Optimization of transplastomic production of hemicellulases in tobacco: effects of expression cassette configuration and tobacco cultivar used as production platform on recombinant protein yields
© Kolotilin et al.; licensee BioMed Central Ltd. 2013
Received: 2 January 2013
Accepted: 29 April 2013
Published: 3 May 2013
Chloroplast transformation in tobacco has been used extensively to produce recombinant proteins and enzymes. Chloroplast expression cassettes can be designed with different configurations of the cis-acting elements that govern foreign gene expression. With the aim to optimize production of recombinant hemicellulases in transplastomic tobacco, we developed a set of cassettes that incorporate elements known to facilitate protein expression in chloroplasts and examined expression and accumulation of a bacterial xylanase XynA. Biomass production is another important factor in achieving sustainable and high-volume production of cellulolytic enzymes. Therefore, we compared productivity of two tobacco cultivars – a low-alkaloid and a high-biomass - as transplastomic expression platforms.
Four different cassettes expressing XynA produced various mutant phenotypes of the transplastomic plants, affected their growth rate and resulted in different accumulation levels of the XynA enzyme. The most productive cassette was identified and used further to express XynA and two additional fungal xylanases, Xyn10A and Xyn11B, in a high-biomass tobacco cultivar. The high biomass cultivar allowed for a 60% increase in XynA production per plant. Accumulation of the fungal enzymes reached more than 10-fold higher levels than the bacterial enzyme, constituting up to 6% of the total soluble protein in the leaf tissue. Use of a well-characterized translational enhancer with the selected expression cassette revealed inconsistent effects on accumulation of the recombinant xylanases. Additionally, differences in the enzymatic activity of crude plant extracts measured in leaves of different age suggest presence of a specific xylanase inhibitor in the green leaf tissue.
Our results demonstrate the pivotal importance of the expression cassette design and appropriate tobacco cultivar for high-level transplastomic production of recombinant proteins.
KeywordsTransplastomic tobacco Recombinant proteins Cellulolytic enzymes Chloroplast expression cassette Cellulosic biofuels
Chloroplasts, the photosynthetic organelles in plant cells, are believed to originate from endosymbiotic cyanobacteria that were incorporated into an ancestral eukaryotic host cell . Although the bulk of the endosymbionts' genome was depleted during evolution, chloroplasts retain a relatively small circular genome (plastome) that is highly polyploid, and the chloroplast genetic machinery for transcription/translation resembles that of prokaryotes [2, 3]. These features make plastome transformation in higher plants an alternative to nuclear genome transformation, and also offer several advantages, such as 1) integration of the transgene into a precise plastome locus by homologous recombination; 2) lack of positional effects and epigenetic factors, such as transgene silencing, often detrimental for foreign protein expression in nuclear transformants; 3) the ability of the plastid genetic machinery to transcribe and translate operons and, 4) transgene containment due to maternal inheritance of the engineered plastome [4–6]; for review see [7–10]. Stable chloroplast genome transformation was achieved in several plant species, where routine generation of transplastomic plants with well-established protocols have been developed mostly in Solanaceae species such as tobacco, tomato and potato [4, 11–16]
Since the development of the plastome transformation techniques more than two decades ago, successful production in chloroplasts of heterologous proteins from various origins has been reported [11, 17–19]. Many chloroplast transformation vectors with different configuration of the chloroplast expression cassettes were designed and applied [7, 11, 16, 17]. A typical cassette would contain a gene of interest (GOI) and a selectable marker - a gene for antibiotic resistance that enables selection of transplastomic clones, most commonly the aminoglycoside adenylyltransferase (aadA) gene conferring resistance to streptomycin/spectinomycin [14, 20]. Expression of these genes is regulated by specific cis-acting elements that are usually adopted from endogenous as well as heterologous plastid genes and include chloroplast promoters, 5'- and 3'-untranslated (UTR) sequences and ribosome-binding sites [11, 16, 18]. Structural design (configuration) of a cassette can vary according to the plastome locus where integration is planned; usually transcriptionally-active or silent intergenic spacer as well as cassettes of different configuration can be introduced into the same plastome locus. Various cassettes, designed by different research groups, have been integrated into several distinct sites in the tobacco plastome, mostly targeting intergenic spacers in the inverted repeat (IR) region between the trnV and rps12 genes, an intron with no read-through transcription, and between the trnI and trnA genes, a transcriptionally-active intron, where endogenous transcriptional activity may be exploited to express foreign genes. In the large single copy (LSC) region a silent intergenic spacer between trnfM and trnG genes has been also extensively utilized [6, 11, 16, 21, 22]. Cassettes integrated into these plastome loci were reported to produce abundant yields of recombinant proteins, some reaching a massive accumulation of 70% of the total soluble protein (TSP) in the plant leaf tissue and overburdening the protein synthesis machinery in the plastid [23–25]. Studies that addressed the reasons of variable levels of recombinant protein accumulation in chloroplasts showed that multiple determinants at transcriptional, translational and post-translational levels are involved in the process. Factors such as mRNA stability, mRNA-rRNA interactions, appropriate codon usage, efficient processing of polycistronic transcripts, the N-terminal amino acid residue and sequences downstream the initial methionine of the nascent polypeptide chain, as well as protein secondary structure - all exert tight control over recombinant protein production and accumulation in chloroplasts [26–30].
Although numerous different cassettes have been constructed by several laboratories and introduced into the tobacco plastome to express various proteins, the assortment of the cis-acting elements used to facilitate the expression of the genes of interest and the selectable marker genes from these cassettes remains limited. Typically, a strong chloroplast ribosomal operon promoter (Prrn) and the promoter for the PSII protein D1 (PpsbA) are used, driving the transcription of the foreign genes [16, 18]. In most constructs reported, the mRNA transcripts of the transgenes were stabilized by 5' and 3' UTRs of the tobacco endogenous plastid psbA, rbcL or rps16 genes; heterologous UTRs originating from different species were also successfully implemented [31–34]. Coding sequences of the genes of interest and the selectable marker may be fused at the 5’ to translational enhancers, also called “downstream boxes” (DB) - specific DNA sequences, that have been previously identified as important regulators of translation efficiency and defined by the 10–15 codons immediately downstream of the initial ATG start codon [16, 26, 27, 35–39]. One of the best-characterized in that context is the N-terminal portion of the protein encoded by gene 10 from bacteriophage T7 (T7g10), which has been shown to increase accumulation of several recombinant proteins produced in chloroplasts [32, 40, 41].
In an attempt to optimise production of cellulolytic enzymes in transplastomic tobacco, we used a set of endogenous and heterologous cis-acting elements to construct several cassettes with varying configuration of the cis-acting regulatory elements and the foreign genes expressed. We introduced four different cassettes containing the aadA gene and the xynA gene encoding a bacterial xylanase from Clostridium cellulovorans into the trnI - trnA intron of the tobacco plastome. We confirmed the functionality of the best cassette with two additional fungal xylanases, Aspergillus niger Xyn10A or Xyn11B using a different, high-biomass tobacco cultivar. Cumulatively, our results demonstrate the importance of two factors for optimization of transplastomic production of recombinant proteins in tobacco: 1) effective structural design of the cassette and 2) the choice of regulatory cis-elements. Developmental restriction of some transplastomic plants may be considered an additional limiting factor to obtainable yields of the recombinant protein.
Results and discussion
Design and construction of the cassettes used in this study
General design and positional configuration of the regulatory cis-elements and foreign genes expressed in all the Chloroplast Expression Cassettes (CECs) was based on previously reported constructs with some modifications (Figure 1A; [11, 16, 18, 33, 42, 43]). Integration of all the CECs was targeted into the trnI - trnA intron in the IR region of the tobacco plastome. No promoters were incorporated into CEC1 and the expression of both the xynA and the aadA genes from CEC1 relied entirely on read-through transcription from the endogenous promoter of the rrn operon (Prrn, ). CEC2 utilized the read-through transcription for expression of xynA, while the psbA gene promoter (PpsbA) along with its 5’ UTR governed the expression of aadA. CEC3 was the only cassette designed to contain two strong chloroplast promoters, PpsbA and mutated Prrn (mPrrn, see Methods for a description of the mutations; ), driving the expression of aadA and xynA, respectively. CEC4 construct utilized the read-through transcription for expression of aadA and the PpsbA/5’ UTR for expression of xynA. The intercistronic expression element (IEE), shown to direct efficient mRNA processing and promote protein expression  was incorporated into CEC1 and CEC4 upstream of the aadA gene. The 5’ end of the xynA reading frame in all the cassettes contained the first 11 codons of the T7g10 as a translational enhancer ; the 3’ end was fused in frame with strepII and c-myc protein tags for detection and purification. The T7g10 5’ UTR and downstream box (DB) was located upstream of xynA in CEC1, CEC2 and CEC3, while the psbA 5’ UTR and T7g10 DB were used in CEC4. In all the cassettes, the 3’ ends of both xynA and aadA reading frames were fused to the same heterologous 3’ UTRs from Populus alba, TrbcL and TpsbC respectively, required for the stabilization of the mRNA [46, 47]. All the described cassettes were cloned into pUC19-based pPT vector , designated pCEC1- through -pCEC4-XynA, and propagated in E. coli. We observed much lower plasmid DNA yields from bacterial cultures bearing pCECs and 3 – 5 times larger culture volume was required to obtain plasmid DNA yields comparable with the yield of unmodified pUC19 or pPT, indicating possible leaky expression of chloroplast elements in E. coli that resulted in probable toxicity and slow growth.
Generation of transplastomic homoplasmic tobacco plants expressing XynA from different cassettes
Our group previously reported efficient rates of chloroplast transformation achieved in two tobacco cultivars: the low-alkaloid cultivar (cv.) 81V9 and the high-biomass cv. I64 . Cv. 81V9  is used as a model plant in our lab and has been characterized extensively as a platform for transient and nuclear-transformed, stable expression systems . Thus, cv. 81V9 was chosen for the initial selection of the most efficient cassette for transplastomic XynA production. Transplastomic tobacco cv. 81V9 plants were obtained following standard bombardment of leaf tissue with the four cassettes and 3 consecutive rounds of regeneration on selective medium [4, 14, 16]. High transformation frequencies were observed for all the cassettes, generating usually 10–15 independent transplastomic clones after bombardment of five sterile-grown tobacco leaves.
After the initial PCR-assisted screening confirming foreign DNA insertion (data not shown), the regenerated T0 plantlets were rooted on selective medium and grown to a size of 5 – 10 cm before transfer to pots in the greenhouse. Differences in regeneration/rooting timing among the T0 plants transformed with different cassettes did not allow for accurate comparison of the growth rate and phenotype, which were observed as roughly similar for CEC1-, CEC2- and CEC4-XynA-transformed plants compared with untransformed wild-type (WT) cv. 81V9 plants. However the CEC3-XynA-transformed plants could be readily distinguished, as they displayed pale-green-to-white leaf color and severely retarded growth (Figure 1B). Two independent T0 clones for each cassette were chosen for further experiments; their homoplastomy was confirmed by a Southern blot RFLP analysis that showed stable integration of the foreign DNA into the plastome (Figure 1C).
For the initial analysis of the XynA protein production in T0 clones transformed with different cassettes, we sampled young, well-developed leaves of the same size (~30 cm long, ~third-fourth leaf from top), thus minimizing possible developmental variations in XynA expression among the clones and focusing on the cassette effect. Equal amounts of extracted leaf tissue were analyzed by SDS-PAGE and immunoblotting (Figure 1D). The results of this analysis confirmed the expression of XynA from all the cassettes; however, differences in accumulated XynA amounts were observed, suggesting varying expression efficiency from different cassettes. Beside the full-size XynA protein product appearing at ~58 kDa, we also observed two abundant bands of ~27 – 28 kDa in size, detectable with anti-c-myc antibody. These bands correspond to the size of the C-terminal NodB domain of XynA .
Effects of different cassettes on transplastomic plant growth/biomass generation and accumulation of the recombinant proteins
Number of days to flowering (DTF) and fresh leaf weight (FLW; kg ± standard error of mean [SEM]; n = 3) at mature plant stage in transplastomic low-alkaloids tobacco T 1 plants (cv. 81V9) transformed with different CECs expressing XynA
CEC3 generated the most xynA transcripts among all the cassettes, with the most abundant transcript size being ~1,800 bp, corresponding to a mPrrn-generated xynA transcript terminated at the TrbcL 3’ UTR. The mPrrn-driven transcription of the xynA gene from CEC3 reached higher levels than CEC1-XynA, which is driven by the endogenous Prrn, or of CEC4-XynA, where xynA is driven by PpsbA, whereas these two promoters are considered among the strongest in chloroplast [44, 45]. Since each of the three triplet mutations introduced into mPrrn was reported to increase transcription (; see Methods section), it is reasonable to suggest that mPrrn created in this study is more powerful than native Prrn; however, additional quantitative experiments are required to validate this assertion.
XynA and AadA enzymes accumulation from each cassette in T1 plants correlated with RNA results (Figure 3B, C). All the cassettes produced AadA at similar levels. CEC2 showed very low xynA RNA and protein amounts, while accumulation of XynA expressed from other cassettes reached similar levels. T0 plants had displayed a similar effect, albeit not as strong, which could be explained by different ages of T0 plants at sampling (compare Figure 3B with Figure 1D). However, although CEC3 appeared to have the highest levels of xynA mRNA, at the protein level it produced similar amounts of XynA enzyme as CEC4. Since both transplastomic genotypes transformed with CEC3 and CEC4 displayed similar accumulation levels of both recombinant proteins, the chlorotic stunted phenotype in CEC3-expressing plants is likely due to a disruption of plastid mRNA homeostasis by massively redirecting mRNA synthesis and probably causing reduced transcription of essential genes due to depleted resources of the genetic machinery inside the organelle. To the best of our knowledge this observation that high levels of foreign mRNA accumulation can cause near-lethality is a novel insight into the complexity of transplastomic production of recombinant proteins. This view is different from previous arguments put forward for explaining stunted growth or lethality observed in transplastomic plants, such as foreign protein toxicity and/or a depletion of resources needed for synthesis of essential plastid proteins [25, 55–57].
Thus, according to the phenotypic and expression data, although CEC3 produces more transcript and as much protein as CEC4, the plants are severely stunted, and although the developmental pattern and biomass of CEC2 is similar to wild type, it produces very little XynA. As well, CEC1 requires 3 weeks more than CEC4 to reach maturity. Therefore, it appears that CEC4 is the best cassette for XynA production.
Generation of transplastomic homoplasmic tobacco plants expressing fungal xylanases and effects of T7g10 translational enhancer
With these new constructs we carried out chloroplast transformation of a high-biomass tobacco, cultivar I64, thus testing the performance of the selected CEC4 in a different genetic background. Southern blot RFLP analysis confirmed uniform homoplastomy of the generated cv. I64 T0 primary transformants that phenotypically resembled cv. I64 WT plants (Figure 5B, C). Transplastomic T0 clones were further examined for the recombinant protein content (Figure 5D). Surprisingly, Xyn10A accumulated only to 13.0 μg/g leaf tissue (0.2% TSP), whereas transplastomic Xyn11B accumulation showed levels reaching 1.3 mg/g fresh leaf tissue (6.0% TSP), consistent with the levels of transiently-expressed, chloroplast-targeted Xyn11B.
Numerous reports found that the N-terminal coding sequence of a protein can strongly affect its accumulation level in chloroplasts [27, 36, 38, 39, 58, 59]. Chloroplast-produced proteins with N-terminal T7g10 fusions usually report high levels of expression [27, 32, 40, 41]. Interestingly however, accumulation of neomycin phosphotransferase (NPTII) reporter enzyme, translationally fused with T7g10 N-terminal portion was significantly improved when the translational enhancer was removed from the expression construct . That result prompted us to scrutinize the impact of the T7g10 translational enhancer N-terminal fusion on the recombinant protein yields. Two additional constructs, namely pCEC5-Xyn10A and pCEC5-Xyn11B, were prepared by eliminating the DNA fragment encoding T7g10 translational enhancer from pCEC4-Xyn10A and pCEC4-Xyn11B, respectively (Figure 5E). Primary cv. I64 clones transformed with pCEC5-Xyn10A and pCEC5-Xyn11B displayed uniform homoplastomy and WT-like phenotype (Figure 5F, G). Strikingly, the removal of the T7g10 translational enhancer greatly increased (more than 16-fold) the accumulation of the Xyn10A, which reached ~0.8 mg/g fresh leaf tissue (3.3% TSP). Contrasting that, the lack of T7g10 N-terminal fusion was unfavourable for Xyn11B accumulation that decreased by more than two-fold to ~0.4 mg/g (2.5% TSP) (Figure 5D, H). Here we show that T7g10 N-terminal fusion displayed an opposite effect on accumulation of two different recombinant proteins in chloroplasts, suggesting protein-specific influence for this cis-acting element. Thus, our results imply that a transplastomic approach for expression of recombinant proteins should include testing of combinations of different types of translation control elements for each individual foreign ORF .
Number of days to flowering (DTF) and fresh leaf weight (FLW; kg ± SEM; n = 3) at mature plant stage in transplastomic high-biomass tobacco T 1 plants (cv. I64) expressing different xylanases from CEC4 and CEC5
Enzymatic activity of crude plant extracts
Xylanolytic activity of crude plant extracts from mature green leaves (GL) and senescing leaves (SL) of cv. I64 transplastomic lines expressing XynA, Xyn10A and Xyn11B
Enzyme Crude Extract
Leaf developmental stage
Enzyme in reaction (μg)
Generated Xylose (μMole)
Generated Xylose (μMole)/enzyme (μg)
The results showed that equivalent amounts of crude extracts containing different amounts of XynA, Xyn10A and Xyn11B, generated 21.8 to 47.7% conversion of xylan. Xyn10A produced the highest conversion efficiency, although it accumulated to lower levels than Xyn11B. Thus, Xyn10A seems to be more catalytically active in crude extracts than Xyn11B. Although the conversion efficiency of XynA appeared lower than that of Xyn10A, when corrected for amount of enzyme present in the reaction, XynA was vastly superior to both fungal enzymes in its ability to hydrolyze xylan and produce xylose, (Table 3). XynA is a major xylanase subunit of the cellulosome from Clostridium cellulovorans and its high enzymatic activity could be attributed to the synergy in action of its two catalytic domains: the N-terminal catalytic domain and C-terminal NodB, with xylanase and acetyl xylan esterase activities, respectively . The domains are separated by a small dockerin domain that “docks” the protein into the cellulosome by its interaction with a receptor domain – cohesin on the cellulosomal structural protein scaffoldin CbpA . That dockerin domain is probably an easy target for plastid proteases – on protein blots from XynA extracts we observed abundant bands corresponding to molecular sizes of the NodB domain with or without the dockerin (~27 – 28 kDa), suggesting it has two protease cleavage sites (Figure 1D, 3B, 4B, 6C). Yet, the separated domains retained their catalytic activity, which was observed in a zymogram (Figure 7B). The intact XynA band could not be distinguished in the zymogram; instead, a smeary clearing appeared in lanes loaded with XynA extracts, indicating presence of partially degraded XynA protein, undetectable with anti-c-myc antibody, and possible failure of XynA to refold in its intact form after denaturing SDS-PAGE. Although the activity assay indicated that Xyn10A is more catalytically active than Xyn11B, the zymogram displayed the clearest band for Xyn11B, correlating with its higher accumulation. This observation implies that crude extracts may have different effects on stability/activity of the fungal xylanases accumulated in chloroplasts, while SDS-PAGE conditions could provide physical segregation from probable inhibiting and/or degrading agents present in crude plant extracts, allowing the separated enzymes to “work” on their substrate in the “protected environment” of the gel matrix.
We observed higher xylanase activity in extracts from SL for all three recombinant enzymes, whereas the amount of the fungal Xyn10A and Xyn11B diminished ~4-fold, compared to GL tissue (Table 3). This result was unexpected and may be due to induction of plant endogenous cellulases/hemicellulases in the SL tissue, which is supported by the elevated levels of reducing sugars obtained in the control reactions with SL extracts from WT leaves. Yet, this increase cannot account for the massive increase in reducing sugars content observed in the reactions with extracts from SL tissue of the transplastomic lines. A more probable explanation to the observed phenomenon is the presence of an inhibitory factor, which acts in the GL tissue and is depleted from the SL tissue. Indeed, several reports described occurrence of specific endogenous protein inhibitors of xylanases in different plant species, including tobacco [65–68]. Although additional studies are required to confirm that the foreign xylanases accumulated in chloroplasts are catalytically subdued in crude extracts by a specific inhibitor(s) found in fresh leaves, it is reasonable to suggest that identification of such inhibitors in tobacco and targeted knock-out of their genes through genetic manipulation could lead to creation of cultivars”tailored” for expression of xylanases belonging to a particular type or family, which would be highly catalytically active in plant crude extracts.
In this study we optimized the transplastomic production of recombinant xylanases in tobacco for a potential application in bioethanol industry. The initial optimization steps focused on selection of the most efficient chloroplast expression cassette, which combined recombinant protein expression/leaf biomass generation maxima as productivity parameters. Using the selected cassette we demonstrated that different genetic backgrounds, chosen as a platform for transplastomic expression in tobacco, allow additional optimization for the production process of recombinant enzymes.
Chloroplast transformation cassettes construction
The sequences of the cis-regulatory elements were chemically-synthesized and assembled into the designed cassettes by a series of restriction/ligation reactions (Figure 1A). A xynA clone (AF435978; ) was a generous gift from Dr. Yutaka Tamaru, Mie University, Japan. Xyn10A and xyn11B sequences were provided by Dr. Adrian Tsang, Concordia University, Canada. Primers used for amplification/cloning of the GOIs into cassettes are listed in Additional file 1: Table S1A in Additional Materials section.
In all the cassettes constructed, the 3' ends of the xynA and the aadA genes were fused to the 3' UTR regions of rbcL (TrbcL) and psbC (TpsbC) plastid genes from White Poplar (Populus alba, chloroplast genome NC008235; nucleotides 56790-to-57022 and 34875-to-35052, respectively).
Three triplet nucleotide mutations (“-58 – -56” ATG to TAC; “-22 – -20” AGG to TCC and “-5 – -7” CTC to AGA mutation; ) were introduced into the sequence of the chloroplast rrn operon promoter (Nicotiana tabacum chloroplast genome NC001879, nucleotides 102565-to-102648) producing mutated Prrn (mPrrn) in order to increase the transcription, also reducing the homology to the endogenous Prrn, thus reducing the chance of deleterious homologous recombination between these sequences.
Integration of the cassettes into the tobacco plastome was designed to occur between the trnI (tRNA-Ile) and trnA (tRNA-Ala) genes. For that, the transformation cassettes were introduced into the Nsi I site in the trnI-trnA intron of the pPT vector, described in , thus creating Chloroplast Expression Cassette vectors (pCECs), designated as pCEC1–C4 (Figure 1A). The sequences of the GOIs were cut with Sap I (Nhe I for CEC5) and Not I and introduced into all the pCECs by direct cloning into the corresponding restriction sites.
Generation of transplastomic plants and confirmation of homoplasmy
Transplastomic tobacco plants (cv. 81V9 and I-64) were obtained by the biolistic method [4, 14, 16]. After 3 rounds of regeneration on selective medium containing 500 μg/mL spectinomycin, homoplasmy of all the clones was confirmed by Southern blot analysis (Figure 1C; Figure 4B, F). Three μg of plant total DNA, extracted from the transplastomic clones as well as from untransformed WT plants (Qiagen DNeasy Plant Mini kit, Qiagen, GmbH), were completely digested with Rsr II enzyme, electrophoresed on 0.8% agarose gel and transferred onto Hybond-N+ membrane (Amersham Biosciences, UK). A DIG-labelled probe was amplified with primers Probe-F: 5’-caccacggctcctctcttctcg-3’ and Probe-R: 5’-ttcctacggggtggagatgatgg-3’ using PCR DIG Probe Synthesis kit (Roche Diagnostics, GmbH) and pPT as the template, according to the manufacturer’s protocol. Hybridization of the probe was carried out at 50°C over-night. Three stringency washes (100 mL of 2XSSC + 0.1% SDS at RT – twice; 100 mL of 0.5XSSC + 0.1% SDS at 68°C – three times) were performed, followed by 30 min blocking at 42°C and 30 min of antibody binding. Detection was carried out with AGFA CURIX ULTRA EJUTK film with different exposures.
RNA extraction and northern blot analyses
Total plant RNA was isolated using the RNeasy Plant Mini Kit (QIAGEN Sciences, Maryland, USA) according to the manufacturer’s instructions. For each RNA sample, 2 μg were electrophoretically separated on a denaturing, 1.2% agarose gel. Following capillary transfer of the RNA to a nylon membrane (Roche Diagnostics, GmbH), the membrane was submerged in a reversible staining solution (0.02% Methylene Blue, 0.3 M sodium acetate, pH 5.5) for 5 minutes. The membrane was then washed in 1× SSC until the background had cleared such that the consistency of the transfer and the quality of the RNA could be visualized (Figure 3A, left panel). Subsequently, the damp membrane was put into the pre-hybridization solution prepared using DIG Easy Hyb Granules (Roche) according to the manufacturer’s instructions. The blot was probed at 50°C with a DNA fragment of Xylanase A that had been DIG-labelled using the PCR DIG Probe Synthesis Kit (Roche Diagnostics, GmbH). Stringency washes were employed (2×5 minutes at room temperature with 2× SSC, 0.1% SDS; 1×15 minutes at 68°C with 0.5× SSC, 0.1% SDS; 1×15 minutes at 68°C with 0.1× SSC, 0.1% SDS) before blocking with Blocking Reagent (Roche Diagnostics, GmbH) and detection with Anti-DIG Fab fragments and CSPD (Roche Diagnostics, GmbH) as described by the manufacturer. The blot was subsequently exposed to X-ray film for various times to visualize the hybridized bands.
Recombinant protein extraction, quantification and functional enzyme analyses
For extraction of total soluble proteins from leaf tissue ~0.05 g samples frozen in liquid N2 were homogenized in Tissuelyser (Qiagen, GmbH) for 2 minutes in 2-mL Eppendorff tubes with 3 silica beads (Biospec, USA), then either ~250 μl or ~500 μl of Extraction Buffer (EB; 50 mM Na-Acetate, 15 mM CaCl2, pH 4.9) were added to the tubes to obtain 1/5 or 1/10 sample weight/extraction buffer volume (w/v) ratios, vortexed for 1 minute and centrifuged for 10 minutes at 14000 X g, 4°C. The supernatant was used as crude extract for quantification of the expressed recombinant proteins as well as for enzymatic activity analyses.
Immunoblot analyses were performed to assess levels of recombinant protein expression. For that, crude extracts were resolved on 12% SDS-PAGE gels, transferred onto a nitrocellulose membrane by semi-dry electroblotting (Biorad, USA). The blots were blocked over night at 4°C in 5% skimmed milk in Tris-buffered Saline (TBS, pH=7.5) and subsequently probed with a primary antibody, either anti-c-myc (Genscript, USA) or anti-AadA (Agrisera, UK), diluted 1:5000 in 0.5% skimmed milk-TBS for 1 hour; the horse radish peroxidase-conjugated goat anti-mouse IgG (secondary antibodies, Biorad, USA) was diluted 1:5000 in 0.5% skimmed milk-TBS and incubated with the blots for 1 hour. The recombinant proteins accumulated in transplastomic leaf tissue were quantified from immunoblots by densitometry with TotalLab TL100 software (Nonlinear Inc., Durham, USA) using intensity analysis of specific bands, where known amounts of a c-myc-tagged CBD protein were used as reference.
Enzymatic hydrolysis of birchwood xylan (Sigma, USA) by crude extracts (w/v = 1/10) of XynA-, Xyn10A- and Xyn11B-expressing plants was carried out in 15 ml tubes. Extract from WT plants was used as negative control. Crude extracts were prepared in EB, 400 μl of each extract representing 40 mg of extracted leaf tissue were mixed with 10 ml of 1% (w/v) xylan as a substrate, diluted in EB. Reactions were set as triplicates for each extraction at 40°C for 24 hours with agitation, and then placed on ice for 30 min. Subsequently tubes were centrifuged and the supernatant (40 μl) was mixed with 70 μl of Dinitrosalicylic Acid (DNS) reagent , boiled for 5 min and examined in a spectrophotometer (Bio-Rad) for reducing sugar content [62, 63].
A zymogram of the xylanolytic activity of crude extracts from XynA-, Xyn10A- and Xyn11B-expressing plants (equivalent of 2.5 mg of extracted leaf tissue) was obtained on 12% SDS-PAGE gel containing 0.1% (w/v) birchwood xylan (Sigma, USA), followed by 3×30 min washes in 100 ml of EB to eliminate SDS and renature the resolved proteins. Subsequently, the gel was incubated in 100 ml of EB at 40°C for 4 hours, stained with 0.1% Congo Red and de-stained in 1M NaCl.
Extractions of total soluble proteins for each experiment were repeated at least 3 times. From those, samples for protein and enzymatic analyses were taken. At least 6 technical repeats were analyzed for each extraction. Collected data were used to express the mean value of a parameter ± standard error of the mean (SEM). Values were analyzed using JMP software (SAS Institute, Cary, USA).
Aminoglycoside adenylyltransferase gene
Gene encoding XynA xylanase fom C. cellulovorans
Gene encoding Xyn10A xylanase fom A. niger
Gene encoding Xyn11B xylanase fom A. niger
Chloroplast expression cassette
Gene of interest
Mature green leaf tissue
Senescing leaf tissue
Total soluble protein
- IR region:
Inverted Repeat region
We would like to thank Dr. Adrian Tsang for critical reading of this manuscript and for support during the course of this project. We acknowledge expert technical assistance from Catherina Loshkin, Kira Liu and Hong Zhu, and help with the figures from Alex Molnar as well as help with bibliography from Tanja Patry. This project was supported by Agriculture and Agri-Food Canada’s Agricultural Bioproducts Innovation Program through the Cellulosic Biofuels Network.
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