- Research article
- Open Access
Positive Darwinian selection is a driving force for the diversification of terpenoid biosynthesis in the genus Oryza
BMC Plant Biology volume 14, Article number: 239 (2014)
Terpenoids constitute the largest class of secondary metabolites made by plants and display vast chemical diversity among and within species. Terpene synthases (TPSs) are the pivotal enzymes for terpenoid biosynthesis that create the basic carbon skeletons of this class. Functional divergence of paralogous and orthologous TPS genes is a major mechanism for the diversification of terpenoid biosynthesis. However, little is known about the evolutionary forces that have shaped the evolution of plant TPS genes leading to terpenoid diversity.
The orthologs of Oryza Terpene Synthase 1 (OryzaTPS1), a rice terpene synthase gene involved in indirect defense against insects in Oryza sativa, were cloned from six additional Oryza species. In vitro biochemical analysis showed that the enzymes encoded by these OryzaTPS1 genes functioned either as (E)-β-caryophyllene synthases (ECS), or (E)-β-caryophyllene & germacrene A synthases (EGS), or germacrene D & germacrene A synthases (DAS). Because the orthologs of OryzaTPS1 in maize and sorghum function as ECS, the ECS activity was inferred to be ancestral. Molecular evolutionary detected the signature of positive Darwinian selection in five codon substitutions in the evolution from ECS to DAS. Homology-based structure modeling and the biochemical analysis of laboratory-generated protein variants validated the contribution of the five positively selected sites to functional divergence of OryzaTPS1. The changes in the in vitro product spectra of OryzaTPS1 proteins also correlated closely to the changes in in vivo blends of volatile terpenes released from insect-damaged rice plants.
In this study, we found that positive Darwinian selection is a driving force for the functional divergence of OryzaTPS1. This finding suggests that the diverged sesquiterpene blend produced by the Oryza species containing DAS may be adaptive, likely in the attraction of the natural enemies of insect herbivores.
Plants produce diverse secondary metabolites that are not essential for growth and development but play important roles in plant interactions with other organisms ,. With over 25,000 representatives , terpenoids constitute the largest class of plant secondary metabolites ,. Synthesized as the components of resins, complex oils, or volatile mixtures (such as floral scents) , terpenoids are involved in diverse biological processes ranging from plant defense to reproduction and symbiosis ,,. Despite the collective diversity of terpenoids in the plant kingdom, for any given plant species, only a subset of terpenoids are produced, some of which may be unique to the taxon ,. Such taxon-specific diversity may be important for the specific biological functions of terpenoids. Therefore, understanding the evolutionary mechanisms underlying the diversification of terpenoid biosynthesis is important for us to understand plant adaptation to specialized niches.
The wealth of structural diversity of plant terpenoids can be mainly attributed to an enzyme class known as terpene synthases (TPSs). TPSs convert the isoprenyl diphosphate precursors geranyl diphosphate (GPP), farnesyl diphosphate (FPP) and geranylgeranyl diphosphate (GGPP) to a multitude of cyclic and acyclic monoterpenes (C10), sesquiterpenes (C15) and diterpenes (C20), respectively ,. The unusual reaction mechanism of TPSs involves the formation of intermediate carbocations that can have multiple metabolic fates, depending on the termination mechanisms ,. As a result, a single TPS can catalyze the formation of multiple terpene products from a single substrate. Therefore, the enormous diversity of plant terpenoids is partly due to the ability of some plant TPSs producing multiple products.
The principal cause of plant terpenoid diversity is the large number of TPSs with different product specificities. In most sequenced plant genomes that have been analyzed, TPSs constitute mid-sized gene families with 30-100 members which are most likely to have evolved through gene duplication followed by functional divergence. These genes can be further divided into subfamilies based on their evolutionary relatedness with individual families generally associated with the formation of a specific class of terpenoids, such as monoterpenes, sesquiterpenes or diterpenes . The individual members in specific TPS subfamilies usually share a specific type of isoprenyl diphosphate as substrate, but exhibit large variations in product profiles . The biochemical basis for such functional divergence has been studied using biochemical and structural approaches. The product profiles of many TPSs have been interconverted by mutating only a small number of amino acid residues within or around the active site cavity -. On the other hand, numerous remote substitutions that result in the repositioning of key residues within the active site cavity can lead to enzymes with moderate level of sequence homology catalyzing similar biochemical reactions . In addition to individual sites, epistasis, which is defined as context dependence for mutational effects, also plays a critical role on product specificity of terpene synthases . Other mechanisms such as losing the N-terminal domain  or fusing two functional domains  have been proposed to be involved in evolving new terpene synthase genes.
In contrast, our knowledge of the molecular evolutionary basis underlying functional divergence of TPSs is very limited. The evolution of the large TPS gene family probably occurred largely through gene duplication followed by functional divergence, but the driving forces behind this process have not been well investigated. In contrast, positive Darwinian selection has been identified to be an important driving force for the evolution of a number of genes of plant secondary metabolism for functional diversification. Such examples include the methylthioalkylmalate synthases involved in the glucosinolate biosynthesis , the shikimate kinase (SK) of the shikimate pathway , the methyltransferases of the SABATH family important for the production of methyl esters , the dihydroflavonol-4-reductase (DFR) involved in anthocyanin biosynthesis  and the homospermidine synthase involved in pyrrolizidine alkaloid biosynthesis . While it may be sensible to propose that positive selection has also played a role in the functional diversification of TPSs, no such evidence has been presented.
We have chosen rice (Oryza) as a model plant to study the molecular evolution of TPS genes for two main reasons. First, rice plants produce a mixture of approximately 20 volatile monoterpenes and sesquiterpenes with a clear biological function. Produced upon herbivore damage, they serve in attracting the natural enemies of herbivores . Second, the molecular basis of volatile terpene production in rice has been well characterized. Three TPS genes Os02g02930, Os08g07100 and Os08g04500 are responsible for production of the majority of the terpenes released from insect-damaged rice plants . This study focused on the sesquiterpene synthase Os08g04500 from O. sativa and its orthologs from selected Oryza species. Os08g04500 produces predominantly (E)-β-caryophyllene and germacrene A . The orthologs of Os08g04500 in maize (TPS23)  and sorghum (SbTPS4)  which also play a role in attracting herbivore enemies produce only (E)-β-caryophyllene as their major product. The common ancestry of these three grasses indicates that functional divergence of the Os08g04500/TPS23/SbTPS4 orthologs has occurred, and such functional changes may have happened within the Oryza genus as well. Biochemical characterization and molecular evolutionary analysis of the orthologs of Os08g04500 (collectively designated as OryzaTPS1) from multiple Oryza species implied that positive Darwinian selection is one evolutionary force driving the functional divergence of OryzaTPS1s.
Functional conservation and divergence of OryzaTPS1s
To detect sequence divergence of OryzaTPS1 in rice, OryzaTPS1s were cloned from six additional Oryza species including O. glaberrima (African cultivated rice), O. rufipogon (a perennial wild relative of O. sativa), O. nivara (an annual wild relative of O. sativa), O. barthii (a wild relative of O. glaberrima), O. glumaepatula and O. officinalis (Additional file 1). All these seven species are diploids. The seven OryzaTPS1s cloned from the seven Oryza species displayed 96-99% similarity at the protein sequence level (Additional file 2). The related sequences have been deposited in the GenBank under accessions KJ415250 to KJ415255.
Our previous study showed that OryzaTPS1 in O. sativa Nipponbare (Os08g04500, renamed as OsTPS1 here) functions as a sesquiterpene synthase catalyzing the formation of multiple sesquiterpenes, with (E)-β-caryophyllene as the major product and germacrene A as the next most abundant . Here it was designated as an (E)-β-caryophyllene/germacrene A synthase (EGS). For functional evaluation, the six OryzaTPS1s other than OsTPS1 were expressed in E. coli and recombinant proteins were tested for terpene synthase activity. All these proteins were biochemically active. These enzymes fell into three categories based on their biochemical activities (Figure 1 and Additional files 3, 4 and 5). Two of them functioned as EGSs, while three others produced (E)-β-caryophyllene as the only dominant product with α-humulene, germacrene A and occasionally germacrene D as minor products. These were designated as (E)-β-caryophyllene synthase (ECS). One other enzyme, OrTPS1, produced germacrenes D and A as major products and was therefore designated as germacrene D & germacrene A synthase (DAS). In addition, as described in our previous reports ,, TPS23 and SbTPS4, the orthologs of OryzaTPS1 in maize and sorghum, are both ECSs. The ancestor of these orthologs occurred before the split of rice (Oryza), maize and sorghum as revealed by collinearity and phylogenetic analysis . Thus, it is most likely that the ECS activity evolved before this split and served as the ancestral activity for the OryzaTPS1s of various Oryza species to diverge after the spilt. The fact that germacrene A and germacrene D were already minor products of ECS catalysis further supports that the sesquiterpene profiles of EGS and DAS evolved from a certain ancestral ECS.
Molecular evolutionary analysis of OryzaTPS1s
To further explore the evolution of OryzaTPS1s, its phylogeny was reconstructed. As shown in Figure 2, a striking feature of this gene tree was the strict clustering of the seven OryzaTPS1 sequences for each of the three different biochemical activities. Several codon-based models implemented in the PAML package  were employed to analyze the evolutionary patterns reflected in this phylogeny. The one-ratio branch model indicated overall purifying selection for OryzaTPS1 evolution (dN/dS (ω) = 0.63, Table 1). However, as selective pressure may diverge along different lineages , we applied the two-ratio models to examine whether positive selection can be detected in lineages A and D (Figure 2) where the original enzyme functional evolution may have occurred. Positive selection was detected in lineage D (ω = 999.0000, P < 0.05) but not in lineage A (Table 1). Failure to detect positive sites in lineage A may be due to the involvement of few substitutions which cannot be detected after the selective pressure was averaged on the branch. Since positive selection typically acts on only a few sites , we then used the branch-site models to examine whether there were signatures for selection at individual sites along lineage D. Likelihood ratio tests showed evidence for significant positive selection in lineage D (P < 0.05, Table 1). Five residues were identified to be under positive selection, including residues 32, 318, 429, 433, and 486 (using the OrTPS1 sequence as a reference, posterior probabilities > 95%, Figure 2 and Table 1). As the gene tree of OryzaTPS1 was different from the canonical Oryza species tree , we also subjected the OryzaTPS1 species tree to the same analysis. This analysis confirmed the outcome of the analysis using the gene tree (Additional file 6). Taken together, these results suggest that at least the evolution from ECS to DAS is adaptive.
Functional validation of the five positively selected sites
Next we tested the role of the five sites at which positive selection was indicated in functional evolution from an (E)-β-caryophyllene-predominating activity to a germacrene D-predominating activity. First, a structural model of OrTPS1 (a DAS) was created based on its homology to the known structure of tobacco 5-epi-aristolochene synthase . The residues 318, 429, 433 of OrTPS1 were located in the active site cavity, while residues 32 and 486 were positioned near the entrance of the active site cavity (Figure 3), providing initial evidence for the importance of all five sites in the functional evolution of OryzaTPS1.
Next, proteins mutated at these sites were produced and analyzed. We focused on the differences between ObTPS1, a typical ECS that produced almost exclusively (E)-β-caryophyllene with traces of α-humulene and germacrene A, but not germacrene D, and OrTPS1, a DAS producing germacrene D and A as its two major products. These enzymes differed in the residues present at all five positively selected sites, so ObTPS1 was used as the starting point for the generation of 31 variants covering all possible intermediates in the complete conversion from these five residues to those present in OrTPS1. All 31 variants were shown to be biochemically active (Figure 4).
To better illustrate the contribution to the functional evolution from each mutant, the product profiles of all the mutants were subject to a clustering analysis based on relative abundance of the four sesquiterpene products. As shown in Figure 4, of the five single mutants, one (ObTPS1-C429G) showed a reduced proportion of (E)-β-caryophyllene and an elevated amount of germacrene A, but not germacrene D, while the other four displayed the wild-type phenotype. The products of three double mutants (ObTPS1-F318L + C429G, ObTPS1-C429G + V433I and ObTPS1-F318L + V433I) included germacrene D (the chromatogram of ObTPS1-F318L + V433I is shown in Figure 4 as an instance) with the first two mutants also producing significant amounts of germacrene A (Figure 4). The triple mutant ObTPS1-F318L + C429G + V433I produced comparable amounts of germacrene A, germacrene D and (E)-β-caryophyllene (Figure 4) and might represent the sequence of an intermediate stage gene prior to full functional divergence. Noticeably, all the proteins were grouped into two major clades. The first clade contained the proteins producing no or just minor amounts of germacrene D while the second clade contained OrTPS1 and four ObTPS1 mutants (1 triple mutant, 2 quadruple mutants and the quintuple mutant) harboring all the following switches: F318L, C429G, and V433I, further supporting the key role of these three switches in the function evolution. Finally, the quintuple mutant gave a product profile similar to that of ObTPS1-F318L + C429G + V433I rather than a true DAS (Figure 4), and thus changes at additional residue(s) are necessary for a complete functional switch from ECS to DAS.
Biological impact of OryzaTPS1 evolution
To determine whether the evolution of the sesquiterpene synthase OryzaTPS1 is reflected in terms of the actual pattern of sesquiterpenes produced in the intact plant, we measured the volatile terpenes emitted from rice plants expressing different OryzaTPS1s. From our previous studies, we know that the products of OryzaTPS1 (Os08g04500) are released after herbivore damage and function together with other volatiles in attracting enemies of attacking herbivores ,. A group of six rice species other than Nipponbare was subject to insect herbivory, and volatiles were sampled by headspace collection and analyzed by GC-MS. All insect-damaged rice plants emitted volatiles, including the sesquiterpene products of OryzaTPS1s (Additional file 7). Cluster analysis of the OryzaTPS1s and the rice species together was performed based on the relative abundance of the four OryzaTPS1 sesquiterpene products produced. As shown in Figure 5, this clustering led to three clades that perfectly represented the three different biochemical activities DAS, ECS and EGS. Specifically, the products of each enzyme clustered closely to the volatile products of its corresponding species. Six OryzaTPS1s, including OrTPS1, clustered immediately next to their corresponding species, while OoTPS1 belonged to the same clade as its species did. Thus, these data demonstrate that evolution of OryzaTPS1 is well correlated with changes in terpene emission profile and thus directly impacts the diversity of terpene biosynthesis of Oryza plants.
This study has demonstrated that positive Darwinian selection is an evolutionary force driving the functional divergence of terpene synthases, the pivotal enzymes for the biosynthesis of the largest class of secondary metabolites made by plants. OryzaTPS1, a terpene synthase found in rice species that produces a mixture of volatile sesquiterpenes, was subject to an overall purifying selection. This pattern is consistent with the evolution of TPS23 in maize, which may suggest that the evolution of the indirect defense traits may have been constrained in grasses. However, it was shown by phylogenetic analysis and functional characterization to have diverged from being an (E)-β-caryophyllene synthase (ECS) making a few other minor products to being an (E)-β-caryophyllene/germacrene A synthase (EGS) or a germacrene D and A synthase (DAS) (Figures 1 & 2) and molecular evolutionary analysis revealed that at least the evolution from ECS to DAS was driven by positive Darwinian selection. Functional divergence from ECS en route to DAS was partially achieved by the effects of mutations at five, particularly three, positively selected codon positions identified through the analysis using the branch-site models of the PAML package (Figures 3 & 4).
It is not particularly surprising that even a quintuple mutant of ECS in which all five target residues have been exchanged did not exhibit exact DAS activity (Figure 4). This suggests that one or more additional amino acids are involved in the activity divergence. Some of those amino acids may have been under positive selection. If so, the failure to detect the signature of positive selection could be due to the relatively small sampling size. On the other hand, the genus Oryza is relatively small with about 20 species; the seven species analyzed in this study account for most of the diploid Oryza species. Two of the five sites identified to be under positive selection exerted minimal, if any, effect on functional changes from ECS to DAS (Figure 4). One explanation for this phenomenon is epistasis, namely the function of these sites can only be manifested with the changes of additional amino acids in the appropriate context . Further systemic creation and analysis of additional mutants may help clarify these possibilities.
The biochemical mechanism of functional divergence for OryzaTPS1 may arise directly from the properties of terpene synthases. While forming hundreds of monoterpene, sesquiterpene and diterpene carbon skeletons from just a few isoprenyl diphosphate substrates ,, terpene synthases, including OryzaTPS1, often produce multiple minor products in addition to their major products, exhibiting a type of product promiscuity attributed to their carbocationic reaction mechanisms . A proposed reaction mechanism for ECS, EGS and DAS is shown in Figure 6. Common to all three enzymes is the ionization of the substrate farnesyl pyrophosphate leading to the farnesyl cation. While ECS converted this cation via a 11,1-cyclization, a subsequent 2,10-cyclization and a deprotonation to (E)-β-caryophyllene, EGS obtained the ability to catalyze also a 10,1-cyclization of the farnesyl cation and the conversion of the resulting germacren-11-yl cation to germacrene A. DAS, however, lost the ability to catalyze the 11,1-cyclization but is able to convert the germacren-11-yl cation via two consecutive 1,2-hydride shifts or a single 1,3-hydride shift and a subsequent deprotonation to germacrene D (Figure 6). As demonstrated by protein engineering of TPSs  and analysis of variants of naturally occurring TPS homologs ,, the proportions of major and minor products of TPSs can sometimes be readily altered by exchanges of a few amino acid residues, which is also the case for OryzaTPS1 as described here (Figure 4). These key amino acid residues are usually located within or around the synthase active site cavity ,. For the functional evolution from ObTPS1 to OrTPS1, three amino acid switches F318L, C429G, and V433I as revealed by the mutagenesis analysis (using the OrTPS1 sequence as a reference, same below) did occur within the enzyme active site cavity as revealed by the structure modeling. However, two other switches, C32R and S486P, which occurred near the entrance of the active site cavity seemed not to contribute directly to enzyme functional evolution as shown by the mutagenesis analysis. This is consistent with the previous studies that the residues located within the TPS active site cavity play a more critical role in deciding the product outcome than those outside the active site cavity ,. The minor activities of promiscuous terpene synthases provide the raw material for the evolution of novel enzymes in which such minor activities can become dominant ones. Functional divergence of (E)-β-caryophyllene/germacrene A synthase (EGS) and germacrene D and A synthase (DAS) activities from (E)-β-caryophyllene synthase (ECS) began with an ancestral activity that already had germacrene D and A as minor products. After functional divergence, the original function may either be retained or become lost. In the case of OryzaTPS1, the co-opted EGS and DAS activities retained the ability to produce (E)-β-caryophyllene, the only predominant product of the ancestral ECS, although with reduced relative abundance (Figure 1 and Additional file 3). The retention of these products may be ascribed either to natural selection or to the restricted flexibility of enzymatic mechanisms.
It should be acknowledged that the evolutionary trajectory for functional divergence of OryzaTPS1s could have occurred in a number of scenarios. If only the seven Oryza species studied in this paper are considered, O. officinalis is sister to the other six species based on the canonical Oryza species tree . Because OoTPS1 from O. officinalis was an EGS, one scenario could be that the ancestral activity of the other six OryzaTPS1s is EGS. In this case, it would suggest that DAS evolved from EGS, which earlier had evolved from ECS. The functional divergence from ECS to EGS was relatively minor, affecting only the relative abundance of germacrene A (Figure 1). The five amino acid residues in ECSs and EGSs that correspond to the five sites under positive selection in DAS were highly similar, providing additional evidence on the importance of these sites on the evolution of the new activity DAS. However, it is still highly possible that DAS evolved from ECS, as inferred in this study, which would represent the ancestral activity of the six OryzaTPS1s sister to OoTPS1. In this case, the EGS activity of OoTPS1 would have evolved from an ECS after the split of O. officinalis from the common ancestor of the other six Oryza species. Functional characterization of OryzaTPS1s from additional Oryza species may provide better answer to this question.
The evidence for positive selection driving the diversification of secondary metabolite biosynthesis has been detected in a number of enzyme systems, such as methylthioalkylmalate synthases involved in glucosinolate biosynthesis  and dihydroflavonol-4-reductases involved in anthocyanin biosynthesis . In all such cases, positive selection has exerted its effect on duplicated genes. In contrast, the positive selection-driven functional divergence of OryzaTPS1 in rice appears to have occurred without the direct involvement of gene duplication. In the sequenced O. sativa cultivar Nipponbare, OryzaTPS1 (Os08g04500 or OsTPS1) and its closest paralog Os08g07100 (50% identity at the amino acid level, Additional file 8) have been demonstrated to be derived from a duplication event that occurred before the divergence of rice (Oryza), maize and sorghum . Os08g04500 and Os08g07100 make two completely different sets of terpene products . Analysis of the whole genome sequence available for another Oryza species O. glaberrima also supported that OryzaTPS1 (gene ID ORGLA08G0019200 in this species) has not been duplicated in rice after the divergence of rice from the common ancestor of maize and sorghum as its closest paralog in this species (gene ID ORGLA08G0035300 in this species) also only possessed 48% similarity at the amino acid level to OryzaTPS1. Analysis of the genome sequences of other Oryza species analyzed in this study will be needed to provide undisputable evidence that the positive selection-driven functional divergence of OryzaTPS1 occurred without the direct involvement of gene duplication.
The divergence of OryzaTPS1 to new biochemical functions was apparent not only from in vitro enzyme assays (Figure 1), but also from whole plant volatile collection. There were strong correlations between the sesquiterpene profiles of individual OryzaTPS1 enzymes and the sesquiterpenes emitted from the plant from which the corresponding OryzaTPS1 was cloned (Figure 5), indicating that functional evolution of OryzaTPS1 directly impacts the phenotype of the plant. What is the biological significance of these alterations in sesquiterpene volatile emission? The volatile sesquiterpenoids emitted from insect-damaged rice and maize plants function in indirect defense as chemical cues to attract natural enemies, such as parasitic wasps ,,. Herbivore enemies have demonstrated the ability to perceive differences in terpene volatile profiles ,. Therefore, the changes in rice sesquiterpene emission profiles caused by functional divergence of OryzaTPS1 may reflect the changing spectra of insect herbivores and their natural enemies present in the environments of different species. For instance, (E)-β-caryophyllene serves as a signal not only for the indirect defense above ground ,, but also for that below ground . However, based on the current literature, germacrene A and germacrene D are specific signals for the indirect defense above ground -. Thus, it's likely that evolution from ECS to DAS & EGS in certain rice lineages is driven by more serious insect challenges above ground.
The detection of positive selection as an evolutionary force driving the functional divergence of OryzaTPS1 (Figure 2) presents the first case that we are aware of in which positive selection drove the evolution of terpene synthase genes for the diversification of terpenoid biosynthesis. This study also strengthens the view that the interactions of plants with their herbivores and pathogens evolve rapidly. In the arms race with pests, plants are continually evolving novel defenses as adaptive traits under positive selection, reflected by such disparate examples as the evolution of glucosinolate biosynthetic genes  and plant resistance (R) genes  for direct defense against insect herbivores and defense against microbial pathogens, respectively. The functional divergence of the terpene synthase gene OryzaTPS1 driven by positive selection implies the adaptive evolution of indirect defense against herbivorous insects.
This study reports that positive Darwinian selection is a driving force for the functional divergence of OryzaTPS1. As the evolution of OryzaTPS1 is well correlated with changes in terpene emission profiles of Oryza plants, these results may imply that the sesquiterpene volatile blend produced by the Oryza species that contains DAS may be adaptive, likely in the attraction of the natural enemies of insect herbivores. This study gains us further insight into the mechanisms shaping the diversity of plant secondary metabolism.
Plants growth and insect treatment
Seeds of the selected Oryza species (Additional file 1) were obtained from the National Plant Germplasm Systems of the USDA Agricultural Research Service (http://www.ars-grin.gov/npgs/). Seeds were de-hulled and germinated at 28°C in the dark for 3 days. Seedlings were planted at eight plants per 200 ml glass jar, and grown at 28°C with 16 h of light per day. The eggs of Spodoptera frugiperda were purchased from Benzon Research Inc (PA, USA). Newly emerged larvae of S. frugiperda were transferred to 37.5 ml cups containing pinto-bean-based artificial diet as a food source in an incubator (28°C). For plant treatment, two second-instar larvae were placed on the leaves of a single 2-week-old rice seedling. After overnight (when approximately 20% of the leaf area had been consumed), insects were removed and the rice plants were subjected to volatile collection and tissue collection for RNA extraction.
Related sequences were obtained and analyzed through the Rice Genome Annotation Project website (http://rice.plantbiology.msu.edu/index.shtml) and http://www.gramene.org/Oryza_glaberrima/Info/Index.
Full-length cDNA cloning
Total RNA was isolated from rice tissues using Qiagen Plant RNeasy Mini Kit. cDNAs were synthesized through GE Healthcare First-Strand cDNA Synthesis Kit. Full-length cDNAs of the TPS genes were cloned into the vector pEXP5-CT/TOPO (Invitrogen, Carlsbad, CA, USA) and fully sequenced. The primers used for CDS cloning were: 5'- ATGGCAACCTCTGTTCCGAG-3' (forward) and 5'-CAGTCACGCTTCATTAGAAG-3' (reverse).
Protein expression in E. coli and terpene synthase assay
An E. coli BL21 Codon Plus strain (Invitrogen), transformed with the appropriate expression construct (including a vector control), was used for protein expression. Expression was induced by addition of isopropyl-1-thio-d-galactopyranoside to a final concentration of 1 mm. The cells were collected by centrifugation at 4000 g for 6 min, and disrupted by a 4 × 30 sec treatment with a sonicator in chilled extraction buffer (50 mm Mopso, pH 7.0, with 5 mm MgCl2, 5 mm sodium ascorbate, 0.5 mm PMSF, 5 mm dithiothreitol and 10% v/v glycerol). The cell fragments were removed by centrifugation at 14 000 g, and the supernatant was desalted into assay buffer (10 mm Mopso, pH 7.0, 1 mm dithiothreitol, 10% v/v glycerol) by passage through a Econopac 10DG column (Bio-Rad). Enzyme assays were performed in a Teflon®-sealed, screw-capped 1 ml GC glass vial containing 50 μl of the bacterial extract and 50 μl assay buffer with 10 μm (E, E)-FPP, 10 mm MgCl2, 0.2 mm NaWO4 and 0.1 mm NaF. An SPME (solid phase micro-extraction) fiber consisting of 100 μm polydimethylsiloxane (Supelco) was placed into the headspace of the vial for 60 min incubation at 30°C and then inserted into the injector of the gas chromatograph for analysis of the adsorbed reaction products. Volatiles were analyzed on a Shimadzu 17A gas chromatograph coupled to a Shimadzu (http://www.shimadzu.com) QP5050A quadrupole mass selective detector. Separation was performed on a Restek SHR5XLB column (30 m × 0.25 mm internal diameter × 0.25 μm thickness, Shimadzu). Helium was used as the carrier gas (flow rate of 5 ml min-1), a splitless injection (injection injector temperature 250°C) was used, and a temperature gradient of 5°C min-1 from 40°C (3 min hold) to 240°C was applied. Products were identified by comparison of retention times and mass spectra with those of authentic reference compounds obtained from Fluka, Sigma (http://www.sigmaaldrich.com/) and W. König at the University of Hamburg.
Plant volatile collection and identification
Volatiles emitted from insect-damaged rice plants and control rice plants were collected in an open headspace sampling system (Analytical Research Systems, Gainesville, FL, USA). Eight plants grown in a single glass jar wrapped with aluminum foil were placed in a glass chamber with a removable O-ring snap lid with an air outlet port. Charcoal-purified air entered the chamber at a flow rate of 0.8 l min-1 from the top through a Teflon® hose. Volatiles were collected for 4 h by pumping air from the chamber through a Super Q volatile collection trap (Analytical Research Systems). Volatiles were eluted with 40 μl of CH2Cl2, and 1-octanol was added as an internal standard for quantification. Volatile identification was conducted as described above.
Hierarchical clustering analysis
Hierarchical clustering analysis was performed in MATLAB using the clustergram function in the bioinformatics toolbox. The Mahalanobis Distance was used to calculate the distance matrix, from which the hierarchical clusters were generated using complete linkage method. The color bar in each figure showed the relative abundance of the four sesquiterpene products (from 0% to 100%).
To perform phylogeny reconstruction, the protein sequence alignment was performed by using the MAFFT program . The phylogenetic tree based on the alignment was reconstructed using the maximum likelihood method in MEGA5  with 1,000 replicates of bootstrap analysis.
Molecular evolutionary analysis
Molecular evolution of OryzaTPS1s was analyzed using the codeml program in the PAML 4.4 package . An unrooted phylogenetic tree reconstructed using the maximum likelihood method and a canonical species tree  containing the seven Oryza species included in this study were subjected to the analysis. A series of branch models were tested: the one ratio model for all the lineages and the two-ratio model for the A and D lineages respectively (labeled in the phylogenetic tree) where the original enzyme functional evolution occurred. Likelihood ratio tests (LRT) were conducted to determine which model fitted the data better. The D lineage was tested for a signature of positive selection using the branch-sites test. The positive sites with high posterior probabilities (>0.95) were obtained through Bayes Empirical Bayes analysis.
For site-directed mutagenesis, the QuickChange site-directed mutagenesis kit (Stratagene, La Jolla, USA) was used according to the manufacturer's instructions. Mutated genes were fully sequenced.
Homology-based structural modeling
Protein structure modeling was performed with the SWISS-MODEL service (http://www.expasy.org/swissmod/SWISS-MODEL.html)  using the previously determined structure of 5-epi-aristolochene synthase M4 mutant (, PDB id, 3lz9) as the modeling template. Models were visualized and analyzed using the program PyMOL.
Author contributions: HC, TGK, JG and FC conceived the project. HC performed gene cloning, enzymes assays, volatile collection from plants and mutagenesis studies. G-LL performed phylogenetic and molecular evolutionary analysis. TGK performed enzyme assays and structure modeling. Q-DJ conducted the clustering analysis. HC and FC wrote the manuscript and all other authors provided critical comments and revisions. All authors read and approved the final manuscript.
Hartmann T: From waste products to ecochemicals: fifty years research of plant secondary metabolism. Phytochemistry. 2007, 68: 2831-2846. 10.1016/j.phytochem.2007.09.017.
Weng JK, Philippe RN, Noel JP: The rise of chemodiversity in plants. Science. 2012, 336: 1667-1670. 10.1126/science.1217411.
Buckingham J: Dictionary of Natural Products. Chapman & Hall, London; New York; 1994.
Gershenzon J, Dudareva N: The function of terpene natural products in the natural world. Nat Chem Biol. 2007, 3: 408-414. 10.1038/nchembio.2007.5.
Tholl D: Terpene synthases and the regulation, diversity and biological roles of terpene metabolism. Curr Opin Plant Biol. 2006, 9: 297-304. 10.1016/j.pbi.2006.03.014.
Harborne JB, Turner BL: Plant Chemosystematics. Academic, London; Orlando; 1984.
Pichersky E, Gershenzon J: The formation and function of plant volatiles: perfumes for pollinator attraction and defense. Curr Opin Plant Biol. 2002, 5: 237-243. 10.1016/S1369-5266(02)00251-0.
Degen T, Dillmann C, Marion-Poll F, Turlings TCJ: High genetic variability of herbivore-induced volatile emission within a broad range of maize inbred lines. Plant Physiol. 2004, 135: 1928-1938. 10.1104/pp.104.039891.
Lou Y, Hua X, Turlings TCJ, Cheng J, Chen X, Ye G: Differences in induced volatile emissions among rice varieties result in differential attraction and parasitism of Nilaparvata lugens eggs by the parasitoid Anagrus nilaparvatae in the field. J Chem Ecol. 2006, 32: 2375-2387. 10.1007/s10886-006-9151-7.
Christianson DW: Unearthing the roots of the terpenome. Curr Opin Chem Biol. 2008, 12: 141-150. 10.1016/j.cbpa.2007.12.008.
Degenhardt J, Köllner TG, Gershenzon J: Monoterpene and sesquiterpene synthases and the origin of terpene skeletal diversity in plants. Phytochemistry. 2009, 70: 1621-1637. 10.1016/j.phytochem.2009.07.030.
Chen F, Tholl D, Bohlmann J, Pichersky E: The family of terpene synthases in plants: a mid-size family of genes for specialized metabolism that is highly diversified throughout the kingdom. Plant J. 2011, 66: 212-229. 10.1111/j.1365-313X.2011.04520.x.
Greenhagen BT, O'Maille PE, Noel JP, Chappell J: Identifying and manipulating structural determinates linking catalytic specificities in terpene synthases. Proc Natl Acad Sci U S A. 2006, 103: 9826-9831. 10.1073/pnas.0601605103.
Keeling CI, Weisshaar S, Lin RP, Bohlmann J: Functional plasticity of paralogous diterpene synthases involved in conifer defense. Proc Natl Acad Sci U S A. 2008, 105: 1085-1090. 10.1073/pnas.0709466105.
Köllner TG, Gershenzon J, Degenhardt J: Molecular and biochemical evolution of maize terpene synthase 10, an enzyme of indirect defense. Phytochemistry. 2009, 70: 1139-1145. 10.1016/j.phytochem.2009.06.011.
Xu M, Wilderman PR, Peters RJ: Following evolution's lead to a single residue switch for diterpene synthase product outcome. Proc Natl Acad Sci U S A. 2007, 104: 7397-7401. 10.1073/pnas.0611454104.
Phillips MA, Wildung MR, Williams DC, Hyatt DC, Croteau R: cDNA isolation, functional expression, and characterization of (+)-alpha-pinene synthase and (+)-alpha-pinene synthase from loblolly pine (Pinus taeda): stereocontrol in pinene biosynthesis. Arch Biochem Biophys. 2003, 411: 267-276. 10.1016/S0003-9861(02)00746-4.
O'Maille PE, Malone A, Dellas N, Andes Hess B, Smentek L, Sheehan I, Greenhagen BT, Chappell J, Manning G, Noel JP: Quantitative exploration of the catalytic landscape separating divergent plant sesquiterpene synthases. Nat Chem Biol. 2008, 4: 617-623. 10.1038/nchembio.113.
Hillwig ML, Xu M, Toyomasu T, Tiernan MS, Wei G, Cui G, Huang L, Peters RJ: Domain loss has independently occurred multiple times in plant terpene synthase evolution. Plant J. 2011, 68: 1051-1060. 10.1111/j.1365-313X.2011.04756.x.
Cseke L, Dudareva N, Pichersky E: Structure and evolution of linalool synthase. Mol Biol Evol. 1998, 15: 1491-1498. 10.1093/oxfordjournals.molbev.a025876.
Benderoth M, Textor S, Windsor AJ, Mitchell-Olds T, Gershenzon J, Kroymann J: Positive selection driving diversification in plant secondary metabolism. Proc Natl Acad Sci U S A. 2006, 103: 9118-9123. 10.1073/pnas.0601738103.
Fucile G, Falconer S, Christendat D: Evolutionary diversification of plant shikimate kinase gene duplicates. PLoS Genet. 2008, 4: e1000292-10.1371/journal.pgen.1000292.
Barkman TJ, Martins TR, Sutton E, Stout JT: Positive selection for single amino acid change promotes substrate discrimination of a plant volatile-producing enzyme. Mol Biol Evol. 2007, 24: 1320-1329. 10.1093/molbev/msm053.
Des Marais DL, Rausher MD: Escape from adaptive conflict after duplication in an anthocyanin pathway gene. Nature. 2008, 454: 762-765.
Kaltenegger E, Eich E, Ober D: Evolution of homospermidine synthase in the convolvulaceae: a story of gene duplication, gene loss, and periods of various selection pressures. Plant Cell. 2013, 25: 1213-1227. 10.1105/tpc.113.109744.
Yuan JS, Köllner TG, Wiggins G, Grant J, Degenhardt J, Chen F: Molecular and genomic basis of volatile-mediated indirect defense against insects in rice. Plant J. 2008, 55: 491-503. 10.1111/j.1365-313X.2008.03524.x.
Köllner TG, Held M, Lenk C, Hiltpold I, Turlings TCJ, Gershenzon J, Degenhardt J: A maize (E)-beta-caryophyllene synthase implicated in indirect defense responses against herbivores is not expressed in most American maize varieties. Plant Cell. 2008, 20: 482-494. 10.1105/tpc.107.051672.
Zhuang X, Köllner TG, Zhao N, Li G, Jiang Y, Zhu L, Ma J, Degenhardt J, Chen F: Dynamic evolution of herbivore-induced sesquiterpene biosynthesis in sorghum and related grass crops. Plant J. 2012, 69: 70-80. 10.1111/j.1365-313X.2011.04771.x.
Yang ZH: Likelihood ratio tests for detecting positive selection and application to primate lysozyme evolution. Mol Biol Evol. 1998, 15: 568-573. 10.1093/oxfordjournals.molbev.a025957.
Zhang JZ, Nielsen R, Yang ZH: Evaluation of an improved branch-site likelihood method for detecting positive selection at the molecular level. Mol Biol Evol. 2005, 22: 2472-2479. 10.1093/molbev/msi237.
Ge S, Sang T, Lu BR, Hong DY: Phylogeny of rice genomes with emphasis on origins of allotetraploid species. Proc Natl Acad Sci U S A. 1999, 96: 14400-14405. 10.1073/pnas.96.25.14400.
Noel JP, Dellas N, Faraldos JA, Zhao M, Hess BA, Smentek L, Coates RM, O'Maille PE: Structural elucidation of cisoid and transoid cyclization pathways of a sesquiterpene synthase using 2-fluorofarnesyl diphosphates. ACS Chem Biol. 2010, 5: 377-392. 10.1021/cb900295g.
Yoshikuni Y, Ferrin TE, Keasling JD: Designed divergent evolution of enzyme function. Nature. 2006, 440: 1078-1082. 10.1038/nature04607.
Sakai H, Ikawa H, Tanaka T, Numa H, Minami H, Fujisawa M, Shibata M, Kurita K, Kikuta A, Hamada M, Kanamori H, Namiki N, Wu J, Itoh T, Matsumoto T, Sasaki T: Distinct evolutionary patterns of Oryza glaberrima deciphered by genome sequencing and comparative analysis. Plant J. 2011, 66: 796-805. 10.1111/j.1365-313X.2011.04539.x.
Schnee C, Köllner TG, Held M, Turlings TC, Gershenzon J, Degenhardt J: The products of a single maize sesquiterpene synthase form a volatile defense signal that attracts natural enemies of maize herbivores. Proc Natl Acad Sci U S A. 2006, 103: 1129-1134. 10.1073/pnas.0508027103.
Clavijo McCormick A, Unsicker SB, Gershenzon J: The specificity of herbivore-induced plant volatiles in attracting herbivore enemies. Trends Plant Sci. 2012, 17: 303-310. 10.1016/j.tplants.2012.03.012.
Fontana A, Held M, Fantaye CA, Turlings TC, Degenhardt J, Gershenzon J: Attractiveness of constitutive and herbivore-induced sesquiterpene blends of maize to the parasitic wasp Cotesia marginiventris (Cresson). J Chem Ecol. 2011, 37: 582-591. 10.1007/s10886-011-9967-7.
Danner H, Boeckler GA, Irmisch S, Yuan JS, Chen F, Gershenzon J, Unsicker SB, Kollner TG: Four terpene synthases produce major compounds of the gypsy moth feeding-induced volatile blend of Populus trichocarpa. Phytochemistry. 2011, 72: 897-908. 10.1016/j.phytochem.2011.03.014.
Arimura G, Huber DP, Bohlmann J: Forest tent caterpillars (Malacosoma disstria) induce local and systemic diurnal emissions of terpenoid volatiles in hybrid poplar (Populus trichocarpa x deltoides): cDNA cloning, functional characterization, and patterns of gene expression of (-)-germacrene D synthase, PtdTPS1. Plant J. 2004, 37: 603-616. 10.1111/j.1365-313X.2003.01987.x.
Lou Y, Baldwin IT: Nitrogen supply influences herbivore-induced direct and indirect defenses and transcriptional responses in Nicotiana attenuata. Plant Physiol. 2004, 135: 496-506. 10.1104/pp.104.040360.
Hammond-Kosack KE, Jones JD: Plant disease resistance genes. Annu Rev Plant Physiol Plant Mol Biol. 1997, 48: 575-607. 10.1146/annurev.arplant.48.1.575.
Katoh K, Misawa K, Kuma K, Miyata T: MAFFT: a novel method for rapid multiple sequence alignment based on fast Fourier transform. Nucleic Acids Res. 2002, 30: 3059-3066. 10.1093/nar/gkf436.
Tamura K, Peterson D, Peterson N, Stecher G, Nei M, Kumar S: MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. Mol Biol Evol. 2011, 28: 2731-2739. 10.1093/molbev/msr121.
Schwede T, Kopp J, Guex N, Peitsch MC: SWISS-MODEL: An automated protein homology-modeling server. Nucleic Acids Res. 2003, 31: 3381-3385. 10.1093/nar/gkg520.
This work was supported by an Innovation grant from the University of Tennessee Experimental Station (to F.C.) and funds from the Max Planck Society (to TGK and JG).
The authors declare that they have no competing interests.
Electronic supplementary material
Additional file 1: Oryza species analyzed and the designation of the OryzaTPS1s genes.(PDF 80 KB)
Additional file 4: Chemical conversion of the sesquiterpene germacrene A to β-elemene at typical GC injector temperatures.(PDF 273 KB)
Additional file 5: Chemical conversion of the sesquiterpene germacrene A to β-elemene at a low GC injector temperature.(PDF 344 KB)
Additional file 7: Relative abundance of individual OryzaTPS1 products emitted from insect-damaged rice plants.(PDF 44 KB)
Additional file 8: The top five paralogs of Os08g04500 by blast search against the rice genome database with the amino acid sequence of Os08g04500 as a query.(PDF 8 KB)
Authors’ original submitted files for images
About this article
Cite this article
Chen, H., Li, G., Köllner, T.G. et al. Positive Darwinian selection is a driving force for the diversification of terpenoid biosynthesis in the genus Oryza. BMC Plant Biol 14, 239 (2014). https://0-doi-org.brum.beds.ac.uk/10.1186/s12870-014-0239-x
- Plant secondary metabolism
- Terpene synthase
- Positive selection