High level expression of Acidothermus cellulolyticusβ-1, 4-endoglucanase in transgenic rice enhances the hydrolysis of its straw by cultured cow gastric fluid
© Chou et al.; licensee BioMed Central Ltd. 2011
Received: 6 August 2011
Accepted: 10 December 2011
Published: 10 December 2011
Large-scale production of effective cellulose hydrolytic enzymes is the key to the bioconversion of agricultural residues to ethanol. The goal of this study was to develop a rice plant as a bioreactor for the large-scale production of cellulose hydrolytic enzymes via genetic transformation, and to simultaneously improve rice straw as an efficient biomass feedstock for conversion of cellulose to glucose.
In this study, the cellulose hydrolytic enzyme β-1, 4-endoglucanase (E1) gene, from the thermophilic bacterium Acidothermus cellulolyticus, was overexpressed in rice through Agrobacterium-mediated transformation. The expression of the bacterial E1 gene in rice was driven by the constitutive Mac promoter, a hybrid promoter of Ti plasmid mannopine synthetase promoter and cauliflower mosaic virus 35S promoter enhancer, with the signal peptide of tobacco pathogenesis-related protein for targeting the E1 protein to the apoplastic compartment for storage. A total of 52 transgenic rice plants from six independent lines expressing the bacterial E1 enzyme were obtained that expressed the gene at high levels without severely impairing plant growth and development. However, some transgenic plants exhibited a shorter stature and flowered earlier than the wild type plants. The E1 specific activities in the leaves of the highest expressing transgenic rice lines were about 20-fold higher than those of various transgenic plants obtained in previous studies and the protein amounts accounted for up to 6.1% of the total leaf soluble protein. A zymogram and temperature-dependent activity analyses demonstrated the thermostability of the E1 enzyme and its substrate specificity against cellulose, and a simple heat treatment can be used to purify the protein. In addition, hydrolysis of transgenic rice straw with cultured cow gastric fluid for one hour at 39°C and another hour at 81°C yielded 43% more reducing sugars than wild type rice straw.
Taken together, these data suggest that transgenic rice can effectively serve as a bioreactor for the large-scale production of active, thermostable cellulose hydrolytic enzymes. As a feedstock, direct expression of large amount of cellulases in transgenic rice may also facilitate saccharification of cellulose in rice straw and significantly reduce the costs for hydrolytic enzymes.
In facing increasing demands for energy and depleting fossil oil reserve, the adoption of alternative, renewable energy is imperative. In the past decade, utilization of biomass for fuel production has been considered not only practical but also extremely vital with respect to the development of sustainable energy [1–3]. Biofuels converted from biomass, considered renewable, environment friendly and carbon neutral, will serve a more important function in the days to come. Although the production of biofuels from starch, sugar or oil from traditional food crops, such as corn, sugarcane, soybean and canola, is relatively simple, it competes with human beings and animals for foods and requires a high energy input for cultivation of these crops. Use of lignocellulosic crops or agricultural residues, such as rice straw or corn stover, for ethanol production is not only economical (high energy output to input ratio) but also environment friendly (that is, carbon neutral and with the emission of less toxic pollutants) and will curtail our reliance on fossil oil and help prevent global warming .
Lignocellulose is the major polysaccharide component of global plant mass, which consists of hemicellulose, lignin and cellulose, a polymer of thousands of 1, 4-β-linked unions of D-glucose [5, 6]. The polymer is arranged in collinear, semi-crystalline bundles and it comprises up to 45% of the dry weight of plant biomass, which is a potentially inexpensive, renewable source of fermentable glucose [7, 8]. Rice is one of the most important food resources in the world, and global rice production has risen steadily from about 200 million metric tons in 1960 to over 660 million metric tons in 2009 . At the same time, about 800 million metric tons of rice straw is also produced annually, which is normally burned or decayed in the field, producing more pollutants and greenhouse gases (for example, methane). Thus, developing rice as a dual-functional crop for solving both the immediate food and energy crisis issues could pave the road toward the successful development of sustainable energy and the prevention of possible pollution from agricultural wastes. However, the conversion of the polysaccharide component of lignocellulose into ethanol for use as an alternative transportation fuel and other useful chemicals requires a series of complete pretreatment and hydrolysis procedures [2, 6, 10]. The complete hydrolysis of cellulose (saccharification) requires at least three different hydrolytic enzymes, including β-1,4-endoglucanse (EC 22.214.171.124), β-1, 4-exoglucanse (EC 126.96.36.199), and β-D-glucosidase (EC 188.8.131.52) [2, 10, 11].
Large-scale production of effective cellulose hydrolytic enzymes is the key to the bioconversion of lignocellulose to fermentative sugars for biofuel and chemical production. Nowadays, production costs and the performance of hydrolytic enzymes from bacterial and fungal sources for cellulosic ethanol production remain the major obstacles because the essential nutrients and the maintenance of optimal conditions are very expensive and laborious [3, 12]. Nevertheless, there has been significant progress in bringing effective and inexpensive means of cellulase production from a large scale bioreactor, in the conversion of low value lignocellulosic material into a cost effective fermentative sugars for producing biofuels. Replacing microorganisms with transgenic plants for the production of cellulose hydrolytic enzymes will significantly reduce the production costs. In other words, manufacturing heterologous cellulases in plants (especially in energy crops) using genetic engineering would lower the expense associated with enzyme production and the amount of enzyme loading required during saccharification [11, 13]. So far, a number of studies have attempted to express cell wall-related degrading enzymes in transgenic plants, such as β-glucosidases [14, 15], ferulic acid esterases [16, 17], xylanases , cellobiohydrase [19, 20] and endoglucanase [7, 21–26]. However, there may be a trade off between expressing foreign cellulases in transgenic plants, obstructing their normal growth  and low level expression [27, 28]. Hence, it is essential to design a proper expression system for the production of plants expressing microbial cellulases, without perturbing their growth and development. This system needs to include a strong promoter with a high-level transcription capacity and an appropriate signal peptide to target the foreign protein into a suitable compartment for high level accumulation .
A. cellulolyticus E1 endoglucanase is a well-known thermostable enzyme, which exhibits low activity at ambient temperatures [21, 22, 29]. This desirable E1 feature might have less deleterious effects on the growth and development of transgenic plants under normal growth conditions. Transgenic expression of thermostable E1 endoglucanase has been examined in Arabidopsis, potato, maize, rice and tobacco [7, 21–25], with the foreign protein accounting for up to 0.01% to approximately 25.7% of the total soluble protein, depending on the host plant and its tissue. In addition, when expressed in plants, the E1 enzyme exhibits high temperature stability (optimum 81°C) and relatively low activity at general room temperatures .
The major objective of this study was to express and accumulate A. cellulolyticus E1 in the apoplastic compartment of rice in large quantities. The expression of the bacterial E1 gene in rice was under the control of the strong constitutive Mac promoter, which has been previously shown to have three- to five-fold higher strength than the cauliflower mosaic virus 35S promoter , and targeted the E1 protein to the apoplast compartment for higher accumulation. We report that high expression levels of active E1 enzyme were achieved in transgenic rice plants, which accumulated up to 6.1% of total leaf soluble protein. Moreover, this thermostable enzyme can be purified from crude extract by a simple heat treatment. In addition, digestion of transgenic rice straw with cultured cow gastric fluid (CGF) for one hour at 39°C and another hour at 81°C yielded 43% more reducing sugars than the wild type rice straw. Thus, the present study demonstrates the technical feasibility and great potential to reduce the cost of producing cell wall-degrading enzymes from transgenic crops.
Rice transformation and transgene confirmation
E1gene expression in transgenic rice
Thermostability of the E1 protein and purification
Enzymatic activity and zymogram analysis of E1 protein
Enzymatic hydrolysis of rice straw with cultured CGF
The presence of free sucrose in the straw could have contributed to the reducing sugars released during the hydrolysis experiment. However, our data showed that air-dried straw from both transgenic and wild type rice plants contained low amounts of reducing sugar, sucrose, glucose and fructose. This is consistent with data from a recent study by Park et al. , which showed that air-dried rice straw contained minimal amounts of sucrose and free glucose and fructose, presumably due to continued respiration and bacterial contamination during drying. Thus, our results demonstrate that, with a starting straw of 10 mg dry matter, after 2 h incubation (at 39°C for 1 h plus 81°C for 1 h) approximately 4.83 mg and 3.52 mg reducing sugars were released from the transgenic and wild type straw, respectively. After correcting for the background amount of reducing sugars in the CGF (0.48 mg/10 mg) this 1.31 mg of additional reducing sugars released through the action of A. cellulolyticus E1 in the transgenic rice straw represented a 43% increase. There were no corresponding increases in glucose and fructose, which may be related to the fact that digestion of cellulose by endoglucanase mainly releases cellobiose.
Global rice production had reached 660 million dry metric tons in 2009, along with 800 million metric tons of straw, and continues to grow at a steady rate . Rice straw contains a high cellulose content (approximately 45%), and is a suitable resource for the large-scale production of biofuels to replace fossil fuels and to reduce environmental pollution caused by agricultural wastes and burning of fossil fuels . Use of cell wall-degrading enzymes from microorganisms for the conversion of cellulosic material to sugars is a limiting step at present. Thus, large-scale production of effective cellulose hydrolytic enzymes is key to the biofuels industry. The expression of heterologous proteins in transgenic plants is an established technology. Consequently, the expression of foreign proteins has been successfully applied in plant systems at various levels, including industrially useful enzymes, viral proteins, pharmaceutical proteins, polypeptides (including antibodies) and various structural proteins [34–37]. The factors influencing the level of accumulation for each of these protein classes vary. Although success depends on the characteristics of the individual protein, protein accumulation has been particularly successful when targeted to the cell wall (apoplast compartment), vacuole or endoplasmic reticulum [11, 38].
This study demonstrated that the E1 gene of A. cellulolyticus integrated into the genome of transgenic rice plants (Figure 1) can be properly transcribed (Figures 2 and 3) and translated into an active enzyme and accumulated at high levels (Figures 4, 5, 6 and 7). We noticed that some of the transgenic rice plants with high E1 activities exhibited a short stature and flowered earlier than wild type plants. However, in a previous study, transgenic rice overexpressing A. cellulolyticus did not show any deleterious effect on plant growth and development . The differences in E1 effect on rice plant growth and development between the present study and that of Oraby et al.  could in part stem from expression level. The highest expression level achieved in our transgenic lines was 6.1% of the total leaf soluble protein, higher than that reported by Oraby et al. . The controversy regarding the effects of E1 on plant growth and development has been reported previously [11, 24]. It also could be related to the difference in the primary structure of cell walls and its composition between monocot (rice) and dicot (tobacco) plants [39, 40] or the position effects of E1 transgene insertion in the genome of transgenic plants. Further study is needed to address the effect of growth temperature on the growth and development of E1 transgenic rice. Most importantly, the E1 protein produced in rice retains its thermostability and can be purified by a simple heat treatment (Figure 5). Also significant is the fact that it remains active in tissues after a long period of storage at room temperature and the presence of E1 in the rice straw increases its hydrolytic efficiency (Figure 8).
The A. cellulolyticus E1 activity could be detected in all tissues of all five transgenic lines. Its activities in the leaves ranged from 60,000 pmol MU/mg protein/min to 79,000 pmol MU/mg protein/min in the homozygous plants derived from the line with the highest expression level (Figure 4). The large (ten-fold) variation in expression among the five transgenic lines containing E1 (Figure 4) was presumably a position effect, as all transgenic lines had one copy of insertion (Figure 1). This highlights the importance of generating as many transgenic plants as possible for selecting high expression lines with a normal phenotype. Transformation of rice with the E1 expression vector under the control of a constitutive Mac promoter  with the tobacco pathogenesis related signal peptide  allowed the heterologous E1 protein to be secreted to and accumulated in the apoplastic compartment at high levels. This is consistent with previous studies reporting that the apoplast can serve as a storage site for large quantities of functional foreign proteins . Based on the zymogram PAGE (Figure 7) and western blot analysis data (Figure 4), E1 protein in all tissue extracts of the transgenic plants was partially degraded to its catalytic domain polypeptide of 38 kDa (Figure 5), in agreement with the observation of previous studies [7, 23, 41, 42]. Obviously, the degraded protein still retains its catalytic activity. The partial degradation of E1 protein may be due to the sensitivity of the cellulose-binding domain to proteases in plant extracts. Further study will be necessary to illustrate the E1 protein degradation pattern in plant tissues.
Although the Mac promoter is known to drive constitutive expression of transgenes in plants and the E1 transcript was detected in all tissues, including the mature seed, floret, leaf, stem and root of transgenic rice (Figures 2,3,4B and 6B), much higher expression levels were found in green tissues, such as leaf, floret and stem (Figure 3). However, a relative large amount of E1 protein was detected in the root soluble protein sample in the western blot analysis (Figure 4B), but a relatively low E1 specific enzyme activity was found in the enzyme activity assay (Figure 6B). This is due to the fact that an equal amount of the total soluble protein for each sample was used in both analyses for comparison but root extract contains a relative low amount of other soluble protein and some potential inhibitors to the activity of E1. The highest amount of E1 protein accumulation, in the leaves of our transgenic rice plants, was up to 6.1% of the total leaf soluble protein (Figure 7), higher than the 4.9% in the transgenic rice plants reported by Oraby et al. , in which the cauliflower mosaic virus 35S promoter was used to drive the expression of the bacterial E1 gene in rice. Thus, the Mac promoter may be more effective for E1 protein production. However, the position of the gene insertion into the genome apparently has a strong influence on transgene expression. With a conservative estimate of ten metric tons of rice straw produced per hectare per year and a 5% E1 protein content in the tissues, 30 kg of very pure E1 protein can be produced annually from a hectare of padding field.
The high thermostability and protease-resistance of A. cellulolyticus E1 protein allows the enzyme to remain active in the tissues for a long period of time. Most importantly, as demonstrated in the digestion experiment with cultured CGF (Figure 8), direct expression of A. cellulolyticus E1 in the transgenic rice straw increases the hydrolytic efficiency of cellulose during saccharification, which can reduce the amount of hydrolytic enzyme needed for the conversion of cellulosic biomass to fermentative sugars. A recent study with transgenic tobacco and maize suggests that the expression of A. cellulolyticus E1 during cell wall construction may alter the inherent recalcitrance of the cell wall . All of these features show the great potential of using transgenic plants as a bioreactor for the large scale production of cellulases and reducing the cost for enzymes through tissue autohydrolysis.
With the anticipation of a fossil fuel shortage in the near future and awareness of the need for environment protection, the use of agricultural wastes and bioenergy crops for biofuel production is considered desirable. Genes coding for many cell wall degradation enzymes have been cloned and sequenced from a wide variety of microbes, and the application of plant genetic engineering in producing these enzymes for biofuel production from lignocellulose has received increasing attention and development in recent years. The most important goals of engineering plants in relation to bioenergy are to reduce the cost of biomass and cellulosic enzyme production and to produce effective cellulose decomposition enzymes on a large scale.
In this study, we adopted a transgene expression constructs that had been previously demonstrated improved A. cellulolyticus E1 expression in transgenic tobacco  for A. cellulolyticus E1 expression in transgenic rice, where the expression of the thermostable A. cellulolyticus E1 gene was under the control of a strong Mac promoter and pathogenesis related protein S signal peptide for apoplast targeting. High levels of A. cellulolyticus E1 protein in transgenic rice plants have been achieved via gene expression, driven by the strong Mac promoter, with accumulation in the apoplast compartment by a proper signal peptide. The bacterial gene was stably integrated into the rice genome, expressed and translated into active protein at high levels, especially in the leaf and stem, with a much higher enzyme activity than those obtained in previous studies. In the transgenic rice line with the highest expression level, the amount of A. cellulolyticus E1 protein accounted for 6.1% of the total soluble leaf protein with a specific activity of 79,000 pmol MU/mg protein/min. Most importantly, high levels of expression of this enzyme did not severely impair the plant growth and development of rice plants. This may be in part due to the high optimum temperatures (81°C) for the E1 activity and the relatively low plant growth temperatures (16°C to 35°C), which may not activate the E1 enzyme substantially and interfere with the cell wall integrity of transgenic plants. Furthermore, the presence of high-level active A. cellulolyticus E1 protein in the transgenic rice straw enhances the hydrolysis of cellulose to reducing sugars.
In the future, the advancement of plant genetic engineering can be tapped to produce biomass or crop plants with increased overall biomass and cellulose content, reduced lignin content  or simplified structure of hemicelluloses. It will also be interesting to simultaneously express both cellulose and hemicellulose degrading enzymes to increase the efficiency of cellulose and hemicellulose conversion into glucose and xylose, respectively. In addition, targeting the same or different foreign cellulose hydrolytic enzymes simultaneously to various cellular compartments of transgenic plants might provide the opportunity for effective production of large quantities of cellulases and increase the efficacy of tissue autohydrolysis. In short, with the advancements in modern plant genetic engineering, many cellulose hydrolysis-related genes from microbes have been cloned and introduced into plants and expressed as active proteins in large quantities. Modifying the genetic make-up for higher thermostability and protein stability during storage and for easy purification will also significantly lower the cost of cellulosic biofuel production.
Transformation vector and bacterial strains
The DNA fragment containing the apoplast transit peptide and mature E1 coding sequence from A. hydrolyticus (1.56 kb) was first fused in frame between the Mac promoter and nos terminator of the pZD264 vector . For selection of transgenic plants, HptII was isolated from the binary vector pCAMBIA1300 and inserted into the pZD264 vector using the PmeI (GTTTAAAC) cloning site, which resulted in a vector of p1500 for rice transformation (Figure 1). The primers used for polymerase chain reaction (PCR) to attach HptII were 5'-CACACAACATACGAGCCGGAAGCAT- 3' and 5'-GCTTAGACAACTTAATAACACATTGCGGACGTT-3'. Escherichia coli strain DH5α was used as the host for cloning plasmid DNA while Agrobacterium tumefaciens AGL0 strain harboring the vector was used for rice transformation.
Plant material, gene transformation and plant growth conditions
Immature embryos of a japonica rice cultivar (Oryza sativa L.), Tainoung 67 (TNG67), were used for induction of embryogenic calli. The Agrobacterium-mediated transformation and regeneration of transgenic plants were performed following the procedure of previous studies [44–48]. Regenerated transgenic rice plants were first cultured in a growth chamber under a day/night temperature regime of 28°C/24°C and a light period of 14 h at 400 μmol/m2/s. For molecular and biochemical studies, all transgenic and wild type rice pants were grown in a greenhouse under natural sun light conditions (12 h-14 h) with day temperature ranging from 25°C to 32°C and night temperature from 20°C to 25°C. Plants were watered and fertilized regularly.
Isolation of rice genomic DNA
For the isolation of genomic DNA, leaf tissues were ground in liquid nitrogen into a fine powder using a pestle and mortar and mixed with extraction buffer containing 100 mM tris-HC1 (pH 7.5), 500 mM NaCl, 50 mM ethylenediaminetetraacetic acid (EDTA), 2% β-mercaptoethanol and 4% sodium dodecyl sulfate (SDS) . The mixture was incubated at 65°C for 15 min and centrifuged (14,000 rpm) at room temperature for 3 min. The supernatant was mixed with 5 M potassium acetate and incubated at -20°C for 15 min. After centrifugation at 4°C for 20 min, the supernatant was passed through a MILLEX-HA filter (Millipore, Billerica, MA, USA; pore diameter 0.45 μm), mixed gently with an equal volume of ice-cold isopropanol, and then incubated at -20°C for 30 min, followed by centrifugation at 4°C for 20 min. The DNA pellet was washed with ethanol, air-dried and dissolved in 5 × TE buffer (50 mM tris-HCl, 10 mM EDTA, pH 8.0). One tenth volumes of 3 M sodium acetate and an equal volume of isopropanol were added and mixed well. After centrifugation at 4°C for 10 min, the DNA pellet was washed sequentially by 70% and 95% ethanol, air-dried, and then dissolved in distilled water.
Southern blot analysis
Southern blot analysis was performed essentially as described by Sambrook et al. . Genomic DNA was first treated with RNase A at 60°C for 2 h. Twenty-five micrograms DNA was digested by HindIII, and DNA fragments separated by electrophoresis on 0.8% agarose gel at 25 V for 15 h. After electrophoresis, the agarose gel was first soaked in 0.25 M HCl for 15 min for depurination, denatured by soaking in the denature solution containing 0.5 N NaOH and 1 M NaCl for 2 h, and then neutralized in 0.5 M tris-HCl (pH 7.4) and 2.5 M NaCl for 2 h. The DNA was transferred to Hybond-N+ membrane (Amersham Biosciences, Little Chalfont, Buckinghamshire) by capillary transfer using 10 × SSC buffer that contains 1.5 M sodium chloride and 0.15 M sodium citrate, pH 7.0 and subsequently fixed by UV cross-linking. Probes were prepared from the PCR products of E1 and HptII independently using genomic DNA isolated from transgenic rice plants as templates. About 200 μg of PCR products and 0.5 μg of random primers were mixed and denatured at 94°C for 3 min. Denatured PCR products were diluted to a final volume of 15 μL in Klenow buffer mixture containing 6 μg of BSA, 0.1 mM deoxyribonucleotide triphosphate without deoxycytidine triphosphate (dCTP) and 5 units of Klenow fragments of DNA polymerase I, kept at room temperature for 1 h after adding 32P-labeled deoxycytidine triphosphate, and then passed through a Sephadex G50 column (Sigma-Aldrich, St. Louis, MO, USA) to purify the probe. The membrane was treated with pre-hybridization solution containing 1 M NaCl, 10% sodium chloride-tris-EDTA buffer (SSTE), 1 × Denhardt's solution, 0.085% dextran sulfate and 1% salmon sperm DNA at 42°C for 4 h, and then hybridized with the probe at 42°C overnight. The hybridized membrane was washed sequentially by 0.1 × SSC containing 0.1% SDS at 42°C for 20 min, and exposed to X-ray film at -80°C for a period of time ranging from 8 h to 2 weeks, depending on radioactivity.
RNA extraction and northern blot analysis
Total RNA was extracted according to Wang and Vodkin  with a modified phenol/chloroform protocol. Leaf tissues were ground in liquid nitrogen with TENS buffer, containing 80 mM tris-HCl, 16 mM EDTA, 160 mM NaCl, 4% SDS and 16 mM dithiothreitol (DTT). Reverse transcriptase-PCR was performed as described by Chen et al.  with slight modification. Total RNA (7.5 μg) was first treated with RNase-free DNase Ι by incubating in a mixture containing 6.7 mM DTT, 20 units RNAsin and 1 unit RNase-free DNase I. The mixture was mixed evenly and incubated at 37°C for 15 min and then at 80°C for 10 min .
RNA gel blot analysis was performed as described by Chao et al. . Total RNA was treated with 3-(N-morpholino)propanesulfonic acid buffer, containing 5% formaldehyde and 40% formamide, and separated by electrophoresis on 1.2% agarose gel. Total RNA in the gel was stained with ethidium bromide and then treated with 50 mM NaOH for 30 min, followed by 10 × SSC for 30 min. The RNA was then transferred to a Hybond-N+ membrane by capillary transfer using 10 × SSC and then fixed onto the membrane by UV cross-linking. Probe preparation and hybridization procedures were the same as described for Southern blot analysis.
Enzyme activity assay
Soluble protein was extracted from newly matured leaf, stem, root, green floret and mature seeds of transgenic and wild type plants by grinding in cold extracting medium containing 80 mM 2-(N-morpholino)ethanesulfonic acid (MES, pH 5.5), 10 mM β-mercaptoethanol, 10 mM EDTA, 0.1% sodium N-lauroylsarcosinate (w/v), 0.1% Triton X-100 (v/v), 1 mM phenylmethylsulfonyl fluoride (PMSF), 10 μM leupeptin, and 1 μg/mL pepsin A. The crude extract was centrifuged at 15,000 g for 10 min at 4°C and the supernatant was used immediately for enzyme assay. Endoglucanase activity was quantitated by its ability to cleave 4-methylumbelliferyl-β-D-cellobioside (MUC) to produce the fluorophore, 4-methylumbelliferone (4-MU), at 65°C . The reaction was initiated by adding 50 μL enzyme extract with an equal volume of 2 × ice cold endoglucanase activity assay buffer containing 4 mM 4-MUC, 160 mM MES (pH 5.5), 20 mM β-mercaptoethanol, 2 mM EDTA, and 2 mM DTT, heated to 65°C, and terminated after 45 min by adding 0.2 M Na2CO3. The peak excitation wavelength was 365 nm and the peak fluorescence emission was 455 nm, measured with a TECAN infinite M200 fluorescence spectrophotometer (Tecan, Gordig/Salzburg, Austria). Enzyme specific activity was expressed on a total soluble protein basis.
For the production of polyclonal antibodies against E1, the coding sequence of mature E1 was PCR amplified with p1500 as a template using a gene specific primer set (forward, 5'-AAGCTTGCGGGCGGCGGCTATTGGCACACGA-3'; reverse, 5'-CTCGAGTGTCGGTGCCGCGTTGCTTCCGGTA-3') with HindIII/XhoI restriction sites. The resulting PCR product was digested with HindIII and XhoI, and inserted into the prokaryote His-tag expression vector pQEtrisystem (Invitrogen, Valencia, CA, USA) to construct the pTRI/E1 vector. E. coli strain BL21 was used for the production of recombinant protein, and overexpression of the truncated protein was induced according to the manufacturer's instructions. The E1 protein from the sonicated cell extract was primarily purified by TALON metal affinity resin (Clontech, Mountain View, CA, USA) and further separated by electrophoresis on 10% SDS-PAGE. Rabbits were immunized with 100 μg of protein in the first injection with four booster injections at one-week intervals, each with 50 μg of protein. After clearance by centrifugation, the crude serum obtained from the rabbits was used for immunological studies. For antibody titer determination, purified E1protein was separated on 10% SDS gels and blotted onto polyvinylidene fluoride (PVDF) membranes (Bio-Rad, Hercules, CA, USA) with electrophoresis. The blots were incubated with the antibody with a series of dilution, and immunodetection was carried out using alkaline phosphatase conjugated goat anti-rabbit immunoglobulin G.
SDS-PAGE, western blot and zymography
The total soluble protein was extracted from newly matured leaves by the same method as described above for enzyme assay. The protein concentration was determined using Quick Start Bradford Protein Assay (Bio-Rad, Hercules, CA, USA) with BSA as standard according to the instruction manual. The lanes were loaded with 20 μg of proteins per lane was loaded onto 10% polyacrylamide gel and separated by electrophoresis . The protein on the gel was transferred on to PVDF membrane (Bio-Rad, Hercules, CA, USA) with electrophoresis, and probed with rabbit antibodies against purified E1 (1:100,000 dilution) and tobacco Rubisco large subunit independently. Goat anti-rabbit immunoglobulin G conjugated to alkaline phosphatase was used as a second antibody. Color formation was developed by adding 5-bromo-4-chloro-3'-indolyphosphate p-toluidine salt/nitro-blue tetrazolium chloride (BCIP/NBT) substrate solution (Sigma-Aldrich, St. Louis, MO, USA) directly onto the membrane at room temperature.
The assay of E1 activity by a zymogram was performed with leaf soluble protein separated in 10% polyacrylamide gel containing 0.1% CMC according to Chavez et al.  with minor modifications. After electrophoresis, the gel was washed with 50 mM phosphate-buffered saline (pH 5.3) for 30 min, 2.5% triton X-100 for 4 h and incubated at 65°C in 50 mM phosphate-buffered saline for 30 min. The gel was stained in 1% Congo red solution for 15 min at room temperature, and then washed with 1 M NaCl to enable visualization of cleared zones, which correspond to the E1 endoglucanase activity. The amount of E1 protein accumulated in the leaves among transgenic plants was estimated with QuantOne software v4.3.0 (BioRad, Hercules, CA, USA) based on the densitometric determination from the zymogram, where the purified E1 protein at 1 μg, 2 μg and 3 μg per lane were included as standards.
Hydrolysis of rice straw with cultured CGF
Fresh CGF was collected from a local abattoir, quickly strained through four layers of cheesecloth, mixed with AS in a 1:5 ratio (v/v) and incubated statically at 39°C in flasks under anaerobic condition by flushing with CO2 gas. The AS was based on McDougall buffer , which contained 117 mM NaHCO3, 26 mM Na2HPO4 · 12H2O, 8 mM NaCl, 8 mM KCl, 0.2 mM CaCl2, 0.3 mM MgCl2 (pH 8.1). The AS also contained 2% napier grass powder as the sole carbon source. A repeated-batch culture was conducted. After 2 days of incubation, the culture medium was centrifuged (3,200 g, 30 min) and the supernatant was used as inoculums for the next culture. The supernatant of the fifth repeated-batch culture was collected, concentrated five times and stored at -20°C until use. The activities of xylanase, cellulase and avicelase in the concentrated supernatant were analyzed based on the amount of liberated reducing sugars by the 3,5-dinitrosalicylic acid method [57–60]. The concentrated supernatant contained approximately 18 U xylanase per mL, and no cellulase activity was detected. The 200-μL reaction mixture contained the same amount of the concentrated supernatant in buffer pH 8.0 and 1% (w/v) of the corresponding substrates: birch wood xylan for xylanase activity, CMC for CMCase activity, and avicel for avicelase activity. The reactions were incubated at 39°C for 10 min and the amount of reducing sugar was determined by absorbance measurements based on standard curves prepared using the corresponding sugars. One unit was defined as the amount of enzyme liberating 1 μmol of reducing sugar, or the corresponding products, per minute under the assay conditions.
For enzymatic hydrolysis of the rice straw, rice straw was harvested without grains at mature stage and dried in air. The entire straw was milled into fine powder (passed through a 1 mm mesh), and 0.1 g straw sample was mixed with 10 mL AS or 10 mL concentrated supernatant of the cultured CGF, and incubated at 39°C for 1 h, 39°C for 2 h, or 39°C for 1 h plus 81°C for 1 h. Each experiment was repeated three times. The amount of sugars released during 1 h and 2 h incubations was determined using a 3,5-dinitrosalicylic acid method, with D-glucose as standard. A Mixed Sucrose-D-fructose- D-glucose Assay Kit (Megazyme, Wicklow, Ireland) was used for quantification of free glucose, sucrose and fructose, according to the manufacture's instructions.
bovine serum albumin
cow gastric fluid
cellulose hydrolytic enzyme β-1, 4-endoglucanase
- saline-sodium citrate.:
This work was supported in part by funds from the Council of Agriculture (97AS-1.2.1-ST-a2) and National Science Council of Taiwan (NSC 99-ET-415-001-ET). We also thank Yi-Chin Wang and Jiun-Hau Lu for the analysis of reducing sugars. Ziyu Dai was supported by the DOE Office of Biomass. The authors also thank Ms. Kathryn S. Panther of Pacific Northwest National Laboratory (PNNL) for her support in construction of transgene expression vector. PNNL is multiprogram national laboratory operated by Battelle for the DOE under Contract No. DE-AC05-76RLO 1830.
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