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Mineral acids have been used effectively for the pretreatment of cellulosic biomass to improve sugar recovery and promote its conversion to ethanol; however, substantial capital investment is required to enable separation of the acid, and corrosion-resistant materials are necessary. Disposal and neutralization costs are also concerns because they can decrease the economic feasibility of the process. In this work, three acid-functionalized nanoparticles were synthesized for pretreatment and hydrolysis of lignocellulosic biomass. Silica-protected cobalt spinel ferrite nanoparticles were functionalized with perfluoroalkylsulfonic acid (PFS), alkylsulfonic acid (AS), and butylcarboxylic acid (BCOOH) groups. These nanoparticles were magnetically separated from the reaction media and reused. TEM images showed that the average diameter was 2 nm for both PFS and BCOOH nanoparticles and 7 nm for AS nanoparticles. FTIR confirmed the presence of sulfonic and carboxylic acid functional groups. Ion exchange titration measurements yielded 0.9, 1.7, and 0.2 mmol H+/g of catalyst for PFS, AS, and BCOOH nanoparticles, respectively. Elemental analysis results indicated that PFS and AS nanoparticles had 3.1 and 4.9% sulfur, respectively. Cellobiose hydrolysis was used as a model reaction to evaluate the performance of acid-functionalized magnetic nanoparticles for breaking β-(1→4) glycosidic bonds. Cellobiose conversion of 78% was achieved when using AS nanoparticles as the catalyst at 175℃ for 1 h, which was significantly higher than the conversion for the control experiment (52%). AS nanoparticles retained more than 60% of their sulfonic acids groups after the first run, and 65 and 60% conversions were obtained for the second and third runs, respectively.

Specific rotation and carbohydrate profile of Croatian black locust (Robinia pseudoacacia), sage (Salvia officinalis) and chestnut (Castanea sativa) honeys were determined. Fructose, glucose, sucrose, maltose (with cellobiose and trehalose), melezitose (with erlose), raffinose, and xylose were evaluated and quantified by HPLC, while specific rotation was determined by using a polarimeter. The differences in the carbohydrate profile, especially in disaccharide and trisaccharide contents, reflected different specific rotation values of the honey types selected. Weak positive correlations between specific rotation and sucrose, melezitose with erlose, and raffinose contents were found.

Markers for evaluating the establishment of cyanobacteria based on their sensitivity or resistance to antibiotics, saccharide utilization patterns and PCR generated fingerprints were developed. Four selected strains (isolates from rhizosphere soils of diverse agro-ecosystems) have shown potential as diazotrophs and exhibited plant growth promoting abilities. Different responses were obtained on screening against 40 antibiotics, which aided in developing selectable antibiotic markers for each strain. Biochemical profiles generated using standardized chromogenic identification system (including saccharide utilization tests) revealed that 53 % of the saccharides tested were not utilized by any strain, while some strains exhibited unique ability for utilization of saccharides such as melibiose, cellobiose, maltose and glucosamine. PCR based amplification profiles developed using a number of primers based on repeat sequences revealed the utility of 3 primers in providing unique fingerprints for the strains.

Cellulose microfibrils with an electron diffraction pattern characteristic of crystalline native cellulose I have been assembled abiotically by means of a cellulase-catalyzed polymerization of beta-cellobiosyl fluoride substrate monomer in acetonitrile/acetate buffer. Substantial purification of the Trichoderma viride cellulase enzyme was found to be essential for the formation of the synthetic cellulose I allomorph. Assembly of synthetic cellulose I appears to be a result of a micellar aggregation of the partially purified enzyme and the substrate in an organic/aqueous solvent system favoring the alignment of glucan chains with the same polarity and extended chain conformation, resulting in crystallization to form the metastable cellulose I allomorph

Ruminococcus albus is an important fibrolytic bacterium in the rumen. Cellobiose is metabolized by this organism via hydrolytic and well as phosphorylytic enzymes, but the relative contributions of each pathway were not clear. The cellobiose consumption rate by exponentially growing cells was less than that of crude extracts (75 versus 243 nmol/min/mg protein). Cellobiose phosphorolytic cleavage was much greater than hydrolytic activity (179 versus 19 nmol/min/mg protein) indicating that phosphorylases were key enzymes in the initial metabolism of the soluble products of cellulose degradation. Cellodextrin phosphorylase appeared to be active against substrates as large as cellohexaose. Phosphorylase activities were cytoplasmic, but hydrolytic activities were associated with both the membrane and cytoplasmic fractions. Free glucose was phosphorylated with a GTP-dependent glucokinase, and this enzyme showed 20-fold higher activity with GTP or ITP (324 nmol/min/mg protein) than with ATP, UTP, CTP, GDP, or PEP. The activity was decreased at least 57% when mannose, 2-deoxyglucose, or fructose was used as substrate compared with glucose. The KmS for glucose and GTP were 321 and 247 micromolar, respectively. Since phosphorolytic cleavage conserves more metabolic energy than simple hydrolysis, it is likely that such pathways provide for more efficient growth of R. albus in substrate-limiting conditions like those found in the rumen

The production of organic acids by two anaerobic ruminal bacteria, Fibrobacter succinogenes S85 and Ruminococcus flavefaciens FD-1, was compared with glucose, cellobiose, microcrystalline cellulose, Walseth cellulose (acid swollen cellulose), pulped paper, and steam-exploded yellow poplar as substrates. The major end product produced by F. succinogenes from each of these substrates was succinate (69.5-83%), the principal secondary product was acetate (16-30.5%). Maximum succinate productivity ranged from 14.1 mg/L.h for steam-exploded yellow Poplar to 59.7 mg/L.h for pulped paper. For R. flavefaciens, the major end product from cellobiose, microcrystalline cellulose, and acid-swollen Walseth cellulose was acetate (39-46%), pulped paper and steam-exploded yellow poplar yielded succinate (42-54%) as the major product. Maximum succinate productivity by R. flavefaciens ranged from 9.21 mg/L.h for cellobiose to 43.1 mg/L.h for pulped paper. In general, much less succinate was produced at a lower maximum productivity by R. flavefaciens than by F. succinogenes under similar fermentation conditions. The maximum succinate productivities by these two organisms are comparable to the previously reported value of 59 mg/L .h for Anderobiospirillum succiniciproducens grown on glucose and corn steep liquor

The regulation and kinetic properties of cellulose synthase as well as beta-1,3-glucan synthase have been studied. The cellulose was detected using acetic/nitric acid insolubility as an indicator of cellulose (this product contained only beta-1,4-linked glucans; K. Okuda, L. Li, K. Kudlicka, S. Kuga, R.M. Brown, Jr. [1993] Plant Physiol 101: 1131-1142). These studies reveal that (a) beta-1,3-glucan synthesis is enhanced up to 31-fold by cellobiose with a Ka of 1.16 mM; (b) cellulose synthesis is increased 12-fold by a combination of cellobiose (Ka = 3.26 mM) and cyclic-3':5'-GMP (Ka = 100 micromolar); (c) the common components in the reaction mixture required by both enzymes are cellobiose, calcium, and digitonin; (d) cellulose synthase has an essential requirement for magnesium (Ka = 0.89 mM); (e) cellulose synthase also requires a low concentration of calcium (Ka = 90 micromolar); (f) the optimal pH for cellulose synthase (7.6-8.0) is slightly higher than that for beta-1,3-glucan synthase (7.2-7.6); (g) the Km for UGP-GLC for cotton (Gossypium hirsutum) cellulose synthase is 0.40 mM; (h) the Km for UDP-GLC for beta-1,3-glucan synthase is 0.43 mM

ENTERORapid 24 kit (PLIVA-Lachema, Czech Republic) was used for the identification of 321 strains isolated from the respiratory tract of different animal species in the Czech Republic and Ethiopia. A total of 207 strains were identified at the species level within 4 to 8 hours of incubation. In the same way, 39 strains were successfully classified at the genus level. The remaining strains (23.4 %) were not identified nor classified to the family Pasteurellaceae. The accuracy of the ENTERORapid 24 kit was compared to the results of the RapiD 20E kit (bioMerieux, France). The ENTERO Rapid 24 kit is the fastest system for the identification of P. multocida and M. haemolytica strains within 4 to 8 hours with a correct identification rate at the species level. We propose its modification for rapid identification of P. multocida, M. haemolytica and related bacterial species from the family Pasteurellaceae isolated from different animal species.

In this paper, we describe cellulase and cellobiose dehydrogenase (CBDH) dynamics in relation to incubation time, mass loss and chemical composition of decomposing deciduous leaf litter. Cellulose disappearance from litter coincided with periods of maximum cellulase activity. CBDH activity peaked later in decomposition after cellulase activity had declined. Enzyme activity patterns differed among litter types when expressed on the basis of decomposition time or cumulative mass loss. The patterns converged when expressed on the basis of chemical composition as indexed by the fraction of cellulose in the lignocellulose complex. We present a three-stage model of decomposition based on temporal changes in cellulase activities and coincident changes in litter chemical composition.