ABC Transport Is Inactivated by the PTSNtr under Potassium Limitation in Rhizobium leguminosarum 3841

PTSNtr is a regulatory phosphotransferase system in many bacteria. Mutation of the PTSNtr enzymes causes pleiotropic growth phenotypes, dry colony morphology and a posttranslational inactivation of ABC transporters in Rhizobium leguminosarum 3841. The PTSNtr proteins EINtr and 2 copies of EIIANtr have been described previously. Here we identify the intermediate phosphocarrier protein NPr and show its phosphorylation by EINtr in vitro. Furthermore we demonstrate that phosphorylation of EINtr and NPr is required for ABC transport activation and that the N-terminal GAF domain of EINtr is not required for autophosphorylation. Previous studies have shown that non-phosphorylated EIIANtr is able to modulate the transcriptional activation of the high affinity potassium transporter KdpABC. In R. leguminosarum 3841 kdpABC expression strictly depends on EIIANtr. Here we demonstrate that under strong potassium limitation ABC transport is inactivated, presumably by non-phosphorylated EIIANtr. This is to our knowledge the first report where PTSNtr dictates an essential cellular function. This is achieved by the inverse regulation of two important ATP dependent transporter classes.


Introduction
Rhizobia are proteobacteria that are best known for their ability to enter a nitrogen fixing symbiosis with legume plants. After an exchange of signaling compounds rhizobia enter the appropriate host plant root in general via plant derived infection threads [1]. These infection threads grow into the root cortex towards a newly induced meristem that forms the basis for a newly developing root structure called a nodule [2]. Inside the nodule the plant cells greatly enlarge and their cytosol fills up with infection thread derived symbiosomes [3]. Symbiosomes are surrounded by a plant derived membrane and contain rhizobia. Inside these symbiosomes rhizobia transform into nitrogen fixing bacteroids. Bacteroids are greatly dependent on plant derived compounds and are therefore considered as plant organelles, called ammoniaplasts [4]. Exchange of molecules requires transport across two membranes, the bacteroid-and the symbiosome membrane. Rhizobia undergo dramatic changes in their lifestyle by turning from an oligotrophic soil bacterium into an intracellular plant symbiont [5].
Rhizobia are also known to be especially rich in ATP binding cassette dependent transporters, so called ABC transporters [6]. ABC transporters are widely spread in all kingdoms of life and have high affinities for the solutes they transport. The Rhizobium leguminosarum 3841 genome sequence contains 269 genes encoding for ATP binding cassettes, which are characteristic for ABC transporters. Together with additional permease-and solute binding proteins, they are thought to make up more than 180 individual ABC transport systems that are largely uncharacterized. This high number of ABC systems probably reflects the requirements of a soil dwelling bacterium competing in a nutrient poor environment. In a systematic approach in Sinorhizobium meliloti 1021 it has been shown that a large fraction of the ABC transport systems can be specifically induced, presumably by the solutes they transport [6]. In R. leguminosarum 3841 it has also been demonstrated that a large number of ABC systems are generally expressed [7,8]. Very recently it has been shown that ABC transport can be regulated post-transcriptionally [9,10].
One of these regulatory circuits involves the PTS Ntr . Phosphotransferase systems (PTS) are known since more than 50 years. The first PTS was described in E. coli as a phosphorylation cascade that transfers phosphate from phosphoenolpyruvate (PEP) to incoming sugars [11]. PTS systems are made up of a core set of three enzyms: Enzyme I (EI), histidine protein (HPr) and Enzyme IIA (EIIA). EI autophosphorylates on a conserved histidine residue in the presence of PEP. This phosphate is then transferred to a conserved histidine on the phosphocarrier protein HPr, which finally phosphorylates the EIIA component, also on a conserved histidine residue. Multiple EIIA components in E. coli interact with multiple EIIBC(D) transport complexes which facilitate uptake and phosphorylation mainly of incoming sugar compounds.
More recently an EIIA homologue (PtsN) was discovered within the rpoN operon in E. coli [12] which also contains an HPr homologue named NPr [13]. A homologous EI component (EI Ntr or PtsP) was later identified [14], which completed the paralogous PTS Ntr system. PTS Ntr does not interact with PTS transport complexes and was named after its presence in the rpoN operon and its probable involvement in regulation of nitrogen (Ntr) metabolism. The PTS Ntr components are specifically named EI Ntr (or PtsP), NPr (or PtsO) and EIIA Ntr (or PtsN). EI Ntr contains an N-terminal GAF domain of 180 aa which separates it from EI proteins of the transport PTS. PTS Ntr is widely distributed in bacteria and it has been suggested that transport PTS components are rather an exception than the rule [15]. In R. leguminosarum 3841 and all other rhizobia sequenced so far PTS transport components are lacking but PTS Ntr components are present [16].
The main functions of PTS Ntr are still largely unknown, although mutants display pleiotropic phenotypes. In recent years, the E. coli PTS Ntr has been linked to potassium homeostasis, because non-phosphorylated PtsN inhibits the low affinity K + transporter Trk via protein-protein interaction with TrkA [17] and at the same time transcriptionally activates the high affinity K + transporter KdpFABC via protein-protein interaction with KdpD, a sensor kinase that acts via the response regulator KdpE [18]. Additionally, non-phosphorylated PtsN also activates the Pho regulon, responsible for phosphate acquisition, via protein-protein interaction with the master regulator PhoR in E. coli [19].
In other bacteria PTS Ntr mutants have exhibited a wide range of diverse phenotypes [20]. These phenotypes are often related to carbon metabolism and protein-protein interactions with central metabolic enzymes have been described very recently [21,22]. PTS Ntr mutants were also investigated in rhizobia. In Sinorhizobium meliloti 1021 PTS mutants were linked to succinate mediated catabolite repression (SMCR) [23,24], in R. etli a ptsN mutant showed reduced growth on dicarboxylates, reduced melanin production and nifH induction [25] and in Bradyrhizobium japonicum I110 a ptsP mutant showed strongly reduced oligopeptide uptake [26].
We have recently demonstrated that PtsP and two copies of PtsN are required for the full activation of a wide range of ABC transporters in R. leguminosarum 3841 [10]. We also showed that PtsN, presumably in its non-phosphorylated form, interacts with KdpD, the sensor kinase that transcriptionally activates the high affinity K + transporter KdpABC via the response regulator KdpE, identically to the situation in E. coli.
Here we identify the missing phosphocarrier protein NPr of the PTS Ntr in Rlv3841 and characterise critical components of the phosphorylation cascade. We also demonstrate that under potassium limitation the phosphorylation state of PTS Ntr dictates the activity of two essential ATP dependent transporter classes. This is to our knowledge the first report of an essential regulation mediated by PTS Ntr .

NPr Candidates in Rhizobium leguminosarum 3841
We have recently described the PTS Ntr phosphorylation cascade in R. leguminosarum 3841 and its role in the activation of ABC transport and regulation of high affinity K + uptake [10]. EI Ntr and two copies of EIIA Ntr are part of this phospho relay and linked by phenotypes, but the intermediate NPr has not been identified. An inspection of the Rlv3841 genome produced two possible candidate genes, RL0032 and RL2903, which are annotated as putative phosphocarrier proteins. RL0032 shows 37% and 33% identity to NPr and HPr from E. coli K12, while RL2903 has 28% and 31% identity, respectively. RL0032 is the last gene in a possible operon that is conserved in many bacteria [24,35,36] and involved in SMCR in Sinorhizobium meliloti 1021 [23]. Upstream of RL0032 is a gene coding for a protein with homology to the Nterminus of EIIA Man , a mannose PTS component, and further upstream is a gene coding for a putative HPr kinase (HprK). Mutants in those genes in S. meliloti 1021 are all linked to SMCR and carbon metabolism, but also to cobalt requirements, succinoglycan production and symbiotic performance [23,24]. The authors describe a possible PTS in S. meliloti starting with the phosphorylation of histidine 22 of HPr by EI Ntr . The final phosphorylation acceptor of this cascade is probably EIIA Man . The second npr candidate, RL2903, is part of a dihydroxy acetone PTS which is likely functional in rhizobia [37].

RL0032 is NPr, the Missing link in the PTS Ntr Phosphorylation Cascade
We mutated RL0032 by replacing the gene with an VTet marker cassette creating strain AA015 (DRL0032). AA015 grew well on TY medium and displayed a dry colony morphology identical to PtsP107 (ptsP::Tn5). We also replaced RL2903, the second phosphocarrier protein candidate gene, with an VSpec cassette, creating strain AA006 (DRL2903) and the double mutant AA016 (DRL0032; DRL2903). Strain AA006 formed mucoid colonies comparable to wild type Rlv3841 and AA016 formed dry colonies identical to AA015 (DRL0032) and PtsP107 (ptsP::Tn5). This clearly links RL0032 by phenotype to PTS Ntr mutants and we therefore tentatively named RL0032: NPr and the AA015 (DRL0032) mutant: AA015 (Dnpr).
The colony morphology and ABC transport phenotypes of the npr (RL0032) mutant AA015 are very similar to the phenotypes of the other PTS Ntr mutants, which suggests that NPr is the missing phosphocarrier protein which should be phosphorylatable by EI Ntr (PtsP).

EI Ntr (PtsP) Autophosphorylates with PEP and Phosphorylates NPr in vitro
To test the hypothesis that EI Ntr (PtsP) can phosphorylate NPr in vitro we purified His-tagged versions of both proteins. 6His-PtsP and 6His-GST-PtsP fusions were not soluble in E. coli BL21 DE3+ cells in sufficient amounts, but 6His-MBP-PtsP (130 kD) and 6His-NPr (10 kD) could be purified using Ni-IDA affinity purification. Both purified proteins showed only very minor contaminations.
6His-MBP-PtsP rapidly autophosphorylated when 33 PEP was added to the assay ( Fig. 2A). This phosphorylation was heat stable at 70uC for 10 min and did not occur when 6His-MBP-PtsP was inactivated by boiling before the reaction start (Fig. 2B). The histidine phosphorylation of the smaller HPr protein of Bacillus subtilis is instable under those conditions [38]. Phosphorylation of 6His-MBP-PtsP did not occur when 33 ATP was used (Fig. 2B). The addition of protein crude extract of the Rlv3841 asparto kinase mutant RU4392 (Dask; [10]) and 33 ATP did also not result in phosphorylation, even though this was reported for purified GST-PtsP protein from B. japonicum I110 [26].

EI Ntr (PtsP) Requires Histidine 367 for ABC Transport Activation, but Autophosphorylation is Probably not Dependent on its GAF Domain
Since we demonstrated that EI Ntr (PtsP) phosphorylates NPr in vitro, we wanted to test which functional properties of EI Ntr (PtsP) are necessary to enable the phosphorylation cascade in vivo. EI Ntr (PtsP) is a multi domain protein with an N-terminal GAF domain and several PEP utilizing domains, including a central domain that contains histidine 367, which is the conserved residue for autophosphorylation with PEP. GAF domains are well known as regulatory small ligand binding domains [20] and they are characteristic for EI Ntr proteins in comparison to EI enzymes of PTS sugar transport systems [14]. The EI Ntr GAF domain is thought to be the regulatory input domain of the phosphorylation cascade, but possible ligands are so far unknown [20]. We have previously shown that we can complement the ptsP mutant PtsP107 in trans, expressing ptsP from the E. coli lacZ promoter on a low copy plasmid pRK415 (pLMB151; [10]). To verify the role of the histidine 367 residue and the GAF domain we constructed two pRK415 derivatives expressing a PtsP with histidine 367 replaced by an alanine (pAA003; PtsPH367A) and a PtsP lacking the N-terminal GAF domain (pAA001; PtsPDGAF). Both plasmids were introduced into the ptsP mutant PtsP107, forming strains PtsP107+PtsPH367A and PtsP107+PtsPDGAF, and were compared to the fully complemented strain (Pts107+PtsP) and an empty vector control (PtsP107+EV). Colonies of Pts107+PtsP and PtsP107+PtsPDGAF showed a surface phenotype identical to wild type Rlv3841. In contrast PtsP107+EV and PtsP107+PtsPH367A looked identical to PtsP107. To further analyse the changes in phenotype we assayed the complemented strains for AIB uptake (Fig. 3). Strains Rlv3841 and Pts107+PtsP showed comparable rates of AIB transport of ,14 nmol min 21 mg protein 21 , while PtsP107, PtsP107+EV and PtsP107+PtsPH367A showed severely reduced transport rates. Interestingly, we measured a small but significant reduction of AIB transport (p,0.001; n = 6) in the PtsP107+PtsPDGAF compared to the fully complemented PtsP107+PtsP strain. Very similar results were obtained when glucose uptake was quantified (data not shown). These results demonstrate that the conserved phosphorylation site histidine 367 of EI Ntr (PtsP) is necessary for ABC transport activation and that a GAF truncated version of PtsP is able to sufficiently activate the PTS Ntr phosphorylation cascade and therefore ABC transport. To further clarify the role of the GAF domain, autophosphorylation of purified GAF truncated PtsP protein needs to be tested in vitro.

NPr Requires Histidine 17 for ABC Transport Activation
Since phosphorylation of PtsP is essential for ABC transport activation, we also wanted to verify that this is true for NPr. NPr contains a conserved histidine at position 17 which is the proposed site of phosphorylation by PtsP. To test the influence of the histidine 17 phosphorylation site we cloned a wild type NPr and a NPrH17A variant into pRK415 to complement an NPr mutant in Rlv3841. For that we first had to replace the VTet marker of AA015 (Dnpr) by an VSpec marker resulting in strain AA031 (Dnpr). AA015 and AA031 exhibited indistinguishable surface and transport phenotypes (data not shown). AA031 (Dnpr) was complemented with NPr (pAA038) and NPrH17A (pAA039) and the empty vector (EV). Complementation with NPr restored the mucoid Rlv3841 surface phenotype, while NPrH17A and the EV produced dry colonies in the AA031 background. Additionally, AIB transport rates of Rlv3841+EV and AA031+NPr were at WT level of ,14 nmol/min/mg protein (Fig. 4), while AA031+NPrH17A and AA031+EV transported with strongly reduced rates comparable to PtsP107+EV (compare to Fig. 3).
We therefore conclude that H17 phosphorylation of NPr is required for ABC transport activation.

ABC Transport Activity is Reduced under K + Limitation
It has previously been shown in E. coli that non-phosphorylated PtsN (EIIA Ntr ) activates the ATP dependent high affinity K + transporter KdpFABC (which is not an ABC transporter) via the stimulation of phosphorylation of the two component transcriptional regulator KdpDE [18]. We have recently demonstrated in R. leguminosarum 3841 that a kdpA mutant shows the same severe growth defects in medium with limiting K + levels (#10 mM KCl) as a ptsN1/N2 double mutant, indicating that PtsN is essential for Kdp activation. In contrast, wild type and a ptsP mutant, which cannot phosphorylate PtsN, grow equally well down to levels of 1 mM KCl [10] indicating that non-phosphorylated PtsN is required for kdpABC expression and therefore activation. Consistent with that, we have shown that kdpAB expression is up regulated in a ptsP mutant and that PtsN1 and PtsN2 can both physically interact with KdpD. Altogether these results demonstrate that as in E. coli non-phosphorylated PtsN is required for full kdpABC transcription and high affinity K + transport. However, in contrast to E. coli, where kdpFABC transcription is only modulated by PtsN dependent on an unknown signal, in R. leguminosarum 3841 K + transport via KdpABC is completely dependent on the presence of PtsN, presumably in its non-phosphorylated form, at growth limiting K + levels.
This allows us to make the following prediction: If nonphosphorylated PtsN is required for growth of wild type Rlv3841 at limiting K + levels (#10 mM KCl), ABC transport rates should be reduced under those conditions.
To test this, we grew Rlv3841 in AMS with normal and limiting K + levels (1 mM and 1 mM KCl, resp.) and compared AIB transport rates to those of the ptsP mutant PtsP107 (Fig. 5A). Rlv3841 grown at 1 mM KCl transported AIB at normal rates (,17 nmol/min/mg protein). At limiting K + levels transport of K + via KdpABC is essential for growth and its transcriptional activation is dependent on the presence of non-phosphorylated PtsN. When Rlv3841 was grown at 1 mM K + , AIB transport rates dropped to the levels present in a ptsP mutant (,5 nmol/min/mg protein), where PtsN cannot be phosphorylated via EI Ntr (PtsP) and Npr. This shows that under K + limitation, ABC transport is inactivated to an extent similar to that in a ptsP mutant. From that result we also expected that Rlv3841 would show difficulties to grow on AMS Glc/Glu medium when potassium is limiting, because glutamate transport is dependent on the ABC transport systems Aap and Bra, while NH 4 + transport is independent from ATP dependent transport systems. Therefore we determined generation times of Rlv3841 grown on AMS Glc/ NH 4 Cl compared to AMS Glc/Glu at non-limiting potassium levels (1 mM KCl) compared to limiting levels (1 mM KCl). Generation times of Rlv3841 are very similar (,4h) when grown on AMS Glc/NH 4 Cl compared to AMS Glc/Glu at 1 mM KCl ( Fig. 5B and [10]). When grown at strong potassium limitation (1 mM KCl) generation times markedly increased ( Fig. 5B and [10]) and this increase was significantly stronger when grown in AMS Glc/Glu (p = 0.009; n = 3 independent experiments with each 2 independent cultures).

Discussion
We have recently identified the EI Ntr and two EIIA Ntr proteins of the PTS Ntr of R. leguminosarum 3841 [10]. EI Ntr and EIIA Ntr   Regulation by PTSNtr in Rhizobium leguminosarum PLOS ONE | www.plosone.org mutants exhibit similar dry surface phenotypes and showed reduced activities of a range of ABC transporters. We suspected that the dry surface is a result of reduced EPS secretion which is likely facilitated via a yet uncharacterised ABC exporter [10,39]. Additionally it was demonstrated that EIIA Ntr , presumably in its non-phosphorylated form, is required for the activation of the high affinity potassium transporter KdpABC and therefore essential for growth on limiting potassium levels. The intermediate HPr homologue of the PTS Ntr phosphorylation cascade was left unidentified.
Here we first identify the missing intermediate phosphocarrier protein NPr that connects the phosphorylation from EI Ntr (PtsP) to EIIA Ntr (PtsN). The npr gene (RL0032) is in R. leguminosarum 3841 not located within the rpoN operon together with ptsN (EIIA Ntr ) as in many other bacterial genomes [20]. In contrast, npr is located within another conserved operon downstream of the two component regulator genes chvI and chvG, a putative hprK gene and a manX homologue which encodes a protein with homologies to EIIA Man proteins. The conservation of this operon has been mentioned previously [24,35,36], and seems to be restricted to aproteobacteria [35]. But it remains to be determined whether the absence of npr (usually named ptsO) within the rpoN operon is strictly linked to the presence of the chvIG, hprK, manX, npr operon. In B. melitensis it has been suggested and demonstrated by RT-PCR that this operon is co-transcribed from a single chvI promoter [21], although the operon structure in R. leguminosarum 3841 and related species allows sufficient space for a manX promoter downstream of hprK. The NPr homologue in S. meliloti 1021 is named HPr [23,24].
The Rlv3841 npr mutants AA015 (npr::VTet) and AA031 (npr::VSpec) exhibit identical surface and transport phenotypes to the ptsP::Tn5 (PtsP107) mutant ( Fig. 1 and 4). Additionally, purified 6His-MBP-PtsP was able to phosphorylate 6His-NPr in vitro (Fig. 2C). This transphosphorylation was also recently demonstrated for the PtsP and NPr homologues of B. melitensis [21]. In this study it was additionally shown that NPr is able to phosphorylate EIIA Ntr as well as EIIA Man . We assume this is also likely the case for the homologous Rlv3841 and S. meliloti 1021 proteins, because a phenotypical link between NPr (called Hpr in the following citation) and EIIA Man (ManX) was also made in Rm1021 [23]. In that study phenotypes of NPr and EIIA Man mutants were linked to SMCR and carbon metabolism. In the next study of this group [24] HprK was also shown to be involved in the regulation of SMCR. The mechanism of this regulation is still largely unknown but it is mediated via a conserved serine residue of NPr, similar to the regulation of carbon catabolite repression in firmicutes [40]. This conserved serine (S48) is also present in the NPr of R. leguminosarum 3841and suggests a second level of PTS Ntr regulation involving carbon metabolism. An interaction of EIIA Ntr (PtsN) with pyruvate dehydrogenase has recently been demonstrated in P. putida [22] and an interaction of EIIA Man (ManX) with a-ketoglutarate dehydrogenase is likely to occur in B. melitensis [21]. A general regulation of central carbon metabolism seems likely.
After the identification of NPr we show direct mechanistic evidence that phosphorylation of the PTS Ntr proteins is required for ABC transport activation in Rlv3841. Non-phosphorylatable versions of ptsP (PtsPH367A) and npr (NPrH17A) are not able to activate AIB (and glucose) transport above the levels of the respective mutants ( Fig. 3 and 4). It was crucial to demonstrate this because these results are in contrast to a previous result presented in Prell et al. 2012, where a non-phosphorylatable version of EIIA Ntr (PtsN1H66A) was able to restore AIB transport almost to wild type levels in an EIIA Ntr double mutant background (LMB272) when expressed from the lacZ promoter of the mid-copy number plasmid pBBR-MCS5. In this study we concluded that non-phosphorylated PtsN must be a weak activator of AIB transport and that a complementation needs to be repeated with reduced copy numbers of PtsN1H66A to make final conclusions. The level of PtsN protein and its relative degree of phosphorylation seems to be absolutely crucial for its function in a physiological context. This is in agreement with recent results in E. coli where non-phosphorylatable PtsN is required to activate PhoR [19]. However, in a physiological condition where E. coli PtsN is shown to be fully phosphorylated [41], both phosphorylatable and non-phosphorylatable PtsN versions were equally able to activate PhoR mediated transcriptional responses when expressed from a plasmid [19]. This clearly shows that absolute levels and relative degree of phosphorylation are essential for PtsN function.
After we show the importance of phosphorylation of the PTS Ntr proteins we also demonstrate that the N-terminal EI Ntr GAF domain is dispensable for ABC transport activation (Fig. 3). We suspect the GAF domain must have a negative regulatory function in the control of EI Ntr phosphorylation, because its removal still allows significant ABC transport activation which is dependent on phosphorylation of the PTS Ntr cascade. In a physiological context, e.g. under potassium limitation, when growth is dependent on kdpABC expression and PtsN should be predominantly nonphosphorylated, the cell must either be depleted in PEP levels or an unknown ligand must bind to the EI Ntr GAF domain and prevent EI Ntr and therefore NPr and EIIA Ntr phosphorylation. We believe that PEP depletion is an unlikely condition, because growth on glucose is not limited in PTS Ntr mutants [10]. We instead predict that a ligand, either building up or depleting under limiting K + conditions, might control EI Ntr autophosphorylation or NPr transphosphorylation. The nature of that ligand might reflect the adenylate charge of the cell as already discussed in Prell et al. 2012, because in R. leguminosarum two ATP dependent transporter classes, ABC transport and KdpABC, are both regulated by PTS Ntr . Such a ligand has so far not been identified [20], although a wide range of obvious candidates were tested with the E. coli EI Ntr [42]. However, the situation in an aproteobacterium might be different from E. coli.
Furthermore, if under conditions of potassium limitation EIIA Ntr phosphorylation is strongly reduced, this should also result in reduced ABC transport activation. We could indeed demonstrate that AIB transport in Rlv3841 was reduced to ptsP mutant levels when potassium concentrations were at 1 mM in the growth medium (Fig. 5A) and that this also caused reduced growth rates when glutamate instead of ammonium was the sole nitrogen source for growth (Fig. 5B). This is a remarkable result, because it shows to our knowledge for the first time a physiological condition, essentially K + limitation, where signaling through the PTS Ntr phosphorylation cascade to PtsN dictates an essential cellular function, namely K + homeostasis. And this is achieved through the strict regulation of two ATP dependent transporter classes. Under potassium limitation where potassium acquisition via the ATP dependent high affinity KdpABC system is essential to maintain intracellular potassium levels for growth, ATP dependent ABC transport is limited. This probably makes sense in a soil dwelling bacterium that is constitutively expressing a high number of ABC transport systems to acquire nutrients in an oligotrophic environment [7,8]. Under K + limitation such energy consuming efforts are shifted to K + homeostasis as the primary need of the cell. In an enterobacterium such as E. coli, which probably rarely faces K + limitation and facilitates transport primarily via PTS systems, PTS Ntr regulation might have only evolved into modulatory roles, e.g. modulation of K + uptake and PO 4 32 acquisition.

Bacterial Growth and Media
The bacterial strains, plasmids and primers used in this study are detailed in Table 1. Rhizobium strains were grown at 28uC in either Tryptone Yeast extract (TY) [27] or acid minimal salts medium (AMS) [28] with 10 mM D-glucose as carbon source and 10 mM NH 4 Cl or 10 mM sodium glutamate as nitrogen sources. In cultures grown in AMS medium with defined potassium levels, K 2 HPO 4 was replaced by Na 2 HPO 4 and KCl added to appropriate concentrations. Antibiotics were used at the following concentrations ( mg ml 21 ): streptomycin (Str), 500; neomycin (Nm), 80; tetracycline (Tet), 5; gentamicin (Gm), 20; ampicillin (Amp) 100 and spectinomycin (Spec), 100.

Mutant and Plasmid Construction
The npr (RL0032) mutant AA015 was isolated as follows. The npr gene was amplified with flanking DNA using primers P1nprforBam/P2nprrevXba (Tab. 1) and Phusion DNA polymerase (Finnzymes Thermo). The resulting PCR product was cloned into pJET1.2 (Fermentas Thermo) following the manufacturer's instructions. An inverse PCR with primers P3nprforinvSac/ P4nprrevinvSac was performed to amplify the vector lacking npr. The resulting PCR product was digested with Ecl136II and a SmaI digested VTet cassette [29] was inserted. From that construct a BamHI/XbaI fragment was cloned into pJQ200SK to form pAA019. Strain AA015 (npr::VTet) was generated in the Rlv3841 wild type background by selecting for recombination using the sac mutagenesis strategy as previously described [30]. Strain AA015 was verified by PCR using primers P1nprforBam/ P2nprrevXba confirming that the 2.3 kb wild type fragment was replaced by a 4 kb fragment. The npr mutant AA031 was isolated in the same way, but by inserting a SmaI digested VSpec cassette [29].
The RL2904 mutant AA006 was isolated as follows. The RL2904 gene was amplified with flanking DNA using primers P1RL2903forXho/P2RL2903frevXba and Phusion DNA polymerase. The resulting PCR product was cloned into pJET1.2 following the manufacturer's instructions. An inverse PCR with primers P3RL2903forinvEco/P4RL2903revinvEco was performed to amplify the vector lacking RL2904. The resulting PCR product was digested with EcoRV and a SmaI digested VSpec cassette [29] was inserted. From that construct an XhoI/XbaI fragment was cloned into pJQ200SK to form pAA006. Strain AA006 (RL2903::VSpec) was generated in the Rlv3841 wild type background by selecting for recombination using the sac mutagenesis strategy as previously described [30]. Strain AA006 was verified by PCR using primers P1RL2903forXho/ P2RL2903frevXba confirming that the 2.3 kb wild type fragment was replaced by a 4 kb fragment.
The complementing plasmids pAA001 and pAA003 were cloned in the following way. The ptsP ORF was amplified using primers ptsPforHind/ptsPrevXba and Phusion DNA polymerase. The resulting PCR product was cloned into pJET1.2 following the manufacturer's instructions. An inverse PCR with primers ptsP-GAFforSpe/ptsP-GAFrevSpe was performed to amplify the vector lacking the ptsP GAF domain (aa 24-160). The resulting PCR product was digested with SpeI and religated. An XbaI/HindIII fragment was then cloned into pRK415 [31] forming pAA001. A second inverse PCR with primers ptsPH367Afor/ptsPH367Arev was performed and digested with DpnI. After transformation a clone was identified by sequencing with the H367A mutation and an XbaI/HindIII fragment was then cloned into pRK415 forming pAA003.
The complementing plasmids pAA038 and pAA039 were cloned in the following way. The npr (RL0032) ORF was amplified using primers nprcompforHind/nprcomprevXba and Phusion DNA polymerase. The resulting PCR product was cloned into pJET1.2. An XbaI/HindIII fragment was then cloned into pRK415 forming pAA038. An inverse PCR with primers nprH17Afor/nprH17Arev was performed using pJET1.2 carrying npr as a template to generate the H17A mutant variant of npr. This was cloned as an XbaI/HindIII fragment into pRK415 forming pAA039.
The expression plasmids pLMB222 and pAA033 were cloned in the following way. The ptsP ORF excluding its stop codon was amplified using primers ptsPexpfor/ptsPexprev and Phusion DNA polymerase. The resulting PCR product was inserted into pHMGWA [32] using Gateway BP Clonase (Invitrogen) forming pLMB222. The npr ORF excluding its stop codon was amplified using primers nprexpforBam/nprexprevHind and Phusion DNA polymerase (Finnzymes). The resulting PCR product was cloned as a BamHI/HindIII fragment into pETduet-1 (Novagen Merck Millipore) forming pAA033.

Transport Assays
R. leguminosarum uptake assays were performed with 25 mM (4.625 kBq of 14 C) solute [33], using cultures grown in AMS with 10 mM glucose and 10 mM NH 4 Cl to an OD 600 of ,0.4 (cultures with limiting K + at ,0.2). AMS medium with defined potassium levels were prepared as described above.

Protein Purification
The expression plasmids pLMB222 (6His-MBP-PtsP) and pAA033 (6His-NPr) were electroporated into E. coli BL21 DE+ cells and LB Amp pre-cultures were grown overnight at 37uC. 500 ml LB Amp cultures were than inoculated and grown for ,4 h at 37uC to an OD600 of 0.5-0.7. Those cultures were induced with 1 mM IPTG and grown over night at 18uC. Cells were harvested by centrifugation at 4uC, washed in 25 ml of PBS buffer and resuspended in 12.5 ml PBS. Cells were disrupted by sonication in extraction buffer (PBS; 0.1% Triton X-100; 10% glycerol; 5 mM b-mercaptoethanol) and extracts were cleared by centrifugation. Cell free extracts were loaded on Protino Ni-IDA 1000 (Macherey+Nagel, Germany) columns and the his-tagged proteins were purified following the manufacturer's instructions (purification using native conditions protocol). The eluates were dialysed against the phosphorylation assay buffer (94 mM Tris HCl, pH8.0; 1.6 mM MgSO 4 ; 10 mM b-mercaptoethanol) and protein purity was checked in an SDS PAGE following Coomassie blue staining (NuSep, Australia, precast gels, following manufacturer's instructions).  [34]. This assay only depends on the PEP/ATP ratio and transfers the vast majority of label from ATP to PEP. The reaction mixture was used as a [ 33 P]PEP source without further purification. The phosphorylation assay was done following the protocol published by [26]. The assay was performed in 20 ml of assay buffer (see above), 2 mg of purified 6His-MBP-PtsP and/or 6His-NPr fusion protein and either 125 mM [ 33 P]PEP (3 Ci/mmol) or 10 mM [c-33 P]ATP (3 Ci/mmol). Reactions were stopped in 6x Laemmli buffer and run on SDS PAGE. Radioactive labeled proteins were visualized on a Phosphoimager (Fujifilm FLA-3000). Gels were stained with Coomassie blue. RU4392 (Dask) crude extract was produced from 20 mL TY cultures by breaking the cells in a FastPrep FP120 instrument (Q-BioGen, USA) in phosphorylation assay buffer (see above).

Phosphorylation Assay
,10 mg of crude extract were used in the [c-33 P]ATP phosphorylation assay.