Enhanced oxygen consumption in Herbaspirillum seropedicae fnr mutants leads to increased NifA mediated transcriptional activation
© Batista et al.; licensee BioMed Central. 2015
Received: 16 December 2014
Accepted: 24 April 2015
Published: 7 May 2015
Orthologous proteins of the Crp/Fnr family have been previously implicated in controlling expression and/or activity of the NifA transcriptional activator in some diazotrophs. This study aimed to address the role of three Fnr-like proteins from H. seropedicae SmR1 in controlling NifA activity and consequent NifA-mediated transcription activation.
The activity of NifA-dependent transcriptional fusions (nifA::lacZ and nifB::lacZ) was analysed in a series of H. seropedicae fnr deletion mutant backgrounds. We found that combined deletions in both the fnr1 and fnr3 genes lead to higher expression of both the nifA and nifB genes and also an increased level of nifH transcripts. Expression profiles of nifB under different oxygen concentrations, together with oxygen consumption measurements suggest that the triple fnr mutant has higher respiratory activity when compared to the wild type, which we believe to be responsible for greater stability of the oxygen sensitive NifA protein. This conclusion was further substantiated by measuring the levels of NifA protein and its activity in fnr deletion strains in comparison with the wild-type.
Fnr proteins are indirectly involved in controlling the activity of NifA in H. seropedicae, probably as a consequence of their influence on respiratory activity in relation to oxygen availability. Additionally we can suggest that there is some redundancy in the physiological function of the three Fnr paralogs in this organism, since altered respiration and effects on NifA activity are only observed in deletion strains lacking both fnr1 and fnr3.
The endophytic diazotroph Herbaspirillum seropedicae SmR1 is a Beta-proteobacterium found in association with economically important crops such as rice, maize, sugar cane and sorghum [1,2]. H. seropedicae can fix nitrogen under micro-oxic and nitrogen limiting conditions and expression of H. seropedicae nitrogen fixation (nif) genes inside plant tissues has been demonstrated . In H. seropedicae the nif genes are clustered in a contiguous region of 46 genes , comprising at least seven operons , whose products are essential for biosynthesis, maturation and assembly of the nitrogenase complex. The nitrogenase structural genes (nifHDK) are located in the nifHDKENXHsero2847Hsero_2846fdxA operon. nifH encodes the iron (Fe) protein while nifDK encodes the molybenum-iron (MoFe) protein.The nifB gene, which encodes a protein involved in the synthesis of FeMoco, is located in an operon with other nif-related genes. The σ54-dependent transcriptional activator, NifA, a member of the bacterial enhancer binding family  is a master regulator of nif gene expression in H. seropedicae SmR1 . Two sites for NifA binding and a consensus binding site for the RNA polymerase σ54 holoenzyme were found in the promoters upstream nifB and nifH [6,7]. NifA responds to both fixed nitrogen and oxygen levels, being activated in response to limitation of these resources . Once active, NifA activates transcription from nif promoters  including nifB and nifH (reviewed in ).
The Fnr protein, is a widespread transcriptional regulator that binds a [4Fe–4S]2+ cluster to monitor the oxygen status in the cell , and regulates the transcription of genes required for the metabolic switch in response to decreasing oxygen levels [11-13]. Orthologous proteins of the Crp/Fnr family [11,14] have been previously implicated in controlling expression and/or activity of the NifA transcriptional activator in some diazotrophs [14-16]. In Klebsiella pneumoniae Fnr influences NifA activity through modulation of the mechanism by which the NifL repressor protein is sequestered to the membrane . In Bradyrhizobium japonicum the Fnr-like protein, FixK1, negatively controls genes that are subject to NifA activation  suggesting that FixK1, can repress transcription at NifA-dependent promoters. Another precedent for Fnr involvement in NifA activity was observed by Monteiro and co-workers , who showed that the activity of an amino-terminally truncated form of H. seropedicae NifA was influenced by Fnr when expressed in an Escherichia coli fnr- background.
The H. seropedicae genome  has three genes encoding for Fnr-like proteins  and a role for these Fnr orthologs in controlling the expression of the complete cytochrome c branch of the electron transport chain has been demonstrated . In this study we aimed to investigate the potential involvement of H. seropedicae Fnr proteins in the expression and activity of NifA and the consequences for transcriptional activation of other nif genes.
We found that combined deletions in both the fnr1 and fnr3 genes lead to higher expression of nifB::lacZ and nifA::lacZ transcriptional fusions and increased nifH transcription. We also show that the oxygen consumption rate in multiple fnr deletion strains is higher than in the wild-type, which we believe to result in either higher stability or activity of the oxygen sensitive NifA protein and consequently increased transcriptional activation of nif genes.
Results and discussion
We considered the possibility that the multiple fnr deletion strains exhaust dissolved oxygen in the media faster than the wild type strain, thus leading to higher activity or stability of NifA in cultures of the fnr deletion mutants. To examine this further, we assayed nifB::lacZ activity in cultures grown in the absence of fixed nitrogen under defined initial oxygen concentrations of oxygen in the gas phase (Figure 1B). As anticipated, nifB expression was not detected under either 8% or 20.8% oxygen in both wild-type and the fnr triple deletion mutant, presumably because H. seropedicae NifA is inactivated at high oxygen concentrations [8,19]. However, the activity of the nifB::lacZ promoter fusion was markedly higher in the triple fnr deletion strain (MB231) compared with the parental strain, when cultures were incubated under an initial oxygen concentration of 4% or 6% in the gas phase (Figure 1B). To ensure that the increase of nifB expression observed in the mutant strains was NifA-dependent, we prepared single nifA − and multiple deletion strains carrying a nifA deletion in addition to the fnr mutations (Additional file 1) and confirmed that the influence of Fnr proteins on nifB promoter activation requires NifA protein (Additional file 2).
Since expression of the nifA gene itself is subject to autoactivation in H. seropedicae , we tested the influence of fnr deletions on nifA expression using various nifA::lacZ promoter constructs (Figure 2). Transcriptional regulation of nifA is complex, since this σ54-dependent promoter is subject to nitrogen regulation by the enhancer binding protein NtrC in addition to autogenous activation by NifA under oxygen-limiting conditions (see Figure 2A). Notably, single deletions in each of the three fnr genes had no apparent influence on nifA expression. However, as in the case of nifB, an increase in promoter activation was apparent in the double fnr1, fnr3 deletion mutant (MB13) and the triple fnr deletion strain (MB231) (Figure 2B). In all cases, promoter activation significantly decreased when cultures were grown in the presence of a high concentration of fixed nitrogen (Figure 2C), or when the −24 to −12 region of the promoter was disrupted (plasmid pRW22, Figure 2B), indicating that activation is rpoN-dependent and subject to nitrogen regulation by NtrC as expected . In all cases, irrespective of the presence of fnr mutations, nifA expression decreased when promoter constructs (plasmids pRWC and pRW3) carried mutations in the upstream activation sequence (UAS2) of the promoter (Figure 2B), presumably as a consequence of decreased autoactivation by NifA . Overall, these results demonstrate that in the absence of both fnr1 and fnr3, activation of the nifA promoter is increased. Since higher expression of the nifA::lacZ fusion is not observed when the NifA binding site (UAS2) is deleted, it is likely that the increased expression results from autoactivation of the nifA promoter due to increased activity or stability of NifA protein.
In a previous study, we showed that the triple fnr mutant is deficient in the expression of the cytochrome c-type branch of the electron transport chain . An alternative route of electron transport from the quinol pool to oxygen via the terminal quinol oxidases is likely to occur in the triple fnr mutant. As the quinol branch of the respiratory chain results in a lower number of proton-translocation events it is conceivable that the activity of this branch, rather than the expression of the bo 3 and bd-type oxidases, is enhanced in the fnr mutant strains to compensate for the lower level of energy production. This may result in increased electron flux through the respiratory chain and hence enhanced oxygen consumption as observed in our experiments.
We demonstrated previously that nitrogenase activity is severely impaired when the triple fnr deletion strain is cultured in ammonium-limiting liquid medium, potentially as a consequence of energy depletion . We also showed that diazotrophic growth is impaired in the fnr ablated strain, after subjecting cultures to severe nitrogen starvation . Under these conditions, cultures divide at extremely low growth rates, requiring 24 days post-inoculation to achieve an OD600 of ~ 1.6 (Additional file 4). However, it is notable that the triple fnr mutant grew faster than the wild-type for the first 12 days of incubation under these conditions. Potentially, the enhanced rate of O2 consumption by the triple fnr deletion allows higher levels of NifA activity and consequently higher nitrogenase activity during the ‘early’ stages of growth. However, it is possible that as the bacterial population increases and the oxygen levels in the culture drop further, the triple fnr mutant strain can no longer maintain the necessary electron flux to support nitrogenase activity and as a consequence, diazotrophic growth is impaired.
In summary, these studies have not identified a direct role for the H. seropedicae Fnr proteins in regulating NifA activity and nitrogen fixation, but rather suggest that they may influence both, by means of altering the composition of the electron transport chain and the oxygen consumption rate. Since we only observe such effects in strains deleted for both fnr1 and fnr3, there is apparently some redundancy in the physiological functions of the three fnr paralogs in H. seropedicae. It is feasible that H. seropedicae can take advantage of the three fnr genes to differentially modulate respiratory chain composition. This is likely to influence nitrogen fixation during different phases of growth and enable efficient adaptation during plant-bacterial colonization.
In this study we have used a combination of transcriptional and physiological approaches to address the role of the H. seropedicae Fnr proteins in influencing the expression and activity of NifA. In summary we found that Fnr1 and Fnr3 participate indirectly in modulating NifA stability as a consequence of alterations in the rate of O2 consumption. This mechanism can potentially allow the bacteria to fine tune nitrogen fixation in response to environmental cues.
Plasmids, bacterial strains and growth conditions
Plasmids and strains used in this study
pLAFR vector containing the polycloning site of pTZ18R, TcR
H.seropedicae NifA expressed from lac promoter
Allelic exchange suicide vector; mobilized by E. coli S17-1 λpir, sacB,KmR
Allelic exchange suicide vector; mobilized by E. coli S17-1, sacB,GmR
H.seropedicae NifA in pT7-7 vector
H.seropedicae NifA with a deletion of 576 bp
XbaI/BamHI fragment from pRAM1T7del
5′-BamHI, KpnI, XhoI – 3xFlag-Stop – HindIII, SalI, XmaI-3′, AmpR
H. seropedicae nifA-3xFlag gene plus 647 bp of the downstream region, AmpR
H. seropedicae nifA-3xFlag gene plus 647 bp of the downstream region, Mob, SacB, KmR
H. seropedicae fnr1-3xFlag gene plus 1000 bp of the downstream region, AmpR
H. seropedicae fnr1-3xFlag gene plus 1000 bp of the downstream region, Mob, SacB, GmR
lacZ fusion vector, TcR, Mob
TcR, Mob, nifB::lacZ fusion, nifB promoter cloned in pPW452
TcR, Mob, nifA::lacZ fusion, nifA promoter cloned in pMP220
pRW1, but with a 49 bp deletion including the UAS 2 site for NifA
pRW1, but with a double mutation at the UAS 2 site for NifA (TGT ->TCT and ACA -> AGA)
pRW1, but with a single mutation at the −24/-12 promoter (G -> T at −25 residues)
Herbaspirillum seropedicae Z78 but SmR 100 μg/mL, Nif+
Derived from SmR1 fnr1 deletion
Derived from SmR1, fnr2 deletion
Derived from SmR1, fnr3 deletion
Derived from MB1, fnr1 and fnr3 double deletion
Derived from MB2, fnr1 and fnr1 double deletion
Derived from MB2, fnr2 and fnr3 double deletion
Derived from MB23, fnr1, fnr2 and fnr3 triple deletion
Derived from SmR1, but with 576 bp deletion in the nifA gene
Double fnr1, fnr3 deletion, plus a 576 bp deletion in the nifA gene
Triple fnr deletion, plus a 576 bp deletion in the nifA gene
Derived from SmR1, but with a C-terminal 3xFlag nifA gene
Double fnr1, fnr3 deletion, plus a C-terminal 3xFlag nifA gene
Triple fnr deletion, plus a C-terminal 3xFlag nifA gene
Derived from SmR1, but with a C-terminal 3xFlag fnr1 gene
Construction of nifA deletion and 3xFlag tagged strains
To construct the C-terminal 3xFlag tagged NifA strains, we generated a nifA-3XFlag gene by cloning the complete nifA gene (1629 bp) in frame with the 3xFlag sequence from a vector synthesized by the GenScript® Corporation (Table 1). To assist homologous recombination, a fragment of 647 bp downstream of nifA was cloned adjacent to the 3xFlag tag sequence to generate an approximately 2.4 Kb fragment containing the nifA-3xFlag allele plus the downstream region. This fragment was then digested with BamHI, and subcloned into pK18mobsacBKm vector  to generate the suicide vector pK18nifAflag. A similar approach was used to generate a vector for C-terminal 3xFlag tagging of the fnr1 gene, but a fragment of 1002 bp downstream of fnr1 gene was cloned adjacent to the 3xFlag tag sequence to generate a fragment of approximately 1.95 kb containing the fnr1-3xFlag allele plus the downstream region. This fragment was then subcloned into pJQ200SK suicide vector  to generate pJQfnr1Flag. To generate the nifA deletion vector, plasmid pRAM1T7 was digested with EcoRI and re-ligated to yield the vector pRAM1T7del containing a deleted copy of nifA lacking 576 bp. Then an XbaI/BamHI fragment from pRAM1T7del was cloned into pK18mobsacB vector to generate the pK18nifAdel suicide vector.
The suicide plasmids generated for both tagging of nifA and fnr1 and also for deletion of nifA gene were transferred to wild type H. seropedicae SmR1, and the fnr deletion strains MB13 and MB231 strains by conjugation as described [18,24]. Single crossover strains were selected by antibiotic resistance. Double crossover strains were selected on plates containing 5% sucrose and then tested for antibiotic marker sensitivity. The mutant strains sensitive to kanamycin or gentamicin and resistant to sucrose were analysed by PCR using specific primers as described (Additional files 1, 3 and 5). All primers used are listed in the Additional file 6.
β-Galactosidase activity and transcriptional fusions
β-Galactosidase activities of various nif promoter:lacZ transcriptional fusions were assayed in H. seropedicae strains as previously described [6,20], except that the strains were grown in NFbHP-Malate liquid medium supplemented with 5 mM NH4Cl (6 ml in 25 ml cylindrical bottles under air). Under these conditions, the cultures exhaust the supply of fixed nitrogen and become oxygen limited resulting in formation of active NifA and nif gene expression.
Alternatively, H. seropedicae strains carrying the nifB::lacZ fusion were assayed for β-galactosidase activity after incubation under defined initial oxygen concentrations. In summary, cultures with an O.D600 adjusted to 0.2, were incubated for six hours in NFbHP-Malate without addition of fixed nitrogen and under the initial oxygen concentrations of 4%, 6% or air (20.8%).
RNA extraction and RT-PCR
Strains were grown under 4% of oxygen for six hours. Cells from 30 mL of culture were collected by centrifugation (7000 rpm, 4°C, 5 minutes) and re-suspended in 200 μL of 10 mM Trizma® (Sigma# T-2694). The cells were then mixed with 700 μL of RLT Buffer (Qiagen Rneasy Mini Kit #74104) containing 1% of β-mercaptoethanol and added to lysing tubes containing zirconia and silica/glass beads in the proportion of 2:1 (Thistle Scientific Ltd). Lysis was carried out with 3 pulses (speed 6.5 with 30 seconds on/1.5 minutes off) using the Thermo Savant FastPrep 120 Cell Disrupter System. Beads and cellular debris were collected by centrifugation (17000 × g, 4°C, 5 min). The supernatant (900 μL) was transferred to a new RNase free tube and 450 μL of ethanol (Sigma #459844) was then added. The samples were applied to the RNeasy columns (Qiagen RNeasy Mini Kit #74104) and total RNA was recovered after on column DNAse treatment with the Qiagen RNase-Free DNase set (#79254) following the manufacturer’s instructions. The quality of purified RNA was accessed by electrophoresis in a 1% agarose gel. RNA was treated with Turbo DNase (Ambion#AM1907) following manufacturer’s instructions and further purified with Qiagen RNeasy columns to avoid carryover of divalent cations.
Approximately 0.25 ng/μL of total RNA was used for direct RT-PCR using the One-Step RT-PCR kit (Qiagen #210210) according to the manufacturer’s instructions. Expression of nifH gene was evaluated using 16S rRNA as endogenous control. The primers are listed in the Additional file 6.
Preparation of protein extracts and western blotting
H. seropedicae cultures adjusted to an O.D600 of 0.2 were grown under 4% of oxygen for six hours. After incubation, approximately 3 mL of cells (volumes were adjusted as necessary) were collected by centrifugation (17000 × g, 2 min), re-suspended in 100 μL of protein sample buffer (120 mM of Tris–HCl pH 6.8, 2% SDS, 20% Glycerol, 9% β-mercaptoethanol and 0.03% bromophenol blue) and boiled for 5 minutes. Subsequently, 10 μL of the resulting extract was loaded onto 12% SDS-PAGE for resolution of the proteins, which were immediately transferred to a PVDF membrane and then hybridized with ANTI-FLAG® (Sigma #7425) primary antibody (1/2500 dilution), followed by secondary anti-rabbit-HRP conjugated antibody (1/10000 dilution). The HRP activity was detected using the ECL Plus Western Blotting detection kit (GE Healthcare #RPN2132) as indicated by the manufacturer and the UVP® gel imaging system.
Oxygen consumption measurements
For determination of the oxygen consumption we designed two assays. First we evaluated the depletion of the oxygen levels in the gas phase of culture flasks sealed with Suba-seal septa. Every hour we took a 0.5 ml gas sample from the growing culture and analyzed the oxygen concentration by gas chromatography (Varian GC-450) coupled to a molecular sieve column and a TCD detector. Oxygen depletion was linear until 10 hours growth. The rate of consumption was calculated as the amount of oxygen consumed in the gas phase normalized by the protein concentration of the culture. A measurement of the dissolved oxygen consumption was also carried out with a Clark-type electrode. After addition of 100 μl of bacterial culture into the chamber, containing 1.6 ml of NFbHP-Malate at 30°C, the consumption of dissolved oxygen in the medium was recorded until the polarizing voltage reached 0 (i.e. 0% oxygen saturation).
This study was supported by the Brazilian Program of National Institutes of Science and Technology-INCT/Brazilian Research Council-CNPq/MCT, CNPq, Fundação Araucária, CAPES. MBB is also grateful to the PhD and academic mobility fellowships provided by CNPq and the Brazilian program Science without Borders, respectively. Roseli A. Prado, Marilza D. Lamour and Valter A. de Baura are acknowledged for the technical assistance.
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