Genome-wide identification and expression analysis revealed key transcription factors as potential regulators of high-temperature adaptation of Coriolopsis trogii.

Transcription factors (TFs) play a crucial role in gene expression, and studying them can lay the foundation for future research on the functional characterization of TFs involved in various biological processes. In this study, we conducted a genome-wide identification and analysis of TFs in the thermotolerant basidiomycete fungus, Coriolopsis trogii. The TF repertoire of C. trogii consisted of 350 TFs, with C2H2 and Zn2C6 being the largest TF families. When the mycelia of C. trogii were cultured on PDA and transferred from 25 to 35 °C, 14 TFs were up-regulated and 14 TFs were down-regulated. By analyzing RNA-seq data from mycelia cultured at different temperatures and under different carbon sources, we identified 22 TFs that were differentially expressed in more than three comparisons. Co-expression analysis revealed that seven differentially expressed TFs, including four Zn2C6s, one Hap4_Hap_bind, one HMG_box, and one Zinc_knuckle, showed significant correlation with 729 targeted genes. Overall, this study provides a comprehensive characterization of the TF family and systematically screens TFs involved in the high-temperature adaptation of C. trogii, laying the groundwork for further research into the specific roles of TFs in the heat tolerance mechanisms of filamentous fungi.

The parallel electron transfer pathways of biofilm and self-secreted electron shuttles in gram-positive strain Rhodococcus pyridinivorans HR-1 inoculated microbial fuel cell.

Microbial fuel cell (MFC) exhibits huge potentials in disposing wastewater and extra energy consumption. Exploring useful microorganisms for MFC is the crucial section. Herein, the electrochemical mechanism of extracellular anaerobic respiration in MFC inoculated with gram-positive Rhodococcus pyridinivorans HR-1, was first revealed. The MFC exhibited rapid recovery of currents on anode, and could recover to maximum output within one hour, with redox peaks near -0.38 and -0.18 V through electron transfer between the biofilm and anode. When the biofilm-based pathway was blocked by wrapping the anode with Millipore filter membrane, HR-1 inoculated MFC could still generate electricity within a longer recovery period (∼35 h) during anolyte exchange. This was proposed as a self-secreted electron shuttle pathway for electron transfer in R. pyridinivorans HR-1. Cyclic voltammetry analysis revealed that the biofilm-based and self-secreted electron shuttle-based pathways co-existed in R. pyridinivorans HR-1 inoculated MFC, which could play synergistic roles in electricity generation.

Revealing the key role of structural cross-link between lignin and polysaccharides during fast pyrolysis of lignocellulose.

Lignin-carbohydrate complex (LCC) is the native existing form of major components in lignocellulose. In this study, the structural cross-link between lignin and polysaccharides in lignocellulose was quantitatively estimated with carboxymethylation-separation (CM-Sep) method, and its influence on lignocellulose pyrolysis was systematically investigated. The cross-linked lignin was found to positively correlate with the production of small molecules and furan derivatives while negatively affecting the generation of anhydrous sugars. Content of small molecules was increased by 97% while that of anhydrous sugars was decreased by 47% in pyrolytic products with levoglucosan yield lowered by 54 wt% in the existence of cross-linked lignin. Furthermore, the impact of cross-linked lignin was revealed to be significantly distinguished from free lignin. Impeded glycosidic end formation and boosted glycosyl ring scission as well as lignin fragmentation were responsible for the distinction. Excellent correlations between structural cross-link and lignocellulose pyrolytome could facilitate product prediction and process design.

Incorporating nanocrystalline cellulose into a multifunctional hydrogel for heart valve tissue engineering applications.

Functional tissue engineered heart valves (TEHV) have been an elusive goal for nearly 30 years. Among the persistent challenges are the requirements for engineered valve leaflets that possess nonlinear elastic tissue biomechanical properties, support quiescent fibroblast phenotype, and resist osteogenic differentiation. Nanocellulose is an attractive tunable biological material that has not been employed to this application. In this study, we fabricated a series of photocrosslinkable composite hydrogels mNCC-MeGel (mNG) by conjugating TEMPO-modified nanocrystalline cellulose (mNCC) onto the backbone of methacrylated gelatin (MeGel). Their structures were characterized by FTIR, 1 HNMR and uniaxial compression testing. Human adipose-derived mesenchymal stem cells (HADMSC) were encapsulated within the material and evaluated for valve interstitial cell phenotypes over 14 days culture in both normal and osteogenic media. Compared to the MeGel control group, the HADMSC encapsulated within mNG showed decreased alpha smooth muscle actin (αSMA) expression and increased vimentin and aggrecan expression, suggesting the material supports a quiescent fibroblastic phenotype. Under osteogenic media conditions, HADMSC within mNG hydrogels showed lower expression of osteogenic genes, including Runx2 and osteocalcin, indicating resistance toward calcification. As a proof of principle, the mNG hydrogel, combined with a viscosity enhancing agent, was used to 3D bioprint a tall, self-standing tubular structure that sustained cell viability. Together, these results identify mNG as an attractive biomaterial for TEHV applications.

Synthesis and characterization of a thermosensitive solid amine biomass adsorbent for carbon dioxide adsorption.

A thermosensitive solid amine fiber SF-AM-co-NIPAM-HBP-NH2 was synthesized by grafting temperature-sensitive monomer N-isopropyl acrylamide (NIPAM) as well as acrylamide (AM) onto the surface of substrate sisal fiber, and further aminating with hyperbranched amine. FTIR, 13C NMR, SEM, EA and TGA were used to confirm the structure and chemical properties of the grafted fibers. Swelling ratio and CO2 adsorption-desorption experiment were investigated to verify the thermo-sensitivity of the grafted fibers and their CO2 adsorption-desorption behavior. Compared with conventional solid amine adsorbents regenerated around 140 °C, SF-AM-co-NIPAM-HBP-NH2 (1:1) with NIPAM could be regenerated at a much lower temperature of 60 °C, while still maintain a high CO2 adsorption capacity (2.61 mmol/g), comparable to that of SF-AM-HBP-NH2 (2.73 mmol/g) before NIPAM introduction. Its excellent regeneration property and the effect of energy consumption reduction make it possible to be used for CO2 adsorption in industrial process.

Preparation and application of bagasse-based adsorbent for highly efficient removal of mercury ions.

A high-performance bagasse-based adsorbent was prepared from agricultural waste bagasse by grafting of acrylamide and aminating with diethylenetriamine. Effects of catalyst dosage, acrylamide concentration, reaction temperature, and bath ratio on the grafting yield were investigated. The adsorption performances for mercury ions were evaluated by batch adsorption experiments and kinetic experiments. The results show that the adsorbent has high adsorption capacity for mercury in a wide range of pH values. The adsorption capacity could be as high as 813.0 mg/g, and the removal percentage for mercury ions can reach 99.9%. The kinetic adsorption experiments show it can achieve adsorption equilibrium rapidly, which implies that the adsorbent has a strong ability to capture mercury ions. Besides, the bagasse-based adsorbent showed promising regeneration performance, and its adsorption amount of regenerated adsorbent only slightly decreased after five recycling. PRACTITIONER POINTS: An amino-rich adsorbent was prepared from bagasse. The adsorbent possesses high adsorption capacity and high removal efficiency for mercury. The aminated bagasse adsorbs mercury rapidly. The adsorbent functionalized with amino possesses strong affinity toward mercury.

Superior removal of Hg (II) ions from wastewater using hierarchically porous, functionalized carbon.

The removal of heavy metal ions from industrial wastewater by adsorption has been central to the environment for decades, where common adsorbent materials are often limited by poor efficiency, complex fabrication and long processing time. Porous carbon derived from biospecies holds promise to address the limitations. In this study we converted bagasse into a carbon composite having hierarchically porous structure; the composite's dispersion phases - iron oxide and manganese oxide - were synthesized by a simple one-step liquid-phase reaction method. Featuring large specific surface area of 350.8 m2 g-1, the composite demonstrated exceptional Hg (II) removal efficiency of 96.8%, adsorption rate of up to 96.8% within 150 min and adsorption capacity of 9.8 mg g-1. In comparison with other removal materials, our work is outstanding in terms of both removal efficiency and synthesis simplicity. The high efficiency is attributed to the synergy between physical adsorption referring to hierarchically porous structure and chemical adsorption relating to functional complexation processes. It provides a new avenue for the development of high-performance adsorbent materials for heavy metal removal from aqueous media.

Preparation and characterization of amine-functionalized sugarcane bagasse for CO2 capture.

A low-cost solid amine adsorbent for CO2 capture was prepared by using sugarcane bagasse (SB), a dominant agro-industrial residue in the sugar and alcohol industry as raw materials. In this preparation process, acrylamide was grafted on SB, and the grafted fiber was then aminated with different type of amine reagents to introduce primary and secondary amine groups onto the surface of SB fibers. The graft and amination conditions were optimized. The prepared solid amine adsorbent showed remarkable CO2 adsorption capacity and the adsorption capacity of the solid amine adsorbent could reach 5.01 mmol CO2/g at room temperature. The comparison of adsorption capacities of amine fibers aminated with various amination agents demonstrated that fibers aminated with triethylenetetramine would obtain higher adsorption capacities and higher amine efficiency. These adsorbents also showed good regeneration performance, the regenerated adsorbent could maintain almost the same adsorption capacity for CO2 after 10 recycles.

Homogeneous acylation of xylan with 3,5-dinitrobenzoyl in ionic liquid and the adsorption property.

A new xylan ester (xylan 3,5-dinitrobenzoate) as a creatinine adsorbent was prepared by the homogeneous acylation of xylan with 3,5-dinitrobenzoyl chloride in 1-butul-3-methylimidazolium chloride ionic liquid. The influences of reaction conditions on the degree of substitution values of xylan esters were discussed. Results indicated that xylan esters with the degree of substitution range from 1.34 to 1.77 were obtained under the given conditions. The FTIR and (13)C NMR spectroscopies provided the evidence of grafting 3,5-dinitrobenzoyl groups onto the backbone of xylan. Moreover, the adsorption properties of the xylan ester for creatinine were also investigated. Isotherm studies showed that the sorption capacities for creatinine were 2.45, 2.08 and 1.86 mg/g for 23, 30 and 37 °C, respectively. Thermodynamic studies performed indicated the sorption process mainly was controlled by the chemical adsorption. Therefore, xylan 3,5-dinitrobenzoate displayed the promising application in the treatment of chronic renal failure by the creatinine adsorption as the new oral adsorbent.

Preparation of amine group-containing chelating fiber for thorough removal of mercury ions.

An aminated chelating fiber (AF) with high adsorption capacity for mercury ions was prepared by grafting copolymerization of acrylonitrile onto polypropylene fiber, followed by aminating with chelating molecule diethylenetriamine. Effects of reaction conditions such as temperature, reaction time, bath ratio and dosage of catalyst on the grafting yield were studied. Chemical structure, tensile strength and thermal stability of AF were characterized. The adsorption performances for mercury were evaluated by batch adsorption experiments and kinetic experiments. The results show that AF is effective for the removal of mercury over a wide range of pH. The chelating fiber also shows much higher adsorption capacities for mercury, the equilibrium adsorption amount could be as high as 657.9 mg/g for mercury. The high adsorption capacity of Hg(2+) on AF is resulted from the strong chelating interaction between amine groups and mercury ions. Two amine groups coordinate with one mercury ion could be speculated from the adsorption capacity and amine group content on AF. The kinetic adsorption results indicate that the adsorption rates of AF for mercury are very rapid. Furthermore, the residual concentration was less than 1 microg/L with feed concentration of mercury below 1mg/L, which can meet the criterion of drinking water, which indicates that the chelating fiber prepared in this study could be applied to low-level Hg contaminated drinking water purification.