- Research article
- Open Access
Integration of deep transcriptome and proteome analyses reveals the components of alkaloid metabolism in opium poppy cell cultures
© Desgagné-Penix et al; licensee BioMed Central Ltd. 2010
- Received: 2 June 2010
- Accepted: 18 November 2010
- Published: 18 November 2010
Papaver somniferum (opium poppy) is the source for several pharmaceutical benzylisoquinoline alkaloids including morphine, the codeine and sanguinarine. In response to treatment with a fungal elicitor, the biosynthesis and accumulation of sanguinarine is induced along with other plant defense responses in opium poppy cell cultures. The transcriptional induction of alkaloid metabolism in cultured cells provides an opportunity to identify components of this process via the integration of deep transcriptome and proteome databases generated using next-generation technologies.
A cDNA library was prepared for opium poppy cell cultures treated with a fungal elicitor for 10 h. Using 454 GS-FLX Titanium pyrosequencing, 427,369 expressed sequence tags (ESTs) with an average length of 462 bp were generated. Assembly of these sequences yielded 93,723 unigenes, of which 23,753 were assigned Gene Ontology annotations. Transcripts encoding all known sanguinarine biosynthetic enzymes were identified in the EST database, 5 of which were represented among the 50 most abundant transcripts. Liquid chromatography-tandem mass spectrometry (LC-MS/MS) of total protein extracts from cell cultures treated with a fungal elicitor for 50 h facilitated the identification of 1,004 proteins. Proteins were fractionated by one-dimensional SDS-PAGE and digested with trypsin prior to LC-MS/MS analysis. Query of an opium poppy-specific EST database substantially enhanced peptide identification. Eight out of 10 known sanguinarine biosynthetic enzymes and many relevant primary metabolic enzymes were represented in the peptide database.
The integration of deep transcriptome and proteome analyses provides an effective platform to catalogue the components of secondary metabolism, and to identify genes encoding uncharacterized enzymes. The establishment of corresponding transcript and protein databases generated by next-generation technologies in a system with a well-defined metabolite profile facilitates an improved linkage between genes, enzymes, and pathway components. The proteome database represents the most relevant alkaloid-producing enzymes, compared with the much deeper and more complete transcriptome library. The transcript database contained full-length mRNAs encoding most alkaloid biosynthetic enzymes, which is a key requirement for the functional characterization of novel gene candidates.
- Opium Poppy
- Fungal Elicitor
- Elicitor Treatment
Opium poppy (Papaver somniferum) remains our most important source for several pharmaceutical benzylisoquinoline alkaloids (BIAs) including the narcotic analgesic morphine, the anti-tussive drug codeine, the vasodilator papaverine and the antimicrobial agent sanguinarine. In opium poppy plants, most BIAs (e.g., morphine, codeine and papaverine) occur in the cytoplasm (i.e. latex) of specialized cells, known as laticifers, that are associated with the phloem in all organs. Although latex and, thus, most BIAs are most abundant on shoot organs of opium poppy, the antimicrobial alkaloid sanguinarine accumulates constitutively in roots possibly in association with cell types other than laticifers. Although opium poppy cell cultures do not produce BIAs constitutively, the biosynthesis of sanguinarine is induced in response to treatment of the cells with a fungal elicitor. As such, opium poppy cell cultures provide an effective model system to investigate the inducible regulation of BIA metabolism and other plant defense pathways. The induction of sanguinarine biosynthesis and supporting metabolism in elicitor-treated opium poppy cell cultures has been characterized using a variety of technologies including EST and species-specific microarray analyses to analyze the transcriptome , LC-MS/MS to survey the proteome , and Fourier-transform ion-cyclotron resonance-mass spectrometry (FT-ICR-MS) to profile the metabolome [1, 3]. Although these studies provided valuable insights into the response of opium poppy cell cultures to fungal elicitor treatment, the technologies used to generate the various databases were limited in terms of the depth of penetration into the transcriptome, proteome and metabolome of the cultured cells. For example, LC-MS/MS peptide analysis of 340 spots isolated by two-dimensional SDS-PAGE led to the identification of 219 proteins using a combination of public and species-specific sequence databases. More extensive genomics resources for opium poppy would improve the downstream identification and discovery of enzymes involved in alkaloid biosynthesis. New sequencing technologies such as 454 pyrosequencing, and advances in LC-MS/MS-based proteomics and bioinformatics, will expand the application of genomics methodologies to a vast array of non-model plants that produce interesting and valuable metabolites.
The berberine bridge enzyme (BBE) converts (S)-reticuline to (S)-scoulerine as the first committed step in sanguinarine biosynthesis (Figure 1) [13, 15–17]. Two P450-dependent enzymes, cheilanthifoline synthase (CheSyn) and the stylopine synthase (StySyn), catalyze the formation of two methylenedioxy bridges and yield (S)-stylopine [18, 19]. Subsequently, tetrahydroprotoberberine cis-N-methyltransferase (TNMT) converts (S)-stylopine to (S)-cis-N-methylstylopine . Two additional P450-dependent enzymes, N-methylstylopine 14-hydroxylase (MSH)  and protopine 6-hydroxylase (P6H) are responsible for the conversion of (S)-cis-N-methylstylopine to 6-hydroxyprotopine, which spontaneously rearranges to yield dihydrosanguinarine [21, 22]. Finally, dihydrosanguinarine is oxidized to sanguinarine by the oxygen-dependent oxidoreductase dihydrobenzophenanthridine oxidase (DBOX) [23, 24]. The biosynthesis of morphine involves the epimerization of (S)-reticuline to (R)-reticuline followed by a series of C-C phenol coupling, two reductions, O-acetylation and two O-demethylations [25–29]. Reticuline 7-O-methyltransferase (7OMT) converts (S)-reticuline to (S)-laudanine , whereas norreticuline 7-O-methyltransferase (N7OMT) yields norlaudanine from norreticuline  (Additional File 1). Cognate cDNAs have been reported for all of the aforementioned enzymes with the exception of MSH, P6H and DBOX.
The standard approach to establish genomics resources for non-model plant species involves the random generation of expressed sequence tags (ESTs) from a cDNA phagemid library using dideoxy chain-termination (Sanger) sequencing technology. Next-generation technologies, such as 454 pyrosequencing, have the potential to dramatically increase the availability of sequence data [31, 32]. The redundancy and depth of coverage of 454 pyrosequencing also provides and unbiased representation of transcript abundance, which is useful for relative gene expression analysis especially in non-model plants that lack complete genome sequence information [33, 34]. However, despite the fundamental importance of transcriptome analysis in genomics-based research, the frequent incongruity between steady-state protein levels and the abundance of cognate gene transcripts  is crucial to the interpretation of relative gene expression profiles in the context of systems biology or gene discovery applications. Complementary analysis of the most abundant proteins combined with a comprehensive transcriptome database provides an important validation tool for the relative importance of gene transcripts within a given cell, tissue or organ. Transcript and protein sequence databases have recently been reported for opium poppy cell cultures using Sanger sequencing of randomly selected cDNAs and first-generation LC-MS/MS analysis of proteins isolated by two-dimensional SDS-PAGE [1, 2]. In terms of the components of sanguinarine metabolism, transcripts corresponding to all known biosynthetic genes were present in the EST database, although some were represented by relatively few sequence reads. Combined with a low-throughput two-dimensional sampling approach the limited availability of sequence data more severely hampered the identification of known sanguinarine biosynthetic enzymes using LC-MS/MS analysis, which yielded only 6OMT .
We report the integration of next-generation 454 pyrosequencing and advanced LC-MS/MS analysis to establish a deep survey of the transcriptome and proteome of opium poppy cell cultures in response to treatment with a fungal elicitor. The effectiveness of 454 pyrosequencing is compared to standard Sanger sequencing with respect to depth of penetration into the transcriptome of elicitor-treated opium poppy cells. Use of the enhanced EST database for the identification of corresponding peptide sequences obtained by one-dimensional SDS-PAGE and LC-MS/MS peptide analysis facilitated the identification of more than 1,000 peptides and polypeptides. Most of the known enzymes involved in sanguinarine biosynthesis and many components of primary metabolic pathways that support alkaloid production are present in the protein database. Several candidate proteins and transcripts that potentially represent novel biosynthetic enzymes involved in the biosynthesis of sanguinarine and other BIAs are also represented.
Induction of sanguinarine accumulation in opium poppy cell cultures
The content of reticuline, protopine and sanguinarine were determined at several time points after elicitor treatment of opium poppy cell cultures to facilitate a correlation of the occurrence of specific transcript and proteins with the abundance of intermediate and end-product alkaloids (Additional File 2). Reticuline was detected at low levels over the entire time course, but the levels of this central pathway intermediate decreased beginning 50 h after elicitor treatment. Protopine and sanguinarine were not detected at early time points after elicitor treatment, but both accumulated later in the time course. Sanguinarine levels began to increase rapidly between 10 and 50 h after the addition of elicitor, and reach a concentration of more than 5 μg/g fresh-weight of cells by the end of the 100-h time course. At 100 h post-elicitation, the level of sanguinarine was 40-fold greater than that of reticuline or protopine. An inverse correlation between the levels of reticuline and protopine/sanguinarine was apparent over the duration of the time course.
Properties of the transcript database generated by 454 pyrosequencing
Summary of the expressed sequence tag databases for elicitor-treated opium poppy cell cultures obtained using 454 GS-FLX Titanium pyrosequencing.
Total number of EST sequences clustered*
Average length of EST sequences (bp)
Number of contigs
Number of singletons
Total number of unigenes**
Number of unigenes blasted with no hits***
An anticipated feature of the EST database is the substantially greater coverage of the 3'-ends of several contigs resulting from (1) the proportionately larger number of partial cDNAs in the library and (2) the relative inefficiency of shearing short cDNAs prior to 454 pyrosequencing (Figure 2). In most cases and as demonstrated for TNMT (Figure 2), relatively few unigenes were assembled from the majority of sequence reads corresponding to the same gene product. Taking this into account, the gene density of opium poppy can be estimated by only dividing the number of contigs (i.e. 37,329) by the size of the opium poppy genome, estimated at 3,724 Mbp , which yields a gene density of approximately 10 genes per Mbp.
Deep transcriptome analysis of elicitor-treated opium poppy cell cultures
The fifty most abundant unigenes in the opium poppy 454 G S-F L X Titanium pyrosequencing database.
Number of reads
Multiprotein bridging factor
Heat shock protein
Chitinase, class IV
Berberine bridge enzyme
60 S ribosomal protein L6
Elongation factor 1α
Heat shock protein 90
40 S ribosomal protein S9
Oryza sativa subsp japonica
Proteasome component protein
Nectarin IV/xyloglucanase inhibitor
Nicotiana langsdorffii × N. sanderae
Luminal-binding protein 5
Elongation factor 1α
Norcoclaurine synthase 1
ADP ribosylation factor
P apaver somniferum
Oryza sativa subsp japonica
Lipid transfer protein
Oryza sativa subsp japonica
Elaeis guineensis var. tenera
Oryza sativa subsp japonica
Tetrahydroprotoberberine N- methyltransferase
Spindle disassembly protein
Transcripts encoding three out of six known enzymes involved in the conversion of (S)-reticuline to morphine were not detected in the database, with ESTs corresponding to the other three enzymes represented at substantially lower levels than enzymes involved in sanguinarine biosynthesis (Figure 3; Additional File 1). Similarly, transcripts encoding two other known BIA biosynthetic enzymes from opium poppy were represented at low levels (e.g., 7OMT, N7OMT) or were not found in the database (Figure 3; Additional File 1). The failure of elicitor-treated opium poppy cell cultures to express genes encoding SalSyn, SalR and CODM explains the absence of morphine in dedifferentiated cells. It is notable that all unigenes encoding enzymes involved in sanguinarine biosynthesis displayed full-length open reading frames, which further supports the depth of transcriptome coverage that is possible using 454 pyrosequencing.
Deep proteome analysis of elicitor-treated opium poppy cell cultures
Integration of transcriptome and proteome databases
The remaining sanguinarine biosynthetic enzymes for which cognate cDNAs have not been isolated catalyze three of the four steps involved in the formation of dopamine and 4-HPAA, and the final three conversions from (S)-cis-N-methylstylopine to sanguinarine (Figure 6). Some of these enzymes likely belong to known protein families including the cytochromes P450 MSH and P6H [21, 22] and the oxidoreductase DBOX [23, 24]. Candidate proteins with substantial identity to oxidoreductase and other enzyme categories potentially involved in BIA metabolism were found in the LC-MS/MS-generated peptide and polypeptide database (Additional File 6).
Integration of 454 pyrosequencing and LC-MS/MS peptide analysis were used to survey the transcriptome and proteome, respectively, of elicitor-treated opium poppy cell cultures. The depth of each database provides new insights into the regulation of BIA metabolism and plant defense responses, establishes valuable resources for the discovery of new alkaloid biosynthetic genes, and allows an assessment of next-generation-omics technologies as tools to study natural product biosynthesis in plants that currently lack genome sequence resources .
Treatment of cell cultures with the elicitor for 10 and 50 h maximized the accumulation of BIA biosynthetic gene transcripts and cognate enzymes, respectively. Using microarray and northern blot analyses, the maximum induction of BIA biosynthetic genes was previously shown to occur 10 h after the elicitor treatment of opium poppy cell cultures . Corresponding western blot analysis showed that BIA biosynthetic enzyme levels were highest 50 h after elicitor treatment [2, 38]. The elicitor-induced accumulation profiles of protopine and sanguinarine (Additional File 2) were in agreement with the temporal induction of BIA products and pathway intermediates determined using FT-ICR-MS .
The EST database generated by 454 pyrosequencing was compared with that established by random sequencing of clones from an elicitor-treated opium poppy cell culture cDNA library using dideoxy chain-termination (Sanger) technology . Although the average read length produced by 454 pyrosequencing was less than that of Sanger-based sequencing (462 bp and 653 bp, respectively), substantially more ESTs were generated (427,369 and 10,224, respectively), which led to the acquisition of a large number of additional unigenes (93,723 and 7,225, respectively; Table 1). The most abundant transcripts in the 454 pyrosequencing database encoded enzymes and proteins involved in metabolism, defense, signaling, transport and cellular structure (Table 2). Transcripts encoding biosynthetic enzymes involved in the regeneration of (S)-adenosylmethionine (i.e. SAM synthetase, S-adenosylhomocyteinase and methionine synthase) were among the most abundant in the database, which is in agreement with their widespread occurrence in an EST database generated by Sanger sequencing .
An EST database was established using 454 pyrosequencing to investigate the flavonoid pathway in the Chinese medicinal plant Epimedium sagittatum. A total of 217,380 reads with an average length of 225 bp were assembled into 76,459 unigenes consisting of 17,231 contigs and 59,228 singletons. Similarly, 454 pyrosequencing of cDNA obtained from the glandular trichomes of Artemisia annua, which produces the antimalarial sesquiterpene artemisinin, yielded 406,044 reads with and average length of 210 bp asembling into 42,678 contigs and 147,699 singletons . Real time-PCR confirmed the expression of all known terpenoid biosynthetic genes and revealed several novel gene transcripts in the 454 pyrosequencing database including putative sesquiterpene synthase homologues. Our opium poppy cell culture library is comparable or superior to these reported databases in terms of sequence coverage (Table 1). The large number singletons in the opium poppy cell culture database was also reported in the other systems and might result from assembly errors due or from the occurrence of low abundance transcripts. As shown for TNMT (Figure 2; Additional file 4) several unigenes were found for most BIA biosynthetic enzymes (i.e. using the criterion of > 90% amino acid identity), which could reflect the occurrence of multiple gene family members. Separate unigenes encoding proteins with 100% amino acid identity could also result from the improper assembly of contigs (Figure 2; Additional file 4). Clearly, the reported 93,723 unigenes is a substantial overestimate of the actual number of transcripts expressed in those cells. The lack of assembly potentially caused by sequencing errors could account for the high number of orphaned ESTs, although some could represent low-expression level genes.
Our 454 pyrosequencing reads showed a substantial bias for the 3'-end of gene transcripts most likely due to the priming of the first-strand cDNA synthesis using oligo-dT (Figure 2). Moreover, the nebulization of relatively short, partial cDNAs process was also inefficient (Figure 2). Comparison of 454 pyrosequencing using California poppy (Eschscholzia californica) cDNA libraries prepared using oligo-dT or random-primers confirmed that the 3'-end bias resulted from priming first-strand cDNA synthesis with oligo-dT . Assembly of both the oligo-dT and random-primed ESTs generated from two full plate of GS-FLX 454 pyrosequencing resulted in 120,585 unigenes with an average length of 157 bp which assembled into 30,603 contigs and 89,892 singletons . Many of the partial ESTs are also truncated at common points at their 5'-end (Figure 2). Genomic 454 pyrosequencing of Escherichia coli showed that 80% of single nucleotide polymorphisms were falsely linked to reads having the same starting point . The high number of replicate sequences suggested that the phenomenon was not random and was associated with the emulsion PCR step and not with nebulization. Similar artefacts were also reported in a metagenomics study on several species, which found systematic errors in genomes sequenced by 454 pyrosequencing technologies (i.e. GS20 or GS-FLX) . Multiple reads from a single template were suggested to occur when amplified DNA attaches to empty beads during emulsion PCR. Although duplicate sequences are occasionally removed prior to assembly, clearly some are still present in our database (Figure 2).
Since the number of 454 pyrosequencing reads in each contig is directly proportional to the abundance of specific cDNAs in the library, quantification of the data provides an accurate measure of the relative expression level of selected transcripts. Comparisons of 454 pyrosequencing and hybridization-based gene expression analyses (i.e. DNA microarray or northern blot) have shown reproducible correlations [32, 35, 44]. The induction of all known genes encoding BIA biosynthetic enzymes involved in the formation of sanguinarine has been shown previously . However, 454 pyrosequencing provides the ability to quantify the relative abundance of different gene transcripts (Figure 3). In the conversion of tyrosine to sanguinarine (Figure 1),454 pyrosequencing reads encoding CNMT and TNMT were most abundant and were represented among the top-50 most highly expressed unigenes (Table 2). In contrast, reads corresponding to the P450-dependent enzymes NMCH, CheSyn and StySyn were the least abundant (Figure 3). Overall, elicitor-treated opium poppy cell cultures show a strong commitment to sanguinarine biosynthesis as demonstrated by the cumulative abundance of 454 pyrosequencing reads corresponding to genes involved in sanguinarine biosynthesis in agreement with previously published reports comparing control and elicitor-treated opium poppy cell cultures . The total number of reads (i.e. 8,505) with greater than 90% amino acid identity to all known BIA biosynthetic enzymes represent approximately 2.0% of the transcriptome. Of these, 62.5% encoded enzymes leading to (S)-reticuline, 35.0% corresponded to enzymes involved in the conversion of (S)-reticuline to sanguinarine, 2.4% represented enzymes in the morphinan alkaloid branch pathway, and 0.1% were relevant to the formation of other BIAs, such as laudanine (Figure 1 and Additional File 1). The absence of any 454 pyrosequncing reads corresponding to three (i.e. SalSyn, SalR and CODM) out of the six enzymes leading from (S)-salutaridine to morphine explains the lack of codeine or morphine in elicitor-treated opium poppy cell cultures (Figure 3). Interestingly, genes encoding other known biosynthetic enzymes in the morphinan alkaloid branch pathway (i.e. SalAT, T6ODM and COR) were expressed, albeit at low levels compared with those involved in the formation of (S)-reticuline or sanguinarine (Figure 3). DNA microarray and northern blot analyses have previously shown that SalAT mRNA levels were induced in opium poppy cell cultures in response to elicitor treatment, whereas COR transcripts are constitutive . Moreover, the recently identified T6ODM cDNA was represented in a Sanger-based opium poppy cell culture EST database, whereas the CODM was only found in an opium poppy stem EST database . The differential expression of genes encoding morphinan biosynthetic enzymes in elicitor-treated opium poppy cells could reflect a requirement for specific cellular or developmental conditions not present in dedifferentiated cell cultures [38, 45].
Two-dimensional (2D) SDS-PAGE is the most commonly used method to separate proteins for plant proteomics applications. However, penetration into the proteome is limited owing mostly to low abundance proteins that are difficult isolate from the 2D gel. Our previous application of LC-MS/MS to analyze the proteome of elicitor-treated opium poppy cell cultures resulted in the identification of 219 proteins based on peptide fragment fingerprint searches using a combination of public and opium poppy EST (i.e. Sanger sequenced) databases . A total of 340 spots were isolated by 2D SDS-PAGE and 6OMT was the only BIA biosynthetic enzyme represented among the identified proteins . Recently, the mass spectral analysis of proteins partially separated by one-dimensional SDS-PAGE was used to assemble an impressive proteome map for Arabidopsis thaliana for different organs, developmental stages, and undifferentiated cultured cells . A total of 86,456 peptide matches yielded 13,029 identified proteins. Proteomics in many plants is typically forced to rely on cross-species identification owing to the lack of genome or transcriptome sequence information, which leads to relatively low numbers of unambiguously identified proteins and the potential for false-positive identification. For example, proteome analysis of banana, which is distantly related to most plant species with substantial DNA sequence data, was used to compare various protein extraction methods and one-dimensional versus 2D SDS-PAGE techniques within the context of cross-species matching of peptide mass spectra. One-dimensional SDS-PAGE on proteins extracted in chloroform:methanol (5:4) followed by LC-MS/MS facilitated the identification of the most proteins, including several hydrophobic proteins that were underrepresented when 2D SDS-PAGE was used .
Our one-dimensional SDS-PAGE, LC-MS/MS proteomics approach coupled with the unambiguous identification of peptide spectra using an extensive opium poppy EST database generated by 454 pyrosequencing led to the identification of five-fold more peptides and polypeptides (1,004 in total) than our previous effort . Most identified proteins are involved in metabolism, defense, signalling, transport and cellular structure (Figure 5, Additional file 5). The majority of identified transcripts (Figure 5A) and proteins (Figure 5B) are involved in metabolism and include enzymes of primary metabolic pathways, such as glycolysis and the tricarboxylic acid cycle, and intermediary metabolic enzymes, such as SAM synthetase and methionine synthase (Additional File 5; Figure 6). Almost all enzymes involved in BIA biosynthesis were identified by LC-MS/MS peptide analysis (Additional File 5; Figure 6). Since the likelihood of identifying a certain protein is proportional to the abundance of specific peptides, the absence of TYDC in the identified protein list (Additional File 5) could be due to the large number of isoforms encoded by the approximately 15-member TYDC gene family . Alternatively, the absence of TYDC in the identified protein list (Additional File 5) could result from issues related to solubility, extraction efficiency, digestion, or the nature of peptide sequences.
With one exception (i.e. 3-dehydroquinate dehydratase), transcripts encoding all enzymes required for the formation of tyrosine and SAM were represented in the EST database (Figure 6) and several were also among the 50 most abundant unigenes (Table 2). Similarly, many of these enzymes were also found in the protein database (Additional File 5; Figure 6). Altogether these results further demonstrate the metabolic commitment of elicitor-treated opium poppy cell cultures to the overall biosynthesis of sanguinarine.
Based on the abundance of characterized mRNAs and enzymes involved in BIA metabolism, the remaining components of sanguinarine biosynthesis for which cognate cDNAs have not been isolated should be represented in the transcript and protein databases at similar levels. The penultimate and third-to-last enzymes in sanguinarine biosynthesis, which catalyze the conversion of (S)-cis-N-methylstylopine to dehydrosanguinarine (Figure 1), are cytochromes P450 [21, 22]. Although the transcript database contains numerous sequences that annotated as cytochromes P450, a more focused number of candidate cytochromes P450 were represented in the protein database (Additional File 6). Cytochromes P450 represented in the 454 pyrosequencing database at levels similar to transcripts encoding NMCH, CheSyn and StySyn coupled with the corresponding representation of the cognate enzymes in the LC-MS/MS protein database provides a basis for the selection of genes putatively involved in BIA biosynthesis.
The integration of state-of-the-art 454 GS-FLX Titanium pyrosequencing and LC-MS/MS-based protein profiling technologies is an effective strategy to establish deep transcriptome and proteome databases for the investigation of natural product metabolism in non-model plant systems. A near-complete transcriptome from relatively homogenous, elicitor-treated opium poppy cell cultures could be achieved by the assembly of fewer than one-half million 454 pyrosequencing reads using the GS-FLX Titanium technology. All known sanguinarine biosynthetic gene transcripts were represented in the database, along with a multitude of transcripts encoding primary and intermediary metabolic enzymes providing precursors and co-substrates in support of alkaloid production. The absence of several transcripts encoding morphinan alkaloid biosynthetic enzymes reveals the transcriptional basis for the lack of morphine production in dedifferentiated opium poppy cell cultures. The establishment of tandem mass spectra derived from predicted peptides represented in the deep transcript database facilitated the empirical identification of a large number of corresponding proteins fractionated by one-dimensional SDS-PAGE. The depth of proteome coverage was dramatically greater than that achieved using 2D SDS-PAGE to isolate individual proteins base on the representation of most sanguinarine biosynthetic enzymes and a substantial number of metabolic enzymes relevant to BIA metabolism. The integration of a near-complete and species-specific transcript database was crucial to the successful identification of multiple peptides. Profiling of the more abundant proteins in elicitor-treated opium poppy cell cultures also revealed a number of uncharacterized enzymes that potentially catalyze steps in sanguinarine biosynthesis.
Cell culture and elicitor treatment
Cell suspension cultures of opium poppy (Papaver somniferum) cv Marianne, cell line 2009 , were grown at 23°C on a gyrotary shaker at 125 rpm in Gamborg 1B5C medium  containing B5 salts and vitamins, 20 g/L sucrose, 1 g/L casein hydrolysate and 1 mg/L 2,4-dichlorophenoxyacetic acid. The cell cultures were sub-cultured biweekly using a 1:3 dilution of inoculum to fresh medium. Elicitor treatment was performed by adding 1 ml of Botrytis cinerea homogenate to 50 ml of cultured cells in rapid growth phase (2 days after sub-culture) and grown for an additional 10 h or 50 h for the isolation of RNA or protein, respectively. Cells were collected by vacuum filtration and stored at -80°C. The fungal elicitor was prepared by inoculating 50 ml of 1B5C medium lacking 2,4-dichlorophenoxyacetic acid with 1 cm3 of B. cinerea mycelium. The fungal culture was grown at 120 rpm on a gyratory shaker at 22°C in the dark for 1 week. Fungal mycelia and medium were homogenized in a blender (Waring Instruments, Torrington, CT), autoclaved at 121°C for 20 min and stored at -20°C.
R NA extraction, cDNA library construction, 454 pyrosequencing and data processing
Cell cultures treated with the fungal elicitor for 10 h were ground to a fine powder under liquid nitrogen and total RNA was isolated according to . Poly(A)+ RNA was extracted by two rounds of Dynabeads oligo(dT)-based purification according to the manufacturer's instruction (Invitrogen, Carlsbad, CA). A double-stranded cDNA library was prepared using a protocol optimized for 454 pyrosequencing developed by the Joint Genome Institute http://www.jgi.doe.gov/. The cDNA library was randomly sheared and sequenced using Titanium FLX series reagents on a Genome Sequencer FLX instrument (454 Life Sciences, Branford, CT). A total of 427,369 high-quality expressed sequence tags (ESTs) with an average read length of 462 bp were obtained after processing the raw data to eliminate low-quality sequences and poly(A) tails. Pre-processing of the data included the removal of reads with BLASTn expectation values of e < 10-20 with respect to a plant repeat sequence database , the trimming of poly(A/T) tails, the removal of low-complexity sequences using the mdust filtering program http://www.tigr.org/tdb/tgi/software, and the elimination of reads shorter than 40 bp. Clustering was done using the TGI Clustering Tools software http://compbio.dfci.harvard.edu/tgi/software. Unigenes were annotated by BLASTx analysis against the Uniprot Plants 9.2 public database.
Protein extraction and SDS-PAGE
Opium poppy cells (1 g) treated with the fungal elicitor for 50 h were ground to a fine powder under liquid nitrogen and extracted in 0.5 M Tris-HCl, pH 7.5, 50 mM EDTA, 1% (w/v) SDS, and 2% (w/v) 2-mercaptoethanol. The extract was centrifuged at 15,000 g and the supernatant extracted with an equal volume of phenol. Subsequently, the emulsion was centrifuged at 15,000 g to separate the phases. The aqueous phase was discarded and an equal volume of extraction buffer was vigorously mixed with the phenol phase. The emulsion was centrifuged and the phenol phase was recovered. Five volumes of methanol containing 0.1 M ammonium acetate and 0.068% (v/v) 2-mercaptoethanol were added, and the mixture incubated overnight at -20 °C. Precipitated proteins were collected by centrifugation at 15,000 g and washed twice with the methanol solution. The pellet was dried and dissolved in rehydration buffer (7 M urea, 2 M thiourea, 56 mM dithiothreitol, and 2.5% (v/v) 3-[(3-cholamidopropyl)dimethylammonio]-1-propane-sulfonic acid (CHAPS)). Protein concentration was determined using the RC DC protein assay (BioRad, Hercules, CA). Ten micrograms of total proteins were separated by SDS-PAGE. To evaluate the quality of the electrophoretic separation, the gel was stained with Coomassie Brilliant Blue. The lane on the gel containing protein was cut into 12 equal segments (Figure 2). Proteins in each gel segment were digested with trypsin prior to LC-MS/MS.
Mass spectrometry and spectrum data analysis
Tryptic protein digests were analyzed using an Agilent 1100 LC-Ion-trap-XCT-Ultrasystem (Agilent Technologies, Santa Clara, CA) fitted with an integrated fluidic cartridge for peptide capture, separation and nanospraying (HPLC-Chip technology) as described previously . Injected protein samples were trapped and desalted on a pre-column channel (40-nl volume; Zorbax 300 SC-C18) for 5 min with 0.2% (v/v) formic acid delivered by an auxiliary pump at 4 μl/min. The peptides were then reverse-eluted from the trapping column and separated on the analytical channel (43-mm channel length; Zorbax 300 SC-C18) at 0.3 μl/min. Peptides were eluted using a 5-70% (v/v) acetonitrile gradient in 0.2% (v/v) formic acid over 10 min. MS/MS spectra were collected by data-dependent acquisition, with parent ion scans of 8100 Th/s over m/z 400-2000 and MS/MS scans at the same rate over m/z 100-2200. Peak-list data were extracted from these files by the DataAnalysis software for the 6300 series ion trap, v3.4 (build 175). Mascot v2.1 (Matrix Science, Boston, MA) was used to search the MS/MS data using the following parameters: 1.6 Da precursor ion mass tolerance, 0.8 Da fragment ion mass tolerance, 1 potential missed cleavage, carbamidomethyl modification of cysteine and variable oxidation of methionine. Peptide sequence data was used to search the Viridiplantae (green plants) database (containing 468,052 sequences) in NCBI http://www.ncbi.nlm.nih.gov. The peptide sequence data was then used to query the elicitor-treated opium poppy cell culture 454 EST database (containing 427,369 sequences) in all potential open reading frames using Mascot v2.1. Results were indexed with the aid of a prior-clustering and annotation exercise. In all cases, human and Botrytis cinerea proteins were included in the searches to avoid contaminant-based erroneous assignment of the data.
Protein hits were scored based on the quality and abundance of the underlying peptide MS/MS data and their scores. A cut-off score (p < 0.012) of 56 with a false discovery rate of 1% was used for all peptides identified through matches in the public databases, and a cut-off score (p < 0.05) of 46 with a false discovery rate of 1.13% was used for all peptides identified through matches in the 454 EST database. The resulting MS/MS spectra were manually assessed for consistency with the proposed sequences and distance from the next highest scoring peptide(s). The protein names associated with each hit were determined by selecting the highest scoring entry and the most common name representing the dataset.
Metabolite extraction and HPLC analysis
Frozen cell cultures (1 g) were ground to a fine powder under liquid nitrogen and extracted for 2 h in 100% (v/v) methanol at room temperature. The extracts were centrifuged for 10 min to pellet debris and the supernatants were reduced to dryness under reduced pressure. Pellets were resuspended in 100 μl 100% (v/v) methanol. Ten microliters of each extract was diluted in 100 μl of 98% (v/v) H2O: 2% (v/v) acetonitrile: 0.04% (v/v) H3PO4 and analyzed using a System Gold HPLC and photodiode array detector (Beckman-Coulter, Mississauga, Canada). All separations were performed at a flow rate of 1.5 ml/min on a LiChrospher RP-Select B 5μ column 150 × 4.6 mm (Alltech, Illinois, USA). Separation was achieved using a gradient of solvent A [98% (v/v) H2O: 2% (v/v) acetonitrile: 0.04% (v/v) H3PO4] and solvent B [98% (v/v) acetonitrile: 2% (v/v) H2O: 0.04% (v/v) H3PO4]. Chromatography was initiated and maintained for 5 min using 90% solvent A. Subsequently, the gradient was ramped to 35% solvent B over 40 min and then to 100% solvent B over 5 min. Peaks corresponding to reticuline, protopine and sanguinarine were monitored at 210 nm and identified on the basis of their retention times and UV spectra compared with authentic standards. Dextromethorphan was used as an internal standard for the quantification of data.
The sequences described in this paper have been submitted to GenBank under the accession numbers GU325749 and GU325750.
This work was funded by a Natural Sciences and Engineering Research Council of Canada Strategic Project Grant to PJF. DCS holds the Canada Research Chair in Chemical Biology. PJF holds the Canada Research Chair in Plant Metabolic Processes Biotechnology.
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