Low Molecular Weight Fraction Research Articles

Hydrothermal processing of β-glucan from Aureobasidium pullulans produces a low molecular weight reagent that regulates inflammatory responses induced by TLR ligands

The Kururu no β-glu® (KBG) is a commercial hydrothermal-treated Aureobasidium pullulans β-glucan produced by a unique hydrothermal process that results in high solubility of the β-glucan. In this study, we examined the biological activities of this reagent. RAW264.7 cells do not express Dictin-1 on the cell surface, but cells still respond to various pathogen molecular patterns. Lipopolysaccharide (LPS) induced nitrogen oxide (NO) synthesis and TNF−α production in RAW264.7 cells, and those were suppressed by KBG in a dose-dependent manner. The major signaling cell surface receptor respond to LPS is the TLR4/MD-2 complex. The UT12 antibody against to the TLR4/MD-2 complex mimics LPS function and induces cell responses. NO generation and TNF-α production were similarly induced in cells by stimulation with the antibody, but those were not suppressed by KBG. Cell responses induced by other TLR ligands, such as CPG (TLR9 ligand) and Pam3CSK4 (TLR1/TLR2 ligand), were also suppressed by KBG. Therefore, the target molecule for KBG is different from TLR receptors and Dictin-1. Although we also examined the suppressive activities of several other β-glucan products, comparable activities were not detected with other reagents. A unique hydrothermal process may produce the active reagent. Reprocessing KBG increased low molecular weight fractions, and suppressive activities were markedly enhanced. Therefore, low molecular weight fractions obtained by hydrothermal processing of KBG may result in potential reagents that control inflammation induced by various pathogens.

Molecular weight-dependent spectral and metal binding properties of sediment dissolved organic matter from different origins

The metal binding potential of dissolved organic matter (DOM) is highly related with its inherent properties such as molecular weight (MW). Here sediment DOMs with different origins, i.e., algae- and macrophyte-dominated sediment DOM (named as ASDOM and MSDOM, respectively), were size-fractionated into low MW (LMW-, <1 kDa) and high MW (HMW-, 1 kDa~0.45 μm) fractions, with the spectral and metal binding properties in different MW fractions exploring via total organic carbon, absorption spectroscopy, fluorescence parallel factor (PARAFAC) analysis, and Cu(II) titration techniques. The MSDOM contained more organic carbon, lower specific UV absorbance, lower fluorescence index, higher humification index, and lower biological index compared to the ASDOM. As for the MW-fractionated samples, the humic- and fulvic-like fluorophores were mainly distributed in the LMW-DOM, while the protein-like ones were located richly in the HMW-DOM. Thus, obvious MW- and origin-dependent heterogeneities in abundance and spectral properties were observed for sediment DOMs. One humic-like, one fulvic-like, and two protein-like fluorescent components were identified by PARAFAC analysis, with different components exhibiting different variable patterns in response to Cu(II) addition. Irrespective of sample sources, humic- and fulvic-like components had higher condition stability constants (logKM > 4.96) than protein-like components (logKM < 4.86). As for the MW-fractionated samples, the HMW-DOM, especially the HMW humic-/fulvic-like components, exhibited higher metal binding potential than the bulk and LMW counterparts. This study highlighted the importance of HMW-DOM in manipulating the behavior, fate, and bioavailability of heavy metals in lake sediments.

Molecular weight-dependent adsorption fractionation of natural organic matter on ferrihydrite colloids in aquatic environment

Natural organic matter (NOM), a heterogeneous mixture with various organic components and continuous molecular weight (MW) distribution, is omnipresent in natural waters. To date, understanding of the MW-dependent adsorption fractionation of NOM samples on colloids is limited due to the lack of NOM fractionation and characterization methods. In this study, the ultrafiltration technique was applied to fractionate the bulk NOM samples into low MW (LMW-, <1 kDa) and high MW (HMW-, 1 kDa–0.45 μm) fractions, whose adsorption behaviors on ferrihydrite colloids were comparatively examined via using total organic carbon, chromophoric, fluorescent emission-excitation matrix-parallel factor (EEM–PARAFAC), and two dimension FTIR correlation spectroscopy (2D–FITR–COS). The adsorption behaviors of all samples can be reasonably explained by Langmuir and Frendlich isotherm models, and the HMW-NOM exhibited higher adsorption capacities and affinities (4.71 mg-C/g) than the bulk (3.88 mg-C/g) and LMW- (2.44 mg-C/g) counterparts. Irrespective of MWs, the non-aromatic moieties were preferentially adsorbed by ferrihydrites, causing an enhanced aromaticity for the residual solutions. Two humic-like and one protein-like component were identified by EEM–PARAFAC, and a increase and decrease trend of Ka (adsorption affinity) were observed for humic- and protein-like components, respectively, in the order of LMW-, bulk, and HMW-NOM, showing obvious MW- and component-dependent adsorption fractionation of NOM on ferrihydrite colloids. 2D–FTIR–COS provided further information that, with increasing site limitation, the C–O in carbohydrate was adsorbed prior to the amide I in proteins, which testified the MW-dependent adsorption fractionation of NOM samples and accounted for the enhanced aromaticity in the residual solutions. This study highlighted the importance of MWs in NOM adsorption, which can enhance our understanding of the biogeochemical cycles of colloids and contaminants in aquatic environments.

Characterization of particulate-bound polycyclic aromatic compounds (PACs) and their oxidations in heavy polluted atmosphere: A case study in urban Beijing, China during haze events

Characterizations on polycyclic aromatic compounds (PACs) during frequent haze periods have been conducted in an urban site of Beijing, China. Particulate polycyclic aromatic hydrocarbons (PAHs) and oxygenated-PAHs (OPAHs) and other carbonaceous matters were quantified. The average PM2.5 during haze events (256.3 ± 103.7 μg/m3) were one magnitude over than that of clear periods (CRs, 24.7 ± 27.7 μg/m3).The average total quantified PAHs (ΣPAHs) and OPAHs (ΣOPAHs) during haze events were 423.9 ± 178.4 ng/m3 and 581.4 ± 299.8 ng/m3, respectively, which were approximately 10 times higher than those of 40.3 ± 68.2 ng/m3 and 54.4 ± 82.4 ng/m3 in clear days. Four-rings PAHs had the highest compositions. 1,8-Naphthalic anhydride (1,8-NA) is the most abundant OPAHs, accounted for 49.8% of ∑OPAHs, followed by 9,10-anthraquinone (9,10-AQ) (13.8%) and benzo(a)anthracene-7,12-dione (BaAQ) (8.31%). In haze events, the contents of 5- to 7-rings PAHs decreased by 2.32% compared with those of clear days, while lower molecular weight fractions of 3- and 4-rings PAHs increased. The relationships between PAHs, OPAHs and relative humidity (RH) were found to be exponential. High oxygenation rate (R0) ratios of OPAH/PAH represents higher rates in secondary formation or degradation and gas- particle conversion for each PAH or OPAH during the wintertime. Significant positive correlation between BeP and OPAHs (r = 0.97), combined with the results of photochemical aging and negatively correlation with O3, suggest that secondary atmospheric reactions of PAHs played an important role in the burden of OPAHs.

Assessment of neuropharmacological potential of low molecular weight components extracted from Rhinella schneideri toad poison.

Background:Studies on toad poison are relevant since they are considered a good source of toxins that act on different biological systems. Among the molecules found in the toad poison, it can be highlighted the cardiotonic heterosides, which have a known mechanism that inhibit Na+/K+-ATPase enzyme. However, these poisons have many other molecules that may have important biological actions. Therefore, this work evaluated the action of the low molecular weight components from Rhinella schneideri toad poison on Na+/K+-ATPase and their anticonvulsive and / or neurotoxic effects, in order to detect molecules with actions of biotechnological interest.Methods: Rhinella schneideri toad (male and female) poison was collected by pressuring their parotoid glands and immediately dried and stored at -20 °C. The poison was dialysed and the water containing the low molecular mass molecules (< 8 kDa) that permeate the dialysis membrane was collected, frozen and lyophilized, resulting in the sample used in the assays, named low molecular weight fraction (LMWF). Na+/K+ ATPase was isolated from rabbit kidneys and enzyme activity assays performed by the quantification of phosphate released due to enzyme activity in the presence of LMWF (1.0; 10; 50 and 100 µg/mL) from Rhinella schneideri poison. Evaluation of the L-Glutamate (L-Glu) excitatory amino acid uptake in brain-cortical synaptosomes of Wistar rats was performed using [3H]L-glutamate and different concentration of LMWF (10-5 to 10 µg/µL). Anticonvulsant assays were performed using pentylenetetrazole (PTZ) and N-methyl-D-aspartate (NMDA) to induce seizures in Wistar rats (n= 6), which were cannulated in the lateral ventricle and treated with different concentration of LMWF (0.25; 0.5; 1.0; 2.0; 3.0 and 4.0 µg/µL) 15 min prior to the injection of the seizure agent.Results:LMWF induced a concentration-dependent inhibition of Na+/K+-ATPase (IC50% = 107.5 μg/mL). The poison induces an increased uptake of the amino acid L-glutamate in brain-cortical synaptosomes of Wistar rats. This increase in the L-glutamate uptake was observed mainly at the lowest concentrations tested (10-5 to 10-2 µg/µL). In addition, this fraction showed a very relevant central neuroprotection on seizures induced by PTZ and NMDA.Conclusions:LMWF from Rhinella schneideri poison has low molecular weight compounds, which were able to inhibit Na+/K+-ATPase activity, increase the L-glutamate uptake and reduced seizures induced by PTZ and NMDA. These results showed that LMWF is a rich source of components with biological functions of high medical and scientific interest.

ЗМІНИ БІЛКОВОГО СКЛАДУ ТКАНИН ПРИ РОЗВИТКУ ЕКСПЕРИМЕНТАЛЬНОГО ОЖИРІННЯ У ЩУРІВ

The problem of obesity in modern world has a leading place along with other pathologies. Contrary to the settled ideas that the reason of obesity is hypodynamia and overeating, leading medical editions claim that investigating pathology has polymorphic origin and are linked to the cascade of various violations in organs and their systems. Recently collected data array on the basis of which participation of tissue-specific peptide pools in maintenance to a homeostasis is being postulated, in particular, their ability to regulate proliferation processes, differentiation and death of cells is established. We have characterized fractions of low-, medium- and high-molecular-weight protein homogenates from liver, kidney, muscle and adipose tissue samples of rats with experimental obesity. Protein fractions were separated by electrophoresis using the Laemmli method in 10 % PAAG with sodium dodecyl sulfate (SDS). Spreading between proteins in control and group of rats with obesity has showed a difference in quantity of fractions. We have investigated quantitative and qualitative composition of protein fractions in rat's tissues. Under experimental obesity conditions protein composition of tissues changes, the content of median-molecular fraction (67-35 kDa) and low molecular weight fraction (35-10 kDa) increases. Experimental data may indicate connection breach in protein-protein interactions in these viscuses and predict the formation of non-specific proteins and their fragments in the bloodstream, as a result of increased activity of proteolytic enzymes and destruction of viscuses cells. Future studies in specifics of protein composition changes and peptide pool of rat's tissues will improve understanding the biochemical processes under the conditions of this pathology, which is important in the development of new approaches to diagnosis and treatment of obesity principles

Characterization and epitope identification of the T cell response in non-allergic individuals exposed to mouse allergen

BackgroundExposure to airborne allergens is a frequent trigger of respiratory allergy and asthma in atopic individuals. While allergic patients suffer hypersensitivity reactions to these allergens, non-allergic individuals do not exhibit clinical symptoms despite environmental exposure to these ubiquitous allergen sources. The aim of this study was to characterize T cell responses in non-allergic laboratory workers, who are heavily exposed to mice allergens (Exposed Non-Allergics, ENA) and compare this data to previously published T cell responses measured in mouse (MO)-allergic patients. METHODS: Peripheral mononuclear cells (PBMC) from ENA subjects were expanded for 2 weeks in vitro with mouse urine extract and screened for IFNγ and IL-5 cytokine production in response to mouse antigen-derived peptides by ELISPOT. Ex vivo T cell reactivity in the ENA cohort was performed after 6hr stimulation with peptide pools by intracellular staining of CD154. ResultsVigorous responses were detected, associated with 147 epitopes derived from 16 mouse antigens. As expected, responses in ENA subjects were somewhat lower than those observed in MO-allergics for both responder frequency and overall response magnitude. While responses in allergics were polarized towards IL-5 production and associated with low IFNγ production, ENA responses were not polarized. The composition of targeted antigens and epitopes was overall similar between the two cohorts, with the majority of T cell reactivity directed against Mus m 1 and other major urinary proteins. However, kappa-casein precursor and odorant binding protein Ib were more abundantly recognized in MO-allergics compared to ENA subjects. Additionally, T cell responses against oligopeptides derived from the low molecular weight fraction of mouse urine were also assessed. Interestingly, no difference in the response frequency, magnitude or polarization between MO-allergic and ENA individuals was observed. Finally, assessment of ex vivo T cell activation also revealed T cell reactivity in the ENA cohort, with a non-significant trend for lower responses compared to MO-allergics. ConclusionExposure to mouse induces potent T cell responses in non-allergic individuals, targeting similar epitopes as seen in allergic patients.

Raman spectroscopic screening of high and low molecular weight fractions of human serum.

This study explores the suitability of Raman spectroscopy as a bioanalytical tool, when coupled with ultra-filtration and multivariate analysis, to detect imbalances in both high molecular weight (total protein content, γ globulins and albumin) and low molecular weight (urea and glucose) fractions of the same samples of human patient serum, in the native liquid form. Ultracentrifugation was employed to separate and concentrate the high and low molecular weight fractions of the serum. Initially, aqueous solutions of the respective molecular species, covering physiologically relevant concentration ranges, were analysed to optimise the measurement protocols. An adapted Extended Multiplicative Signal Correction (EMSC) algorithm was applied to raw spectra to remove water background signal and spectral interferents (β-carotene). Using a validated partial least squares regression modelling method, R2 values, Root Mean Square Error of Cross Validation (RMSECV) and standard deviations were established for the quantification of γ globulin, total protein, albumin, urea and glucose content of the patient serum samples. The study demonstrates that Raman spectroscopy in the liquid form is a viable alternative and/or adjunct to current clinical practice for the parallel analysis of high and low molecular weight fractions, and simultaneous analysis of multiple analytes in the low molecular weight fraction, of human serum for diagnostic applications.

Effects of one-step alkaline and two-step alkaline/dilute acid and alkaline/steam explosion pretreatments on the structure of isolated pine lignin

Biological valorization of biomass most often depends on the efficient reduction of plant cell wall recalcitrance and conversion of lignin – the most recalcitrant constituent – to fuels, chemicals and/or value-added substances. Lignin conversion to fuels and value-added chemicals requires a sound understanding of the structure of lignin before and after different pretreatments. In the current work, an effort has been made to compare the structural differences in isolated pine lignin after one- (alkaline) and two-step (alkaline/dilute acid and alkaline/steam explosion) pretreatments. Our results indicate removal of the low molecular weight fraction of lignin after an initial alkaline pretreatment. A subsequent dilute acid pretreatment resulted in the loss of lignin inter-unit linkages such as β-O-4’ aryl ethers. However, with a steam explosion pretreatment, lignin exhibited a competing condensation process leading to increased condensed lignin structures.

Lower molecular weight fractions of PolyDADMAC coagulants disproportionately contribute to N-nitrosodimethylamine formation during water treatment

N-nitrosodimethylamine (NDMA) is a chloramine disinfection by-product, and its formation in drinking waters can increase due to the addition of cationic polydiallyldimethylammonium chloride (polyDADMAC). PolyDADMAC is a cationic polymer added as a coagulant or coagulant aid to enhance turbidity removal during sedimentation and filtration. This paper answers two central questions to understanding the nature of the NDMA precursors in polyDADMAC. First, what is the reactivity of different molecular weight (MW) fractions of polyDADMAC with chloramines? NDMA formation potential (NDMAFP) and kinetic experiments with chloramines were conducted for non-fractionated (raw) and size-excluded fractions (<3K, 3–10K, and >10K Da.) of polyDADMAC. The lower MW fraction (<3K Da.) of polyDADMAC solutions was responsible for forming 64 ± 6% of the NDMA, despite containing only 8.7 and 9.8% of the carbon or nitrogen present in the bulk polymer. The chloramine demand kinetics of the lowest MW fraction were also >2× faster than the higher MW fractions. Therefore, in a water treatment application the lower MW polyDADMAC likely contributes to most of the NDMA attributed to the use of polyDADMAC. The second question was: can 1H and 13C nuclear magnetic resonance spectroscopy (NMR) be used to characterize the molecular structures in polyDADMAC that react with chloramines? A peak for 1H NMR dimethylamine (DMA), a known low MW NDMA precursor, was found in a commercial polyDADMAC solution and decreased upon chloramination. The estimated DMA alone could not account for the observed NDMAFP, indicating the presence of other low MW precursors. Diffusion order spectroscopy (DOSY) NMR also showed multiple lower MW organics in polyDADMAC that change upon chloramination, including a 1.5× decrease in MW, suggesting chloramines cleave CC or CN bonds. These reactions may produce intermediates responsible for NDMA formation. Polymer manufacturers could use NMR to synthesize polyDADMAC with less DMA and other low MW compounds that produce NDMA upon chloramination.

Biodegradation of humic substances by microscopic filamentous fungi: chromatographic and spectroscopic proxies

The study of interactions between humic substances (HSs) and soil filamentous fungi is the key to understanding the sustainable soil functioning. The present work aims to examine the decomposition of HSs by filamentous dark-pigmented fungus Alternaria alternatа under the laboratory conditions and to determine the effect of easily assimilable organic carbon on this process. Analyzing such polydisperse substances like HSs by a complex integrated methodology makes it possible to explore the data on their decomposition by microorganisms. To achieve the aforementioned goals, we used chromatographic and spectroscopic approaches: low-pressure size-exclusion and hydrophobic interaction chromatography accompanied by absorption and fluorescence spectroscopy. To determine the effect cometabolism conditions produced on HS decomposition, two types of carbon substrates were added to the nutrient media: easily assimilable organic carbon (standard 0.3% or reduced 0.03% sucrose content) and hardly assimilable organic carbon (HSs), as well as their combinations. Five HS samples of different organic matter origin have been inspected: potassium humates (HPs) and humic acids (HAs) from coal, peat, and lignosulfonate. Correlation matrix and principal component analysis (PCA) were calculated for comprehensive data analysis. Transformations of the investigated HSs under fungal cultivation lead to the increase in the low molecular weight fraction, rise of hydrophilic fraction, enlargement of absorbance ratio A250/A365, shortening of the emission wavelength of the humic-type fluorescence, and growth in the fluorescence quantum yield measured with excitation at 355 nm. A positive correlation was observed between the accumulation of fungal biomass and the degree of HS decomposition. PCA analysis confirms that the difference in the results of HS decomposition largely depends on the sucrose content and the nature of HSs. We divided all the HS samples into four groups according to the degree of HS decomposition: original HS solutions, HPs altered using fungal cultivation at 0.03% sucrose, HAs after fungal cultivation at 0.03% sucrose, and finally, HSs (both HPs and HAs) after fungal cultivation at 0.3% sucrose. In the laboratory experiments, we showed that (1) the isolated HAs were more effectively degraded than the parent HPs, and this process was more pronounced at a reduced sucrose content, and (2) the decomposition of stable organic compounds (HSs) was activated by the easily assimilable carbon sources (especially 0.3% sucrose) being present. We assume that it is the easily assimilable organic carbon that most likely triggers the HS degradation working as the priming effect in natural environments.

Impact of nanoparticles on transcriptional regulation of catabolic genes of petroleum hydrocarbon-degrading bacteria in contaminated soil microcosms.

This study was conducted to determine what effects nanoparticles (NPs) like TiO2 , ZnO, and Ag may pose on natural attenuation processes of petroleum hydrocarbons in contaminated soils. The solid NPs used were identified using x-ray diffraction technique and their average size was certified as 18.2, 16.9, and 18.3 nm for Ag-NPs, ZnO-NPs, and TiO2 -NPs, respectively. NPs in soil microcosms behave differently where it was dissolved as in case of Ag-NPs, partially dissolved as in ZnO-NPs or changed into other crystalline phase as in TiO2 -NPs. In this investigation, catabolic gene encoding catechol 2,3 dioxygenase (C23DO) was selected specifically as biomarker for monitoring hydrocarbon biodegradation potential by measuring its transcripts by RT-qPCR. TiO2 -NPs amended microcosms showed almost no change in C23DO expression profile or bacterial community which were dominated by Bacillus sp., Mycobacterium sp., Microbacterium sp., Clostridium sp., beside uncultured bacteria, including uncultured proteobacteria, Thauera sp. and Clostridia. XRD pattern suggested that TiO2 -NPs in microcosms were changed into other non-inhibitory crystalline phase, consequently, showing the maximum degradation profile for most low molecular weight oil fractions and partially for the high molecular weight ones. Increasing ZnO-NPs concentration in microcosms resulted in a reduction in the expression of C23DO with a concomitant slight deteriorative effect on bacterial populations ending up with elimination of Clostridium sp., Thauera sp., and uncultured proteobacteria. The oil-degradation efficiency was reduced compared to TiO2 -NPs amended microcosms. In microcosms, Ag-NPs were not detected in the crystalline form but were available in the ionic form that inhibited most bacterial populations and resulted in a limited degradation profile of oil, specifically the low molecular weight fractions. Ag-NPs amended microcosms showed a significant reduction (80%) in C23DO gene expression and a detrimental effect on bacterial populations including key players like Mycobacterium sp., Microbacterium sp., and Thauera sp. involved in the biodegradation of petroleum hydrocarbons.

Fucoidan Extracted from the New Zealand Undaria pinnatifida-Physicochemical Comparison against Five Other Fucoidans: Unique Low Molecular Weight Fraction Bioactivity in Breast Cancer Cell Lines.

Fucoidan, the complex fucose-containing sulphated polysaccharide varies considerably in structure, composition, and bioactivity, depending on the source, species, seasonality, and extraction method. In this study, we examined five fucoidans extracted from the same seaweed species Undaria pinnatifida but from different geological locations, and compared them to the laboratory-grade fucoidan from Sigma (S). The five products differed in molecular composition. The amount of over 2 kDa low molecular weight fraction (LMWF) of the New Zealand crude fucoidan (S1) was larger than that of S, and this fraction was unique, compared to the other four fucoidans. The difference of molecular compositions between S and S1 explained our previous observation that S1 exhibited different anticancer profile in some cancer cell lines, compared with S. Since we observed this unique LMWF, we compared the cytotoxic effects of a LMWF and a high molecular weight fucoidan (HMWF) in two breast cancer cell lines—MCF-7 and MDA-MB-231. Results indicated that the molecular weight is a critical factor in determining the anti-cancer potential of fucoidan, from the New Zealand U. pinnatifida, as the LMWF exhibited a dose-dependent inhibition on the proliferation of breast cancer cells, significantly better than the HMWF, in both cell lines. A time-dependent inhibition was only observed in the MCF-7. Induction of caspase-dependent apoptosis was observed in the MDA-MB-231 cells, through the intrinsic apoptosis pathway alone, or with the extrinsic pathway. LMWF stimulated a dose-dependent NOS activation in the MDA-MB-231 cells. In conclusion, the fucoidan extracted from the New Zealand U. pinnatifida contains a unique LMWF, which could effectively inhibit the growth of breast cancer cell lines. Therefore, the LMWF from New Zealand U. pinnatifida could be used as a supplement cancer treatment.

Quantity and Functionality of Protein Fractions Isolated from 3 Ecotypes of Indigenous Chicken in Kenya

&lt;p&gt;&lt;em&gt;The aim of this study was to evaluate the effect of the cluster ecotype and the part of chicken on nutritional composition, and functionality of sarcoplasmic and myofibrillar proteins that are most relevant to the technological features of chicken meat. Over 50 chickens from each ecotype cluster purchased, slaughtered and the meat stored under refrigeration at -20&lt;sup&gt;o&lt;/sup&gt;C and later on transferred in cooler box on ice and flown to South Africa, at the Durban University of Technology. Protein fractions were extracted with a cocktail of Sodium Chloride buffer (50mM NaCl, 50mM Tris HCl; 75mM DTT and 1mM EDTA at pH 7) and quantified by Bradford method. One dimensional Sodium Dodecyl Polyacrylamide Gel Electrophoresis (SDS PAGE) was applied to separate protein fractions. Emulsifying capacity, emulsifying stability, solubility, and in vitro digestibility were determined on the total protein isolates. Significant differences in band expressions were recorded for the myofibrillar and the sarcoplasmic proteins. The three ecotypes had high quality proteins with all the limiting and essential amino acids at concentrations higher than FAO/WHO recommended daily allowance for adults and children. Distinct protein bands at larger molecular weight proteins &amp;gt;100 kDa, corresponding to Myosin Heavy Chain, medium fractions 75 kDa and 45 kDa and even lower molecular weight fraction &amp;lt;25 kDa were present in the chicken breast and the thighs. It concludes that Indigenous chicken protein isolates’ nutritional and functional properties are affected by part of chicken and ecotype clusters. &lt;/em&gt;&lt;/p&gt;

Laser-assisted oxidative polymerization of 3-octylthiophene (3OT) and its characterization

Regioramdom poly(3-octylthiophene) (P3OT) was successfully synthesized by laser assisted oxidative polymerization of 3-octylthiphene monomer. The polymerization reaction mixture was irradiated using a 532-nm laser source at different output power, from 0.5 W to 3 W. Results indicate that laser irradiation favors the growth of low molecular weight fractions during the polymerization reaction, promoting changes in the morphology and crystal size, with a significant reduction in process duration, from 24 h to 10 min. This polymerization route could have important industrial applications in optolectronic devices due to the widening of absorption spectrum and short synthesis time.

Seasonal characteristics of particulate polycyclic aromatic hydrocarbons (PAHs) in a petrochemical and oil refinery industrial area on the west coast of South Korea

The Daesan industrial complex is one of the largest petrochemical and oil refinery industrial complexes in South Korea, which is believed to be a major source of polycyclic aromatic hydrocarbons (PAHs). Total suspended particle (TSP) samples (n = 84) were seasonally collected at two industrial sites and one residential site, and 19 PAHs were analyzed. Concentrations of individual PAHs ranged from 0.01 to 2.52 ng/m3, and annual mean concentrations of Σ19 PAHs at Sites 1, 2, and 3 were 5.88, 4.52, and 5.08 ng/m3, respectively. The concentrations of Σ19 PAHs in warm seasons (spring and summer) were lower than those in cold seasons (autumn and winter). Annual fractions of low molecular weight (LMW)-PAHs (2–3 rings, 12.1%) and high molecular weight (HMW)-PAHs (4–7 rings, 87.9%) indicated a strong contribution of thermal processes. Significant correlations between Σ19 PAHs and TSP (p < 0.01) at all the sampling sites were observed, implying that increased TSP levels were responsible for elevated levels of PAHs. There were strong seasonal variations in the profiles of PAHs, and they were clearly reflected in the results of the principal component analysis. Diagnostic ratios and backward air trajectories suggested seasonal variations in the contribution of local emissions and long-range transport. The diagnostic ratios suggested that mixed sources were dominant in cold seasons, while coal/biomass burning and non-traffic sources were prevailing in warm seasons. BeP/BaP ratios indicated that local emissions were major sources compared with long-range transport except for summer. Backward air trajectories in winter suggested the influence of long-range transport, but local emissions were more important in this study area.

Combination of Chemical Coagulation and Photo-Fenton Oxidation Process for the Treatment of Beet Sugar Industry Wastewater: Optimization of Process Conditions by Response Surface Methodology

ABSTRACTThe beet sugar industry generates large volumes of wastewater with high levels of chemical oxygen demand (COD) and color content, which are discharged into the nearby environment without adequate treatment. The aim of this study was to investigate the treatment possibility of this wastewater by using the photo-Fenton oxidation combined with a coagulation process. Central composite design and response surface methodology were used to evaluate the relationships between color and COD reduction and the photo-Fenton oxidation parameters (i.e. Fenton’s reagent dosage, pH, and reaction time).The combined treatment results showed 59% of COD and 83.9% of color removal were obtained at optimum conditions (pH: 6.2; Fe2+ dosage: 20 ppm; H2O2 dosage: 1500 ppm; and reaction time of 15 min). Finally, the results of gel permeation chromatography showed that low molecular weight fraction of the wastewater impurities is more degraded than high molecular weight fraction during oxidation/coagulation process. Therefore, the results obtained from this study showed that an appropriate combined method for the treatment of beet sugar industry wastewater can be designed and implemented.

Fractionation of three different lignins by thermal separation techniques—A comparative study

AbstractSeparation of the heterogeneous lignin macromolecule in fractions with increased homogeneity, as well as different structural (molar mass) and functional (hydroxy groups, ‐OH) features is important in terms of its use as a chemical building block. For this purpose, three thermal separation techniques were investigated and compared: solvent extraction, successive precipitation and ultrafiltration. One important issue in this context is the utilization of organic solvents with low boiling points to ensure a simple and efficient recovery. In addition to a softwood Kraft lignin (Indulin AT) as reference lignin, two sulfur‐free Organosolv lignins from short rotation coppice (“poplar with bark”) and from the energy grass Miscanthus × gigantheus were investigated. The lignins were separated into low, medium and high molecular weight fractions. Due to the different initial structural features and the associated varying solubility properties in such lignins, different organic solvents were needed for dissolution and precipitation of the individual lignin fractions. The polarity of the used solvent is one key factor regarding the yield of the soluble fraction and the success of molecular sorting into low, medium, and high molecular weight. Further structural features, for example the aliphatic OH‐group content increased with rising molecular weight of poplar, miscanthus, and Kraft lignin from minimum 0.72, 0.3, and 1.6 mmol/g to maximum 2.4, 1.6, and 2.8 mmol/g, respectively. The number of phenolic OH‐groups decreased from maximum 3.8, 4.3, and 4.2 to minimum 1.4, 2.7, and 2.9, respectively. The presented work illustrate options regarding the molecular sorting of several lignin types with three thermal techniques into fractions differing in key properties (yield, molecular weight, polydispersity, functional groups) for material applications.

A mechanistic microbial underpinning for the size-reactivity continuum of dissolved organic carbon degradation

The reservoir of dissolved organic carbon (DOC) in the ocean is modified by multiple input and removal processes. Incubation experiments as well as measurements of oceanic DOC have demonstrated that the high molecular weight (HMW) fraction of DOC typically has a younger radiocarbon age and is more reactive biologically than the low molecular weight (LMW) fraction of DOC. These observations have been summarized as a ‘size-reactivity continuum’ of DOC reactivity, but mechanistic explanations for these observations have been lacking. Here we describe how our recent discovery of ‘selfish’ HMW organic matter uptake among bacteria in surface ocean waters may help explain the rapid removal of HMW DOC. ‘Selfish’ substrate uptake by bacteria encompasses rapid binding and partial hydrolysis of intact polysaccharides on the outer membrane of bacteria, seamlessly followed by the transport of large oligosaccharide fragments into the periplasm with little to no loss of LMW hydrolysis products. ‘Selfish’ bacteria therefore process HMW substrates in a manner distinct from bacteria that carry out extracellular hydrolysis that yields LMW hydrolysis products in the environment. Recognition of the presence and prevalence of selfish bacteria in the ocean has profound implications for carbon flow – the source and quantity of LMW substrates made available to non-extracellular-enzyme producing bacteria – as well as for efforts to model and measure bacterial interactions during organic matter degradation. This discovery also highlights the importance of targeted substrate binding and uptake as key (often understudied) factors in geochemical investigations of microbially driven carbon cycling in the ocean. We conclude with some speculative thoughts about the factors that may determine the prevalence of selfish substrate uptake in the environment.

Monitoring WWTP performance using size-exclusion chromatography with simultaneous UV and fluorescence detection to track recalcitrant wastewater fractions

A trial monitoring of a typical full-scale municipal WWTP in Central Finland was aimed to explore applicability of high performance liquid chromatography – size exclusion chromatography (HPSEC) with simultaneous UV and fluorescence detection as a tool for advanced routine monitoring of wastewater treatment. High, intermediate, and low molecular weight (MW) fractions of untreated wastewater (influent) and treated wastewater (secondary effluent) were characterized in terms of UV absorbance at 254 nm (UVA254) and specific fluorescence representing tyrosine-like, tryptophan-like, and humic/fulvic-like compounds.The activated sludge treatment removed 97 ± 1% of BOD, 93 ± 2% of COD, 71 ± 7% of DOC, and 24 ± 7% of TN, while the overall reduction of UVA254 was 50 ± 6%. Total fluorescence signal declined by ∼80% for tyrosine-like, by 60–70% for tryptophan-like, and by 7–36% for humic/fulvic-like compounds. Low and intermediate MW humic/fulvic-like compounds fluorescing at λex/λem = 390/500 nm demonstrated recalcitrant behavior. Protein-like and humic/fulvic-like fractions of low MW < 1 kDa accounted for 60–65% of total UVA254 and 50–70% of total fluorescence of whole influent and effluent samples. Strong linear correlations were observed between wastewater BOD, COD, DOC, UVA254 and tyrosine-like, tryptophan-like fluorescence.