A Conserved Rubredoxin Is Necessary for Photosystem II Accumulation in Diverse Oxygenic Photoautotrophs*

Background: Photosystem II is an essential component of oxygenic photosynthesis. Results: Photosystem II is specifically decreased in rubredoxin mutants of the green alga Chlamydomonas reinhardtii, the cyanobacterium Synechocystis sp. PCC 6803, and the plant Arabidopsis thaliana. Conclusion: Rubredoxin is required for photosystem II, and not photosystem I, accumulation in these organisms. Significance: Rubredoxin was likely important in the evolution of oxygenic photosynthesis.

In oxygenic photosynthesis, two photosystems work in tandem to harvest light energy and generate NADPH and ATP. Photosystem II (PSII), the protein-pigment complex that uses light energy to catalyze the splitting of water, is assembled from its component parts in a tightly regulated process that requires a number of assembly factors. The 2pac mutant of the unicellular green alga Chlamydomonas reinhardtii was isolated and found to have no detectable PSII activity, whereas other components of the photosynthetic electron transport chain, including photosystem I, were still functional. PSII activity was fully restored by complementation with the RBD1 gene, which encodes a small iron-sulfur protein known as a rubredoxin. Phylogenetic evidence supports the hypothesis that this rubredoxin and its orthologs are unique to oxygenic phototrophs and distinct from rubredoxins in Archaea and bacteria (excluding cyanobacteria). Knockouts of the rubredoxin orthologs in the cyanobacterium Synechocystis sp. PCC 6803 and the plant Arabidopsis thaliana were also found to be specifically affected in PSII accumulation. Taken together, our data suggest that this rubredoxin is necessary for normal PSII activity in a diverse set of organisms that perform oxygenic photosynthesis.
Photosystem II (PSII) 3 uses absorbed light energy to catalyze the splitting of water into molecular oxygen and protons and is the only enzyme complex known to be capable of this energetically unfavorable process. Working together with photosystem I (PSI), the cytochrome b 6 f complex and the ATP synthase, PSII drives oxygenic photosynthesis and is responsible for producing most, if not all, of the oxygen present in the Earth's atmosphere (1,2). Recent work has further refined our knowledge of the structure (3) and biogenesis (4 -11) of PSII, but a complete understanding of how the 20 -30 protein subunits and ϳ70 cofactors are correctly assembled into a functional light-driven water:plastoquinone oxidoreductase remains elusive (12)(13)(14).
The structural and functional homology between PSII and the pheophytin-quinone (type II) reaction center of anoxygenic photosynthetic bacteria, along with many geological and biological lines of evidence, indicates that these two complexes share a common evolutionary origin and that this ancestral complex was almost certainly anoxygenic (15). Despite the availability of crystal structures for both reaction centers (3,16), knowledge of their common ancestor is remarkably limited and therefore the evolutionary inventions and innovations that enabled a proto-PSII to use water as an electron donor (and to concomitantly release molecular oxygen) are poorly understood.
Rubredoxins are [1Fe-0S] proteins in which one iron atom is coordinated by four cysteine residues (17,18). Most studied rubredoxins exist as small soluble proteins that act as electron carriers in a variety of biochemical processes including carbon fixation (19), detoxification of reactive oxygen species (20 -22), and fatty acid metabolism (23,24). The distribution of rubredoxins within the tree of life is distinct in that these proteins appear to be limited to divergent groups within the archaea and bacteria, whereas they are found in only one group of eukaryotes: plants and photosynthetic algae that contain a plastid derived ultimately from primary endosymbiosis of a cyanobacterium. Interestingly, this eukaryotic "photosynthetic" rubredoxin is thylakoid membrane-associated and, together with the homologous protein found in cyanobacteria, appears to represent a class of rubredoxins unique to the oxygenic pho-toautotrophs that is distinct from all other known rubredoxins (25,26).
Previous studies of thylakoid membrane rubredoxins have yielded conflicting results. Analysis of a mutant strain of the cyanobacterium Synechococcus sp. PCC 7002 lacking rubA, the membrane-bound rubredoxin, led to the conclusion that the function of this protein was to aid in iron-sulfur cluster assembly of PSI and that it had little or no effect on PSII (26,27). Surprisingly, however, an antibody raised against the membrane-bound rubredoxin from the photosynthetic cryptophyte Guillardia theta was found to react with a homologous protein in PSII-enriched particles from spinach (28).
Here we report the characterization of mutants lacking the thylakoid membrane-associated rubredoxin in the green alga Chlamydomonas reinhardtii, the cyanobacterium Synechocystis sp. PCC 6803 and the flowering plant Arabidopsis thaliana. We show that these mutants exhibit a PSII-specific defect and that the role of this rubredoxin in contributing to the assembly or stability of PSII is likely conserved in oxygenic photoautotrophs.

EXPERIMENTAL PROCEDURES
Strains, Mutant Generation, and Growth Conditions-Chlamydomonas reinhardtii wild-type strain 4Aϩ and the mutant strains 2pac, gRBD1-1, gRBD1-2, and Fud7 (29) were maintained on Tris acetate-phosphate (TAP) medium (30) in the dark and at 25°C unless otherwise indicated. The 2pac mutant (CAL028.03.28) was generated by insertional mutagenesis of the 4Aϩ strain with linearized pBC1 plasmid encoding paromomycin resistance (31), and flanking sequence was isolated by SiteFinding PCR (32) using the primers listed in supplemental Table S1. SiteFinding PCR products were separated by gel electrophoresis and isolated using the QIAquick gel extraction kit (Qiagen) before sequencing. Generation of gRBD1 complemented lines was achieved by transformation of the 2pac mutant with a 1.75 kb fragment of genomic DNA (for primers see supplemental Table S1) that includes the 510 bp coding sequence of the RBD1 gene cloned into the Gateway vector pENTR-D (Invitrogen), as described (33). After transformation, cells were allowed to recover in 10 ml of TAP overnight in the dark with shaking at 110 rpm. Cells were then collected by centrifugation (1,300 ϫ g, 3 min), resuspended in 300 l of high-salt (HS) medium (34), and plated onto HS agar plates. The plates were maintained under 50 mol of photons m Ϫ2 s Ϫ1 for 3 to 4 weeks before the autotrophic transformed colonies were picked.
The glucose-tolerant strain of the cyanobacterium Synechocystis sp. PCC 6803 (35) was used as a parental strain for generation of the ⌬rubA (⌬slr2033) mutant and as a wild-type control. All strains were grown on solid or in liquid BG-11 medium (36) buffered with 25 mM Hepes-NaOH, pH 7.5 and supplemented with 5 mM glucose at 32°C under constant illumination (30 mol of photons m Ϫ2 s Ϫ1 ) unless otherwise indicated.
The ⌬rubA mutant was obtained via transformation of wildtype cells as described (36) with a construct consisting of the 5Ј and 3Ј flanking regions of the rubA (slr2033) coding sequence directly fused with a cassette containing nptI (encoding resist-ance to kanamycin) and sacB (conferring lethality in the presence of sucrose) (37). Transformants were selected on BG-11 plates supplemented with 5 mM glucose, 5 M DCMU, and 50 M kanamycin. Segregation was analyzed by PCR amplification of both the flanking region and the coding sequence of rubA (for primers, see supplemental Table S1). Complementation of the ⌬rubA mutant was achieved by transformation with a plasmid containing the 5Ј and 3Ј flanking regions of the slr0168 coding sequence surrounding a construct consisting of the psbA2 promoter (38) fused with the coding sequence of rubA, allowing for incorporation into a neutral site as described (39).
Seeds from Arabidopsis thaliana wild type (Col-0) and from mutant GT12976 obtained from the Cold Spring Harbor Gen-eTrap collection (40,41) were sterilized and plated on plant nutrient plates (42) supplemented with 0.5% sucrose (5g/liter) (and kanamycin (50 g/ml), where indicated). Primers used for genotyping are listed in supplemental Table S1.
Chlorophyll Fluorescence-Minimum (F o ), maximum (F m ), and variable (F v /F m ) chlorophyll fluorescence of Chlamydomonas, Synechocystis, and Arabidopsis lines were measured after 15 min of dark acclimation with a pulse-amplitude-modulated fluorescence imaging system (MAXI-IMAGING-PAM, Heinz Walz, Effeltrich, Germany).
Fluoresence induction kinetics were monitored before and after addition of 10 M DCMU on custom-built equipment as described (43).
Protein Analysis-For all samples, chlorophyll concentration was determined as described (44). For isolation of total protein from Chlamydomonas, cells were pelleted and washed in wash buffer (5 mM Hepes-NaOH, pH 7.5, 10 mM EDTA, 1 mM benzamidine-HCl, 5 mM aminocaproic acid and 200 M PMSF). After washing, cells were pelleted and resuspended in resuspension buffer (200 mM DTT, 200 mM Na 2 CO 3 , 1 mM benzamidine-HCl, 5 mM aminocaproic acid, and 200 M PMSF) and solubilized by further addition of 5% SDS/30% sucrose solution to final concentration of 2% SDS/12% sucrose. Samples were mixed, boiled for 50 s, placed on ice and centrifuged. For isolation of total protein from Synechocystis, cells were harvested and incubated with lysozyme (0.05% w/v) at 37°C for 45 min before sonicating to break open cells. Supernatant was isolated and solubilized in 2ϫ Laemmli buffer (45) for 30 min at 55°C. Arabidopsis protein extraction was performed as described (46). 2 g (Chlamydomonas) or 0.5 g (Synechocystis) of chlorophyll were loaded per "100%" lane while loading based on equal amounts of AtpB was performed for each "100%" Arabidopsis lane. Samples were run on 10 -20% Tris-Glycine gels (Invitrogen) followed by semi-dry transfer to a PVDF membrane. Specific polyclonal antibodies were used and signals were visualized by Supersignal West Femto Chemiluminescent substrate detection system (Thermo Scientific). Polyclonal antibodies against AtpB, D2, RbcL, and CP43 were obtained from Agrisera (Sweden). The antibodies against D1, PsaA/ PsaD, cytochrome f, PsaC, and RubA were kind gifts from Profs. A. Melis, J.-D. Rochaix, R. Malkin, A. Haldrup, and D. Bryant, respectively. For the production of an antibody against the RBD1 and AtRBD1 proteins (excluding the transmembrane helix), portions of the RBD1 and AtRBD1 cDNA were sub-cloned (using the primers listed in supplemental Table S1) into the pET28 (aϩ) vector (Novagen). These constructs were introduced into Escherichia coli strain BL21 (DE3) (Novagen), and protein expression was induced by addition of IPTG. The Histagged RBD1 and AtRBD1 proteins were purified under native conditions through a Ni-NTA column (Qiagen) according to the manufacturer's instructions. Specific polyclonal antibodies were generated in rabbits by ProSci Inc.
Absorption Spectroscopy-Electrochromic band shift and redox changes of P700 were assessed by monitoring absorbance at 520 and 705 nm, respectively, with a JTS-10 spectrophotometer (BioLogic) as previously described (43,47,48). Chlamydomonas and Synechocystis cells were dark-acclimated for 10 min in 20 mM Hepes, 20% Ficoll, pH 7.2. A 5 ns and 1 mJ cm Ϫ2 laser flash was used to activate light reactions for electrogenicity measurements. To achieve mildly reducing conditions, cells were thoroughly mixed and aerated before absorbance measurement for each wavelength probed. PSII was inhibited by addition of 1 mM HA and 10 M DCMU. P700 measurements of Arabidopsis were performed on a one leaf-thick array of leaves after 10 min of dark acclimation.
Phylogenetic Tree Construction-The indicated sequences were retrieved from UniProt and aligned using PRANK (49). Putative transit peptides and poorly aligning regions were manually removed and the remaining sequences were realigned (supplemental Dataset S1). PhyML 3.0 (50) was used to construct a maximum likelihood tree from the alignment file and an SH-like approximate likelihood ratio test (51) was performed to calculate support for each branch. Support for the oxygenic photoautotroph branch was consistently over 0.85 and was not substantially changed by the removal of any one sequence.

The 2pac Mutant Exhibits No Detectable PSII Activity-A
collection of acetate-requiring Chlamydomonas insertional mutants (52) was grown in the dark and screened for mutants displaying a very low maximum efficiency of PSII (F v /F m ). One such mutant, CAL028.03.28, was renamed second photosystem assembly component (2pac) and selected for further characterization. The 2pac mutant was unable to grow photoautotrophically on minimal medium and grew more slowly than the wildtype strain when grown mixotrophically (Fig. 1A). Analysis of chlorophyll a fluorescence revealed an initial fluorescence (F o ) level that was equivalent to the maximum fluorescence (F m ), resulting in a lack of variable fluorescence (F v ) from PSII and an F v /F m value of 0 (Fig. 1A).
Steady-state levels of proteins from the photosynthetic electron transport chain were assayed by immunoblot analysis, and a ϳ90% decrease in the levels of the PSII reaction center proteins D1, D2, and CP43 in the 2pac mutant was observed (Fig.  1B). These immunoblot data, along with the growth and chlorophyll fluorescence results, indicate that the 2pac insertional mutant is unable to perform photosynthesis and that this is likely due to the absence of PSII activity.
The PSII-deficient Phenotype of 2pac Is Due to the Absence of the RBD1 Gene-Tetrad analysis of a backcross of the 2pac mutant to the wild-type strain showed that the mutant phenotypes (acetate requirement and absence of variable fluorescence) segregated together in a 2:2 pattern, indicating that they are due to a single nuclear mutation ( Fig. 2A). Both phenotypes were linked to the paromomycin resistance that was used as the selectable marker for insertional mutagenesis ( Fig. 2A), suggesting that the 2pac mutation was tagged by the insertion of the antibiotic resistance gene.
SiteFinding PCR (32) was used to identify the location of the insertion in the 2pac mutant. Sequence flanking the insertion was recovered that corresponded to a region on chromosome 7 within a gene encoding a putative ␥-glutamyl hydrolase (Cre07.g315050). Amplification of small (Յ400 bp) segments of genomic DNA upstream and downstream of the insertion revealed an adjacent deletion of ϳ12.5 kb affecting three additional genes: Cre07.g315100, Cre07.g315150/RBD1, and Cre07.g315200/NRM3 (Fig. 2B). BLAST searches revealed that only one of these genes, RBD1, has homologs in all oxygenic photoautotrophs. This gene encodes a 169 amino acid protein that includes a predicted N-terminal chloroplast transit peptide, a rubredoxin domain and a predicted C-terminal transmembrane helix (Fig. 1C). Using a specific antibody raised against recombinant RBD1, the RBD1 protein was detected in the wild type but not in the 2pac mutant (Fig. 1B).
To test whether or not the absence of RBD1 was responsible for the PSII-deficient phenotype of 2pac, a 1.75-kb fragment of genomic DNA containing the RBD1 gene was amplified from the wild type. This fragment, which included ϳ1 kb of sequence upstream of the predicted start codon, the coding sequence and ϳ200 bp downstream of the predicted stop codon, was used to transform the 2pac mutant. Two strains independently generated by this transformation, denoted gRBD1-1 and gRBD1-2, showed wild-type levels of variable fluorescence and photoautotrophic growth (Fig. 1A), as well as restored levels of D1, D2, CP43 and the RBD1 protein (Fig. 1B). Both complemented lines also retained resistance to paromomycin and the 12.5 kb deletion, indicating that the restoration of photoautotrophic growth and variable fluorescence was due specifically to complementation of the 2pac mutation by the RBD1 gene (Fig. 2, C  and D).
PSII, but Not Other Major Photosynthetic Electron Transport Complexes, Is Defective in 2pac-Because previous work had shown that the homolog of RBD1 (RubA) was essential for PSI assembly in the cyanobacterium Synechococcus sp. PCC 7002 (26,27), we assayed the activity of other complexes functioning in the photosynthetic electron transport chain. Photosynthetic electron transport results in a trans-thylakoid electric field that alters the absorbance spectra of pigments within the membrane, a phenomenon known as electrochromism (53). To determine the relative contributions of PSII and PSI to the light-induced electrochemical gradient across the thylakoid membrane, we measured these changes in absorbance at 520 nm (⌬A 520 nm ) upon excitation with a saturating laser pulse. Addition of PSII-specific inhibitors DCMU and HA to wildtype cells eliminated the contribution of PSII to the ⌬A 520 nm , with the remaining activity attributable to PSI (Fig. 1D). The 2pac mutant showed only a contribution of PSI to ⌬A 520 nm , since it was not affected by addition of DCMU and HA (Fig.  1D), demonstrating that PSII does not contribute to the electrochemical gradient in 2pac. To further assay PSI activity, light-induced absorbance changes at 705 nm (P700) were meas-FIGURE 2. The absence of the RBD1 gene is responsible for the loss of variable fluorescence. A, representative tetrad obtained from the backcross of 2pac with 4A-(wild-type) indicates that the insertion cosegregates with the PSII-deficient phenotype. A total of 45 progeny were obtained (some from incomplete tetrads), and 19 were found to retain resistance to paromomycin and have no variable fluorescence. The remaining 26 were susceptible to paromomycin and displayed wild-type levels of variable fluorescence. B, PCR amplification of small fragments of genomic DNA showed that the 2pac mutant contains a ϳ12.5 kb deletion spanning four genes. C, two independent lines generated by transformation of 2pac with a construct containing RBD1 (gRBD1-1 and gRBD1-2) retained resistance to paromomycin. D, PCR analysis showed that gRBD1-1 and gRBD1-2 also have the deletion present in 2pac. ured at both 56 and 340 mol photons m Ϫ2 s Ϫ1 in the presence of DCMU and HA. In both cases, P700 absorbance and oxidation/reduction kinetics in 2pac were indistinguishable from that of wild-type (Fig. 1E). Altogether, these spectroscopic data are consistent with the specific absence of a functional PSII in 2pac.

RBD1 and Its Homologs Have a Unique Domain Architecture and Are Present in All Sequenced PSII-containing Organisms-
Genes encoding proteins with high identity to RBD1 were found in all sequenced organisms known to perform oxygenic photosynthesis. RBD1 and its orthologs in oxygenic phototrophs have a rubredoxin domain fused to a C-terminal transmembrane helix (25). This helix likely anchors RBD1 in the thylakoid membrane as evidenced by detection of the RBD1 homolog in highly-purified thylakoid membranes from Synechococcus sp. PCC 7002 (26) and in the thylakoid membrane proteome of Arabidopsis thaliana (54). The canonical rubredoxin from other bacteria and archaea, however, is usually found as a soluble protein consisting almost entirely of the rubredoxin domain, although a number of other forms of rubredoxin domain-containing proteins are also found, most notably rubrerythrins (55). A phylogenetic reconstruction of the relationship between representative rubredoxins from different species shows that those from PSII-containing organisms (RBD1 homologs) form a clade distinct from all others (Fig. 3A), suggesting that a membrane-bound rubredoxin was almost certainly present in the most recent common ancestor of all oxygenic cyanobacteria and plastids.

RBD1 Knockouts in Synechocystis sp. PCC 6803 and Arabidopsis thaliana Also Display a PSII-specific Phenotype-
The phylogenetic analysis of rubredoxins and the phenotype of the 2pac mutant led us to hypothesize that RBD1, and its homologs might have a conserved function in all oxygenic phototrophs. To test this hypothesis, we analyzed rbd1 mutants in a model cyanobacterium (Synechocystis sp. PCC 6803) and plant (A. thaliana). First, we produced a ⌬rubA mutant strain of the glucose-tolerant cyanobacterium Synechocystis sp. PCC 6803 in which the gene rubA/RBD1(slr2033) was replaced with a cassette encoding resistance to the antibiotic kanamycin (nptI) and sensitivity to sucrose (sacB). After multiple rounds of restreaking on kanamycin plates, full segregation for the deletion was achieved and confirmed via PCR (Fig. 4A). The ⌬rubA strain was able to grow photoautotrophically but showed reduced variable fluorescence relative to wild-type (ϳ70%) under both mixotrophic and photoautotrophic growth (Fig. 4B), suggesting a defect in PSII. Immunoblot analysis of wild-type and ⌬rubA strains revealed that the ⌬rubA strain has highly reduced levels of D1 and D2 (ϳ 40%), lacks the RubA protein, but retains wild-type levels of cytochrome f and PSI subunits PsaC and PsaD (Fig. 4C). To directly assess the functionality of PSI, we measured changes of absorbance at 705 nm (P700) at 80 and 500 mol of photons m Ϫ2 s Ϫ1 in the presence of DCMU on equal cell densities of wild-type and ⌬rubA. Both strains showed P700 redox changes of similar amplitude and kinetics (Fig. 4D), pointing to the presence of wild-type levels of functional PSI in ⌬rubA cells. To ensure the PSII defect was due specifically to the loss of RubA, the ⌬rubA mutant was transformed with a construct that allowed for overexpression of rubA in a neutral site in the genome, generating the RubA OE strain. The RubA OE strain displayed variable fluorescence that was restored to approximately wild-type levels (Fig. 4B). Immunoblot analysis of the RubA OE strain showed that the RubA protein was present at much higher levels than in the wild-type and that PSII subunits D1 and D2 were restored to wild-type levels (Fig. 4C). While overexpression of RubA appears to have caused a reduction in levels of cytochrome f and PSI subunits, it did not affect photosynthetic electron transport downstream of PSII, as fluorescence induction kinetics were indistinguishable between the wild-type and RubA OE strains (data not shown). The ortholog of RBD1 in the flowering plant A. thaliana is encoded by the gene At1g54500. An Arabidopsis mutant heterozygous for a transposon insertion within At1g54500 was obtained, and seeds harvested from the self-fertilized plant were grown on plates containing 0.5% sucrose to support growth of potential non-photosynthetic mutants. Seedlings were genotyped by PCR (data not shown), and those homozygous for the insertion were pale green, showed no detectable variable chlorophyll a fluorescence and had an F v /F m value of 0 (Fig. 5A), indicating a lack of PSII activity. The F v /F m values of homozygous wild-type progeny were ϳ0.75 (Fig. 5A), the same value as measured for heterozygous progeny (data not shown). Immunoblot analysis showed that subunits of PSII (D1 and D2) were also severely reduced in the mutant while other components of the photosynthetic apparatus (PSI, cytochrome b 6 f and the ATP synthase) were unaffected (Fig. 5B). Furthermore, using an antibody raised against recombinant AtRBD1, we were able to detect the AtRBD1 protein in the wild-type but not in the mutant. We measured PSI activity by examining the kinetics of P700 oxidation and reduction and found that plants homozygous for the insertion exhibited wild-type kinetics, although with a weaker amplitude (Fig. 5C), similar to recent results with a mutant specifically lacking PSII (48). To ensure that the insertion and PSII phenotype were genetically linked, we grew seedlings on plates containing 0.5% sucrose and kanamycin (to select for plants harboring the insertion). Nineteen out of 58 plants (ϳ33%) were kanamycin sensitive and died at the cotyledon stage, which was the same phenotype exhibited by the wild-type controls (data not shown). 26 out of 58 plants (ϳ45%) were kanamycin resistant and displayed wild-type levels of variable fluorescence (F v /F m ϳ 0.75). The remaining 13 plants (ϳ22%) grew past the cotyledon stage but were pale and lacked PSII activity, as evidenced by high initial levels of fluorescence and no detectable variable fluorescence. The observed results are consistent with a 1:2:1 Mendelian ratio (X 2 ϭ 1.862, p Ͻ 0.39), suggesting that the PSII deficiency is caused by a single, recessive mutation in At1g54500.

DISCUSSION
Several lines of evidence show that the thylakoid-associated rubredoxin encoded by RBD1 is necessary specifically for PSII activity in Chlamydomonas. Without RBD1, the 2pac mutant does not accumulate PSII as assayed by chlorophyll a fluorescence (Fig. 1A), immunodetection of PSII subunits (Fig. 1B), and measurements of ⌬A 520 nm (Fig. 1D). PSII accumulation is clearly restored via transformation of the 2pac mutant with a small fragment of DNA containing only RBD1, its putative promoter and its 3Ј UTR (Fig. 1). The mature RBD1 protein is small (ϳ16 kDa) and is a membrane-associated rubredoxin (Fig. 1B). Membrane-bound rubredoxins are found exclusively in PSIIcontaining organisms and are distinct from the well-studied soluble rubredoxins found in many archaea and bacteria (Fig.  3A). The PSII-specific defect of Synechocystis (Fig. 4) and Arabidopsis (Fig. 5) mutants lacking a RBD1 homolog indicates that the role of RBD1 in PSII assembly or stability is broadly conserved in a diverse group of oxygenic photoautotrophs. The residual amount of PSII in the cyanobacterial mutant compared with the complete absence in eukaryotic mutants is consistent with previously observed mutants in PSII assembly factors (4,7,9) and is thought to be due, at least in part, to more efficient quality control mechanisms in plastids than in their cyanobacterial relatives (4,57). Interestingly, PSII activity as assayed by variable fluorescence is lower than in the wild-type but apparently sufficient to support photoautotrophic growth (Fig. 4B), providing an opportunity for future studies into the precise functional role of RBD1 in the proper biogenesis of PSII.
Our results are in agreement with previous work showing that the membrane-bound rubredoxin is present in spinach PSII preparations (28). However, our findings with Chlamydomonas, Synechocystis, and Arabidopsis differ from reports on a rubA mutant of the cyanobacterium, Synechococcus sp. PCC 7002, which lacked PSI but not PSII activity due to a defect in iron-sulfur cluster assembly (26,27). This discrepancy could simply be due to a difference in RubA function in different cyanobacterial species, despite the conserved genomic location of the rubA gene next to five other genes involved in PSII function (Fig. 3B). In Chlamydomonas and Arabidopsis, there appear to be multiple chloroplast-localized rubredoxins, so it is possible that one of these other homologs functions in PSI assembly. However, Chlamydomonas RBD1 (and its Arabidopsis and Synechocystis homologs encoded by At1g54500 and rubA, respectively) does not seem to play a major role in PSI assembly as evidenced by measurements of ⌬A 520 nm (Fig. 1D), P700 redox changes (Figs. 1E, 4D, and 5C), as well as PsaA, PsaC and PsaD protein accumulation (Figs. 1B, 4C, and 5B).
Because PSII activity is fully restored in the complemented lines gRBD1-1 and gRBD1-2 despite relatively low levels of RBD1 protein accumulation (Fig. 1), RBD1 is unlikely to be a subunit of PSII, rather it may have a catalytic, substoichiometric role in promoting PSII assembly or stability. This is further supported by the detection of wild-type levels of RBD1 in the Fud7 mutant lacking the D1 protein (Fig. 1B). It is known that rubredoxins participate in electron transport reactions in some Archaea and bacteria. Indeed, the midpoint redox potential of the RBD1 homolog from the cryptophyte alga Guillardia theta was found to be ϳ ϩ125 mV (25), a value that could enable it to participate in electron transport with, or perhaps bypassing, plastoquinone (E m ϳ ϩ100 mV, (1)). In fact, a similar role has been suggested for a pair of flavodiiron proteins that function in the photoprotection of PSII in Synechocystis (58).
Rubredoxins have also been previously described as aiding in oxygen tolerance, either by reacting with reactive oxygen species directly or by helping to maintain the appropriate redox state of Fe-containing active sites in some enzymes (20 -22). PSII, which generates oxygen and contains both a redox-active non-heme Fe as well as a redox-active heme (cytochrome b 559 ), would certainly fit the profile of a protein complex that might benefit from the presence of such an enzyme. In many microbes, the active site of superoxide reductase (SOR) contains a non-heme iron that, after catalyzing the reduction of superoxide to hydrogen peroxide, is thought to be reactivated via rubredoxin-mediated re-reduction (59,60). Cytochrome b 559 has recently been shown to have superoxide reductase and oxidase activity (61) and the presence of RBD1/rubA in a highly conserved gene cluster with the two subunits of this transmembrane cytochrome might also be taken to suggest an as yet unidentified interaction between these proteins.
Another possible clue regarding the function of RBD1 may be found by examination of the synthesis of the membrane-bound [NiFe] uptake hydrogenase. The gene cluster required for synthesis of this hydrogenase is well conserved among anaerobic and aerobic species, but aerobic species with this enzyme contain an additional operon in which one of the genes (hupI or hoxR) encodes a rubredoxin (20,22). These rubredoxins appear to contribute to oxygen tolerance of the hydrogenase, and it is of note that some of these species are photosynthetic purple bacteria that contain type II reaction centers, which are believed to be similar to the ancestral state of PSII (1). Although they are not required for assembly of anoxygenic type II reaction centers in bacteria, it is tempting to speculate that these types of soluble rubredoxins might be representative of the ancestral state of the rubredoxin motif and that the membranebound rubredoxin found in the oxygenic phototrophs might be an evolutionary innovation co-opted from a soluble ancestral protein during the transition from anoxygenic to oxygenic photosynthesis.