- Short Report
- Open Access
Transcript analysis of the extended hyp-operon in the cyanobacteria Nostoc sp. strain PCC 7120 and Nostoc punctiforme ATCC 29133
© Lindblad et al; licensee BioMed Central Ltd. 2011
- Received: 7 February 2011
- Accepted: 14 June 2011
- Published: 14 June 2011
Cyanobacteria harbor two [NiFe]-type hydrogenases consisting of a large and a small subunit, the Hup- and Hox-hydrogenase, respectively. Insertion of ligands and correct folding of nickel-iron hydrogenases require assistance of accessory maturation proteins (encoded by the hyp-genes). The intergenic region between the structural genes encoding the uptake hydrogenase (hupSL) and the accessory maturation proteins (hyp genes) in the cyanobacteria Nostoc PCC 7120 and N. punctiforme were analysed using molecular methods.
The five ORFs, located in between the uptake hydrogenase structural genes and the hyp-genes, can form a transcript with the hyp-genes. An identical genomic localization of these ORFs are found in other filamentous, N2-fixing cyanobacterial strains. In N. punctiforme and Nostoc PCC 7120 the ORFs upstream of the hyp-genes showed similar transcript level profiles as hupS (hydrogenase structural gene), nifD (nitrogenase structural gene), hypC and hypF (accessory hydrogenase maturation genes) after nitrogen depletion. In silico analyzes showed that these ORFs in N. punctiform e harbor the same conserved regions as their homologues in Nostoc PCC 7120 and that they, like their homologues in Nostoc PCC 7120, can be transcribed together with the hyp-genes forming a larger extended hyp- operon. DNA binding studies showed interactions of the transcriptional regulators CalA and CalB to the promoter regions of the extended hyp-operon in N. punctiforme and Nostoc PCC 7120.
The five ORFs upstream of the hyp-genes in several filamentous N2-fixing cyanobacteria have an identical genomic localization, in between the genes encoding the uptake hydrogenase and the maturation protein genes. In N. punctiforme and Nostoc PCC 7120 they are transcribed as one operon and may form transcripts together with the hyp-genes. The expression pattern of the five ORFs within the extended hyp-operon in both Nostoc punctiforme and Nostoc PCC 7120 is similar to the expression patterns of hupS, nifD, hypF and hypC. CalA, a known transcription factor, interacts with the promoter region between hupSL and the five ORFs in the extended hyp-operon in both Nostoc strains.
- Electrophoretic Mobility Shift Assay
- Nitrogen Depletion
- Uptake Hydrogenase
- Transcription Start Point
Cyanobacteria are an ancient group of organisms capable of both oxygenic photosynthesis and hydrogen evolution. Molecular hydrogen (H2) is produced by nitrogenases as a by-product when fixing atmospheric dinitrogen (N2) while uptake hydrogenases recapture the molecular hydrogen and oxidize it, to prevent energy losses from the cells. In addition, if present bidirectional hydrogenases have the capacity to both produce and oxidize H2[1–3]. Hydrogenases and nitrogenases are oxygen sensitive enzymes [1, 2] and therefore cyanobacteria have developed different strategies to maintain enzyme activity by separating the enzymes from oxygenic photosynthesis either spatially, e.g. in heterocysts [2, 4, 5], or temporally . In heterocystous cyanobacteria nitrogenase and uptake hydrogenase are expressed in heterocysts, while the bidirectional hydrogenase is present in both heterocysts and vegetative cells. Neither the uptake nor the bidirectional hydrogenases are universally present among cyanobacteria. However, all filamentous strains examined so far capable of N2-fixation contain an uptake hydrogenase [2, 3, 6].
All cyanobacterial hydrogenases belong to the NiFe class of hydrogenases [3, 6]. The uptake hydrogenase consists of a small and a large subunit, encoded by hupS and hupL, respectively [1, 2, 5]. The large subunit, HupL, harbors the Ni and Fe containing active site [3, 6]. The assembly of the active site and correct folding of HupL is a complex process, requiring assistance of accessory proteins, encoded by at least hypABCDEF, and a hydrogenase specific protease, encoded by hupW[3, 7]. The hyp-genes (hyp for hy drogenase p leiotropic) and the Hyp-proteins have been studied mainly in Escherichia coli. However, mutational analyses in e.g. Synechocystis sp. PCC 6803 have shown that the corresponding cyanobacterial hyp-genes most likely have similar function [6, 8].
The small subunit, HupS, mediates electron transport from the active site located in the large subunit to redox partners and downstream reactions through a set of FeS clusters [3, 7]. Little is known about the cyanobacterial maturation process and assembly of FeS clusters in the small subunit. Three different kinds of FeS cluster biosynthesis systems have been identified in bacteria, the ISC (i ron-s ulphur c luster), SUF (mobilization of su lf ur) and NIF (ni trogen f ixation) system. They all have in common that they require a FeS cluster scaffolding protein (IscU and IscA, SufA, NifU) and a cysteine desulfurase (IscS, SufS, NifS), providing elemental sulphur [3, 9]. Cyanobacteria lack homologues to iscU but the gene nfu, encoding a protein with high similarity to the C-terminal domain of NifU, is present. In cyanobacteria SufA and IscA seem to have a more regulatory function, e.g. sensing of redox stress and being involved in FeS cluster assembly under iron homeostasis. Nfu has been suggested to be involved in general FeS cluster assembly and is considered to be an essential FeS cluster scaffold protein .
There have been reports of proteins participating in the maturation process of the small subunit of uptake hydrogenases. The legume endosymbiont Rhizobium leguminosarum bv. viciae strain UPM791 harbors a subcluster of five genes, hupGHIJK, which has been connected to the maturation of the small subunit of the uptake hydrogenase. The subcluster is part of the hydrogenase gene cluster due to its location between the structural genes and the hyp-genes, and is preceded by a promoter (P3) upstream of hupG[11–13]. Homologues can be found in other aerobic, NiFe-type uptake hydrogenase containing bacteria such as Azotobacter vinelandii, Rhodobacter capsulatus, Ralstonia eutropha H16, Azotobacter chroococcum and Bradyrhizobium japonicum[14–16]. The presence of HupGHIJ appears to be connected to oxygen dependent microorganisms, since no homologues have been found in strictly anaerobic bacteria [11, 16]. HupH forms a direct complex with the small subunit precursor, pre-HupS . In addition, an interaction between the uptake hydrogenase small subunit Tat signal peptide and the HupH and HupG homologues, HoxQ and HoxO, has been shown in Ralstonia eutropha H16 [14, 17, 18]. The proposed functions of HupGHIJ in R. leguminosarum and HoxOQ in R. eutropha are to protect the FeS clusters in the small subunit from oxygen, stabilizing the small subunit complexes and preventing premature translocation of the small subunit to the periplasm by masking the Tat signal peptide [11, 18].
The ORFs upstream of the hyp-genes in Nostoc sp. strain PCC 7120 and their homologues in Nostoc punctiforme ATCC 29133
Nostoc sp. strain PCC 7120
Nostoc punctiforme ATCC 29133
N. punctiforme and Nostoc PCC 7120 are two filamentous, heterocyst forming cyanobacterial strains used in the present study. Both possess an uptake hydrogenase while Nostoc PCC 7120 in addition possesses a bidirectional enzyme [2, 24, 25]. This makes the two strains interesting to compare due to the presence of only one set of hyp-genes in both genomes [19, 26, 27]. In this study we have further investigated the ORFs upstream of the hyp-genes by examining their transcript level pattern after nitrogen depletion in N. punctiforme and Nostoc PCC 7120. The results were compared to the transcript level pattern for genes known to be involved in hydrogen metabolism, such as hupS (encoding the uptake hydrogenase small subunit), nifD (encoding a nitrogenase subunit) and hypC and hypF (encoding Hyp-proteins). We also tested if the ORFs upstream of the hyp-genes in N. punctiforme may be, like in Nostoc PCC 7120, transcribed together with the hyp-operon. The ORFs upstream of the hyp-genes in N. punctiforme were analyzed in silico and the region examined experimentally for transcription start points. In addition, different DNA affinity studies were used to analyze binding of transcriptional regulators to the promoter region of the extended hyp-operon in both N. punctiforme and Nostoc PCC 7120.
Strains and culture conditions
The filamentous heterocystous cyanobacterial strains Nostoc punctiforme ATCC 29133 and Nostoc sp. strain PCC 7120 (also named Anabaena sp. strain PCC 7120) were cultured in BG110 medium , sparged with air and grown at 25°C, at a continuous irradiance of 40 μmol of photons m-2 s-1. For non N2-fixing conditions the BG110 medium was supplemented with 5 mM NH4Cl and 5 mM MOPS (pH 7.8).
In silico genome analyses of the ORFs upstream of the hyp-genes
Sequence homology search for conserved domains in the ORFs upstream of the hyp-genes of N. punctiforme was performed in Cyanobase (http://genome.kazusa.or.jp/cyanobase/), UniProt Knowledgebase (Swiss-Prot and TrEMBL at http://www.expasy.org/sprot/) and Pfam (http://pfam.sanger.ac.uk). The deduced protein sequences of HupGHIJ were blasted against the N. punctiforme and Nostoc PCC 7120 and protein database at Cyanobase (http://genome.kazusa.or.jp/cyanobase) and National Center for Biotechnology Information (NCBI) (http://0-www.ncbi.nlm.nih.gov.brum.beds.ac.uk/).
Heterocysts from Nostoc PCC 7120 were isolated as previously described with a few modifications [30, 31]. The incubation step with lysozyme was prolonged to 2 hours and the sonication step decreased to 3 intervals of 10 s. The pellet, containing heterocysts, were washed 4 times in extraction buffer and centrifugated at 4°C at, in order, 1000 × g, 1000 × g, 750 × g, 500 × g and 250 × g for 5 min respectively.
Nucleic acid isolation and analysis
Genomic DNA and RNA were isolated from N. punctiforme and Nostoc PCC 7120 cultures as previously described [19, 29]. The rRNA quality was analyzed with the Experion System (Bio-Rad Laboratories) according to the manufacturer's instructions. The concentration was determined by absorbance measurements using Cary Win UV (Varian). Prior to RT-reactions RNA was treated with DNaseI (Fermentas) according to the instructions of the manufacturer.
Primer oligonucleotides designed and used to generate or amplify cDNA from cyanobacterial cell cultures after nitrogen depletion
N. punctiforme primers
Nostoc PCC 7120 primers
RT primers N. punctiforme
Primer oligonucleotides designed and used to locate novel transcription start points in Nostoc punctiforme ATCC 29133 and to amplify DNA probes for DNA affinity assay and electrophoretic mobility shift assay (EMSA) from N. punctiforme and Nostoc sp. strain PCC 7120 genomic DNA
N. punctiforme F-bio
N. punctiforme R
N. 7120 F-bio
N. 7120 R
EMSA PhupS F
EMSA PhupS R
EMSA hupL F
EMSA hupL R
Reverse transcription (RT) reactions were performed according to the manufacturer's instructions with either the iScript™ cDNA Synthesis Kit (Bio-Rad Laboratories) containing random primers, using 0.25 μg total RNA from N. punctiforme and 0.5 μg total RNA from Nostoc PCC 7120, or the RevertAid™ First Strand cDNA Synthesis Kit (Fermentas) and gene specific primers, using 0.5 μg total RNA from N. punctiforme. The cultures were grown under either N2-fixing or non N2-fixing conditions. PCR amplifications using cDNAs of the respective genes were performed using corresponding primers (Table 2). To ensure that the PCR reaction of the reference gene, 23S, were not saturated a semi-quantitative analysis of 23S PCR product from N. punctiforme and Nostoc PCC 7120 were done by removing a sample every 2nd cycle from, cycle 8 to 26, and comparing the amount of transcript (data not shown). PCR were used to amplify the regions between hupS to Npun_R0367 (using primers hupS forward and Npun_R0367 reverse), Npun_R0367 to Npun_R0366 (using primers Npun_R0367 forward and Npun_R0366 reverse), Npun_R0366 to Npun_R0365 (using primers Npun_R0366 forward and Npun_R0365 reverse), Npun_R0365 to Npun_R0364 (using primers Npun_R0365 forward and Npun_R0364 reverse), Npun_R0364 to Npun_R0363 (using primers Npun_R0364 forward and Npun_R0363 reverse) and Npun_R0363 to hypF (using primers Npun_R0363 forward and hypF reverse). Negative controls for the RT-reaction were RT-PCR on DNaseI treated RNA without RT-enzyme. Negative controls for the PCR reactions included PCR amplification without cDNA added and positive controls were made with genomic DNA from N. punctiforme and Nostoc PCC 7120 using the corresponding forward and reverse primer.
PCR and agarose gel electrophoresis
PCR amplifications were carried out using the enhanced thermostable Taq DNA Polymerase DreamTaq™ (Fermentas), according to manufacturer's protocol, in a UnoCycler Thermal Cycler (VWR) according to the guidelines provided by the suppliers. For the transcript level analysis an annealing temperature of 60°C and 0.8 μl or 0.4 μl cDNA were used (N. punctiforme and Nostoc PCC 7120 respectively) in 10 μl reactions. The amount of cycles varied from 15 to 30 cycles for the different samples to avoid saturation of the PCR product in the reactions. The products were visualized on 1% agarose gels containing thiazole-orange. The gels were run with 1x sodium boric acid buffer at 160 V for 15 minutes.
Identification of transcription start points
Transcription start points were located with the 5'RACE System for Rapid Amplification of cDNA Ends, Version 2.0 (Invitrogen), according to the manufacturer's instructions using 1 μg total RNA and gene specific primers (Table 3). The resulting PCR products were gel purified using the NucleoSpin® Extract II (Macherey-Nagel) according to protocol and cloned into the pCR® 2.1-TOPO® vector (Invitrogen), following to the manufacturer's instructions, before being sequenced at Macrogen Inc. The sequences were subsequently analyzed with BioEdit Sequence Alignment Editor 184.108.40.206. Negative controls included RT-PCR on DNaseI treated RNA without RT-enzyme, dC-tailing without TdT enzyme and PCR amplification without cDNA. Positive controls were made with genomic DNA from N. punctiforme using the corresponding forward and reverse primer.
Protein extraction, DNA affinity assays and mass spectrometry
Cells from N. punctiforme and Nostoc PCC 7120 cultures were harvested by centrifugation at 3300 × g for 10 minutes at 4°C and washed once in protein buffer (100 mM Tris-HCl pH 7.5, 1 mM EDTA, 2 mM DTT, 0.5% Triton X-100, 10% glycerol and 1 mM PMSF). Proteins were extracted using 0.2 g of 0.6-mm-diameter glass beads and a Precellys® 24 homogenizer (Bertin Technologies) at a speed of 5500 for 6 × 30 s keeping samples on ice between runs. After centrifugation at 10000 × g for 10 minutes at 4°C, the supernatants were transferred to new tubes and subjected to further separation by centrifugation at 30000 × g for 20 minutes at 4°C. The supernatant was once more transferred to new tubes and the protein concentration was determined using a Bio-Rad Protein Assay Dye Reagent (Bio-Rad Laboratories) according to manufacturer's protocol. For the DNA affinity assay a DNA fragment stretching from ATG (translation start point) for hupS to ATG for Npun_R0367 in N. punctiforme (from now on referred to as PhupS/Npun_R0367) and DNA fragment stretching ATG for hupS to ATG for asr0689 for Nostoc PCC 7120 (from now on referred to as PhupS/asr0689), were amplified by PCR using the proofreading Phusion High Fidelity polymerase (Finnzymes) and the corresponding oligonucleotides (Figure 1, Table 3). The biotin labeled DNA fragments were incubated with streptavidin coated magnetic beads (Dynabeads® M-280, Dynal Biotech) and subsequently with protein extracts as previously described . For each reaction 1.5 μg DNA, 500 μg beads and 1000 μg proteins were used. Finally the beads were resuspended in 1x SDS loading buffer containing 62.5 mM Tris-HCl pH 6.8, 2% SDS, 2.5% 2-mercaptoethanol, 7,5 mM Ditiotreitol (DTT), 10% glycerol and 5 × 10-3 % Bromphenol blue, and heated at 95°C for 5 minutes. The samples were excised from a 15% denaturing polyacrylamide gel, SDS-PAGE, stained with Brilliant Blue-G Colloidal (Sigma). Bands containing protein was cut from the gel and washed with water. The proteins were reduced by DTE and alkylated with iodoacetamide. After washing the proteins were digested with trypsin (Promega modified trypsin) in 50 mM NH4HCO3 at 37°C over night. Peptides were extracted and the extract was subjected to MALDI-Tof analysis using a Bruker Ultraflex-Tof/Tof instrument. Proteins were identified by using the peptide maps for search in the NCBInr database using the Mascot search engine (http://matrixscience.com). If needed for identification, MS/MS analysis was performed using the same MS instrument and search engine. The regions upstream of 16S (Npun_r084 and rrn16Sc for N. punctiforme and Nostoc PCC 7120, respectively) were used as a negative control as well as beads incubated without DNA but with protein extract.
Electrophoretic mobility shift assay
For electrophoretic mobility shift assays, a fragment of the N. punctiforme hupS immediate upstream region was amplified by PCR using the proofreading Phusion High Fidelity polymerase (Finnzymes). The primers used were PhupS F and PhupS R yielding the 558 bp DNA fragment PhupS. Two control fragments, C1 and C2, were generated using primers against a region within the hupL gene, hupL F and hupL R. C1 was amplified with wild type N. punctiforme ATCC 29133 DNA as template, resulting in a 308 bp fragment, and C2 was amplified using template DNA where the hupL gene has been interrupted by an antibiotic resistance cassette , resulting in a 1350 bp fragment. Histidine-tagged Nostoc PCC 7120 CalA was expressed in Nostoc PCC 7120 as described previously . After expression, the protein was purified on a Superflow Ni-NTA column (Qiagen) according to the manufacturer's instructions. Binding of the protein to the DNA fragments was performed as described previously , using 100 ng of each DNA fragment per 20 μl reaction, and different amounts, from 0 to 45 ng, of purified His-tagged CalA. After incubation at room temperature for 1 h, the assay mixtures were separated on an 8% non-denaturing polyacrylamide gel. The gel was subsequently stained with thiazole orange to visualize DNA bands.
In silico genome analyses of the ORFs upstream of the hyp-genes demonstrates a conserved arrangement
To investigate if the same, or similar, conserved domains as reported for the five ORFs upstream of the hyp-genes in Nostoc PCC 7120 , asr0689 to alr0693, can be identified in the ORFs upstream of the hyp-genes in N. punctiforme, Npun_R0367 to Npun_R0363 (Figure 1), computational analyzes was performed. Indeed, in the deduced amino acid sequences of Npun_R0366 and Npun_03 65, being the counterparts to asr0689 and asr0690 in Nostoc PCC 7120, putative transmembrane regions can be identified. Furthermore, in accordance to the findings in Nostoc PCC 7120 the deduced amino acid sequence of the alr0691 homologue Npun_R0367 and the alr0693 homologue Npun_0363 harbor TPR and NHL repeats, respectively. The deduced amino acid sequence of alr0692 was described as being similar to the C-terminal of NifU. When analyzing the homologue of alr0692 in N. punctiforme we found that Npun_R0364 as well was annotated as being similar to the C-terminal of NifU (Table 1).
The ORFs upstream of the hyp-genes show the same pattern of transcription as the hyp genes
The genes upstream of the hyp-genes can be transcribed together with the hyp-genes as one operon
CalA is binding to the hupSL Npun_R0367 promoter region in N. punctiforme and the hupSL asr6890 promoter region in Nostoc PCC 7120
Here we show that the five ORFs upstream of the hyp-genes in N. punctiforme harbors the same conserved regions as reported for Nostoc PCC 7120 . The homologues alr0691 and Npun_R0367 contains TPR domains . TPR domains mediate protein-protein interactions and are evolutionary conserved. They have been found in a variety of proteins involved in a wide range of cellular processes, for example protein folding. The numbers of TPR repeats differ between proteins, normally 3-16, and they are not connected to any specific position in primary protein sequences [20–22]. Likewise the homologues alr0639 and Npun_R0363 harbor NHL repeats also believed to be involved in protein-protein interactions . FeS clusters are important for electron transfer to and from the active site in hydrogenases. Assembly and insertion of FeS clusters is a complex process; Fe and S atoms must be mobilized from storages, transported to the correct cellular localization and inserted into the correct apoprotein. In the three FeS cluster assembly systems found so far the assistance of a scaffold protein and a cysteine desulfurase is needed [3, 9]. Interestingly, homologue genes alr0692 and Npun_R0364 contain a conserved domain that is similar to the C-terminal domain of NifU. Proteins of the NifU family function as a scaffolds for FeS cluster assembly but another protein family, Nfu, with sequence similarity to the C-terminal domain of NifU has also been reported to function as biosynthetic scaffolds . In cyanobacteria, Nfu have been proposed to be the primary FeS cluster scaffold protein .
The transcript level analysis of the ORFs upstream of the hyp-genes showed, as expected, an upregulation of transcripts for the control genes, nifD and hupS (nitrogenase and uptake hydrogenase structural genes) and hypF and hypC (hydrogenase maturation genes) when going from non N2 to N2-fixing conditions in both N. punctiforme and Nostoc PCC 7120. This increase in transcript levels was expected and has been shown before [6, 27]. Similarly, an upregulation of the transcript levels for all five ORFs upstream of the hyp-genes were seen after nitrogen depletion in both organisms while the amount of transcript of the control, 23S (ribosomal subunit), were constant. For Npun_0363 this is in accordance with the earlier finding that this gene is expressed as one transcript with the hyp-genes . Nostoc PCC 7120 harbors a bidirectional hydrogenase. To distinguish if an increase in transcript levels after a shift to N2-fixing conditions was connected to hydrogen metabolism in the heterocysts and not to bidirectional hydrogenase activity in the vegetative cells, heterocysts were isolated 48 hours after nitrogen depletion. The presence of transcripts of all genes tested in the heterocyst sample strongly indicates that expression takes place in the heterocysts. Since the ORFs upstream of the hyp-genes are not present in cyanobacterial strains containing only the bidirectional hydrogenase this points to a function related to the uptake hydrogenase. In Nostoc PCC 7120 the highest transcript levels of most genes investigated were detected 72 hours after nitrogen depletion while the highest transcript levels of most genes were detected already after 48 hours in N. punctiforme. The five ORFs upstream of the hyp-operon in N. punctiforme were shown to have, as hupGHIJK in R. leguminosarum, a tsp located upstream the gene cluster. In addition, as in Nostoc PCC 7120 , they are transcribed as a single operon and can form a transcript together with the hyp-genes in an extended hyp-operon. In bacterial genomes, genes that are functionally related are often clustered together and transcribed from the same promoter. By coordinating protein activities with gene regulation, genes expressed during different growth conditions, e.g. N2-fixation, can be turned on and off efficiently with minimal energy expenditure .
In Nostoc PCC 7120 a putative tsp was found upstream of asr0689 and in the promoter region a putative NtcA binding site and an extended -10 box were identified. In addition, tsps upstream of hypF and hypC were identified suggesting transcripts of varying sizes . Occurrence of several tsps in one operon has been shown before in cyanobacteria and might allow for a more fine tuned regulation [39, 40]. In N. punctiforme a tsp has been identified upstream of Npun_R0363 together with a putative -10 box and a putative NtcA binding site. No tsp has been found upstream of hypF or hypC. In this study we found a novel tsp 170 bp upstream of the translation start point, ATG, of Npun_R0367 as well as a - 10 and possibly a -35 box. NtcA is a global regulator of nitrogen metabolism in cyanobacteria [41, 42]. The -10 box in the Npun_R0367 promoter match the consensus sequence (TAN3T) reported for Class II NtcA activated promoters [41, 42], but there is no NtcA binding site overlapping the area of the -35 box. There is, however, a NtcA binding site located further upstream and we have earlier reported that NtcA does indeed interact specifically in EMSAs with this proposed binding site . This NtcA binding motif was first associated transcription of hupSL and is centered at -258.5 in the hupSL promoter . However, the promoter regions of hupSL and Npun_R0367 are located in the same intergenic region, although in opposite direction (Figure 1). In the Npun_R0367 promoter region the NtcA binding site is centered at - 64.5 from the tsp. This shorter distance from the NtcA binding site to the tsp fits better, although not perfect, with the -41.5 distance reported for NtcA regulated promoters . Interestingly, 10.5 base pairs approximately correspond to one helical turn of the DNA  which means that the NtcA site will have almost the reported angular orientation compared to the Npun_R0367 tsp. This, together with the importance of the NtcA binding site to the transcription of hupSL being low , supports our earlier suggestion that NtcA might not be involved in the regulation of hupSL but rather Npun_R0367, or putatively that NtcA is involved in the regulation of transcription from both promoters .
DNA binding assays showed that the novel transcriptional regulator CalA interacts specifically with the promoter region of the extended hyp-genes in both N. punctiforme and Nostoc PCC 7120 (Figure 5). Interestingly, two different bands were both identified as CalA. They may be either intact, cleaved, or partly degraded CalA, or different forms of CalA Furthermore, the CalA homologue, CalB, is also binding to the extended hyp promoter regions, or alternatively to CalA, in the respective strains (Figure 5). The c yanobacterial A brB l ike Cal proteins belong to the transcription regulator family AbrB (A ntib iotic r esistance). They have a conserved DNA binding region in the C-terminal part of the protein, and the cyanobacterial Cal proteins may be classified into two separate clades, CalA and CalB [34, 44]. AbrB is a global transition-state regulator well studied in Bacillus subtilis, that directly, or indirectly, regulates more than 60 different genes . No consensus sequence for AbrB binding has been identified, instead the protein is believed to recognize a specific DNA 3D-conformation [46, 47] and regulating by binding to promoter regions with different affinities  thereby fine-tuning the regulatory process. The functions of CalA and CalB in cyanobacteria are largely unknown, but parts of it are starting to be revealed. CalA appears to be essential, since no attempts to create a fully segregated knock-out mutant have been successful [37, 44], and have been shown to interact with the promoter regions of genes involved in hydrogen metabolism in Nostoc PCC 7120  and Synechocystis PCC 6803 , toxin production in Aphanizomenon ovalisporum, and with the promoter regions of FtsZ  and FeSOD in Nostoc PCC 7120 . Fully segregated knock-out mutants of CalB have, however, been constructed in Synechocystis PCC 6803  and it appears to play an important role in the regulation of genes involved in nitrogen uptake  and carbon concentrating mechanisms . Since CalA interacts with the promoter region of hypC in Nostoc PCC 7120  it makes sense that CalA also is involved in the regulation of the upstream of the hyp-operon in N. punctiforme and Nostoc PCC 7120. Furthermore, due to the fact that the genes in the extended hyp-operon are expressed during nitrogen depletion, together with many other genes involved in N2-fixation and nitrogen metabolism, interaction of CalB with the extended hyp promoter region is not unreasonable. Whether CalA or CalB activates or represses transcription of the extended hyp-operon in N. punctiforme and Nostoc PCC 7120 remains to be revealed.
The five ORFs upstream of the hyp-genes in several filamentous N2-fixing cyanobacteria have an identical genomic localization, in between the uptake hydrogenase structural genes, hupSL, and the maturation protein genes, hypABCDEF. These ORFs are not present in strains harboring only the bidirectional hydrogenase. In N. punctiforme and Nostoc PCC 7120 they are transcribed as one operon and may form transcripts together with the hyp-genes. The homologues alr0691 and Npun_R0364 both contain a domain that is similar to NifU, a FeS cluster scaffold protein believed to be involved in the maturation of FeS cluster containing subunits. The expression pattern of the five ORFs within the extended hyp-operon in both Nostoc punctiforme and Nostoc PCC 7120 is similar to the expression patterns of hupS, nifD, hypF and hypC. CalA, a known transcription factor, interacts with the promoter region between hupSL and the five ORFs within the extended hyp-operon in both Nostoc strains.
This work was supported by the Swedish Energy Agency, the Knut and Alice Wallenberg Foundation, the Nordic Energy Research Program (project BioH2) and the European Union/Energy FP7 project SOLAR-H2 (contract # 212508).
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