Evolutionary origins, molecular cloning and expression of carotenoid hydroxylases in eukaryotic photosynthetic algae
- Hongli Cui†1, 2,
- Xiaona Yu†3,
- Yan Wang1,
- Yulin Cui1,
- Xueqin Li4,
- Zhaopu Liu3 and
- Song Qin1Email author
© Cui et al.; licensee BioMed Central Ltd. 2013
Received: 16 January 2013
Accepted: 12 June 2013
Published: 8 July 2013
Xanthophylls, oxygenated derivatives of carotenes, play critical roles in photosynthetic apparatus of cyanobacteria, algae, and higher plants. Although the xanthophylls biosynthetic pathway of algae is largely unknown, it is of particular interest because they have a very complicated evolutionary history. Carotenoid hydroxylase (CHY) is an important protein that plays essential roles in xanthophylls biosynthesis. With the availability of 18 sequenced algal genomes, we performed a comprehensive comparative analysis of chy genes and explored their distribution, structure, evolution, origins, and expression.
Overall 60 putative chy genes were identified and classified into two major subfamilies (bch and cyp97) according to their domain structures. Genes in the bch subfamily were found in 10 green algae and 1 red alga, but absent in other algae. In the phylogenetic tree, bch genes of green algae and higher plants share a common ancestor and are of non-cyanobacterial origin, whereas that of red algae is of cyanobacteria. The homologs of cyp97a/c genes were widespread only in green algae, while cyp97b paralogs were seen in most of algae. Phylogenetic analysis on cyp97 genes supported the hypothesis that cyp97b is an ancient gene originated before the formation of extant algal groups. The cyp97a gene is more closely related to cyp97c in evolution than to cyp97b. The two cyp97 genes were isolated from the green alga Haematococcus pluvialis, and transcriptional expression profiles of chy genes were observed under high light stress of different wavelength.
Green algae received a β-xanthophylls biosynthetic pathway from host organisms. Although red algae inherited the pathway from cyanobacteria during primary endosymbiosis, it remains unclear in Chromalveolates. The α-xanthophylls biosynthetic pathway is a common feature in green algae and higher plants. The origination of cyp97a/c is most likely due to gene duplication before divergence of green algae and higher plants. Protein domain structures and expression analyses in green alga H. pluvialis indicate that various chy genes are in different manners response to light. The knowledge of evolution of chy genes in photosynthetic eukaryotes provided information of gene cloning and functional investigation of chy genes in algae in the future.
KeywordsCarotenoid hydroxylase Xanthophylls biosynthesis Structure and evolution Molecular cloning Expression profiles Algae
Carotenoids are isoprenoids which derived from the precursor molecule isopentenyl pyrophosphate and its isomer dimethylallyl diphosphate. All photosynthetic organisms including cyanobacteria, algae, and higher plants synthesize carotenoids [1, 2]. Carotenoids are divided into two major groups: carotenes, which are enriched in the centers of photosystem reaction [3, 4], and xanthophylls (including lutein, zeaxanthin, antheraxanthin, violaxanthin, and neoxanthin), oxygenated carotenoids that serve various functions in photosynthetic organisms and are essential for survival of the organism [5–8]. Of xanthophylls, lutein is the most abundant xanthophyll in all plant photosynthetic tissues, where it plays an important role in assembly and function of light harvesting complexes II (LHC II) [6–8]. Zeaxanthin is a structural isomer of lutein and a mainly component of the non-photochemical quenching (NPQ) mechanism involved in protecting the organism from photo-damage [9–11].
Untangling the phylogenomics of xanthophylls biosynthesis in eukaryotic algae requires basic knowledge of their evolutionary histories. Three algal phyla, the Rhodophyta (red algae), Glaucophyta, and Viridiplantae (land plants and green algae) acquired their plastids during primary endosymbiosis starting a heterotrophic eukaryote as a host and a phototrophic cyanobacterium as an endosymbiont [12–18]. Viridiplantae is comprised of two major evolutionary lineages that split in early: the Chlorophyta (Chlorophyceae, Ulvophyceae, Trebouxiophyceae, and Prasinophyceae) and the Streptophyta (Charophyte and Embryophytes) [19–21]. Subsequently, secondary endosymbiosis from green or red algae occurred, producing the extant diverse algal groups (for reviews, see [22, 23]). Algae comprise a paraphyletic and polyphyletic group , as they do not include all the descendants of the last universal ancestor nor do they all descend from a common algal ancestor, although their plastids seem to have a single origin . From an evolutionary perspective, carotenoid biosynthesis in photosynthetic organisms has become increasingly more complex and diverse . Some photosynthetic bacteria, e.g., cyanobacteria contain carotenoids with β-rings (e.g. β-carotene), and many of them produce various mono- or di-hydroxy xanthophyll derivatives (e.g. zeaxanthin) [27, 28]. In addition, pathway bifurcation occurred in some red algae and cyanobacteria (i.e. Acaryochloris and Prochlorococcus), and all green algae, and higher plants at the level of lycopene cyclization, yielding α-carotene from which α-carotene-derived xanthophylls (e.g. lutein) are synthesized [29–32]. As a consequence, the origins and evolution of xanthophylls biosynthetic pathway in algae lineages is of particular interesting.
Carotenoid hydroxylases (CHYs) comprise an important hydroxylase protein family performing the key enzymatic steps, hydroxylation reactions for α- and β-branch xanthophylls biosynthesis in photosynthetic organisms . In higher plants, production of α-xanthophylls from α-carotene requires one β- and one ϵ-ring hydroxylation, while synthesis of β-xanthophylls from β-carotene requires two β-ring hydroxylations. Two classes of structurally unrelated enzymes catalyze these ring hydroxylations: two heme-containing cytochrome P450 hydroxylases (CYP97A3 and CYP97C1) and a pair of non-heme/di-iron hydroxylases (BCH1 and BCH2) [34–37]. Two β-ring hydroxylations in β-carotene are mediated by either P450-type CYP97A or BCH enzyme, during which zeaxanthin is produced [34–36]. Hydroxylations of β-ring and ϵ-ring in α-carotene are performed by CYP97A and CYP97C, respectively, producing lutein . It is unknown why two different β-ring hydroxylases could have been maintained throughout the evolution. Probably, their own respective activities are not entirely interchangeable . Different chy genes in higher plants are up-regulated often differentially, depending on environmental conditions or developmental stage of various tissues [6, 8, 26, 33, 36–40]. For algae, however, the research on xanthophylls biosynthesis is still in its infancy. For unicellular green algae, bch genes were investigated such as in Haematococcus pluvialis and Chlamydomonas reinhardtii[41–43]. Although lutein and its derivatives are detected in Rhodophyta (macrophytic type), Cryptophyta, Euglenophyta, Chlorarachniophyta, and Chlorophyta, enzymes involving in hydroxylation of α-carotene remains unknown . Recently, a new P450 protein responsible for the hydroxylation of ϵ–ring of α-carotene in Arabidopsis thaliana was reported [37, 45]. In addition, two genes encoding cytochrome P450-type carotenoid hydroxylases (cyp97a4 and cyp97c2) were isolated from Oryza sativa and their functions were investigated in a β-carotene producing Escherichia coli strain . Moreover, 25 cytochrome P450 oxidoreductases have been discovered so far in the green alga Ulva linza. Therefore, it is evident that P450-type monooxygenases, in addition to non-heme hydroxylases such as BCH, are involved in carotenoid hydroxylation, which identified one of the missing pieces of carotenoid biosynthetic enzyme and provided valuable clues to study chy genes in algae in the future.
Recently, the genome sequences of a number of microalgae became available from the DOE Joint Genome Institute (http://genome.jgi.doe.gov/). Proteins coding sequences of each filtered model of these algae genomes with representatives from very different groups such as green algae, red algae, diatoms, and Haptophytes was performed to identify their chy genes. Details of the completeness of genome sequences used in this study were taken from DOE Joint Genome Institute project list (project list: http://genome.jgi.doe.gov/genome-projects/) [see Additional file 1: Table S1]. A BLASTp-HMMER-plus-phylogeny reconstruction approach was employed to analyze CHYs in focus of their distribution, structure, evolution, origins, and expression. In order to study the evolutionary histories of xanthophylls biosynthetic pathway from cyanobacteria to modern algae, candidate genes were then compared with known sequences of other organisms. Based on the predicted putative CHY-encoding genes, two full-length sequences of CYP97-encoding cDNA (Haecyp97a and Haecyp97b) were isolated from high-astaxanthin-production green alga H. pluvialis strain Flotow 1844 . Expression profiles of different chy genes under high light stress of different wavelength were observed by means of relative quantitative real-time RT-PCR (Reverse Transcription-Polymerase Chain Reaction). Light is considered an effective stimulus inducing the expression of carotenoid biosynthesis-related genes and the astaxanthin accumulation in economic green alga H. pluvialis[47, 48]. These studies provide significant insight into the origins and evolution of chy genes in photosynthetic eukaryotes and provide information for further gene cloning, functional characterization, and expression analysis of chy genes in algae. A better understanding of algal CHYs can help us to comprehend the roles of CHYs in xanthophylls biosynthetic under different adverse conditions.
Results and discussion
Identification, classification, and distribution of CHY proteins
Putative carotenoid hydroxylase genes identified in 18 algae genomes
Gene locations (Locations are indicated by positions on either chromosomes or scaffolds)
Chlorophyta---- Chlamydomonas reinhardtii
Chlorophyta---- Volvox carteri
Chlorophyta---- Chlorella NC64A
Chlorophyta---- Chlorella vulgaris
Chlorophyta---- Coccomyxa sp c-169
Chlorophyta---- Ostreococcus lucimarinus
Chlorophyta---- Osetrococcus tauri
Chlorophyta---- Osetrococcus RCC809
Chlorophyta---- Micromonas pusilla
Chlorophyta---- Micromonas sp. RCC299
Rhodophyta---- Cyanidioschyzon merolae
gnl|CMER|CMV041C [pt] beta-carotene hydroxylase
Bacillariophyta---- Thalassiosira pseudonana
Bacillariophyta---- Phaeodactylum tricornutum
Bacillariophyta---- Fragilariopsis cylindrus
Haptophyceae---- Emiliania huxleyi
Cryptophyta---- Guillardia theta
Cercozoa---- Bigelowiella natans CCMP2755
Stramenopiles---- Aureococcus anophagefferens
Homologs of cyp97a and cyp97c genes are found in green algae, but absent in other algae, including red algae (C. merolae), Heterokontophyta (P. tricornutum, F. cylindrus and T. pseudonana), Haptophyta (E. huxleyi), Cryptophyta (G. theta), and Stramenopiles (A. anophagefferens). Interestingly, two cyp97a genes were predicted in C. reinhardtii and O. lucimarinus, indicating that lineage-specific gene duplications occurred during the evolution of these algae. Due to gene loss or the incompletely sequenced genome, only genes encoding CYP97B and CYP97C homologs and none gene encoding CYP97A homolog were predicted in B. natans CCMP2755. Moreover, none gene encoding CYP97A homolog has been discovered in Chlorella sp. NC64A. In this study, at least one copy of the gene encoding CYP97B was found to be widely distributed in most of algae, except for red algae, indicating that the originations of this gene is not due to secondary endosymbiosis.
Domain structures of BCH-type CHYs in algae
β-Xanthophylls (zeaxanthin) are widely distributed in nature, and they are common in all photosynthetic eukaryotes, and many photosynthetic, or non-photosynthetic prokaryotes [26, 52]. Non-heme/di-iron β-ring carotenoid hydroxylase (BCH) has long been regarded as the only enzyme involved in zeaxanthin synthesis by hydroxylating β–carotene. Genes encoding β-carotene hydroxylases have been identified and characterized from bacteria [53, 54], cyanobacteria , algae [41, 42] and higher plants . The bch genes of algae and higher plants encode the members of the fatty acid hydroxylase superfamily [PF04116] that also includes fatty acid and carotene hydroxylases and sterol desaturases. Members of this superfamily are integral membrane proteins and contain two copies of histidine-rich iron-binding motifs (HXXHH), needed for binding this cofactor with enzymes [34, 56].
Origins and evolution of BCHs in algae
As shown in Figure 3, difference between CrtRs of cyanobacteria and BCHs of algae, bacteria, and higher plants is very clear. Genes encoding BCHs from bacteria, green algae, and higher plants build a monophyletic group (Bootstrap [BS]: 100%), and the phylogenetic relationship present here indicates that they share a common ancestor and strongly supports a non-cyanobacterial origin. In contrast to the apparently widespread retention of BCH paralogs in higher plants, the gene encoding BCH is a single copy in each algal genome sequences (Figure 3). In higher plants, duplication of the ancestral bch gene took place most probably via whole-genome or segmental genome duplication  and the duplicates seem to have functionally diverged primarily at the gene expression level [60–62]. It is worth mentioned, however, that the gene encoding BCH (CrtR-type) of red algae forms another monophyletic group (BS: 97%) with CrtRs of cyanobacteria, suggesting that the red alga obtained this gene via the primary endosymbiotic event from cyanobacteria and retained it over the course of evolution persistently. However, the activity of this encoded enzyme was not demonstrated when expressed in E. coli[57, 58]. Therefore, hydroxylation of β-carotene in red algae remains unclear, calling for more red-algal genomes sequences to elucidate. In this study, no BCH- or CrtR-type CHY-encoding gene was discovered in algae of Chromalveolates, except for a partial sequence of bch-type gene in the genome sequences of T. pseudonana. This result is consistent with observations from a previous study, in which only a partial sequence of BCH-type gene was found in the genome sequences of T. pseudonana and no one was detected from the P. tricornutum genome . Unfortunately, the enzymatic activity of this putative carotene hydroxylases (BCH) from T. pseudonana has not yet been reported anywhere to the best knowledge of authors. Therefore, the hydroxylation of β-carotene in Chromalveolates remains unknown, resulting from genomes of the few organisms currently sequenced lack entire hydroxylation families and, enzymatic activity of putative carotene hydroxylases has not yet been reported at present [51, 57, 63–65].
As mentioned above, it is difficult to fully understand the evolution of β-xanthophylls biosynthesis with limited available data, but some hypotheses were proposed based on the tree topology. Firstly, it is presumed that CrtR-type CHY was originated in all algae as the result of primary endosymbiosis. In such a scenario, CrtR-type CHY proteins were lost in extant green algae and higher plants, and these organisms acquiring another BCH from bacteria by lateral gene transfer or from the host during the primary endosymbiosis event. Secondly, red algae have CrtR-type CHY-encoding gene, while Chromalveolates do not have them due possibly to gene lost during the secondary endosymbiosis event. In addition, BCH-type CHYs are also absent in Chromalveolates, which may be resulted from the replacement of algal CrtR- and BCH-type CHYs by another unidentified novel lineage-specific CHY in strains that derived from the red algal secondary endosymbiosis. Previous studies of the diatom P. tricornutum, however, have demonstrated the presence of a xanthophyll cycle (zeaxanthin-antheraxanthin-violaxanthin), with violaxanthin the putative precursor of both diadinoxanthin and fucoxanthin, implying this enzymatic reaction may therefore be catalyzed by other unrelated enzymes, such as LUT-like P450 proteins . Therefore, we speculate that the bch genes in Chromalveolates have not been under a strong pressure of natural selection like in green algae and higher plant lineages, and they may have instead evolved different ways for β-xanthophylls biosynthesis.
Domain structures of CYP97s in algae
The alignment (Figure 4) reveals 11 domains in strongly conserved amino acid sequences from all CYP97 protein sequences. All conserved domains are highly similar between CYP97As and CYP97Cs of green algae except for CD1 (QPVFVPLYKLPLXYG) (Figure 4), indicating that they share a common ancestor. In addition, the conserved domains in CYP97Bs of distinct algae phyla are also similar, implying that this gene occurred before the formation of extant diverse algal groups. Degenerate primers for cloning genes encoding CYP97 homologs were designed from these conserved amino acid residues. P450s catalytic motifs were found as expected in all CYP97A/B/C protein sequences including I-helix involved in oxygen binding (CD6 in CYP97B and CD5 in CYP97A and CYP97C), an ERR triad (CD7 in CYP97A/B/C) responsible for locking the heme pockets into position and assuring stabilization of the conserved core structure, and CD10 associated with the conserved heme-binding cysteine. In addition, many amino acids were conserved in each CYP97 subfamily such as CD4 (LLRFLVDXR) and CD9 (LYPXE) were conserved in CYP97B subfamily only. The conserved domains associated with active sites suggest that these protein sequences are members of the P450 family, and that conserved domains within each CYP97 subfamily proteins are responsible for the specificity with respect to the β- or ϵ-ring of different carotenes.
Origins and evolution of CYP97s in algae
Production of α-xanthophylls (lutein) in higher plants requires four reaction steps: β- and ϵ-ring formation from lycopene by the action of β- and ϵ-cyclases (LYCB and LYCE); and subsequently, hydroxylation of each ring of α-carotene by β- and ϵ-ring hydroxylases (CYP97A and CYP97C) . Ample evidence shows that genes encoding CYP97A and CYP97C homologs are only present in green algae and higher plants, but not in Chromalveolates, indicating that α-xanthophylls biosynthesis occurs only in green algae and higher plant lineages. In our results, this biosynthetic pathway is also absent in red algae. In contrast to a previous study postulated that synthesis of α-xanthophylls occurs in only a few lineages of photosynthetic eukaryotes, namely, some red algae, all green algae, and higher plants . An insufficient number of red algal species (only a red alga used in this study) may be responsible for these different conclusions. In addition, our previous and other studies have demonstrated that β-cyclases (LYCBs) genes are widely distributed in nature, and ϵ-cyclase (LYCEs) genes were identified only in green algae, higher plants, and some cyanobacteria (e.g. Prochlorococcus marinus MED4). LYCE genes seems to come from β-cyclases by gene duplication and subsequently functional divergence [30, 57, 74–77], which indirectly manifests that α-xanthophylls are synthesized only in green algae and higher plants. No CYP97A and CYP97C homologs are detected in algal genome sequences from Chromalveolates, and these algae cannot synthesize α-xanthophylls (lutein), which is consistent with previous studies .
As it shows in maximum likelihood tree, CYP97 proteins constitute three distinct monophyletic groups: CYP97A, CYP97B, and CYP97C. Two of these groups (CYP97A and CYP97C) form a sister group that are composed of proteins from green algae and higher plants. CYP97A and CYP97C sequences in Chromalveolates, including Heterokontophyta (P. tricornutum, F. cylindrus, and T. pseudonana), Haptophyta (E. huxleyi), Cryptophyta (G. theta), and Stramenopiles (A. anophagefferens) are absent in the cluster. Genes encoding CYP97B homologs from all organisms form a monophyletic group (BS: 92%). Surprisingly, algal CYP97Bs from Chromalveolates and green algae (Prasinophyceae) build another monophyletic group (BS: 95%). This phylogenetic relationship and the lack of CYP97B homologs in C. merolae point to a “green” origin of this gene in Chromalveolates, similar to the origin and evolution of hydroxypyruvate reductase . Alternatively, this gene represents early eukaryotic innovations in the Plantae although lacking CYP97B homolog in C. merolae. Further investigations are needed to support this hypothesis.
The topology of the phylogenetic tree shows that the CYP97B is an ancient gene emerging before the divergence of extant algae groups during evolution, and represents an ancient eukaryotic innovation. Our results indicate that CYP97A is evolutionarily more closely to CYP97C than to CYP97B (Figure 5). Therefore, we believe that the CYP97A and CYP97C genes were originated by gene duplication before the split between green algae and higher plants, and were subjected to purifying selection in a lineage-specific fashion (Figure 5). Alternatively, these genes may have been originally present in all algae, and then they were lost gradully from red algae and Chromalveolates. This scenario is similarity to that of Arabidopsis whose evolution and functional divergence of two duplicate gene pairs, CYP97A3/C1 and BCH1/2 involved in carotenoid hydroxylation occurred . Additional lineage- or organism-specific gene duplications have occurred during the evolution of CYP97A in green algae (C. reinhardtii and O. lucimarinus), and CYP97B in most algae, except for C. reinhardtii, C. sp. NC64A, C. vulgaris, C. sp. C-169, V. carteri, M. pusilla, E. huxleyi, and B. natans CCMP2755. Duplication and subsequent functional divergence of genes have been recognized increasingly as an important mechanism of evolution [80–83].
Isolation and characterization of cyp97 genes from H. pluvialis
Listed of three full-length of HaeCYP97A/B/C from Haematococcus pluvialis
The degree of identity and similar between the predicted amino acid sequences for each isolated CYP97 genes and corresponding CYP97 from other eukaryotes
Expression analysis of four chy genes in H. pluvialisunder high light stress
Studies showed that high light (HL) effectively induces carotenoid biosynthesis-related gene expression and astaxanthin accumulation in H. pluvialis[47, 48], indicating that light plays an important role in controlling green algal carotenoid biosynthesis. Although the regulatory role of light in the expression of nuclear-encoded plastid-targeted proteins has been studied for decades in green algae and higher plants, elucidation of effects of light on transcriptional levels of three novel cyp97 genes in green algae is still in its infancy. In a previous study on diatom P. tricornutum, a blue-light library was found to be the most enriched in carotenogenesis-related ESTs . For more detail in the transcriptional regulatory role of light on green algae, we studied the gene transcriptional expression profiles of bch, Haecyp97a, Haecyp97b, and Haecyp97c genes in response to white and blue HL conditions.
Expression levels of Haecyp97a, Haecyp97b, and Haecyp97c began with a slight decrease followed by a dramatic increase (Figure 6B-D). Strongly steady increase in transcriptional levels of Haecyp97a and Haecyp97b were observed during 4–28 h of both HL (white and blue) treatments. Then, they dropped sharply after 28 h of exposure. It is also intriguing that different conditions had various impacts on Haecyp97a and Haecyp97b mRNA levels. For instance, transcriptional levels of Haecyp97a and Haecyp97b under blue HL were higher than that of under white HL during 4–10 h of exposure, and the contrary tendency was observed during 13–28 h of exposure (Figure 6B and C). The maximum transcriptional levels of Haecyp97c under both the blue and white HL treatments occurred at hour 13 and 10, and transcriptional levels were 4.5- and 2.8-fold higher than that of control, respectively (Figure 6D). Blue HL appeared to have stronger effects on Haecyp97c transcriptional level than that of white HL (Figure 6D). Studies on mutant of higher plants showed that CYP97A3 and CYP97C1 are the enzymes primarily responsible for catalyzing hydroxylation of β- and ϵ-ring of α-carotene, respectively, producing α-branch xanthophylls (lutein), the most abundant carotenoids in light-harvesting complexes (LHCs) which is key structural and functional components of light harvesting [6, 8, 26, 33, 37, 39, 59, 72]. During early stages (0–4 h) of HL (blue and white) treatments, lutein concentrations were lower than that of the control , which is listed in Figure S5 for details [see Additional file 9: Figure S5]. This result is consistent with the decreased transcriptional levels of Haecyp97a and Haecyp97c observed in H. pluvialis (Figure 6B and D). Although Haecyp97a and Haecyp97c transcriptional levels increased over time, lutein concentration level remained rather stable but was lower than the control. When considering that CYP97A is also involved in hydroxylation of β-carotene into zeaxanthin, the level of Haecyp97a increase is understandable . Previous studies have demonstrated there was a cytochrome P450 involved in astaxanthin biosynthesis in H. pluvialis by the use of ellipticine . Therefore, we speculate that CYP97A may be the cytochrome P450 involved in astaxanthin biosynthesis in H. pluvialis. According to our results, however, it is unclear why and how the levels of Haecyp97b and Haecyp97c increased. The function of CYP97B is currently unknown and they (CYP97B and CYP97C) may play some additional roles (aside from CHY ϵ–ring) in algae under adverse conditions. An earlier study reported that cytochrome P450 reductase is also co-up-regulated with enzymes involved in DNA repair under light/dark cycles .
Our data (Figure 6) reveal that mRNA levels of different chy genes increase rapidly under HL exposure and varied with light wavelength. For instance, our results indicate that blue HL very significantly increased Haebch and Haecyp97c genes expression, and produced similar effects on Haecyp97a and Haecyp97b genes expression compare with white HL treatment. Young et al.  have demonstrated that different carotenoid metabolic gene isoforms typically had distinctly different expression patterns. Previous study has demonstrated that zeaxanthin and astaxanthin concentrations were more efficiently enhanced for H. pluvialis under blue HL treatment than white . Therefore, we propose that Haematococcus cells are more sensitive to blue induction compare with white. Similar phenomena were reported red Light Emitting Diodes (LEDs) operated at a relatively low light intensity were found to be suitable for cell growth; and LEDs emitting short wavelength (380–470 nm) can induce morphological changes in H. pluvialis and enhance astaxanthin accumulation [92–94]. It is well known that strong light (blue) enhances astaxanthin accumulation, because astaxanthin is produced by H. pluvialis cells to protect cells from the strong intensity of the light . Although blue light contains more energy than red light, according to Planck’s law , in fact only energy associated to the S1 transition level of chlorophyll (Chl) can be used for photosynthesis . On this bottom line, the fact that the efficiency of energy transfer from carotenoid to Chl a is far lower (40%) with respect to Chl b to Chl a or Chl a to Chl a. Thus it can easily be concluded that less energy used for photosynthesis is available from blue light than from red or white light under the same light intensity. According to above conclusions, we speculate that astaxanthin accumulation for H. pluvialis depends on not only light intensity, but also light quality (i.e. blue light might be a more useful wavelength to enhance astaxanthin accumulation in H. pluvialis under HL intensity). Therefore, we believe that the response of H. pluvialis Flotow 1844 to high light stress is a complicated process involving bch, Haecyp97a, Haecyp97b, and Haecyp97c.
Our study provided a genome-wide comparative analysis of genes encoding CHYs in algae, with a focus on their distribution, structure, evolution, origins, and expression. As part of this study, we provided a summary of currently known distributions of chy genes in eukaryotic photosynthetic algae, and constructed hypotheses regarding xanthophylls biosynthetic pathways. Genes encoding BCHs of green algae and higher plants were determined to be non-cyanobacterial origin, whereas those from red algae were derived from cyanobacteria. Genes involved in β-xanthophylls biosynthetic pathway in Chromalveolates remains unknown. CYP97B genes are likely an innovation of eukaryotic algae, whereas genes of CYP97A and CYP97C initiated by gene duplication events before the split of green algae and higher plants. The biosynthesis of α-xanthophylls is characteristic of green algae and higher plants. Although transcriptional levels of bch, Haecyp97a, Haecyp97b, and Haecyp97c were up-regulated by blue and white HL treatments, the amplitude and kinetics of mRNA accumulation varied among different chy genes. Compare with white light, blue light may play a more important role in controlling green algal carotenoid biosynthesis. The response of H. pluvialis Flotow 1844 to different HL stresses is a complicated course involving bch, Haecyp97a, Haecyp97b, and Haecyp97c. The observed increase in Haecyp97b transcriptional level implies that this gene may be another carotenoid biosynthetic-related gene, perhaps a novel chy gene in Chromalveolates. Further investigations are needed to test this hypothesis.
Identification of chygenes encoding CHY proteins
The genomes of 18 eukaryotic photosynthetic algae included Chlamydomonas reinhardtii, Chlorella sp. NC64A, Chlorella vulgaris, Coccomyxa sp. C-169, Volvox carteri, Micromonas pusilla, Micromonas sp. RCC299, Ostreococcus sp. RCC809, Ostreococcus tauri, Ostreococcus lucimarinus, Phaeodactylum tricornutum, Thalassiosira pseudonana, Fragilariopsis cylindrus, Aureococcus anophagefferens, Emiliania huxleyi, Guillardia theta and Bigelowiella natans CCMP2755 were obtained from the website of the DOE Joint Genome Institute (Walnut Creek, CA, USA; http://genome.jgi.doe.gov/). The genome of the red alga Cyanidioschyzon merolae was obtained from the C. merolae Genome Project (http://merolae.biol.s.u-tokyo.ac.jp). The protein coding sequences of each genome was fed into the program makeblastdb to create an organism-species database .
Two methods were applied to identify the putative CHY homologs genes. Firstly, we followed JGI’s or the C. merolae Genome Project’s annotation to determine the number of chy present in the algal genomes. Then, eight previously characterized CHYs from Haematococcus pluvialis [GenBank: BCH, ABB70496.1], Chlamydomonas reinhardtii [GenBank: BCH, AAX54907.1], Synechocystis sp. PCC 6803 [GenBank: CrtR, BAA17468.1] and Arabidopsis thaliana [GenBank: BCH1, sp|Q9SZZ8.1; BCH2, sp|Q9LTG0.1; CYP97A3, NP_564384.1; CYP97B3, NP_193247.2, and CYP97C1, NP_190881.2] were used to construct a query protein set. BLASTp [97, 98] and HMMER  programs were then conducted locally to identify all chy genes in all 18 algal genomes using a threshold e-value of 1e-10. Finally, we manually checked the extracted proteins by SMART and Pfam analyses to avoid false positive hits that commonly arise during large-scale automated analyses. Putative chy genes found by this method were added to the query set for another round of BLASTp searches. This procedure was iterated until no newly retrieved sequences that belonged to chy homologs. Moreover, in order to check for false negatives, two HMM models [Pfam: PF04116] and [Pfam: PF00067] derived from known bch and cyp97 genes were applied to search for genes encoding chy on all proteins encoded in the 18 algal genomes [100, 101]. All translated protein sequences of CHYs-encoding genes used in this paper were listed in more detail [see Additional file 2]. CHY proteins from higher plants and cyanobacteria were also downloaded from National Center for Biotechnology Information GenBank database and Cyanobase (http://bacteria.kazusa.or.jp/cyanobase/).
Multiple sequence alignment and phylogenetic analysis
Proteins identified by the BLAST and HMM searches were aligned using ClustalW [102, 103] with a gap opening penalty of 10, a gap extension penalty of 0.2, and Gonnet as the weight matrix. The SMART  and Pfam 26.0  databases were applied to delete false positives. Phylogenetic trees were constructed using Maximum likelihood (ML) method that implemented in PhyML . ML trees were built in particular models of amino acid substitutions chosen according to PROTTEST AIC results . The Le and Gascuel evolutionary model  was selected to analyze the protein phylogenies by assuming an estimated proportion of invariant sites and a gamma correction (four categories). Bootstrap values (BS) were inferred from 400 replicates. Graphical representation and edition of the phylogenetic tree were performed with TreeDyn (v198.3) .
Algal strains and culture conditions
H. pluvialis strain Flotow 1844 was obtained from Culture Collection of Algae and Protozoa, Dunstaffnage Marine Laboratory, and maintained at the Biological Resources Laboratory, Yantai Institute of Costal Zone Research, Chinese Academy of Science. Algae were incubated in 250-ml erlenmeyer flasks, each containing 100-ml BBM, and placed in an illuminating incubator (Ningbo Jiangnan Instrument Factory, GXZ-380, Ningbo, China) under a light intensity of 25 μmol photons m–2 s–1 in 14 h:10 h diurnal scheme at temperature of 22 ± 1°C without aeration.
For high light stress conditions, exponentially growing cultures (cell density approximately 5 × 107 cells ml–1) were harvested, and then transferred to 500-ml erlenmeyer flasks (named, 1–9), each containing 250-ml BBM (fresh medium) under continuous exposure of white light (390–770 nm) or blue light (420–500 nm) in light intensity of 1,000 μmol photons m–2 s–1 without day/night cycle. Algal cells collected (20-mL sample at some selected time) were rinsed with PBS, stored at −80°C if not immediately used. All experimental chemicals and reagents were of analytical grade.
Cloning and characterization of the CYP97 genes
H. pluvialis strain flotow 1844 in the exponential growth phase were harvested. Total RNA was extracted from fresh cells of H. pluvialis using Trizol reagent (TaKaRa D9108B, Dalian, China) according to the user manual. RNA solutions were stored at −80°C, if not immediately used. First-strand cDNAs were synthesized from 2 μg total RNA with PrimeScript® RT Enzyme Mix I (TaKaRa DRR047A, Dalian, China) according to the manufacturer′s instructions.
The CODEHOP (Consensus-degenerate hybrid oligo-nucleotide primers) strategy (http://blocks.fhcrc.org/blocks/codehop.html) was used to generate degenerate primers [110, 111] for the cloning of core partial sequences of HaeCYP97A/B/C basing on the highly conserved regions of predicted putative genes encoding CYP97 homologs from some green algae. The nucleotide sequences of the 3’- and 5’-ends of HaeCYP97A/B/C were amplified by the RACE method [112, 113]. Gene-specific primers were designed from the amplified core cDNA sequence of HaeCYP97A/B/C and their 3’- and 5’-ends were obtained using SMARTTM RACE cDNA Amplification Kit (Clontech) according to the manual. All primers used in this study were listed in more [see Additional file 5: Table S3]. The PCR products were resolved by electrophoresis on 1% agarose gel. The fragment of interest was excised and purified using agarose gel DNA fragment recovery kit (TaKaRa D823A, Dalian, China). Finally, the fragment was cloned into PMD-18T vector (TaKaRa D101A, Dalian, China) and sequenced (Invitrogen, Beijing, China).
The full-length cDNA sequence of HaeCYP97A/B/C was spliced according to the RACE-PCR results by the SeqMan software of DNAStar 7.1 (DNASTAR Inc., USA). The theoretical molecular weight (Mw) and isoelectric point (pI) of HaeCYP97A/B/C protein were computed by ExPASy Compute pI/Mw tool . Transmembrane regions were predicted by "DAS"-Transmembrane Prediction server . Prediction of sub-cellular localization of the deduced amino acids was conducted using ChloroP and TargetP Servers [82, 83].
Gene expression profiling: Real-time RT-PCR
Total RNA from different samples was extracted using Trizol reagent (TaKaRa D9108B, Dalian, China) according to the user manual. Total RNA was treated with RNase-free DNase I (Fermentas, Glen Burnie, MD) to remove any residual genomic DNA that might be carried through the extraction process. Nuclear acids were quantified by NanoDrop 2000c (Thermo Scientific, USA). The first-strand cDNA synthesis for quantitative Real-time RT-PCR (qRT-PCR) was obtained from 1 μg total RNA with PrimeScript® RT Enzyme Mix I (TaKaRa DRR047A, Dalian, China) according to the manufacturer’s instructions.
Gene-specific primers were designed with Primer5 and are listed in more [see Additional file 5: Table S3]. All primer pairs were initially tested by standard RT-PCR and the amplification of single products of the correct size was verified on 2% (w/v) agarose gels (data not shown). The actin gene  has been proven experimentally in this study [see Additional file 10: Figure S6]. The qRT-PCR amplifications were carried out in triplicate in a total volume of 20 μL according to the manufacturer’s instructions of SYBR® Premix Ex Taq™ (Tli RNaseH Plus) (TaKaRa DRR420A, Dalian, China). The qRT-PCR program was holding stage, 50°C for 20 s and 95°C for 10 min, followed by 40 cycles of 95°C for 15 s, 60°C for 1 min, and melt curve stage, 95°C for 15 s, 60°C for 1 min, 95°C for 30 s, and 60°C for 15 s. Real-time RT-PCR analysis was performed on an ABI fast 7500 Sequence Detection System (Applied Biosystems) following the protocol previously described using actin gene as the internal control. The relative steady state mRNA transcript levels were normalized to the respective actin transcripts. The 2–ΔΔCT method  was used to analyze quantitative real-time PCR data based on the cycle threshold (C T ) values. The ΔΔC T is represented as the following formula: ΔΔC T = (C T , target gene (test group) - C T , actin gene (test group)) time x - (C T , target gene (control group) - C T , actin gene (control group)) times x, where x is the time of selected sample. Therefore, the relative expression level of chy genes has been normalized to control group (normal light regime).
All exposure experiments were repeated three times independently, and data were recorded as the mean with standard deviation (SD). For gene expression experiments, quantitative real-time PCR analysis was performed using software BioRAD iQ5. For each gene, the expressed as the mean ± SD (% control) was calculated using the (standard curve) approximation corrected for primer efficiency and normalized to housekeeping gene actin expression values.
Nucleotide sequencing and accession numbers
The cDNA nucleotide sequences of HaeCYP97A/B/C have been deposited and assigned the accession number AFR31786, AFR36909, and AFQ31612, respectively, in the EMB/GenBank/DDBJ database.
Non-heme/di-iron β-ring hydroxylase
Cytochrome P450 proteins
Cytochrome P450 protein, 97 family
Rapid Amplification of cDNA Ends
This work was supported by the National Natural Science Foundation of China (No. 41176144); Ocean Public Welfare Scientific Research Project, State Oceanic Administration of China (No. 201205027); the Natural Science Foundation of Shandong Province (No. ZR2012DQ015); Project of the Guangdong Provincial Comprehensive Strategic Cooperation with the Chinese Academy of Sciences (No. 2011A090100040); Science and Technology Planning Project of Yantai, China (No. 2010247); and Nature Science Funds for Distinguished Young Scholar of Shandong Province (JQ200914).
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