- Research article
- Open Access
Overexpression of a rice BAHD acyltransferase gene in switchgrass (Panicum virgatum L.) enhances saccharification
BMC Biotechnology volume 18, Article number: 54 (2018)
Switchgrass (Panicum virgatum L.) is a promising bioenergy feedstock because it can be grown on marginal land and produces abundant biomass. Recalcitrance of the lignocellulosic components of the switchgrass cell wall to enzymatic degradation into simple sugars impedes efficient biofuel production. We previously demonstrated that overexpression of OsAT10, a BAHD acyltransferase gene, enhances saccharification efficiency in rice.
Here we show that overexpression of the rice OsAT10 gene in switchgrass decreased the levels of cell wall-bound ferulic acid (FA) in green leaf tissues and to a lesser extent in senesced tissues, and significantly increased levels of cell wall-bound p-coumaric acid (p-CA) in green leaves but decreased its level in senesced tissues of the T0 plants under greenhouse conditions. The engineered switchgrass lines exhibit an approximate 40% increase in saccharification efficiency in green tissues and a 30% increase in senesced tissues.
Our study demonstrates that overexpression of OsAT10, a rice BAHD acyltransferase gene, enhances saccharification of lignocellulosic biomass in switchgrass.
Bioenergy derived from plant biomass is a renewable energy resource widely used for heat, electricity and transportation fuels . Biofuels have the potential to reduce greenhouse gas emissions by reducing the use of fossil fuels . First generation biofuels (i.e. biodiesel, bioethanol, and biogas) are mainly derived from starch, sugar and vegetable oil. Because these biofuels are produced from food or feed crops, less land is available to produce food, raising concerns about the effects of biofuels on food security. In contrast, second generation biofuels are derived from lignocellulosic feedstocks , most of which are non-food grasses such as Panicum virgatum (switchgrass) and Miscanthus x giganteus, woody plants such as Populus trichocarpa (poplar) and Eucalyptus grandis (eucalyptus), or crop residues such as corn stover .
Switchgrass, a fast-growing perennial C4 grass native to the United States, is considered a prime lignocellulosic feedstock for production of second generation biofuels . Switchgrass is highly tolerant to water-deficit conditions and can be grown at large scale on marginal land. Switchgrass produces abundant lignocellulose, however, this biomass is not easily converted to simple sugars. This recalcitrance is due mainly to the structure of lignocellulose, including cellulose crystallinity, lignin, and lignin-carbohydrate complexes . Knowledge of the genetic basis of cell wall composition and biosynthesis in switchgrass can help advance strategies to improve switchgrass as a bioenergy source.
Diverse approaches have been used to reduce the recalcitrance of plant cell walls. For example, researchers have reduced lignin content, altered lignin composition, structure and distribution in the cell wall [6,7,8], reduced inhibitors derived from biomass , increased the abundance of easily fermentable sugars [10, 11], and manipulated other components of the plant cell wall such as hemicellulose and pectin [12,13,14]. Genes controlling lignin biosynthesis that have been used in switchgrass engineering include 4-coumarate: coenzymeA ligase (4CL) , cinnamyl alcohol dehydrogenase (CAD) , and caffeic acid O-methyltransferase (COMT) [17,18,19]. Transcription factors related to cell wall biosynthesis and modification have also been used to engineer switchgrass, including a WRKY family transcription factor , an ERF gene (PvERF001) , a Knotted1-like gene PvKN1 , two SBP-box-like genes PvSPL1/2 , and a PvMYB4 gene that encodes a general transcriptional repressor of the phenylpropanoid/lignin biosynthesis pathway [24, 25]. Researchers have also engineered switchgrass using microRNAs including miR156/Corngrass1 (Cg1) to improve saccharification efficiency [26, 27].
BAHD acyltransferases utilize CoA thioesters and transfer an acyl group to oxygen and nitrogen molecules of diverse plant metabolites, and are important enzymes in cell wall modifications in grasses . The ‘Mitchell clade’ of BAHD acyltransferases (ATs) is characterized by an expansion in the number of genes and by high gene expression in grasses relative to dicots . Members of the Mitchell clade have been shown to play critical roles in biomass accumulation, cell wall polymer modification, and hydrolysis of lignocellulosic materials in grasses and are thus good candidates in feedstock engineering [28, 30,31,32]. In rice, overexpression of OsAT10 has been used to enhance saccharification . OsAT10 is a putative p-coumaroyl coenzyme A transferase that modifies glucuronoarabinoxylan (GAX) by altering the content of ferulic acid (FA) and p-coumaric acid (p-CA). FA and p-CA are phenylpropanoid-derived hydroxycinnamates (HCAs) that are a distinguishing feature of grass cell walls and other recently evolved commelinid monocots. FA is predominantly esterified to arabinose moieties on GAX in grasses  and p-CA is predominantly esterified to lignin . However, FA has also been found to be incorporated into lignin in comelinids and other species, and p-CA also links to GAX [34, 35]. Feruloyl esters undergo oxidative coupling with neighboring phenylpropanoids on GAX and cause lignin polymerization, which strengthens both primary and secondary cell walls and increases recalcitrance . Overexpression of OsAT10 in rice increases the content of cell wall-bound p-CA and reduces the content of cell wall-bound FA. Biomass extracted from the OsAT10 overexpression lines displayed up to a 40% increase in saccharification efficiency. Introduction of the p-CA monolignol transferases (PMTs) of rice or Brachypodium, another cell wall BAHD acyltransferase, into Arabidopsis and poplar promotes para-coumarylation of lignin and also improves saccharification [31, 37, 38]. These examples demonstrate the importance of the BAHD acyltransferases in modifying cell walls of grasses as well as dicots and illustrate their potentials in feedstock engineering to improve saccharification.
While the positive effect of increasing endogenous OsAT10 expression in the model grass species rice has been studied, it has not been determined if the same approach can be used to improve saccharification in bioenergy grass species. In this study, we overexpressed the rice BAHD acyltransferase gene OsAT10 in switchgrass. One of the two switchgrass lines overexpressing OsAT10 showed no change in plant growth and development. Overexpression of the OsAT10 gene in switchgrass significantly increased in the level of cell wall-bound p-CA in green leaves but decreased its level in senesced tissues, whereas the levels of cell wall-bound FA are decreased in green leaves and to a lesser extent in senesced tissues. The engineered switchgrass lines display 40% and 30% enhanced saccharification efficiency in green and senesced tissues, respectively. Thus, the OsAT10 gene is a valuable target for improving biofuel production in bioenergy feedstocks.
The OsAT10 orthologs are conserved in grasses
To facilitate the transfer of the OsAT10 engineering approach to other putative bioenergy crops, we analyzed OsAT10 orthologs from multiple plant species, including switchgrass, sorghum and maize (Fig. 1). All selected grass species have one OsAT10 ortholog except switchgrass, which has two. The highly-expressed switchgrass orthologs (Pavir.J252500.1) is named as PvAT10 (Additional file 1: Figure S1). PvAT10 and OsAT10 share an 81% identity in their protein sequences (Additional file 2: Figure S2). PvAT10 is highly similar to its putative orthologs in other grass species as well, including Panicum hallii (91% identity), Setaria viridis (91% identity), Sorghum bicolor (84% identity) and Brachypodium distachyon (79% identity). The homolog confidence in P. trichocarpa and E. grandis is low (37% identity), consistent with OsAT10 being commelinid-specific. The PvAT10 and its homologs from other grass species contain a conserved transferase domain. PvAT10 and OsAT10 share an 86% identity in the transferase domain (Additional file 2: Figure S2), suggesting that these two encoded proteins should share similar functions.
Overexpression of OsAT10 in switchgrass
To overexpress OsAT10 in switchgrass, we transformed the wild-type switchgrass line ‘Alamo’ with a construct expressing the OsAT10 gene driven by the maize Ubi1 promoter . We generated two independent transformed lines that possess the transgene (Additional file 3: Figure S3). Quantitative RT-PCR of green leaves revealed that lines FT2 and FT8 express OsAT10 approximately 8- and 6-fold higher, respectively, than the reference ubiquitin gene, while the wild-type plants show no expression of OsAT10 (Fig. 2). Line FT8 displays normal growth and development (Fig. 2); line FT2 is slightly shorter than the wild-type line and shows a slight decrease (14%) of biomass yield (Table 1).
The OsAt10 overexpression lines display alterations in cell wall-bound phenolics in green leaves and to a lesser extent in senesced tissues
The grass cell wall is rich in hydroxycinnamic acids that affect cell wall recalcitrance [36, 39]. We evaluated the amount of FA and p-CA in green leaves of transgenic plants. Levels of cell wall-bound FA and p-CA are altered in alcohol insoluble residue (AIR) samples from green leaves (Fig. 3a and Additional file 4: Figure S4). The transgenic plants show higher levels of p-CA, an 18% increase in FT2 and a 28% increase in FT8. However, levels of FA are reduced in green leaves of transgenic plants- a 21% decrease in FT2 and a 27% decrease in FT8- compared with the wild-type control line (Fig. 3a). In senesced tissues of lines FT2 and FT8, the approximate 15% decrease in p-CA content is statistically significant (p < 0.05) compared with the wild type control. For FA, a statistically significant difference was observed in line FT8 (19% lower) but not in line FT2 (Fig. 3b).
Overexpression of OsAT10 does not alter the xylan sugar substitution pattern in switchgrass
FA and p-CA are important in cell wall polymer modification and can be ester linked to xylan [30, 40]. We used polysaccharide analysis by carbohydrate gel electrophoresis (PACE) to determine the xylan structure of the OsAT10 overexpression switchgrass . For this analysis, AIR samples of two-week-old leaves were prepared and digested with a GH11 xylanase. The digested samples were used to run the PACE gel. Compared to the wild-type line, OsAT10 overexpression lines FT2 and FT8 do not show significant differences in the pattern of xylanase-released oligosaccharides (Fig. 4). The number of fragments and the intensity of each band for lines FT2 and FT8 are similar to those of the wild-type line, indicating that overexpression of OsAT10 had no obvious impact on the xylan sugar substitution pattern in switchgrass.
Overexpression of OsAT10 results in enhanced saccharification
To evaluate the effect of overexpression of OsAT10 on cell wall recalcitrance in switchgrass, we conducted saccharification assays on green leaves and senesced tissues using a hot water pretreatment. Enhanced saccharification was observed in both green leaves and senesced tissues (Fig. 5). In green leaf tissues, lines FT2 and FT8 released 40% and 33% more reducing sugars, respectively, compared to the wild-type line (Fig. 5a). Similarly, approximately 30% more reducing sugars were released from senesced tissues of FT2 and FT8 than the wild-type line (Fig. 5b). These data demonstrate that biomass from the OsAT10 overexpression lines are less recalcitrant to enzymatic digestion, leading to higher sugar yields after saccharification.
In this study, we show that overexpression of a rice BAHD acyltransferase, OsAT10, in switchgrass reduces recalcitrance and enhances biomass saccharification efficiency, demonstrating that OsAT10 functions similarly in rice and switchgrass and that the OsAT10 engineering approach is feasible in switchgrass and possibly in a wide variety of other bioenergy feedstocks as well. Moreover, overexpression of OsAT10 has no or marginal effects on plant growth and development, similar to the observation in the OsAT10 overexpression rice lines . One of the OsAT10 overexpression switchgrass lines (FT8) displays normal plant growth and line FT2 is slightly reduced in biomass yield. The reduced yield observed in line FT2 may be due to somatic variations induced during the transformation process, but not the transgene per se. Nonetheless, the negative effect of the OsAT10 overexpression, if any, is manageable, which indicates the feasible application of OsAT10 to other biofuel feedstocks.
Both the OsAT10 overexpression rice and switchgrass lines show enhanced saccharification. However, different from the rice OsAT10 lines that show a 20% increase in cell wall glucose content, the cell wall composition of the OsAT10 overexpression switchgrass lines is the same as the wild-type line (Additional files 5: Table S1 and Additional file 6: Table S2), indicating that the glucose content is not the major reason for enhanced saccahrification of the engineered switchgrass lines.
The enhanced saccharification of the OsAT10 switchgrass lines is negatively correlated with cell wall-bound FA, consistent with the findings in rice  and a previous study in which overexpression of a transcription factor PvMYB4 reduces cell wall-bound phenolics and enhances saccharification . Different from that observed in the OsAT10 overexpression rice lines in which the levels of p-CA are increased both in the young seedlings and mature plant biomass, the level of p-CA is increased in green leaf tissues but decreased in senesced tissues in the OsAT10 switchgrass lines. However, in all the rice and switchgrass tested, the level of FA is reduced compared to the control lines. Taken all together, cell wall-bound FA rather than p-CA should be the major factor of the biomass recalcitrance.
The improved enzyme accessibility due to the reduced level of cell wall-bound FA could be the major reason for enhanced saccharification of the OsAT10 switchgrass lines. Cell wall-bound FA is an important component of recalcitrance because FA typically forms linkages between cell wall polymers . The reduced level of cell wall-bound FA in the engineered switchgrass lines reduces the association between lignin and polysaccharides such as arabinoxylans, and in turn improves saccharification. Cell wall-bound FA as an important component of recalcitrance is also shown in studies using feruloyl esterases. The feruloyl esterase cleaves the ester linkage between hydroxycinnamoyl substrates and polysaccharides, which enhances the access of hydrolases to the polysaccharide. When added to the enzyme cocktail, feruloyl esterase shows synergy with cellulases, xylanases, pectinases, and accessory enzymes in degrading cell walls and enhancing saccharification . Compromised plant cell wall integrity and disease resistance is associated with decreased levels of polysaccharide feruloylation or cell wall phenolics in several plant species [42,43,44], indicating the importance of cell wall phenolics in maintaining the proper cell wall structure, biotic stress resistance, and recalcitrance. FA and p-CA can be ester linked to xylan [30, 40]. While overexpression of OsAT10 clearly alters the FA and p-CA content in xylan, assays in the current study are not sufficient to explain the mechanism. Moreover, one puzzle is that the BAHD acyltransferases are cytoplasmic but esterification of xylan takes place inside the Golgi . Based on these results, it has been hypothesized that acyltransferases such as OsAT10 transfer the FA or p-CA to a cytoplasmic intermediate, for example a protein or UDP-arabinofuranose [40, 46], but so far such activity has not been demonstrated and needs to be studied in the future.
Overexpression of the rice BAHD acyltransferase gene OsAT10 alters the levels of cell wall-bound FA and p-CA and enhances saccharification with no or minimal negative effects on plant growth, suggesting that this approach may be useful for future engineering of bioenergy feedstocks.
The lowland-type switchgrass (Panicum virgatum L.) cultivar ‘Alamo’  was used in this study. Switchgrass plants were grown and propagated in the greenhouse at the University of California, Davis. The light intensity was maintained at approximately 250 μmol m− 2 s− 1 with the supplement of artificial lights during the winter time and the day/night period was set to 14/10 h. The temperature was ~ 28–30 °C. In this study, biological replicates of the same line were clonally propagated from a single plant and were grown in different pots. When plants were fully senesced (tillers that senesce and become dry after flowering), the R4 stage , 20 tillers from each line, that is, five top tillers per plant and four plants per line, were measured for plant height and dry weight.
Phylogenetic analysis of the OsAT10 orthologs
The predicted protein sequence of OsAT10 (LOC_Os06g39390)  was used to search the protein databases of Arabidopsis thaliana, Brachypodium distachyon, Eucalyptus grandis, Glycine max, Hordeum vulgare, Panicum hallii, Panicum virgatum, Populus trichocarpa, Setaria viridis, Sorghum bicolor, Triticum urartu, and Zea mays at Phytozome (http://jgi.doe.gov/) or Ensembl Plants (http://plants.ensembl.org/index.html) [50, 51]. The identified protein sequences were aligned with the ClustalX2.1 program and the phylogenetic tree was generated using the neighbor-joining (NJ) method with 1000 bootstraps and was visualized using FigTree 1.4.2. The transferase domain of OsAT10 orthologs was identified using the SMART program  and aligned with the ClustalX2.1 program .
Generation of Ubipro: OsAT10 switchgrass lines
The binary vector containing the rice OsAT10 gene under control of the maize Ubiquitin promoter was described in a previous study . For switchgrass transformation, fresh calli were induced from inflorescences of switchgrass and transformed with the OsAT10 construct using Agrobacterium-mediated transformation as described . Regenerated plantlets were rooted in a mixture containing equal volumes of liquid MP media, topsoil, and Sunshine Mix. Hygromycin was used as the selection antibiotic to select putative transgenic lines. Positive transformants were identified using regular PCR with OsAT10-specific primers FT/1F (5′-cgtcgagccgcacaacag-3′) and FT/1R (5′-gatgaggtcgca gttcacca-3′). The positive transgenic lines were then transferred to greenhouses under the conditions described above. Genomic DNA was isolated from young leaves using the CTAB method . The ubiquiin gene was used as the DNA quality control and the primers were Ubi/QF (5′-agaagcgcaagaagaagacg-3′) and Ubi/QR (5′-ccaccttgtagaactggagca-3′). The PCR was conducted on the T100 thermal cycler (Bio-Rad) using the DreamTaq polymerase (Thermo Scientific).
The expression level of the OsAT10 gene in the transgenic switchgrass lines was analyzed using quantitative reverse transcription polymerase chain reaction (qRT-PCR). Green leaves were sampled with liquid nitrogen and stored in a − 80 °C freezer. Total RNAs were isolated with TRIzol (Invitrogen, CA) as described . RNA was treated with DNase I (Ambion) to remove residual DNA. cDNA synthesis was conducted using the high-capacity cDNA reverse transcription kit (Applied BioSystems) following the manufacturer’s instructions. qRT-PCR was performed on a Bio-Rad CFX96 Real-Time System coupled to a C1000 Thermal Cycler (Bio-Rad). The Bio-Rad SsoFast EvaGreen Supermix was used in qRT-PCR reactions. The qRT-PCR condition was set as 40 cycles with denaturation at 95 °C for 5 s and annealing together with amplification at 60 °C for 30 s. The relative quantification of each transcript was calculated using the 2-ΔCT method, normalized to the internal control ubiquitin gene (accession number: FE609298). The results were fromthree biological replicates for the wild-type line, and four biological replicates for each of the FT2 and FT8 lines. Three technical replicates were used for each biological replicate. OsAT10-specific primers used in the qRT-PCR assays were FT/QF (5′-gtacgtgtcggactggagcaa-3′), FT/QR (5′-gacgatcaccgacgagatgag-3′). The ubiquitin-specific primers of switchgrass were Ubi/QF (5′-agaagcgcaagaagaagacg-3′) and Ubi/QR (5′-ccaccttgtagaactggagca-3′).
Cell wall-bound phenolics extraction
Biomass of green leaf tissues was used to measure cell wall-bound phenolics. Green leaf tissues were collected and snap frozen in liquid nitrogen prior to being dried in the lyophilizer (Labconco) at − 80 °C overnight. Dried samples were homogenized with a sample mill and then were ground on a tissue homogenizer in 2-mL polypropylene tubes at 1200 rpm with one stainless-steel ball for four times, 90 s each time. Alcohol insoluble residue (AIR) preparation and the de-starch procedure was conducted as described . Briefly, tissues were processed following instructions described above. Ground tissue (30 mg) was treated with 95% ethanol at 100 °C for 30 min. After the treatment, the supernatant was discarded by centrifugation (10,000 g, 8 min), and the residue was washed three times with 70% ethanol and dried at approximately 35 °C under vacuum. The dried powder obtained after 70% ethanol wash is designated as alcohol insoluble residues (AIR). The dried AIR sample was de-starched with amylase (Novozymes), amyloglucosidase (Megazyme) and pullulanase (Megazyme) as described . De-starched AIR sample (10 mg) was mixed with 500 μL of 2 M NaOH and incubated at 1400 rpm at 30 °C for 24 h. Concentrated HCl (100 μL) was added to the mixture and then subjected to three ethyl acetate partitioning steps. Ethyl acetate fractions were pooled, dried and suspended in 50% methanol for the subsequent LC-MS analysis . Senesced tissues were processed in the same procedure except being dried in the oven. The numbers of biological replicates of green leaf tissues of lines WT, FT2 and FT8 are 3, 4, and 4, respectively. The numbers of biological replicates of senesced tissues for lines WT, FT2 and FT8 are 4, 5, and 5, respectively. No technical replicates were used in the assays.
Polysaccharide analysis by carbohydrate gel electrophoresis (PACE)
PACE was performed as described . Briefly, 100 μg AIR of each sample was pre-treated with 4 M NaOH (20 μl) for 1 h at 21 °C. Following neutralization with 1 M HCl, each sample was suspended in a final concentration of 100 mM ammonium acetate, pH 6.0 (500 μl). Samples were hydrolyzed to completion with 10 μl (8.5 mg/mL) CAZy (www.cazy.org) GH11 family endo-β-1, 4-xylanase (Prozomix) from Neocallimastix patricarium (accession number: CAA46498). The released oligosaccharides, along with appropriate controls and xylo-oligosaccharide standards (Megazyme) were dried in vacuuo, and were reductively aminated with 8-aminonaphthalene-1, 3, 6-trisulfonic acid (ANTS; Invitrogen, www.life technologies.com) as follows: to each tube was added 5 μl of 0.2 M ANTS solution (resuspended in 17:3, water: acetic acid) and 5 μl of 0.2 M 2-picoline borane (Sigma, resuspended in DMSO). Samples were incubated overnight in the dark in a 37 °C waterbath, then dried in vacuuo and resuspended in 100 μl of 3 M urea. The samples (2 μl) were analyzed by separation on large format Tris-borate acrylamide gel prepared as described . The PACE gels were visualized with a G-box (Syngene, www.syngene.com) equipped with a UV detection filter and long-wave UV tubes (365 nm emission). Experiments were performed on three biological replicates of the wild-type line and four biological replicates for each of the FT2 and FT8 lines and a representative gel was shown.
Compositional analysis of switchgrass lines was conducted according to the NREL acidolysis protocol (LAP) LAP-002 [58, 59]. Fully senecesed tissues were used. Three biological replicates for each of the wild-type and FT8 lines and four biological replicates for line FT2 were used in the assay. Homogenized switchgrass biomass (100 mg) and 1 mL of 72% H2SO4 were incubated in a shaker at 300 rpm and 30 °C for 1 h. The sample was diluted to 4% H2SO4 by adding 28 mL distilled water and autoclaved at 121 °C for 1 h. After autoclaving, the sample was placed in ice to quench the reaction and was filtered. The filtrate was used to measure the carbohydrate concentration on an Agilent HPLC 1200 Series equipped with a Bio-Rad Aminex HPX-87H column and a Refractive Index detector. A 4 mM H2SO4 solution was used as the mobile phase in running the machine at the speed of 0.6 mL min− 1. The column temperature was set at 60 °C. The injection volume was 20 μL with a run time of 25 min. The solid part was heated at 105 °C overnight to measure the combined weight of lignin and ash.
Monosaccharide composition analysis
Senesced switchgrass tissues, three biological replicates per line, were used in the monosaccharide composition analysis. De-starched AIR (10 mg) was hydrolyzed with 2 M Trifluoroacetic acid (TFA) at 121 °C for 1 h. The hydrolysate was dried in a CentriVap at 32 °C overnight and then dissolved in water. The dissolved hydrolysate was filtered through a 0.45 μm PVDF filter and the filtrate was analyzed by high-performance anion-exchange chromatography with pulsed amperometric detection (HPAEC-PAD) on a Dionex ICS-3000 system with the CarboPac PA20 column (3 × 150 mm) .
Cell wall pretreatments and saccharification
Liquid hot water pretreatment was used in the saccharification assay . Water (340 μL) was added to 10 mg de-starched AIR samples made from senesced tissues and green leaves as previously described . The biomass mixture was shaken at 1400 rpm at 30 °C for 30 min and autoclaved at 120 °C for 1 h. In saccharification, pretreated biomass was hydrolyzed with 650 μL of 100 mM sodium citrate buffer pH 5 containing 80 μg/mL tetracycline and 1% w/w Cellic CTec2 enzyme mixture (Novozymes), which contains cellulases, β-glucosidases, and hemicellulases. After incubation at 50 °C with shaking (800 rpm) for 95 h, samples were centrifuged at 20000 g for 3 min and 10 μL of the supernatant was used for measurement of reducing sugars using the 3,5-dinitrosalicylic acid (DNS) assay . The absorbance of the samples was measured in a spectrophotometer at 540 nm. Glucose solutions were used for the standard curve. The number of biological replicates and technical replicates for each line was the same as the one for the assay of cell wall-bound phenolics.
4-Coumarate: coenzymeA ligase
Alcohol insoluble residue
The initials of the first four biochemically characterized enzymes in this class, benzylalcohol O-acetyltransferase (BEAT), anthocyanin O-hydroxycinnamoyltransferase (AHCT), anthranilate N-hydroxycinnamoyl/benzoyltransferase (HCBT) and deacetylvindoline 4-O-acetyltransferase (DAT)
Cinnamyl alcohol dehydrogenase
Caffeic acid O-methyltransferase
Polysaccharide analysis by carbohydrate gel electrophoresis
Quantitative reverse transcription polymerase chain reaction
Yuan JS, Tiller KH, Al-Ahmad H, Stewart NR, Stewart CN Jr. Plants to power: bioenergy to fuel the future. Trends Plant Sci. 2008;13:421–9.
Wang M, Hong MW, Huo H. Life-cycle energy and greenhouse gas emission impacts of different corn ethanol plant types. Environ Res Lett. 2007;2:024001.
Vega-Sanchez ME, Ronald PC. Genetic and biotechnological approaches for biofuel crop improvement. Curr Opin Biotechnol. 2010;21:218–24.
David K, Ragauskas AJ. Switchgrass as an energy crop for biofuel production: a review of its lignocellulosic chemical properties. Energy Environ Sci. 2010;3(9):1182–90.
McCann MC, Carpita NC. Biomass recalcitrance: a multi-scale, multi-factor, and conversion-specific property. J Exp Bot. 2015;66:4109–18.
Wang P, Dudareva N, Morgan JA, Chapple C. Genetic manipulation of lignocellulosic biomass for bioenergy. Curr Opin Chem Biol. 2015;29:32–9.
Zhao Q. Lignification: flexibility biosynthesis and regulation. Trends Plant Sci. 2016;21(8):713–21.
Chen F, Dixon RA. Lignin modification improves fermentable sugar yields for biofuel production. Nat Biotechnol. 2007;25:759–61.
Eudes A, Sathitsuksanoh N, Baidoo EE, George A, Liang Y, Yang F, Singh S, Keasling JD, Simmons BA, Loque D. Expression of a bacterial 3-dehydroshikimate dehydratase reduces lignin content and improves biomass saccharification efficiency. Plant Biotechnol J. 2015;13:1241–50.
Vega-Sanchez ME, Loque D, Lao J, Catena M, Verhertbruggen Y, Herter T, Yang F, Harholt J, Ebert B, Baidoo EE, et al. Engineering temporal accumulation of a low recalcitrance polysaccharide leads to increased C6 sugar content in plant cell walls. Plant Biotechnol J. 2015;13:903–14.
Loque D, Scheller HV, Pauly M. Engineering of plant cell walls for enhanced biofuel production. Curr Opin Plant Biol. 2015;25:151–61.
Lee C, Teng Q, Huang W, Zhong R, Ye ZH. Down-regulation of PoGT47C expression in poplar results in a reduced glucuronoxylan content and an increased wood digestibility by cellulase. Plant Cell Physiol. 2009;50:1075–89.
Chiniquy D, Sharma V, Schultink A, Baidoo EE, Rautengarten C, Cheng K, Carroll A, Ulvskov P, Harholt J, Keasling JD, et al. XAX1 from glycosyltransferase family 61 mediates xylosyltransfer to rice xylan. Proc Natl Acad Sci U S A. 2012;109:17117–22.
Biswal AK, Atmodjo MA, Li M, Baxter HL, Yoo CG, Pu Y, Lee YC, Mazarei M, Black IM, Ji-Yi Zhang JY, et al. Sugar release and growth of biofuel crops are improved by downregulation of pectin biosynthesis. Nature Biotech. 2018;36:249–57.
Xu B, Escamilla-Trevino LL, Sathitsuksanoh N, Shen Z, Shen H, Zhang YH, Dixon RA, Zhao B. Silencing of 4-coumarate:coenzyme a ligase in switchgrass leads to reduced lignin content and improved fermentable sugar yields for biofuel production. New Phytol. 2011;192:611–25.
Saathoff AJ, Sarath G, Chow EK, Dien BS, Tobias CM. Downregulation of cinnamyl-alcohol dehydrogenase in switchgrass by RNA silencing results in enhanced glucose release after cellulase treatment. PLoS One. 2011;6:e16416.
Fu C, Mielenz JR, Xiao X, Ge Y, Hamilton CY, Rodriguez M Jr, Chen F, Foston M, Ragauskas A, Bouton J, et al. Genetic manipulation of lignin reduces recalcitrance and improves ethanol production from switchgrass. Proc Natl Acad Sci U S A. 2011;108:3803–8.
Baxter HL, Mazarei M, Labbe N, Kline LM, Cheng Q, Windham MT, Mann DG, Fu C, Ziebell A, Sykes RW, et al. Two-year field analysis of reduced recalcitrance transgenic switchgrass. Plant Biotechnol J. 2014;12:914–24.
Shen H, Mazarei M, Hisano H, Escamilla-Trevino L, Fu C, Pu Y, Rudis MR, Tang Y, Xiao X, Jackson L, et al. A genomics approach to deciphering lignin biosynthesis in switchgrass. Plant Cell. 2013;25:4342–61.
Gallego-Giraldo L, Shadle G, Shen H, Barros-Rios J, Fresquet Corrales S, Wang H, Dixon RA. Combining enhanced biomass density with reduced lignin level for improved forage quality. Plant Biotechnol J. 2016;14:895–904.
Wuddineh WA, Mazarei M, Turner GB, Sykes RW, Decker SR, Davis MF, Stewart CN Jr. Identification and molecular characterization of the switchgrass AP2/ERF transcription factor superfamily, and overexpression of PvERF001 for improvement of biomass characteristics for biofuel. Front Bioeng Biotechnol. 2015;3:101.
Wuddineh WA, Mazarei M, Zhang JY, Turner GB, Sykes RW, Decker SR, Davis MF, Udvardi MK, Stewart CN Jr. Identification and overexpression of a Knotted1-like transcription factor in switchgrass (Panicum virgatum L.) for lignocellulosic feedstock improvement. Front Plant Sci. 2016;7:520.
Wu Z, Cao Y, Yang R, Qi T, Hang Y, Lin H, Zhou G, Wang ZY, Fu C. Switchgrass SBP-box transcription factors PvSPL1 and 2 function redundantly to initiate side tillers and affect biomass yield of energy crop. Biotechnol Biofuels. 2016;9:101.
Baxter HL, Poovaiah CR, Yee KL, Mazarei M, Rodriguez M, Thompson OA, Shen H, Turner GB, Decker SR, Sykes RW, et al. Field evaluation of transgenic switchgrass plants overexpressing PvMYB4 for reduced biomass recalcitrance. Bioenergy Res. 2015;8:910–21.
Shen H, Poovaiah CR, Ziebell A, Tschaplinski TJ, Pattathil S, Gjersing E, Engle NL, Katahira R, Pu Y, Sykes R, et al. Enhanced characteristics of genetically modified switchgrass (Panicum virgatum L.) for high biofuel production. Biotechnol Biofuels. 2013;6:71.
Chuck GS, Tobias C, Sun L, Kraemer F, Li CL, Dibble D, Arora R, Bragg JN, Vogel JP, Singh S, et al. Overexpression of the maize Corngrass1 microRNA prevents flowering, improves digestibility, and increases starch content of switchgrass. Proc Natl Acad Sci U S A. 2011;108:17550–5.
Fu C, Sunkar R, Zhou C, Shen H, Zhang JY, Matts J, Wolf J, Mann DG, Stewart CN Jr, Tang Y, Wang ZY. Overexpression of miR156 in switchgrass (Panicum virgatum L.) results in various morphological alterations and leads to improved biomass production. Plant Biotechnol J. 2012;10:443–52.
Bontpart T, Cheynier V, Ageorges A, Terrier N. BAHD or SCPL acyltransferase? What a dilemma for acylation in the world of plant phenolic compounds. New Phytol. 2015;208:695–707.
Mitchell RA, Dupree P, Shewry PR. A novel bioinformatics approach identifies candidate genes for the synthesis and feruloylation of arabinoxylan. Plant Physiol. 2007;144:43–53.
Bartley LE, Peck ML, Kim SR, Ebert B, Manisseri C, Chiniquy DM, Sykes R, Gao L, Rautengarten C, Vega-Sanchez ME, et al. Overexpression of a BAHD acyltransferase, OsAt10, alters rice cell wall hydroxycinnamic acid content and saccharification. Plant Physiol. 2013;161:1615–33.
Petrik DL, Karlen SD, Cass CL, Padmakshan D, Lu F, Liu S, Le Bris P, Antelme S, Santoro N, Wilkerson CG, et al. P-Coumaroyl-CoA:monolignol transferase (PMT) acts specifically in the lignin biosynthetic pathway in Brachypodium distachyon. Plant J. 2014;77:713–26.
Withers S, Lu F, Kim H, Zhu Y, Ralph J, Wilkerson CG. Identification of grass-specific enzyme that acylates monolignols with p-coumarate. J Biol Chem. 2012;287:8347–55.
Ralph J. Hydroxycinnamates in lignification. Phytochem Rev. 2010;9:19.
Mueller-Harvey I, Hartley RD, Harris PJ, Curzon EH. Linkage of p-coumaroyl and feruloyl groups to cell-wall polysaccharides of barley straw. Carbohydr Res. 1986;148:71–85.
Karlen SD, Zhang C, Peck ML, Smith RA, Padmakshan D, Helmich KE, Free HC, Lee S, Smith BG, Lu F, et al. Monolignol ferulate conjugates are naturally incorporated into plant lignins. Sci Adv. 2016;2:e1600393.
de O Buanafina MM. Feruloylation in grasses: current and future perspectives. Mol Plant. 2009;2:861–72.
Smith RA, Gonzales-Vigil E, Karlen SD, Park JY, Lu F, Wilkerson CG, Samuels L, Ralph J, Mansfield SD. Engineering monolignol p-coumarate conjugates into poplar and Arabidopsis lignins. Plant Physiol. 2015;169:2992–3001.
Sibout R, Le Bris P, Legee F, Cezard L, Renault H, Lapierre C. Structural redesigning Arabidopsis lignins into alkali-soluble lignins through the expression of p-coumaroyl-CoA:monolignol transferase (PMT). Plant Physiol. 2016;170(3):1358-66.
Vogel J. Unique aspects of the grass cell wall. Curr Opin Plant Biol. 2008;11:301–7.
de Oliveira DM, Finger-Teixeira A, Rodrigues Mota T, Salvador VH, Moreira-Vilar FC, Correa Molinari HB, Craig Mitchell RA, Marchiosi R, Ferrarese-Filho O, Dantas dos Santos W. Ferulic acid: a key component in grass lignocellulose recalcitrance to hydrolysis. Plant Biotechnol J. 2015;13:1224–32.
Mortimer JC, Faria-Blanc N, Yu X, Tryfona T, Sorieul M, Ng YZ, Zhang Z, Stott K, Anders N, Dupree P. An unusual xylan in Arabidopsis primary cell walls is synthesised by GUX3, IRX9L IRX10L and IRX14. Plant J. 2015;83:413–26.
Reem NT, Pogorelko G, Lionetti V, Chambers L, Held MA, Bellincampi D, Zabotina OA. Decreased polysaccharide Feruloylation compromises plant Cell Wall integrity and increases susceptibility to Necrotrophic fungal pathogens. Front Plant Sci. 2016;7:630.
Santiago R, Reid LM, Arnason JT, Zhu X, Martinez N, Malvar RA. Phenolics in maize genotypes differing in susceptibility toGibberellaStalk rot (Fusarium graminearumSchwabe). J Agric Food Chem. 2007;55:5186–93.
Buanafina MMO, Fescemyer HW. Modification of esterified cell wall phenolics increases vulnerability of tall fescue to herbivory by the fall armyworm. Planta. 2012;236:513–23.
Rennie EA, Scheller HV. Xylan biosynthesis. Curr Opin Biotechnol. 2014;26:100–7.
Scheller HV, Ulvskov P. Hemicelluloses. Annu Rev Plant Biol. 2010;61:263–89.
Liu Y, Zhang X, Tran H, Shan L, Kim J, Childs K, Ervin EH, Frazier T, Zhao B. Assessment of drought tolerance of 49 switchgrass (Panicum virgatum) genotypes using physiological and morphological parameters. Biotechnol Biofuels. 2015;8:152.
Hardin CF, Fu C, Hisano H, Xiao X, Shen H, Stewart CN Jr, Parrott W, Dixon RA, Wang ZY. Standardization of Switchgrass sample collection for Cell Wall and biomass trait analysis. Bioenerg Res. 2013;6:755–62.
Kawahara Y, de la Bastide M, Hamilton JP, Kanamori H, McCombie WR, Ouyang S, Schwartz DC, Tanaka T, Wu J, Zhou S, et al. Improvement of the Oryza sativa Nipponbare reference genome using next generation sequence and optical map data. Rice (N Y). 2013;6:4.
Goodstein DM, Shu S, Howson R, Neupane R, Hayes RD, Fazo J, Mitros T, Dirks W, Hellsten U, Putnam N, Rokhsar DS. Phytozome: a comparative platform for green plant genomics. Nucleic Acids Res. 2012;40:D1178–86.
Kersey PJ, Allen JE, Armean I, Boddu S, Bolt BJ, Carvalho-Silva D, Christensen M, Davis P, Falin LJ, Grabmueller C, et al. Ensembl Genomes 2016: more genomes more complexity. Nucleic Acids Res. 2016;44:D574–80.
Letunic I, Doerks T, Bork P. SMART: recent updates, new developments and status in 2015. Nucleic Acids Res. 2015;43:D257–60.
Larkin MA, Blackshields G, Brown NP, Chenna R, McGettigan PA, McWilliam H, Valentin F, Wallace IM, Wilm A, Lopez R, et al. Clustal W and Clustal X version 2.0. Bioinformatics. 2007;23:2947–8.
Li RY, Qu RD. High throughput Agrobacterium-mediated switchgrass transformation. Biomass Bioenergy. 2011;35:1046–54.
Li G, Chern M, Jain R, Martin JA, Schackwitz WS, Jiang L, Vega-Sanchez ME, Lipzen AM, Barry KW, Schmutz J, Ronald PC. Genome-wide sequencing of 41 Rice (Oryza sativa L.) mutated lines reveals diverse mutations induced by fast-neutron irradiation. Mol Plant. 2016;9:1078–81.
Chern M, Bai W, Ruan D, Oh T, Chen X, Ronald PC. Interaction specificity and coexpression of rice NPR1 homologs 1 and 3 (NH1 and NH3), TGA transcription factors and negative regulator of resistance (NRR) proteins. BMC Genomics. 2014;15:461.
Goubet F, Jackson P, Deery MJ, Dupree P. Polysaccharide analysis using carbohydrate gel electrophoresis: a method to study plant cell wall polysaccharides and polysaccharide hydrolases. Anal Biochem. 2002;300:53–68.
Sluiter A: National Renewable Energy Laboratory (NREL) analytical procedures. 2004.
Parthasarathi R, Sun J, Dutta T, Sun N, Pattathil S, Murthy Konda NV, Peralta AG, Simmons BA, Singh S. Activation of lignocellulosic biomass for higher sugar yields using aqueous ionic liquid at low severity process conditions. Biotechnol Biofuels. 2016;9:160.
J OB, Harholt J, Scheller HV, Orfila C. Rhamnogalacturonan I in Solanum tuberosum tubers contains complex arabinogalactan structures. Phytochemistry. 2004;65:1429–38.
Miller GL. Use of dinitrosalicylic acid reagent for determination of reducing sugar. Anal Chem. 1959;31:426–8.
The authors thank Maria E. Hernandez, Sasha Yogiswara, Rick A. Rios, Ning Sun, and Miguel E. Vega-Sánchez for plant maintenance and assistance in saccharification assays, and Drs. Catherine Nelson and Brittany Anderton for critical reading of the manuscript. We are grateful for Novozymes for providing Cellic CTec2. We thank the Joint Genome Institute (JGI) for sharing the switchgrass genome (https://phytozome.jgi.doe.gov/pz/portal.html).
This work was part of the DOE Joint BioEnergy Institute (http://www.jbei.org) supported by the U. S. Department of Energy, Office of Science, Office of Biological and Environmental Research, through contract DE-AC02-05CH11231 between Lawrence Berkeley National Laboratory and the U. S. Department of Energy. Work at OU was funded through the DOE Feedstock Genomics program (DOE BER Office of Science DE-SC006904). The United States Government retains and the publisher, by accepting the article for publication, acknowledges that the United States Government retains a non-exclusive, paid-up, irrevocable, world-wide license to publish or reproduce the published form of this manuscript, or allow others to do so, for United States Government purposes.
Availability of data and materials
The authors ensure the availability of supporting data and materials.
Ethics approval and consent to participate
Consent for publication
The authors have consented for publication.
DL and HVS have financial conflict of interests in Afingen. PCR, LEB and HVS have intellectual property related to the research.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Additional file 1:
Figure S1. Gene expression levels of the two PvAT10 genes from different switchgrass tissues. (DOCX 68 kb)
Additional file 2:
Figure S2. Sequence alignment of the acyl transferase domain from OsAT10 orthologs of selected grasses. (DOCX 629 kb)
Additional file 3:
Figure S3. Analysis of the OsAT10 transgene in switchgrass lines. (DOCX 33 kb)
Additional file 4:
Figure S4. Representative LC-MS chromatograms of p-coumarate (a, b) and ferulate (c, d) obtained from a plant extract (a, c) and authentic standards (b, d). (DOCX 59 kb)
Additional file 5:
Table S1. Compositional analysis of senesced tissues of the wild-type and OsAT10 overexpression switchgrass lines. (DOCX 20 kb)
Additional file 6:
Table S2. Cell wall monosaccharide composition of senesced switchgrass tissues. (DOCX 21 kb)
Rights and permissions
Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
About this article
Cite this article
Li, G., Jones, K.C., Eudes, A. et al. Overexpression of a rice BAHD acyltransferase gene in switchgrass (Panicum virgatum L.) enhances saccharification. BMC Biotechnol 18, 54 (2018). https://doi.org/10.1186/s12896-018-0464-8
- Ferulic acid
- p-coumaric acid