP-SaNPF6.3 revealed GFP (green fluorescent protein) fluorescence localized predominantly in the cytoplasm and/or vacuoles. Apparently, in the heterologous expression system used, only a relatively small fraction of the GFP-SaNPF6.3 reached the plasma membrane of yeast cells. In S. altissima plants grown in media with either low (0.5 mM) or high (15 mM) NO3−; concentrations, SaNPF6.3 was expressed at various ontogenetic stages in different organs, with the highest expression levels in roots, pointing to an important role of SaNPF6.3 in nitrate uptake. SaNPF6.3 expression was induced in roots of nitrate-deprived plants in response to raising the nitrate concentration in the medium and was suppressed when the plants were transferred from sufficient nitrate to the lower concentration. When NaCl concentration in the nutrient solution was elevated, the SaNPF6.3 transcript abundance in the roots increased at the low nitrate concentration and decreased at the high one. We also determined nitrate and chloride concentrations in the xylem sap excreted by detached S. altissima roots as a function of their concentrations in the root medium. Based on a linear increase in Cl− concentrations in the xylem exudate as the external Cl− concentration increased and the results of SaNPF6.3 expression experiments, we hypothesize that SaNPF6.3 is involved in chloride transport along with nitrate transport in S. altissima plants.

In other experiments, A. thaliana, O. sativa and Nicotiana benthamiana plants grown in a nutrient solution with NH 4 + as a nitrogen source were found to be hypersensitive to NaCl stress [33].For AtNPF6.3 mutant plants, the authors showed that the salt hypersensitivity was a result of Cl − overaccumulation due to AtNPF6.3Cl − transport activity, which was upregulated by NH 4 + ; salt stress hypersensitivity was alleviated in the presence of competing NO 3 − anion.Under saline conditions, halophytes, plants inhabiting saline soils, are suggested to regulate the absorption of nutrients more efficiently than glycophytes, plants that are not salt-tolerant [32,[34][35][36].However, available information on anion-transporting proteins of halophytes is scarce.Gene cloning and elucidation of functional features of anion transporters from halophytes are important for unraveling the mechanisms of plant salinity tolerance and improving crop salt tolerance by genetic engineering (reviewed by [37][38][39][40]).
Here, we describe cloning SaNPF6.3, a putative ortholog of A. thaliana NPF6.3/NRT1.1, from the euhalophyte Suaeda altissima.The genus Suaeda belongs to the Amaranthaceae (Chenopodiaceae), many members of which inhabit highly saline soils and are characterized by extreme salt tolerance [41,42].S. altissima is one of the most salt tolerant plants and is able to perform its life cycle at NaCl concentrations up to 1M [43].The ability of SaNPF6.3 to transport nitrate was examined by functional complementation analysis in the mutant strain ∆ynt1 of the yeast Hansenula (Ogatae) polymorpha.H. polymorpha is a suitable model organism to study nitrate assimilation pathways in plants since it is able to take up and metabolize nitrate as the only nitrogen source [44][45][46][47][48]. Gene YNT1 (yeast nitrate transporter 1) encodes the only high-affinity nitrate transporter in H. polymorpha.In the mutant strain ∆ynt1, the gene YNT1 has been deleted.The nitrate transporting activity of SaNPF6.3 was also validated by checking the ability of ∆ynt1 expressing SaNPF6.3 to absorb NO 3 − from nitrate-containing media.The relative SaNPF6.3 transcript abundance in S. altissima organs was measured for plants grown at various nitrate and chloride concentrations in nutrient solutions.The changes in SaNPF6.3expression which were induced by changing the nitrate availability and salinity in the medium were also studied.

Plant Material
Seeds of Suaeda altissima (L.) Pall.were collected from plants growing in the wild on the shores of the salt lake Elton, located in the Volgograd region in Russia.Seeds were stratified at +4 • C over 3 days and then germinated in wet sand.Seed germination and further plant growth were carried out in a growth chamber under controlled conditions at 24 • C and relative humidity of 60-70%.The plants were illuminated with high pressure sodium lamps DNaZ_400 (Reflux, Novocherkassk, Russia) at a light flux of 300 µmol photons m −2 s −1 and photoperiod of 16 h, with an 8 h dark period.Fourteen days after germination, the seedlings were transplanted to an aerated Robinson and Downton nutrient solution (NS) [49] in 3-L opaque glass containers (5 plants per container) with low (0.5 mM) or high (15 mM) nitrate concentrations.Plants were grown hydroponically under the same environmental conditions until they were 45 days old, when they were used in most experiments.For total RNA extraction, organs of S. altissima plants (roots, leaves, stems, flowers) were sampled (approximately 1 g fresh weight of each sample) and frozen in liquid nitrogen for further use.
To study the long-term salinity effect on the expression of SaNPF6.3 in Suaeda organs, NaCl was applied to the NS after 7 d.To avoid salt shock, NaCl was added gradually in increments of 50 or 100 mM per day, up to the final concentrations of 250 or 750 mM; no NaCl was added to the NS for control plants.To study the effect of salt shock on the expression of SaNPF6.3,NaCl was raised to 250 mM in a single addition.SaNPF6.3 transcript levels were determined after 31 d for both the long-term NaCl treatment and for the NaCl shock, when the plants had reached 45 d of age.In order to investigate the effects of changes in nitrite and ammonium ions on the expression of SaNPF6.3,KNO 2 and (NH 4 ) 2 SO 4 were added to the NS at a final concentration of 5 mM after 31 d of plant growth in NS, with both a low (0.5 mM) or a high (15 mM) nitrate concentration.The effects of an increase in nitrate concentration in the NS from 0.5 mM up to 5 mM and the transfer of plants grown at 15 mM nitrate to the non-nitrate medium were also studied using plants of the same age.A comparative assessment of SaNPF6.3 expression levels in different organs of S. altissima was performed for 21-and 45-day-old plants (7 and 31 days of growth in hydroponics, respectively) in roots, stems and leaves and for 60-day-old plants (at 46 day of growth in hydroponics) in flowers.
To obtain xylem exudates, the shoots of 55-day-old S. altissima plants grown under standard conditions in the NS medium but supplemented with nitrate and chloride at various concentrations (the ion concentrations are indicated in the corresponding figure), were cut off 2 cm above the root collar.Silicone tubes were placed on the stem stumps, and the exudates were collected in the tubes for 48 h at 24 • C. In the experiments where the dependence of NO 3 − concentration in the xylem exudate on NO 3 − concentration in the medium was determined, the plants were grown in the presence of 100 mM NaCl in NS.Two days before the exudate collection, the plants were transferred to modified NS, in which 1 mM KH 2 PO 4 and 4 mM Ca(NO 3 ) 2 were replaced by 1 mM NaH 2 PO 4 and 4 mM CaCl 2 , respectively, while KNO 3 was added in various concentrations.In order to investigate the dependence of Cl − concentration in the xylem exudate on Cl − concentration in the medium, NaCl was applied to the NS gradually after 7 days of plant growth in hydroponics without NaCl, as indicated above.

Yeast Strain and Vectors Used in the Study
Methylotrophic yeast (Hansenula polymorpha) double auxotrophic strains DL-1 (leu2 ura3 genotype) (wild-type strain, WT strain) and yeast integrative vectors pCCUR2 and pCHLX were used in this study.The strain DL-1 (leu2 ura3) was transformed with plasmids pCCUR2 and pCHLX carrying the URA and LEU genes, respectively, to ensure the growth of the yeast strains without additional nitrogen sources, leucine and uracil, when performing complementation tests.Plasmids pCCUR2 and pCHLX were kindly provided by Dr. Michael Agafonov (Federal Research Center "Fundamentals of Biotechnology", Russian Academy of Sciences, Moscow, Russia).Yeast cells were transformed by the lithium method [50] or by electroporation [51] using an Eppendorf device (Eppendorf, Framingham, MA, USA).

Extraction of Total RNA from Plant Material and the First-Strand cDNA Synthesis
Total RNA from S.altissima plant organs was isolated by the hot phenolic method [52] and used as a template for the total first-strand cDNA synthesis.For amplification of the 3 -and 5 -ends of the SaNPF6.3transcript by the Step-Out RACE method, the firststrand cDNA was synthesized on the total RNA template, isolated from Suaeda roots, using MINT revertase (Evrogen, Moscow, Russia).Full-length cDNA of SaNPF6.3 gene was also amplified on the total RNA template, isolated from Suaeda roots.To obtain full-length cDNA of SaNPF6.3 and quantify the representation of the gene transcripts in S. altissima organs, first-strand cDNA synthesis was performed on total RNA templates using (dT)15 primer and MMLV revertase (Evrogen, Moscow, Russia).

Identification of the Full Length SaNPF6.3 Coding Sequence
Partial coding sequence (the middle fragment) of the SaNPF6.3gene was obtained by us previously (GenBank ID: MK580125.1)[53].Here, based on this sequence, the forward and reverse primer sets were designed for amplification of the 5 -and 3 -end sequences of SaNPF6.3 cDNA.The 5 -and 3 -end sequences of SaNPF6.3 cDNA were determined by the Step-Out RACE technology (kit #SKS03, Evrogen, Moscow, Russia).The cDNA fragments were amplified on the total cDNA template using Encyclo DNA polymerase (#PK002, Evrogen, Moscow, Russia).The 5 -sequence of SaNPF6.3 cDNA (1152 bp) was amplified with primers SaNPF6.3_r(round 1) and SaNPF6.3_5RACE_R1 (round 2).The 3 -sequence of SaNPF6.3 cDNA (722 bp) was amplified with SaNPF6.3_f(round 1) and SaNPF6.3_F1(round 2).All amplicons obtained, including also the middle cDNA fragment amplified from the cDNA template with a primer pair SaNPF6.3_f and SaNPF6.3_r,were cloned into pAL2-T vector (Evrogen, Moscow, Russia) for replication in E. coli cells and the following sequencing.Subsequently, the partial sequences (middle fragment, 5 -and 3 -ends of SaNPF6.3 cDNA) were assembled in silico using SnapGene software 5.0.8 (https://www.snapgene.com/snapgene-viewer(accessed on 29 July 2023)).The resulting coding sequence of 1788 bp contained open reading frame (ORF) for the protein of 596 aa.This sequence was used for the design of primers for the amplification of full-length SaNPF6.3cDNA on the total first-strand cDNA template.

Cloning of the Full-Length SaNPF6.3 cDNA in the Yeast Vector pCHLX
The full-length coding sequence of SaNPF6.3 was amplified from the total first-strand cDNA using primer pairs SaNPF6.3_Gib_F and SaNPF6.3_Gib_R.The full-length SaNPF6.3cDNA was cloned into the yeast integrative vector pCHLX [54] under the control of the inducible nitrate reductase promoter pYNR1 and terminator tYNR1 of H. polymorpha.Promoter pYNR1 and terminator tYNR1 sequences were amplified from the H. polymorpha genomic DNA template using primer pairs pYNR1_F and pYNR1_R, and tYNR1_F and tYNR1_R.The first 10 cycles of amplification of the promoter, terminator and gene coding sequences were performed using Encyclo polymerase (No.PK002, Evrogen, Moscow, Russia); the next 25 cycles were performed using CloneAmp HiFi PCR Premix kit (No. 639298, Clontech, Mountain View, CA, USA).The pCHLX vector was linearized in the Hind III and EcoRI restriction sites and ligated with the synthesized pYNR1, tYNR1 and SaNPF6.3sequences using a Gibson assembly kit (No. E5510, SkyGen, NEB, Ipswich, MA, USA) to produce the pCHLX-pYNR1-SaNPF6.3-tYNR1construct (further denoted as pCHLX-SaNPF6.3).The cloned sequences were verified by sequencing.The SaNPF6.3 cDNA sequence (1788 bp) was deposited in GenBank (GenBank ID: OQ330855).
The pCHLX-GFP-SaNPF6.3 construct was also obtained for the expression of SaNPF6.3 fused at the N-terminus with green fluorescent protein (GFP) in yeast cells.To achieve this, three fragments were ligated in one reaction: (1) GFP coding sequence amplified from pTR vector [55] with pYNR1_GFP_F and TEV_GFP_R primers (2) SaNPF6.3coding sequence amplified from the first cDNA strand with TEV_SaNPF6.3_F and SaNPF6.3_Gib_Rprimers; (3) plasmid pCHLX linearized by inverted PCR from the pCHLX-SaNPF6.3construct with the pYNR1_R3 and tYNR1_F primer pair.Ligation was carried out using Gibson assembly kit (NEB, Ipswich, MA, USA).

Cloning of AtNPF6.3 Coding Sequence in the Yeast Vector pCHLX
To control the functional complementation of the H. polymorpha mutant ∆ynt1, the mutant was transformed by the construct carrying the known nitrate transporter gene At-NPF6.3(GenBank ID: NP_563899.1)from Arabidopsis.The coding sequence of AtNPF6.3 was amplified from the Arabidopsis total first-strand cDNA, using primer pairs AtNPF6.3_Gib_F and AtNPF6.3_Gib_R.The total first-strand cDNA was synthesized on the total RNA template, isolated from roots of adult Arabidopsis plants.Like SaNPF6.3 cDNA, full-length AtNPF6.3coding sequence was cloned into the vector pCHLX [54] under the control of the inducible nitrate reductase promoter pYNR1 and terminator tYNR1 of H. polymorpha.
For ligation with AtNPF6.3,nitrate reductase promoter and terminator sequences were amplified from the H. polymorpha genomic DNA template using primer pairs pYNR1_F and pYNR1_R2, and tYNR1_F2 and tYNR1_R.All stages of the amplification and ligation of the sequences were similar to how it was carried out during the amplification and ligation of the sequences in the case of SaNPF6.3 cloning.The construct pCHLX-pYNR1-AtNPF6.3-tYNR1(pCHLX-AtNPF6.3) was obtained for the transformation of mutant ∆ynt1 cells.

Implementation of Amino Acid Substitutions in the Amino Acid Sequence of the SaNPF6.3 Protein
To obtain point amino acid substitutions of Tyr358His, Thr106Asp and Thr106Ala in the SaNPF6.3protein sequence, the pCHLX-pYNR1-SaNPF6.3-tYNR1construct was linearized by inverse PCR with primer pairs SaNPF6.3_1074_F and SaNPF6.3_Tyr358His_R,SaNPF6.3_318_F and SaNPF6.3_Thr106Asp_R,and SaNPF6.3_318_Fand SaNPF6.3_Thr106Ala_R,respectively, using a ready-to-use CloneAmp HiFi PCR Premix kit (TakaraBio, San Jose, CA, USA).The resulting linear forms of PCR products with corresponding nucleotide substitutions were converted into circular forms.For this purpose, the 5 -ends of the linearized plasmid DNA were phosphorylated using T4-polynucleotide kinase.The reaction mixture for the phosphorylation, containing T4 DNA-ligase buffer, 250 ng linearized DNA and 10 U T4-polynucleotid kinase (SibEnzyme, Novosibirsk, Russia), was incubated for 15 min at 37 • C. The phosphorylated product was ligated by adding 2.5 U T4 ligase (Fermentas, Thermo Fisher Scientific, Waltham, MA, USA) to the reaction mixture and incubating the mixture for 16-18 h at room temperature.The ligase was inactivated by incubation of the mixture at 65 • C for 15 min.Plasmid pCHLX-SaNPF6.3,which served as a template for amplification, was removed from the mixture by treatment with methyl-dependent DNA endonuclease Mal I (SibEnzyme, Novosibirsk, Russia).The mixture was purified from proteins by treatment with phenol-chloroform, and plasmid DNA was resuspended in mQH 2 O for subsequent transformation of competent E. coli cells.

Production of a Deletion Mutant ∆ynt1 of H. polymorpha
A mutant with a deleted YNT1 gene (GenBank ID: CP080316.1),ynt1::BleoR(ZeoR), was derived from the wild-type strain DL-1 (leu2, ura3) of H. polymorpha through homologous recombination by an "one-step gene disruption" method [56].To carry out the knockout of the gene YNT1, the zeocin resistance gene (ZeoR) was incorporated into the YNT1 locus through homologous recombination at the YNT1 gene sites [44].For this purpose, PCR fragments corresponding to "left" and "right" flanking parts of the YNT1 gene and the zeocin resistance gene ZeoR amplified from the pVR2 vector [57] were cloned into the bacterial vector pBlueScript KS(II)+ using Gibson assembly kit (NEB, Ipswich, MA, USA)."Left" and "Right" fragments of the YNT1 gene and the gene ZeoR were amplified using primer pairs ZeoYNTRfl_F and pBlueYNTRfl_R, pBlueYNTLfl_F and YNTLflZeo_R, and ZeoCas1 and ZeoCas2, respectively.From the resulting construct, pBlueScript KS(II)+ YNT1_L-ZeoR-YNT1_R, a fragment of YNT1_L-ZeoR-YNT1_R, was excised by Hind III and Pst I restriction endonucleases (SibEnzym, Novosibirsk, Russia) and transferred into DL1 cells.The presence of the insert in the zeocin-resistant yeast clones was validated by PCR screening using the primer pair pBlueYNTLfl_F and pBlueYNTRfl_R.Growth of the selected colonies was tested on the agarized media containing nitrate and nitrite (in the concentration range of 0.2-5 mM) to exclude the occurrence of other spontaneous mutations in the genome which may occur when yeast is transformed by the lithium method.
The mutant strain ∆ynt1 (ynt1: BleoR(ZeoR), leu2, ura3) was additionally transformed with pCCUR2 and pCHLX integrative plasmids carrying the URA and LEU genes, respectively, to ensure the growth of the yeast strains without additional nitrogen sources in the selective media, namely, leucine and uracil, when performing complementation tests.

Cultivation of H. polymorpha and Transformants of ∆ynt1 Strain
Cells of H. polymotpha WT strain, mutant strain ∆ynt1, and transformants of the ∆ynt1 strain were grown on a rich YPD medium (1% yeast extract, 2% peptone, 2% glucose) or a minimal synthetic SD medium (0.67% yeast nitrogen base without amino acids, 2% glucose) with (NH 4 ) 2 SO 4 addition (medium SD + AS) or KNO 3 addition (medium SD + KNO 3 ) as nitrogen sources.The KNO 3 concentrations ranged from 0.2 to 5 mM.The media contained or did not include auxotrophic additions (0.02 mg/mg leucine, 0.04 mg/mL uracil).The yeast growth occurred at 37 • C for 2-3 days.All manipulations with H. polymorpha were performed according to the protocols generally accepted for the yeast [51].Yeast transformants were selected on minimal selective media in the absence of leucine and/or uracil.Transformants that contained the insertion in the genome were validated by PCR with DL-1_Chr2_HpURA3_F or Hp_DL-1_Chr1_R primers for genomic DNA and standard M13_R or M13_F primers for pCCUR2 and pCHLX vectors.

Study of nitrate uptake by H. polymorpha cells expressing SaNPF6.3 and AtNPF6.3 Genes
Cells of H. polymorpha knockout mutant strains ∆ynt1 expressing SaNPF6.3 and At-NPF6.3, as well as WT cells, were grown to approximately 20 mg fresh weight/mL in a minimal SD medium (2% dextrose and 0.67% YNB containing sulphate ammonium) at 37 • C for 2 days.To induce the expression of nitrate transporter genes, cells were precipitated, washed with water, and cultured for 24 h (37 • C) in a minimal SD-AS medium (2% dextrose, 0.67% YNB without ammonium sulphate) supplemented with 20 mM NaNO 3 as the only nitrogen source.After induction of the nitrate transporter genes, yeast cells were repeatedly washed with water and resuspended in a minimal SD-AS medium (2% dextrose; 0.176% YNB without sulphate ammonium) supplemented with 0.5 mM or 2 mM NaNO 3 .The yeast cultures were left to grow in these media for 18 h (37 • C); the absorption of nitrate by the cells was determined by measuring nitrate concentration decline in incubation media using an Elite-021 NO 3 − selective electrode (Niko-Analit, Moscow, Russia).

Immunoblotting
For SDS-PAAG protein electrophoresis and the following immunoblot analysis, H. polymorpha WT cells and cells transformed with pCHLX-GFP-SaNPF6.3 were grown in 10 mL of SD + AS medium (0.67% yeast nitrogen base without amino acids, 2% glucose; ammonium sulphate as a nitrogen source was a component of the yeast nitrogen base) for 24 hr.Then, the yeast cells were transferred to SD + KNO 3 medium (0.17% yeast nitrogen base without amino acids and ammonium sulphate, 2% glucose + 10 mM KNO 3 as a sole nitrogen source).After cultivation for 24 h in the NO 3 − -containing medium, leading to the induction of nitrate transporter genes, the cells were precipitated and lysed in 300 µL of A buffer (20 mM Tris-HCl, pH 8.0, 100 mM NaCl, 1% SDS, 1 mM PMSF) with 300 µL glass beads using Vortex.The lysate was centrifuged (13,000× g, 10 min, +4 • C) and the proteins from the supernatant were analyzed by SDS-PAAG electrophoresis and immunoblotting.The protein concentration in the supernatant was determined by the bicinchoninic acid method [58].Electrophoresis was performed in 8% separating gel, loading 50 µg of protein per lane.The semi-dry transfer of the proteins from PAAG matrix to the nitrocellulose membrane (NC) (pore diameter of 0.45 µm; Schleicher & Schuell, Dassel, Germany) was carried out at 100 mA for 1 h using transfer device (Helicon, Moscow, Russia).For immunodetection of the recombinant protein GFP-SaNPF6.3, polyclonal anti-GFP antibodies (Evrogen, Moscow, Russia) were used as primary antibodies and horseradish peroxidase-conjugated (HRP) antibodies (Imtek Ltd., Moscow, Russia) as secondary ones.After treatment with a blocking solution (5% Carnation non-fat dry milk (Nestle, Vevey, Switzerland) in TBS with 0.1% Tween-20), the membrane was incubated with the primary antibodies (overnight at +4 • C) and then with the secondary antibodies (2 h).Primary antibodies were used at a 1:2000 dilution in TBS-Tw-BSA solution (1×TBS, 0.2% Tween 20, 1% BSA, 0.01% NaN 3 ), and secondary antibodies were used at a 1:10,000 dilution in the TBS-Tw-DM solution (1×TBS, 0.2% Tween 20, 5% Carnation non-fat dry milk).After incubation with the antibodies, the membrane was washed with TBS-Tw solution (1×TBS, 0.1% Tween 20) and immunoreactive bands were visualized using an ECL kit (GE Healthcare, Piscataway, NJ, USA).A ChemiDoc XRS+ System gel documentation system (BioRad, Hercules, CA, USA) was used for visualization.

Determination of SaNPF6.3 Localization in Yeast Cells
The images of yeast cells transformed with pCHLX-GFP-SaNPF6.3 were obtained with a laser scanning confocal microscope LSM-710-NLO (Carl Zeiss, Jena, Germany) equipped with a 63x oil immersion objective Plan-Apochromat, with numerical aperture of 1.4 and ZEN 2010 software 1.1.2.0 (Carl Zeiss, Jena, Germany).For analysis, the suspension of yeast cells was transferred to sterilized Petri dishes with a thin glass bottom.The fluorescence signals were detected in confocal channel mode with a confocal diaphragm of 46 µm in diameter, image size 1024 × 1024 pixels (132 nm/pixel), and a scanning rate of 1.27 µs/pixel (1.33 s/image).The GFP fluorescence was excited at λ ex = 488 nm and visualized in the 490-555 nm range.The transmitted laser light was recorded with a separate T-PMT detector.

Quantitative Analysis of SaNPF6.3 Transcripts in S. altissima Organs
Quantitative analysis of SaNPF6.3 transcripts was performed by qRT-PCR using a LightCycler ® 96 System (Roche Diagnostics Corporation, Indianapolis, IN, USA).The cDNA templates for the amplification of SaNPF6.3 fragments were synthesized on total RNAs templates, isolated from different organs of S. altissima plants grown in the NS with various nitrate and NaCl concentrations or the plants subjected to NaCl shock.A readyto-use reaction mixture with intercalating dye SYBR Green I (Evrogen, Moscow, Russia) was used.The S. altissima gene of elongation factor 1 alpha SaeEF1alpha (GenBank ID: MN076325.1)and protein phosphatase gene SaPP2A (GenBank ID:OP752355) were used as the reference genes.To amplify the SaeEF1alpha and SaPP2A fragments, SaeEF1alfa_F1 and SaeEF1alfa_R1, and SaPP2A_F1 and SaPP2A_R1 primer pairs, respectively, were used.The results are based on three replicates.The results obtained were processed by the LightCycler 96SW 1.1 software.Similar results were obtained with SaeEF1alpha and SaPP2A, hence, the data are presented only for the former gene.For the amplification of SaNPF6.3 fragment, the primer pair SaNPF6.3_F1 and SaNPF6.3_R1was used.

Determination of NO 3
− and Cl − Concentrations in Xylem Exudates Xylem exudates were mineralized at 400 • C, the solid residues obtained were diluted with mQ water and the nitrate concentrations in the solutions were determined using an Elite-021 NO 3 − -selective electrode (Niko-Analit, Moscow, Russia).Cl − was assayed by titration with Hg 2+ using a Top Buret H digital burette (Eppendorf, Wesseling-Berzdorf, Germany).

Statistics
Data processing (mean, standard errors) and the production of graphs were performed using Sigma Plot software (version 14.0).Statistical analysis of the data was made by one-way analysis of variance (ANOVA).Statistical calculations were carried out in the Microsoft Excel program (version 2019).Standard errors are given.Different letters indicate significant difference (p-value < 0.05).

Results
3.1.Full-Length Cloning and in Silico Analysis of the Protein SaNPF6.3 We had earlier obtained the partial coding sequence (CDS) of SaNPF6.3 (GenBank ID: MK580125.1),the gene of a nitrate transporter from the halophyte S. altissima, based on the assumed similarity of SaNPF6.3 to the gene of a nitrate transporter from the closely related species S. fruticosa [53].Here, based on the partial CDS of SaNPF6.3,we determined the full-length cDNA of SaNPF6.3 by a rapid amplification of 3 -and 5 -ends of cDNA.The entire coding sequence of SaNPF6.3,1788-bp in size, was cloned into the yeast integrative vector pCHLX [54] and sequenced.The cloned SaNPF6.3sequence contained an open reading frame encoding a protein of 596 aa in size, with a calculated molecular mass of 66.0 kDa.

Functional Complementation of the Yeast Mutant Δynt1 by SaNPF6.3 Expression in the Yeast Cells
Most of the NPF6 members are thought to be nitrate transporters [61].To demon-

Functional Complementation of the Yeast Mutant ∆ynt1 by SaNPF6.3 Expression in the Yeast Cells
Most of the NPF6 members are thought to be nitrate transporters [61].To demonstrate the nitrate transporting function of the SaNPF6.3coding sequence, SaNPF6.3 was expressed in the cells of the knockout mutant strain ∆ynt1 of the methylotrophic yeast H. polymorpha.Growth of ∆ynt1 strain was inhibited on a minimal SD medium containing NO 3 − at concentrations ranging from 0.2 to 5 mM (SD + nitrate media) (Figure 3a).As a positive control for the complementation of the ∆ynt1 mutation, heterologous expression of AtNPF6.3 cloned from A. thaliana was used.Expression of AtNPF6.3 in the mutant yeast cells, as in the earlier study [48], resulted in the recovery of the ∆ynt1 colony growth on the (SD + nitrate) media.When ∆ynt1 cells were transformed with SaNPF6.3, a recovery of the ∆ynt1 growth on the (SD + nitrate) media also occurred (Figure 3a), indicating the involvement of SaNPF6.3 protein in NO 3 − transport.To validate a nitrate transporting function of SaNPF6.3,nitrate absorption by the cells of yeast transformants expressing SaNPF6.3 was studied (Figure 3b).As a positive control, the yeast transformant expressing AtNPF6.3 was used.In these experiments, the yeast cells were grown initially in the medium containing ammonium as the only nitrogen source, and then, nitrate transporting systems were induced by cell transfer to the nitrate medium.The WT yeast cells took up nitrate from the media containing this anion at concentrations of both 0.5 mM and 2 mM.The knockout mutation ∆ynt1 resulted in a sharp decrease in nitrate uptake by the cells compared to WT at both nitrate concentrations, indicating the essential contribution of YNT1 in nitrate absorption by this organism.Expression of SaNPF6.3,like AtNPF6.3, in the mutant strain cells resulted in a recovery of nitrate uptake; the recovery occurred to an even higher level than in WT cells (Figure 3b).The results obtained indicate the ability of SaNPF6.3 to transport nitrate at nitrate concentrations in both high-and low-affinity ranges in the medium.Unfortunately, we were not able to assess the SaNPF6.3chloride transport properties in the experiments with H. polymorpha mutant strain ∆ynt1 expressing SaNPF6.3,presumably because of the endogenic Cl − -transporting activity of yeast cells (Figure S3).
We also examined the effects of substitutions of Thr106 by Ala disrupting phosphorylation and Thr106 by Asp mimicking constitutive phosphorylation on the growth of the yeast transformants as well as the substitution of Tyr358 by His, found in a number of NPF6.3 homologs.However, SaNPF6.3 with the above substitutions complemented the growth defect phenotype of the yeast mutant as effectively as the wild-type SaNPF6.3.
We investigated the localization of SaNPF6.3 in the cells of ∆ynt1 transformants.For this purpose, the GFP coding sequence was fused to the 5 -end of the SaNPF6.3.and cells of the ∆ynt1 mutant strain were transformed with the recombinant gene.At first, the presence of the GFP-SaNPF6.3 protein in cell lysates of the transformants obtained was determined by Western blotting with antibodies to GFP (Figure 4a).There was no band with a calculated molecular mass of 94.1 kDa for the GFP-SaNPF6.3 chimeric protein.However, a band of approximately 110 kDa was observed.The higher molecular mass of the observed band than the calculated molecular mass for GFP-SaNPF6.3 could be explained by an additional phosphorylation and glycosylation of the protein in the yeast heterologous system [62].
Using the approach based on the Western blot analysis, we selected colonies of the yeast transformants with the highest GFP-SaNPF6.3 expression.Confocal laser microscopy of the transformant cells revealed GFP fluorescence as clusters with a dot structure, localized in the cytoplasm and/or vacuoles.(Figure 4b).We did not observe significant GFP fluorescence in the plasma membranes of the transformants.Apparently, in the used heterologous expression system, just a small fraction of the fused GFP-SaNPF6.3 protein reaches the plasma membrane, which is insufficient to see intensive GFP fluorescence in the PM.Nevertheless, it seems that even a relatively small fraction of the transporter that was delivered to the PM provided complementation of the ∆ynt1 growth-defect phenotype and observed nitrate uptake (Figure 3).To validate a nitrate transporting function of SaNPF6.3,nitrate absorption by the cells of yeast transformants expressing SaNPF6.3 was studied (Figure 3b).As a positive control, the yeast transformant expressing AtNPF6.3 was used.In these experiments, the yeast cells were grown initially in the medium containing ammonium as the only nitrogen source, and then, nitrate transporting systems were induced by cell transfer to the nitrate medium.The WT yeast cells took up nitrate from the media containing this anion at concentrations mined by Western blotting with antibodies to GFP (Figure 4a).There was no band with a calculated molecular mass of 94.1 kDa for the GFP-SaNPF6.3 chimeric protein.However, a band of approximately 110 kDa was observed.The higher molecular mass of the observed band than the calculated molecular mass for GFP-SaNPF6.3 could be explained by an additional phosphorylation and glycosylation of the protein in the yeast heterologous system [62].

Quantitative Analysis of SaNPF6.3 Transcripts in S.altissima Organs
We investigated expression of SaNPF6.3 in organs of S. altissima at different stages of plant growth, at different nitrate concentrations in the NS and at different salinities (Figure 5).SaNPF6.3 was expressed in all S. altissima organs tested: roots, stems, leaves and flowers.The expression levels were higher in the roots and stems than in the leaves and flowers (Figure 5a,b).SaNPF6.3 was expressed both at a sufficient supply of nitrate to plants (15 mM NO 3 − ) and under nitrate deficient conditions (0.5 mM NO 3 − ) in the NS (Figure 5b).SaNPF6.3expression in the roots was significantly influenced by NaCl and depended on the NO 3 − concentration in the nutrient solution.The SaNPF6.3 transcript abundance in the roots increased at the low NO 3 − concentration but decreased at the high concentration, when NaCl concentration increased from 0 mM to 750 mM NaCl (Figure 5b), mainly confirming the earlier results [53].In the leaves, SaNPF6.3expression did not change significantly with variations of NaCl or NO 3 − concentrations in the NS.In the stems, SaNPF6.3expression increased with increasing NO 3 − concentration but was not influenced by NaCl concentration in the NS (Figure 5b).
We also examined the dynamics of SaNPF6.3 expression changes in the roots of plants grown in the presence of either low (0.5 mM) or high (15 mM) NO 3 − concentrations, following the additions of NaCl (250 mM), NaNO 2 ( 5 mM) or (NH 4 ) 2 SO 4 (5 mM) to the NS (Figure 5c,d; the final concentrations are indicated).For plants grown at 0.5 mM NO 3 − (Figure 5c), the concentration of KNO 3 was also increased up to 5 mM.The expression of SaNPF6.3 changed most significantly in the roots of plants grown in the NS with low NO 3 − in response to an increase in NO 3 − concentration (Figure 5c).Salt shock also led to increased SaNPF6.3 expression, while nitrite inhibited it.In the roots of plants grown in the NS with 15 mM NO 3 − , the addition of nitrite and, to a lesser extent, NaCl shock, lowered SaNPF6.3 transcript abundance.The transfer of plants grown in the NS containing 15 mM NO 3 − to the NS without NO 3 − led, in general, to decreasing SaNPF6.3expression in the roots (Figure 5e).

Discussion
From the euhalophyte Suaeda altissima, we cloned the coding sequence of the SaNPF6.3gene, homologous to the AtNPF6.3/AtNRT1.1 encoding a dual-affinity nitrate transporter/transceptor in the model plant A. thaliana.The protein SaNPF6.3belongs to

Discussion
From the euhalophyte Suaeda altissima, we cloned the coding sequence of the SaNPF6.3gene, homologous to the AtNPF6.3/AtNRT1.1 encoding a dual-affinity nitrate transporter/ transceptor in the model plant A. thaliana.The protein SaNPF6.3belongs to the large NPF/NRT1/PTR family of transporters, including proteins involved in the transport of nitrate, nitrite, peptides, amino acids, glucosinolates, auxin, ABA and gibberellins [10,13,65].Phylogenetic analysis showed evolutionary relations of SaNPF6.3 to NPF6.3 family proteins (Figure 1) and displayed a larger similarity of SaNPF6.3 to NPF6.3 members from other families of dicotyledonous plants rather than families of monocotyledons.A SaNPF6.3 topological model matched those of the NPF6.3 proteins from other plants, in particular AtNPF6.3(Figure 2b).In silico analysis based on SaNPF6.3multiple sequence alignment with homologous proteins from other plants (Figure 2) revealed that SaNPF6.3 has features inherent in the NRT1/NPF/PTR family of anion transporters.
(1) A conserved threonine residue, Thr106, in the motif RxxT (Figure 2), a putative phosphorylation site, is found at the N-terminus of SaNPF6.3 in TMH3 (Figure 1c).Similar threonine residues are present at equivalent positions in other NPF6.3 transporters.In AtNPF6.3, an equivalent Thr101 was shown to be responsible for switching between a highand a low-affinity AtNPF6.3mode [14,60].The switching was accomplished through alterations in the Thr101 phosphorylation status which was dependent on nitrate availability in the growth medium.At low nitrate concentrations (<1 mM), Thr101 is phosphorylated by CBL-INTERACTING PROTEIN KINASE 23 (CIPK23) and AtNPF6.3operates as a high-affinity transporter.In the range of millimolar nitrate concentrations, Thr101 is dephosphorylated and AtNRT1.1 operates as a low-affinity nitrate transporter [14,60].However, the anion-transporting activities of Zea mays proteins, ZmNPF6.6 and ZmNPF6.4,unlike AtNPF6.3,appear unlikely to be regulated by the phosphorylation status of equivalent threonine residues [26].In ZmNPF6.6, the point mutations Thr104Ala disrupting phosphorylation and Thr104Asp mimicking a phosphorylation event retained the highaffinity nitrate transport activity, although with a lower Km for nitrate.Thr106Ala and Thr106Asp substitutions in chloride-transporting ZmNPF6.4eliminated the saturable curve in chloride uptake, with influx activity becoming linear as external chloride concentrations increased [26].The authors suggested that the transport activity of ZmNPF6.6 and Zm-NPF6.4 changed in a phosphorylation-independent but threonine-dependent manner.We made similar substitutions in the S. altissima protein: Thr106Ala and Thr106Asp.Growth of the mutant yeast strain ∆ynt1 transformed with the modified and unmodified versions of SaNPF6.3 on the minimal SR medium containing nitrate did not differ markedly (data not presented), testifying against the role of a Thr106 phosphorylation status in switching SaNPF6.3affinity to nitrate.
(2) In TMH7 of SaNPF6.3,there is tyrosine residue Tyr358 (Figures 1c and 2), the equivalent position of which is occupied by His in a number of NPF6.3 homologues including AtNPF6.3 [11], ZmNPF6.6 [26] and several others [16].The mutation of His356Ala abolished both high-and low-affinity nitrate transporter activities in AtNPF6.3,suggesting that His356 is required for nitrate binding [15,16].SaNPF6.3 is not the only NPF6.3 transporter containing Tyr at the equivalent positions (Figure 2, Table S3).Tyr was also found in dualaffinity nitrate transporters MtNPF6.8(Tyr350) [27] and OsNPF6.3(Tyr366) [25], as well as in the high-affinity chloride and low-affinity nitrate transporter ZmNPF6.4(Tyr370) [26].In a comparative study of anion transport by ZmNPF6.6 containing His362 and ZmNPF6.4 containing Tyr370, the authors found that in the absence of chloride, ZmNPF6.6 operates as a pH-dependent non-biphasic high-affinity nitrate-specific transporter, while ZmNPF6.4acts as a low-affinity nitrate transporter.In the presence of chloride, ZmNPF6.6 switched to low-affinity, while ZmNPF6.4 to a high-affinity chloride transporter [26].The authors hypothesized that ZmNPF6.4 in planta is likely to be a component of the root chloride uptake system.SaNPF6.3bearing Tyr358 should presumably share more features with ZmNPF6.4 than with ZmNPF6.6 and function more as a transporter of chloride than of nitrate.However, SaNPF6.3 transported nitrate in a test with functional complementation of the yeast mutant ∆ynt1, lacking the only nitrate transporter (Figure 3a,b).(3) Analogs of the conserved residues (Lys165 and Glu476), forming ionic bonds to maintain the AtNPF6.3 in a functional state [15,16], were found in SaNPF6.3(Lys168 and Glu482) (Figure 2).(4) In TMH1 of SaNPF6.3,there is an ExxER motif (EACER) conserved among NPF6.3family members (Figure 2), an analog of which (EAVER) in AtNPF6.3 is involved in proton binding and the coupling of anion and proton transport [15,16].(5) The presence of conserved proline residue between TMH10 and TMH11 was found to be a common property of all examined NPF6.3 homologs including AtNPF6.3 (Pro492) (Figure 2) [15,16].This proline residue is essential for signaling functions of AtNPF6.3 [18].We found an analog of this residue in SaNPF6.3(Pro498) (Figure 2).SaNPF6.3 is likely an ortholog of AtNPF6.3/NRT1.1, a dual-affinity nitrate transporter/transceptor from A. thaliana.The latter assumption is based on several points.(I) The SaNPF6.3 expression occurred under a variety of environmental conditions similar to the expression of the AtNPF6.3, the gene encoding dual-affinity nitrate transporter At-NPF6.3.The expression of SaNPF6.3 was observed under external nitrate concentrations corresponding to both high-and low-affinity modes of the protein operation, as well as in the presence of the reduced nitrogen compounds, ammonium and nitrite ions, at salinization of the medium and without it (Figure 5).The gene was transcribed in the root, stem, leaf and flower; the transcription occurred at different ontogenetic stages (Figure 5).Expression levels were higher in the roots and stems than in the other organs, indicating a particularly important role of SaNPF6.3 in nitrate uptake and transfer.(II) The recovery of H. polymorpha mutant strain ∆ynt1 growth on the minimal SD medium, in the presence of nitrate, when SaNPF6.3 was expressed in the yeast cells, demonstrated clearly the nitrate transport properties of the S. altissima protein (Figure 3a).It should be noted that the nitrate concentrations applied, from 0.2 to 5 mM NO 3 − , covered both high-and low-affinity ranges.The lack of full growth recovery of the ∆ynt1 mutant transformed with SaNPF6.3 may be due to a limited expression of this gene in the heterologous system used.Also, it is possible that only a small fraction of the synthesized SaNPF6.3 protein is delivered to the plasma membrane in the yeast cells, or a rapid degradation of the protein occurred.In line with this assumption, laser confocal microscopy demonstrated that in the mutant yeast cells expressing GFP-SaNPF6.3, the recombinant protein was localized in the cytoplasm and vacuole (Figure 4b).(III) Nitrate uptake by the mutant ∆ynt1 cells expressing SaNPF6.3demonstrated directly a nitrate-transporting function of SaNPF6.3 (Figure 4b).The yeast transformants took up nitrate from the media containing this anion in concentrations of both 0.5 mM and 2.0 mM.(IV) Like AtNPF6.3 [11,66], the induction of SaNPF6.3 expression in response to an increase in nitrate concentration in the NS, when plants are grown at a low nitrate availability (Figure 5c), and the suppression of SaNPF6.3 expression following the plants being transferred from sufficient nitrate supply to nitrate starvation (Figure 5e) support also the participation of SaNPF6.3 in nitrate uptake.The decreased expression of SaNPF6.3 in response to a nitrite addition at low nitrate availability (Figure 4c) may be the result of an increased fraction of reduced nitrogen compounds in the cells during nitrate assimilation, which inhibits SaNPF6.3expression by the feedback.
It is possible that SaNPF6.3mediates a low-affinity transport of chloride ions in addition to the dual-affinity transport of nitrate.The involvement of SaNPF6.3 in a lowaffinity chloride transport is supported by increasing expression of the transporter gene in the response to NaCl addition to the NS.The stimulation of SaNPF6.3 expression by NaCl in the presence of 0.5 mM nitrate observed at both the long-term salinity and under the salt shock conditions suggests the involvement of the transporter in the transport of chloride.S. altissima, like other salt-accumulating halophytes, absorbs chloride in large quantities as a counter-ion for Na + passively entering the root cells.Further root-to-shoot translocation of Cl − and Na + , which play a role of 'cheap' osmotic compounds, contributes to maintaining the water potential gradient in the soil-root-shoot system [43,67,68].Another possible reason for the stimulation of SaNPF6.3 expression in response to increasing NaCl

Figure 1 .
Figure 1.Phylogenetic analyses for plant NPF/NRT1/PTR family nitrate transporters (a,b) and SaNPF6.3 and AtNPF6.3membrane topology (c).The phylogenetic trees (a,b) were built in the MEGA 11 using the maximum likelihood method based on the Jones-Taylor-Thornton model.The number of bootstrap replicates was 1000; the values of bootstrap support are indicated near the nodes.Scale: 0.2 (a) and 0.2 (b) substitutions per site.The protein sequences were taken from NCBI, UniProtKB and Salicornia DB.Names of plant objects and protein IDs are given in the Tables S2 and S3.The membrane topology of SaNPF6.3(c) was predicted by DeepTMHMM software (version 1.0.24,https://dtu.biolib.com/DeepTMHMM;accessed on 26 September 2023).For comparison, AtNPF6.3topology predicted by the same software is given.

Figure 1 .
Figure 1.Phylogenetic analyses for plant NPF/NRT1/PTR family nitrate transporters (a,b) and SaNPF6.3 and AtNPF6.3membrane topology (c).The phylogenetic trees (a,b) were built in the MEGA 11 using the maximum likelihood method based on the Jones-Taylor-Thornton model.The number of bootstrap replicates was 1000; the values of bootstrap support are indicated near the nodes.Scale: 0.2 (a) and 0.2 (b) substitutions per site.The protein sequences were taken from NCBI, UniProtKB and Salicornia DB.Names of plant objects and protein IDs are given in the Tables S2 and S3.The membrane topology of SaNPF6.3(c) was predicted by DeepTMHMM software (version 1.0.24,https://dtu.biolib.com/DeepTMHMM;accessed on 26 September 2023).For comparison, AtNPF6.3topology predicted by the same software is given.

Figure 3 .
Figure 3. Complementation of growth and nitrate absorption defects of the yeast mutant strain Δynt1 by expression of SaNPF6.3 gene in the mutant cells.(a) Growth of the yeast mutant cells expressing SaNPF6.3 on an agarized minimal SD media (0.17% yeast nitrogen base without amino acids and sulphate ammonium, 2% dextrose) containing NaNO3 in concentrations ranged from 0.2 to 5 mM.Approximately 10 5 of the yeast cells were plated on the agarized selective media.The yeast colonies grew for 3 days at 37 °C.(b) Nitrate absorption from the liquid minimal SD media, containing NaNO3 in concentrations 0.5 or 2 mM, by the yeast mutant Δynt1 transformed with the SaNPF6.3gene; the initial wet weight of the yeast suspension was 10 mg/mL.The yeast cells grew in the liquid media for 18 h at 37 °C.Controls: wild-type DL-1 strain and the mutant Δynt1 strain, transformed with vectors pCHLX and pCCUR2, and the mutant Δynt1 strain transformed with pCHLX-AtNPF6.3and pCCUR2.Different letters indicate significant difference (p-value < 0.05).

Figure 3 .
Figure 3. Complementation of growth and nitrate absorption defects of the yeast mutant strain ∆ynt1 by expression of SaNPF6.3 gene in the mutant cells.(a) Growth of the yeast mutant cells expressing SaNPF6.3 on an agarized minimal SD media (0.17% yeast nitrogen base without amino acids and sulphate ammonium, 2% dextrose) containing NaNO 3 in concentrations ranged from 0.2 to 5 mM.Approximately 10 5 of the yeast cells were plated on the agarized selective media.The yeast colonies grew for 3 days at 37 • C. (b) Nitrate absorption from the liquid minimal SD media, containing NaNO 3 in concentrations 0.5 or 2 mM, by the yeast mutant ∆ynt1 transformed with the SaNPF6.3gene; the initial wet weight of the yeast suspension was 10 mg/mL.The yeast cells grew in the liquid media for 18 h at 37 • C. Controls: wild-type DL-1 strain and the mutant ∆ynt1 strain, transformed with vectors pCHLX and pCCUR2, and the mutant ∆ynt1 strain transformed with pCHLX-AtNPF6.3and pCCUR2.Different letters indicate significant difference (p-value < 0.05).

Figure 5 .
Figure 5. Relative abundance of SaNPF6.3 transcripts in S. altissima plants.(a) SaNPF6.3expression in different organs and at different stages of the plant growth.(b) SaNPF6.3expression in roots, stems and leaves at different NaCl concentrations in NS, at the background of either low (0.5 mM) or high (15 mM) nitrate availability.(c) Dynamics of SaNPF6.3 expression in roots of plants grown under conditions of low nitrate availability, following addition to the nutrient solution of 250 mM NaCl, 5 mM KNO2, 5 mM (NH4)2SO4) or adjustment of KNO3 concentration up to 5 mM.(d) Dynamics of SaNPF6.3 expression in roots of plants grown under conditions of high nitrate availability, following addition to NS of 250 mM NaCl, 5 mM KNO2 or 5 mM (NH4)2SO4.(e) Dynamics of SaNPF6.3 expression in roots of plants grown under conditions of high nitrate availability, following the transfer of the plants to the same medium but without nitrate.Data shown are mean ± SD from three independent experiments.Bars with different letters are significantly different at p < 0.05.The results were deduced from three biological replicates and each of them was performed in three analytical replicates.

Figure 5 .
Figure 5. Relative abundance of SaNPF6.3 transcripts in S. altissima plants.(a) SaNPF6.3expression in different organs and at different stages of the plant growth.(b) SaNPF6.3expression in roots, stems and leaves at different NaCl concentrations in NS, at the background of either low (0.5 mM) or high (15 mM) nitrate availability.(c) Dynamics of SaNPF6.3 expression in roots of plants grown under conditions of low nitrate availability, following addition to the nutrient solution of 250 mM NaCl, 5 mM KNO 2 , 5 mM (NH 4 ) 2 SO 4 ) or adjustment of KNO 3 concentration up to 5 mM.(d) Dynamics of SaNPF6.3 expression in roots of plants grown under conditions of high nitrate availability, following addition to NS of 250 mM NaCl, 5 mM KNO 2 or 5 mM (NH 4 ) 2 SO 4 .(e) Dynamics of SaNPF6.3 expression in roots of plants grown under conditions of high nitrate availability, following the transfer of the plants to the same medium but without nitrate.Data shown are mean ± SD from three independent experiments.Bars with different letters are significantly different at p < 0.05.The results were deduced from three biological replicates and each of them was performed in three analytical replicates.

3. 4 . 24 Figure 6 .
Figure 6.Concentrations of NO3 − and Cl − in xylem exudate of S. altissima as functions of these anion concentrations in the nutrient solutions.(a) Dependence of NO3 − concentration in xylem exudate on NO3 − concentration in NS.(b) Dependence of Cl⁻ concentration in xylem exudate on Cl − concentration in NS.(c) The same as (b), but the dependence is presented in a smaller range of the external concentrations.Cl⁻ concentrations are indicated in the medium along abscissa and in the xylem exudate along ordinate.

Figure 6 .
Figure 6.Concentrations of NO 3 − and Cl − in xylem exudate of S. altissima as functions of these anion concentrations in the nutrient solutions.(a) Dependence of NO 3 − concentration in xylem exudate on NO 3 − concentration in NS.(b) Dependence of Cl − concentration in xylem exudate on Cl − concentration in NS.(c) The same as (b), but the dependence is presented in a smaller range of the external concentrations.Cl − concentrations are indicated in the medium along abscissa and in the xylem exudate along ordinate.