Switchgrass Lignin Research Articles

Optimization of Cosolvent Enhanced Lignocellulosic Fractionation for Isolating Switchgrass Lignin with Distinct Structural Features Using Response Surface Methodology

Optimization of Cosolvent Enhanced Lignocellulosic Fractionation for Isolating Switchgrass Lignin with Distinct Structural Features Using Response Surface Methodology

Catalytic Transfer Hydrogenolysis of Switchgrass Lignin with Ethanol Using Spinel-Type Mixed-Metal Oxide Catalysts Affords Control of the Oxidation State of Isolated Aromatic Products

Catalytic Transfer Hydrogenolysis of Switchgrass Lignin with Ethanol Using Spinel-Type Mixed-Metal Oxide Catalysts Affords Control of the Oxidation State of Isolated Aromatic Products

Atomistic Simulations of Polydisperse Lignin Melts Using Simple Polydisperse Residue Input Generator.

Understanding the physics of lignin will help rationalize its function in plant cell walls as well as aiding practical applications such as deriving biofuels and bioproducts. Here, we present SPRIG (Simple Polydisperse Residue Input Generator), a program for generating atomic-detail models of random polydisperse lignin copolymer melts i.e., the state most commonly found in nature. Using these models, we use all-atom molecular dynamics (MD) simulations to investigate the conformational and dynamic properties of polydisperse melts representative of switchgrass (Panicum virgatum L.) lignin. Polydispersity, branching and monolignol sequence are found to not affect the calculated glass transition temperature, Tg. The Flory-Huggins scaling parameter for the segmental radius of gyration is 0.42 ± 0.02, indicating that the chains exhibit statistics that lie between a globular chain and an ideal Gaussian chain. Below Tg the atomic mean squared displacements are independent of molecular weight. In contrast, above Tg, they decrease with increasing molecular weight. Therefore, a monodisperse lignin melt is a good approximation to this polydisperse lignin when only static properties are probed, whereas the molecular weight distribution needs to be considered while analyzing lignin dynamics.

Natural Variation in Lignin and Pectin Biosynthesis-Related Genes in Switchgrass (Panicum virgatum L.) and Association of SNP Variants with Dry Matter Traits

Switchgrass (Panicum virgatum), a C4 perennial grass native to North America and developed as a sustainable biofuel feedstock, occurs in two ecotypes, lowland and upland, which vary in their architecture as well as their range of adaptation. In this study, we assessed single nucleotide polymorphism (SNP) variation in 372 switchgrass genotypes for nine genes involved in lignin and pectin biosynthesis. STRUCTURE results at K = 3 differentiated the genotypes into three genetic subpopulations that corresponded largely to the previously characterized upland C1 and lowland C2 and C3 subpopulations. Out of the 146 SNPs identified, 19 SNPs were non-synonymous, including two non-conservative and common SNPs in cinnamyl alcohol dehydrogenase (CAD, Chr01N) and p-coumarate3-hydroxylase (C3H, Chr09N), two genes in the lignin biosynthesis pathway. Allele status at seven of the 19 non-synonymous SNPs, including the non-conservative SNP in C3H, was significantly associated with four dry matter traits within subpopulations. Dry matter traits appeared to be mostly dominant and three of them (acid detergent fiber, non-fiber carbohydrate, water-soluble carbohydrates) were the most frequently differentiated traits. In addition, a heterosis effect was detected at the non-conservative SNP in phenylalanine ammonia-lyase (PAL) for neutral detergent fiber. Association analysis revealed the CAD gene on Chr01N, its homoeolog on Chr01K and cinnamate 4-hydroxylase (C4H, Chr03K) as potential candidates associated with dry matter traits. Further analyses are needed to determine whether these candidate genes play a role in switchgrass lignin content and could be exploited to reduce recalcitrance in this bioenergy crop.

Gene regulatory networks for lignin biosynthesis in switchgrass (Panicum virgatum).

SummaryCell wall recalcitrance is the major challenge to improving saccharification efficiency in converting lignocellulose into biofuels. However, information regarding the transcriptional regulation of secondary cell wall biogenesis remains poor in switchgrass (Panicum virgatum), which has been selected as a biofuel crop in the United States. In this study, we present a combination of computational and experimental approaches to develop gene regulatory networks for lignin formation in switchgrass. To screen transcription factors (TFs) involved in lignin biosynthesis, we developed a modified method to perform co‐expression network analysis using 14 lignin biosynthesis genes as bait (target) genes. The switchgrass lignin co‐expression network was further extended by adding 14 TFs identified in this study, and seven TFs identified in previous studies, as bait genes. Six TFs (PvMYB58/63, PvMYB42/85, PvMYB4, PvWRKY12, PvSND2 and PvSWN2) were targeted to generate overexpressing and/or down‐regulated transgenic switchgrass lines. The alteration of lignin content, cell wall composition and/or plant growth in the transgenic plants supported the role of the TFs in controlling secondary wall formation. RNA‐seq analysis of four of the transgenic switchgrass lines revealed downstream target genes of the secondary wall‐related TFs and crosstalk with other biological pathways. In vitro transactivation assays further confirmed the regulation of specific lignin pathway genes by four of the TFs. Our meta‐analysis provides a hierarchical network of TFs and their potential target genes for future manipulation of secondary cell wall formation for lignin modification in switchgrass.

Biomass augmentation through thermochemical pretreatments greatly enhances digestion of switchgrass by Clostridium thermocellum

BackgroundThe thermophilic anaerobic bacterium Clostridium thermocellum is a multifunctional ethanol producer, capable of both saccharification and fermentation, that is central to the consolidated bioprocessing (CBP) approach of converting lignocellulosic biomass to ethanol without external enzyme supplementation. Although CBP organisms have evolved efficient machinery for biomass deconstruction, achieving complete solubilization requires targeted approaches, such as pretreatment, to prepare recalcitrant biomass feedstocks for further biological digestion. Here, differences between how C. thermocellum and fungal cellulases respond to senescent switchgrass prepared by four different pretreatment techniques revealed relationships between biomass substrate composition and its digestion by the two biological approaches.ResultsAlamo switchgrass was pretreated using hydrothermal, dilute acid, dilute alkali, and co-solvent-enhanced lignocellulosic fractionation (CELF) pretreatments to produce solids with varying glucan, xylan, and lignin compositions. C. thermocellum achieved highest sugar release and metabolite production from de-lignified switchgrass prepared by CELF and dilute alkali pretreatments demonstrating greater resilience to the presence of hemicellulose sugars than fungal enzymes. 100% glucan solubilization and glucan plus xylan release from switchgrass were achieved using the CELF–CBP combination. Lower glucan solubilization and metabolite production by C. thermocellum was observed on solids prepared by dilute acid and hydrothermal pretreatments with higher xylan removal from switchgrass than lignin removal. Further, C. thermocellum (2% by volume inoculum) showed ~ 48% glucan solubilization compared to < 10% through fungal enzymatic hydrolysis (15 and 65 mg protein/g glucan loadings) of unpretreated switchgrass indicating the effectiveness of C. thermocellum’s cellulosome. Overall, C. thermocellum performed equivalent to 65 and better than 15 mg protein/g glucan fungal enzymatic hydrolysis on all substrates except CELF-pretreated substrates. CELF pretreatments of switchgrass produced solids that were highly digestible regardless of whether C. thermocellum or fungal enzymes were chosen.ConclusionsThe unparalleled comprehensive nature of this work with a comparison of four pretreatment and two biological digestion techniques provides a strong platform for future integration of pretreatment with CBP. Lignin removal had a more positive impact on biological digestion of switchgrass than xylan removal from the biomass. However, the impact of switchgrass structural properties, including cellulose, hemicellulose, and lignin characterization, would provide a better understanding of lignocellulose deconstruction.

A novel flocculant prepared by lignin nanoparticles-gelatin complex from switchgrass for the capture of Staphylococcus aureus and Escherichia coli

Lignin nanoparticles (L-NPs) were firstly prepared from switchgrass lignin by using ultrasonic-assisted alkali method, after which L-NPs were assembled with gelatin to constitute L-NPs-gelatin complex as a novel flocculant. Both Gram-positive (Staphylococcus aureus, S.aureus) and Gram-negative (Escherichia coli, E.coli) strains were used to investigate the flocculation property of L-NPs and L-NPs-gelatin complex. It was found that L-NPs-gelatin complex exhibited relatively better flocculation capacity than L-NPs, in which the flocculation efficiency was greatly affected by pH and dosage. For both indicator strains, flocculation efficiency (>95%) was achieved within 30 min at pH 4.5, while the flocculation efficiency of 90% costed 60 min at pH 5. The L-NPs-gelatin complex was promising to be applied for flocculating bacteria in wastewater treatment, enrichment and detection of microorganism, etc.

Effect of in Vivo Deuteration on Structure of Switchgrass Lignin

Biomass deuteration is an effective engineering method that can be used to provide key insights into understanding of biomass recalcitrance and the complex biomass conversion process. In this study, production of deuterated switchgrass was accomplished by growing the plants in 50% D2O under hydroponic conditions in a perfusion chamber. Cellulolytic enzyme lignin was isolated from deuterated switchgrass, characterized by Fourier transform infrared (FTIR), gel permeation chromatography (GPC), and nuclear magnetic resonance (NMR) and compared with its protiated control sample to determine the effect of in vivo deuteration on the chemical structure of lignin. FTIR results showed that D2O can be taken up by the roots and transported to the leaves, and deuterium was subsequently incorporated into hydroxyl and alkyl groups in the plant and its lignin through photosynthesis. According to GPC results, deuterated lignin had slightly higher molecular weight, presumably due to isotope effects. 31P and heteronuclear s...

Switchgrass forage yield and biofuel quality with no-tillage interseeded winter legumes in the southern Great Plains

ABSTRACTInformation is limited on using winter legumes as a source of nitrogen (N) intercropped with switchgrass in the southern Great Plains of the United States. The objectives of this study were to evaluate N contribution of several winter legumes to switchgrass, and to determine the influence of winter legumes on biofuel quality and soil fertility status. Field experiments were conducted at two locations in Oklahoma in which six winter legumes and four rates of N fertilizer were studied over a 3-year period. Winter legumes did not increase switchgrass forage yield, cellulose, lignin, and hemicellulose concentrations at any location. Soil organic matter (OM), nitrate-N (NO3-N), soil test phosphorus (P), soil test potassium (K), and soil pH remained unchanged. In contrast, applying inorganic N only increased switchgrass yield. This study demonstrated that southern Great Plains may not be conducive to utilizing legumes as the primary N source for switchgrass.

Lignin‐based carbon fibers: Accelerated stabilization of lignin fibers in the presence of hydrogen chloride

ABSTRACTOrganosolv switchgrass lignin (SGL) and hardwood lignin (HWL) polymers are used as precursors to prepare low cost carbon fibers (CFs). Lignin powder and fiber samples are stabilized and carbonized at different conditions to investigate the effect of HCl on thermal‐oxidative stabilization time, mass yield, fiber diameter, and mechanical properties. The results show that HCl can accelerate stabilization and reduce the stabilization time from many hours to 75 min for the SGL fibers, and to 35 min for the HWL fiber. The rate of rapid stabilization in HCl/air is at least four times faster than conventional stabilization in air. The CFs prepared with two different stabilization methods have almost the same strength and modulus, but higher carbon yield is obtained with the rapid stabilization due to a short time of oxidation. Pores and defects observed on the surface and the cross‐section of the CFs across all stabilization conditions contribute to low fiber strength. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017, 134, 45507.

Improving Processing and Performance of Pure Lignin Carbon Fibers through Hardwood and Herbaceous Lignin Blends.

Lignin/lignin blends were used to improve fiber spinning, stabilization rates, and properties of lignin-based carbon fibers. Organosolv lignin from Alamo switchgrass (Panicum virgatum) and yellow poplar (Liriodendron tulipifera) were used as blends for making lignin-based carbon fibers. Different ratios of yellow poplar:switchgrass lignin blends were prepared (50:50, 75:25, and 85:15 w/w). Chemical composition and thermal properties of lignin samples were determined. Thermal properties of lignins were analyzed using thermogravimetric analysis and differential scanning calorimetry. Thermal analysis confirmed switchgrass and yellow poplar lignin form miscible blends, as a single glass transition was observed. Lignin fibers were produced via melt-spinning by twin-screw extrusion. Lignin fibers were thermostabilized at different rates and subsequently carbonized. Spinnability of switchgrass lignin markedly improved by blending with yellow poplar lignin. On the other hand, switchgrass lignin significantly improved thermostabilization performance of yellow poplar fibers, preventing fusion of fibers during fast stabilization and improving mechanical properties of fibers. These results suggest a route towards a 100% renewable carbon fiber with significant decrease in production time and improved mechanical performance.

Characteristic properties of organosolv lignin/polylactide copolymers

A polylactide (PLA)/switchgrass organosolv lignin graft copolymer was synthesized via ring-opening polymerization. The resulting copolymer was characterized by size exclusion chromatography (SEC), differential scanning calorimetry, tensile testing, and hydrogen nuclear magnetic resonance spectroscopy. Phenolic hydroxyl content, percent lignin retained, and ultraviolet (UV) light transmission were investigated by UV light spectroscopy. Hydrolytic degradation and water vapor transmission rates were also investigated.It was found that the addition of organosolv switchgrass lignin to the polymer slowed the rate of degradation and water vapor transmission rate of the copolymer compared to the PLA homopolymer at varying temperatures. UV light transmission was also reduced with the addition of lignin.

Effect of torrefaction temperature on lignin macromolecule and product distribution from HZSM-5 catalytic pyrolysis

Torrefaction is a low-temperature process considered as an effective pretreatment technique to improve the grindability of biomass as well as enhance the production of aromatic hydrocarbons from Catalytic Fast Pyrolysis (CFP). This study was performed to understand the effect of torrefaction temperature on structural changes in the lignin macromolecule and its subsequent influence on in-situ CFP process. Lignin extracted from southern pine and switchgrass (via organosolv treatment) was torrefied at four different temperatures (150, 175, 200 and 225°C) in a tubular reactor. Between the two biomass types studied, lignin from pine appeared to have greater thermal stability during torrefaction when compared with switchgrass lignin. The structural changes in lignin as a result of torrefaction were followed by using FTIR spectroscopy, solid state CP/MAS 13C NMR, 31P NMR spectroscopy and it was found that higher torrefaction temperature (200 and 225°C) caused polycondensation and de-methoxylation of the aromatic units of lignin. Gel permeation chromatography analysis revealed that polycondensation during torrefaction resulted in an increase in the molecular weight and polydispersity of lignin. The torrefied lignin was subsequently used in CFP experiments using H+ZSM-5 catalyst in a micro-reactor (Py-GC/MS) to understand the effect of torrefaction on the product distribution from pyrolysis. It was observed that although the selectivity of benzene-toluene-xylene compounds from CFP of pine improved from 58.3% (torrefaction temp at 150°C) to 69.0% (torrefaction temp at 225°C), the severity of torrefaction resulted in a loss of overall aromatic hydrocarbon yield from 11.6% to 4.9% under same conditions. Torrefaction at higher temperatures also increased the yield of carbonaceous residues from 63.9% to 72.8%. Overall, torrefying lignin caused structural transformations in both type of lignins (switchgrass and pine), which is ultimately detrimental to achieving a higher aromatic hydrocarbon yield from CFP.

Structural Analysis of Pyrolytic Lignins Isolated from Switchgrass Fast-Pyrolysis Oil

Structural characterization of lignin extracted from the bio-oil produced by fast pyrolysis of switchgrass (Panicum virgatum) is reported. This is important for understanding the utility of lignin as a chemical feedstock in a pyrolysis-based biorefinery scheme. Pyrolysis induces a variety of structural changes to lignin in addition to reduction in molecular weight. The guaiacol structural units remain largely intact, and some hemicellulose stays covalently linked to the lignin. However, two-dimensional 1H–13C HSQC NMR analysis shows an absence of γ-methylene hydrogens from β-O-4 linkages, implying that rearrangements in the propyl linking chains have occurred. Ferulate and hydroxyl phenol esters are still present in the pyrolyzed lignin, but at lower concentrations than in unpyrolyzed switchgrass lignin.

Structural Characterization of Lignin in Wild-Type versus COMT Down-Regulated Switchgrass

This study examined the chemical structural characteristics of cellulolytic enzyme lignin isolated from switchgrass focusing on comparisons between wild-type control and caffeic acid 3-O-methyltransferase (COMT) down-regulated transgenic line. Nuclear magnetic resonance (NMR) techniques including 13C, 31P, and two-dimensional 13C-1H heteronuclear single quantum coherence (HSQC) as well as gel permeation chromatography (GPC) were employed. Compared to the wild-type, the COMT down-regulated transgenic switchgrass lignin demonstrated a decrease in syringyl (S): guaiacyl (G) ratio and p-coumarate:ferulate ratio, an increase in relative abundance of phenylcoumaran unit, and a comparable content of total free phenolic OH groups along with formation of benzodioxane unit. In addition, COMT down-regulation had no significant effects on the lignin molecular weights during its biosynthesis process.

Characterization of organosolv switchgrass lignin by using high performance liquid chromatography/high resolution tandem mass spectrometry using hydroxide-doped negative-ion mode electrospray ionization

Method for identification of compounds in organosolv lignin.

Depolymerization and Hydrodeoxygenation of Switchgrass Lignin with Formic Acid

Organosolv switchgrass lignin is depolymerized and hydrodeoxygenated with a formic acid hydrogen source, 20 wt % Pt/C catalyst, and ethanol solvent. The combination of formic acid and Pt/C is found to promote production of higher fractions of lower molecular weight compounds in the liquid products. After 4 h of reaction, all of the switchgrass lignin is solubilized and 21 wt % of the biomass is shown to be converted into seven prominent molecular species that are identified and quantified. Reaction time is shown to be an important variable in affecting changes in product distributions and bulk liquid product properties. At 20 h of reaction, the lignin is significantly depolymerized to form liquid products with a 76 % reduction in the weighted average molecular weight. Elemental analysis also shows that the resultant liquid products have a 50 % reduction in O/C and 10 % increase in H/C molar ratios compared to the switchgrass lignin after 20 h.

Structural Characterization of Switchgrass Lignin after Ethanol Organosolv Pretreatment

Kanlow switchgrass was subjected to aqueous ethanol organosolv pretreatment, and ethanol organosolv lignin (EOL) was recovered through precipitation of pretreatment effluents. Ball-milled switchgrass lignin was also isolated from unpretreated and pretreated switchgrass. The obtained switchgrass lignins were characterized using Fourier transform infrared (FTIR) spectroscopy, 31P nuclear magnetic resonance (NMR), two-dimensional (2D) heteronuclear single-quantum coherence (HSQC) NMR spectroscopy, and gel permeation chromatography (GPC). The results showed that the molecular weight of switchgrass EOL lignin decreased while polydispersity increased. The pretreatment resulted in an increase of free phenolic guaiacyl and syringyl units and a decrease of the β-O-4 linkage content.

Structural changes in switchgrass lignin and hemicelluloses during pretreatments by NMR analysis

Switchgrass is currently being developed as a sustainable bio-energy crop due to its broad adaptability, high mass yield and low agricultural input. Its current conversion to biofuels is detrimentally impacted by its native recalcitrance which is typically addressed using chemical and/or biological pretreatments. In this study, extractives free switchgrass was pretreated with steam, dilute H 2SO 4 and lime at 160 °C for 1 h. The degradation and impact of pretreatment was estimated semi-quantitatively by 13C– 1H HSQC (heteronuclear single quantum coherence) NMR analysis of ball milled untreated and pretreated switchgrass samples in perdeuterated pyridinium chloride–DMSO-d 6 solvent system. As a result of steam pretreatment the resulting switchgrass was depleted of xylan and a slight degradation of lignin were observed. This was confirmed by the relative decrease of cross peak intensity for β-aryl ether, phenylcoumaran, resinol and dibenzodioxocin units. Significant structural changes observed due to the lime pretreatment of switchgrass was deacetylation/dissolution of hemicellulose and the extent of delignification was less however, a preferential removal p-hydroxy of benzoyl ester, ferulate and coumarate type linkages were notified from the HSQC studies. Finally the most significant degradation resulted in acid pretreatment involving ∼90% loss of hemicellulose and a substantial degradation of various lignin sub-units. These results are further supported by the composition analysis of the respective switchgrass samples.

Chemical compositions of four switchgrass populations

Four populations of switchgrass (Alamo, GA993, GA992, Kanlow), Panicum virgatum L., were studied for the difference of their chemical constituents. The extractives, Klason lignin, and carbohydrates compositions of the stem portion of these switchgrass populations were determined by gas chromatography mass spectroscopy (GC-MS) and high performance anion exchange chromatography with pulsed amperometric detection (HPAEC-PAD) respectively. Ball milled grass lignin (BMGL) was isolated and analyzed by NMR spectroscopy. The results demonstrated that the chemical compositions of four switchgrass populations were similar with the exception of the lignin content and chemical composition of extractives. The results of quantitative C-13 NMR spectroscopy indicated that switchgrass lignin consisted of p-hydroxylphenyl, guaiacyl, and syringyl units in an average ratio of 26:42:32 and incorporated with p-coumaric acid and ferulic acid at a level of approximately 0.20 per aromatic ring. The lignin structure of four switchgrass cultivars was comparable.