Reeselohse2723

The dual roles of H2S as an endogenously synthesized respiratory substrate and as a toxin raise questions as to how it is cleared when the electron transport chain is inhibited. Sulfide quinone oxidoreductase (SQOR) catalyzes the first step in the mitochondrial H2S oxidation pathway, using CoQ as an electron acceptor, and connects to the electron transport chain at the level of complex III. We have discovered that at high H2S concentrations, which are known to inhibit complex IV, a new redox cycle is established between SQOR and complex II, operating in reverse. Under these conditions, the purine nucleotide cycle and the malate aspartate shuttle furnish fumarate, which supports complex II reversal and leads to succinate accumulation. Complex II knockdown in colonocytes decreases the efficiency of H2S clearance while targeted knockout of complex II in intestinal epithelial cells significantly decreases the levels of thiosulfate, a biomarker of H2S oxidation, to approximately one-third of the values seen in serum and urine samples from control mice. These data establish the physiological relevance of this newly discovered redox circuitry between SQOR and complex II for prioritizing H2S oxidation and reveal the quantitatively significant contribution of intestinal epithelial cells to systemic H2S metabolism.Mitotic catastrophe (MC) is a newly identified type of anticancer mechanism for multidrug resistance (MDR) prevention. However, the long cellular death process resulting from MC is not beneficial for anticancer treatment. BZML is a novel colchicine-binding site inhibitor which can overcome MDR by inducing MC; however, BZML-induced MC cells underwent a long cellular death process. Thus, to improve anticancer therapies based on drug-induced MC, BZML-induced MC was served as a model to further study the underlying molecular mechanisms in the process of MC. Here, BZML could induce p53-dependent senescence in A549/Taxol cells, a MDR cell line. This senescence was a secondary effect of MC in overcoming MDR. During MC, BZML-induced destruction of protein-degradation system contributed not only to an increase of p53 protein but also to the accumulation of survivin in nucleus of A549/Taxol cells. Importantly, the nuclear accumulation of survivin was not the inducer but the result of BZML-induced MC, and it promoted the survival of senescent cells. Moreover, it provided additional vulnerability and critical opportunities for sequentially applied therapies. Further, targeting survivin with YM155 accelerated the death of MC cells by timely eliminating therapy-induced senescent cells and strengthening the efficiency of BZML in overcoming MDR in A549/Taxol cells. Collectively, nuclear accumulation of survivin delayed cellular death during MC by promoting the survival of BZML-induced senescent A549/Taxol cells. Moreover, "one-two punch" approach to cancer treatment based on combination therapy with YM155 for survivin suppression might be a new strategy for potentiating MC to overcome MDR.The photo-Fenton-like catalytic process has shown great application potential in environmental remediation. Herein, a novel photo-Fenton-like catalyst of Bi2WO6 nanosheets decorated hortensia-like CoAl-layered double hydroxides (Bi2WO6/CoAl-LDHs) was synthesized via hydrothermal process. The optimized Bi2WO6/CoAl-LDHs composite performed the high-efficiency photo-Fenton-like catalytic performance for oxytetracycline (OTC) removal (98.47%) in the mediation of visible-light and H2O2. The comparative experiment, technical characterization and density functional theory calculation results indicated that the efficient photo-Fenton-like catalytic performance of Bi2WO6/CoAl-LDHs was attributed to the synergistic action of the Fenton-like process of cobalt ions in CoAl-LDHs, an internal electric field and the S-scheme heterojunction form between Bi2WO6 and CoAl-LDHs, which could significantly promote the active substance formation and the photocatalytic process in the catalytic system. This study will stimulate the new inspiration of designing the efficient catalytic system for environmental remediation and other fields.In the present work, the effect of ether oxygen atom introduction in a furan ring-containing polymer has been evaluated. Solvent-free polycondensation process permitted the preparation of high molecular weight poly(diethylene 2,5-furandicarboxylate) (PDEF), by reacting the dimethyl ester of 2,5-furandicarboxylic acid with diethylene glycol. After molecular and thermal characterization, PDEF mechanical response and gas barrier properties to O2 and CO2, measured at different temperatures and humidity, were studied and compared with those of poly(butylene 2,5-furandicarboxylate) (PBF) and poly(pentamethylene 2,5-furanoate) (PPeF) previously determined. Both PDEF and PPeF films were amorphous, differently from PBF one. Glass transition temperature of PDEF (24 °C) is between those of PBF (39 °C) and PPeF (13 °C). As concerns mechanical response, PDEF is more flexible (elastic modulus [E] = 673 MPa) than PBF (E = 1290 MPa) but stiffer than PPeF (E = 9 MPa). Moreover, PDEF is the most thermally stable (temperature of maximum degradation rate being 418 for PDEF, 407 for PBF and 414 °C for PPeF) and hydrophilic (water contact angle being 74° for PDEF, 90° for PBF and 93° for PPeF), with gas barrier performances very similar to those of PPeF (O2 and CO2 transmission rate being 0.0022 and 0.0018 for PDEF and, 0.0016 and 0.0014 cm3 cm/m2 d atm for PPeF). Lab scale composting experiments indicated that PDEF and PPeF were compostable, the former degrading faster, in just one day. The results obtained are explained on the basis of the high electronegativity of ether oxygen atom with respect to the carbon one, and the consequent increase of dipoles along the macromolecule.An amphiphilic cellulose aerogel (HCNC-TPB/TMC) was fabricated by grafting 1,3,5-Tris (4-aminophenyl)benzene (TPB) and trimesoyl chloride (TMC) onto the aldehyde nanocellulose through Schiff alkali and substitution reaction. The obtained HCNC-TPB/TMC exhibited good morphology with cellulose fiber and owned abundant hydrophilic amino and carboxyl groups and hydrophobic aromatic groups. The batch adsorption experiments demonstrated that HCNC-TPB/TMC showed excellent adsorption performance (Qmax = 526.32 mg g-1) for sodium diclofenac (DCF), wide pH applicability (4-10) and outstanding stability and reusability. The DCF adsorption obeyed the pseudo-second-order kinetic model and the Langmuir isotherm, and underwent a spontaneous exothermic process. The main adsorption mechanisms involved electrostatic interaction, hydrogen bonds, π-π stacking interaction and hydrophobic effect. Importantly, the introduced carboxyl aromatic groups on TMC could effectively strengthen the hydrogen bonds and the π-π stacking between HCNC-TPB/TMC and DCF.The effects of pyrolysis temperature on properties and adsorption performance of carbonized bacterial cellulose (CBC) produced from bacterial cellulose at 300, 400, 600 and 800 °C were investigated. As pyrolysis temperature increased, the BET surface area, C and ash contents of CBC increased while its mass yield and the contents of H, N and O decreased. Higher pyrolysis temperature resulted in CBC having more aromatic structure and less hydrophilic. The impacts of pyrolysis temperature, solution pH, contact time and initial concentration on the absorption of Cr(VI) onto CBC were systematically studied as well. The results showed that CBC400 prepared at 400 °C exhibited the highest Cr(VI) adsorption capacity for Cr(VI) up to 250.0 mg/g. selleck products The equilibrium adsorption and adsorption kinetics fitted the Langmuir isotherm and pseudo-second-order kinetic models well. The mechanisms of adsorption of Cr(VI) on CBC included electrostatic interaction, π-π interaction and functional groups complexation.The research on preparing high-quality pellets by combining torrefaction and densification of biomass has received widespread attention. This paper investigated the influence of torrefaction temperature on biomass and evaluated the quality of three kinds of pellets (raw pellets, ex-situ torrefied densified pellets and in-situ torrefied densified pellets). When the torrefaction temperature was raised to 300 °C, the energy yield of rice straw (RS) and rice husk (RH) quickly decreased to 71.08% and 77.62%, and the cellulose was decomposed significantly. The results proved that 250 °C was an optimum temperature for RS and RH torrefaction. The densities of RS and RH in-situ torrefied densified pellets were 1236.84 kg/m3 and 1277.50 kg/m3 under 150 MPa, respectively. The density, Meyer hardness, hydrophobicity, and mechanical specific energy consumption of the pellet increased with the increase of molding pressure. The in-situ pellets had higher Meyer hardness, hydrophobicity, and lower mechanical specific energy consumption under the same molding pressure than raw pellets and ex-situ torrefied densified pellets. In addition, the bonding mechanism was studied by using scanning electron microscopy and ultraviolet auto-fluorescence. In-situ torrefaction and densification facilitated the formation of self-locking and the migration of lignin between particles. Compared with RH pellets, RS pellets had higher quality due to the higher hemicellulose content, which was necessary for forming stable hydrogen bonds.The United Nations estimates the rate of deforestation over 10 million hectares per year, with additional infested wood available due to drought, bark beetle calamity and other damage vectors. Processing the hard-to-reach infested wood into biochar via mobile pyrolysis units seems to be a good option for fire prevention. However, since most biochar is currently produced mainly from biological waste, there is not enough experience with wood biochar on a large scale. Review of current knowledge, followed by techno-economic assessment reveals that following the chemical composition of the feedstock, wood biochar outperforms other types of biochar in terms of high porosity. Therefore, wood biochar shows excellent results in increasing the amount of plant-available water content in soil and appears to be an excellent tool for recycling nutrients (especially into plant-available forms of phosphorus and nitrogen). The overall positive effects of biochar application change from abiotic to biotic over time because as it decays, many of its physical properties disappear, but it can boost soil microbial communities on which soil fertility depends. As global climate change creates a wide range of factors that damage forest cover, wood biochar consequently represents untapped potential in the field of soil, nutrient, and energy management.Pseudomonas brassicacearum LZ-4 is a facultative anaerobic bacterium, can efficiently degrade naphthalene and reduce chromate simultaneously. In this study, we showed that the naphthalene degradation enzyme NahAa from P. brassicacearum LZ-4 can reduce Cr(VI). Heterologous expression in E. coli S17-1 along with RNA interference of NahAa in strain LZ-4 showed the enzyme can reduce chromate in vivo. In vitro, purified NahAa was identified and can catalyze Cr(VI) reduction by 64.2%. Flavin adenine dinucleotide (FAD) was identified as a cofactor of NahAa, which Cr(VI) could obtain electrons from NADH through NahAa-associated FAD for reduction. Immobilized NahAa on functional multi walled carbon nanotubes via physical adsorption method to produce a stable, high efficient composite MWCNT-NahAa. The maximum efficiency of MWCNT-NahAa composite was obtained in enzyme concentrations of 6 mg/mL and 20 min immobilization time. The optical reaction conditions for MWCNT-NahAa were pH 7.0 and 30 °C, still retaining 50% of its initial activities after five consecutive cycles.