- Open Access
Fate of p-hydroxycinnamates and structural characteristics of residual hemicelluloses and lignin during alkaline-sulfite chemithermomechanical pretreatment of sugarcane bagasse
Biotechnology for Biofuelsvolume 11, Article number: 153 (2018)
Preparing multiple products from lignocellulosic biomass feedstock enhances the profit and sustainability of future biorefineries. Grasses are suitable feedstocks for biorefineries as they permit a variety of possible by-products due to their particular chemical characteristics and morphology. Elucidating the fate of p-hydroxycinnamates (ferulates—FAs and p-coumarates—pCAs) and major structural components during bioprocessing helps to discriminate the sources of recalcitrance in grasses and paves the way for the recovery of p-hydroxycinnamates, which have multiple applications. To address these subjects, we assessed sugarcane bagasse biorefining under alkaline-sulfite chemithermomechanical (AS-CTM) pretreatment and enzymatic saccharification.
The mass balances of the major bagasse components were combined with 2D-NMR structural evaluation of process solids to advance our understanding of sugarcane bagasse changes during biorefining. AS-CTM pretreatment provided a high yield and thoroughly digestible substrates. The pretreated material was depleted in acetyl groups, but retained 62 and 79% of the original lignin and xylan, respectively. Forty percent of the total FAs and pCAs were also retained in pretreated material. After pretreatment and enzymatic hydrolysis, the residual solids contained mostly lignin and ester-linked pCAs, with minor amounts of FAs and non-digested polysaccharides. Saponification of the residual solids, at a higher alkali load, cleaved all the ester linkages in the pCAs; nevertheless, a significant fraction of the pCAs remained attached to the saponified solids, probably to lignin, through 4-O ether-linkages.
AS-CTM pretreatment provided soundly digestible substrates, which retain substantial amounts of xylans and lignin. Acetyl groups were depleted, but 40% of the total FAs and pCAs remained in pretreated material. Ester-linked pCAs detected in pretreated material also resisted to the enzymatic hydrolysis step. Only a more severe saponification reaction cleaved ester linkages of pCAs from residual solids; nevertheless, pCAs remained attached to the core lignin through 4-O ether-linkages, suggesting the occurrence of an alkali-stable fraction of pCAs in sugarcane bagasse.
Biorefining lignocellulosic biomass to produce fuel, chemicals and heat has been the target of extensive research and development during the last few decades. Due to the high costs of biomass processing via biochemical routes, including pretreatment and enzymatic saccharification steps, multiple-product biorefineries have been noted to enhance the profit and sustainability of the process [1, 2]. For biochemical routes of biomass processing, at least one pretreatment step is necessary to enhance access to the structural polysaccharides . Elucidating the physico-chemical mechanisms that describe the changes in biomass structure during pretreatment can help to reinforce biorefinery designs producing multiple products from the original feedstock.
Given their long-term use in the pulp and paper industry, pulping processes have served as the base for pretreatment in wood chips biorefining [4,5,6]. Sulfite chemithermomechanical (CTM) pulping is one of the industrially developed processes [7, 8] that have been successfully tuned for wood pretreatment . However, lignocellulose from grasses, a relevant raw material for large biorefineries , differs from wood feedstocks concerning morphology and chemical composition and thus requires tailored investigations . Grass internode morphology includes epithelial cells, and vascular bundles, which are rich in fibers and vessels, as well as large areas that are occupied by parenchymal cells [11, 12]. Nodes are even more complex and have been reported to be extremely recalcitrant . The singular morphology of grasses makes them very heterogeneous material for pretreatment purposes.
From a chemical point of view, in addition to cellulose, hemicelluloses and lignin, p-hydroxycinnamates (ferulates and p-coumarates) comprise a significant portion of the aromatic compounds present in grass cell walls [14,15,16]. Ferulates (FAs) and p-coumarates (pCAs) form esters predominantly with hemicelluloses and lignin, respectively [16, 18], which contribute to cell wall recalcitrance . Indeed, part of the p-hydroxycinnamates is detected as lignin via routine analytical techniques [14, 19].
In sugarcane, a detailed study discriminated lignin and p-hydroxycinnamates as core lignin and non-core lignin, respectively . The authors suggested that approximately 60% of the original aromatics in sugarcane are non-core lignin based on the relative abundances of pyrolysis products detected by gas chromatography coupled with mass spectrometry. Non-core lignin was the first aromatic fraction to be released during the alkaline treatment of sugarcane bagasse, providing a less recalcitrant pretreated material, whereas core-lignin was shown to be more resistant . UV microspectrophotometry also indicated that some of the p-hydroxycinnamates present in the fiber cell walls of sugarcane bagasse are resistant to alkaline-sulfite pretreatment . Another study using rice straw treatment under mild alkaline conditions revealed that ester-linked FAs were promptly released into the treatment liquor, whereas ester-linked pCAs decreased simultaneously with lignin at a slower rate . Under more severe reaction conditions, the 2D-NMR evaluation of sugarcane bagasse lignins recovered from soda/anthraquinone pulping liquors presented pCAs with “free” carboxylic acids linked to the core lignin through 4-O ether-linkages, suggesting the occurrence of an alkali-resistant pCA fraction in sugarcane .
Available data from the alkaline treatment of grasses suggest that some of the p-hydroxycinnamates remain attached to the pretreated material. Elucidating the fate of p-hydroxycinnamates and the structural characteristics of the residual lignin and xylan under these pretreatment conditions could help to discriminate sources of recalcitrance in sugarcane, which would enable new biorefinery models that include the recovery of p-hydroxycinnamates from grasses for multiple applications . These subjects were assessed in the current work using alkaline-sulfite CTM (AS-CTM) pretreatment of sugarcane bagasse under increasing loads of chemicals to provide a set of samples suitable for showing progressive changes in the structural characteristics of the pretreated materials. The enzymatic saccharification, chemical composition and mass balance of the main bagasse components were combined with a detailed structural evaluation of the pretreated materials based on 2D-NMR experiments to advance understanding of sugarcane bagasse changes that occur during AS-CTM pretreatment.
Sugarcane bagasse and pretreatments
Sugarcane bagasse was obtained from a local mill, and it was air dried and stored under dry conditions. Table 1 includes the chemical composition of the studied sugarcane bagasse sample. The AS-CTM pretreatment was based on a previous report . In the current study, sugarcane bagasse (air dried, non-milled material) was pre-cooked for 2 h at 120 °C using a solid:liquid ratio of 1:10 and three different alkaline-sulfite loads. In all experiments, the Na2SO3 load was twice that of NaOH and corresponded to 10, 5 or 2.5 g of Na2SO3 for each 100 g of dried sugarcane bagasse. Initial liquor pHs were 13.3, 13.0, and 12.7, respectively. Alkaline-sulfite pre-cooked sugarcane bagasse was separated from the cooking liquor by centrifugation, avoiding a washing step . Retained solids were refined at 2.4% (w/v) solids in a disk refiner up to 250 Wh of energy consumption . Pretreated material was recovered as a pulp slurry, which was dewatered by centrifugation up to a final humidity of 70%. Chlorite treatment was used to produce a reference sugarcane bagasse sample with reduced lignin content as previously described . The reaction time was 2 h and the temperature was set to 70–80 °C.
Chemical characterization, sugarcane bagasse component mass balance and sample microscopic evaluation
Before chemical characterization, all samples were air dried and milled to pass through a 0.84-mm screen. Untreated samples were extracted with 95 vol% ethanol for 6 h in a Soxhlet apparatus to characterize the extractives. Extracted samples and pretreated samples were hydrolyzed with sulfuric acid to determine their major components (lignin, glucan, xylan, arabinosyl groups and acetyl groups) as described elsewhere . Triplicate analyses were performed for each sample. The reported data correspond to the average values and their standard deviations. Ash content in the sugarcane bagasse sample was 2.8 ± 0.7%. Owing to this low ash content, acid insoluble ash present in klason lignin was not discounted in the total lignin contents reported in the text.
Ferulic and p-coumaric acids were determined after the alkaline treatment of milled samples at mild (1 M NaOH at 30 °C for 24 h) and severe (4 M NaOH at 170 °C for 2 h) reaction conditions as previously described . Triplicate analyses were performed for each sample. The reported data correspond to the average values and their standard deviations.
Mass balances for the major bagasse components, as well as for the FAs and pCAs, were calculated based on the initial contents that were recorded for the untreated samples and the final contents that were calculated as the percent composition multiplied by the solids yield recorded for each treatment condition.
Microscopic evaluation of the untreated sugarcane bagasse was performed after the samples were fixed in epoxy resin, cut along the transversal axes using a Leica EM UC7 ultramicrotome (1 µm thick), stained with toluidine blue and evaluated under an Olympus BX53 microscope as previously described . After AS-CTM pretreatment, fibrous pretreated material was suspended in water and visualized under an Olympus BX53 microscope. After enzymatic hydrolysis of the pretreated material, the residual solids were air dried and macerated in a mortar and pestle. Milled solids were suspended in water and visualized under an Olympus BX53 microscope.
Enzymatic hydrolysis of the pretreated materials
Pretreated bagasse samples were air dried, milled to pass through a 0.84-mm screen, and hydrolyzed with a commercial cellulase blend, Cellic CTec2 (SAE0020, SIGMA). The FPU activity of the commercial preparation was determined as described elsewhere . Pretreated samples were suspended in 50-mL Falcon tubes with 50 mM acetate buffer containing 0.01% sodium azide (w/v), pH 4.8, at 2% solids (w/v). The suspended samples were mixed with commercial enzymes to assure 10 FPU/g of substrate in a total reaction volume of 10 mL. Samples were taken after different hydrolysis periods, with up to 72 h of reaction time. Samples were boiled at 100 °C for 5 min to stop enzymatic activity. The glucose and xylose contents were determined by HPLC . Triplicate hydrolysis experiments were performed for each sample. The reported data correspond to the average values and their standard deviations. Cellulose and xylan conversions were calculated, respectively, from the amounts of glucose and xylose released during the hydrolysis, and they are expressed as a percentage of the theoretical maximum based on the glucan and xylan content of the pretreated material. To determine the yield of residual solids after 72 h of enzymatic digestion, the solids were washed 3 times with water, air dried and weighed.
Saponification reactions of the solids remaining after enzymatic hydrolysis
The residual solids formed after enzymatic hydrolysis were crushed in a mortar and pestle and submitted to saponification at 90 °C for 48 h. Each reaction was performed inside a 10-mL Falcon tube containing 50 mg of sample and 5 mL of 1 M NaOH. After completion, the reaction mixture was adjusted to pH 2.0 with 6 M HCl, and water was added to a final volume of 10 mL. The mixture was stored at 4 °C overnight and was then filtered through a 0.45-μm membrane and analyzed by HPLC to measure the ferulic and p-coumaric acid contents as previously described . To determine the yield of solids that remained after saponification, one analysis set was performed for each sample as described before, but residual solids were washed 3 times with water, air dried, and weighed.
2D-NMR characterization of pretreated materials and residual solids
2D-NMR characterization of the samples was performed using procedures already described [21, 24]. Briefly, approximately 50 mg of each biomass sample was dissolved in 0.75 mL of DMSO-d6, and NMR spectra were recorded at 25 °C using a Bruker AVANCE III 500 MHz instrument equipped with a cryogenically cooled 5-mm TCI gradient probe with inverse geometry (proton coils closest to the sample). Heteronuclear single quantum coherence (HSQC) experiments used Bruker’s ‘hsqcetgpsisp2.2’ pulse program (adiabatic-pulsed version) with spectral widths of 5000 Hz (from 10 to 0 ppm) and 23,843 Hz (from 165 to 0 ppm) for the 1H- and 13C-dimensions, respectively. The central solvent peak was used as an internal reference (δC 39.5; δH 2.49). HSQC correlation signals were assigned by comparing the results with previous evaluations of sugarcane bagasse samples [18, 21]. The 1H/13C correlation signals of H2,6, G2 and S2,6 in the aromatic region of the spectra were used to estimate the content of the respective H-, G- and S-lignin units (relative to the content of amorphous carbohydrates, estimated from the signals of the anomeric carbons in xylose, glucose and 4-O methyl-α-d-glucuronic acid). The signals for pCA2,6 and FA2 were used to estimate the abundance of the different p-hydroxycinnamates. The Cα/Hα correlation signals of the β-O-4′ alkyl aryl ethers (Aα) and phenylcoumarans (Bα) in the aliphatic-oxygenated region of the spectra were used to estimate their relative abundances (as per 100 aromatic units), whereas the Cγ/Hγ correlation signals were used to estimate the relative abundance of the cinnamyl alcohol end-units (as per 100 aromatic units).
Results and discussion
Pretreatment and enzymatic digestibility of pretreated samples
AS-CTM pretreatment performed with increasing alkaline-sulfite loads provided a set of pretreated sugarcane bagasse samples to investigate the fate of p-hydroxycinnamates (FAs and pCAs) and the structural characteristics of the residual hemicelluloses and lignin. A chlorite-delignified bagasse sample served as a reference material in the chemical characterization procedures and enzymatic hydrolysis experiments (Table 1).
Sulfite pretreatment enhances the efficiency of the enzymatic conversion of polysaccharides in several lignocellulosic materials [6, 29, 30]. In the case of sugarcane biomass, we demonstrated that this pretreatment can provide readily digestible materials depending on the chemical load used in the pretreatment and on the sugarcane cultivar . In the current work, sugarcane bagasse from the industrial production of sugar and ethanol was pretreated with increasing alkaline-sulfite loads to generate a single set of results in which the same sugarcane bagasse lot was pretreated, digested with highly active commercial enzymes  and chemically characterized in detail.
Enzymatic hydrolysis of the pretreated samples corroborated previous data , showing improved hydrolysis efficiency with increased chemical loads in the pretreatment (Additional file 1: Figure S1). The initial enzymatic hydrolysis rates and extent of polysaccharide conversion after 72 h of incubation are summarized in Table 2. The initial hydrolysis rates for xylan were lower than those for glucan, probably because xylo-oligosaccharides accumulate in the reaction medium and thus require the inclusion of hemicellulases for a better hydrolysis response . At a longer reaction time (72 h), the xylan conversion efficiency increased significantly but was still lower than that of glucan conversion. The glucan and xylan conversions reached their maximal values after pretreatment with the highest alkaline-sulfite load (95.6 and 78.9%, respectively). These glucan and xylan conversion efficiencies were slightly higher than those of a previous report . The use of a highly active enzymatic cocktail in the current work seemed to yield improved enzymatic hydrolysis efficiency . The reference chlorite-delignified sample was completely digested by the commercial enzymes after 72 h of incubation (Additional file 1: Figure S1).
Mass balance and structural modifications of sugarcane bagasse during AS-CTM pretreatment
The chemical composition of the pretreated materials and a mass balance of bagasse components confirmed that lignin removal was the main effect of the AS-CTM pretreatment. Limited washing of the pretreated solids avoided excessive dissolution of xylan, providing high solids yields after pretreatment (Table 1). The highest Na2SO3/NaOH load used in the current experiments provided 38% lignin removal and xylan losses were limited to 20.6%. Acetyl groups were also extensively hydrolyzed, reaching up to 97% removal at the highest alkaline-sulfite load. Glucans were almost completely preserved. Selective lignin removal is characteristic of alkaline- and neutral-sulfite processes performed with less than 50% delignification. Higher delignification levels usually cause the simultaneous loss of polysaccharides . In this context, alkaline-sulfite processes are suitable for biomass pretreatment purposes because 40–50% delignification has been proven to be enough to decrease biomass recalcitrance in a significant manner, permitting efficient polysaccharide conversion by commercial enzymes [25, 34, 35]. In the current work, the 2 h chlorite-delignified sample demonstrated this assertion for sugarcane bagasse, as lignin removal was selective, yet achieved 56% (Table 1), providing a substrate readily digestible by commercial enzymes (Table 2 and Additional file 1: Figure S1).
During AS-CTM pretreatment of sugarcane bagasse and after acid-chlorite delignification, FAs and pCAs were progressively removed at increasing chemical loads (Table 3). In grasses, FA is generally esterified to hemicelluloses (acylating the O-5 position of arabinosyl residues in arabinoxylans) with possible 4-O-β and 8-β cross-linkages to the lignin backbone; conversely, pCA is mainly esterified to the γ-OH of the syringyl (S) lignin units, typically as a terminal group in the polymer [16, 17].
The fate of FA and pCA during sugarcane bagasse pretreatment was initially evaluated by analytical determinations using mild (1 M NaOH at 30 °C) and severe (4 M NaOH at 170 °C) reaction conditions. These procedures would account for alkali-labile and total amounts of p-hydroxycinnamates, respectively [14, 36, 37]. Alkali-labile FA intensely decreased with increasing chemical loads in the pretreatment, whereas labile pCA decreased more gradually (Table 3). The total p-hydroxycinnamate content decreased with increasing alkaline-sulfite loads in the pretreatment but were detectable at high concentrations even after the most severe pretreatment (Table 3). Mass balances for total p-hydroxycinnamates indicated that 40% of the original FA and pCA content remained in the sample pretreated at the highest alkaline-sulfite load. It is noteworthy that alkaline conditions were maintained up to the end of each pretreatment condition (the final pH values of the pretreatment liquors were, respectively, 8.0, 8.5 and 9.8 for the increasing chemical loads used in the pretreatments). Nonetheless, some of the p-hydroxycinnamates remained attached to the pretreated materials. These data indicate that a significant fraction of the p-hydroxycinnamates was inaccessible to the alkaline liquor and/or that their ester linkages were cleaved, but they remained linked to the residual lignin and/or carbohydrates through 4-O ether cross-linkages.
2D-NMR-HSQC characterization of the pretreated samples clarified the fate of p-hydroxycinnamates as well as the structural characteristics of the residual hemicelluloses and lignin after pretreatment. Figure 1 presents the HSQC spectra of the untreated and AS-CTM pretreated sugarcane bagasse samples together with the chlorite-delignified reference sample. The main lignin and carbohydrate substructures that were found are also depicted in Fig. 1 and their correlation signals that were assigned in the HSQC spectra are listed in Additional file 2: Table S1. The HSQC spectra of the untreated and AS-CTM pretreated bagasse samples showed strong carbohydrate and lignin signals, whereas the spectrum of the reference-delignified sample essentially showed carbohydrate signals with a weak residual guaiacyl (G) lignin signal; the low concentrations of FA and pCA detected during wet chemical characterization of the chlorite-delignified sample (0.16 and 0.02%, respectively) were not detectable in the HSQC spectra. A semiquantitative analysis of the abundances of the different lignin units (H, G, S), p-hydroxycinnamates (pCA, FA), carbohydrates, and lignin inter-unit linkages and end groups was performed by volume integration of the respective correlation signals in the HSQC spectra and is shown in Table 4.
The most important hemicellulose signals in the spectra corresponded to the C2/H2, C3/H3, C4/H4, and C5/H5 correlations for xylans (X2, X3, X4, and X5) and the C4/H4 correlation for 4-O methyl-α-d-glucuronic acid (U4). Arabinosyl side groups were detected in the sugarcane samples only in low amounts (Table 1), but below the minimum needed to be detected in the HSQC spectra. Signals from O-acetylated xylans (3-O-acetyl-β-d-xylopyranoside, X′3, and 2-O-acetyl-β-d-xylopyranoside, X′2) were evident in the untreated sugarcane bagasse spectra. Other carbohydrate signals included the C1/H1 correlations for the anomeric carbons of β-d-xylopyranoside (X1), 2- and 3-O-acetyl-β-d-xylopyranosides (X′1), β-d-glucopyranoside (Gl1) and 4-O methyl-α-d-glucuronic acid (U1). All signal assignments for xylans confirmed that partially acetylated O-methylglucuronoxylans were the predominant hemicelluloses in sugarcane bagasse. Most of the carbohydrate signals observed in the HSQC spectra of the reference-delignified bagasse were also present in the spectra of the untreated bagasse and pretreated bagasse samples.
The signals from acetylated xylans (X′1, X′2 and X′3), which were present with substantial intensities in the spectra of the untreated bagasse and reference chlorite-delignified bagasse, gradually disappeared from the spectra of the pretreated bagasse samples as the alkaline-sulfite load increased (Fig. 1a–d). These data corroborated the wet chemical characterization results of the samples (Table 1), which indicated that the acetyl groups attached to the xylans were hydrolyzed and removed during the alkaline-sulfite pretreatment, but that part of the acetate was resistant to the treatment with up to 5% Na2SO3 and 2.5% NaOH (Fig. 1c). FA that usually esterifies arabinosyl side groups of hemicellulose in grasses  followed the same trend of the acetyl groups, as aromatic carbons from FA were detected with treatment at up to 5% Na2SO3 and 2.5% NaOH (Fig. 1c), corroborating the labile-FA contents determined using the mild hydrolysis procedure (Table 3). However, the residual total FA detected in the sample pretreated at the highest chemical load corresponded to 0.7% (Table 3), which was below the limit of detection of the HSQC (Fig. 1d, Table 4). U1 and U4 signals from O-methylglucuronic acid substituents were readily observed in HSQC spectra of the untreated sugarcane bagasse (Fig. 1a). After the mildest pretreatment (2.5% Na2SO3 and 1.25% NaOH), these signals were not detectable (Fig. 1b), suggesting that the O-methylglucuronic acid branched xylan fractions were preferentially solubilized during pretreatment.
Lignin signals were also observed in the HSQC spectra of the bagasse samples. The main lignin inter-unit linkages observed were β-O-4′ alkyl-aryl ethers (A). Intense signals in the δC/δH 62.7/3.83–4.30 range (which partially overlapped with the carbohydrate signals) from the Cγ/Hγ correlations of γ-acylated units demonstrated that pCA partially acylated the γ-OH in the lignin side-chains of some β-O-4′ substructures (A′) . Detection of A′ substructures by HSQC spectra corroborates the high contents of total pCA determined by wet chemical characterization (Table 3). Signals assigned to either Cβ/Hβ or Cα/Hα in β-O-4′ substructures (A and A′) decreased in intensity in the samples pretreated at the highest alkaline-sulfite loads, indicating that residual lignins were progressively depleted in β-O-4′ substructures (Table 4). Signals corresponding to phenylcoumaran structures (B) were also detected in the spectra and could be readily observed after magnification of the corresponding regions; contrary to β-O-4′ substructures, the abundance of phenylcoumarans remained essentially constant during the different treatments (Table 4). Signals corresponding to the Cγ/Hγ correlations of cinnamyl alcohol end groups (I) were also detectable in samples treated with up to 5% Na2SO3 and 2.5% NaOH (Fig. 1c, Table 4).
The main cross-signals in the aromatic regions of the HSQC spectra corresponded to the different lignin units and to the p-hydroxycinnamates. Signals from H-, G- and S-units were observed in the spectra of untreated (Fig. 1a) and AS-CTM pretreated samples (Fig. 1b–d). Although the total abundance of lignin units gradually decrease with alkaline-sulfite loads (Table 4), it appears that the S-units decrease more rapidly than H- and G-units with increasing alkaline-sulfite loads; this is particularly evident at the highest alkaline-sulfite loads, where the S/G ratios decrease from 1.2 to 1.0, reflecting the preferential removal of S-lignin units. This preferential removal is because S-lignin units are mostly involved in β-O-4′ ether linkages, which are more amenable to alkaline cleavage.
The HSQC data also corroborate that significant amounts of pCA remain in the pretreated samples, even after pretreatment at the highest alkaline-sulfite concentration. Characteristic signals from Cβ/Hβ correlations at δC/δH 113.5/6.27 were consistent with the esterified form of pCA in all bagasse samples, including the pretreated materials. The rest of the correlation signals observed in the spectra were also characteristic of pCA acylating the γ-OH in the lignin sidechain, as previously observed [18, 38]. From these data, it is possible to conclude that a part of the ester bonds between pCA and γ-OH in the lignin sidechain were resistant to the highest alkaline-sulfite load used in the pretreatment. The single explanation for preserved ester linkages after the alkaline-sulfite pretreatment under evaluation is limited accessibility to the pCA esters in the thick secondary cell walls present in sugarcane fibers . Prompt alkali consumption by alkali-labile groups, such as free carboxylic acids, acetyl groups, phenolic structures in the extractives, phenolic lignin and the labile p-hydroxycinnamates, could compete with saponification of the less accessible pCA esters during pretreatment.
To advance structural information on the residual lignin in the pretreated samples as well as the fate of pCA under severe alkaline-sulfite pretreatment conditions, the sample pretreated with 10% Na2SO3 and 5% NaOH was hydrolyzed with commercial enzymes for 72 h at preparative scale (Additional file 3: Figure S2). Assaying the enzymatic hydrolysis liquid for FAs and pCAs resulted in non-detectable peaks using the HPLC procedure, suggesting that most of the p-hydroxycinnamates present in the pretreated material accumulated in the residual solids. Residual solids of the enzymatic hydrolysis procedure represented 16% of the initial mass of the pretreated sugarcane bagasse sample and mostly corresponded to lignin with pCAs as well as minor amounts of non-digested polysaccharides and FAs. The residual solids were further saponified at 90 °C, and they released only minimal amounts of pCAs and FAs to the reaction solution (10.8 and 4.8% of the total contained in the residual solids, respectively).
The aromatic/unsaturated regions of the HSQC spectra of the residual solids (Fig. 2) helped to explain the fate of pCAs and FAs in the pretreated samples. Figure 2a corresponds to the spectrum of residual solids after enzymatic digestion of the polysaccharides. The Cβ/Hβ and Cα/Hα correlation signals of pCA esters were still observed, corroborating that the ester linkages of pCA acylating the lignin γ-OH were resistant to the most severe pretreatment as well as the enzymatic hydrolysis of the polysaccharide fraction. FA signals were not detectable due to their low amounts in the residual solids. After analytical saponification of the residual solids at 90 °C, the signals assigned to pCA esters were not detectable (Fig. 2b); instead, a characteristic shift of the Cβ/Hβ signal to 116.3/6.32 ppm (pCAβ(f)), together with a minor shift of the Cα/Hα signal to 143.5/7.45 ppm (pCAα(f)), was observed and assigned to pCA units that bear a “free” carboxylic group, pCA(f), but are etherified at the 4-OH position . However, from the NMR data, it is not possible to conclude whether these pCA units are etherified to lignin or to carbohydrates. The abundances of the different lignin units (H, G, S), etherified p-hydroxycinnamic acids (pCA), carbohydrates, and lignin inter-unit linkages and end-groups in this sample (RES-sap), estimated from volume integration of the respective signals in the HSQC spectrum, are also shown in Table 4.
The compiled HSQC data demonstrate that all pCAs detected in the untreated sugarcane bagasse were originally γ-OH esterified to lignin. A fraction of these pCAs presented free OH groups at C-4 (representing mostly the labile pCA fraction released during pretreatment, which corresponded to 59% of the original amount—Table 3), whereas another fraction was also 4-O etherified to lignin and/or to carbohydrates at the same time (representing a less labile pCA fraction that was retained in the pretreated sample). Data from the residual solids after pretreatment and enzymatic hydrolysis indicated that the less labile pCAs retained ester linkages likely because the linkages were inaccessible to the alkaline-sulfite liquor owing to the complex cell wall structure of the biomass. After cell wall collapse due to polysaccharide dissolution (Additional file 3: Figure S2), these esters were promptly hydrolyzed by saponification reactions to pCAs bearing “free” carboxylic acids. However, the pCAs bearing “free” carboxylic acids remained linked to the residual lignin and or non-digested carbohydrates through 4-O ether-linkages.
Mass balances for total pCAs and FAs along treatments and analytical procedures are illustrated in Additional file 3: Figure S2. From 100 g of untreated sugarcane bagasse, the total pCAs and FAs corresponded to 3.7 and 1.5 g, respectively. After severe alkaline-sulfite pretreatment, labile pCAs and FAs were released into the pretreatment liquor, whereas the pretreated solids contained a residual amount of p-hydroxycinnamates corresponding to 1.5 and 0.6 g of pCAs and FAs, respectively. These amounts were still present in the residual solids used in the enzymatic hydrolysis procedure. When these residual solids were analytically saponified, 1.3 g of pCAs and 0.5 g of FAs remained attached to the solids, representing the less labile ether-linked pCAs and FAs.
The current data strengthen evidence indicating AS-CTM pretreatment as a high-yield process that provides soundly digestible substrates, which can be converted to monosaccharides using a commercial cellulase cocktail. The pretreated material prepared at the highest alkaline-sulfite load retained high amounts of xylans that were depleted in acetyl groups. Part of the original lignin (62%) and 40% of the total FAs and pCAs were also retained in the pretreated material. The partial removal of lignin, xylans and p-hydroxycinnamates, and complete deacetylation (at the highest alkaline-sulfite load) proved to be sufficient to result in an almost completely digestible pretreated material. None of the isolated biomass modifications would improve digestibility to values as high as 80–95% for polysaccharide conversion. Combined transformations of the substrate after pretreatment were decisive for improving digestibility. Deacetylation, deferuloylation, and the preferential dissolution of O-methylglucurono-xylans should enhance the enzymatic hydrolysis of residual xylan, thus contributing to increased access to cellulose. Simultaneous lignin and p-hydroxycinnamates removal also increased cellulose accessibility. After pretreatment and enzymatic hydrolysis, residual solids contained mostly lignin and ester-linked pCAs, with minor amounts of FAs and non-digested polysaccharides. Saponification of the residual solids cleaved all the ester linkages in the pCAs; nevertheless, a significant fraction of pCAs remained attached to the core lignin and/or non-digested carbohydrates through 4-O ether-linkages.
Elucidating the fate of p-hydroxycinnamates and the structural characteristics of residual lignin and xylans under these pretreatment conditions helped to discriminate sources of recalcitrance in sugarcane and will inform new biorefinery models for grasses, which should include p-hydroxycinnamate recovery (from pretreatment liquor and residual lignin) for multiple applications.
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FR performed pretreatment, enzymatic hydrolysis, chemical characterization, and data interpretation and discussion. JR, AG and JCR designed and performed NMR studies, data interpretation and discussion. AF and AMFM conceived the study, participated in data interpretation, and prepared the manuscript. All authors read and approved the final manuscript.
The authors thank José M. Silva and José C. Tavares for technical assistance. We also thank Dr. Manuel Angulo (University of Seville) for performing the NMR analyses that were acquired on a Bruker Avance III 500 MHz instrument at the NMR facility at the General Research Services of the University of Seville (SGI-CITIUS).
The authors declare that they have no competing interests.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Consent for publication
Ethics approval and consent to participate
This work was supported by FAPESP (Contract Number 14/06923-6), CNPq, and CAPES. Felipe AM Reinoso thanks CAPES for his student fellowships. JCdR, JR, and AG were funded by the Spanish Projects AGL2014-53730-R, CTQ2014-60764-JIN and AGL2017-83036-R (financed by Agencia Estatal de Investigación, AEI, and Fondo Europeo de Desarrollo Regional, FEDER), and the CSIC Project 2014-40E-097.
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