Impact of Dilute Sulfuric Acid,Ammonium Hydroxide,and Ionic Liquid Pretreatments on the Fractionation and Characterization of Engineered Switchgrass

Improving plant characteristics for better environmental resilience and more cost-effective transformation to fuels and chemicals is one of the focus areas in biomass feedstock development. In order to bridge lignin engineering and conversion technologies, this study aimed to fractionate and characterize lignin streams from wild-type and engineered switchgrass using three different pretreatment methods, i.e., dilute sulfuric acid (DA), ammonium hydroxide (AH), and aqueous ionic liquid (IL). Results demonstrate the low lignin content and high S/G ratio switchgrass mutant (4CL) was more susceptible to pretreatment and subsequently more digestible by enzymes as compared to wild-type switchgrass and AtLOV1 mutant. In addition, when compared to DA and AH pretreatment, aqueous IL (cholinium lysinate) was demostrated to be an efficient lignin solvent, as indicated by the high (> 80%) lignin solubility and reduced lignin molecular weight. FTIR and differential scanning calorimetry measurements suggest that pretreatment chemistry greatly influenced the structural and compositional changes and thermal properties of the pretreated switchgrass and recovered lignin-rich streams. The comparative data obtained from this work deepen our understanding of how lignin modification impacts the fractionation and properties of biomass feedstocks.     

Comparing the Recalcitrance of Eucalyptus, Pine, and Switchgrass Using Ionic Liquid and Dilute Acid Pretreatments

Pine, eucalyptus, and switchgrass were evaluated for the production of fermentable sugars via ionic liquid and dilute acid pretreatments and subsequent enzymatic hydrolysis. The results show that among the three feedstocks, switchgrass has the highest sugar yields and faster hydrolysis rates for both pretreatment technologies by achieving 48 % (dilute acid) and 96 % (ionic liquid) sugar yields after 24 h. Of the two wood species, eucalyptus has a higher and faster sugar recovery after ionic liquid pretreatment than pine (93 vs. 62 % in 24 h) under 160 °C for 3 h with [C₂mim][OAc]. Pretreatment of pine and eucalyptus is observed to be ineffective under 1.2 % dilute acid condition and 160 °C for 15 min, indicating that further enhancement of reaction temperature or acid concentration is necessary to increase the digestibility of pretreated materials. Raman spectroscopy data show that the extent of lignin depolymerization that occurs during pretreatment also varies for the three different feedstocks. Under similar hemicellulose removal conditions, lignin removal in ionic liquid pretreatment can help improve cellulose conversion. This finding may help explain the observed variation in the saccharification yields and kinetics. These results indicate that ionic liquid pretreatment not only improved saccharification over dilute acid for all three feedstocks but also better dealt with the differences among them, suggesting better tolerance to feedstock variability.     

Investigation of Thermal Decomposition of Ascorbic Acid by TG-FTIR and Thermal Kinetics Analysis Shi Jingyan

The thermal behavior of dry solid ascorbic acid in nitrogen atmosphere in the temperature range of 25~800℃was investigated by TG-FTIR.During the thermal decomposition process,five evolved gaseous species,including H_2O,CO_2,CO,CH_4 and HCOOH,were identified and monitored,in which HCOOH was detected for the first time.The results indicated that ascorbic acid began to decompose at 191℃.Its decomposition process consisted of three stages,and dehydration and decarboxylation to form furfural were the possible principal mechanism.The kinetic analysis for the first decomposition stage was also carried out by the isoconversional method and the master plots method.The results indicated that this process can be described by the model of 1st order reaction.     

Properties of Soil Pore Space Regulate Pathways of Plant Residue Decomposition and Community Structure of Associated Bacteria

Physical protection of soil carbon (C) is one of the important components of C storage. However, its exact mechanisms are still not sufficiently lucid. The goal of this study was to explore the influence of soil structure, that is, soil pore spatial arrangements, with and without presence of plant residue on (i) decomposition of added plant residue, (ii) CO₂ emission from soil, and (iii) structure of soil bacterial communities. The study consisted of several soil incubation experiments with samples of contrasting pore characteristics with/without plant residue, accompanied by X-ray micro-tomographic analyses of soil pores and by microbial community analysis of amplified 16S–18S rRNA genes via pyrosequencing. We observed that in the samples with substantial presence of air-filled well-connected large (>30 µm) pores, 75–80% of the added plant residue was decomposed, cumulative CO₂ emission constituted 1,200 µm C g^-1 soil, and movement of C from decomposing plant residue into adjacent soil was insignificant. In the samples with greater abundance of water-filled small pores, 60% of the added plant residue was decomposed, cumulative CO₂ emission constituted 2,000 µm C g^-1 soil, and the movement of residue C into adjacent soil was substantial. In the absence of plant residue the influence of pore characteristics on CO₂ emission, that is on decomposition of the native soil organic C, was negligible. The microbial communities on the plant residue in the samples with large pores had more microbial groups known to be cellulose decomposers, that is, Bacteroidetes, Proteobacteria, Actinobacteria, and Firmicutes, while a number of oligotrophic Acidobacteria groups were more abundant on the plant residue from the samples with small pores. This study provides the first experimental evidence that characteristics of soil pores and their air/water flow status determine the phylogenetic composition of the local microbial community and directions and magnitudes of soil C decomposition processes.     

Effects of Inorganic Oxides, Sulfides, Chlorides, and Acid Chlorides on Metachromasia and Other Staining Properties

The ability of 17 inorganic compounds (POCl₃, PSC1₃, PC1₃, P₂O₅, P₂S₅, P₄S₃, P₄S₇, PC1₅, Sb₂O₅, As₂O₅, BiOC1₂, SeOC1₂, SO₂C1₂, Sb₂S₅, VOC1₂, SiC1₄ and CrO₂Cl₂) dissolved in pyridine or 2,2,4-trimethyl pentane, to enhance subsequent staining of tissue components with toluidine blue, phosphotungstic acid-hematoxylin (PTAH), leukofuchsin, and dihydroxydinaphthyl-disulfide (DDD) was studied. Eight of these compounds were also tested for ability to enhance staining with Alcian blue 8GN and Luxol fast blue MBS. Nine of the 17 compounds produced increased staining of certain tissue components with leukofuchsin, 13 with toluidine blue, 16 with PTAH, and 16 with DDD. The results suggest additional approaches to identification of tissue entities by induced metachromatic basophilia and leukofuchsin positivity as well as by the other stains studied, and also suggest a number of hitherto unstudied modes of reaction between the dyes used and reactive groups of tissue components. Many reactions of the compounds tested, with reactive groups known to be present in tissue components, are basecatalyzed, so that choice of solvent can influence the results obtained.     

Effects of Inorganic Oxides,Sulfides, Chlorides,and Acid Chlorides on Metachromasia and Other Staining Properties

The ability of 17 inorganic compounds (POCl₃, PSC1₃, PC1₃, P₂O₅, P₂S₅, P₄S₃, P₄S₇, PC1₅, Sb₂O₅, As₂O₅, BiOC1₂, SeOC1₂, SO₂C1₂, Sb₂S₅, VOC1₂, SiC1₄ and CrO₂Cl₂) dissolved in pyridine or 2,2,4-trimethyl pentane, to enhance subsequent staining of tissue components with toluidine blue, phosphotungstic acid-hematoxylin (PTAH), leukofuchsin, and dihydroxydinaphthyl-disulfide (DDD) was studied. Eight of these compounds were also tested for ability to enhance staining with Alcian blue 8GN and Luxol fast blue MBS. Nine of the 17 compounds produced increased staining of certain tissue components with leukofuchsin, 13 with toluidine blue, 16 with PTAH, and 16 with DDD. The results suggest additional approaches to identification of tissue entities by induced metachromatic basophilia and leukofuchsin positivity as well as by the other stains studied, and also suggest a number of hitherto unstudied modes of reaction between the dyes used and reactive groups of tissue components. Many reactions of the compounds tested, with reactive groups known to be present in tissue components, are basecatalyzed, so that choice of solvent can influence the results obtained.     

Ultrasonic and Thermal Pretreatments on Anaerobic Digestion of Petrochemical Sludge: Dewaterability and Degradation of PAHs

Effects of different pretreatment methods on sludge dewaterability and polycyclic aromatic hydrocarbons (PAHs) degradation during petrochemical sludge anaerobic digestion were studied. Results showed that the total biogas production volume in the thermal pretreatment system was 4 and 5 times higher than that in the ultrasound pretreatment and in the control system, and the corresponding volatile solid removal efficiencies reached 28%, 15%, and 8%. Phenanthrene, paranaphthalene, fluoranthene, benzofluoranthene, and benzopyrene removal rates reached 43.3%, 55.5%, 30.6%, 42.9%, and 41.7%, respectively, in the thermal pretreatment system, which were much higher than those in the ultrasound pretreatment and in the control system. Moreover, capillary suction time (CST) of sludge increased after pretreatment, and then reduced after 20 days of anaerobic digestion, indicating that sludge dewaterability was greatly improved after anaerobic digestion. The decrease of protein and polysaccharide in the sludge could improve sludge dewaterability during petrochemical sludge anaerobic digestion. This study suggested that thermal pretreatment might be a promising enhancement method for petrochemical sludge solubilization, thus contributing to degradation of the PAHs, biogas production, and improvement of dewaterability during petrochemical sludge anaerobic digestion.     

Impact of Simulated Acid Rain on Trace Metals and Aluminum Leaching in Latosol from Guangdong Province,China

Acid rain is one of the most serious ecological and environmental problems worldwide. This study investigated the impacts of simulated acid rain (SAR) upon leaching of trace metals and aluminum (Al) from a soil. Soil pot leaching experiments were performed to investigate the impacts of SAR at five different pH levels (or treatments) over a 34-day period upon the release of trace metals (i.e., Cu, Ni, Pb, Zn, and Fe) and Al from the Latosol (acidic red soil). The concentrations of trace metals in the effluent increased as the SAR pH level decreased, and were highest at the SAR pH = 2.0. In general, the concentrations of Cu, Pb, Fe, and Al in the effluent increased with leaching time at the SAR pH = 2.0, whereas the concentrations of Zn, Fe, and Al in the effluent decreased with leaching time at the SAR pH ≥ 4.0. The increase in electrical conductivity (EC) with leaching time at five different SAR pH levels was primarily due to the concentrations of Al and Fe in the effluent. There were good linear correlations between the effluent Al concentrations and the effluent pH at the SAR pH = 2.0 (R² = 0.87) and pH = 3.0 (R² = 0.83). More soil trace metals and Al were activated and released into the soil solution as the SAR pH level decreased.     

The Impact of Corn Residue Removal on Soil Aggregates and Particulate Organic Matter

Removal of corn (Zea mays L.) stover as a biofuel feedstock is being considered. It is important to understand the implications of this practice when establishing removal guidelines to ensure the long-term sustainability of both the biofuel industry and soil health. Aboveground and belowground plant residues are the soil’s main sources of organic materials that bind soil particles together into aggregates and increase soil carbon (C) storage. Serving to stabilize soil particles, soil organic matter (SOM) assists in supplying plant available nutrients, increases water holding capacity, and helps reduce soil erosion. Data obtained from three Corn Stover Regional Partnership sites (Brookings, SD; Morris, MN; and Ithaca, NE) were utilized to evaluate the impact of removing corn stover on soil physical properties, including dry aggregate size distribution (DASD), erodible fraction (EF), and SOM components. Each site consisted of a combination of three residue removal rates (low—removal of grain only, intermediate—approximately 50 % residue removal, and high—maximum amount of residue removal). Results showed that the distribution of soil aggregates was less favorable for all three locations when residue was removed without the addition of other sources of organic matter such as cover crops. Additionally, we found that when residue was removed and the soil surface was less protected, there was an increase in the EF at all three research sites. There was a reduction in the EF for both the Brookings, SD, and Ithaca, NE sites when cover crops were incorporated or additional nitrogen (N) was added to the system. Amounts of SOM, fine particulate organic matter (fPOM), and total particulate organic matter (tPOM) consistently decreased as greater amounts of residue were removed from the soil surface. Across these three locations, the removal of crop residue from the soil surface had a negative impact on measured soil physical properties. The addition of a cover crop or additional N helped reduce this impact as measured through aggregate size distribution and EF and SOM components.     

Heavy Metals in Agricultural Soils of the Mouriki-Thiva Area (Central Greece) and Environmental Impact Implications

The heavy metal content of 51 surface soil samples from the agricultural region of Mouriki-Thiva (central Greece) was investigated by a combination of mineralogical (X-ray diffraction and scanning electron microscopy) and geochemical (aqua regia and 0.5 M HCl extractions) methods in order to determine the levels of contamination, as well as the origin, distribution and mobility of selected metals. The geology of the area includes ultrabasic rocks, and consequently the soils have anomalous values in Ni (621-2639 mg/kg) and Cr (134-856 mg/kg). Whereas Cr is mainly hosted in the crystal structure of chromite, Ni is primarily mobilized from olivine and serpentine. Nickel, and to a lesser extent Cr, were also found to be absorbed in Fe oxides. The results of a single 0.5 HCl leach revealed significant differences in the mobility and potential bioavailability of Ni and Cr in representative soil samples; Nickel is substantially more labile, and as a result a potential amount of this metal is readily available to the plants. The whole area is heavily contaminated by Ni and Cr and consequently the monitoring of the agricultural products of the region for their heavy metal content is strongly recommended.     

Subcellular Localization of Inorganic Pyrophosphatases in Rabbit Skeletal Muscle and Some Properties of a Microsomal Acid Pyrophosphatase

Subcellular localization of muscle inorganic pyrophosphatase was examined using rabbit skeletal muscle homogenates. The pyrophosphatases were found to be contained in the microsomal, mitochondrial, and cytosol fractions. The microsomal and mitochondrial pyrophosphatases were most likely bound to the respective subcellular fractions. The pyrophosphatases associated with microsome and mitochondria showed their optimal activities at about pH 5.5 and 7, respectively. They were not dissociated from the particles by washing with salt solution or by ten times freezing-thawing. The activity of microsomal acid pyrophosphatase was not affected by Mg,²⁺ Ca,²⁺ or EDTA, but that of the mitochondrial neutral pyrophosphatase was enhanced by the addition of Mg.²⁺ The microsomal acid pyrophosphatase was stable between pH values of 5.5 and 8.5 during storage at 4°. The activity was inhibited by p-chloromercuribenzoate. The activity was irreversibly inhibited by sodium dodecyl sulfate, but reversibly inhibited by neutral salts and membrane solubilizing detergents such as Triton X-100, octaethylene glycol mono-n-dodecylether, and sodium cholate.     

The Regulation of Surface Charged Residues on the Properties of Cytochrome b5

To understand the roles of negatively surface charged residues, the cytochrome b₅ (Cyt b₅) E48A/D60A mutant was constructed. UV-visible and CD spectra confirmed that the mutation did not cause overall structural changes of the protein. The mutant presents an unexpected high stability toward the thermal and denaturant compared with the wild type Cyt b₅, which shows that these surface charged residues can influence the interactions between the heme b group and the polypeptide chain. Functional properties were clarified through the electron transfer reactions between Cyt b₅ and Cyt c. The driving force of the electron transfer reactions is conservative. Although the association constant of Cyt b₅ E48A/D60A with Cyt c is much lower than that of the wild type Cyt b₅, their electron transfer rate constants do not differ significantly. The results show that these surface charged residues play important roles in regulating both the stability and functional properties of Cyt b₅.     

Biosynthesis and Thermal Properties of PHBV Produced from Levulinic Acid by Ralstonia eutropha

Levulinic acid (LA) can be cost-effectively produced from a vast array of renewable carbohydrate-containing biomaterials. LA could facilitate the commercialization of the polymer poly(hydroxybutyrate-co-hydroxyvalerate) (PHBV) and PHBV-based products as carbon substrates. Therefore, this paper focused on the production of PHBV by Ralstonia eutropha with LA for hydroxyvalerate (HV) production, which plays an important role in enhancing the thermal properties of PHBV. Accordingly, the HV content of PHBV varied from 0–40.9% at different concentrations of LA. Stimulation of cell growth and PHBV accumulation were observed when 2–6 g L⁻¹ LA was supplied to the culture. The optimal nitrogen sources were determined to be 0.5 g L⁻¹ ammonium chloride and 2 g L⁻¹ casein peptone. It was determined that the optimal pH for cell growth and PHBV accumulation was 7.0. When the cultivation was performed in large scale (2 L fermenter) with a low DO concentration of 30% and a pH of 7.0, a high maximum dry cell weight of 15.53 g L⁻¹ with a PHBV concentration of 12.61 g L⁻¹ (53.9% HV), up to 81.2% of the dry cell weight, was obtained. The melting point of PHBV found to be decreased as the fraction of HV present in the polymer increased, which resulted in an improvement in the ductility and flexibility of the polymer. The results of this study will improve the understanding of the PHBV accumulation and production by R. eutropha and will be valuable for the industrial production of biosynthesized polymers.     

玉米淀粉渣中玉米黄色素的提取及性质测定

利用玉米生产葡萄糖工艺中的淀粉渣提取的玉米黄色素 ,主要成分是一种脂溶性色素和少量的极性较大的色素 ,呈血红色 ,其稀释液呈柠檬黄色。高醇和石油醚提取色素液在 2 41nm和 2 80～ 32 7nm之间有最大吸收值 ,水提色素液在 2 13nm有最大吸收值。通过不同的方法进行了对比提取 ,并作了酸碱和热等稳定性的测定     

The Role of Nonconserved Residues of Archaeoglobus fulgidus Ferritin on Its Unique Structure and Biophysical Properties

Archaeoglobus fulgidus ferritin (AfFtn) is the only tetracosameric ferritin known to form a tetrahedral cage, a structure that remains unique in structural biology. As a result of the tetrahedral (2-3) symmetry, four openings (∼45 Å in diameter) are formed in the cage. This open tetrahedral assembly contradicts the paradigm of a typical ferritin cage: a closed assembly having octahedral (4-3-2) symmetry. To investigate the molecular mechanism affecting this atypical assembly, amino acid residues Lys-150 and Arg-151 were replaced by alanine. The data presented here shed light on the role that these residues play in shaping the unique structural features and biophysical properties of the AfFtn. The x-ray crystal structure of the K150A/R151A mutant, solved at 2.1 Å resolution, indicates that replacement of these key residues flips a “symmetry switch.” The engineered molecule no longer assembles with tetrahedral symmetry but forms a typical closed octahedral ferritin cage. Small angle x-ray scattering reveals that the overall shape and size of AfFtn and AfFtn-AA in solution are consistent with those observed in their respective crystal structures. Iron binding and release kinetics of the AfFtn and AfFtn-AA were investigated to assess the contribution of cage openings to the kinetics of iron oxidation, mineralization, or reductive iron release. Identical iron binding kinetics for AfFtn and AfFtn-AA suggest that Fe²⁺ ions do not utilize the triangular pores for access to the catalytic site. In contrast, relatively slow reductive iron release was observed for the closed AfFtn-AA, demonstrating involvement of the large pores in the pathway for iron release.