BackgroundThe efficiency of enzymatic hydrolysis is reduced by the structural properties of cellulose. Although efforts have been made to explain the mechanism of enzymatic hydrolysis of cellulose by considering the interaction of cellulolytic enzymes with cellulose or the changes in the structure of cellulose during enzymatic hydrolysis, the process of cellulose hydrolysis is not yet fully understood. We have analysed the characteristics of the complex supramolecular structure of cellulose on the nanometre scale in terms of the spatial distribution of fibrils and fibril aggregates, the accessible surface area and the crystallinity during enzymatic hydrolysis. Influence of the porosity of the substrates and the hydrolysability was also investigated. All cellulosic substrates used in this study contained more than 96% cellulose.ResultsConversion yields of six cellulosic substrates were as follows, in descending order: nano-crystalline cellulose produced from never-dried soda pulp (NCC-OPHS-ND) > never-dried soda pulp (OPHS-ND) > dried soda pulp (OPHS-D) > Avicel > cotton treated with sodium hydroxide (cotton + NaOH) > cotton.ConclusionsNo significant correlations were observed between the yield of conversion and supramolecular characteristics, such as specific surface area (SSA) and lateral fibril dimensions (LFD). A strong correlation was found between the average pore size of the starting material and the enzymatic conversion yield. The degree of crystallinity was maintained during enzymatic hydrolysis of the cellulosic substrates, contradicting previous explanations of the increasing crystallinity of cellulose during enzymatic hydrolysis. Both acid and enzymatic hydrolysis can increase the LFD, but no plausible mechanisms could be identified. The sample with the highest initial degree of crystallinity, NCC-OPHS-ND, exhibited the highest conversion yield, but this was not accompanied by any change in LFD, indicating that the hydrolysis mechanism is not based on lateral erosion.Electronic supplementary materialThe online version of this article (doi:10.1186/s13068-015-0236-9) contains supplementary material, which is available to authorized users.

The industrial production of cellulolytic enzymes is dominated by the filamentous fungus Trichoderma reesei (anamorph of Hypocrea jecorina). In order to develop optimal enzymatic cocktail, it is of importance to understand the natural regulation of the enzyme profile as response to the growth substrate. The influence of the complexity of cellulose on enzyme production by the microorganisms is not understood. In the present study we attempted to understand how different physical and structural properties of cellulose-rich substrates affected the levels and profiles of extracellular enzymes produced by T. reesei. Enzyme production by T. reesei Rut C-30 was studied in submerged cultures on five different cellulose-rich substrates, namely, commercial cellulose Avicel® and industrial-like cellulosic pulp substrates which consist mainly of cellulose, but also contain residual hemicellulose and lignin. In order to evaluate the hydrolysis of the substrates by the fungal enzymes, the spatial polymer distributions were characterised by cross-polarisation magic angle spinning carbon-13 nuclear magnetic resonance (CP/MAS (13)C-NMR) in combination with spectral fitting. Proteins in culture supernatants at early and late stages of enzyme production were labeled by Tandem Mass Tags (TMT) and protein profiles were analysed by liquid chromatography-tandem mass spectrometry. The data have been deposited to the ProteomeXchange with identifier PXD001304. In total 124 proteins were identified and quantified in the culture supernatants, including cellulases, hemicellulases, other glycoside hydrolases, lignin-degrading enzymes, auxiliary activity 9 (AA9) family (formerly GH61), supporting activities of proteins and enzymes acting on cellulose, proteases, intracellular proteins and several hypothetical proteins. Surprisingly, substantial differences in the enzyme profiles were found even though there were minor differences in the chemical composition between the cellulose-rich substrates.

Birch chips were subjected to pilot-scale pre-hydrolysis under various sets of conditions to mimic a pre-hydrolysis step in a dissolving pulp process. The process generates residual process liquor, a wood hydrolysate, and the treated chips may be directly utilized in a dissolving process. The wood hydrolysates were rich in xylan and utilized in the production of fully renewable films that provide very good oxygen barrier function and mechanical integrity also at high relative humidity. Membrane filtration had an effect in enriching higher molecular weight fractions from the hydrolysates, but noteworthy, a hydrolysate used in the crude state without any membrane filtration performed just as well as upgraded fractions in forming films providing acceptable tensile properties and a good barrier against oxygen permeation.

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The bark of trees contains an interesting mixture of bioactive compounds, or so-called extractives. The use of supercritical carbon dioxide (sc-CO2) eliminates both the need for organic solvents as extractants and the danger that solvent traces might compromise the purity of the extracts. Unfortunately, the complexity and natural variability of extracts’ composition render any utilization attempts rather challenging. Thus, in order to implement exploitation concepts in a meaningful way, appropriate analytical techniques for characterizing extracts must be available beforehand. In our work, we explored gas chromatography coupled to both mass spectrometry and a flame ionization detector (GC-MS/FID), in combination with ultraperformance convergence chromatography and quadrupole time-of-flight mass spectrometry (UPC2-QTof-MS), for the characterization of bark extracts from pine (Pinus sylvestris L.) in both qualitative and quantitative terms. Although the conventional GC-MS/FID approach is a robust method for overall quantification of extractives, it fails to provide ample information about native sterol esters and triglycerides. These data are provided by a new, complementary analytical technique based on supercritical carbon dioxide, as the chromatographic eluant, coupled to a high-resolution mass spectrometer. The combination of both techniques and the use of sc-CO2 as both an extraction solvent and eluant made this combined tool especially powerful. The most prominent triglycerides in the extract were identified qualitatively and quantitatively, and the dominating sterol esters were identified qualitatively, by UPC2-QTof-MS.