Metagenomic studies recently uncovered form II/III RubisCO genes, originally thought to only occur in archaea, from uncultivated bacteria of the candidate phyla radiation (CPR). There are no isolated CPR bacteria and these organisms are predicted to have limited metabolic capacities. Here we expand the known diversity of RubisCO from CPR lineages. We report a form of RubisCO, distantly similar to the archaeal form III RubisCO, in some CPR bacteria from the Parcubacteria (OD1), WS6 and Microgenomates (OP11) phyla. In addition, we significantly expand the Peregrinibacteria (PER) II/III RubisCO diversity and report the first II/III RubisCO sequences from the Microgenomates and WS6 phyla. To provide a metabolic context for these RubisCOs, we reconstructed near-complete (>93%) PER genomes and the first closed genome for a WS6 bacterium, for which we propose the phylum name Dojkabacteria. Genomic and bioinformatic analyses suggest that the CPR RubisCOs function in a nucleoside pathway similar to that proposed in Archaea. Detection of form II/III RubisCO and nucleoside metabolism gene transcripts from a PER supports the operation of this pathway in situ. We demonstrate that the PER form II/III RubisCO is catalytically active, fixing CO2 to physiologically complement phototrophic growth in a bacterial photoautotrophic RubisCO deletion strain. We propose that the identification of these RubisCOs across a radiation of obligately fermentative, small-celled organisms hints at a widespread, simple metabolic platform in which ribose may be a prominent currency.
The vast majority of the organisms in the environment have not been cultivated, obscuring our knowledge of their physiology. Recent metagenomic investigations have revealed the presence of a large diversity of uncultivated organisms in marine and terrestrial subsurface environments (Castelle et al., 2013, 2015; Lloyd et al., 2013; Baker et al., 2015). For example, in a metagenomic study of a shallow alluvial aquifer, we determined that many of the uncultivated bacteria were associated with the candidate phyla radiation (CPR), a monophyletic group of at least 35 phyla that accounts for >15% of all bacterial diversity (Brown et al., 2015). Metagenomic sampling of almost 800 CPR bacteria suggested that members of this radiation consistently have small genomes with many metabolic limitations, including lack of an electron transport chain, no more than a partial tricarboxylic acid cycle and mostly incomplete nucleotide and amino-acid biosynthesis pathways. Using metabolic predictions from complete and near-complete genomes (Wrighton et al., 2012), we inferred that members of the CPR are fermenters whose primary biogeochemical impact is primarily on subsurface organic carbon and hydrogen cycling (Wrighton et al., 2014). However, many of the genes in these genomes remain poorly annotated and the metabolic platform of CPR bacteria remains uncertain. Further, no transcription and enzyme activities have been validated, hindering knowledge of the actual reactions catalyzed by these organisms.
The incorporation of CO2 into organic carbon is a critical step in the carbon cycle. Ribulose-1,5-bisphophate carboxylase-oxygenase (RubisCO) is the most abundant enzyme on earth and is integral to the fixation of carbon dioxide. Currently four forms of RubisCO can fix atmospheric carbon dioxide (I, II, II/III and III) (Tabita et al., 2007; 2008). Forms I and II are used by plants, algae and some chemoautotrophic and phototrophic bacteria for CO2 fixation during primary production via the Calvin Benson Bassham (CBB) cycle. Forms III and II/III, found primarily in archaea, enable light-independent CO2 incorporation into sugars derived from nucleotides like adenosine monophosphate (AMP) (Sato et al., 2007; Tabita et al., 2007). Form II/III RubisCOs, which were primarily known in methanogens, have greater overall similarity to bacterial Form II RubisCO but have specific residues, structural and catalytic features that more closely resemble archaeal form III (Alonso et al., 2009).
Previously, we reported the first evidence of form II/III RubisCO genes in partial genomes from the Peregrinibacteria (PER) phylum in the CPR radiation (Wrighton et al., 2012). Additionally, three bacterial form II/III RubisCOs were recovered from genomes of members of the SR1 phylum that also are inferred to be fermentative (Wrighton et al., 2012; Campbell et al., 2013; Kantor et al., 2013). The presence of these annotated RubisCO genes in small genomes that house few ancillary genes suggests that RubisCO may have an important role in the metabolism of some of these bacteria.
To more comprehensively explore the diversity and potential role of CPR RubisCOs, we reproduced the prior experiment from which we first identified bacterial form II/III RubisCO sequences (Wrighton et al., 2012). Size filtration was used to increase the relative abundance of the small-celled CPR organisms in samples used for sequencing (Luef et al., 2015). Here we investigate CPR genomes that encode RubisCO genes, report a new RubisCO sequence type diverged from Archaeal form III and propose a broader metabolic context in which these genes occur. By detecting in situ transcripts and through directly cloning one CPR form II/III RubisCO sequence into an expression host, we suggest the potential functionality of this bacterial enzyme. This study represents the first enzymatic activity demonstrated from these broadly distributed but metabolically enigmatic candidate phyla bacteria.
Materials and methods
Groundwater field experiment and sample collection
The field experiment was carried out between 25 August and 12 December 2011 at the US Department of Energy Rifle Integrated Field Research Challenge site adjacent to the Colorado River, CO, USA as recently described (Brown et al., 2015; Castelle et al., 2015; Luef et al., 2015). In brief, biostimulation experiments were performed by adding approximately 15 mm acetate to the groundwater over the course of 72 days to maintain an average in situ concentration of ~3 mM acetate during peak stimulation. Six microbial community samples (A–F) were collected over 93 days, including 3 days prior to acetate stimulation and after acetate addition ceased (amendment ceased on day 72). Ferrous iron and sulfide concentrations were analyzed immediately after sampling using the HACH phenanthroline assay and methylene blue sulfide reagent kit, respectively (HACH, Loveland, CO, USA). Acetate and sulfate concentrations were determined using a Dionex ICS-2100 ion chromatograph (Sunnyvale, CA, USA) equipped with an AS-18 guard and analytical column (Williams et al., 2011). Microbial cells from pumped groundwater that passed through a 1.2-μm prefilter (Pall, Port Washington, NY, USA) were retained on 0.2- and 0.1-μm filters (Pall). Filters were flash-frozen in liquid nitrogen immediately upon collection.
Nucleic acid extraction and sequencing
Approximately a 1.5-g sample from each frozen filter was used for genomic DNA extraction. DNA was extracted using the PowerSoil DNA Isolation Kit (MoBio Laboratories, Inc., Carlsbad, CA, USA). Illumina HiSeq 2000 2 × 150 paired-end sequencing was conducted by the Joint Genome Institute on extracted DNA. Sequencing amounts for samples A–F from 0.1- and 0.2-μm filters ranged from 9.5 to 40.7 Gbp, as described in Castelle et al. (2015). RNA was extracted using Invitrogen TRIzol Reagent (Carlsbad, CA, USA) followed by genomic DNA removal and cleaning using Qiagen RNase-Free DNase Set Kit (Valencia, CA, USA) and Qiagen Mini RNeasy Kit (Valencia, CA, USA). An Agilent 2100 Bioanalyzer (Santa Clara, CA, USA) was used to assess the integrity of the RNA samples. Only RNA samples having RNA Integrity Number between 8 and 10 were used. The Applied Biosystems SOLiD Total RNA-Seq Kit (Invitrogen/LifeTechnologies, Carlsbad, CA, USA) generated the cDNA template library. The SOLiD EZ Bead system was used to perform emulsion clonal bead amplification to generate bead templates for SOLiD platform sequencing. Samples were sequenced on the 5500XL SOLiD platform (LifeTechnologies). The 75-bp sequences produced were mapped in color space using the SOLiD LifeScope software version 2.5 (Life Technologies/Invitrogen) using the default parameters against the reference genome set of 2 302 715 separate gene FASTA entries. Corresponding GTF files were built to record the position of each gene on the set of artificial chromosomes.
Genome assembly, binning and functional annotations
Methods for assembly, binning and annotation are described from methods described in detail in prior publications (Wrighton et al., 2012; Castelle et al., 2015). Reads were quality trimmed using Sickle (https://github.com/najoshi/sickle) with default settings. Trimmed paired-end reads were assembled using IDBA_UD (Peng et al., 2012) with default parameters. Genes on scaffolds >5 kb in length were predicted using Prodigal (Hyatt et al., 2012) with the metagenome procedure (-p meta), and then USEARCH (–ublast) (Edgar, 2010) was used to search protein sequences against UniRef90 (Suzek et al., 2007), KEGG (Kanehisa and Goto, 2000; Kanehisa et al., 2012) and an in-house database composed of open reading frames from candidate phyla genomes. The in-house database includes previously published genomes (Wrighton et al., 2012; Castelle et al., 2013; Hug et al., 2013; Kantor et al., 2013; Wrighton et al., 2014) and genomes from ongoing work and primarily aiding in identifying putative CPR scaffolds. For each scaffold, we determined the GC content, coverage and profile of phylogenetic affiliation based on the best hit for each gene against the Uniref90 (Suzek et al., 2007) database. Scaffolds were binned to specific organisms by using coverage across the samples, phylogenetic identity and GC content, both automatically with the ABAWACA algorithm and manually using ggKbase (http://ggkbase.berkeley.edu/). ABAWACA is an algorithm that generates preliminary genome bins based on different characteristics of assembled scaffolds (https://github.com/CK7/abawaca). Six genome bins generated by ABAWACA were manually inspected within ggKbase. Binning purity was confirmed using an Emergent Self-Organizing Map (Dick et al., 2009). Our primary method for assessing genome completeness was based on the presence or absence of orthologous genes representing a core gene set that are widely conserved as single-copy genes among bacterial candidate phyla, but we also assessed global markers. All single copy and metabolic analyses reported here and summarized in the Supplementary Figures are reported in ggKbase (FASTA files can be accessed via links provided in the Supplementary Figures). Manual assembly curation improved some genome bins by extending and joining scaffolds, removing local scaffolding errors and, in some cases, bringing in small previously unbinned fragments. One genome was curated to closure and completion.
Inventory of the RubisCO genes
All putative RubisCO genes on genome fragments assembled from the 12 separate groundwater filter samples were recovered first by BLAST search (Altschul et al., 1990) against an in-house database that included candidate phyla sequences from prior studies (Wrighton et al., 2012; Campbell et al., 2013; Kantor et al., 2013; Castelle et al., 2015). The taxonomic affiliation of these putative RubisCO CPR scaffolds was confirmed based on phylogenetic analysis of genes included on the same genome fragment as the RubisCO or in the same genome bin. We then used these RubisCO sequences to recruit additional CPR sequences from currently unreported groundwater and sediment genomic data sets from the same field site.
16S rRNA gene recovery and phylogenetic analyses
16S rRNA gene sequences were identified in assembled scaffolds based on Hidden Markov Model searches using the cmsearch program from the Infernal package (cmsearch –hmmonly –acc –noali –T –1) (Nawrocki et al., 2009). This protocol is described in detail in Brown et al. (2015). Searches were conducted using the manually curated structural alignment of the 16S rRNA provided with SSU-Align (Nawrocki, 2009). Sequences corresponding with CPR genomes were aligned using SSU-Align along with the best hits of these sequences in the Silva database (v1.2.11) (Quast et al., 2013), a curated set of reference sequences associated with candidate phyla of interest, and a set of archaea sequences to serve as a phylogenetic root. Sequences with ⩾800 bp aligned in the 1582-bp alignment were used to infer a maximum-likelihood phylogeny using RAxML (Stamatakis, 2014) with the GTRCAT model of evolution selection via ProTest and 100 bootstrap re-samplings.
Protein phylogenetic analyses and modeling
For single protein trees (for example, RubisCO large subunit), the phylogenetic pipeline was performed as previously described (Wrighton et al., 2012). Briefly, protein sequences were aligned using MUSCLE version 3.8.31 (Edgar, 2004) with default settings. Problematic regions of the alignment were removed using very liberal curation standards with the program GBlocks (Talavera and Castresana, 2007). Alignments with and without GBlocks were confirmed manually. Best models of amino-acid substitution for each protein alignment were estimated using ProtTest3 (Abascal et al., 2005). Phylogenetic trees were generated using RAxML with the PROTCAT setting for the rate model and the best model of amino-acid substitution specified by ProtTest. Nodal support was estimated based on 100 bootstrap replications using the rapid bootstrapping option implemented in RAxML. Three-dimensional structure predictions were generated by SWISS-MODEL (an automated protein homology-modeling server) and i-tasser based on protein alignment and secondary structure prediction. The alignment mode was based on a user-defined target-template alignment. Conservation of key catalytic residues and the secondary structure for each model was confirmed by manual inspection.
Plasmids and cloning
Rifle metagenomic DNA was used as the template to amplify the exact coding regions for the RubisCO genes from PER genome PER_GWF2_38_29 (PER-2), the OD-1 genome GWE1_OD1_1_1_39 and WS6 genomes GWC1_1_418 and GWC1_33_22_1_93. Primer sequences used for RubisCO amplification are included (Supplementary Table S1). PCR was performed using the PrimeStar GXL (Clontech, Mountain view, CA, USA) high-fidelity polymerase. PCR products for all genes were cloned between NdeI and BamHI sites in plasmid pet11a (Novagen/EMD Millipore, Billerica, MA, USA), which does not incorporate an N-terminal hexa-histadine tag. For the PER, the PCR product was also cloned between KpnI and BamHI sites in plasmid p80, a high copy plasmid 3716-based vector (a derivative of pLO11 obtained from Oliver Lenz and Bärbel Friedrich, Berlin, Germany), which contained the Rhodospirillum rubrum CbbR/cbbM promoter region, for expression in vivo. This promoter has been used previously in the broad-host range vector pRPS-MCS3 to drive the expression of RubisCO genes to complement RubisCO deletion strain Rhodobacter capsulatus strain SB I/II (Smith and Tabita, 2003). Constructs for the coding regions of archaeal form III Archaeoglobus fulgidus RbcL2 (Kreel and Tabita, 2007), archaeal form II/III Methanococcoides burtonii rbcL and bacterial form II R. rubrum cbbM (Falcone and Tabita, 1993) were used for comparison and served as positive controls. The sequences of all constructs were verified at the Plant-Microbe Genomics Facility at The Ohio State University.
Growth and culture conditions
To test for in vitro activity, RubisCO proteins from pet11a constructs were expressed in Escherichia coli strain Rosetta 2 (DE3) pLysS (Novagen), which uses the pRARE plasmid to accommodate expression of rare codons such as those from candidate phyla and archaeal RubisCO sequences. Cells were grown in 50 ml lysogeny broth supplemented with 150 μg ml−1 ampicillin and 12.5 μg ml−1 chloramphenicol in 125-ml flasks. After reaching an optical density of 0.6–0.8 (at 600 nm), RubisCO gene expression was induced by adding IPTG to a final concentration of 1 mM. After 5–16 h of shaking at room temperature, cells were harvested, flash frozen and stored at −80 °C prior to analysis. To ensure that candidate phyla RubisCOs were exposed to minimal amounts of oxygen, cell lysis and assay conditions were performed under strict anaerobic conditions. Using an anaerobic chamber, cell pellets were resuspended in 50 mM bicine-NaOH, 10 mM MgCl2, at pH 8.0, supplemented with 2 mM NaHCO3 and 1 mM dithiothreitol; crude protein lysates were obtained via bead beating with 0.1-mm beads for 3–4-min intervals in tightly capped tubes.
To test for in vitro activity from complemented autotrophic cultures, p80::PER, p80::R. rubrum and pRPS-MCS3::A. fulgidus RubisCO constructs were transformed into E. coli strain S17-1 (ATCC47055) and mobilized into R. capsulatus SB I/II− via biparental matings (Smith and Tabita, 2003; Satagopan et al., 2009, 2014). Plasmid-complemented strain SB I/II− colonies were first selected on peptone yeast extract plates followed by streaking onto Ormerod’s minimal medium (Ormerod et al., 1961) agar plates with no added organic carbon. To test for photoautotrophic growth complementation, plates were incubated in illuminated anaerobic jars, which were periodically flushed with a gas mixture of 5% CO2/H2 as previously described (Satagopan et al., 2009, 2014). Anaerobic CO2-dependent photoautotrophic growth was obtained using Ormerod’s minimal medium agar plates in a sealed jar flushed with a 5% CO2/95% H2 gas mixture. Colonies on minimal plates under these conditions were used to inoculate liquid photoautotrophic cultures bubbled continuously with 5% CO2/H2 for growth analysis; cells were harvested anaerobically for RubisCO activity assays, as described above.
In vitro RubisCO assays
RubisCO assays with activated enzyme preparations were performed according to Satagopan et al. (2014) with modifications to ensure anaerobiosis. All crude protein lysates, reagents and supplies were prepared in an anaerobic chamber and crimped in sealed glass vials prior to conducting the assays in a hood using gas-tight Hamilton syringes (Hamilton Robotics, Reno, NV, USA). Assay reaction mixtures contained 50 mM NaHCO3 (~2 μCi of NaH 14CO3), 10 mM MgCl2 and 0.8 mM ribulose 1,5 bisphosphate (RuBP) in 50 mM bicine-NaOH buffer, pH 8.0. RubisCO activity is initiated by addition of its physiological substrate, RuBP. Reactions were initiated with the addition of crude protein lysate to its physiological substrate, RuBP, at 30 °C and incubated for 5–30 min. Negative control reactions consisted of no RuBP or no crude protein lysate added. Carboxylase activities were determined following the equimolar conversion of 14C from NaHCO3 into acid-stable 3-phosphoglycerate (3-PGA), as measured via radioactive scintillation counting. Protein was determined via the Bradford method and specific activities (nmol CO2 fixed per min per mg protein) were calculated consistent with prior publications (Satagopan et al., 2009).
Results and discussion
Recovery of CPR genomes that contain RubisCO
We reconstructed CPR genomes from sequence data sets for samples collected over 93 days (Brown et al., 2015; Castelle et al., 2015). As previously reported, bacteria from CPR phyla WS6, OD1 and OP11 were enriched (>75% 16S rRNA relative abundance) on the 0.1-μm filter, and some members were shown to have ultra-small cells (median cell volume of 0.009±0.002 μm3) (Luef et al., 2015). Multiple genomes belonging to the CPR phylum PER were recovered from all six 0.2-μm filter data sets, suggesting that these cells may be larger in size than other CPR bacteria (for example, OD1, WS6) enriched on the 0.1-μm filters.
Taxonomic identifications of the CPR organisms from which we recovered RubisCO genes are provided in Supplementary Figures S1 and S2. The emergent self-organizing map clustered genome fragments based on their tetranucleotide sequence composition (Supplementary Figure S3) and validated 16 unique CPR genomes that ranged in estimated completion from near-complete (>94%) to complete (Supplementary Figure S4). Here we report RubisCO sequences from five genomic bins assigned to the PER phylum, two to the Parcubacteria (OD1), five to the Microgenomates (OP11) and six to the WS6 phylum (Table 1). We also report RubisCO from additional scaffolds assigned to these CPR phyla.
The five WS6 genomes reported here span multiple taxonomic classes (Supplementary Figure S1 and Supplementary Table S2) (Brown et al., 2015). The manually curated and closed WS6 genome is 0.896 Mbp in length and is the first complete genome reconstructed for a member of this lineage. The mapped read file confirming the assembly and the annotations can be accessed via ggKbase (see Methods section). Given the level of genome completion and the breadth of phylogenetic diversity sampled here (Konstantinidis and Rosselló-Móra, 2015), we propose the name Candidatus Dojkabacteria for the WS6 phylum to honor the memory of Michael A Dojka, who first reported this lineage based on 16S rRNA gene sequence data (Dojka et al., 2000)
We recovered five distinct PER genomes that we estimated to be >93% complete (Table 1; Supplementary Figure S4). This data set augments the three partial PER genomes analyzed from samples collected from the same aquifer 5–7 days after acetate stimulation, two of which (ACD51, ACD65) encoded RubisCO genes (Wrighton et al., 2012). Phylogenetic analyses that include these and other recently reported sequences (Rinke et al., 2014; Brown et al., 2015) support the identification of this lineage as a separate phylum (Candidatus Peregrinibacteria). Based on sequence divergence, the five Peregrinibacterial genomes reported here represent multiple taxonomic classes in this newly designated phylum.
CPR genomes contain novel and diverse RubisCO sequences
Fifty-one new RubisCO genes were identified from these CPR genomes. Some sequences, for example, from the WS6-1 and OD1-1 genomes, were independently reconstructed from multiple data sets. Ultimately, 18 representative unique sequences were manually confirmed by read mapping to verify their accuracy (Figure 1). These sequences were most similar to previously reported CPR or archaeal RubisCO sequences (and not bacterial RubiscCO sequences) (Supplementary Table S3) and the majority harbor the key active-site residues (Figure 2).
Phylogenetic analyses revealed that the seven bacterial CPR RubisCO sequences reported here are members of the previously defined archaeal intermediate form II/III RubisCOs (Figure 1) (Tabita et al., 2007, 2008). Recent metagenomic studies reported the form II/III RubisCOs from PER and SR1 uncultivated bacterial lineages (Wrighton et al., 2012; Campbell et al., 2013; Kantor et al., 2013). Although the overall sequence similarity is most closely related to type II, protein sequence alignment confirmed the presence of form III-specific residues (Supplementary Figure S5), validating the form II/III phylogenetic placement of these bacterial sequences. Our results expand the bacterial members of this form by four additional PER sequences, add the first three Dojkabacteria sequences and add a single-cell unpublished Microgenomates (OP11) sequence. Originally, two form II/III RubisCO subgroups were described based on the absence (PER) or the presence (SR1 and archaea) of a 29 amino-acid N-terminal insert sequence (Wrighton et al., 2012; Campbell et al., 2013; Supplementary Figures S5 and S6). Here our additional sampling of the PER RubisCO confirms this earlier discovery, as all PER genomes to date lack the insertion. The Microgenomates and two of the Dojkabacteria RubisCOs reported here have the 29 amino-acid insertion found in the SR1 and archaeal II/III form, while the closed WS6 genome (WS6-1) encodes a RubisCO with a novel 48 amino-acid insertion (Figure 1,Supplementary Figures S5 and S6). Both the 29 and 48 amino-acid insertion sequences are located in the same position as previously identified insertions. Similar to the methanogen sequences, the insertion is sandwiched between catalytic sites of the enzyme (Supplementary Figure S5), yet impact of these insertions on enzyme biochemical properties is currently unknown.
In addition to the form II/III sequences, nine of our newly recovered bacterial sequences form a distinct and strongly supported monophyletic group that branches deeply from, yet is most similar to, the form III RubisCO sequences found in archaea. This current CPR clade includes RubisCO sequences from Dojkabacteria (3), Parcubacterium (1) and Microgenomates (5). Although the extent of sequence divergence between these bacterial sequences and the archaeal form III sequences is considerable, additional taxon sampling is needed to resolve this clade as completely distinct RubisCO form (Figure 1,Supplementary Figure S7). In our analyses, we have identified other bacterial genomes that contain homologs to archaeal form III sequences in public databases (for example, from a partial single-cell Parcubacteria genome and in two Firmicutes draft genomes; Supplementary Figure S7). Notably, these bacterial form III are not monophyletic with the CPR RubisCOs described here but clade with the canonical archaeal form III.
The parcubacterial sequence from the OD1-1 genome contains two, an 8 and 24 amino acid, insertions between alpha-helix 6 and beta-sheet 7 (Figure 1, Supplementary Figures S5 and S6). The WS6 genome containing divergent form III also contains the eight amino-acid insertion. To further confirm analyses indicating that these insertions were not due to sequencing or assembly error, we designed specific PCR primers for the gene encoding for the large RubisCO subunit and confirmed the insertions via cloning and sequencing. Prior sequence analyses demonstrated that this region was involved in interactions with the neighboring subunit (Satagopan et al., 2014); however, these insertions have not been previously identified in other RubisCO sequences.
CPR RubisCO is inferred to support a heterotrophic nucleoside pathway
Previously studied archaeal form III (Finn and Tabita, 2004; Sato et al., 2007; Estelmann et al., 2011) and form II/III (Tabita et al., 2008; Alonso et al., 2009) RubisCOs are not associated with the CBB pathway but instead function in a nucleoside-salvaging pathway. Consistent with the archaeal genomes that contain RubisCO, all bacterial CPR genomes containing RubisCOs sampled to date lack the gene encoding phosphoribulokinase, a key gene of the CBB pathway (Wrighton et al., 2012; Campbell et al., 2013; Kantor et al., 2013). However, we note these genomes contain many genes that are too novel to be identified based on sequence similarity and thus we cannot eliminate the possibility that they contain new enzymes or divergent phosphoribulokinase homologs (Ashida et al., 2008). Consistent with our hypothesis that these RubisCO function in archaeal nucleoside pathway, outside other CPR sequences, these RubisCO proteins have the closest homologs to similar archaeal and not bacterial RubisCOs (Supplementary Table S3). Thus we suggest RubisCOs studied here also function in a nucleoside/nucleotide metabolism pathway analogous to archaea.
Rather than using phosphoribulokinase, there are two proposed pathways to generate RuBP, the substrate for RubisCO in Archaea. In the first pathway, identified in Thermococcus kodakarensis, nucleosides are converted into 3-PGA. The first step in this short pathway dephosphorylates the nucleotide (AMP, CMP, UMP) to release the base (for example, adenine), yielding ribose-1,5-bisphosphate, which an isomerase converts to ribulose-1,5-bisphosphate (RuBP) (that is, AMP→ribose 1,5 bisphosphate→RuBP). From RuBP and CO2, the type III or II/III archaeal RubisCO generate two molecules of 3-PGA, a central intermediate of core carbon metabolism (Aono et al., 2012).
All CPR genomes with RubisCO reported here and studied previously possesses the two archaeal AMP pathway homologs (Figure 4), with the best hits to the AMP phosphorylase and the isomerase outside the CPR are largely from archaeal genomes (Supplementary Table S3). For both proteins in this pathway, the most similar sequences outside the CPR are to homologs in archaeal genomes, often times to methanogens (PER) or to uncultivated archaeal lineages such as the DPANN (Castelle et al., 2015). We used an amino-acid alignment and protein modeling to confirm that the CPR isomerase has all residues for catalytic activity and is specific for ribose 1,5 bisphophate and not another substrate, for example, 5-methylthioribose-1-phosphate isomerase (Supplementary Figures S8 and S9). Based on the genomic evidence to date, we propose that the CPR bacteria likely use a RubisCO pathway analogous to that of T. kodakarensis (Figure 3, denoted in green).
In contrast to Thermococcus pathway, other thermophilic archaeal (Methanocaldococcus jannaschii, Methanosarcina acetivorans and Archaeoglobus lithotrophicus) use a second pathway. In this pathway, ribose-phosphate pyrophosphokinase (PRPP) is suggested to be desphophorylated to ribose 1,5 bisphosphate via an abiotic reaction that is facilitated by high temperatures. In archaea, the non-enzymatically produced ribose 1,5-bisphosphate is then converted to RuBP by an enzyme annotated to function in thiamine monophosphate formation (Figure 3, unique pathway denoted in yellow; Finn and Tabita, 2004) (that is, PRPP→ribose 1,5 bisphosphate→RuBP). Given that only one Peregrinibacterium genome contains a distant homolog of this RuBP-forming enzyme, and all of these CPR were recovered from an ~14 °C aquifer, this pathway seems less likely in most CPR bacteria whose genomes encode RubisCO. However, we note many PER genomes encode an enzyme that can convert PRPP to AMP. This enzyme, adenine phosphoribosyltransferase, may represent an alternative mechanism by which PER genomes can use PRPP via the AMP pathway and not the pathway previously reported in thermophilic archaea (that is, PRPP→AMP→ribose 1,5 bisphosphate →RuBP). Thus we cannot rule out that PRPP may also be used as a source for RuBP in some members of the CPR via a T. kodakarensis-like pathway (Figure 3).
Very recently, Aono et al. (2015) identified alternative enzymes involved in the nucleoside metabolism pathway in T. kodakarensis, linking nucleoside moieties to central carbon metabolism. Instead of AMP phosphorylase (step 1 T. kodakarensis pathway), the ribose moieties of adenosine, guanosine and uridine are converted to ribose-1-bisphosphate (R1P) by three nucleoside phosphorylases. R1P is converted to ribose-1,5-bisphosphate (R15P) via a nucleoside kinase (ADP-dependent ribose-1-phosphate kinase). R15P is likely directed to glycolysis via the R15P isomerase and RubisCO. In this metabolic context, using phosphate and ADP, the ribose moieties of adenosine, guanosine and uridine are converted to R15P via R1P by nucleoside phosphorylases and ADP-R1P kinase (Aono et al., 2015) (Figure 3, blue dotted line). Finally, R15P can be directed to glycolysis via the functions of R15P isomerase and RubisCO (Aono et al., 2015). We examined the CPR genomes for this alternative T. kodakarensis pathway and found some (albeit weak) support for this pathway in Microgenomates and most PER genomes. Thus it cannot be ruled out that some CPR bacteria could use an alternative route through which R15P is generated from the phosphorolysis of nucleosides (Figure 3).
CPR organisms that contain RubisCO are inferred to be obligate fermenters (Supplementary Figure S10), consistent with prior metabolic analyses (Wrighton et al., 2012; Campbell et al., 2013; Kantor et al., 2013; Wrighton et al., 2014). All of the genomes lack a complete tricarboxylic acid cycle, NADH dehydrogenase (complex I) and most other complexes from the oxidative electron transport phosphorylation chain (for example, complex II, complex III, complex IV and quinones). All CPR genomes included in this study, besides the Dojkabacteria (WS6), have complete or near-complete glycolysis and/or pentose phosphate pathway(s) and the capacity to produce acetate, lactate and/or hydrogen as byproducts of fermentation. Notably, the PER, in contrast to bacteria of the other CPR genomes with RubisCO described here, seem to have the capacity to synthesize nucleotides and some amino acids (Supplementary Figure S11).
The metabolic information gleaned from the first complete WS6 genome is sparse compared with that for the other CPR genomes. Enzymes that were identified include those required for the last steps of glycolysis from PGA to pyruvate and ultimately fermentation to acetate and ATP. Notably, PGA is the product of RuBP conversion by RubisCO (Figure 3). We failed to identify genes for upper glycolysis, gluconeogenesis and the pentose phosphate pathway in the WS6 genomes (Supplementary Figure S10). Gene and protein sequences discussed in this manuscript can be accessed through links in Supplementary Figures S10 and S11. This finding is similar to reports of bacteria of the SR1 phylum (placement within the CPR is uncertain) that also encode form II/III RubisCO and lack these pathways (Campbell et al., 2013; Kantor et al., 2013) (Supplementary Figure S10). Complete and closed SR1 and WS6 genomes also lack pathways for biosynthesis of nucleotides (purines and pyrimidines) and amino acids (Kantor et al., 2013). Consistent with reports for SR1 and some small CPR genomes (Kantor et al., 2013; Gong et al., 2014; Brown et al., 2015; He et al., 2015; Luef et al., 2015), we suggest that WS6 bacteria reported here have an obligatory symbiotic or parasitic lifestyle and are not free-living.
It is possible that WS6 and other CPR that encode RubisCO may be reliant on other members of the community for external ribose, which is utilized as carbon and energy sources. A bacterial or archaeal cell is on average 20% by weight RNA, and RNA is 40% by weight ribose, meaning that a cell is roughly 8% pure ribose. A recent paper used this information to suggest that ribose was likely an abundant sugar available on early earth for fermentation and that the archaeal type III RubisCO pathway of nucleoside monophosphate conversion to 3-PGA might be a relic of ancient heterotrophy (Schönheit et al., 2015). In a similar manner, we suggest that in WS6 the ribose moiety can be funneled into RuBP via the two gene AMP pathway and converted to PGA via RubisCO to ultimately yield ATP and acetate via substrate-level phosphorylation. This use of ribose would minimize the energetic cost of upper glycolysis, maximizing energy yields for these organisms such as WS6 with tiny genomes.
CPR RubisCO transcripts detected in the environment
We examined the metatranscriptomic sequence data set collected from the 0.2-μm filter samples for reads that mapped uniquely to PER-1 genome (Supplementary Table S4), given that these organisms were enriched on this filter (there was insufficient biomass after metagenomics to investigate the 0.1-μm filters). In the sample collected prior to acetate amendment (sample A), we confirmed the expression of RubisCO (Scaffold 3_gene102) and the surrounding gene neighborhood (3_105, 3_107, 3_109) (Figure 4a). Notably, besides RubisCO, all of these transcribed genes were annotated as hypothetical. Also in sample A, we detected transcripts for step 1 of the AMP pathway (AMP phosphorylase (Scaffold 5_gene7)) and energy generation via acetate production (phosphotransacetylase (Scaffold 5_gene5)), as well as a poorly annotated phosphoesterase (Scaffold 5_gene4) (Figure 4b). The expression of RubisCO, a key gene in the AMP pathway, and genes for acetate production from the same genome prior to stimulation suggests a role for the RubisCO and likely the AMP pathway in bacteria under natural aquifer conditions.
The PER RubisCO can support autotrophic CO2-dependent growth
We synthesized a recombinant protein in E. coli of the PER-1 form II/III RubisCO that was transcribed in situ. We demonstrated CO2 fixation activity from the crude extract using RuBP as a substrate (Kreel and Tabita, 2007; Supplementary Table S5). In contrast to the PER results, the OD1 and WS6 recombinant proteins failed to support comparable (OD1) or detectable (WS6) RuBP-dependent CO2 fixation under these conditions. This latter WS6 finding is consistent with the missing catalytic residues and thus their annotation as RubisCOs remains uncertain (Figure 2).
More importantly, we demonstrated that the PER form II/III enzyme could complement a Rhodobacter capsulatus RubisCO-deletion host strain to support autotrophic CO2-dependent growth, much like archaeal form III RubisCO (Finn and Tabita, 2003) (Figure 5). However, while under the conditions tested RubisCO fixed extracellular CO2, we cannot rule out the possibility that in situ this RubisCO may scavenge intracellular CO2 pools to support heterotrophic metabolism as previously reported (Joshi and Tabita, 1996; Tachi and Tabita, 2001; Kresge et al., 2005; McKinlay and Harwood, 2010; Aono et al., 2015).
Given that RubisCO is exceptionally well studied owing to its central role in CO2 fixation in the Earth’s biosphere, it is significant that this analysis of subsurface sediments has yielded many new sequence types. We expand the phylogenetic membership of CPR genomes known to contain RubisCO sequences from the PER to include members of the Dojkabacteria (WS6), Parcubacteria (OD1) and Microgenomates (OP11). We provide the first demonstration that genes of this pathway are transcribed in situ in bacteria. We also verified the first physiological complementation of a novel RubisCO that can support CO2 fixation from a metagenomically derived sequence from the bacterial candidate phylum radiation. Future research is needed to identify the currently unknown but co-expressed flanking genes to better understand the regulatory as well as complete metabolic role for RubisCO in these small, apparently obligatory fermentative bacteria.
The presence of form II/III and a currently novel, undefined form of RubisCO in bacteria with a similar metabolic context (for example, anaerobic, non-CBB functionality) to RubisCO in archaea suggests a deep ancestry of this non-CBB cycle enzyme. Of particular note is that these bacterial RubisCOs occur in organisms with strikingly limited metabolic potential and no detected respiratory capacity. This metabolism, where ribose is suggested to have a key role in carbon compound transformations and energy generation, may have been important in organisms that existed before the emergence of respiration (Schönheit et al., 2015).
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This work is partially based upon work supported through the Lawrence Berkeley National Laboratory’s (LBNL) Sustainable Systems Scientific Focus Area. The US Department of Energy (DOE), Office of Science, Office of Biological and Environmental Research funded the work under contract DE-AC02-05CH11231 (LBNL; operated by the University of California) and DE-SC0004918 to JB and NIH grant R01GM095742 to FRT. DNA sequencing was conducted by the DOE Joint Genome Institute through the Community Science Program. RNA sequencing was performed at the DOE-supported Environmental Molecular Sciences Laboratory at PNNL as part of an award to JFB, KCW, MJW and KHW. We thank Lye Meng Markillie and Ronald C Taylor for transcriptomic sequencing. We thank Professor B Alber at the Ohio State University for discussions on microbial metabolism. Genomes and raw reads in this manuscript are deposited in NCBI under the accession numbers (pending) OP11_GWA2_42_18: LCDD00000000; OP11_GWA2_43_14: LCFP00000000; PER_GWA2_38_35: LBUV00000000; PER_GWF2_38_29: LBUS00000000; PER_GWF2_39_17: LBWM00000000; WS6_GWF2_39_15: LBWK00000000; WS6_GWC1_33_20: LBOV00000000 (BioProject: PRJNA273161 and BioSample: SAMN03319638). RNA sequences have been deposited in the NCBI Sequence Read Archive under accession number SRP050083. The genomes and relevant fasta files for all mentioned proteins are available via the website: http://ggkbase.berkeley.edu/, under the project name ‘RubiscO’ under the link entitled ‘Rifle groundwater metagenome’.
The authors declare no conflict of interest.
Supplementary Information accompanies this paper on The ISME Journal website
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