Comparison between the univariate and multivariate analysis on the partial characterization of the endoglucanase produced in the solid state fermentation by Aspergillus oryzae ATCC 10124

Endoglucanase production by Aspergillus oryzae ATCC 10124 cultivated in rice husks or peanut shells was optimized by experimental design as a function of humidity, time, and temperature. The optimum temperature for the endoglucanase activity was estimated by a univariate analysis (one factor at the time) as 50°C (rice husks) and 60°C (peanut shells), however, by a multivariate analysis (synergism of factors), it was determined a different temperature (56°C) for endoglucanase from peanut shells. For the optimum pH, values determined by univariate and multivariate analysis were 5 and 5.2 (rice husk) and 5 and 7.6 (peanut shells). In addition, the best half-lives were observed at 50°C as 22.8?hr (rice husks) and 7.3?hr (peanut shells), also, 80% of residual activities was obtained between 30 and 50°C for both substrates, and the pH stability was improved at 5–7 (rice hulls) and 6–9 (peanut shells). Both endoglucanases obtained presented different characteristics as a result of the versatility of fungi in different substrates.     

Heavy metal accumulation in rice (Oryza sativa) near electronic waste dumps and related human health risk assessment

This research was conducted to assess heavy metal contamination in the environment and within Oryza sativa. The translocation factors (TFs) and bioaccumulation factors (BAFs) for heavy metals in O. sativa and estimated daily intake (EDI) and health risk index (HRI) were measured. The samples were analyzed for heavy metals using inductively coupled plasma optical emission spectrometry (ICP-OES). Pb and Cr concentrations in water samples within and near the electronic-waste dumping area exceeded water quality standards for surface water sources from the Pollution Control Department in the Ministry of Natural Resources and Environment of Thailand (PCD). The Pb concentration in soil samples within the area also exceeded soil quality standards for habitat and agriculture from PCD. Most of the metals were highly concentrated in roots, except for Mn which has the highest concentration in leaves. Pb concentrations in rice grains exceeded the FAO/WHO standard (0.2 mg/kg). The average TF values for heavy metals from the soil to roots, roots to stems, stems to leaves, and stems to grains were Mn > Pb > Ni > Cr, Mn > Cr > Ni > Pb, Ni > Pb > Mn > Cr, and Pb > Ni > Cr > Mn, respectively. The average BAF values in O. sativa were Mn > Ni > Pb > Cr. The EDI for Cr, Pb, Mn, and Ni via O. sativa consumption were 6.19, 6.02, 370.57, and 3.80 µg/kg/day, respectively. The HRI for Cr, Pb, Mn, and Ni via O. sativa consumption were 0.30, 1.50, 2.60, and 0.002, respectively.     

Nitrogen amendment of green waste impacts microbial community,enzyme secretion and potential for lignocellulose decomposition

Microorganisms involved in biomass deconstruction are an important resource for organic waste recycling and enzymes for lignocellulose bioconversion. The goals of this study were to examine the impact of nitrogen amendment on microbial community restructuring, secretion of xylanases and endoglucanases, and potential for biomass deconstruction. Communities were cultivated aerobically at 55 °C on green waste (GW) amended with varying levels of NH₄Cl. Bacterial and fungal communities were determined using 16S rRNA and ITS region gene sequencing and PICRUSt (Phylogenetic Investigation of Communities by Reconstruction of Unobserved States) was applied to predict relative abundance of genes involved in lignocellulose hydrolysis. Nitrogen amendment significantly increased secretion of xylanases and endoglucanases, and microbial activity; enzyme activities and cumulative respiration were greatest when nitrogen level in GW was between 4.13–4.56 wt% (g/g), but decreased with higher nitrogen levels. The microbial community shifted to one with increasing potential to decompose complex polymers as nitrogen increased with peak potential occurring between 3.79–4.45 wt% (g/g) nitrogen amendment. The results will aid in informing the management of nitrogen level to foster microbial communities capable of secreting enzymes that hydrolyze recalcitrant polymers in lignocellulose and yield rapid decomposition of green waste.     

Extraction of peroxidase from bitter gourd (Momordica charantia) by three phase partitioning with dimethyl carbonate (DMC) as organic phase

Three phase partitioning (TPP) is most renowned technique used for extraction and purification of natural products. In previous studies of TPP, t-butanol is mainly used as an organic phase. This is the first report that explores ability of dimethyl carbonate (DMC) in the field of TPP as an alternate solvent for t-butanol. In the present study TPP process with t-butanol and DMC as organic phase along with different salts was applied to waste bitter gourd powder to obtained peroxidase enzyme. DMC was found to be compatible with most of salts such as ammonium sulphate and sodium citrate and explored as more efficient solvent than t-butanol. This TPP system provides 4.84 fold purity of peroxidase enzyme at optimum source concentration of 0.15 g/mL, with a system comprising DMC as organic phase, sodium citrate (20%) as salt, agitation speed 120 rpm, pH 7, temperature 30 °C and extraction time of 3 h. Present study has aimed for extraction and separation of peroxidase from bitter gourd waste with TPP technique and ensures the scope of carbonated solvents in extraction and purification of proteins.     

茶废弃物对溶液中重金属的生物吸附研究进展

茶废弃物是农业固体废弃物的一个重要组成部分,来源广泛,数量庞大.由于其具有吸附特性,利用茶废弃物作吸附剂去除废水中的重金属受到了国内外学者的广泛关注.本文从影响因素、吸附机理、吸附剂制备和脱附再生等方面综述了茶废弃物吸附去除溶液中重金属的最新研究进展,认为吸附机理、制备、脱附再生、工艺参数和后处理等是今后实现茶废弃物吸附剂工业化应用的主要研究方向.     

The Effect of Compost Treatments and A Plant Cover with Agrostis tenuis on the Immobilization/Mobilization of Trace Elements in a Mine-Contaminated Soil

A semi-field experiment was conducted to evaluate the use of mixed municipal solid waste compost (MMSWC) and green waste-derived compost (GWC) as immobilizing agents in aided-phytostabilization of a highly acidic soil contaminated with trace elements, with and without a plant cover of Agrostis tenuis. The compost application ratio was 50 Mg ha^–1, and GWC amended soil was additionally limed and supplemented with mineral fertilizers.Both treatments had an equivalent capacity to raise soil organic matter and pH, without a significant increase in soil salinity and in pseudo-total As, Cu, Pb, and Zn concentrations, allowing the establishment of a plant cover. Effective bioavailable Cu and Zn decreased as a consequence of both compost treatments, while effective bioavailable As increased by more than twice but remained as a small fraction of its pseudo-total content. Amended soil had higher soil enzymatic activities, especially in the presence of plants.Accumulation factors for As, Cu, Pb, and Zn by A. tenuis were low, and their concentrations in the plant were lower than the maximum tolerable levels for cattle. As a consequence, the use of A. tenuis can be recommended for assisted phytostabilization of this type of mine soil, in combination with one of the compost treatments evaluated.     

Optimization of Chromium(VI) Detoxification by Pseudomonas aeruginosa and Its Application for Treatment of Industrial Waste and Contaminated Soil

The reduction of Cr(VI) to Cr(III) is a potential detoxification process. In this study, seven Pseudomonas spp. were isolated and screened for chromium reduction. Isolate P4 was able to grow in the presence of 8000 μM chromium, in spite of the fact that the isolate was not previously exposed to any metal stress. Isolate P4 was identified as Pseudomonas aeruginosa strain SRD chr3 by 16S rDNA sequence analysis. Shake flask study showed 78% reduction of 1000 μM Cr(VI) after 6 h of incubation. The optimum pH for chromium reduction by the isolate was between 6 and 8. Isolate Pseudomonas aeruginosa gave 50–80% Cr(VI) reduction even in the presence of 100 mM of Cu, Mn, Ni, and Zn and 300–800 mM NaCl in 24 h, compared with the absence of any of these metals. In a 5-L reactor, the isolate showed 84.85% reduction of Cr(VI) even at the 70th cycle, with a hydraulic retention time of 24 h from the effluent of a hard chrome plating (electroplating) industry, which contained 2100 mg L^?1 hexavalent chromium. The chromate-amended soil inoculated with the isolate showed 2800 μM chromium removal from 4000 μM Cr(VI) kg^?1 of soil, which corresponds to 70% removal. The isolate had the ability to degrade stimulated waste containing 10,000 μM chromium.     

Estimates of Lost Material Stock of Buildings and Roads Due to the Great East Japan Earthquake and Tsunami

This article describes research conducted for the Japanese government in the wake of the magnitude 9.0 earthquake and tsunami that struck eastern Japan on March 11, 2011. In this study, material stock analysis (MSA) is used to examine the losses of building and infrastructure materials after this disaster. Estimates of the magnitude of material stock that has lost its social function as a result of a disaster can indicate the quantities required for reconstruction, help garner a better understanding of the volumes of waste flows generated by that disaster, and also help in the course of policy deliberations in the recovery of disaster‐stricken areas. Calculations of the lost building and road materials in the five prefectures most affected were undertaken. Analysis in this study is based on the use of geographical information systems (GIS) databases and statistics; it aims to (1) describe in spatial terms what construction materials were lost, (2) estimate the amount of infrastructure material needed to rehabilitate disaster areas, and (3) indicate the amount of lost material stock that should be taken into consideration during government policy deliberations. Our analysis concludes that the material stock losses of buildings and road infrastructure are 31.8  and 2.1 million tonnes, respectively. This research approach and the use of spatial MSA can be useful for urban planners and may also convey more appropriate information about disposal based on the work of municipalities in disaster‐afflicted areas.     

Carbon Recycling for Renewable Materials and Energy Supply

The current flow of carbon for the production, use, and waste management of polymer‐based products is still mostly linear from the lithosphere to the atmosphere with rather low rates of material recycling. In view of a limited future supply of biomass, this article outlines the options to further develop carbon recycling (C‐REC). The focus is on carbon dioxide (CO₂) capture and use for synthesis of platform chemicals to produce polymers. CO₂ may be captured from exhaust gases after combustion or fermentation of waste in order to establish a C‐REC system within the technosphere. As a long‐term option, an external C‐REC system can be developed by capturing atmospheric CO₂. A central role may be expected from renewable methane (or synthetic natural gas), which is increasingly being used for storage and transport of energy, but may also be used for renewable carbon supply for chemistry. The energy input for the C‐REC processes can come from wind and solar systems, in particular, power for the production of hydrogen, which is combined with CO₂ to produce various hydrocarbons. Most of the technological components for the system already exist, and, first modules for renewable fuel and polymer production systems are underway in Germany. This article outlines how the system may further develop over the medium to long term, from a piggy‐back add‐on flow system toward a self‐carrying recycling system, which has the potential to provide the material and energy backbone of future societies. A critical bottleneck seems to be the capacity and costs of renewable energy supply, rather than the costs of carbon capture.     

Synthesis and in vitro antioxidant functions of protein hydrolysate from backbones of Rastrelliger kanagurta by proteolytic enzymes

Every year, a huge quantity of fishery wastes and by-products are generated by fish processing industries. These wastes are either underutilized to produce low market value products or dumped leading to environmental issues. Complete utilization of fishery wastes for recovering value added products would be beneficial to the society and individual. The fish protein hydrolysates and derived peptides of fishery resources are widely used as nutritional supplements, functional ingredients, and flavor enhancers in food, beverage and pharmaceutical industries. Antioxidants from fishery resources have attracted the attention of researchers as they are cheaper in cost, easy to derive, and do not have side effects. Thus the present investigation was designed to produce protein hydrolysate by pepsin and papain digestion from the backbones of Rastrelliger kanagurta (Indian mackerel) and evaluate its antioxidant properties through various in vitro assays. The results reveal that both hydrolysates are potent antioxidants, capable of scavenging 46% and 36% of DPPH (1,1-diphenyl-2 picrylhydrazyl) and 58.5% and 37.54% of superoxide radicals respectively. The hydrolysates exhibit significant (p < 0.05) reducing power and lipid peroxidation inhibition. Among the two hydrolysates produced, pepsin derived fraction is superior than papain derived fraction in terms of yield, DH (Degree of hydrolysis), and antioxidant activity.