Comparative genomic analysis of carbon and nitrogen assimilation mechanisms in three indigenous bioleaching bacteria: predictions and validations
- Gloria Levicán†1, 4,
- Juan A Ugalde†2, 5,
- Nicole Ehrenfeld1, 6,
- Alejandro Maass2, 3 and
- Pilar Parada1Email author
© Levicán et al; licensee BioMed Central Ltd. 2008
Received: 11 August 2008
Accepted: 03 December 2008
Published: 03 December 2008
Carbon and nitrogen fixation are essential pathways for autotrophic bacteria living in extreme environments. These bacteria can use carbon dioxide directly from the air as their sole carbon source and can use different sources of nitrogen such as ammonia, nitrate, nitrite, or even nitrogen from the air. To have a better understanding of how these processes occur and to determine how we can make them more efficient, a comparative genomic analysis of three bioleaching bacteria isolated from mine sites in Chile was performed. This study demonstrated that there are important differences in the carbon dioxide and nitrogen fixation mechanisms among bioleaching bacteria that coexist in mining environments.
In this study, we probed that both Acidithiobacillus ferrooxidans and Acidithiobacillus thiooxidans incorporate CO2 via the Calvin-Benson-Bassham cycle; however, the former bacterium has two copies of the Rubisco type I gene whereas the latter has only one copy. In contrast, we demonstrated that Leptospirillum ferriphilum utilizes the reductive tricarboxylic acid cycle for carbon fixation. Although all the species analyzed in our study can incorporate ammonia by an ammonia transporter, we demonstrated that Acidithiobacillus thiooxidans could also assimilate nitrate and nitrite but only Acidithiobacillus ferrooxidans could fix nitrogen directly from the air.
The current study utilized genomic and molecular evidence to verify carbon and nitrogen fixation mechanisms for three bioleaching bacteria and provided an analysis of the potential regulatory pathways and functional networks that control carbon and nitrogen fixation in these microorganisms.
The employment of microorganisms for metal recovery from low-grade ores and mineral concentrates and secondary materials, has developed into a successful and expanding area of biotechnology. In association with this interest, microbial communities of extreme acidophilic prokaryotes from bioleaching environments have long been the subject of active research; however, the components and interactions within these microbial communities' remains poorly understood. Recent acquisition of genomic data directly from organisms living in naturally extreme environments [1–4] in combination with genome sequencing projects of individual species [5, 6] provides a novel opportunity for prediction and exploration of the metabolic details that control both individual microorganisms and microorganism communities.
Acidophilic prokaryotes involved in metal recovery from sulfide minerals include members of the Bacteria and Archaea domains. Three species of chemolithotrophic bacteria are mainly involved: Acidithiobacillus ferrooxidans, Acidithiobacillus thiooxidans and Leptospirillum sp., all of which obtain energy primarily from iron and/or sulfur oxidation. A. ferrooxidans is capable of oxidizing reduced sulfur compounds and Fe2+ ions to form sulfate and Fe3+, respectively [7–10]. A. thiooxidans can only oxidize reduced sulfur compounds such as thiosulfate, tetrathionate, metal sulfides and elemental sulfur to form sulfate [7–9, 11]. Leptospirillum sp. is solely capable of oxidizing Fe2+ ions to form Fe3+ . These autotrophic microorganisms utilize the energy and reducing power derived from iron and/or sulfur oxidation for several metabolic processes, including CO2 fixation and acquisition of several sources of nitrogen. In both Acidithiobacillus species, CO2 fixation occurs via the Calvin-Benson-Bassham cycle [5, 13, 14] whereas Leptospirillum sp. grows autotrophically; however the molecular mechanisms involved in carbon fixation remain obscure.
In acidic bioleaching environments, dissolved inorganic carbon can reach levels below atmospheric concentrations average. Therefore, it is not surprising that CO2 concentrating mechanisms have been identified in autotrophic prokaryotes present in such environments [15, 16]. In A. ferrooxidans (ATCC 23270), the presence of carboxysomes has been inferred from genome annotation , but the physiological role of this compartment and characterization of global CO2 concentrating mechanisms in bioleaching bacteria are yet to be determined.
Nitrogen plays an important role in the ecology of microbial communities. Therefore, understanding the molecular mechanisms involved in nitrogen fixation and assimilation are critical to understand how microorganisms adapt themselves to changes in environmental nitrogen. Ammonium, nitrate, nitrite and glutamine are the main nitrogen sources used by microorganisms in natural environments. Under low nitrogen levels, diazotrophic bacteria can fix atmospheric nitrogen under anaerobic or microaerobic conditions through the action of the nitrogenase complex. Because reduction of N2 to ammonium is an energy-demanding process and because the nitrogenase enzyme is very sensitive to oxygen, biological N2 reduction is a tightly regulated process [18, 19].
The capability of microorganisms to fix atmospheric nitrogen plays an important role in recycling scarce nitrogen existing in nutrient-poor acidic conditions; however, the availability of nitrogen and the energy required for its fixation may limit bacterial growth and adversely affect the efficiency of bioleaching operations. The study of nitrogen metabolism in members of microbial communities is therefore of both fundamental and applied interest. In bioleaching communities N2 fixation has been predicted for A. ferrooxidans [5, 20–22] and members of groups I [23, 4] and III  of the Leptospirillum genus. Genomic analysis of these bacteria revealed the presence of genes involved in N2 fixation (nif), ammonium transport (amt) and genes encoding the regulatory proteins NtrC and NifA (specific activators of nif genes). Genes encoding the regulatory PII protein, which plays a controlling role in the nitrogen metabolism coupled to the central carbon metabolism [25, 26], have also been identified.
Although carbon and nitrogen fixation has been predicted for A. ferrooxidans and members of the Leptospirillum genus, the physiology and regulation of these processes are still poorly understood. Here we report a comparative genomic analysis of the carbon and nitrogen metabolism carried out on three sequenced bacterial genomes (A. ferrooxidans, A. thiooxidans and Leptospirillum group II) isolated from naturally extreme environments in the north of Chile.
Results and discussion
Molecular mechanisms involved in CO2fixation
CO2fixation by the Calvin-Benson-Bassham (CBB) cycle
CBB is composed of 13 enzymatic reactions, 12 of which are involved in regeneration of ribulose 1,5-bisphosphate (RuBP) and one of which is responsible for CO2 fixation catalyzed by ribulose 1,5-bisphosphate carboxylase/oxygenase (Rubisco). The key CO2 fixation enzymes in the CBB cycle are Rubisco, Phosphoribulokinase (PRK) and Sedoheptulose 1,7-bisphosphatase (SBP) . We searched in the genomes of Acidithiobacillus ferrooxidans, Acidithiobacillus thiooxidans and Leptospirillum ferriphilum for genes encoding these CBB enzymes (See additional file 1: CarbAsilProts.csv for the list and sequence of these proteins). PRK and SBP genes were identified in the Acidithiobacillus strains as single copies but not in the Leptospirillum strain. We identified canonical forms of Rubisco encoded in the genomes of both Acidithiobacillus species inspected. In A. ferrooxidans DSM 16786, two gene copies encoding Rubisco form I (cbbSL1 and cbbSL2) and one copy encoding Rubisco form II (cbbM) were identified, as described previously , whereas in A. thiooxidans DSM 17318, Rubisco forms I and II were each encoded by one gene. The presence of multiple sets of genes for Rubisco is well documented in the literature. For example, in Hydrogenovibrio marinus it has been proposed that the expression of three Rubisco genes (two of form I and one of form II) is dependent on the environmental CO2 concentration and that there is an interactive regulation among these genes . It is interesting to note that both Acidithiobacillus strains examined in this study contain a cbbR gene upstream of the cbbSL1 and cbbM genes. CbbR is a positive regulator of cbb operon that coordinates the expression of three Rubisco genes [29–31]. It is likely that the presence of multiple forms and gene copies of Rubisco and a controlled Rubisco expression system allow these bacteria to rapidly respond to environmental changes in the CO2/O2 concentrations.
In the Leptospirillum DSM17947 strain only the non-canonical Rubisco-like protein (RLP) was identified, which is similar to Rubisco form IV of the photosynthetic thermophilic purple sulfur bacteria Chromatium tepidum . RLP has not been demonstrated to catalyze CO2 fixation and therefore the enzyme may not take part in the CBB cycle .
The genomic analysis performed on these three genomes suggested that the two γ-proteobacteria strains from the Acidithiobacillus genus (strains DSM 16786 and DSM 17318) can fix CO2 via the CBB cycle. This is based on the identification of all 13 genes encoding enzymes required for this cycle; however, distinct forms and copy numbers of the Rubisco genes were identified. We did not identify genes encoding the key CO2 fixation enzymes of the CBB cycle in Leptospirillum DSM 17947.
CO2fixation by the RTCA cycle
These findings represent the first evidence of the reductive tricarboxylic acid cycle as being the autotrophic CO2 fixation mechanism in a member of Leptospirillum genus.
Genetic characterization of L. ferriphilumgenes encoding enzymes of the RTCA cycle
Bioinformatic analysis of the L. ferriphilumRTCA cycle predicted proteins
The RTCA cycle operates in phylogenetically diverse autotrophic bacteria and archaea [36–41]. Due to this high diversity, it is not surprising to find some differences among these organisms with respect to the catalytic mechanisms and enzymes involved in each step of the cycle. Two examples of these differences are demonstrated by conversion reactions of citrate, which form acetyl-CoA plus oxaloacetate and carboxylation of 2-oxoglutarate which forms isocitrate. Both conversions can be catalyzed in only one reaction as its described for most bacteria, or in two reactions as has been described for Hydrogenobacter thermophilus . To elucidate the nature of the RTCA cycle enzymatic reactions for L. ferriphilum DSM 17947, we analyzed the deduced amino acid sequences of the predicted proteins using a bioinformatics approach.
The first key enzyme of the RTCA pathway is fumarate reductase (Figure 1, reaction 3), which catalyzes the reduction of fumarate to succinate using ubiquinol as an electron donor. This enzyme is a transmembrane protein comprised of two domains; the soluble N-terminal domain (subunit A) which is exposed to the cytoplasm and contains a covalently linked FAD, and the membrane-bound C-terminal domain (subunit B) which contains three iron-sulfur centers. Based on amino acid comparisons of these core subunits and on comparison of the metal centers and membrane anchors, fumarate reductase has been subdivided into five classes, types A-E . The type E group is comprised of those enzymes that lack a canonical membrane-anchoring domain but contain amphipathic subunits that ensure interaction with the membrane. Although we searched the complete genome of L. ferriphilum DSM 17947 for specific sequences to each class of fumarate reductase , only the frdA and frdB genes were detected, which encode the flavoprotein and iron-sulfur protein subunits respectively, and were located in tandem in the ccl operon (Figure 2). We did not detect orthologs for any of the known membrane anchoring subunits. The FdrA and FdrB candidate proteins showed overall similarity to the corresponding subunits of Geobacter metallireducens (70% and 59%, respectively). In addition, FdrA has a high similarity to the SdhA subunit of succinate dehydrogenase from the cyanobacteria Synecchocystis sp., which resembles type E enzymes that contain a non-canonical amphipathic subunit structure . Taken together, these data suggest that the fumarate reductase from L. ferriphilum is a new member of the fumarate reductase type E family . In addition, using bioinformatics procedures, the polypeptide encoded by orf1 located upstream of frdA and frdB was predicted to contain four putative amphipathic helices and to be targeted towards the inner membrane of the cell. We therefore believe that orf1 is a candidate gene for the anchor subunit of fumarate reductase. Further research will be required to evaluate the subunit composition and the catalytic properties of the Frd enzyme from the Leptospirillum genus.
Another key enzyme of the RTCA pathway is 2-oxoglutarate ferredoxin oxidoreductase (OGOR) (Figure 1, reaction 5), which catalyzes the reductive carboxylation of succinyl-CoA to 2-oxoglutarate. In H. thermophilus, a chemolithoautotrophic hydrogen-oxidizing bacterium that fixes carbon dioxide via the RTCA cycle, two different OGOR polypeptide complexes have been reported: one with two subunits (encoded by korAB) and the other with five subunits (encoded by forDABGEF) . A search of the L. ferriphilum DSM 17947 genome showed five similar genes to those in the for operon, including forABGE, which encode the α, β, γ, and ε subunits of OGOR (Figure 2), and two non-identical copies of forD (encoding the δ subunit). These latter non-identical copies of forD (forD1 and forD2) were identified in a different genomic loci which is strikingly different from other models described and will therefore require further analysis to confirm the nature of this putative δ subunit and its possible role in the enzymatic activity of the OGOR complex. The deduced amino acid sequences of these six OGOR subunits showed high overall similarity (66–80%) to the corresponding OGOR subunits of H. thermophilus and also to the conserved protein motifs common to 2-oxoacid acceptor oxidoreductases in the Prosite database (α: PF01855, β: PF02775, γ: PF01558, ε: PF00037, δ1 and δ2: PF02552). No evidence of korAB genes encoding a two-subunit OGOR was found.
In prokaryotes, isocitrate dehydrogenase (ICDH) (Figure 1, reaction 6) is mainly an oligomeric enzyme that catalyzes the reversible conversion of isocitrate to 2-oxoglutarate. ICDH has been mainly studied as a catabolic enzyme of TCA cycle; nonetheless, in some CO2-fixing organisms that utilize the RTCA cycle, special properties of the ICDH enzyme have become evident . For illustration, ICDH from Clorobium limicola  is a monomeric enzyme that works more favorably fixing CO2 in anabolic way than in catabolic decarboxylating way, contrary to that for the ICDH enzyme from E. coli. In addition, a novel mechanism for efficient conversion of 2-oxoglutarate to isocitrate has been recently described for ICDH from H. thermophilus  and involves two distinct and consecutive reactions catalyzed by 2-oxoglutarate carboxylase (OGC) and oxalosuccinate reductase (OSR). In L. ferriphilum DSM 17947, we identified isocitrate dehydrogenase genes similar to those from E. coli. This suggests that L. ferriphilum does not utilize ICDH for anabolic CO2 fixation, as described for C. limicola or H. thermophilus. Experimental methods will be required to determine whether the ICDH from L. ferriphilum functions in a manner similar to that from E. coli or whether this enzyme catalyzes the reductive carboxylation of 2-oxoglutarate in a novel manner.
An important reaction in carbon metabolism is the condensation of acetyl-CoA and oxaloacetate to citrate via the TCA cycle. This reaction is catalyzed by citrate synthase; however, in the case of the RTCA cycle, the reverse reaction is catalyzed by ATP citrate lyase (ACL). ACL is a key enzyme of the RTCA cycle and is unique to organisms that utilize the RTCA cycle. ACL has also been reported in eukaryotes [47–50], where it plays an important role in supplying acetyl-CoA for fatty acid biosynthesis. ACL from Chlorobium  and fungi  is composed of a small and a large subunit with similarity to the N- and C-terminal half, respectively, of the mammalian single polypeptide ACL . On the other hand, in the Aquifex and Hydrogenobacter genera, a novel and ACL-independent citrate cleavage pathway has been described [54, 55]. In these organisms, the ATP-dependent cleavage of citrate is catalyzed by the combined action of the citryl-CoA synthetase (Ccs) and citryl-CoA lyase (Ccl) enzymes (Figure 1, reactions 8 and 9). Ccs is composed of a 46 kDa β subunit and a 36 kDa α subunit. Ccl is a single polypeptide protein of 30 kDa.
Inspection of the L. ferriphilum DSM 17947 genome revealed the presence of ccsAB and ccl, but not aclAB, suggesting that in this bacterium, citrate cleavage occurs via two successive reactions catalyzed by the enzymes Ccs and Ccl, as described for the Aquifex and Hydrogenobacter genera and for H. thermophilus [54, 55]. In addition, the predicted polypeptide sequences of CcsA, CcsB and Ccl displayed high amino acid similarity to the corresponding proteins of H. thermophilus (CcsA: 74% similarity, CcsB: 75% similarity and Ccl: 66% similarity).
Pyruvate ferredoxin oxidoreductase (POR) is another key enzyme in the RTCA pathway and catalyzes the reductive carboxylation of acetyl-CoA to pyruvate (Figure 1, reaction 10). POR, like OGOR, is a member of the 2-oxoacid oxidoreductase family and both enzymes are structurally similar, making sequence comparisons difficult; fortunately, the POR and OGOR enzymes of H. thermophilus have been enzymatically characterized [56–59], and the amino acid sequences are available in the NCBI database. We identified five putative por genes (porABGED) in the L. ferriphilum genome, and based upon the similarity of their deduced amino acid sequences to those from H. thermophilus we assigned a putative function to these genes. The predicted proteins PorA, PorB, PorG, PorE and PorD were similar (65–79%) to α, β, γ, ε and δ subunits of the POR enzyme from H. thermophilus and has the conserved pattern of 2-oxoacid: acceptor oxidoreductases (Prosite database). Additionally, the POR subunit genes were clustered downstream of the for operon (Figure 2).
Our genomic analysis suggests that completely different regulatory mechanisms exist for microorganisms that fix CO2 via alternative mechanisms. Specifically, the Acidithiobacillus and Leptospirillum strains examined in this study fix CO2 by altering the direction of the central carbon metabolism.
Molecular mechanisms involved in CO2concentrating mechanisms
Carbon concentrating mechanisms are present in many species of chemolithoautotrophic bacteria, enabling them to grow in the presence of low concentrations of CO2. They mainly utilize bicarbonate transporters and CO2 traps to generate high intracellular concentrations of dissolved inorganic carbon.
Inorganic carbon transporters that deliver intracellular HCO3 - represent an important carbon concentrating mechanism within a diverse group of microorganisms . In cyanobacteria at least five distinct enzymes for active inorganic carbon uptake have been described, including BCT1 (High affinity Bicarbonate Transporter 1), SbtA (Sodium bicarbonate transporter A), BicA (Low affinity Na+-dependent Bicarbonate Transporter), NDH-14 and NDH-13 (NAD(P)H dehydrogenase type 1) (Reviewed in ). BicA is a Na+-dependent HCO3 - transporter belonging to the widespread SulP (Sulphate Transporter or Permease) family . In the Acidithiobacillus DSM 16786 and DSM 17318 strains analyzed in this work, a putative gene for the BicA transporter was identified, whereas in L. ferriphilum putative genes for the BCT1 transporter (cmpABCD) were detected.
The carboxysome is a polyhedral micro compartment located in the cytoplasm of most autotrophic bacteria and is surrounded by a proteinaceous monolayer that reportedly contains Rubisco and carbonic anhydrase (CA) . CA converts accumulated cytosolic HCO3 - into CO2 within the carboxysome, elevating the CO2 concentration in the vicinity of Rubisco . Previous reports described the A. ferrooxidans ATCC 23270 carboxysome as being composed of at least seven peptides, all encoded by genes located in a carboxysome operon . Similarly, seven candidate genes potentially involved in carboxysome formation were identified immediately downstream of the cbbLS1 genes in both Acidithiobacillus strains examined in the present report. The cbbLS2 and cbbM genes from these strains are followed by the cbbQO genes, which are involved in posttranslational regulation of Rubisco. Carbonic anhydrases are classified in four main forms: α-CA, β-CA, γ-CA and ε-CA [67–69]. ε-CA has been described as a novel form that corresponds to carboxysomal shell protein CsoS3 . The β-CA family is comprised of enzymes from four evolutionarily distinct clades (A through D). Candidate genes for β-CA (Clade B), γ-CA and ε-CA, but not for α-CA, were identified in the A. ferrooxidans DSM 16786 genome. This is consistent with that reported for A. ferrooxidans ATCC 23270 . In A. thiooxidans DSM17318, we only identified a single candidate gene for ε-CA, located in the putative carboxisome gene cluster. In L. ferriphilum DSM 17947, we identified putative genes for β-CA (clade D) and γ-CA, but not for ε-CA (encoded by the csoS3 gene) or for any of the carboxysome genes (cso genes).
Differences in CO2 concentrating mechanisms were also predicted from genomic analysis of the bioleaching bacteria examined herein. In both Acidithiobacillus strains, HCO3 - transport via carboxysomes and the BicA-type protein was inferred. Because CO2 concentrating mechanisms have been described mainly among organisms that utilize the CBB cycle, such as cyanobacteria, comparative analysis with microorganisms that use the RTCA cycle is not possible. Further analysis will be necessary to determine whether L. ferriphilum truly lacks carboxysomes or whether an analogous structure is encoded by unidentified genes to improve the efficiency of RTCA cycle enzymes that fix CO2.
Nitrogen uptake mechanisms
To gain a better understanding of the mechanisms by which the microorganisms examined herein fulfill their nitrogen requirements, we searched the genomic sequences for genes involved in the uptake of different nitrogen compounds (See additional file 2: NitAsilProts.csv for the list and sequence of proteins involved in nitrogen assimilation). From this search we identified genes that encode for the nitrogenase complex in A. ferrooxidans DSM 16786, genes encoding proteins involved in the assimilation of nitrate and nitrite in A. thiooxidans DSM 17138, and genes coding for ammonia permeases (amtB) in the three microorganisms.
In the A. ferrooxidans DSM 16786 genome, we identified a region in which genes of the nitrogenase complex and all the necessary assembly proteins are located (Figure 3), consistent with what has been reported in other strains of A. ferrooxidans . In this region we found the nitrogenase genes nifHDK next to several tandem genes important for assembly of the nitrogenase MoFe cofactor (fdxD, C1499, nifE, nifN and nifX). Interestingly, the genes draGT, the products of which are associated with post-translational regulation of nitrogenase in α-proteobacteria [19, 71] were situated in reverse orientation to the nifHDK operon. In contrast, we did not find any homologous genes in the A. thiooxidans DSM 17318 and L. ferriphilum DSM 17947 genomes, which suggests that these microorganisms utilize alternative mechanisms for assimilation of nitrogen from the environment, consistent with what has been reported for members of Leptospirillum Group II [2, 3], and A. thiooxidans .
Nitrate and nitrite assimilation
We examined whether A. thiooxidans DSM17318 was capable of utilizing nitrate as the sole nitrogen source by monitoring the growth of this strain in a shaking flask experiment under aerobic conditions. Preliminary data showed that this bacterium cannot grow using nitrate as nitrogen source but can grow normally in the presence of ammonia (data not shown). Most bacteria that assimilate nitrate do so under aerobic conditions; in contrast, dissimilatory nitrate metabolism only occurs under anaerobic or microaerophilic conditions. Genome analysis of A. thiooxidans DSM 17138 showed that conserved genes involved in nitrate and nitrite assimilation as narB and nirBD are present. This evidence suggests that this bacterium has the ability to assimilate both nitrate and nitrite from the environment (Fig. 4). Nevertheless, experimental evidence under anaerobic conditions would be required to verify this.
Ammonia transporters (Amt) have been described for almost all organisms, including bacteria , and catalyze the movement of ammonia across the cell membrane. We identified genes encoding ammonia permeases (amtB) in all three microorganisms examined in this study. However, assimilation of ammonia from the environment appears to be the only source of nitrogen for L. ferriphilum DSM 17947, consistent with that reported for Leptospirillum sp. Group II [2, 3].
Regulation of nitrogen assimilation
The process of nitrogen uptake, particularly nitrogen fixation, is energetically costly, and has therefore been shown to be tightly regulated [[18, 19], and ]. To assess the regulatory mechanisms for nitrogen uptake in A. ferrooxidans DSM 16787, A. thiooxidans DSM 17318 and L. ferriphilum DSM 17947, we compared the genetic information from these three organisms to genomic information from microorganisms with previously described regulatory systems, focusing in particular on the genome of A. ferrooxidans DSM 16786, which we determined to be capable of nitrogen fixation.
Nitrogen fixation (NifA, DraTG)
The lack of nifL in the A. ferrooxidans DSM 16786 genome makes it difficult to discern the manner in which oxygen levels affect the regulation of nitrogen fixation in this microorganism. Nitrogenase is very sensitive to oxygen levels, and microorganisms cope with this problem via strategies such as anaerobiosis, high rates of oxygen consumption, and compartmentalization. In γ-proteobacteria, the NifL protein responds to high oxygen by inactivating the NifA protein, whereas in low oxygen conditions, the NifL protein activates the NifA regulator to stimulate expression of the nitrogenase genes [18, 79]. It has been reported that in some microorganisms such as Rhizobia, which also lacks nifL, NifA directly responds to oxygen levels via an N-terminal cysteine motif (CXXXXC) [18, 79]. We identified a similar N-terminal cysteine motif in the translated A. ferrooxidans nifA sequence, suggesting that this microorganism circumvents the need for NifL by utilizing NifA for direct response to oxygen levels.
In the A. ferrooxidans DSM 16786 genome, we also identified genes encoding dinitrogenase reductase-activating glycohydrolase (DraG) and dinitrogenase reductase ADP-ribosyltransferase (DraT) proteins near the nitrogenase operon (Figure 5). These gene products are involved in post-translational regulation of the nitrogenase complex in α-proteobacteria [18, 80]. Under high nitrogen conditions, DraT inactivates nitrogenase via ADP-ribosylation . Under low nitrogen conditions, DraG catalyzes removal of the ADP-ribose from nitrogenase to activate the enzyme . Only recently, the presence of these genes was described in the ATCC23270 strain of A. ferrooxidans , making this microorganism the first reported γ-proteobacteria to be carrying such genes, again suggesting lateral transfer from other microorganisms.
Although nitrogenase genes were not identified in the A. thiooxidans DSM 17318 and L. ferriphilum DSM 17947 genomes, we searched these genomes for nitrogenase regulatory elements. In L. ferriphilum DSM 17947, we identified a candidate nifA homolog, annotated as a NifA-like transcriptional regulator, but the gene was located in a region containing genes involved in the synthesis of flagella. This NifA candidate has an 82% identity with the NifA transcriptional regulator from Leptospirillum sp. Group II. In Leptospirillum sp. Group II, nifA is also located in a region containing genes involved in the synthesis of flagella. It is possible that in L. ferriphilum, this NifA-like protein regulates the synthesis and/or the assembly of flagella, but this needs to be explored further. Of note, the NifA gene in L. ferriphilum DSM 17947 is distinct from that in L. ferrooxidans, an organism previously shown to participate in nitrogen fixation in the Tinto River [23, 112], and from that in L. ferrodiazotrophum, an organism previously connected to nitrogen fixation in the acid mine drainage .
The NtrB/NtrC two-component system
Another important regulatory system in the assimilation of nitrogen compounds is the NtrB/NtrC (Part of the nitrogen regulation system Ntr) two-component system [18, 19]. This system is involved in bacterial response to different nitrogen sources, such as molecular nitrogen, ammonia, or nitrate, and is present in great number of microorganisms . The NtrB protein is a kinase, which activates NtrC via phosphorylation under low nitrogen conditions. NtrC is a transcription factor that not only regulates the glnA gene, which encodes the glutamine synthetase enzyme required for metabolic incorporation of ammonia, and the glnK-amtB operon, which encodes a PII regulatory protein and an ammonia permease protein, but also regulates its own operon (ntrBC). Positive regulation of ntrBC is triggered in response to low intracellular levels of glutamine via the PII sensory system [18, 81, 82]. We identified genes encoding proteins of the NtrB/NtrC two-component system in the A. ferrooxidans DSM 16786 and A. thiooxidans DSM 17318 genomes. In contrast, we identified genes from the NtrY/NtrX two-component nitrogen assimilation system in the L. ferriphilum DSM 17947 genome. NtrX is a transcriptional regulator similar to members of the Fis family (53% identity with a protein from Geobacter uraniireducens) whereas NtrY is a membrane-bound sensor kinase protein. The NtrY/NtrX system has been described in Azorhizobium caulinodans and Azospirillum brasilense (both diazotrophs), and in A. brasilense, where it was shown to participate in the regulation of nitrogen assimilation via detection of ammonia . This suggests that in L. ferriphilum DSM 17947, NtrY detects ammonia levels and regulates the transcription factor NtrX accordingly.
Because amtB is present in all three organisms examined in this study, this suggests a common mechanism for regulation of ammonia uptake [18, 84]. In A. ferrooxidans DSM 16786 and A. thiooxidans DSM 17318, ammonia levels are detected in response to glutamine concentrations and uptake is controlled by the NtrB/NtrC system. In L. ferriphilum DSM 17947, ammonia levels are directly detected by NtrY and uptake is controlled by the NtrY/NtrX system. Nonetheless, both systems likely control similar target genes.
PII protein family
The PII family of signal transduction proteins are found in eukarya, bacteria and archaea [81, 82]. These proteins comprise one of the central mechanisms for controlling the metabolism of nitrogen and carbon in the cell [26, 85] via detection of intracellular levels of different compounds, like glutamine, ATP, and 2-oxoglutarate . This allows them to integrate the information from nitrogen (glutamine, ATP) and the carbon metabolism (ATP, 2-oxoglutarate), thus activating or inactivating several enzymes and transcription factors according to the requirements of the cell [18, 19, 26, 81, 82, 85].
An unexplored issue for nitrogen fixation in A. ferrooxidans is the oxygen sensitivity of the nitrogenase enzyme. A. ferrooxidans typically uses oxygen as its terminal electron acceptor during nitrogen fixation, although it reportedly grows under anaerobic conditions using a ferric ion as the terminal electron acceptor . We have recent evidence that this nitrogenase enzyme is functioning under aerobic conditions on some substrates (data not shown). We believe that in A. ferrooxidans, inactivation of nitrogenase may be prevented by two parallel mechanisms: increased activity of the terminal cytochrome oxidase bd protein may impart respiratory nitrogenase protection  and a ferrodoxin "FeSII"-like protein may provide conformational protection of nitrogenase. Both protective mechanisms have been described for Azotobacter vinelandii [88, 89]. A homolog of the A. vinelandii FeSII gene was identified two open reading frames downstream of the nitrogenase gene nifK, and would likely be co-expressed with the complete nif operon (data not shown). This putative ferredoxin protein may protect nitrogenase from irreversible inactivation mediated by oxygen, as has also been described for Gluconobacter diazotrophicus . More experimental data is necessary to confirm this hypothesis.
Although this study provides important genetic information regarding L. ferriphilum DSM 17947, there is insufficient information for development of a nitrogen metabolism regulatory model. For example, a possible interaction between the NtrX/NtrY system and the PII proteins has been recently explored in Rhodobacter capsulatus ; for L. ferriphilum DSM 17947, it is unclear which nitrogenous species is detected by NtrX/NtrY. In addition, other Leptospirillum species [4, 24] are reportedly capable of nitrogen fixation, in contrast to L. ferriphilum, making extrapolation from one species to another difficult.
Recently it has been reported the genome sequence of another strain of Acidithiobacillus ferrooxidans, which was released by the Joint Genome Institute and named as A. ferrooxidans ATCC 53993. This strain was previously characterized as L. ferrooxidans, but now with the genome available it has been reclassified as a member of the Acidithiobacillus genus. Comparing the genome sequence of the ATCC 53993 strain and our A. ferrooxidans DSM 16786 strain, we observed some differences related with the genome organization (manuscript in preparation), but the genes and mechanisms involved in carbon and nitrogen fixation that we are discussing in this paper, are also present in the ATCC 53993 strain. A similar situation occurred when we compared the genome sequence of our L. ferriphilum strain DSM 17947, against the genome sequence of the microorganism Leptospirillum sp. Group II UBA (92), where the same genes that we described in this work for the carbon and nitrogen assimilation, are also present in this microorganism, confirming that our findings are conserved in microorganisms from the same specie.
Based on our genomic analysis, an ecological role for each of these three microorganisms within a bioleaching community can be proposed. In this type of environment, energy is not the limiting factor for the development of the microbial community, as sulfur or iron minerals are abundant and can be used as electron donors. Therefore, carbon and/or nitrogen are likely the most limiting elements for the development of the microbial biomass. Given this limitation, A. ferrooxidans DSM 16786, or other nitrogen fixing microorganism, may act as the primary supplier of nitrogen (either in the form of nitrate or ammonia) and may therefore be essential for the establishment of a microbial community in this system.
Although each of the strains analyzed in this study is capable of carbon fixation, different pathways are employed to accomplish this purpose. The Calvin-Benson-Bassham cycle represents the most important extant autotrophic carbon fixation pathway. Despite its global significance, it is restricted to organisms with high-energy yield from a chemotrophic or phototrophic lifestyle. Microorganisms present in extreme environments (e.g., high temperature, anaerobic, or acidic conditions) generally utilize different CO2 fixation pathways . Thus, the presence of the RTCA cycle in Leptospirillum reflects the fact that these microorganisms are more metabolically restricted than A. ferrooxidans or A. thiooxidans; Leptospirillum is the only genus which strictly uses ferrous iron as an electron donor. Additionally, the presence of two completely different CO2 fixation mechanisms in the Acidithiobacillus and Leptospirillum genera likely reflects the distinct growth and colonization capacities of these bacteria in extreme environmental conditions. This might also explain the dominance of the Leptospirillum genus reported in bioleaching communities from industrial operations or from naturally extreme environments [93, 94].
To date, a lack of mutational studies and/or knockout strains has prohibited analysis of CO2 and nitrogen metabolisms in A. ferrooxidans, A. thiooxidans, and L. ferriphilum. However, as demonstrated here and elsewhere [3, 24], genomic and other global (transcriptomic and metatranscriptomic) approaches (1,4) can bypass this limitation to provide relevant information regarding individual and community metabolisms.
The genomic study presented here, is the first attempt to describe the metabolic tactics used by a community of three chemolitotrophic bacteria found in a Chilean biomining environment. Acidithiobacillus ferrooxidans is capable of oxidizing iron and sulfides as energy source, whereas Acidithiobacillus thiooxidans only oxidizes sulfides and Leptospirillum ferriphilum only oxidizes iron. These three organisms often share the same environmental niche, but their relative abundance differs depending on whether their surroundings are natural or modified by operations such as mining, likely because the nutrient sources in both cases are completely different. To have a deeper insight on how microorganisms take advantage of the CO2 and nitrogen resources present in their environment we performed this comparative analysis concluding the following main facts:
A. ferrooxidans fixes CO2 by the Calvin-Benson-Bassham (CBB) cycle, the same mechanism used by A. thiooxidans, but the latter has only 1 copy of Rubisco type I instead of the 2 copies found in A. ferrooxidans. A different and novel situation was discovered for Leptospirillum ferriphilum that is fixing CO2 by the reductive tricarboxylic acid cycle.
With respect to nitrogen source assimilation we discovered that while all the species analyzed can incorporate ammonia by their ammonia transporter, Acidithiobacillus thiooxidans can assimilate nitrate and nitrite and only Acidithiobacillus ferrooxidans is able to fix nitrogen directly from the air
Strains and culture conditions
A. ferrooxidans DSM 16786, A. thiooxidans DSM 17318 and L. ferriphilum DSM 17947 (all strains owned by BioSigma SA) were grown at 30°C with shaking (200 rpm) in basal 9 K medium ((NH4)SO4: 0.4 g/L, K2HPO4: 0.4 g/L, MgSO4-7H2O: 0.4 g/L) adjusted to pH 1.8 with concentrated sulfuric acid and supplemented with i) FeSO4-7H20: 30 g/L, ii) S°: 1% w/v and iii) FeSO4-7H20: 15 g/L plus Fe2(SO4)3: 12,4 g/L, respectively. Cell number was determined by chamber counting under microscope (Thoma Chamber, depth 0.010 mm). Cultures were harvested by centrifugation at 12,000 × g for 20 min at 4°C.
To evaluate the growth of A. thiooxidans DSM 17318 on nitrate, cells were grown in 9 K medium with or without ammonia and supplemented with 0.5–4.0 g/L KNO3, above described. Nitrate and nitrite concentrations were quantified using Nitratest (Merck) according to manufacturer's instructions.
Generation of Genomics Library and Sequence Analysis
Sequencing of A. ferrooxidans DSM 16786 performed using a shotgun library of 5,568 clones (2,000 bp each) sequenced by Seqwrite (Houston, TX) and a second library of 1,433 fosmids (40,000 bp each) sequenced by Agencourt (Boston, MA), with an estimated coverage 2.79 folds. The final assembly contained 764 contigs forming 286 scaffolds; the biggest scaffolds covered 62% of the total sequence, while the general coverage of all the assembled contigs is estimated to be near a 94% of the total sequence. The genome of A. thiooxidans DSM 17318 was sequenced using a shotgun library of 18,0480 plasmid clones (4,000 bp each) and 11,088 fosmid clones (40,000 bp each) sequenced by Agencourt (Boston, MA), with an estimated coverage of 4.5×. The final assembly contained 882 contigs forming 283 scaffolds; the seven biggest scaffolds covered the 75% of the sequence, while the general coverage of all the assembled contigs is estimated to be near 92% of the total sequence. The genome of L. ferriphilum DSM 17947 was sequenced using a shotgun library 13,645 plasmid clones (2,000 bp each) and 10,088 fosmids clones (40,000 bp each) sequenced by Agencourt (Boston MA), with an estimated coverage of 5.47×. The final assembly contained 321 contigs forming 89 scaffolds; the five biggest scaffolds covered 87% of the sequence, while the general coverage of all the assembled contigs is estimated to be near a 94% of the total sequence. For all the three genomes, base calling was performed using Phred [95, 96] and resulting reads were assembled using a two-stage method: contigs were formed using Arachne , consensus sequences of each contig were obtained using Phrap . Scaffolds were formed using the Bambus software  based on read mate-pairing. Ambiguities were solved by comparison to the reference sequences and by manual curation.
The assembled sequences of the three genomes were annotated using the GenDB annotation system . Candidate ORFs were marked using Glimmer/Critica  and annotated by homology to the COG database , to non-redundant proteins from NCBI and to previously described proteins from the literature. Protein domains were marked using InterPro . Afterwards automatic annotation was manually cured.
PCR and RT-PCR
Reverse transcriptase PCR (RT-PCR) was carried out in order to identify co-transcribed genes of L. ferriphilum DSM 17947. PCR reactions were carried out to characterize the nirB gene of A. thiooxidans DSM 17318. For RT-PCR, total RNA was isolated from cells in late exponential phase using the protocol described in  Briefly, cell pellets were washed with a solution of 10 mM H2SO4 (pH1.2) followed by PBS buffer (pH 1.2) and suspended in Tris buffer (pH 8.0) containing EDTA, SDS, Triton X-100, and Tween 20 (STT buffer) . The suspension was treated with proteinase K and phenol: chloroform extracted. The total RNA was precipitated using isopropanol as described in . Genomic DNA for PCR amplification of nirB was obtain using the same protocol in , for total RNA extraction described previously. PCR and RT-PCR were carried out by standard procedures and included various control reactions that accompanied each experiment. The DNA sequences of the various primers used for both RT-PCR and PCR and their locations on the genomic open reading frame context are provided (See additional file 3: OligoList.pdf for the list of primers used).
Bioinformatics sequence analysis
The genomic sequences from the three microorganisms under investigation were examined. Proteins involved in known carbon fixation pathways were obtained from the KEGG database . Amino acid sequences derived from genes identified as being involved in the Calvin cycle and the RTCA cycle were used as query sequences to search the translated nucleotide database from the genomes of the A. ferrooxidans DSM 16786, A. thiooxidans DSM 17318 and L. ferriphilum DSM 17947 strains using tBlastn  with default parameters. When a prospective candidate gene was identified, its predicted amino acid sequence was used to formulate a BlastP  search of the NCBI non-redundant data base. Only the best hits were accepted as evidence for putative orthologs. Candidate genes and their corresponding translated proteins were further characterized using the following bioinformatics tools: primary structure similarity relations were determined using ClustalW 1.8 , structural motif predictions were determined using Prosite  and peptide domain predictions were determined using ProDom .
This work was supported by BioSigma 'S. A.'. The authors thank the company for authorizing the submission of the manuscript for publication. Also, this work was partially supported by FONDEF D04I1257, R18, FONDAP and BASAL-CMM projects.
The authors also thank Carolina Burgos and Valeria Espinoza for their technical support.
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