Structural characterization of alkaline hydrogen peroxide pretreated grasses exhibiting diverse lignin phenotypes
© Li et al.; licensee BioMed Central Ltd. 2012
Received: 23 December 2011
Accepted: 27 February 2012
Published: 6 June 2012
For cellulosic biofuels processes, suitable characterization of the lignin remaining within the cell wall and correlation of quantified properties of lignin to cell wall polysaccharide enzymatic deconstruction is underrepresented in the literature. This is particularly true for grasses which represent a number of promising bioenergy feedstocks where quantification of grass lignins is particularly problematic due to the high fraction of p- hydroxycinnamates. The main focus of this work is to use grasses with a diverse range of lignin properties, and applying multiple lignin characterization platforms, attempt to correlate the differences in these lignin properties to the susceptibility to alkaline hydrogen peroxide (AHP) pretreatment and subsequent enzymatic deconstruction.
We were able to determine that the enzymatic hydrolysis of cellulose to to glucose (i.e. digestibility) of four grasses with relatively diverse lignin phenotypes could be correlated to total lignin content and the content of p-hydroxycinnamates, while S/G ratios did not appear to contribute to the enzymatic digestibility or delignification. The lignins of the brown midrib corn stovers tested were significantly more condensed than a typical commercial corn stover and a significant finding was that pretreatment with alkaline hydrogen peroxide increases the fraction of lignins involved in condensed linkages from 88–95% to ~99% for all the corn stovers tested, which is much more than has been reported in the literature for other pretreatments. This indicates significant scission of β-O-4 bonds by pretreatment and/or induction of lignin condensation reactions. The S/G ratios in grasses determined by analytical pyrolysis are significantly lower than values obtained using either thioacidolysis or 2DHSQC NMR due to presumed interference by ferulates.
It was found that grass cell wall polysaccharide hydrolysis by cellulolytic enzymes for grasses exhibiting a diversity of lignin structures and compositions could be linked to quantifiable changes in the composition of the cell wall and properties of the lignin including apparent content of the p-hydroxycinnamates while the limitations of S/G estimation in grasses is highlighted.
KeywordsAlkaline hydrogen peroxide pretreatment Cellulosic biofuels Lignin Plant cell wall analysis Analytical pyrolysis
Biofuels and green chemicals from plant lignocellulose offer the promise of decreased petroleum consumption with the caveat that technological and economic barriers remain that impede large-scale industrial implementation. The polysaccharide portion of plant cell walls (cellulose and hemicellulose) is ideally suited to conversion via biochemical transformations due to the central placement of carbohydrates in cellular metabolism. A diverse set of enzymes and metabolic pathways currently exist that are capable of converting carbohydrates to a wide range of useful metabolites and recent progress in metabolic and protein engineering is expanding this range. The challenge to realizing the potential of plant cell wall polysaccharides is primarily due to the set of plant properties collectively known as “biomass recalcitrance”  that limit the availability of polysaccharides for biological conversion by enzymatic or catabolic routes. This recalcitrance is primarily derived from the heterogeneous supramolecular organization of the plant cell wall matrix or higher order structures in the plants and necessitates a chemical or physical pretreatment step prior to biological conversion . These higher order structures include considerations such as overall plant anatomy, cell wall thickness, covalent and non-covalent interactions between macromolecules (cellulose, hemicellulose, and lignin) as well as distribution of these macromolecules within the cell wall matrix.
Polysaccharides within secondary cell walls are embedded within a matrix of lignin that limits their accessibility. Lignin’s physiological role in the plant cell wall and the reason for its contribution to recalcitrance is to protect vulnerable carbohydrates from attack by pathogens, provide structural stability to the cell wall, and present a hydrophobic barrier to water penetration through cell types that serve the purpose of fluid transport. While lignin’s role in cell wall recalcitrance is universally accepted, the precise set of factors that contribute to this recalcitrance are not universally acknowledged. Factors specific to lignin’s role in recalcitrance have been proposed to include the total lignin abundance [3–5], lignin location within the cell wall , and the properties of lignin such as hydrophobicity , as well as indirect impacts such as lignin’s ability to bind enzymes .
Lignin is a polymer composed primarily from three “canonical” p-hydroxycinnamyl alcohols (monolignols) including coniferyl, sinapyl, and to a lesser extent p- coumaryl alcohols which form the guaiacyl (G), sinapyl (S), and p-hydroxyphenyl (H) units in lignin . Other “non-canonical” aromatic monomers taken from other points of the monolignol biosynthesis grid are known to be incorporated into the lignin polymeric framework as well [10, 11]. The linkages between monolignols can be through ethers such as the β-O-4 (β-aryl ether) and 5-O-4 (biphenyl ether) linkages, C-C (“condensed”) bonds such as 5–5 (biphenyl) linkages, or a combination of C-C and ether linkages as in β–5 + α-O-4 (phenylcoumaran) and β–β + γ-O-α + α-O-γ (resinol) among others , as well as ester linkages involving, for example, p-hydroxycinnamates . The total content and relative abundance of monolignols, their linkages, and degree of crosslinking with polysaccharides varies by plant taxa, plant developmental stage, and plant tissue [14–16]. Other features of lignin that differ between plant source include potentially the degree of polymerization (although this is not clear) and the number of free phenolic groups. Free phenolics provide initiation sites for alkaline and oxidative delignification and contribute to lignin’s alkali solubility [17, 18] due to deprotonation of phenolic hydroxyls at a lower pH than aliphatic hydroxyls.
A significant number of promising bioenergy feedstocks are commelinid monocots, specifically the Poaceae or grasses, and include agricultural wastes  such as corn stover, wheat straw, rice straw, and sugar cane bagasse and dedicated perennial energy crops such as switchgrass and Miscanthus spp. among others. Lignin composition and cell wall structural organization in grasses is significantly different from herbaceous and woody dicots (forbs and hardwoods, respectively) or gymnosperm lignins. One distinguishing feature of the monocot lignins is the considerable incorporation of the p-hydroxycinnamic acids including ferulic and p-coumaric acids [13, 20, 21]. Ferulate monomers and dimers are known to be ester-linked to glucuronoarabinoxylan  and are proposed to be involved in ether and C-C linkages to the lignin polymer that act as crosslinks between hemicellulose and lignin polymer chains [11, 13, 23]. Monomers of p- coumaric acid are proposed to be esterified to the lignin polymer at the γ-carbon of the side chain region of β-O-4 linked syringyl moieties  and to a lesser degree esterified to glucuronoarabinoxylan. Grass lignins are significantly more condensed (i.e. contain more C-C linkages between monolignols) and have higher phenolic hydroxyl contents than the lignins of dicots [21, 25] and an important implication of this is that more than 50% of grass lignins can be solubilized by treatment with alkali  due to the destruction of alkali-labile ester linkages along with the high free phenolic content improving lignin solubility in alkali .
Plants have typically neither been under selective evolutionary constraint nor bred to yield phenotypes that would yield high polysaccharide conversion for a bioenergy process, although the identification and propagation of forage crops with the phenotype for high digestibility in ruminants [27, 28] represents an important starting point. Examples include forage improvement studies on corn stover  and the identification of the brown midrib mutations in grasses including maize, millet, and sorghum  which have been known as having the phenotype for improved ruminant digestibility in corn for more than 50 years [30–32]. The brown midrib lines of maize are known to contain less lignin as well as altered monolignol ratios, and altered inter-monolignol linkages which the present work aims to exploit in comparing differences in the lignin contents and structures.
Alkaline hydrogen peroxide (AHP) pretreatment has been studied as a chemical pretreatment [33–36] and as a delignifying post-treatment [37, 38] and is based on treatment of biomass with hydrogen peroxide at alkaline pH (optimally at pH 11.5) at ambient or near-ambient temperatures and pressures. Due to the distinctive properties of their lignins and structural organization of their cell walls as described above, alkaline pretreatments are particularly effective for grasses, and it is known that AHP is less effective on forbs  and woody dicots (unpublished observations). We hypothesize that the cellulose enzymatic digestibility improvement resulting from AHP pretreatment may be attributable to the destruction of ferulate crosslinks as well as mild oxidation and solubilization of lignin. These outcomes have the net effect of improving the overall hydrophilicity of the cell wall matrix which can allow for water and hydrolytic enzyme penetration.
In this work, AHP pretreatment is used to generate a set of biomass samples exhibiting a diverse range of lignin contents and abundance of the p-hydroxycinnamates with the goal of better characterizing the relationship between a delignifying pretreatment, the composition and properties of the cell wall, and the digestibility by cellulolytic enzymes in grasses displaying a diverse natural range of lignin phenotypes. These lignin phenotypes include differences in total lignin content, differences in the relative abundance of monolignols incorporated into the cell wall with the consequence of altered linkages between monolignols, and differences in the ferulate content resulting in differences in the extent of cross-linking between cell wall polymers. Specifically, these biomass types consist of a switchgrass cultivar, a commercial hybrid corn stover, and two inbred brown midrib lines of maize (bm1 and bm3). The relationship between S/G ratios as determined by Py-GC/MS, thioacidolysis-GC/MS, and HSQC NMR are compared in parallel for the first time for grasses, while HSQC NMR is applied to characterize structural changes associated with the whole cell wall, with the overall intention of identifying and linking properties associated with grass lignins to improved cellulolytic enzyme digestibility.
Relationship between pretreatment, composition, and glucan enzymatic digestibility
Data plotted in Figure 2 represents the same data as in Figure 1 re-plotted to distinguish pretreatment condition. This shows an obvious ranking of the biomass types by both lignin removal and glucan digestibility, with the general trend that the corn stovers and, in particular, the lower lignin stovers show both improved glucan digestibility and lignin removal relative to the switchgrass, which can be considered more recalcitrant to both pretreatment and hydrolysis. Additionally, these data show that while the values differ, the responses of the four biomass types show similar trends.
Lignin characterization by py-GC/MS
Biomass-Derived Aromatic Monomers Quantified by Py-GC/MS
Retention Time (min)
Major Mass Fragment (m/z)
Another important finding from the data in Figure 3 is that 50–70% of the pyrolytically-derived aromatics initially present in the grasses consist of 4-vinylguaiacol and 4-vinylphenol, while the p- hydroxycinnamic acids may account for approximately 10–25% of grass lignins [25, 46]. This implies a higher fraction of these p-hydroxycinnamic acids are involved in pyrolytically-labile ester and/or ether bonds than the bulk lignin which is consistent with the literature [29, 42, 47–49]. While not representing only FA in the cell wall, the estimated pyrolytic FA may provide a good proxy of its content in addition to standard guaiacyl monolignols.
Lignin characterization by thioacidolysis-GC/MS
Thioacidolysis is based on the cleavage of ether inter-unit linkages in lignin by boron trifluoride in ethanethiol-dioxane, followed by derivatization of the released lignin fragments and identification and quantification by GC/MS . The thioacidolysis yield is dependent on the β-O-4 content of the lignin and since the β-O-4 content is dependent on S content (among others), grass lignins are known to have low monomer yields from thioacidolysis  relative to lignins from dicots, that typically have higher syringyl contents. Guaiacyl monolignols can be involved in much greater diversity of condensed C-C bonds at the C5 site on the aromatic ring and an increase in the G lignin content increases the potential for condensed bonds between monolignols, branching, and free phenolic hydroxyl groups. Additionally, the C-C linkages between monolignols are considerably more resistant to cleavage during alkaline chemical pulping  as well as during analytical methods such as thioacidolysis and pyrolysis .
Non-quantitative thioacidolysis was performed on all of the samples to generate the S/G ratios with the result plotted in Figure 5B. This shows that most of the samples have apparently higher S/G by thioacidolysis than by pyrolysis, especially for bm1 stover. One likely explanation for this discrepancy is that the ferulates which are liberated disproportionally to their abundance will contribute to guaiacyl-lignin products in pyrolysis that will artificially inflate the apparent guaiacyl-lignin content. Values obtained in the literature for typical S/G ratios of midrib and non-midrib corn stovers by thioacidolysis are slightly higher than our values . Another trend from Figure 5B is that the S/G ratios increase with increasing pretreatment. It is known that p-coumarates are esterified primarily to the γ-position of syringyl moieties and that this acylation has been shown to reduce the thioacidolysis yield of β-O-4 linked syringyl moieties by 40% . This could be a second interpretation for the trend of increasing S/G ratio as quantified by thioacidolysis, since removal of acylated p-coumarate during pretreatment will increase the syringyl yield during thioacidolysis. A third possible reason for the apparent enrichment in syringyl lignins by thioacidolysis for the hybrid stover and bm1 is if pretreatment is inducing condensation reactions, then only guaiacyl (and p-hydroxyphenyl) lignins would be able to participate in these and the corresponding thioacidolysis yield of guaiacyl and p-hydroxyphenyl lignins would decrease. This apparent increase in S/G ratio has been identified previously for the alkaline hydrogen peroxide bleaching of Kraft eucalypytus lignin .
Another significant result from Figure 6B is that the AHP-pretreated corn stovers have much lower thioacidolysis monomer yields relative to the untreated corn stovers (i.e. 1.0–1.2% vs. 5–12%) indicating that the lignin remaining in the cell wall is even more condensed after pretreatment. Three scenarios that may explain this are that AHP pretreatment may be preferentially solubilizing the less condensed lignins, cleaving β-O-4 bonds, or inducing condensation reactions comparable to, for example, oxidative laccase or peroxidase-mediated lignin polymerization [57, 58]. To determine whether lignin condensation was an important outcome of AHP pretreatment, a material balance on condensed lignin was performed using the data for mass loss during pretreatment, the Klason lignin content, and the thioacidolysis yield to estimate whether the total condensed lignin mass after pretreatment is greater than before pretreatment. The material balance did not show that the overall condensed lignin mass was increased so that pretreatment-induced condensation is presumably minimal.
It is known that in addition to coniferyl alcohol, bm1 lines incorporate coniferyl aldehyde into their lignins due to a presumed deficiency cinnamyl alcohol dehydrogenase (CAD), while caffeic acid O-methyltransferase (COMT) deficiency in bm3 lines results in benzodioxane structures in lignin deriving from incorporation 5-hydroxyguaiacyl moieties  in addition to a significantly reduced syringyl lignin content. These examples of alternate monolignol incorporation are known to yield distinct thioacidolysis products [55, 60] other than what are quantified in the present work and could contribute to both lower S/G ratios and the lower total thioacidolysis yields. We were able to identify peaks in only the untreated bm1 stover thioacidolysis chromatograms (data not shown) exhibiting an m/z of 354 and 384 which are proposed to be indene markers representing incorporation of coniferaldehyde and sinapaldehyde, respectively, into the growing lignin polymer due to CAD defficiency . The coniferaldehyde response was approximately 4.3% of the guaiacyl signal while the sinapaldehyde response was approximately 1.5% of the syringyl signal. These markers are only present in the untreated bm1stover which indicates these monomers are removed during AHP pretreatment.
Lignin characterization by HSQC NMR
Comparison of Methods for Estimation of S/G Ratios in the Residual Cell Wall
2D HSQC NMR
Hybrid corn stover, untreated
0.88 ± 0.097
0.64 ± 0.019
Hybrid corn stover, treated
1.01 ± 0.044
0.68 ± 0.031
Inbred bm3 stover untreated
0.26 ± 0.061
0.20 ± 0.015
Inbred bm3 stover, treated
0.27 ± 0.059
0.23 ± 0.036
In the aliphatic region of the spectrum (not shown), the peaks for 2-acetyl β-D xylopyranose units and 3-acetyl β-D-xylopyranose units were observed to disappear following pretreatment while the β-D-xylopyranose was retained, indicating that acetyl groups on xylans were cleaved by alkali and solubilized in both hybrid corn stover and bm3 stover which is consistent with HPLC data from our lab (not shown).
Lignocellulosic biomass represents a vast resource of reduced carbon that is overwhelming used for its existing structural value (as fiber and as a building material), for combustion, or as livestock forage rather than for the value of its chemical constituents. This is due to the challenges of deconstruction and fractionation of the biopolymer components of the plant cell wall, in particular due to the impact of lignin. Lignin structure, composition, and distribution within the cell wall of plants has obvious important economic implications for ruminant digestibility, chemical pulping, and cellulosic biofuels based on the biological conversion of plant cell wall polysaccharides. This work addresses this challenge by applying the generated data to relate glucan enzymatic digestibility to lignin and plant cell wall properties, to better characterize and understand the mechanism of AHP pretreatment for improved cell wall deconstruction, and to compare three analytical platforms (HSQC NMR, Py-GC/MS, and thioacidolysis) for the analysis of grass lignins.
Relating cell wall enzymatic digestibility to lignin properties
A number of recent reviews have provided an insightful assessment for what properties comprise a promising lignin phenotype for ease of polysaccharide enzymatic deconstruction [10, 24, 31]. From these it is possible to distinguish four lignin properties that may impact the enzymatic digestibility and/or the pretreatability of a plant cell wall: (1) total lignin content; (2) ratio of monolignols and the corresponding degree of condensed linkages between monolignols; (3) the location of the lignin; and (4) for grasses, the abundance of p- hydroxycinnamates and their makeup. To illustrate the impact of these lignin properties in the context of our work, a number of studies can be highlighted. For dicots, where ferulate crosslinking is not as significant a feature of cell walls, strong negative correlations have been shown between initial lignin content and cellulolytic enzyme digestibility for dilute acid pretreated alfalfa (Medicago sativa L)  and hot water  or dilute acid  pretreated Populus spp. For grasses, however, Iiyama and Lam  found that in vitro ruminant digestibility of untreated rye grass (Lolium sp.) displaying a diverse range of initial lignin contents (18–25% w/w) was not dependent on initial lignin content while the initial content of ferulate bridges was strongly, negatively correlated to digestibility. Similar trends have been shown previously in the literature  where both the cellulase degradability and the in vitro ruminant digestibility of bm3 and a “normal” cultivar of maize were strongly negatively correlated to the total content of alkali-labile p- hydroxycinnamates independent of lignin content over a wide range of Klason lignin contents (5.5% to 14.2%). Zhang et al. found that cellulolytic enzyme digestibility in 10 maize lines could be strongly negatively correlated to Klason lignin content (in the range of 12.4–15.2%), total etherified and esterified p-coumaric acid content, and β-O-4 abundance, but not to etherified ferulate content and S/G ratio. Other work has found unpretreated grasses with initial lignin contents in the range of 2–8% to be a strong predictor of in vitro ruminant digestibility . Taken together these results may indicate that for grasses at higher Klason lignin contents, cell wall digestibility is a strong function of the content of p- hydroxycinnamates, while at lower lignin contents, Klason lignin seems to be a better predictor of digestibility. Lignin removal or redistribution has an obvious impact of polysaccharide accessibility and enzymatic digestibility. Acid chlorite delignification of orchardgrass (Dactylis glomerata L) was found to significantly improved its rate of in vitro rumen digestibility . Yang and Wyman  showed that lignin removal in corn stover by hot water pretreatment in a flow-through reactor could be correlated to enzymatic digestibility, while hot water batch pretreatment could achieve comparable enzymatic digestibility without concomitant lignin removal. Because these pretreatments are performed above the glass transition temperature of lignin, the lignin is presumably relocalized outside the cell wall. Properties of lignin (e.g. β-O-4 content, free phenolics, S/G ratio, and ferulate content) other than those that are important for untreated cell wall digestibility may become important for pretreatment or delignification and result in improved digestibility after pretreatment.
Our results in Figures 123 and 4 indicate that the relationship between lignin content, ferulate and p-coumarate content (indirectly inferred from pyrolytic 4-vinylguaiacol and 4-vinylphenol abundance), and glucan enzymatic digestibility are all correlated. In particular it can be seen that functionalities between these properties are that Klason lignin and p- hydroxycinnamate content are linearly correlated which reveals their concurrent removal from the cell wall during AHP pretreatment. While it is not possible to determine directly which of these is the causal factor, it can be proposed that a combination of ferulate crosslink destruction and β-O-4 scission and a concomitant increase in free phenolics allows for lower molecular weight oligomers of lignin to be solubilized (but not necessarily significantly degraded) and removed from the cell wall. As stated previously, one interpretation of the digestibility “threshold” value in Figure 1 between a Klason lignin content of 10–15% may be the point where the internal environment of the cell wall becomes hydrophilic enough to allow water (and enzyme) penetration. Grabber et al. identified a similar digestibility threshold value for enzymatic sugar release at approximately 15% lignin content in plant cell cultures artificially lignified with p-hydroxycinnamate esters.
The relationship between S/G ratio and enzymatic digestibility is less straightforward than the total lignin content due to multiple confounding factors including the fact that the largest differences in S/G ratios are between dicots which typically contain the highest S/G ratios have significantly different cell wall organization and structures and grasses or gymnosperms (softwoods) which typically contain a high fraction of guaiacyl units in their lignins. The S/G ratios in grasses and herbaceous dicots have been proposed to be correlated to the susceptibility of the plant cell wall to enzymatic deconstruction either positively, negatively, or not at all as reviewed by Méchin et al.. As another example, after hot water pretreatment, cellulolytic glucose release was higher for natural Populus trichocarpa variants with higher S/G ratios  while total lignin content was a good predictor of cellulose conversion only at S/G ratios of less than 2.0. For alfalfa cell walls pretreated with dilute acid, large differences in enzymatic saccharification efficiencies were observed between various transgenic lines with significantly altered monolignol biosynthesis pathways, and in lines containing high H content, S/G ratio alone didn’t correlate with sugar yield . For hot water-pretreated Arabidopsis, cell walls with higher S/G ratio gave a much higher glucose yield . In grasses, Chen et al.,  correlated higher S/G ratios in untreated tall fescue (Festuca arundinacea) to decreased in vitro ruminant digestibility, although this result was confounded by total lignin content since increasing S/G was also correlated to increased total lignin content during plant maturation. Based on a study of 22 inbred maize lines, including four bm3 lines, Méchin  proposed that increasing the S/G ratio in grasses would improve the cellulolytic enzyme digestibility of grass cell walls and that p-coumarate acylation of syringyl moieties improved digestibility by decreasing interaction with carbohydrates. Our data in Figures 56 and 7 presenting the relative abundance of monolignols and their alteration and response to AHP pretreatment does not provide conclusive evidence of any strong influence of S/G ratio on lignin removal by pretreatment or on enzymatic conversion to glucose for any of the four grasses tested.
Mechanisms of pretreatment by AHP against plant cell wall polymers
AHP pretreatment solubilizes a fraction of the lignin in the cell wall which, by itself, improves enzymatic glucan digestibility. Based on our data in Figure 6 we can propose that AHP pretreatment destroys alkyl-aryl ether linkages and potentially results in recondensation reactions. In comparing the impacts of other pretreatments on lignin, Glasser et al. found similar results where steam explosion, dilute sulfuric acid, and organosolv pretreatments result in the destruction of alkyl-aryl ethers which lowered lignin monomer and dimer yields following permanganate oxidation and decreased the degree of polymerization of lignin remaining in the cell wall. They also found that considerable recondensation took place following dilute acid pretreatment. Our thioacidolysis lignin monomer yields for AHP pretreatment were significantly lower than the permanganate oxidation lignin monomer plus dimer yields of Glasser et al. for other pretreatments (including only one grass, barley straw) and may indicate that AHP pretreatment is particularly effective at β-O-4 scission.
During an AHP pretreatment performed at a pH near the pKa of H2O2 (pKa = 11.5), hydrogen peroxide is decomposed to several important lignin-acting species including the perhydroxyl anion (OOH–) and by a secondary decomposition to hydroxyl (·OH) and superoxide anion (·O2-) radicals . This β-O-4 scission by alkaline hydrogen peroxide is known from the literature on oxidative delignification and pulp bleaching . In alkaline hydrogen peroxide bleaching, which is performed at a pH lower than 11.5, the perhydroxyl anion is presumably the dominant reactive oxidant rather than oxidative radical species. The perhydroxyl anion is proposed to attack conjugated carbonyl bonds and is important for pulp brightening during bleaching rather than delignification . However, it has been shown that alkaline hydrogen peroxide bleaching can destroy internal alkyl-aryl ether bonds in lignin, while destruction of C-C bonds in the aliphatic region is possible in lignin subunits containing an adjacent phenolic hydroxyl moiety . Because of this, alkaline hydrogen peroxide delignification is improved in lignins with a high phenolic hydroxyl content . While initially grass lignins contain high phenolic hydroxyl contents, destruction of alkyl-aryl ethers in lignin would generate even more free phenolic groups and improve the solubilization of lignin in alkali and would presumably result in more sites of attack for delignification reactions.
It is also well-accepted that during alkaline oxygen or hydrogen peroxide bleaching, oxygen radical species are capable of lignin side chain cleavage and aromatic ring opening reactions [74, 75] that would result in lignin depolymerization and increasing lignin hydrophilicity. At a pH close to 11.5 or at lower pH in the presence of Fenton’s-inducing transition metals, free radical chemistry becomes an important contribution to oxidative lignin reactions. Recent work has demonstrated selective scission of β-O-4 bonds in aspen lignin by brown rot fungi followed by a concomitant increase in benzaldehydes, benzoic acids, and phenylglycerols in the side chain regions of the monolignols resulting from these cleavages . The proposed mechanism was through the Fenton’s generation of hydroxyl radicals from hydrogen peroxide which may be similar to the mechanism of AHP pretreatment.
In addition to alkyl-aryl ether scission, a wide range of reactions with lignin can take place during AHP pretreatment that increase lignin’s hydrophilicity . Recently, alkaline hydrogen peroxide bleaching of eucalyptus Kraft lignin was found to carboxylate the α-C  of the lignin side chain region using NMR. In addition to the previously identified delignification, increasing lignin hydrophilicity (e.g. through carboxylation) is another proposed mechanism for enzymatic digestibility improvement by AHP, whereby the mechanism of improved digestibility could be through a combination of increasing cell wall water swelling with ensuing improvement in enzyme penetration into the cell wall and through a decrease enzyme adsorption onto less hydrophobic lignins . Recently, lignin sulfonation or lignin removal and carboxylation through acid chlorite or AHP delignification were all found to improve the enzymatic digestibility of SO2-impregnated, steam-pretreated softwood presumably due to increased cell wall hydrophilicity  imparted by lignin functionalization. Nakagame et al. utilized dehydrogenative polymer (DHP) lignins synthesized from ferulic acid and coniferyl alcohol to determine that the increasing carboxylic acid content of the artificial lignins reduced the non-productive binding of cellulases to improve cellulolytic activity.
Comparison of lignin methods
Methods for determining the relative abundance of monomers in lignin include, among others, wet chemical lignin degradation techniques such as thioacidolysis , CuO oxidation , permanganate oxidation  and whole-cell wall methods such as analytical pyrolysis  and NMR [61–64]. One challenge to lignin characterization is that each method will have its own drawbacks and qualifications which, at a minimum, should be acknowledged when they are applied. As one example, degradative lignin analysis methods generally overestimate S-lignin  since these are less condensed and more prone to release monomers. As another example, p-hydroxycinnamates should ideally be distinguished from other monolignols in grasses when using NMR or analytical pyrolysis since response factors are significantly different . Using GC/MS analysis of the products of CuO lignin degradation, the 3 pools of monolignols (H, G, S) as well as p-hydroxycinnamic acids were distinguished for white rot fungi degradation of wheat straw  or wheat straw cell wall fractions . These were compared with results for analytical pyrolysis, which did not distinguish p-hydroxycinnamates from other lignins and found that the G + FA fraction was consistently significantly higher by analytical pyrolysis than by CuO degradation, presumably due to the disproportionate contribution by ferulates. This finding is in confirmation of our results in Figure 5 comparing S/G ratios where Py-GC/MS overestimates the guaiacyl fraction. One solution to this problem that has been proposed is to perform pyrolysis in the presence of tetramethylammonium hydroxide (TMAH) which yields distinctive markers for p-hydroxycinnamates  and allows estimation of their abundance relative to other lignin-derived aromatics. Determination of S/G ratios in dicots, where p-hydroxycinnamates are relatively insignificant, has resulted in much better agreement between methods. Recently, Py-GC/MS, thioacidolysis-GC/MS, and HSQC NMR have been used in parallel to characterize the lignins in woody [63, 64] and herbaceous  dicots with good agreement between S/G ratios estimated by each method. Our results in Figure 4 and Table 2 highlights this difficulty in obtaining convergent results between methods for grasses where p-hydroxycinnamates confound the analysis, although the results are likely to be internally consistent.
A number of notable findings were made in this work. The first is that total lignin content, pyrolytic 4-vinylguaiacol fractional yield (as a proxy for ferulate content), and pyrolytic 4-vinylphenol yield (as a proxy for p-coumarate content) were demonstrated to be negatively correlated to glucan digestibility for four grasses. Correlations were found between lignin content and glucan digestibility for these four species of grasses under different AHP pretreatments approximating a sigmoidal function with significant increases in digestibility occurring between 10 and 15% lignin content. We suspect that this threshold value may represent a critical level for cell wall hydrophobicity. The higher lignin content of the switchgrass was presumably the reason for its increased resistance to both pretreatment and digestibility. Another finding is that while S/G ratios for the grasses tested ranged from 0.2 to 2.2 as quantified by thioacidolysis, this parameter did not have any apparent quantifiable impact on either AHP pretreatment or enzymatic glucan digestibility although other significant differences in lignins between plant types may mask the effect of S/G ratio.
Another contribution of this work are the findings that the lignins of brown midrib corn stovers were significantly more condensed than a commercial hybrid corn stover (which is known from the literature) and that pretreatment with alkaline hydrogen peroxide under conditions that solubilizes approximately 50% of the lignin results in the fraction of condensed lignin increasing from 88–95% w/w to 99% w/w. This has the implication that, in addition to alkaline saponification of ester-linked p-hydroxycinnamates, one of the major impacts of AHP pretreatment is to decrease the β-O-4 content of the lignin remaining in the cell wall and potentially to induce lignin condensation reactions with the net result of dramatically decreasing the lignin monomers releasable by thioacidolysis.
Additionally, this work compared three methods for S/G ratio estimation in untreated and AHP-pretreated grasses for the first time and highlighted the limitations and challenges due to the confounding influence of p-hydroxycinnamates. Specifically, Py-GC/MS results indicated that the majority of pyrolyzable aromatics from grass lignins are likely p-hydroxycinnamates which are liberated disproportionately to their abundance rather than S, G and H lignin units. Removal of the 4-vinylguaiacol contribution still resulted in significantly lower S/G ratios by pyrolysis than by thioacidolysis or whole-cell wall NMR. However, the results do indicate that methods should be internally consistent and yield relatively similar trends between biomass samples and between pretreatment conditions.
The biomass used in this study included switchgrass (Panicum virgatum cv. Cave-In-Rock) obtained from the Michigan Biotechnology Institute (Lansing, MI) and corn stovers (Zea mays L.) obtained from Natalia de Leon (University of Wisconsin, Madison). The corn stovers included a commercial hybrid (Pioneer Hi-Bred 36 H56) and two near-isogenic inbred lines of W64A maize containing the brown midrib alleles for bm1 and bm3 and were generated by introduction of the bm1 and bm3 mutations into the W64A background with 8 backcrosses followed by 6 self-pollinations. Biomass was initially milled with a Wiley MiniMill (Thomas Scientific) to pass a 2 mm screen and air-dried to ~5% moisture.
AHP pretreatment, composition analysis, and enzymatic glucan digestibility
The biomass samples were subjected to pretreatments corresponding to “low NaOH” (0.1 g NaOH/g biomass), “high NaOH” (2.2 g NaOH/g biomass), and pH 11.5 (corresponding to slightly more than 0.1 g NaOH/g biomass) where the pH was adjusted by addition of 5 M NaOH during pretreatment. The H2O2 loading was 0.125 g H2O2/g biomass with additional conditions for hybrid corn stover using loadings of 0.25 and 0.50 g H2O2/g biomass at a controlled pH of 11.5. Biomass concentration was 2% (w/w) biomass in 100 mL total volume, and the pretreatment was performed for 24 hours in a temperature-controlled incubator at 30°C with orbital shaking at 170 rpm. Pretreatments were performed in duplicate and the untreated biomass was used as the control. Following pretreatment, biomass was subjected to vacuum filtration with simultaneously washing by deionized water until neutral, then was air-dried to ~5% moisture content. The pretreated biomass was subsequently ball-milled with a QIAGEN TissueLyser II equipped with 25 mL stainless steel jars and 20 mm diameter stainless steel balls at 25 Hz for 2 minutes with liquid nitrogen cooling. Compositional analysis was performed according to Sluiter et al. with the difference that an Aminex HPX-87 H (Bio-Rad, Hercules, CA) column was used. Duplicate compositional analysis was performed for each pretreatment condition and the results are presented on a total composition basis rather than an extractives-free basis. Mass decrease as a result of AHP pretreatment was determined gravimetrically after washing and filtration of the residual insoluble material. For enzymatic digestibility determination, the washed and pretreated biomass samples were incubated at 50°C for 24 hours with Accellerase 1500 (Genencor Inc., Palo Alto, CA) at a loading of 50 mg protein/g glucan, which was chosen with the assumption that this would be above a “saturation” limit for enzyme loading which might give the highest possible conversions for a pretreatment condition such that only substrate effects could be evaluated. The conditions for hydrolysis were 10% solid loading at 5 mL total volume in 0.05 M Na-citrate buffer pH 4.8 for 24 hours. The enzymatic yield of glucose was determined by the HPLC analyzable glucose concentration after incubation divided by the original glucan content in the pretreated samples. Our previous work has demonstrated that approximately 5% of the glucan content may be solubilized during AHP pretreatment  possibly as sucrose, β-glucans, starch, or by oxidative modification of glucan.
Thioacidolysis was used to estimate the relative abundance and total yield of β-O-4 linked S, G, and H monolignols according to Foster et al.. A 60 mg aliquot of the dried biomass was first ball milled in the iWall grinding and feeding robot using three 5 mm stainless steel ball bearings. Using the ball-milled biomass, three replicate assays of 2 mg each were weighed into glass screw cap reaction vials. To the vials, 200 μL of anhydrous 1,4-dioxane containing 2.5% (v/v) borontrifluoride diethyl etherate and 10% (v/v) ethanethiol was added and incubated at 100°C for 4 hours in a heating block. After cooling the samples on ice, 150 μL of 0.4 M sodium bicarbonate was added and then the reaction is extracted with 1 mL of water and 0.5 mL of ethyl acetate. A 150 μL aliquot of the organic phase was transferred to a 2 mL vial and evaporated under a gentle stream of dry air. An addition of 200 μL of dry acetone was added and evaporated twice to help rid the samples of residual water. The dried monomer residue was dissolved in 500 μL of ethyl acetate and transferred to a GC vial to which 20 μL of pyridine and 100 μL of N,O-bis(trimethylsilyl)acetamide is added. The reaction was left to incubate at room temperature for 2 hours before injecting onto the GC/MS (Agilent 6890 GC/Agilent 5975B MSD, Column: Agilent HP-5MS). To determine the quantitative yield of the monomers, synthetic thiol derivatives of the S, G, and H lignin monomers were graciously provided by Dr. John Ralph (University of Wisconsin, Madison) and an alternate method (manuscript in preparation) was adapted from Foster et al.  and Robinson and Mansfield  for quantitative analysis. Mass yields of thioacidolysis-liberated monomers were determined by conversion from the molar concentrations of the standards using the following conversion factors for the assumption that the monolignol is involved in only β-O-4 linkages: syringyl, 223 g/mol; guaiacyl, 192 g/mol; p-hydroxyphenyl, 161 g/mol. All samples were run in triplicate.
Ball-milled control and pretreated samples (500–1000 μg) were pyrolyzed in a quartz tube in a CDS AS 5250 Pyroprobe (Chemical Data Systems Analytical, Inc., Oxford, PA) at 650°C for 20 seconds at a filament heating rate of 1000°C/s using helium as the carrier gas with a flow rate of 1 mL/min. The sample was carried onto a 60 m × 0.25 μm × 0.25 μm Restek 1701 column fitted in a Shimadzu GC/MS-QP5050 with a 100 split ratio. The temperature was programmed to rise from 40°C to a final temperature of 270°C at 8°C/min, and held at that temperature for a total run time of 45 minutes. The injector and detector temperatures were set at 280°C. Mass spectra were recorded in electron ionization mode for m/z 40 to 400. Peaks were quantified by integrated area of each peak divided by the total peak area and the average of duplicates were taken, and identified based on the compound library of Shimadzu GCMSsolution software and by comparison to the NIST database or the literature  for 4-vinylphenol. The majority of the pyrolytic compounds in those chromatograms were identified with compound similarities greater than 80%.
Cell wall 2D HSQC NMR profiling
The pre-milled commercial hybrid and bm3 corn stover samples were sequentially extracted by 70% ethanol, methanol/chloroform (1:1 v/v) and acetone. Approximately 30–50 mg of extractives-free sample were ball-milled for a total of 15 min in a Retsch Mixer Mill MM-200 (Retsch GmbH, Düsseldorf, Germany) and dissolved in anhydrous perdeuterated pyridinium chloride/DMSO-d6 bisolvent system (700 mg, 1:3 w/w) for 2D heteronuclear single quantum correlation (HSQC) 13 C-1 H NMR experiments which were carried out at 65 °C in a Bruker Avance 400 MHz NMR spectrometer equipped with a z-gradient triple-resonance probe [62, 83]. A 1JCH coupling constant of 145 Hz was used for all the HSQC experiments. The HSQC acquisitions were carried out with the following conditions: 10-ppm spectra width in F2 (1 H) dimension with 2048 data points, 210-ppm spectra width in F1 (13 C) dimension with 128 data points, 1.5-s pulse delay, and 380 scans. The DMSO solvent peak (i.e. δC 39.5 ppm and δH 2.5 ppm) was used for the chemical shift calibration. Bruker TopSpin 2.1 software was used to process NMR spectra data.
Alkaline hydrogen peroxide
Gas chromatography mass spectrometry
High performance liquid chromatography
Heteronuclear single-quantum correlation
Nuclear magnetic resonance
The authors would like to thank Dr. Natalia de Leon (University of Wisconsin, Madison) for generously providing corn stover samples, Dr. Farzaneh Teymouri at the Michigan Biotechnology Institute for the donation of switchgrass samples, and Dr. John Ralph (University of Wisconsin, Madison) for synthesizing thioacidolysis standards. This work was funded by the DOE Great Lakes Bioenergy Research Center (DOE BER Office of Science DE-FC02-07ER64494).
- Himmel ME, Ding SY, Johnson DK, Adney WS, Nimlos MR, Brady JW, Foust TD: Biomass Recalcitrance: Engineering Plants and Enzymes for Biofuels Production. Science 2007, 315: 804-807.View ArticleGoogle Scholar
- Wyman CE, Balan V, Dale BE, Elander RT, Falls M, Hames B, Holtzapple MT, Ladisch MR, Lee YY, Mosier N, et al.: Comparative data on effects of leading pretreatments and enzyme loadings and formulations on sugar yields from different switchgrass sources. Biores Technol 2011, 102: 11052-11062.View ArticleGoogle Scholar
- Chen F, Dixon RA: Lignin modification improves fermentable sugar yields for biofuel production. Nat Biotechnol 2007, 25: 759-761.View ArticleGoogle Scholar
- Studer MH, DeMartini JD, Davis MF, Sykes RW, Davison B, Keller M, Tuskan GA, Wyman CE: Lignin content in natural Populus variants affects sugar release. Proc Nat Acad Sci USA 2011, 108: 6300-6305.View ArticleGoogle Scholar
- Van Soest PJ: Nutritional Ecology of the Ruminant. 2nd edition. Cornell University Press, Ithaca, New York; 1994.Google Scholar
- Yang B, Wyman CE: Effect of xylan and lignin removal by batch and flowthrough pretreatment on the enzymatic digestibility of corn stover cellulose. Biotechnol Bioeng 2004, 86: 88-98.View ArticleGoogle Scholar
- Nakagame S, Chandra RP, Kadla JF, Saddler JN: Enhancing the enzymatic hydrolysis of lignocellulosic biomass by increasing the carboxylic acid content of the associated lignin. Biotechnol Bioeng 2011, 108: 538-548.View ArticleGoogle Scholar
- Rahikainen J, Mikander S, Marjamaa K, Tamminen T, Lappas A, Viikari L, Kruus K: Inhibition of enzymatic hydrolysis by residual lignins from softwood—study of enzyme binding and inactivation on lignin-rich surface. Biotechnol Bioeng 2011, 108: 2823-2834.View ArticleGoogle Scholar
- Adler E: Lignin chemistry-past, present and future. Wood Sci Technol 1977, 11: 169-218.View ArticleGoogle Scholar
- Bonawitz ND, Chapple C: The Genetics of Lignin Biosynthesis: Connecting Genotype to Phenotype. Annu Rev Gen 2010, 44: 337-363.View ArticleGoogle Scholar
- Ralph J: Hydroxycinnamates in lignification. Phytochemistry Reviews 2010, 9: 65-83.View ArticleGoogle Scholar
- Ralph J, Lundquist K, Brunow G, Lu F, Kim H, Schatz PF, Marita JM, Hatfield RD, Ralph SA, Christensen JH, Boerjan W: Lignins: Natural polymers from oxidative coupling of 4-hydroxyphenyl- propanoids. Phytochem Rev 2004, 3: 29-60.View ArticleGoogle Scholar
- Iiyama K, Lam TBT, Stone BA: Phenolic acid bridges between polysaccharides and lignin in wheat internodes. Phytochem 1990, 29: 733-737.View ArticleGoogle Scholar
- Chen L, Auh C, Chen F, Cheng X, Aljoe H, Dixon RA, Wang Z: Lignin Deposition and Associated Changes in Anatomy, Enzyme Activity, Gene Expression, and Ruminal Degradability in Stems of Tall Fescue at Different Developmental Stages. J Agric Food Chem 2002, 50: 5558-5565.View ArticleGoogle Scholar
- Terashima N, Nakashima J, Takabe K: Proposed Structure for Protolignin in Plant Cell Walls. Lignin and Lignan Biosynthesis, American Chemical Society 1998, 697: 180-193.View ArticleGoogle Scholar
- Grabber JH, Ralph J, Lapierre C, Barrière Y: Genetic and molecular basis of grass cell-wall degradability. I. Lignin-cell wall matrix interactions. C R Biol 2004, 327: 455-465.View ArticleGoogle Scholar
- Lapierre C, Jouin D, Monties B: On the molecular origin of the alkali solubility of Gramineae lignins. Phytochem 1989, 28: 1401-1403.View ArticleGoogle Scholar
- Froass PM, Ragauskas AJ, Jiang J-E: Nuclear Magnetic Resonance Studies. 4. Analysis of Residual Lignin after Kraft Pulping. Ind Eng Chem Res 1998, 37: 3388-3394.View ArticleGoogle Scholar
- Sun R (Ed): Cereal Straw as a Resource for Sustainable Biomaterials and Biofuels. Elsevier, Oxford, UK; 2010.Google Scholar
- Carpita NC: Structure and biogenesis of the cell walls of grasses. Annu Rev Plant Physiol Plant Molec Biol 1996, 47: 445-476.View ArticleGoogle Scholar
- Hatfield RD, Ralph J, Grabber JH: Cell wall cross-linking by ferulates and diferulates in grasses. J Sci Food Agric 1999, 79: 403-407.View ArticleGoogle Scholar
- Saulnier L, Crépeau M-J, Lahaye M, Thibault J-F, Garcia-Conesa MT, Kroon PA, Williamson G: Isolation and structural determination of two 5,5′-diferuloyl oligosaccharides indicate that maize heteroxylans are covalently cross-linked by oxidatively coupled ferulates. Carb Res 1999, 320: 82-92.View ArticleGoogle Scholar
- Bunzel M: Chemistry and occurrence of hydroxycinnamate oligomers. Phytochem Rev 2010, 9: 47-64.View ArticleGoogle Scholar
- Mechin V, Argillier O, Rocher F, Hebert Y, Mila I, Pollet B, Barriere Y, Lapierre C: In Search of a Maize Ideotype for Cell Wall Enzymatic Degradability Using Histological and Biochemical Lignin Characterization. J Agric Food Chem 2005, 53: 5872-5881.View ArticleGoogle Scholar
- Higuchi T, Ito Y, Kawamura I: p-hydroxyphenylpropane component of grass lignin and role of tyrosine-ammonia lyase in its formation. Phytochem 1967, 6: 875-881.View ArticleGoogle Scholar
- Hartley RD: Degradation of cell walls of forages by sequential treatment with sodium hydroxide and a commercial cellulase preparation. J Sci Food Agric 1983, 34: 29-36.View ArticleGoogle Scholar
- Vermerris W, Sherman DM, McIntyre LM: Phenotypic plasticity in cell walls of maize brown midrib mutants is limited by lignin composition. J Exp Bot 2010, 61: 2479-2490.View ArticleGoogle Scholar
- Findley W: Report of the corn improvement conference of the north central region. USDA Bureau of Plant Industry, Chicago, IL; 1953.Google Scholar
- Lam TBT, Iiyama K, Stone BA: Lignin and Hydroxycinnamic Acids in Walls of Brown Midrib Mutants of Sorghum, Pearl Millet and Maize Stems. J Sci Food Agric 1996, 71: 174-178.View ArticleGoogle Scholar
- Barrière Y, Argillier O: Brown-midrib genes of maize: a review. Agronomie 1993, 13: 865-876.View ArticleGoogle Scholar
- Barrière Y, Ralph J, Méchin V, Guillaumie S, Grabber JH, Argillier O, Chabbert B, Lapierre C: Genetic and molecular basis of grass cell wall biosynthesis and degradability. II. Lessons from brown-midrib mutants. C R Biol 2004, 327: 847-860.View ArticleGoogle Scholar
- Marita JM, Vermerris W, Ralph J, Hatfield RD: Variations in the cell wall Composition of maize brown midrib mutants. J Agric Food Chem 2003, 51: 1313-1321.View ArticleGoogle Scholar
- Saha BC, Cotta MA: Ethanol production from alkaline peroxide pretreated enzymatically saccharified wheat straw. Biotechnol Prog 2006, 22: 449-453.View ArticleGoogle Scholar
- Sun R, Lawther JM, Banks WB: Influence of alkaline pre-treatments on the cell wall components of wheat straw. Ind Crop Prod 1995, 4: 127-145.View ArticleGoogle Scholar
- Banerjee G, Car S, Scott-Craig J, Hodge D, Walton J: Alkaline peroxide pretreatment of corn stover: effects of biomass, peroxide, and enzyme loading and composition on yields of glucose and xylose. Biotechnol Biofuels 2011, 4: 16.View ArticleGoogle Scholar
- Gould JM: Enhanced polysaccharide recovery from agricultural residues and perennial grasses treated with alkaline hydrogen peroxide. Biotechnol Bioeng 1985, 27: 893-896.View ArticleGoogle Scholar
- Yang B, Boussaid A, Mansfield SD, Gregg DJ, Saddler JN: Fast and efficient alkaline peroxide treatment to enhance the enzymatic digestibility of steam-exploded softwood substrates. Biotechnol Bioeng 2002, 77: 678-684.View ArticleGoogle Scholar
- Kumar L, Chandra R, Saddler J: Influence of steam pretreatment severity on post-treatments used to enhance the enzymatic hydrolysis of pretreated softwoods at low enzyme loadings. Biotechnol Bioeng 2011, 108: 2300-2311.View ArticleGoogle Scholar
- Ralph J, Hatfield RD: Pyrolysis-GC-MS characterization of forage materials. J Agric Food Chem 1991, 39: 1426-1437.View ArticleGoogle Scholar
- Calvo AM, Terrón MC, Fidalgo ML, Pelayo JM, Galletti GC, González AE: Pyrolysis-gas chromatography–mass spectrometry characterization of wheat straw alkaline-cooking effluents after biological treatment with the fungi Phanerochaete chrysosporium and Ganoderma australe. Anal Chim Acta 1995, 309: 145-152.View ArticleGoogle Scholar
- Camarero S, Bocchini P, Galletti GC, Martínez AT: Pyrolysis-gas chromatography/Mass spectrometry analysis of phenolic and etherified units in natural and industrial lignins. Rap Com Mass Spectrom 1999, 13: 630-636.View ArticleGoogle Scholar
- del Río JC, Gutiérrez A, Rodríguez IM, Ibarra D, Martínez ÁT: Composition of non-woody plant lignins and cinnamic acids by Py-GC/MS, Py/TMAH and FT-IR. J Anal Appl Pyrolysis 2007, 79: 39-46.View ArticleGoogle Scholar
- Rodrigues J, Meier D, Faix O, Pereira H: Determination of tree to tree variation in syringyl/guaiacyl ratio of Eucalyptus globulus wood lignin by analytical pyrolysis. J Anal Appl Pyrolysis 1999, 48: 121-128.View ArticleGoogle Scholar
- Sykes R, Yung M, Novaes E, Kirst M, Peter G, Davis M: High-Throughput Screening of Plant Cell-Wall Composition Using Pyrolysis Molecular Beam Mass Spectroscopy. In Volume 2009, 581: 169-183.Google Scholar
- Camarero S, Bocchini P, Galletti GC, Martínez MJ, Martínez AT: Compositional changes of wheat lignin by a fungal peroxidase analyzed by pyrolysis-GC-MS. J Anal Appl Pyrolysis 2001, 58–59: 413-423.View ArticleGoogle Scholar
- Hatfield RD, Chaptman AK: Comparing Corn Types for Differences in Cell Wall Characteristics and p-Coumaroylation of Lignin. J Agric Food Chem 2009, 57: 4243-4249.View ArticleGoogle Scholar
- Camarero S, Galletti GC, Martínez AT: Preferential degradation of phenolic lignin units by two white rot fungi. Appl Environ Microbiol 1994, 60: 4509-4516.Google Scholar
- Fidalgo ML, Terron MC, Martinez AT, Gonzalez AE, Gonzalez-Vila FJ, Galletti GC: Comparative study of fractions from alkaline extraction of wheat straw through chemical degradation, analytical pyrolysis, and spectroscopic techniques. J Agric Food Chem 1993, 41: 1621-1626.View ArticleGoogle Scholar
- Zhang Y, Culhaoglu T, Pollet B, Melin C, Denoue D, Barrière Y, Baumberger Sp, Méchin Vr: Impact of Lignin Structure and Cell Wall Reticulation on Maize Cell Wall Degradability. J Agric Food Chem 2011, 59: 10129-10135.View ArticleGoogle Scholar
- Alves A, Schwanninger M, Pereira H, Rodrigues J: Analytical pyrolysis as a direct method to determine the lignin content in wood. J Anal Appl Pyrolysis 2006, 76: 209-213.View ArticleGoogle Scholar
- Robinson AR, Mansfield SD: Rapid analysis of poplar lignin monomer composition by a streamlined thioacidolysis procedure and near-infrared reflectance-based prediction modeling. Plant J 2009, 58: 706-714.View ArticleGoogle Scholar
- Lu F, Ralph J: Chapter 6 - Lignin, Cereal Straw as a Resource for Sustainable Biomaterials and Biofuels. Elsevier, Amsterdam; 2010:169-207.View ArticleGoogle Scholar
- Grabber JH, Quideau S, Ralph J: p-coumaroylated syringyl units in maize lignin: Implications for β-ether cleavage by thioacidolysis. Phytochem 1996, 43: 1189-1194.View ArticleGoogle Scholar
- Ibarra D, Chávez MI, Rencoret J, Del Río JC, Gutiérrez A, Romero J, Camarero S, Martínez MJ, Jiménez-Barbero J, Martínez AT: Lignin Modification during Eucalyptus globulus Kraft Pulping Followed by Totally Chlorine-Free Bleaching: A Two-Dimensional Nuclear Magnetic Resonance, Fourier Transform Infrared, and Pyrolysis − Gas Chromatography/Mass Spectrometry Study. J Agric Food Chem 2007, 55: 3477-3490.View ArticleGoogle Scholar
- Chabbert B, Tollier MT, Monties B, Barrière Y, Argillier O: Biological variability in lignification of maize: Expression of the brown midrib bm3 mutation in three maize cultivars. J Sci Food Agric 1994, 64: 349-355.View ArticleGoogle Scholar
- Barriere Y, Emile J, Traineau R, Surault F, Briand M, Gallais A: Genetic variation for organic matter and cell wall digestibility in silage maize. Lessons from a 34-year long experiment with sheep in digestibility crates. MYDCAH 2004, 49: 115-126.Google Scholar
- Martin-Sampedro R, Capanema EA, Hoeger I, Villar JC, Rojas OJ: Lignin Changes after Steam Explosion and Laccase-Mediator Treatment of Eucalyptus Wood Chips. J Agric Food Chem 2011, 59: 8761-8769.View ArticleGoogle Scholar
- Martin H: Review: lignin conversion by manganese peroxidase (MnP). Enz Microb Technol 2002, 30: 454-466.View ArticleGoogle Scholar
- Lu F, Marita JM, Lapierre C, Jouanin L, Morreel K, Boerjan W, Ralph J: Sequencing around 5-Hydroxyconiferyl Alcohol-Derived Units in Caffeic Acid O-Methyltransferase-Deficient Poplar Lignins. Plant Physiol 2010, 153: 569-579.View ArticleGoogle Scholar
- Lapierre C, Pilate G, Pollet B, Mila I, Leplé J-C, Jouanin L, Kim H, Ralph J: Signatures of cinnamyl alcohol dehydrogenase deficiency in poplar lignins. Phytochem 2004, 65: 313-321.View ArticleGoogle Scholar
- Kim H, Ralph J: Solution-state 2D NMR of ball-milled plant cell wall gels in DMSO-d6/pyridine-d5. Org Biomol Chem 2010, 8: 576-591.View ArticleGoogle Scholar
- Samuel R, Foston M, Jaing N, Cao S, Allison L, Studer M, Wyman C, Ragauskas AJ: HSQC (heteronuclear single quantum coherence) 13 C–1H correlation spectra of whole biomass in perdeuterated pyridinium chloride–DMSO system: An effective tool for evaluating pretreatment. Fuel 2011, 90: 2836-2842.View ArticleGoogle Scholar
- Rencoret J, Gutiérrez A, Nieto L, Jiménez-Barbero J, Faulds CB, Kim H, Ralph J, Martínez AT, del Río JC: Lignin composition and structure in young versus adult Eucalyptus globulus plants. Plant Physiol 2010, 155: 667-682.View ArticleGoogle Scholar
- Rencoret J, Marques G, Gutiérrez A, Ibarra D, Li J, Gellerstedt G, Santos JI, Jiménez-Barbero J, Martínez ÁT, del Río JC: Structural characterization of milled wood lignins from different eucalypt species. Holzforschung 2008, 62: 514-526.View ArticleGoogle Scholar
- Davison BH, Drescher SR, Tuskan GA, Davis MF, Nghiem NP: Variation of S/G ratio and lignin content in a Populus family influences the release of xylose by dilute acid hydrolysis. Appl Biochem Biotechnol 2006, 130: 427-435.View ArticleGoogle Scholar
- Iiyama K, Lam TBT: Structural characteristics of cell walls of forage grasses: their nutritional evaluation for ruminants. Asian-Aust J Anim Sci 2001, 14: 862-879.View ArticleGoogle Scholar
- Hartley RD, Jones EC: Phenolic components and degradability of the cell walls of the brown midrib mutant, bm3, of Zea mays. J Sci Food Agric 1978, 29: 777-782.View ArticleGoogle Scholar
- Jung HG, Vogel KP: Influence of Lignin on Digestibility of Forage Cell Wall Material. J Anim Sci 1986, 62: 1703-1712.Google Scholar
- Darcy BK, Belyea RL: Effect of Delignification upon In Vitro Digestion of Forage Celluloses. J Anim Sci 1980, 51: 798-803.Google Scholar
- Li X, Ximenes E, Kim Y, Slininger M, Meilan R, Ladisch M, Chapple C: Lignin monomer composition affects Arabidopsis cell-wall degradability after liquid hot water pretreatment. Biotechnol Biofuels 2010, 3: 1-7.View ArticleGoogle Scholar
- Glasser WG, Barnett CA, Muller PC, Sarkanen KV: The chemistry of several novel bioconversion lignins. J Agric Food Chem 1983, 31: 921-930.View ArticleGoogle Scholar
- Kadla John F, Chang Hm: The Reactions of Peroxides with Lignin and Lignin Model Compounds. Oxidative Delignification Chemistry, American Chemical Society 2001, 785: 108-129.View ArticleGoogle Scholar
- Gellerstedt G, Zhang L: Chemistry of TCF-Bleaching with Oxygen and Hydrogen Peroxide. Oxidative Delignification Chemistry, American Chemical Society 2001, 785: 61-72.View ArticleGoogle Scholar
- Gierer J: Formation and Involvement of Superoxide (O2-/HO2·) and Hydroxyl (OH·) Radicals in TCF Bleaching Processes: A Review. Holzforschung 1997, 51: 34-46.View ArticleGoogle Scholar
- Northey Robert A: A Review of Lignin Model Compound Reactions under Oxygen Bleaching Conditions. Oxidative Delignification Chemistry, American Chemical Society 2001, 785: 44-60.View ArticleGoogle Scholar
- Yelle DJ, Wei D, Ralph J, Hammel KE: Multidimensional NMR analysis reveals truncated lignin structures in wood decayed by the brown rot basidiomycete Postia placenta. Environ Microbiol 2011, 13: 1091-1100.View ArticleGoogle Scholar
- Pan XJ, Xie D, Gilkes N, Gregg DJ, Saddler JN: Strategies to enhance the enzymatic hydrolysis of pretreated softwood with high residual lignin content. Appl Biochem Biotechnol 2005, 121: 1069-1079.View ArticleGoogle Scholar
- Obst JR: Analytical pyrolysis of hardwood and softwood lignins and its use in lignin-type determination of hardwood vessel elements. J Wood Chem Technol 1983, 3: 377-397.View ArticleGoogle Scholar
- del Río JC, Rencoret J, Marques G, Li J, Gellerstedt Gr, Jiménez-Barbero Js, Martínez AnT, Gutiérrez A: Structural Characterization of the Lignin from Jute (Corchorus capsularis) Fibers. J Agric Food Chem 2009, 57: 10271-10281.View ArticleGoogle Scholar
- Sluiter A, Hames B, Ruiz R, Scarlata C, Sluiter J, Templeton D: Determination of Structural Carbohydrates and Lignin in Biomass. NREL Analytical Procedure National Renewable Energy Laboratory, Golden, CO; 2004.Google Scholar
- Banerjee G, Car S, Liu T, Williams DL, Meza SL, Walton JD, Hodge DB: Scale-up and integration of alkaline hydrogen peroxide pretreatment, enzymatic hydrolysis, and ethanolic fermentation. Biotechnol Bioeng 2011, 104: 922-931.Google Scholar
- Foster CE, Martin TM, Pauly M: Comprehensive Compositional Analysis of Plant Cell Walls (Lignocellulosic biomass) Part I Lignin. J Vis Exp 2010, 37: 5-8.Google Scholar
- Jiang N, Pu Y, Samuel R, Ragauskas AJ: Perdeuterated pyridinium molten salt (ionic liquid) for direct dissolution and NMR analysis of plant cell walls. Green Chem 2009, 11: 1762-1766.View ArticleGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.