Suppression of PtrDUF579-3 Expression Causes Structural Changes of the Glucuronoxylan in Populus

DUF579 (domain unknown function 579) genes have been reported to play diverse roles in cell wall biosynthesis, such as in glucuronoxylan (GX) synthesis. As GX is a major type of hemicelluloses in hard wood species, how DUF579 genes function in wood formation remains to be demonstrated in planta. This study reports a Populus DUF579 gene, PtrDUF579-3, which is characterized for its function in wood cell wall formation. PtrDUF579-3 is localized in Golgi apparatus and catalyzes methylation of the glucuronic acid (GlcA) in GX biosynthesis. Suppression of PtrDUF579-3 expression in Populus caused a reduction in both the GlcA side chain number and GlcA side chain methylation on the GX backbone. The modified GX polymer through PtrDUF579-3 suppression was more susceptible to acid treatment and the PtrDUF579-3 suppressed plants displayed enhanced cellulose digestibility. These results suggest that PtrDUF579-3 is involved in GX biosynthesis and GX structure can be modified through PtrDUF579-3 suppression in Populus.

In addition to GX backbone synthesis, GX is typically modified with GlcA side chains which appears to be methylated or not. In Arabidopsis, methylation of the GlcA side chain in GX was found to be mediated by DUF579 family proteins. Double mutant of DUF579 genes irx15 and irx15l show an increase of GX methylation and decrease of GX content, which causes secondary cell wall defects (Brown et al., 2011;Jensen et al., 2011). Whereas, some other studies showed that DUF579 proteins have a catalytic activity to methylate GlcA residue in GX and mutation of the DUF579 genes led to reduction of GX methylation (Lee et al., 2012b;Urbanowicz et al., 2012). It is unclear whether these different DUF579 genes have different catalytic activities in the GX biosynthesis.
DUF579 gene family consists of 10 members in Arabidopsis and 12 members in Populus. Our study suggests Populus DUF579 genes play diverse roles in affecting wood formation in Populus (Song et al., 2014). They display a variety of expression patterns across various tissues and their encoded proteins are localized in different types of cells. PtrDUF579-1 suppression specifically affected cambium cell wall formation (Song et al., 2014), while PtrDUF579-3 and PtrDUF579-4 are specifically expressed in xylem cells. In another study, PtrDUF579-3 and PtrDUF579-4 are reported to catalyze the GlcA methylation of GX in vitro (Yuan et al., 2014). However, it remains to be demonstrated how these DUF579 genes function in regulating GX methylation in planta.
Here we show that regulation of PtrDUF579-3 expression resulted in GX structure modification in Populus. This study provides a line of new evidence for elucidation of the PtrDUF579-3 function in GX biosynthesis during wood formation.

Plant Materials and Growth Condition
Populus trichocarpa was used for gene cloning. Populus × euramericana cv. 'Nanlin895' was used for genetic transformation analysis. Young Populus plants were grown in a phytotron with a light and dark cycle of 16 and 8 h at 22 • C. Populus trees at 3-months were grown in a greenhouse as described (Song et al., 2014).

Gene Constructs and Genetic Transformation
Total RNA was extracted from developing xylem using modified CTAB method (Chang et al., 1993). The total RNA used for gene cloning and gene expression analysis was extracted from developing xylem tissues of WT or anti-PtrDUF579-3 transgenic plants. After removing DNA contamination, 1 µg of total RNA was reversely transcribed into cDNAs using HiScript II 1st Strand cDNA Synthesis Kit (R211, Vazyme, Nanjing, China). The full coding sequences of PtrDUF579-3 and PtrDUF579-4 were amplified and cloned from cDNA of P. trichocarpa. To construct antisense vector, the coding sequences of PtrDUF579-3 was reversely inserted into pBI121 binary vector under a constitutive CaMV35S promoter. The constructs were transferred into Populus × euramericana cv. 'Nanlin895' by Agrobacterium mediated transformation according to the protocol adopted in our lab (Li et al., 2003).

Subcellular Localization and Colocalization Experiment
PtrDUF579-3 and PtrDUF579-4 gene cloned above were fused with mCherry gene and inserted into pm-rk binary vector after removing PIP2A gene, respectively (Nelson et al., 2007; primer sequences for constructs supplied in Supplementary Table S1). The constructs of G-gk (Nelson et al., 2007) were used for Golgi identification. The two constructs and G-gk were then transformed into Agrobacterium, co-injected into tobacco leaves and were observed under laser confocal scanning microscopy (LCSM; LSM510 META, ZEISS, Germany) according to previous procedure (Song et al., 2014).

Gene Expression Analysis
Gene-specific primers were designed to amplify a specific fragment (100-300 bp in length) of the PtrDUF579-3, PtrDUF579-4, and PtrDUF579-9 genes (Supplementary Table  S1). Using the cDNA prepared above as template, quantitative real-time PCR was performed using Hieff TM qPCR SYBR R Green Master Mix (11201ES03, Yeasen, Shanghai, China) on a MyiQ Real-Time PCR Detection System (Bio-Rad, Winston-Salem, NC, USA). The gene expression was normalized against PtrActin2 expression and analyzed by Delta CT method using three biological replicates from independent plants.

Microscopy Analysis of Populus Secondary Growth
For light microscopy analysis, the 12th internode of Populus stems were cut into 2 mm lengths and fixed by FAA solution (5% formaldehyde, 10% acetic acid, and 50% ethanol), dehydrated with ethanol and embedded in paraffin. After obtaining 10-µm sections with a Leica RM2235 rotary microtome and removing of paraffin, sections were stained with 0.05% toluidine blue and analyzed using an OLYMPUS BX51 light microscope according to previous protocol (Song et al., 2014).

Measurement of Mechanical Strength
Mechanical strength was measured using a material tester (Instron 5867, Norwood, MA, USA). The mechanical strength was measured as the force required for breaking a fresh stem segment with a diameter about 1 cm and length about 10 cm. The mechanical strength was assayed using Young's modulus, Y = (F/S)/( L/L) (Mishra et al., 2000). Y, Young's modulus; F, force; S, cross-sectional area; L,

Chemical Analysis of Secondary Cell Wall Components
Wood developing xylem tissues (5-6 g) collected from stems of 1-year-old trees were ground in liquid nitrogen into a fine powder to prepare alcohol insoluble residues (AIRs) according to (Foster et al., 2010). After de-starched procedure, the cell walls AIR were subjected to determination of the chemical composition. The AIRs were hydrolyzed with 2 M trifloroacetic acid (TFA) at 120 • C for 1.5 h. The produced monosaccharides were then dried in a rotatory evaporator and subjected to mercaptalation and silylation as described (Lluveras-Tenorio et al., 2012;Song et al., 2014). The final reaction mixture was dried with nitrogen flow, reconstituted in hexane and then were subjected to GC-MS analysis. The sugars and uronic acids were separated by HP-5 column, and detected by Agilent 5975 inert MSD system (Agilent, Santa Clara, CA, USA). Crystalline cellulose content and monosaccharide composition was analyzed according to the protocol previously described (Li et al., 2009). Lignin content was determined by Klason method and lignin subunit S/G-ratio was analyzed by thioacidolysis according to our previous protocol (Gui et al., 2011).

GX Oligosaccharide Preparation
Above prepared AIR (1 g) was sequentially extracted with 50 mM ammonium oxalate and 1 M KOH, containing 1.0% (w/v) sodium borohydride. The KOH extracts were neutralized, dialyzed, and lyophilized. GX oligosaccharides were generated by digestion of the lyophilized KOH extracts (20 mg) with a Trichoderma viride endoxylanase (Megazyme) in 0.1 M ammonium formate buffer (pH 5.0) for 24 h at 37 • C as described (Mazumder et al., 2012). The reaction mixture was neutralized with ammonia and passed through a cut-off ultrafiltration tube (3 KD, Millipore) to remove residual polysaccharides. Then the percolate was repurified by adding ethanol to a final concentration of 65% (vol/vol) and concentrated to remove precipitates. The soluble fraction was subjected to liquid chromatography-quadrupoletime-of-flight-mass spectrometry (LC-QTOF-MS) analysis. GX oligosaccharides (about 25-30 mg) generated from digestion of 100 mg KOH extracts were desalted and lyophilized for 1 H NMR analysis.

GX Glucuronosyltransferase and Methyltransferase Assay
Microsomal proteins from developing xylem tissue were prepared according to previous method (Suzuki et al., 2006). The microsomes were washed three time with ice cold Milli-Q water and dissolved in protein extraction buffer containing 100 mM NaAc, pH 7.0, 0.5% w/v dodecyl-β-D-maltoside (DDM) and 1 mM protease inhibitor cocktail (Sigma). After centrifuged at 10000 g for 10 min at 4 • C, the supernatant containing microsomal protein was collected and subjected to protein concentrations determination using Bio-Rad protein assay system. Glucuronoxylan glucuronosyltransferase activity of microsomal proteins was assayed in a 100 µl reaction mixture with 100 mM NaAc, pH 7.0, 100 µg microsomal proteins, 1 mM UDP-GlcA (Sigma), 2 mM xylohexaose (Megazyme) and 5 mM MnCl 2 . For GX methyltransferase activity assay, the reaction mixture was added with 1 mM S-(5 -adenosyl)-Lmethionine chloride dihydrochloride (Sigma) and 1 mM CoCl 2 . After incubation at 23 • C for 3 h, the reaction mixtures were passed through a cut-off ultrafiltration tube (3 KD, Millipore). The percolate was directly subjected to LC-QTOF-MS for product identification. Percolate of GX glucuronosyltransferase activity assay mixture was stored at −20 • C for the following methyltransferase assays.

Methyltransferase Assay of Recombinant
PtrDUF579-3 and PtrDUF579-9 Proteins The DUF579 domain sequence of PtrDUF579-3 and PtrDUF579-9 was amplified using specific primer (Supplementary Table S1). The PCR products were sequenced and then cloned into the NheI and SalI sites of pET28b (Novagen). Recombinant proteins were induced in Escherichia coli BL21(DE3), purified with Ni-NTA Superflow (Qiagen) and examined by SDS-PAGE and Western blot using produced antibody according to the protocol (Song et al., 2010(Song et al., , 2014. Methyltransferase activity of the recombinant PtrDUF579-3 and PtrDUF579 proteins were analyzed in above 100 µl percolate containing glucuronxylohexaose by adding 100 µg recombinant PtrDUF579-3 protein or 100 µg cell lysates of E. coli BL21(DE3) as control, 1 mM SAM and 1 mM CoCl 2 . After incubation at 23 • C for 3 h, the reaction mixtures were passed through a cut-off ultrafiltration tube (3 KD, Millipore) and the percolate was directly subjected to LC-QTOF-MS for product identification.

Liquid Chromatography-Quadrupole-Time-of-Flight-Mass Spectrometry
The product of methyltransferase assay were directly identified through LC-QTOF MS analysis using an Agilent 6520 series LC 1200 MS 6520 QTOF system packed with a ZORBAX Extend-C18 column (3.0 mm × 50 mm, 1.8 µm, Agilent, Palo Alto, CA, USA) as our previous protocol (Zhao et al., 2013). Briefly, 3 µl of xylo-oligosaccharides was injected with a constant mobile phase flow rate of 0.3 ml min −1 . The mobile phase consisted of 10 mM ammonium acetate in H 2 O (A) and 20 mM ammonium acetate in acetonitrile (B) using a gradient elution of buffer B. GX oligosaccharides (1 µg/µl) extracted from wild type and transgenic plants were separated by XBRIDGE amide column (4.6 mm × 250 mm, 3.5 µm Waters, Milford, MA, USA) for structure characterization. The mobile phase consisted of 0.2% NH 4 OH in H 2 O (A) and pure acetonitrile (B) using a gradient elution of buffer B by a linear decrease from 80 to 50% in 30 min. The TOF mass spectrometer was set as scan range from 200 to 1700 at 160 V and radiofrequency (Sanderfoot et al., 1998) at 750 V in positive scan mode at 4 GHz resolution. The temperature of dry gas of electrospray ionization (ESI) was set at 350 • C with holding flow at 9 L min −1 .

H-NMR Spectroscopy
Xylo-oligosaccharides used for NMR analysis were prepared from wild type plants or five plants of individual transgenic lines. Xylooligosaccharides samples (20 mg) were prepared with 100% D 2 O (0.6 mL, 99.9 atom % D; Sigma) in 5 mm standard NMR tubes. A total of 0.5 µl of acetone (δ 2.225) was added for measurement of chemical shifts. High-resolution NMR spectra were acquired at 303 K with a Varian Inova-NMR spectrometer (Varian, Palo Alto, CA, USA) operating at 600 MHz using a 5-mm NMR cold probe (Agilent). For all examination, 128 transients were collected and an acquisition time of 3-s. Residual water resonance was suppressed using the NOESYPR1D (1D Nuclear Overhauser effect spectroscopy with water pre-saturation) pulse sequence with a mixing time of 100 ms. 1D spectra were phased, baseline corrected for integral analysis using MestRe-Nova software (MestreC Research). All NMR spectra were compared with the spectra data for xylan structure analysis (Pena et al., 2007;Lee et al., 2011).

GX Release and Cellulose Hydrolysis Assay
For GX release assay, wood samples collected from 1-year-old trees were milled to pass the 80 mesh screen for preparing AIRs according to (Foster et al., 2010). After de-starched procedure and iodine test, 2 mg of wood mill per reaction was weighted into a 2 mL screw cap tube with 300 µL 2% sulfuric acid, 20 ul of inositol (1 µg/µl) was used as an internal standard. After set at room temperature for 20 min, the reactions were heated to 121 • C for 15, 25, 35, 45, 55 min. The reactions were immediately cooled down on ice after heated with various time intervals and neutralized with ammonium hydroxide. After centrifugation, 200 ul of supernatant was collected and dried in a rotatory evaporator and subjected to alditol acetate derivatization followed by acetylation procedure according to (Foster et al., 2010). Xylose content was detected and quantified using an Agilent GC-MS system equipped with a SP-2380 capillary column (Foster et al., 2010). For 60 min acid treatment, 0.5 g of wood residue was collected by centrifugation and washed, and then suspended in 10 mL of 0.1 M sodium citrate buffer at pH 4.8. Cellulase (E.C. 3.2.1.4) from T. viride (Yakult Honsha, Tokyo, Japan) of 20 filter paper units (FPUs) was added to each sample and the volume was adjusted to 30 mL for digestion at 50 • C for 1, 8, and 72 h. The glucose concentration in the reaction was measured by dinitrosalicylic acid (DNS) method using glucose as standard according to (Hou and Li, 2011).

Catalytic Activity of GX Glucuronosyltransferases and Methyltransferase in Populus Developing Xylem Tissue
To examine the GX methylation process during wood formation, the microsomal proteins from developing xylem tissue of Populus was isolated and determined for enzyme activities. Using UDP-GlcA and xylohexaose as substrates, glucuronoxylohexaose (GlcA)Xyl 6 (m/z [M+ NH 4 ] + = 1004.33; m/z [M+Na] + = 1009.28; Figure 1A) was detected as a reaction product, indicating that the microsomal proteins contained a catalytic activity of glucuronosyltransferase. When UDP-GlcA, xylohexaose and S-adenosyl methionine (SAM) were used as substrates, both GlcAXyl 6 and methyl-glucuronoxylohexaose (MeGlcA)Xyl 6 (m/z [M+NH 4 ] + = 1018.33; m/z [M+Na] + = 1023.28) was produced (Figure 1B), while the (MeGlcA)Xyl 6 product was not be detected in the absence of SAM (Figure 1D), indicating the microsomal proteins have methylation activity on glucuronoxylohexaose using SAM as a methyl group donor. In this reaction, methylated UDP-GlcA was not found to be a product (Figure 1C), suggesting that UDP-GlcA may not be directly methylated in Populus xylem tissue, instead that the methylation may occur after the GlcA group is added onto GX polymers. These results revealed that the developing xylem microsomal protein contains catalytic activities for transferring the GlcA residues onto GX polymers as well as for catalyzing the methylation on the GlcA side chains.
In our previous study, PtrDUF579-3 and PtrDUF579-9 were identified for their high expression in developing xylem (Song et al., 2014). To examine PtrDUF579-3 and PtrDUF579-9 catalytic activity, their recombinant proteins were expressed in E. coli and purified (Figure 2A, Supplementary  Figures S1A,C). The recombinant proteins were examined with their enzymatic activity in the reaction system containing GlcA-Xyl 6 and SAM (methyl group donor) as substrates. PtrDUF579-3 displayed a catalytic activity in producing MeGlcA-Xyl 6 (Figures 2B,C). However, PtrDUF579-9 was unable to catalyze the MeGlcA-Xyl 6 production (Supplementary Figure S1B), indicating that PtrDUF579-9 was deficient in such methylation under the experimental conditions. These suggest that the PtrDUF579-3 but not PtrDUF579-9 was able to methylate glucuronoxylan. PtrDUF579-3 protein was further examined for its subcellular location. The Golgi apparatus markers GmMan1 were co-expressed with PtrDUF579-3:mCherry in tobacco leaf.
PtrDUF579-3:mCherry shows colocalization with the Golgi apparatus markers (Figures 3A-D). The results indicated PtrDUF579-3 localized in Golgi apparatus and mediated GX methylation process in Populus xylem cell.

Suppression of PtrDUF579-3 Affected the GX Components
To investigate the PtrDUF579-3 function in planta, an antisense PtrDUF579-3 construct was transferred into Populus to generate PtrDUF579-3 suppressed plants. Thirty-four independent transgenic lines were generated and confirmed. Expression of PtrDUF579-3 was found to be down-regulated in twenty of the transgenic lines, among which two transgenic lines (Line 1 and line 2) were multiplied through cutting propagation and used for detailed analysis (Figure 4A). In the transgenic plants, expression of PtrDUF579-3 and PtrDUF579-4 was found to be simultaneously down-regulated, while the expression of PtrDUF579-9 gene was not affected (Figure 4A). Western blot analysis demonstrated that PtrDUF579-3 protein was dramatically reduced in the xylem tissue of transgenic plants ( Figure 4B). Results also showed that both PtrDUF579-3 and PtrDUF579-4 share high protein sequence identity and same subcellular localization (Supplementary Figure S2). Likely PtrDUF579-3 and PtrDUF579-4 may play redundant roles. The transgenic plants did not show apparent growth alterations in terms of plant height, stem diameter, internode length, and leaf size compared to those in wild type plants ( Figure 4C). Cross-section of the transgenic plant stem showed that the xylem cell morphology was not affected when observed under light microscope (Figures 4D,E). However, the mechanical strength of the stem was slightly reduced in the transgenic plants ( Figure 4F). Changes of the stem mechanical property could be due to the alteration occurred in wood tissues.
The chemical composition of the wood was analyzed in transgenic plants. Compared to control plants, GlcA content was significantly decreased, while other monosaccharide composition was generally not changed in the transgenic plants, except a slight decrease in mannose content (Table 1). Furthermore, cellulose content and Klason lignin content were not significantly changed in the transgenic plants. Lignin S/G ratio was also not changed ( Table 1). These results suggest suppression of PtrDUF579-3 did not affect biosynthesis of cellulose and lignin but mainly affected the GlcA content in xylem cell walls.
PtrDUF579-3 protein displayed a catalytic activity of GX methyltransferase. Then we examined the methylation of the GX polymer in Populus wood cell walls. After GX was isolated and digested by endoxylanase, the released oligosaccharides were analyzed using a liquid chromatography quadrupole time-of-flight mass spectrometry (LC-QTOF-MS). The detected oligosaccharides from wild type Populus contained abundant MeGlcA-Xyl 4 along with trivial GlcA-Xyl 4 (Figures 5A,B). However, the GlcA-Xyl 4 abundance was increased in the transgenic plants compared to wild type (Figures 5A,B), indicating a reduction of GlcA-Xyl 4 methylation in the PtrDUF579-3-suppressed transgenics.
The GX structures in the transgenic plants were further examined by nuclear magnetic resonance (NMR). GX oligosaccharides from wild Populus displayed abundant MeGlcA residues with minor GlcA residues ( Figure 5C). In the transgenic plant, un-methylated GlcA side chains on GX oligosaccharides were increased, while the methylated GlcA side chains were relatively reduced ( Figure 5C; Table 2). This further verifies that PtrDUF579-3 suppression resulted in reduction of the GlcA side chain methylation. Meanwhile, in GX polymers, the branched β-Xyl residues were reduced about 12% suggesting a reduction of GlcA/MeGlcA branches on the xylan backbone ( Table 2). These results together suggest that PtrDUF579-3 suppression led to reduction of GlcA methylation and branches on GX backbone. In addition, the α-GalA and α-Rha at GX reducing ends were not changed in the transgenic plant ( Figure 5C; Table 2). As tetrasaccharide at the reducing ends can be referred to be correlated with the average degree of polymerization of GX (Pena et al., 2007), this indicated that the elongation of GX backbone was not affect in the PtrDUF579-3 suppressed plants.

Analysis of Polysaccharide Hydrolysis of Wood Tissue
Glucuronoxylan is involved in connecting lignin and cellulose fibrils together in wood and is thought to be a main factor limiting the hydrolytic efficiency during biomass conversion (Laureano-Perez et al., 2005;Himmel et al., 2007). We examined GX hydrolysis during acid treatment and cellulose digestibility after the treatment. The xylose release was significantly enhanced (average 29.9% in 15 min, 22.4% in 25 min, and 18.9% in 35 min) from PtrDUF579-3 suppressed plants compared to the wild type plants during the course of treatment, but not significant after 45 min ( Figure 6A). After treatment for 60 min, wood residues were subjected to cellulose digestibility assay. The glucose release was increased (average 38.3% in 1 h and 13.5% in 8 h) from PtrDUF579-3 suppressed plants compared to the wild type plants with cellulase hydrolysis (Figure 6B). The results revealed that the PtrDUF579-3 suppression enhances GX susceptibility to acid treatment and increased cellulose digestibility, which could attribute to the alteration of GX structure in the PtrDUF579-3 suppressed plants.

DISCUSSION
In Populus, 12 DUF579 genes have been identified, of which individual members play diverse roles in various developing processes (Song et al., 2014). In this study, evidence showed that PtrDUF579-3 functions with an enzymatic activity in catalyzing methylation of GX side chains and plays a role in planta for affecting GX biosynthesis during wood formation.
In another study, PtrDUF579-1 protein was reported to display GX methyltransferase activity, while its substrate affinity and catalytic efficiency were rather lower than those of PtrDUF579-3 (Yuan et al., 2014). In our previous study, PtrDUF579-1 was found to be localized in cambium cells. Suppression of PtrDUF579-1 expression affected cambium pectin composition, suggesting its role in association with pectin formation in primary cell wall (Song et al., 2014). Here, the evidence suggests a possibility that DUF579 family members may have different catalyzing properties or catalyze methylation using different polysaccharide substrates. Certainly this remains to be further investigated.

Roles of PtrDUF579-3 in the GX Biosynthesis Process
In Arabidopsis (Columbia type), about 63% of the GlcA side chains on the GX backbone is methylated (Urbanowicz et al., 2012). In our study, about 97% of the GlcA side chains in Populus xylem tissue are found to be methylated. The different degree of GlcA side chain methylation between Arabidopsis and Populus may indicate a difference of GX polymer structures in the two plants.
Activity analysis indicated that the Populus microsomal proteins contain glucuronosyltransferases and methyl transferases. Recombinant PtrDUF579-3 protein displayed GX methyltransferase activity. Consistent with this, genetic suppression of PtrDUF579-3 caused the GlcA methylation reduction of GX polymers in planta. In addition, branches on GX polymers were also decreased in the PtrDUF579-3 suppressed plants. In Arabidopsis, knocking-out of a DUF579 gene, GXMT1 affected the methylation of GlcA, but did not affect the addition of GlcA onto GX backbone (Lee et al., 2012b;Urbanowicz et al., 2012). A recent study shows that PtrDUF579-3 could only restore a small fraction of GlcA side chains of GX in the gxm1/2/3 mutant suggesting a possibility that GlcA methylation is carried out by a protein complex containing DUF579s and other xylan biosynthetic enzymes (Yuan et al., 2014). Thus, how GlcA methylation and its addition onto GX are carried out in a coordinated manner remains to be further characterized in Populus.
PtrDUF579-3 and PtrDUF579-4 share 90% sequence identity, with a similar expression and same subcellular localization. Suppression of PtrDUF579-3 affected PtrDUF579-4 but not other family members. Due to the difficulty in individual regulation of the two genes, the phenotypes of the PtrDUF579-3-suppressed plants could be due to simultaneous suppression of both PtrDUF579-3 and PtrDUF579-4 expression. Actually PtrDUF579-3 and PtrDUF579-4 form a pair of DUF579 genes (Song et al., 2014) with similar enzyme activity (Yuan et al., 2014). Likely, they may play redundant roles.

GX Structure and Wood Formation
As a potential feedstock for biofuel industry, wood is mainly composed of three types of biopolymers, cellulose, hemicellulose and lignin. Among these polymers, cellulose and lignin are connected by hemicelluloses in wood secondary cell walls (Fengel and Wegener, 1983). In hard wood species, GX is a major hemicellulose and affects conversion of wood biomass into biofuel (Laureano-Perez et al., 2005;Himmel et al., 2007;Lee et al., 2011). Engineering of the GX structure through genetically manipulating genes involved in GX biosynthesis may contribute to improvement of the wood conversion efficiency for biofuel production. In Populus, alteration of the GX content and structure through down-regulation of GT43B and GAUT12 gene enhanced sugar release from wood biomass (Lee et al., 2011;Biswal et al., 2015). In this study, suppression of a glucuronoxylan methyltransferase gene, PtrDUF579-3, enhances GX susceptibility to acid treatment which would be beneficial for pentose separation in the process of pretreatment.
In secondary walls, it is thought that GX interacts with cellulose and lignin. The backbone of GX interacts with cellulose microfibrils through hydrogen-bond (Laureano-Perez et al., 2005), while the substituted GX with negatively charged MeGlcA side residues has low affinity with cellulose (Linder et al., 2003;Kabel et al., 2007). The GlcA substitutions may allow xylan backbone to fold as a twofold helical screw to form an uncharged surface to facilitate GX-cellulose interaction or to fold as threefold helical screw to form a charged surface for interaction of GlcA residue with other cell wall components (Szabo et al., 2001;Bromley et al., 2013). The twofold helical screw conformation allows the xylan to interact with both hydrophilic and hydrophobic faces of cellulose (Busse-Wicher et al., 2014). In addition, the MeGlcA side residues on GX polymers are reported to be able to interact with lignin through covalent ester linkages (Takahashi and Koshijima, 1988). Regulation of PtrDUF579-3 in Populus caused GX methylation and substitution changes. The change of GX structure may affect the direct linkages between xylan, cellulose microfibrils, lignin, and other cell wall components. The enhanced cellulose accessibility by cellulase in the PtrDUF579-3 suppressed plants could be caused by alternation of the linkage networks, suggesting that suppression of PtrDUF579-3 can be a useful approach for wood property engineering, which would be beneficial for industrial biofuel production.