- Original article
- Open Access
Cloning and characterization of the lignin biosynthesis genes NcCSE and NcHCT from Neolamarckia cadamba
AMB Express volume 9, Article number: 152 (2019)
Neolamarckia cadamba is an important fast growing tree species used for pulping and wood material in industry for it’s desirable wood properties. As one of the most important content in wood, lignin provides structural integrity, strength, and hydrophobicity to the thickened cell walls and is the major factor contributing to biomass recalcitrance. It does not reduce the palatability of forage grass for animals, but it hinders the isolation of cellulose fibers and the efficient enzymatic depolymerization of cellulose and hemicellulose into fermentable sugars in biorefining processes by limiting the access by hydrolytic enzymes to their polysaccharide substrates. This work focused on analyzing the functions of NcCSE (Caffeoyl Shikimate Esterase, GenBank accession number: MG739672) and NcHCT (Hydroxycinnamoyl Transferase,GenBank accession number: MG739673) in the lignin biosynthetic process in order to improve the potential for utilization of leaves and wood from N. cadamba. The mutant phenotype of cse-2 was dramatically complemented to WT in the stable transgenic lines cse-35S::NcCSE, but overexpression of NcHCT in the cse-2 mutant did not have the same result as cse-35S::NcCSE, providing only partial complementation.
Neolamarckia cadamba (Rubiaceae, Anthocephalus) is a tropical evergreen tree species with a natively distribution in South and Southeast Asia. It is famous for its fast growing and perfect trunk, which can reach a height of 45 m with a DBH (diameter at breast height) of 100–160 cm (Krisnawati et al. 2011). It is excellent for use in building, furniture fabrication and papermaking. Moreover, it is characterized by an abundance of alkaloids in the leaves and bark, such as cadambine and dihydroconchonine, which can be used as treatments for several diseases like fever, anemia, diabetes, tumors, and have been studied for more than 100 years (Dwevedi et al. 2015). In our previous research, we found that the leaves of N. cadamba contained an abundance of protein and fat, and the compositional parameter index as a forage is even better than that of the common forage species Alfalfa (Medicago sativa Linn) (Additional file 1: Table S1), so it is also good as a woody forage plant.
The plant cell wall, which is the most abundant renewable energy in nature, the main component of plant biomass and essential mechanical support for the plant, is a complex matrix of several different polymers enclosing the plasma membrane, maintaining cell shape and protecting the cell (Hückelhoven 2007). The major components making up the framework of the cell wall are cellulose organized into microfibrils, hemicelluloses and lignin filling the space between the microfibrils (Salmén 2015; Adel et al. 2016). Of these compounds, lignin is the major factor limiting the digestibility of forage dry matter, the conversion of lignocellulosic biomass to fermentable sugars, and the effectiveness of pulping in papermaking (Powell et al. 2017; Zeng et al. 2014; Constant et al. 2016).
Lignin is a complex polymer made from different kinds of monomeric subunits linked via ether bonds or carbon–carbon bonds, and the most abundant of these units are guaiacyl (G), syringyl (S), and p-hydroxyphenyl (H) groups (Shuai et al. 2016). Lignin is synthesized via shikimate through the general phenylpropanoid pathway and a monolignol-specific pathway, which include 10 well-known enzymes (PAL, phenylalanine ammonia-lyase; C4H, cinnamate 4-hydroxylase; 4CL, 4-coumarate: CoA ligase; HCT, p-hydroxycinnamoyl-CoA: quinate shikimate p-hydroxycinnamoyltransferase; C3H, p-coumarate 3-hydroxylase; CCoAOMT, caffeoyl-CoA O-methyltransferase; CCR, cinnamoyl-CoA reductase; F5H, ferulate 5-hydroxylase; COMT, caffeic acid O-methyltransferase; CAD, cinnamyl alcohol dehydrogenase) (Boerjan et al. 2003; Vanholme et al. 2010; Ouyang et al. 2016), and a more recently identified enzyme, CSE (Caffeoyl shikimate esterase), which also participates in this process (Vanholme et al. 2013). Many studies have identified the role of the first 10 enzymes in lignin biosynthesis process, and the model of lignin biosynthesis based on these 10 enzymes has been accepted for more than 10 years. However, for the new member, more work needs to be done in order to verify its position in lignin biosynthesis. It is believed that CSE and HCT may have a similar function in this biosynthetic process, as both of them can hydrolyze caffeoyl shikimate, a well-known intermediate in lignin biosynthesis, to produce caffeic acid or caffeoyl-CoA (Vanholme et al. 2013). In Saleme’s study, down-regulation of CSE in hybrid poplar result in a reduced lignin deposition and relatively higher cellulose content (Saleme et al. 2017). But, the relation of CSE and HCT is not mentioned. In this study, we are trying to determine the functions and relationship of NcCSE and NcHCT in the process of lignin biosynthesis and there potential influence in biomass accumulation, cell wall deposition, lignin per percentage and composition by heterologous express the NcCSE and NcHCT in Arabidopsis cse-2 mutant and wild type plant. We find that NcCSE can fully complement ate the cse-2 while NcHCT can only providing partial complementation.
Materials and methods
Plant materials and growth conditions
Neolamarckia cadamba plants were cultivated in an open field in 5-l pots for 2 years, and A. thaliana was cultivated in a growth chamber at a light intensity of 150 µM m2/s under a 16 h light/8 h dark photoperiod and a temperature setting of 22 ± 1 °C light/20 ± 1 °C dark with 80% humidity. All the plants were generated from seed. N. cadamba seeds were collected from Guangzhou, China, and A. thaliana mutant seeds were ordered from ABRC. In this study, the cse-2 (SALK_023077) T-DNA insertion mutant and Col-0 wild type Arabidopsis were used. The insertion locus of the cse-2 is shown in Additional file 1: Fig. S1.
Gene cloning and vector construction
According to our previous RNA-sequence analysis, based on the A. thaliana AtCSE (AT1G52760) sequence, NcCSE and NcHCT were identified from our RNA-seq database (NCBI BioProject Accession: PRJNA232616) through blastx homology searching (The e-value cut-off is 1e-10, those with the highest homology were chose). These two genes were amplified by nested PCR, firstly using the gene specific primer pair N1, then the PCR product was used as the template for amplification with the gene specific primer pair N2 which contained the attB1 and attB2 adapter at the 5′ end for NcCSE and NcHCT respectively. All primers used in this study are listed in Additional file 1: Table S2. The product was subcloned with a BP reaction (Gateway cloning) into the pDONR221 vector after purification. Sequence identity was confirmed by sequencing and the fragment was subsequently introduced into the pEarley100 vector by means of LR Clonase (Invitrogen, USA). In the final construct, expression of the gene was driven by a CaMV 35S promoter with a basta-resistance (bar) gene as plant selection marker. Two vectors, 35S::NcCSE and 35S::NcHCT, were constructed in this study and transferred into Agrobacterium tumefaciens strain GV3101.
Generation of transgenic Arabidopsis
The floral dip method was used for cse mutant transformation (Zhang et al. 2006). Two different transgenic plant lines, cse-35S::NcCSE and cse-35S::NcHCT, were generated and the seeds of each transformed T0 line were harvested after maturation. The herbicide basta (glufosinate ammonium) was used for screening the positive transgenic plants. For each transformation, three independent homozygous transgenic lines were used for experimentation, after selfing for two generations and genotyping.
Co-expression analysis of lignin biosynthesis genes
To investigate the expression profile of genes related to lignin biosynthesis, especially genes related to AtCSE, in both wild type and transgenic plants, co-expression analysis basedon the Topology Overlap Matrix (WGCNA) was used to identify those genes. Microarray data downloaded from GEO (https://www.ncbi.nlm.nih.gov/geo/) consisted of 53 stem samples in 7 datasets, GSE53580 (GSM1296372-GSM1296383), GSE5633 (GSM131643-GSM131645, GSM131655-GSM131660), GSE6151 (GSM142623-GSM142625, GSM142629-GSM142631, GSM142635-GSM142637), GSE23801 (GSM587036, GSM587037), GSE24763 (GSM609886-GSM609891), GSE24781 (GSM610374-GSM610385), GSE2848 (GSM62697, GSM62701, GSM62705), and the raw data were normalized with the Robust Multichip Average (RMA) normalization protocol. The fifteen genes showing the strongest relationship with AtCSE, five lignin biosynthesis genes sharing co-expression with AtCSE, and six cellulose biosynthesis genes that also showed strong correlation with AtCSE were selected for qRT-PCR analysis.
Phenotype analysis of T3 generation transgenic plants
Hypocotyl length was measured by ImageJ (https://imagej.net/) on the 7th day and 14th day after planting under the culture conditions described above; leaf area was measured by ImageJ on the 21st day, with the mean area of the 4th, 5th and 6th true leaves representing the leaf area;, and at the same time the number of rosette leaves was counted for each plant. The rosette leaf biomass was measured on the 35th day after oven drying at 40 °C, and the plant height and dry above ground biomass were measured on the 50th day. The stem thickness was expressed as the cross sectional area of the main stem at 3–4 mm above ground level on the 50th day, which was embedded in 3% (W/V) agar and cut using a LeicaVT1000S vibratome equipped with a razor blade. The stem sections were observed under an Olympus BX43F light microscope and measured with ImageJ.
RNA extraction and quantitative Real-Time PCR (qRT-PCR)
Neolamarckia cadamba total RNA was extracted with a protocol using CTAB plus an OMEGA Plant RNA Isolation Kit (Ouyang et al. 2014); A. thaliana total RNA was extracted with an OMEGA Plant RNA Isolation Kit alone (Omega Bio-Tek, Doraville, CA) following the manufacturer’s instructions. First-strand cDNA was synthesized from 1 μg RNA with Prime Script™ RT Master Mix (Takara, Japan) according to the manufacturer’s instructions. The cDNA was diluted with a 14-fold volume of ddH2O for use as the template in qRT-PCR. SYBR Premix Ex Taq™ Kit (Takara, Japan) was used in the qRT-PCR, and the amplification conditions were as follows: initial denaturation at 95 °C for 30 s, amplification and quantification at 95 °C for 5 s, 58 °C for 30 s, and 72 °C for 15 s for 40 cycles (with a single fluorescence measurement), and an indefinite hold at 10 °C. After the final PCR cycle, a melting curve program was performed to determine the specificity of the PCR products by heating from 65 to 95 °C with a heating rate of 0.1 °C/s and continuous fluorescence measurement. The primers used for qRT-PCR are listed in Additional file 1: Table S3; the N. cadamba gene Cyclophilin (JX902587) and the A. thaliana gene PP2AA3 (AT1G13320) were included as internal references. The relative levels of expression of the two genes NcCSE and NcHCT in the basal, middle and apical stem segments of N. cadamba were analyzed by qRT-PCR. All of the 26 genes selected by co-expression analysis in A. thaliana were analyzed by qRT-PCR in the basal stem (1st and 2st internode) on the 7th day after bolting and in rosette leaves on the 21st day after germination.
Microscopic evaluation and visualizing of lignin content by histochemical staining
The stem of 1 cm above the cotyledonary node were embedded and cut using a LeicaVT1000S vibratome as described above or fixed with FAA (formaldehyde:glacial acetic acid:70% ethanol [1:1:18]), embedded in paraffin and cut with a rotary slicer (RM 2235, LEICA, Germany). Safranin and fast green staining was used to differentiate lignified and non-lignified tissues (Mason 1961). Lignin and cellulose are stained from red to pink and blue to green respectively, depending on their content, and the lignin content can be roughly determined after staining.
Cell wall characterization and lignin composition
Determination of lignin content was based on the protocol of Ververis with minor modifications (Ververis et al. 2007). The samples were dried at 40 °C, and ground to a fine powder. Then each sample (1.000 ± 0.050 g powder; W1) was incubated in 10 ml 72% (v/v) H2SO4 solution at 100 °C for 5 h to degrade the cellulose and hemi-cellulose, and filtered through a sintered glass crucible. The solid residue (W2) obtained after drying at 105 °C for 24 h was heated at 600 °C for 5 h and the weight of the residue (W3) after cooling down was measured. The acid insoluble lignin content (%) is given by (W2–W3)/W1.
To calculate the weight of the cell wall residue (CWR), about 2 g (W4) of the powder described above was extracted sequentially with water, ethanol, chloroform, and acetone to obtain the residue (weight W5) after drying at 40 °C, and CWR (%) was calculated as W5/W4. The content of cellulose is determined totally follow the method descript by Ouyang (Ouyang et al. 2013).
Wiesner’s staining combined with Maule’s reagent was used for roughly determining the S/G lignin composition ratio (Lewis and Yamamoto 1990; Guo et al. 2001; Trabucco et al. 2013). However, lignin monomer composition was more accurately quantified by Gas Chromatography (HP 5890 series II Plus GC Systems) according to a protocol for analysis of DFRC monomers (20 mg stem CWR samples for each measurement; with 0.05 mg tetracosane as internal standard) (Lu and Ralph 1997). All the measurements above were carried out in triplicate.
Lignin content and model of gene expression in N. cadamba
Both NcCSE and NcHCT had a higher expression level in the basal and middle segments than in the top segment of the N. cadamba stem, which was consistent with the trend of lignin content in these three segments (Table 1).
Transgenic plant lines generated
The seedlings were screen with basta, six (cse-35S::NcCSE1, cse-35S::NcCSE2, cse-35S::NcCSE3, cse-35S::NcHCT1, cse-35S::NcHCT2, cse-35S::NcHCT3 six overexpression lines WT-35S::NcCSE1, WT-35S::NcCSE2, WT-35S::NcCSE3, WT-35S::NcHCT1, WT-35S::NcHCT2 and WT-35S::NcHCT3) of the complementary transgenic lines generated were randomly choosed for phenotyping, the presence of the insertion was confirmed by PCR with gene specific primers, all of the six lines were single-copy insertion (verified by Chi square test, Additional file 1: Tables S4, S5). T3 generation transgenic plants were used for the following analysis.
Co-expression analysis of CSE and lignin biosynthesis related genes and qRT-PCR
In the results of co-expression analysis of all genes in the lignin biosynthesis pathway, four of them, F5H, C3H, C4H and CCoAOMT1 shared many more co-expressed genes with CSE compared with the other lignin biosynthesis pathway genes (Additional file 1: Figs. S2, S3). The 15 genes having the strongest relationship with CSE, and the other six genes that correlated with CSE in the cellulose biosynthesis pathway (Additional file 1: Table S6), were selected for analysis with qRT-PCR. However, many of the genes above showed no significant difference between transgenic lines and WT or the cse mutant in either stem or rosette leaves, the exceptions were C3H, C4H, HCT and CCoAOMT1, which had lower expression levels in the cse mutant compared with WT and cse-35S::NcCSE lines (Fig. 1), suggesting that genes other than these four were not influenced by the gene overexpression or the cse mutation and would not be likely to influence the phenotypes of those lines. In transgenic NcCSE and NcHCT overexpression plants, the overexpressed genes had a very high expression level in every line (Fig. 2).
Hypocotyl and inflorescence stem analysis
The hypocotyl length in seedlings by the 7th day and 14th day showed no significant difference between transgenic plants and WT or cse mutant plants (Figs. 3b, 4c, Additional file 1: Table S7), but the cse mutant was significantly shorter, by 34.3%, than the WT by day 50. However, the height of NcCSE complemented cse lines was restored to that of WT plants. Although the NcHCT complemented cse lines also significantly increased (by 11.4%, 11.4%, 8.7%, p < 0.01) in height, they did not reach the WT height. The similarity in hypocotyl length during early growth of the plants and the difference between the height of the plants at day 50 (Fig. 3a, d, Additional file 1: Table S7) suggested that CSE does not affect stem tissue development during the period of primary growth (Sibout et al. 2008), but after bolting, when secondary growth and deposition of lignin occur, differences in the lignification process mediate the different heights of these lines. The stem cross-section area of the cse mutant was a little smaller (4.9%, p = 0.049) than that of WT, but it was restored by complementation in all the transgenic lines (Fig. 3e, Additional file 1: Table S7).
Biomass is another index used to evaluate plant development. None of the lines had any significant difference in the dry weight of rosette leaves, though the dry weight varied among the different lines (Additional file 1: Table S8). However, the dry weight of the main inflorescence stem of the cse mutant was significantly less than that of WT. NcCSE overexpression could restore it to the WT level in cse-35S::NcCSE lines, and cse-35S::NcHCT lines were significantly heavier than the cse mutant but significantly lighter than WT. In addition, the dry weight of the total aboveground part of the cse mutant was less than those of the other lines at day 50, but there was no significant difference between WT and the transgenic lines (Additional file 1: Table S8). At the 21st day after planting, the area and number of leaves of the cse mutant were similar to those of WT and the transgenic lines (Additional file 1: Table S8). The dry weight, and number and area of leaves, in the cse mutant were not significantly different compared with WT and the transgenic lines, suggesting that leaf development is not severely affected by the cse mutation although the growth and development of the main inflorescence stem are severely inhibited by this mutation. Furthermore, the transgenic lines showed complete or partial restoration of the height and dry weight of the main inflorescence stem, so that the final dry weight of the total aboveground part of the cse mutant was less than in the other lines.
Cell wall residue comparison
Cell wall residue (CWR) extraction is a good way to explore the composition of plant dry weight. The CWR of the dry weight of cse mutant rosette leaves and main inflorescence stem was reduced by, respectively, about 14.3% and 10.5% compared with WT. The overexpression of NcCSE in the three independent cse-35S::NcCSE lines restored the CWR of the main inflorescence stem to the WT level in all cases (Additional file 1: Table S8). However, two of the three cse-35S::NcCSE lines still had significantly less CWR than WT in the rosette leaves, but all of them had significantly more CWR than the cse mutant. There was no significant difference between cse-35S::NcHCT and the cse mutant with respect to the CWR of either the main inflorescence stem or the rosette leaves (Additional file 1: Table S8).
The lignin content always changes along with CWR (Shinya et al. 2016). To observe the difference in content between the different lines microscopically, safranin and fast green staining as described in “Materials and methods” section was used. Comparing the staining of the cse, cse-35S:NcCSE and cse-35S:NcHCT lines, the xylem of the cse mutant was almost blue, while that of the cse-35S::NcCSE was red, and the color of cse-35S::NcHCT xylem was intermediate between blue and red. WT was stained a red color (Fig. 4). Furthermore, when Wiesner’s phloroglucinol-based staining method was applied to representative lines, including the cse mutant, cse-35S::NcHCT lines, cse-35S::NcCSE lines and WT, the xylem was stained in colors ranging from light red in the cse mutant to dark red in WT. The color of cse-35S::NcHCT and cse-35S::NcCSE lines was intermediate, but cse-35S::NcCSE lines were much darker in color than cse-35S:NcHCT lines. When stained with Maule’s reagent, the xylem of the cse mutant was brown while that of WT was stained red; the color of the xylem in cse-35S::NcCSE lines was similar to but not identical with that of WT, but the color of the cse-35S::NcHCT lines was an orange shade in between red and brown (Fig. 5).
Lignin content analysis
In this study, the lignin content was reduced by 23.3% and 31.7% in, respectively, the stems and leaves of the cse mutant compared with WT (Additional file 1: Table S8). This severe deficiency was completely complemented by NcCSE overexpression. For instance, the lignin content of both stems and leaves of the three cse-35S::NcCSE lines was not significantly different from WT levels. Although all three cse-35S::NcHCT lines had significantly more lignin than the cse mutant, except that the stem lignin content of cse-35S::NcHCT2 was at the same level as that in cse, the lignin contents of these line, were not restored to WT level, apart from the stem lignin content of cse-35S::NcHCT1 which was not significantly less than WT (Additional file 1: Table S8).
Lignin monomer composition analysis
The cse mutant was found to have a dramatic increase in H monomer but a decrease in G monomer and S monomer in the stem. This change in lignin monomer composition resulted in the S/G ratio increasing from 0.44 (WT) to 0.84 (cse). The S/G ratio (0.57) was partially restored to, but was still significantly higher than, the WT level in cse-35S::NcCSE lines. In cse-35S::NcHCT lines, both the decrease in H monomer content and the increase in G monomer content were at a significant level compared with cse, but S monomer content showed no significant change, so the S/G ratio was intermediate between that of cse mutant and that of the cse-35S::NcCSE line (Table 2, Additional file 1: Fig. S4).
CSE is a key enzyme in lignin biosynthesis
The lignin biosynthetic pathway has been well known for years, but it was not found that CSE, together with 4CL, bypassed the second HCT reaction, or that its preferred substrate was caffeoyl shikimate, until 2013 (Vanholme et al. 2013). The cse mutation was shown to reduce the expression levels of lignin biosynthesis genes upstream of it, and so block the lignin biosynthetic pathway (Vargas et al. 2016). Similarly, in this study, the lignin biosynthesis genes upstream of AtCSE, including C3H, C4H, HCT, were down regulated, but the gene CCoAOMT1, which lies downstream of CSE in the pathway, was not, the inflorescence stems were smaller and lighter, the CWR and lignin content were reduced in both the leaves and the stem, and the S/G ratio increased dramatically in the cse mutant compared with WT. However, the increases in expression levels of C3H, C4H, HCT and CCoAOMT1 (Fig. 1), and the restoration of lignin deposition (Additional file 1: Table S8) in cse-35S::NcCSE lines were also accompanied by restored plant growth (Fig. 3a, d). The mutant phenotype of cse was thus complemented in stable transgenic lines expressing NcCSE. All of these findings indicate that the N. cadamba gene NcCSE has a similar function to AtCSE in A. thaliana.
CSE affects lignin monomer content
In this study, the cse mutant was found to have a much higher content of H monomer and lower content of G and S monomer in the stem compared with WT, resulting in the S/G ratio increasing from 0.44 (WT) to 0.84 (cse). This is likely to be because CSE plays an important role in the part of the phenylpropanoid pathway leading to the G and S units after the branching off of H unit biosynthesis (Vanholme et al. 2013). The mutant phenotype of cse was greatly complemented but not completely restored to WT in the stable transgenic lines cse-35S::NcCSE, though there was still a significant difference in the amount of each lignin unit between WT and cse-35S::NcCSE. The lignin unit content of cse was less fully restored in the stable transgenic lines cse-35S::NcHCT, which had more H units, less of the G and S units and a higher S/G ratio compared with WT (Table 2, Fig. 5). Furthermore, lignin biosynthesis genes including C3H, C4H, HCT, CCoAOMT1 were up regulated in the stable transgenic lines cse-35S::NcCSE but were not affected in the transgenic lines cse-35S::NcHCT compared with the cse mutant (Fig. 1), and alterations in the activity of these related enzymes is also likely to have affected the composition of lignin units (Franke et al. 2002; Besseau et al. 2007; Li et al. 2010). These findings again suggest that NcCSE has a similar function to AtCSE and also that it is more effective than NcHCT in restoring the distribution of lignin units content in A. thaliana, and that NcCSE may be more active than NcHCT in the section of the N. cadamba phenylpropanoid pathway that leads to to G and S units after the branching off of of H unit biosynthesis.
NcCSE may be more active than NcHCT
In the study, the mutant phenotypes of cse-2 were complemented, either completely or partially, in the stable transgenic lines cse-35S::NcCSE; these characters included height and dry weight of the main inflorescence stem, dry weight of the total aboveground part of the plant, and CWR and lignin content of stems and rosette leaves. However, the phenotypes of the stable transgenic lines cse-35S::NcHCT were not restored to WT, in comparison to which they showed significant differences (Additional file 1: Tables S7, S8). Additionally, the xylem of cse-35S::NcCSE and WT was red, but the color of cse-35S::NcHCT xylem lay in between blue and red, in the safranin and fast green staining experiment (Fig. 4). When stained with phloroglucinol, the xylem of the cse mutant was light red but the the xylem of WT was dark red. The color of cse-35S:NcHCT and cse-35S:NcCSE lines was intermediate, but cse-35S:NcCSE lines were much darker in color compared with cse-35S:NcHCT lines (Fig. 5). All of these observations indicate that the lignin content was higher in the cse-35S::NcCSE lines compared with the cse-35S::NcHCT lines. When lignin content was measured, the results showed that it was reduced by 23.3% in the stem of the cse mutant compared with WT and this severe deficiency was completely complemented by NcCSE overexpression, but cse-35S::NcHCT lines did not show full complementation, with the exception of cse-35S::NcHCT1 (Additional file 1: Table S8). CSE and HCT have the same substrate, caffeoyl shikimate (Vanholme et al. 2013). Both NcCSE and NcHCT were expressed at the highest level in the stem segment of N. cadamba with the greatest degree of lignification; however, the expression level of NcCSE was much higher than that of NcHCT in the same segment (Table 1) (Ouyang et al. 2016). These results suggest that NcCSE may be more active than NcHCT in lignin biosynthesis in N. cadamba.
Potential application of NcCSE down-regulation
Lignin does not reduce the palatability of forage grass for animals (Cornelissen et al. 2014), but it hinders the isolation of cellulose fibers and the efficient enzymatic depolymerization of cellulose and hemicellulose into fermentable sugars by limiting the access of the hydrolytic enzymes to their polysaccharide substrate in the biorefining industry (Vanholme et al. 2013). In a previous study, silencing CSE in poplar did not drastically affect plant growth or development, but it reduced lignin deposition and flux into G and S units, increased the cellulose content and improved the saccharification efficiency for stems (Saleme et al. 2017). We found that the function of NcCSE was similar to that of AtCSE in lignin biosynthesis. A highly efficient in vitro regeneration system has been successfully established for N. cadamba (Huang et al. 2014), and in recent years the CRISPR–Cas9 system for genome editing has been established and applied widely to create a loss-of-function mutants affecting of specific genes (Mali et al. 2013; Hsu et al. 2014). These factors suggest that the lignin content in both stems and leaves of N. cadamba could be reduced by creating the loss-of-function mutant nccse with the CRISPR–Cas9 system, resulting in improvements in the nutrient absorption of the leaves for animals and in the total saccharification yield from the stems.
Availability of data and materials
All the gene sequence is deposited into NCBI, all the vectors and materials are stored in our lab, all the data are either in the manuscript or the additional data.
Adel AM, El-Gendy AA, Diab MA, Abou-Zeid RE, El-Zawawy WK, Dufresne A (2016) Microfibrillated cellulose from agricultural residues. Part I: papermaking application. Ind Crops Prod 93:161–174
Besseau S, Hoffmann L, Geoffroy P, Lapierre C, Pollet B, Legrand M (2007) Flavonoid accumulation in Arabidopsis repressed in lignin synthesis affects auxin transport and plant growth. Plant Cell 19:148–162
Boerjan W, Ralph J, Baucher M (2003) Lignin biosynthesis. Annu Rev Plant Biol 54:519–546
Constant S, Wienk HLJ, Frissen AE, Peinder PD, Boelens R, Es DSV, Grisel RJH, Weckhuysen BM, Huijgen WJJ, Gosselink RJA (2016) New insights into the structure and composition of technical lignins: a comparative characterisation study. Green Chem 18:2651–2665
Cornelissen P, Bokdam J, Sykora K, Berendse F (2014) Effects of large herbivores on wood pasture dynamics in a European wetland system. Basic Appl Ecol 15:396–406
Dwevedi A, Sharma K, Sharma YK (2015) Cadamba: a miraculous tree having enormous pharmacological implications. Pharmacogn Rev. 9:107
Franke R, Hemm MR, Denault JW, Ruegger MO, Humphreys JM, Chapple C (2002) Changes in secondary metabolism and deposition of an unusual lignin in the ref8 mutant of Arabidopsis. Plant J 30:47–59
Guo D, Chen F, Wheeler J, Winder J, Selman S, Peterson M, Dixon RA (2001) Improvement of in-rumen digestibility of alfalfa forage by genetic manipulation of lignin O-methyltransferases. Transgenic Res 10:457–464
Hsu PD, Lander ES, Zhang F (2014) Development and applications of CRISPR–Cas9 for genome engineering. Cell 157:1262–1278
Huang H, Li J, OuYang K, Zhao X, Li P, Liao B, Chen X (2014) Direct adventitious shoot organogenesis and plant regeneration from cotyledon explants in Neolamarckia cadamba. Plant Biotechnol-Nar 31:115–121
Hückelhoven R (2007) Cell wall-associated mechanisms of disease resistance and susceptibility. Annu Rev Phytopathol 45:101–127
Krisnawati H, Kallio M, Kanninen M (2011) Anthocephalus cadamba Miq.: ecology, silviculture and productivity. CIFOR, Bogor
Lewis NG, Yamamoto E (1990) Lignin: occurrence, biogenesis and biodegradation. Annu Rev Plant Biol 41:455–496
Li X, Bonawitz ND, Weng JK, Chapple C (2010) The growth reduction associated with repressed lignin biosynthesis in Arabidopsis thaliana is independent of flavonoids. Plant Cell 22:1620–1632
Lu F, Ralph J (1997) Derivatization followed by reductive cleavage (DFRC method), a new method for lignin analysis: protocol for analysis of DFRC monomers. J Agric Food Chem 45:2590–2592
Mali P, Esvelt KM, Church GM (2013) Cas9 as a versatile tool for engineering biology. Nat Methods 10:957–963
Mason R (1961) Dispersal of tropical seeds by ocean currents. Nature 191:408
Ouyang KX, Liu MQ, Pian RQ, Liu SS, Chen XY (2013) Isolation and analysis of α-expansin genes in the tree Anthocephalus chinensis (rubiaceae). Genet Mol Res 2:1061–1073
Ouyang K, Li J, Huang H, Que Q, Li P, Chen X (2014) A simple method for RNA isolation from various tissues of the tree. Biotechnol Biotechnol Equip 28:1008–1013
Ouyang K, Li J, Zhao X, Que Q, Li P, Huang H, Deng X, Singh SK, Wu A, Chen X (2016) Transcriptomic analysis of multipurpose timber yielding tree Neolamarckia cadamba during Xylogenesis using RNA-Seq. PLoS ONE 11:e159407
Powell JB, Johnson KA, Komplin GC et al (2017) Methods and systems for processing lignin during hydrothermal digestion of cellulosic biomass solids. US Patent 9,562,160
Saleme M, Cesarino I, Vargas L, Kim H, Vanholme R, Goeminne G, Van Acker R, Fonseca F, Pallidis A, Voorend W, Junior JN, Padmakshan D, Van Doorsselaere J, Ralph J, Boerjan W (2017) Silencing caffeoyl shikimate esterase affects lignification and improves saccharification in poplar. Plant Physiol 175:1040–1057
Salmén L (2015) Wood morphology and properties from molecular perspectives. Ann Forest Sci 72:679–684
Shinya T, Iwata E, Nakahama K, Fukuda Y, Hayashi K, Nanto K, Rosa AC, Kawaoka A (2016) Transcriptional profiles of hybrid Eucalyptus genotypes with contrasting lignin content reveal that monolignol biosynthesis-related genes regulate wood composition. Front Plant Sci 7:443
Shuai L, Amiri MT, Questell-Santiago YM, Héroguel F, Li Y, Kim H, Meilan R, Chapple C, Ralph J, Luterbacher JS (2016) Formaldehyde stabilization facilitates lignin monomer production during biomass depolymerization. Science 354:329–333
Sibout R, Plantegenet S, Hardtke CS (2008) Flowering as a condition for xylem expansion in Arabidopsis hypocotyl and root. Curr Biol 18:458–463
Trabucco GM, Matos DA, Lee SJ, Saathoff AJ, Priest HD, Mockler TC, Sarath G, Hazen SP (2013) Functional characterization of cinnamyl alcohol dehydrogenase and caffeic acid O-methyltransferase in Brachypodium distachyon. BMC Biotechnol 13:61
Vanholme R, Demedts B, Morreel K, Ralph J, Boerjan W (2010) Lignin biosynthesis and structure. PLANT PHYSIOL 153:895–905
Vanholme R, Cesarino I, Rataj K, Xiao Y, Sundin L, Goeminne G, Kim H, Cross J, Morreel K, Araujo P (2013) Caffeoyl shikimate esterase (CSE) is an enzyme in the lignin biosynthetic pathway in Arabidopsis. Science 341:1103–1106
Vargas L, Cesarino I, Vanholme R, Voorend W, de Lyra Soriano Saleme M, Morreel K, Boerjan W (2016) Improving total saccharification yield of Arabidopsis plants by vessel-specific complementation of caffeoyl shikimate esterase (cse) mutants. Biotechnol Biofuels 9:139
Ververis C, Georghiou K, Danielidis D, Hatzinikolaou DG, Santas P, Santas R, Corleti V (2007) Cellulose, hemicelluloses, lignin and ash content of some organic materials and their suitability for use as paper pulp supplements. Bioresource Technol 98:296–301
Zeng Y, Zhao S, Yang S, Ding SY (2014) Lignin plays a negative role in the biochemical process for producing lignocellulosic biofuels. Curr Opin Biotech 27:38
Zhang X, Henriques R, Lin S, Niu Q, Chua N (2006) Agrobacterium-mediated transformation of Arabidopsis thaliana using the floral dip method. Nat Protocol 1:641
This study was funded by Science and Technology Program of Guangdong, China (2017B020201008), National Natural Science Foundation of China (31600525), Extension and demonstration project of forest science and technology from China state financial budget ((2018)GDTK-08), Guangdong natural science foundation (2015A030313419), Science and Technology Program of Guangzhou (201607020024), Science and Technology Program of Guangxi (2018GXNSFAA138094).
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Li, J., Huang, X., Huang, H. et al. Cloning and characterization of the lignin biosynthesis genes NcCSE and NcHCT from Neolamarckia cadamba. AMB Expr 9, 152 (2019). https://doi.org/10.1186/s13568-019-0860-z
- Neolamarckia cadamba