Lipid Biology of ArchaeaView this Special Issue
Review Article | Open Access
Jonathan Lombard, Purificación López-García, David Moreira, "Phylogenomic Investigation of Phospholipid Synthesis in Archaea", Archaea, vol. 2012, Article ID 630910, 13 pages, 2012. https://doi.org/10.1155/2012/630910
Phylogenomic Investigation of Phospholipid Synthesis in Archaea
Archaea have idiosyncratic cell membranes usually based on phospholipids containing glycerol-1-phosphate linked by ether bonds to isoprenoid lateral chains. Since these phospholipids strongly differ from those of bacteria and eukaryotes, the origin of the archaeal membranes (and by extension, of all cellular membranes) was enigmatic and called for accurate evolutionary studies. In this paper we review some recent phylogenomic studies that have revealed a modified mevalonate pathway for the synthesis of isoprenoid precursors in archaea and suggested that this domain uses an atypical pathway of synthesis of fatty acids devoid of any acyl carrier protein, which is essential for this activity in bacteria and eukaryotes. In addition, we show new or updated phylogenetic analyses of enzymes likely responsible for the isoprenoid chain synthesis from their precursors and the phospholipid synthesis from glycerol phosphate, isoprenoids, and polar head groups. These results support that most of these enzymes can be traced back to the last archaeal common ancestor and, in many cases, even to the last common ancestor of all living organisms.
Archaea were identified as an independent domain of life in the late 1970s thanks to the characterization of differences between their ribosomal RNA molecules and those of bacteria and eukaryotes . At that time, it was already known that the so-called “archaeabacteria” held several atypical biochemical characteristics, of which the most remarkable was their unusual membrane phospholipids. Whereas all bacteria and eukaryotes were known to have membranes based on fatty acids linked by ester bonds to glycerol-phosphate, archaea appeared to have phospholipids composed of isoprenoid chains condensed with glycerol-phosphate by ether linkages [2–6]. Moreover, the archaeal glycerol ethers contained sn-glycerol-1-phosphate (G1P), whereas bacterial and eukaryotic ones contained sn-glycerol-3-phosphate (G3P) (for review, see [7, 8]). These differences, which have been at the center of an intense debate about the nature of the first cell membranes , have progressively been shown to be not so sharp: ether-linked lipids are common both in eukaryotes (up to 25% of the total lipids in certain animal cells, ) and in several thermophilic bacteria [11–13]; fatty acid phospholipids have been found in diverse archaea ; conversely, isoprenoids are known to be universal although they are synthesized by non-homologous pathways in the three domains of life, ; even the stereochemistry of the glycerol phosphate has some exceptions, as shown by the recent discovery of archaeal-like sn-glycerol-1-phosphate specific lipids in some bacteria  and in eukaryotic endosomes .
Today, thanks to the significant accumulation of complete genome sequence data for a wide variety of species, it is possible to study the major pathways of phospholipid synthesis and their exceptions by looking at the presence or absence of the corresponding genes in the different genomes. In addition, these data allows reconstructing the evolutionary history of each gene by combining comparative genomics and phylogenetics, namely, by using a phylogenomic approach. In this paper, we summarize the results concerning the phylogenomic studies of the biosynthesis pathways of archaeal phospholipid components and provide some new evolutionary data about the enzymes reviewed in Koga and Morii  and Matsumi et al.  as likely responsible for the assembly of archaeal lipids from these building blocks.
2. Archaea Possess an Atypical Pathway of Biosynthesis of Isoprenoid Precursors
Isoprenoids are chains of isoprene units and their derivatives and are found ubiquitously in all living beings. They are involved in very diverse functions, such as photosynthetic pigments, hormones, quinones acting in electron transport chains, plant defense compounds, and so forth [15, 20]. In archaea, isoprenoids also make up the hydrophobic lateral chains of phospholipids . Isoprenoid biosynthesis requires two isoprene activated precursors, called isopentenyl pyrophosphate (IPP) and dimethylallyl diphosphate (DMAPP), which act as building parts. The first metabolic pathway responsible for the biosynthesis of isoprenoid precursors was discovered in yeasts and animals in the 1950s and named mevalonate (MVA) pathway in reference to its first committed precursor. Since its first description, the MVA pathway was thought to synthesize the isoprenoid precursors in all organisms , but closer scrutiny showed its absence in most bacteria . An elegant series of multidisciplinary approaches allowed in the late 1990s and early 2000s describing an independent and non-homologous pathway in bacteria, the methylerythritol phosphate (MEP) pathway (see  for review). The MEP pathway was found to be widespread in bacteria and plastid-bearing eukaryotes, whereas the MVA pathway was assumed to operate in archaea and eukaryotes [15, 23]. In the early 2000s, archaeal isoprenoids were thought to be synthesized through the MVA pathway because the 14C-labelled intermediates of this pathway were shown to be incorporated into the archaeal phospholipids . However, only two of the enzymes of the eukaryotic pathway have been described in archaea [25, 26]. Moreover, the search of MVA pathway enzyme sequences in archaeal genomes revealed that from the seven enzymes acting on this pathway, most archaeal species lack the last three of them: phosphomevalonate kinase (PMK), mevalonate diphosphate decarboxylase (MDC), and isopentenyl diphosphate isomerase (IDI1), involved in the conversion of phosphomevalonate into IPP and DMAPP . Attempts to characterize these missing archaeal enzymes revealed two new enzymes: the isopentenyl phosphate kinase (IPK) and an alternative isopentenyl diphosphate isomerase (IDI2) [28–30]. Although the decarboxylation reaction required to synthesize isopentenyl phosphate from phosphomevalonate has not been described yet, an alternative final MVA pathway involving IPK and IDI2 was then proposed to exist in archaea (Figure 1, ).
Taking advantage of the recent accumulation of genomic data, we carried out a thorough phylogenomic analysis of the pathways of isoprenoid precursor synthesis . Concerning archaea, our presence-and-absence analysis extended the presence of the proposed archaeal alternative pathway to a wide archaeal diversity. The main exception to these observations was Nanoarchaeum equitans, which explains the dependence of this organism to obtain its lipids from its crenarchaeal host, Ignicoccus hospitalis . Phylogenetic reconstructions of the MVA pathway enzymes present in archaea systematically revealed a clade independent from the other domains of life, representative of the archaeal diversity and generally respecting the main archaeal taxonomic groups . These results are consistent with the presence of a distinctive archaeal MVA pathway in the last archaeal common ancestor (LACA) and support that different isoprenoid precursor biosynthesis pathways are characteristic of each domain of life: the classical MVA pathway in eukaryotes, the alternative MVA pathway in archaea, and the MEP pathway in bacteria.
The origin of the archaeal MVA pathway appears to be composite. The enzymes shared with the classical eukaryotic MVA pathway were also ancestral in eukaryotes and bacteria and, therefore, they can be inferred to have been present in the last common ancestor of all living organisms (the cenancestor), from which the archaeal lineage would have inherited them. The last enzymes of the eukaryotic MVA pathway were most likely present in the respective ancestors of eukaryotes and bacteria, but their distribution in archaea is scarce and complex: homologues of MDC can be detected in Haloarchaea and Thermoplasmatales and some IDI1 genes have been identified in Haloarchaea and Thaumarchaeota, although they most likely reflect recent horizontal gene transfer (HGT) events from bacterial donors, as deduced from their position well nested among bacterial sequences in phylogenetic analyses [23, 31]. In contrast, the class Sulfolobales contains PMK and MDC homologues which robustly branch in an intermediate position between the eukaryotic and the bacterial sequences, suggesting that these sequences could be ancestral versions that would have been lost in the rest of archaea . If this is the case, a eukaryotic-like pathway (except for the IDI function, which remains ambiguous) can be proposed to have existed in the cenancestor. This pathway would have been replaced by the MEP pathway in the bacterial lineage, whereas in archaea only the last steps were replaced by non-homologous enzymes. We do not know the evolutionary forces that drove these changes; however, the mevalonate kinase (MVK), PMK, and MDC belong to a large family of kinases, namely the GHMP kinases , which is characterized by a high structural and mechanistic conservation that contrasts with the large range of substrates that they can use . If we assume that ancestors of these enzymes were not very specific, this could have allowed some tolerance to recruitment of evolutionary unrelated enzymes not only in archaea but also in some eukaryotes that have replaced their ancestral PMK by a non-homologous one [35, 36]. In agreement with this idea, the archaeal IPK itself appears to be able to use different substrates , which could have made the replacement easier.
3. Early Evolution of Isoprenoid Chain Synthesis
Once the isoprenoid precursors, IPP and DMAPP, have been synthesized, they still have to be assembled to make isoprenoid chains. The prenyltransferases responsible for this function are the isoprenyl diphosphate synthases (IPPS). Since many more complete genome sequences are now available than at the time of previous IPPS phylogenetic analyses, we present here an updated survey of the evolution of these enzymes. Although many different enzymes are required to synthesize the wide diversity of isoprenoids, the first steps are widely shared among the three domains of life . They consist of the progressive addition of IPP units (5 carbons each) to an elongating allyl polyisoprenoid diphosphate molecule. Starting with DMAPP (5 carbons), consecutive condensation reactions produce geranylgeranyl diphosphate (GPP, 10 carbons), farnesyl diphosphate (FPP, 15 carbons), geranylgeranyl diphosphate (GGPP, 20 carbons), and so forth. Different IPPSs are characterized by the allylic substrate that they accept (DMAPP, GPP, FPP, …) and by the stereochemistry of the double bonds, but the main characteristic used to classify them is the size of the products that they synthesize: they can be short-chain IPPS (~up to 25 carbons) or long-chain IPPS (>25 carbons). All IPPS are homologous and share a common reaction mechanism. Short-chain IPPS mainly differ in the size of their substrate-binding hydrophobic pocket (the smaller the pocket, the shorter the final product, ), but point mutations have been shown to importantly impact the size of the pocket and, thus, of their final products [39, 40]. Description of equivalent natural mutations have been reported in archaea , which argues against the possibility of inferring the precise product of a given IPPS only based on its phylogenetic position [41, 42].
The first published IPPS phylogenetic trees  only used 13 sequences (of which 12 were short-chain enzymes) and supported a split between prokaryotic and eukaryotic enzymes. At that time, archaeal IPPS were assumed to be more ancient because they were known to provide isoprenoids for several pathways while bacteria and eukaryotes were thought to have more specialized enzymes. Later phylogenetic analyses with more sequences showed two groups corresponding to the functional split between short and long-chain enzymes . This was expected since the long-chain IPPS use supplementary proteins to stabilize the hydrophobic substrate , which would logically impact the protein structure and therefore trigger the large divergence between the short- and the long-chain enzymes. In that work, the short-chain enzymes formed three groups according to the three domains of life, which could be considered as evidence for the presence of one short-chain enzyme in the cenancestor and its subsequent inheritance in modern lineages, including archaea. Furthermore, in that phylogeny archaea did not branch as a basal lineage, disproving their previously assumed ancient character. In addition, enzymes with different product specificities branched mixed all over the tree, supporting the product plasticity of the ancestral short-chain enzyme and the subsequent evolution of particular specificities according to biological requirements in modern organisms . Archaeal long-chain IPPS had not been detected in that study, but some of them were incorporated in phylogenetic studies some years later .
We have searched for homologues of IPPS in a representative set of 348 complete genomes from the three domains of life (including 88 archaea). A preliminary phylogenetic analysis showed that, in agreement with previous reports , the resulting sequences split into two clades mainly related to the short- or long-chain product specificity (data not shown). To avoid the phylogenetic artifacts that can be introduced by the high sequence divergence between short- and long-chain enzymes, we carried out independent phylogenetic analyses for each one of the two paralogues, to which we will refer as short- or long-chain IPPS with regard to dominant functions of the characterized enzymes. However, as previously mentioned [39–41], substrate specificity exchange between short and long substrates appears to be relatively common, so these partial trees must be acknowledged mainly as phylogenetic groups related to the most widespread biochemical function, but do not definitely determine the substrate specificity of all their sequences, which can only be established by biochemical studies. In preliminary short-chain IPPS phylogenies, long branches at the base of several eukaryotic paralogues evidenced for the high divergence of these sequences. Since we were here mainly interested in the archaeal sequences, we removed the divergent eukaryotic sequences from our analyses. Figure 2 and Supplementary Figure 1 (see Supplementary Material available online at http://dx.doi.org/10.1155/2012/630910) present the phylogeny of some representative prokaryotic short-chain enzyme sequences. Most archaeal sequences branch together in a monophyletic group largely congruent with the main archaeal phyla and orders, which suggests that this enzyme was present in LACA and was vertically inherited in most archaeal lineages. Most bacterial sequences also cluster together according to the main bacterial taxonomic groups, suggesting the ancestral presence of this enzyme in the last bacterial common ancestor and, given its presence also in LACA, most likely also in the cenancestor. However, some recent HGTs can also be pointed out from this phylogeny. Concerning archaea, Thermoproteales, some Desulfurococcales, some Thermoplasmatales, Methanocella paludicola and Aciduliprofundum boonei branch within the bacterial group, so several HGTs can be invoked to explain this pattern, although in most cases the support is weak and does not allow confidently determining the identity of the bacterial donors (Figure 2).
As in the case of the short-chain enzymes, most archaeal sequences also group together in our long-chain IPPS phylogenies and, despite the weakly supported paraphyly of the euryarchaeotal sequences, the main archaeal taxonomic groups are observed (Figure 3 and Supplementary Figure 2). Bacterial sequences also group together according to main taxa, supporting that the respective common ancestors of bacteria and archaea, and thus likely also the cenancestor, had a long-chain IPPS enzyme that was inherited in modern organisms. Contrary to short-chain IPPS, eukaryotic long-chain IPPS are less divergent, so they were conserved in our analyses. Surprisingly, all the eukaryotic sequences, including those from plastid-lacking eukaryotes, branch together as the sister group of cyanobacteria, except for some algae that branch within the cyanobacterial group. In addition, some other more recent HGTs are observed, especially in the archaeal Thermococcus genus, which branches close to a very divergent sequence from the delta-proteobacterium Bdellovibrio bacteriovorus.
Altogether, these results support that in spite of some recent HGTs from bacteria to archaea, most archaea have homologues of both the short- and the long-chain IPPS that were inherited from LACA and that, most likely, were already present in the cenancestor.
4. Archaea May Have an ACP-Independent Fatty Acid Biosynthesis Pathway
In bacteria and eukaryotes, fatty acids are components of membrane phospholipids, energy-storage molecules, substrates for post-translational modifications of proteins, secondary metabolites, and components of coenzymes and messenger compounds. Despite the general assumption that archaeal lipid metabolism is based on isoprenoids, a variety of experimental approaches have shown that fatty acids (FA) also exist in these organisms. Archaea show variable concentrations of free FA or their derivatives [4, 24, 43–45], which has stimulated some attempts to biochemically characterize an archaeal FA synthase [46, 47]. Archaeal FA can participate in protein structure [48–50] and acylation  but they have also been found as components of membrane phospholipids in very diverse euryarchaeotes . Therefore, it is not surprising that homologues of several of the enzymes involved FA biosynthesis in bacteria had been detected in archaeal genomes [8, 51]. In bacteria, FA biosynthesis occurs through multiple condensations of acyl groups (malonyl-CoA) in a series of cyclical steps. The building blocks necessary to the activity of the FA synthases are provided by several reactions. First, the acetyl-CoA carboxylase (ACC) converts acetyl-coenzyme A (CoA) into malonyl-CoA. Second, the peptide cofactor acyl carrier protein (ACP), which is required to channel the elongating intermediates among the FA synthase enzymes, has to be activated through the addition of a phosphopantetheine group from CoA to the apo-ACP by an ACP synthase. Finally, the malonyl-CoA: ACP transacylase (MCAT) charges the malonyl-CoA to holo-ACP, resulting in malonyl-ACP.
Since no archaeal FA synthase system has been described in detail yet, we recently studied the evolution of the archaeal homologues of the bacterial genes involved in FA synthesis. First, many archaea possess ACC homologues that are closely related in phylogenetic analyses, suggesting their possible monophyletic origin and, consequently, the presence of this enzyme in LACA [52, 53]. Second, only a few unrelated archaeal species have ACP and the ACP-processing machinery (ACP synthase and MCAT) and phylogenetic analysis suggests that they acquired them by HGTs from bacteria. As a result, ACP and its related enzymes are missing in most archaea and appear not to have been present in LACA . For the rest of enzymes involved in the cyclic steps of FA synthesis (see Figure 1), phylogenetic analyses support that the archaeal sequences are more closely related to bacterial enzymes that are active on substrates linked to CoA than to enzymes that use substrates linked to ACP. Taking this into account, we have proposed that the ACP processing system has specifically evolved in the bacterial lineage and that archaea carry out FA synthesis using a likely ancient ACP-independent pathway . Although ACC exists in archaea, the hypothetical archaeal FA synthesis pathway probably involves two acetyl-CoA instead of using malonyl and acetyl thioesters as in bacteria, since the thiolases that carry out this function are known to be decarboxylative in bacteria but non-decarboxylative in archaea .
Interestingly, it has been unclear for a long time if either the bacterial FA synthesis pathway specifically recognizes each acyl-ACP intermediate or if its enzymes randomly fix these intermediates, modifying the correct ones and releasing the inappropriate ones. Recent work has shown that ACP carries out its channeling function by adopting unique conformations for each enzyme of the FA elongation cycle . Yet, it can be reasonably assumed that a putative ACP-independent mechanism would rather use random interactions between intermediate metabolites and enzymes, which might be assumed to be less efficient than the bacterial ACP-mediated system. Although this remains speculative and needs biochemical confirmation, the high efficiency of the ACP-mediated machinery may explain the preeminence of FA in bacterial membranes, whereas archaea would have opted by the alternative ancestral mechanism of synthesis of lateral chains for membrane phospholipids, namely, the isoprenoids , relegating FA to different cellular functions and, only to a small extent, to membrane synthesis .
5. Linking Glycerol Phosphate with the Lateral Chains
Although archaeal phospholipids were already known to use G1P instead of G3P as bacteria and eukaryotes do, the recent characterization and sequencing of the enzyme responsible for its synthesis in archaea (G1P dehydrogenase [57, 58]) was astonishing because this enzyme appeared to be totally unrelated to the canonical G3P dehydrogenase . Since then, very little exceptions to this clear-cut distinction between archaea and bacteria have been described (the most remarkable is probably the description of an archaeal-like G1P dehydrogenase in the bacterium Bacillus subtilis, ), but the fact that the two dehydrogenases belong to large enzymatic superfamilies from which they were recruited has provided a model for the independent origin of these dehydrogenases from likely ancient promiscuous enzymes .
Geranylgeranylglyceryl diphosphate and di-O-geranylgeranylglyceryl phosphate synthases (GGGPS and DGGGPS, resp.) are the enzymes that subsequently link isoprenoids to glycerol phosphate in archaea . Boucher et al.  found that GGGPS are widespread in archaea whereas, among bacteria, it was found only in Bacillales and in one Bacteroidetes species. They also described a very divergent homologue in halophilic archaea and in Archaeoglobus. Despite their divergence, these enzymes appear to carry out the same function . Using an updated genome sequence database, we also retrieve the very divergent GGGPS in Methanomicrobiales, confirm that GGGPS is present in Bacillales, and extend this observation to a surprising diversity of Bacteroidetes (Supplementary Figure 3. This suggests that GGGPS plays an important role in these two bacterial groups and, indeed, it has recently been shown to participate in the synthesis of archaeal-type lipids of unknown function in these bacteria . In conclusion, at least one GGGPS gene appears to have been present in LACA, whereas the divergent copy of this gene probably emerged later in a more recent group of euryarchaeota. GGGPS were probably independently transferred to the respective ancestors of Bacillales and Bacteroidetes.
Hemmi et al.  carried out the first phylogenetic analysis of the DGGGPS sequences and their superfamily, the UbiA prenyltransferase family (17 sequences branching in 6 different groups). Using all sequences available at present, we retrieve similar but much more diversified groups (Supplementary Figure 4. Archaeal sequences cluster together in a monophyletic assemblage, suggesting common ancestry, although crenarchaeota are paraphyletic probably as a result of reconstruction artifacts. A number of bacteroidetes sequences branch among the crenarchaeota, reflecting an HGT event to an ancestor of this bacterial group. In addition several bacterial phyla (Chlorobi, Cyanobacteria, Chloroflexi, Planctomycetales, and some proteobacterial species) possess UbiA-related homologues. However, in several of these bacterial species, these enzymes are involved in photosynthesis (they take part in the synthesis of respiratory quinones, hemes, chrolophylls, and vitamin E ) and it is difficult to determine if the widespread distribution in bacteria is due to the ancestral presence of a homologue of this enzyme in the last common bacterial ancestor or to several recent HGTs to these bacterial groups from archaeal donors.
The search of homologues of the bacterial glycerol phosphate acyl transferases PlsX, PlsY, PlsB, and PlsC, which carry out the addition of fatty acids to glycerol phosphate [63, 64], in the available archaeal genome sequences allowed retrieving very few homologues, all of them most likely acquired by HGT from bacterial donors (not shown).
6. Linking the Polar Head Groups
Once the two hydrocarbon chains are linked to the phospholipid backbone, two additional steps are required to add the polar head group (Figure 1). First, an enzyme replaces the phosphate linked to the glycerol moiety by a CDP group; then, this CDP is replaced by the final polar head group, which can be very diverse (glycerol, myo-inositol, serine, and so forth) . The first step has been biochemically described in archaea but the enzyme that carries out this function remains unknown . The bacterial counterpart is the CDP diglyceride synthetase (CdsA) [66, 67]. We looked for archaeal homologues of the bacterial enzyme and retrieved several sequences that we used as queries for exhaustive searches in archaeal genomes. This allowed us to observe that this enzyme is widespread both in bacteria and archaea. Our phylogenetic trees show two clades that correspond to archaea and bacteria and the phylogenetic relationships within each of them are congruent with the main accepted taxonomic groups (Figure 4). This supports the vertical inheritance of this gene from the cenancestor and, consequently, its presence in LACA. However, to our knowledge no archaeal CdsA has been biochemically characterized so far, which would be required to confirm that these archaeal homologues are responsible for the biochemical activity described by Morii et al. .
Two enzymes involved in the second step of the attachment of polar head groups have been characterized in archaea [68, 69]. These enzymes belong to the large family of the CDP alcohol phosphatidyltransferases and have homologues in bacteria . The bacterial members of this enzyme family are known to have different specificities in order to add different polar head groups on phospholipids. A previous phylogenomic survey carried out by Daiyasu et al.  showed that the different sequences group in phylogenetic trees according to their predicted substrates. In addition, the groups of bacterial sequences were in agreement with the main bacterial taxonomic groups. Our analysis with a larger taxonomic sample confirms that homologues of these genes are widespread in archaea. All sequences group into three main categories (data not shown), one related to the addition of serine as a polar head group , another related to myo-inositol-phosphate transfer  (and maybe also glycerol in archaea, according to classification in ), and the last one using glycerol. Archaea are found in the first two groups but not in the last one. In order to avoid artifacts due to extreme sequence divergence, we carried out phylogenies for each of the two groups containing archaeal representatives. In the first phylogeny, archaeal sequences predicted to use serine  as a substrate are limited to Euryarchaeota (Supplementary Figure 5). This tree shows a poorly supported group of slow evolving bacteria together with several divergent bacterial, eukaryotic and archaeal (Methanococcoides burtonii and haloarchaea) sequences. Such mixed distribution dominated by strong sequence divergence and HGTs contrasts with the rest of the phylogeny, which is congruent with the main accepted taxonomic groups. Especially, one monophyletic group of euryarchaeota can be pointed out, supporting that this enzyme probably existed at least in the last euryarchaeotal common ancestor. In the second tree, a larger group of archaeal enzymes, predicted to use glycerol phosphate or myo-inositol-phosphate as substrates [69, 70], cluster in our analysis with bacterial enzymes that use myo-inositol, but these bacterial sequences are scarce and appear to have been acquired from archaea by HGT (Supplementary Figure 6). The phylogeny of archaeal sequences supports the monophyly of Crenarchaeota and a patchy distribution of several paralogues in Euryarchaeota, which makes difficult the analysis of the evolution of these enzymes in archaea without incorporating supplementary biochemical information. At any rate, the wide distribution of this enzyme family in archaea strongly suggests that at least one representative of these enzymes was already present in LACA. Whereas it was conserved in Crenarchaeota, it was subjected to several duplication and neofunctionalization events in Euryarchaeota, which would explain the complex distribution pattern observed in euryarchaeotal species.
7. Saturation of Isoprenoid Chains
So far, we have described the main synthesis and link mechanisms of archaeal phospholipid components, but a wide diversity of phospholipids actually exists in archaea . A substantial characteristic of archaeal membranes is their saturation rate, since double bonds have a prominent influence on membrane stability . Most archaea contain saturated phospholipids and the geranylgeranyl reductase (GGR), the enzyme responsible for the reduction of isoprenoid chains, has been recently described in the euryarchaeota Thermoplasma acidophilum and Archaeoglobus fulgidus and the crenarchaeote Sulfolobus acidocaldarius [73–75]. These studies show that archaeal GGR are able to use geranylgeranyl chains either isolated or attached to phospholipids as substrates. When GGPP is used as a substrate, all bonds but the one in position C2 are reduced, allowing the incorporation in phospholipids, but isoprenoids chains that are already attached to glycerol phosphate can have all their double bonds reduced by this enzyme. As a result, isoprenoid reduction can happen at different steps of the phospholipid biosynthesis pathway (Figure 1).
Archaeal GGRs are homologous to previously reported cyanobacterial and plant GGRs involved in chlorophyll synthesis [76, 77] and many different GGR paralogues have been identified in archaeal genomes that could carry out independent isoprenoid chain reductions . Our phylogeny of GGRs confirms that GGRs are widespread among crenarchaeota and that at least two paralogues exist in a wide diversity of euryarchaeota, although some archaeal groups also bear supplementary GGR genes (Supplementary Figure 7). This supports the ancestral presence of at least one GGR gene in archaea, followed by a complex history of duplications and HGTs. GGRs are also present in many bacterial genomes, but several HGTs can be observed, probably related to the function of this gene in photosynthesis, making uncertain the primary origin of this gene in bacteria. Among eukaryotes, only sequences from plastid-bearing organisms were detected and these sequences clearly branched within one group of cyanobacterial sequences, thus supporting the plastidial origin of these genes in eukaryotes.
In contrast with the rather impressive knowledge about the biochemistry and biosynthesis of bacterial cell membranes, many aspects of their archaeal counterparts remain to be elucidated. Even the synthesis of the most canonical archaeal membrane lipids, the phospholipids based on isoprenoid lateral chains, still has some unresolved points, such as the identity of the enzyme carrying out the phosphomevalonate decarboxylase activity necessary for the final steps of the synthesis of isoprenoid precursors. Moreover, it is becoming clear that archaeal membranes incorporate components that were supposed to be restricted to the other two domains of life, bacteria and eukaryotes. This is notably the case of fatty acids that, despite being relatively widespread in membrane phospholipids of euryarchaeotal species , are synthesized by a pathway that, most likely, has important differences with the bacterial counterpart .
Comparative genomics and phylogenomics provide a powerful way to address these questions, in particular by the detection of potential candidates to carry out missing enzymatic functions thanks to similarities with bacterial and eukaryotic enzymes. This has allowed us to propose, for example, the existence of an ACP-independent pathway of fatty acid synthesis in archaea  and allows us to propose here that archaeal CdsA homologues could carry the same function as in bacteria. This approach has also provided evidence supporting that lipid membranes were already evolved long ago, at the time of the cenancestor . Thus, rather than radical inventions of new phospholipid biochemistries, bacteria and archaea appear to have specialized their cell membranes by tuning the relative importance of the different components, with isoprenoids becoming dominant in archaea and fatty acids in bacteria. Nevertheless, these bioinformatic approaches have limitations and biochemical investigation remains crucial to characterize the different missing activities (the uncharacterized MVA pathway enzymes in archaea, the hypothetical ACP-independent FA synthesis pathway, the characterization of the archaeal CdsA, and a larger diversity of CDP alcohol phosphatidyltransferases) in order to complete the puzzle of archaeal membrane synthesis.
9. Material and Methods
Sequence seeds for similarity searches were retrieved from the KEGG database (http://www.genome.jp/kegg/). Searches were carried out with BLASTp  against a list of completely sequenced genomes available in GenBank (Supplementary Table 1). The resulting sequences were aligned with by default parameters with Muscle 3.6 . Redundant and partial sequences were removed and ambiguously aligned regions were discarded prior to phylogenetic analyses using the NET program from the MUST package . Phylogenetic trees were reconstructed with the approximately maximum likelihood approach with FastTree 2.1.3 .
The authors thank A. Corcelli for the invitation to contribute this paper. This work was supported by the interdisciplinary programs Origine des Planètes et de la Vie and InTerrVie (Interactions Terre-Vie) of the French Centre National de la Recherche Scientifique and Institut National des Sciences de l’Univers and by French National Agency for Research (EVOLDEEP Project, contract no. ANR-08-GENM-024-002). J. Lombard is recipient of a Ph.D. fellowship of the French Research Ministry.
The supplementary material contains a list of the completely sequenced genomes used in this study and the detailed phylogenies of the short and long chain IPPS, the GGGPS, the DGGGPS, the CDP alcohol phosphatidyltransferases probably related to serine transfer, the CDP alcohol phosphatidyltransferases probably related to myo-inositol transfer and the GGR.
- C. R. Woese and G. E. Fox, “Phylogenetic structure of the prokaryotic domain: the primary kingdoms,” Proceedings of the National Academy of Sciences of the United States of America, vol. 74, no. 11, pp. 5088–5090, 1977.
- M. Kates, L. S. Yengoyan, and P. S. Sastry, “A diether analog of phosphatidyl glycerophosphate in Halobacterium cutirubrum,” Biochimica et Biophysica Acta, vol. 98, no. 2, pp. 252–268, 1965.
- T. A. Langworthy, P. F. Smith, and W. R. Mayberry, “Lipids of Thermoplasma acidophilum,” Journal of Bacteriology, vol. 112, no. 3, pp. 1193–1200, 1972.
- T. A. Langworthy, W. R. Mayberry, and P. F. Smith, “Long chain glycerol diether and polyol dialkyl glycerol triether lipids of Sulfolobus acidocaldarius,” Journal of Bacteriology, vol. 119, no. 1, pp. 106–116, 1974.
- C. R. Woese, L. J. Magrum, and G. E. Fox, “Archaebacteria,” Journal of Molecular Evolution, vol. 11, no. 3, pp. 245–252, 1978.
- T. G. Tornabene and T. A. Langworthy, “Diphytanyl and dibiphytanyl glycerol ether lipids of methanogenic archaebacteria,” Science, vol. 203, no. 4375, pp. 51–53, 1979.
- M. De Rosa, A. Gambacorta, and A. Gliozzi, “Structure, biosynthesis, and physicochemical properties of archaebacterial lipids,” Microbiological Reviews, vol. 50, no. 1, pp. 70–80, 1986.
- J. Peretó, P. López-García, and D. Moreira, “Ancestral lipid biosynthesis and early membrane evolution,” Trends in Biochemical Sciences, vol. 29, no. 9, pp. 469–477, 2004.
- J. Lombard, P. López-García, and D. Moreira, “The early evolution of lipid membranes and the three domains of life,” Nature Reviews Microbiology, vol. 10, no. 7, pp. 507–515, 2012.
- H. K. Mangold and F. Paltauf, Ether Lipids: Biochemical and Biomedical Aspects, Academic Press, 1983.
- R. Huber, T. Wilharm, D. Huber et al., “Aquifex pyrophilus gen.nov. sp.nov., represents a novel group of marine hyperthermophilic hydrogen-oxidizing bacteria,” Systematic and Applied Microbiology, vol. 15, no. 3, pp. 340–351, 1992.
- J. S. S. Damsté, W. I. C. Rijpstra, E. C. Hopmans, S. Schouten, M. Balk, and A. J. M. Stams, “Structural characterization of diabolic acid-based tetraester, tetraether and mixed ether/ester, membrane-spanning lipids of bacteria from the order Thermotogales,” Archives of Microbiology, vol. 188, no. 6, pp. 629–641, 2007.
- T. A. Langworthy, G. Holzer, J. G. Zeikus, and T. G. Tornabene, “Iso- and anteiso-branched glycerol diethers of the thermophilic anaerobe Thermodesulfotobacterium commune,” Systematic and Applied Microbiology, vol. 4, no. 1, pp. 1–17, 1983.
- A. Gattinger, M. Schloter, and J. C. Munch, “Phospholipid etherlipid and phospholipid fatty acid fingerprints in selected euryarchaeotal monocultures for taxonomic profiling,” FEMS Microbiology Letters, vol. 213, no. 1, pp. 133–139, 2002.
- B. M. Lange, T. Rujan, W. Martin, and R. Croteau, “Isoprenoid biosynthesis: the evolution of two ancient and distinct pathways across genomes,” Proceedings of the National Academy of Sciences of the United States of America, vol. 97, no. 24, pp. 13172–13177, 2000.
- H. Guldan, F. M. Matysik, M. Bocola, R. Sterner, and P. Babinger, “Functional assignment of an enzyme that catalyzes the synthesis of an archaea-type ether lipid in bacteria,” Angewandte Chemie, vol. 50, no. 35, pp. 8188–8191, 2011.
- H. H. Tan, A. Makino, K. Sudesh, P. Greimel, and T. Kobayashi, “Spectroscopic evidence for the unusual stereochemical configuration of an endosome-specific lipid,” Angewandte Chemie, vol. 51, no. 2, pp. 533–535, 2012.
- Y. Koga and H. Morii, “Biosynthesis of ether-type polar lipids in archaea and evolutionary considerations,” Microbiology and Molecular Biology Reviews, vol. 71, no. 1, pp. 97–120, 2007.
- R. Matsumi, H. Atomi, A. J. M. Driessen, and J. van der Oost, “Isoprenoid biosynthesis in Archaea—biochemical and evolutionary implications,” Research in Microbiology, vol. 162, no. 1, pp. 39–52, 2011.
- D. J. McGarvey and R. Croteau, “Terpenoid metabolism,” The Plant Cell, vol. 7, no. 7, pp. 1015–1026, 1995.
- D. Zhou and R. H. White, “Early steps of isoprenoid biosynthesis in Escherichia coli,” The Biochemical Journal, vol. 273, part 3, pp. 627–634, 1991.
- M. Rodríguez-Concepción and A. Boronat, “Elucidation of the methylerythritol phosphate pathway for isoprenoid biosynthesis in bacteria and plastids. A metabolic milestone achieved through genomics,” Plant Physiology, vol. 130, no. 3, pp. 1079–1089, 2002.
- Y. Boucher, M. Kamekura, and W. F. Doolittle, “Origins and evolution of isoprenoid lipid biosynthesis in archaea,” Molecular Microbiology, vol. 52, no. 2, pp. 515–527, 2004.
- M. Kates, M. K. Wassef, and D. J. Kushner, “Radioisotopic studies on the biosynthesis of the glyceryl diether lipids of Halobacterium cutirubrum,” Canadian Journal of Biochemistry, vol. 46, no. 8, pp. 971–977, 1968.
- W. L. Lam and W. F. Doolittle, “Mevinolin-resistant mutations identify a promoter and the gene for a eukaryote-like 3-hydroxy-3-methylglutaryl-coenzyme A reductase in the archaebacterium Haloferax volcanii,” The Journal of Biological Chemistry, vol. 267, no. 9, pp. 5829–5834, 1992.
- D. Yang, L. W. Shipman, C. A. Roessner, A. Ian Scott, and J. C. Sacchettini, “Structure of the Methanococcus jannaschii mevalonate kinase, a member of the GHMP kinase superfamily,” The Journal of Biological Chemistry, vol. 277, no. 11, pp. 9462–9467, 2002.
- A. Smit and A. Mushegian, “Biosynthesis of isoprenoids via mevalonate in archaea: the lost pathway,” Genome Research, vol. 10, no. 10, pp. 1468–1484, 2000.
- S. J. Barkley, R. M. Cornish, and C. D. Poulter, “Identification of an Archaeal type II isopentenyl diphosphate isomerase in Methanothermobacter thermautotrophicus,” Journal of Bacteriology, vol. 186, no. 6, pp. 1811–1817, 2004.
- L. L. Grochowski, H. Xu, and R. H. White, “Methanocaldococcus jannaschii uses a modified mevalonate pathway for biosynthesis of isopentenyl diphosphate,” Journal of Bacteriology, vol. 188, no. 9, pp. 3192–3198, 2006.
- R. Dutoit, J. de Ruyck, V. Durisotti, C. Legrain, E. Jacobs, and J. Wouters, “Overexpression, physicochemical characterization, and modeling of a hyperthermophilic Pyrococcus furiosus type 2 IPP isomerase,” Proteins, vol. 71, no. 4, pp. 1699–1707, 2008.
- J. Lombard and D. Moreira, “Origins and early evolution of the mevalonate pathway of isoprenoid biosynthesis in the three domains of life,” Molecular Biology and Evolution, vol. 28, no. 1, pp. 87–99, 2011.
- U. Jahn, R. Summons, H. Sturt, E. Grosjean, and H. Huber, “Composition of the lipids of Nanoarchaeum equitans and their origin from its host Ignicoccus sp. strain KIN4/I,” Archives of Microbiology, vol. 182, no. 5, pp. 404–413, 2004.
- P. Bork, C. Sander, and A. Valencia, “Convergent evolution of similar enzymatic function on different protein folds: the hexokinase, ribokinase, and galactokinase families of sugar kinases,” Protein Science, vol. 2, no. 1, pp. 31–40, 1993.
- J. L. Andreassi II and T. S. Leyh, “Molecular functions of conserved aspects of the GHMP kinase family,” Biochemistry, vol. 43, no. 46, pp. 14594–14601, 2004.
- S. M. Houten and H. R. Waterham, “Nonorthologous gene displacement of phosphomevalonate kinase,” Molecular Genetics and Metabolism, vol. 72, no. 3, pp. 273–276, 2001.
- T. J. Herdendorf and H. M. Miziorko, “Phosphomevalonate kinase: functional investigation of the recombinant human enzyme,” Biochemistry, vol. 45, no. 10, pp. 3235–3242, 2006.
- M. Chen and C. D. Poulter, “Characterization of thermophilic archaeal isopentenyl phosphate kinases,” Biochemistry, vol. 49, no. 1, pp. 207–217, 2010.
- B. A. Kellogg and C. D. Poulter, “Chain elongation in the isoprenoid biosynthetic pathway,” Current Opinion in Chemical Biology, vol. 1, no. 4, pp. 570–578, 1997.
- S. I. Ohnuma, K. Hirooka, H. Hemmi, C. Ishida, C. Ohto, and T. Nishino, “Conversion of product specificity of archaebacterial geranylgeranyl- diphosphate synthase. Identification of essential amino acid residues for chain length determination of prenyltransferase reaction,” The Journal of Biological Chemistry, vol. 271, no. 31, pp. 18831–18837, 1996.
- S. I. Ohnuma, K. Hirooka, N. Tsuruoka et al., “A pathway where polyprenyl diphosphate elongates in prenyltransferase: insight into a common mechanism of chain length determination of prenyltransferases,” The Journal of Biological Chemistry, vol. 273, no. 41, pp. 26705–26713, 1998.
- A. Tachibana, Y. Yano, S. Otani, N. Nomura, Y. Sako, and M. Taniguchi, “Novel prenyltransferase gene encoding farnesylgeranyl diphosphate synthase from a hyperthermophilic archaeon, Aeropyrum pernix. Molecular evolution with alteration in product specificity,” European Journal of Biochemistry, vol. 267, no. 2, pp. 321–328, 2000.
- A. Chen, P. A. Kroon, and C. D. Poulter, “Isoprenyl diphosphate synthases: protein sequence comparisons, a phylogenetic tree, and predictions of secondary structure,” Protein Science, vol. 3, no. 4, pp. 600–607, 1994.
- T. G. Tornabene, R. S. Wolfe, W. E. Balch, G. Holzer, G. E. Fox, and J. Oro, “Phytanyl-glycerol ethers and squalenes in the archaebacterium Methanobacterium thermoautotrophicum,” Journal of Molecular Evolution, vol. 11, no. 3, pp. 259–266, 1978.
- M. Nishihara, S. Nagahama, M. Ohga, and Y. Koga, “Straight-chain fatty alcohols in the hyperthermophilic archaeon Pyrococcus furiosus,” Extremophiles, vol. 4, no. 5, pp. 275–277, 2000.
- N. M. Carballeira, M. Reyes, A. Sostre, H. Huang, M. F. J. M. Verhagen, and M. W. W. Adams, “Unusual fatty acid compositions of the hyperthermophilic archaeon Pyrococcus furiosus and the bacterium Thermotoga maritima,” Journal of Bacteriology, vol. 179, no. 8, pp. 2766–2768, 1997.
- E. L. Pugh, M. K. Wassef, and M. Kates, “Inhibition of fatty acid synthetase in Halobacterium cutirubrum and Escherichia coli by high salt concentrations,” Canadian Journal of Biochemistry, vol. 49, no. 8, pp. 953–958, 1971.
- E. L. Pugh and M. Kates, “Acylation of proteins of the archaebacteria Halobacterium cutirubrum and Methanobacterium thermoautotraphicum,” Biochimica et Biophysica Acta, vol. 1196, no. 1, pp. 38–44, 1994.
- M. Colella, S. Lobasso, F. Babudri, and A. Corcelli, “Palmitic acid is associated with halorhodopsin as a free fatty acid radiolabeling of halorhodopsin with 3H-palmitic acid and chemical analysis of the reaction products of purified halorhodopsin with thiols and NaBH4,” Biochimica et Biophysica Acta, vol. 1370, no. 2, pp. 273–279, 1998.
- A. Corcelli, S. Lobasso, M. Colella, M. Trotta, A. Guerrieri, and F. Palmisano, “Role of palmitic acid on the isolation and properties of halorhodopsin,” Biochimica et Biophysica Acta, vol. 1281, no. 2, pp. 173–181, 1996.
- M. Kolbe, H. Besir, L. O. Essen, and D. Oesterhelt, “Structure of the light-driven chloride pump halorhodopsin at 1.8 Å resolution,” Science, vol. 288, no. 5470, pp. 1390–1396, 2000.
- V. Iverson, R. M. Morris, C. D. Frazar, C. T. Berthiaume, R. L. Morales, and E. V. Armbrust, “Untangling genomes from metagenomes: revealing an uncultured class of marine Euryarchaeota,” Science, vol. 335, no. 6068, pp. 587–590, 2012.
- J. Lombard and D. Moreira, “Early evolution of the biotin-dependent carboxylase family,” BMC Evolutionary Biology, vol. 11, article 232, 2011.
- J. Lombard and D. Moreira, “Correction: early evolution of the biotin-dependent carboxylase family,” BMC Evolutionary Biology, vol. 12, no. 1, p. 117, 2012.
- J. Lombard, P. López-García, and D. Moreira, “An ACP-independent fatty acid synthesis pathway in archaea: implications for the Origin of Phospholipids,” Molecular Biology and Evolution, vol. 29, no. 11, pp. 3261–3265, 2012.
- C. Jiang, S. Y. Kim, and D. Y. Suh, “Divergent evolution of the thiolase superfamily and chalcone synthase family,” Molecular Phylogenetics and Evolution, vol. 49, no. 3, pp. 691–701, 2008.
- E. Płoskoń, C. J. Arthur, A. L. P. Kanari et al., “Recognition of intermediate functionality by acyl carrier protein over a complete cycle of fatty acid biosynthesis,” Chemistry & Biology, vol. 17, no. 7, pp. 776–785, 2010.
- M. Nishihara and Y. Koga, “Purification and properties of sn-glycerol-1-phosphate dehydrogenase from Methanobacterium thermoautotrophicum: characterization of the biosynthetic enzyme for the enantiomeric glycerophosphate backbone of ether polar lipids of archaea,” Journal of Biochemistry, vol. 122, no. 3, pp. 572–576, 1997.
- Y. Koga, T. Kyuragi, M. Nishihara, and N. Sone, “Did archaeal and bacterial cells arise independently from noncellular precursors? A hypothesis stating that the advent of membrane phospholipid with enantiomeric glycerophosphate backbones caused the separation of the two lines of descent,” Journal of Molecular Evolution, vol. 46, no. 1, pp. 54–63, 1998.
- H. Daiyasu, T. Hiroike, Y. Koga, and H. Toh, “Analysis of membrane stereochemistry with homology modeling of sn-glycerol-1-phosphate dehydrogenase,” Protein Engineering, vol. 15, no. 12, pp. 987–995, 2002.
- H. Guldan, R. Sterner, and P. Babinger, “Identification and characterization of a bacterial glycerol-1-phosphate dehydrogenase: Ni2+-dependent AraM from Bacillus subtilis,” Biochemistry, vol. 47, no. 28, pp. 7376–7384, 2008.
- J. Payandeh, M. Fujihashi, W. Gillon, and E. F. Pai, “The crystal structure of (S)-3-O-geranylgeranylglyceryl phosphate synthase reveals an ancient fold for an ancient enzyme,” The Journal of Biological Chemistry, vol. 281, no. 9, pp. 6070–6078, 2006.
- H. Hemmi, K. Shibuya, Y. Takahashi, T. Nakayama, and T. Nishino, “(S)-2,3-Di-O-geranylgeranylglyceryl phosphate synthase from the thermoacidophilic archaeon Sulfolobus solfataricus. Molecular cloning and characterization of a membrane-intrinsic prenyltransferase involved in the biosynthesis of archaeal ether-linked membrane lipids,” The Journal of Biological Chemistry, vol. 279, no. 48, pp. 50197–50203, 2004.
- M. Yoshimura, T. Oshima, and N. Ogasawara, “Involvement of the YneS/YgiH and PlsX proteins in phospholipid biosynthesis in both Bacillus subtilis and Escherichia coli,” BMC Microbiology, vol. 7, article 69, 2007.
- Y. J. Lu, Y. M. Zhang, K. D. Grimes, J. Qi, R. E. Lee, and C. O. Rock, “Acyl-phosphates initiate membrane phospholipid synthesis in Gram-positive pathogens,” Molecular Cell, vol. 23, no. 5, pp. 765–772, 2006.
- H. Morii, M. Nishihara, and Y. Koga, “CTP:2,3-di-O-geranylgeranyl-sn-glycero-1-phosphate cytidyltransferase in the methanogenic archaeon Methanothermobacter thermoautotrophicus,” The Journal of Biological Chemistry, vol. 275, no. 47, pp. 36568–36574, 2000.
- T. Icho, C. P. Sparrow, and C. R. H. Raetz, “Molecular cloning and sequencing of the gene for CDP-diglyceride synthetase of Escherichia coli,” The Journal of Biological Chemistry, vol. 260, no. 22, pp. 12078–12083, 1985.
- C. P. Sparrow and C. R. H. Raetz, “Purification and properties of the membrane-bound CDP-diglyceride synthetase from Escherichia coli,” The Journal of Biological Chemistry, vol. 260, no. 22, pp. 12084–12091, 1985.
- H. Morii and Y. Koga, “CDP-2,3-di-O-geranylgeranyl-sn-glycerol:L-serine O-archaetidyltransferase (archaetidylserine synthase) in the methanogenic archaeon Methanothermobacter thermautotrophicus,” Journal of Bacteriology, vol. 185, no. 4, pp. 1181–1189, 2003.
- H. Morii, S. Kiyonari, Y. Ishino, and Y. Koga, “A novel biosynthetic pathway of archaetidyl-myo-inositol via archaetidyl-myo-inositol phosphate from CDP-archaeol and D-glucose 6-phosphate in methanoarchaeon Methanothermobacter thermautotrophicus cells,” The Journal of Biological Chemistry, vol. 284, no. 45, pp. 30766–30774, 2009.
- H. Daiyasu, K. I. Kuma, T. Yokoi, H. Morii, Y. Koga, and H. Toh, “A study of archaeal enzymes involved in polar lipid synthesis linking amino acid sequence information, genomic contexts and lipid composition,” Archaea, vol. 1, no. 6, pp. 399–410, 2005.
- Y. Koga and H. Morii, “Recent advances in structural research on ether lipids from archaea including comparative and physiological aspects,” Bioscience, Biotechnology and Biochemistry, vol. 69, no. 11, pp. 2019–2034, 2005.
- O. Dannenmuller, K. Arakawa, T. Eguchi et al., “Membrane properties of archaeal macrocyclic diether phospholipids,” Chemistry, vol. 6, no. 4, pp. 645–654, 2000.
- Y. Nishimura and T. Eguchi, “Biosynthesis of archaeal membrane lipids: digeranylgeranylglycerophospholipid reductase of the thermoacidophilic archaeon Thermoplasma acidophilum,” Journal of Biochemistry, vol. 139, no. 6, pp. 1073–1081, 2006.
- M. Murakami, K. Shibuya, T. Nakayama, T. Nishino, T. Yoshimura, and H. Hemmi, “Geranylgeranyl reductase involved in the biosynthesis of archaeal membrane lipids in the hyperthermophilic archaeon Archaeoglobus fulgidus,” FEBS Journal, vol. 274, no. 3, pp. 805–814, 2007.
- S. Sato, M. Murakami, T. Yoshimura, and H. Hemmi, “Specific partial reduction of geranylgeranyl diphosphate by an enzyme from the thermoacidophilic archaeon Sulfolobus acidocaldarius yields a reactive prenyl donor, not a dead-end product,” Journal of Bacteriology, vol. 190, no. 11, pp. 3923–3929, 2008.
- H. A. Addlesee, L. C. D. Gibson, P. E. Jensen, and C. N. Hunter, “Cloning, sequencing and functional assignment of the chlorophyll biosynthesis gene, chlP, of Synechocystis sp. PCC 6803,” FEBS Letters, vol. 389, no. 2, pp. 126–130, 1996.
- R. Tanaka, U. Oster, E. Kruse, W. Rüdiger, and B. Grimm, “Reduced activity of geranylgeranyl reductase leads to loss of chlorophyll and tocopherol and to partially geranylgeranylated chlorophyll in transgenic tobacco plants expressing antisense RNA for geranylgeranyl reductase,” Plant Physiology, vol. 120, no. 3, pp. 695–704, 1999.
- S. F. Altschul, W. Gish, W. Miller, E. W. Myers, and D. J. Lipman, “Basic local alignment search tool,” Journal of Molecular Biology, vol. 215, no. 3, pp. 403–410, 1990.
- R. C. Edgar, “MUSCLE: multiple sequence alignment with high accuracy and high throughput,” Nucleic Acids Research, vol. 32, no. 5, pp. 1792–1797, 2004.
- H. Philippe, “MUST, a computer package of management utilities for sequences and trees,” Nucleic Acids Research, vol. 21, no. 22, pp. 5264–5272, 1993.
- M. N. Price, P. S. Dehal, and A. P. Arkin, “FastTree 2—approximately maximum-likelihood trees for large alignments,” PLoS One, vol. 5, no. 3, Article ID e9490, 2010.
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