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The widespread application of neonicotinoid insecticides (NEOs) in agriculture causes a series of environmental and ecological problems. Microbial remediation is a popular approach to relieve these negative impacts, but the associated molecular mechanisms are rarely explored. Nitrile hydratase (NHase), an enzyme commonly used in industry for amide production, was discovered to be responsible for the degradation of acetamiprid (ACE) and thiacloprid (THI) by microbes. Since then, research into NHases in NEO degradation has attracted increasing attention. In this review, microbial degradation of ACE and THI is briefly described. We then focus on NHase evolution, gene composition, maturation mechanisms, expression, and biochemical properties with regard to application of NHases in NEO degradation for bioremediation.

Purpose: To study the inhibitory effect of different doses of tetramethylpyrazine (TMP) combined with the beta-blocker, propranolol (Pro) on hemangioma endothelial (EOMA) cells. Methods: EOMA cells were cultured in vitro with varying doses of TMP and Pro (5, 10, 20 and 40 uM). The effect of treatments on cell proliferation was assessed by MTT assay, while cell apoptosis was assayed by flow cytometry. The expressions of Bcl-2, Bax, p-mTOR), total-mammalian target of rapamycin (t-mTOR, p-p70S6) and total-p70 ribosomal protein S6 (t-p70S6) proteins were determined using Western blot. Results: MTT data showed that when used alone, TMP had no significant inhibitory effect on EOMA cells (p > 0.05). However, when TMP was combined with propranolol, there was significant inhibition of EOMA cells, and that the inhibition is dependent on TMP dose. Flow cytometry results showed that the combination of TMP and Pro induced EOMA cell apoptosis dose-dependently (p < 0.05). Moreover, TMP dose-dependently inhibited the phosphorylation of mTOR and p70S6 in EOMA cells, and enhanced Bax expression, but downregulated Bcl-2 (p < 0.05). Conclusion: These results suggest that TMP enhances the inhibitory influence of Pro p-mTOR and pp-70S6 in EOMA cells in a dose-dependent manner. Thus, TMP may enhance Pro-induced inhibition of the growth of endothelial cells, and promote apoptosis through suppression of activation of PI3K/AKT signal route. These findings provide a theoretical basis for the clinical application of TMP/Pro combination for the treatment of hemangioma.

Chemical additives of magnesium chloride (MaC) and ferrous sulfate (FS) were investigated in sewage sludge composting. A treatment without chemical additive was used as the control group (CK). The effects of MaC and FS on ammonia (NH3) and greenhouse gases (CO2, N2O and CH4) emissions were evaluated. The results showed that the addition of MaC and FS promoted the degradation of organic matter and increased the ammonium concentration of the compost product. The maximum pH values decreased from 8.98 (CK) to 8.49 and 8.0 in MaC and FS treatments, respectively. In addition, the NH3 emission for the MaC and FS treatments reduced by 58.3 % and 82.9 %, respectively, whereas the methane (CH4) emission decreased by 22.9 % and 24.9 %, respectively. However, in FS treatment, the carbon dioxide (CO2) and nitrous oxide (N2O) emissions were higher than those in CK. Furthermore, the FS treatment exhibited lower germination index values (71.4 %) and higher electrical conductivity (6.62 mS/cm). Therefore, MaC is suggested as an additive for reducing greenhouse gas emission and conserving nitrogen during sewage sludge composting.

WRKY transcription factors play a critical role in metabolism and stress responses in plants, but few WRKYs have been reported in Taraxacum antungense. Here, a multiple stress-inducible gene, TaWRKY14, was isolated from T. antungense. TaWRKY14 was localized to the nuclei, and phylogenetic analysis indicated that TaWRKY14 shared the highest identity to WRKY40 in Salvia miltiorrhiza. TaWRKY14 was highly expressed in roots, and up-regulated by salt and drought stress, salicylic acid treatment and powdery mildew. TaWRKY14-overexpressing transgenic lines had higher chlorogenic acid concentration and high expression of TaPAL1. The yeast one-hybrid assay proved that TaWRKY14 bond to the W-box of proTaPAL1. Additionally, field experiments showed that TaWRKY14-overexpressing T. antungense lines have higher powdery mildew resistance than the wild-type. Our results demonstrated that TaWRKY14 can regulate CGA biosynthesis and play an important role in resistance to powdery mildew in T. antungense. TaWRKY14 transgenic T. antungense can be used for further evaluation as a new germplasm resource. We analyzed and evaluated the biological function of TaWRKY14 in Taraxacum antungense, and determined that TaWRKY14-overexpressing lines have higher chlorogenic acid concentration and stronger resistance to powdery mildew.

A new class of chiral cyclopentadienyl rhodium(I) complexes (CpRhI ) bearing C2 -symmetric chiral bridged-ring-fused Cp ligands was prepared. The complexes were successfully applied to the asymmetric C-H activation reaction of N-methoxybenzamides with quinones, affording a series of chiral hydrophenanthridinones in up to 82 % yield with up to 99 % ee. Interestingly, structure analysis reveals that the side wall of the optimal chiral CpRhI catalyst is vertically more extended, horizontally less extended, and closer to the metal center in comparison with the classic binaphthyl and spirobiindanyl CpRhI complexes, and may thus account for its superior catalytic performance.

A new class of C2 -symmetric, chiral cyclopentadienyl ligand based on planar chiral ferrocene backbone was developed. A series of its corresponding rhodium(I), iridium(I), and ruthenium(II) complexes were prepared as well. In addition, the rhodium(I) complexes were evaluated in the asymmetric catalytic intramolecular amidoarylation of olefin-tethered benzamides via C-H activation.

A flexible-robust copper(II) metal-organic framework, denoted as LIFM-100, has been successfully synthesized using a fluorinated linear dicarboxylate to link copper ions. LIFM-100 exhibits a breathing effect, which can transform reversibly between a large form (lp) and a narrow form (np) from single crystal to single crystal. In addition, LIFM-100 shows good thermal and chemical stability. By the introduction of trifluoromethyl functional groups and uncoordinated carboxyl acids, LIFM-100 features a good CO2/R22 adsorption/separation performance at 298 K, showing potential in natural gas purification and CO2/R22 capture.

Bulking agents are particularly important for sewage sludge composting. In this study, reusable polypropylene packing (RPP) was mixed with sawdust to improve composting. The effect of the mix ratio of sawdust and RPP on the physicochemical characteristics, nitrogen transformation, and emissions of greenhouse gas (GHG) as well as differences in the germination index values was detected in a lab-scale composting experiment. The results showed that the unique use of RPP as a bulking agent increased the moisture content over 70%, which resulted in poorer porosity and a less efficient O2 utilization environment and thus suppressed the degradation of organic matter. The highest CH4 9275.8 mg and lowest CO2 202.6 g emissions were detected after 25 days of composting in the treatment with RPP used as a bulking agent. When the mixing ratio of sawdust and RPP was 1:1, the temperature, oxygen supply, and dissolved organic carbon degradation were improved. The NH3, N2O, and CH4 emissions were reduced by 32.2, 18.3, and 90.7% compared with a treatment with RPP as a unique bulking agent. The RPP had no effect on conserving nitrogen during sludge composting; the total nitrogen loss was reduced from 29.3 to 18.2% when sawdust was mixed with RPP in a ratio of 1:1. Therefore, mixing RPP and sawdust in the dry weight ratio of 1:1 (sawdust: RPP) can be potentially used for reducing composting cost and improving the sewage sludge composting by reducing the amount of sawdust mixed and mitigating GHG and NH3 emissions.

Known for excellent stability, porosity and functionality, the high-valent Zr4+ metal-organic frameworks (Zr-MOFs) still meets synthetic challenge in modulating the strength of Zr-Ocarboxylate linkage. Herein we explore the unusual coordination dynamics of fluorinated Zr-MOFs by designing two trifluoromethyl modified ligands with distinct geometry preference to form a family of thermodynamic and kinetic products. The low-connecting kinetic Zr-MOFs possess substitutable coordination sites to endow Zr6 -cluster with extra dynamic behaviors, thus opening a post-synthetic pathway to sequential reassembly/disassembly processes. Comprehensive factors, including ligand geometry, Zr6 -cluster connectivity, acid modulator and reaction temperature/concentration, have been studied for controllable syntheses. The stability, hydrophobicity and gas adsorption/separation properties of obtained Zr-MOFs are explored. This work sheds light on the understanding of the dynamic coordination chemistry of Zr-MOFs beyond strong Zr-O bond, which poses a versatile platform for modification and functionalization of Zr-MOFs.

International audience; Calix[4]arenes have the ability to encapsulate biomimetic guests, offering interesting opportunities to explore their molecular recognition, very close to biological scenarios. In this study, p-sulfonatocalix[4]arene (C4 A) anions and hydrated alkali cations have been used for the in situ recognition of cationic 1,ω-diammonium-alkanes and 1,ω-amino-acids of variable lengths. NMR spectroscopy illustrates that these systems are stable in aqueous solution and the interaction process involves several binding states or stabilized conformations within the C4 A anion, depending of the nature of the guest. DOSY experiments showed that monomeric 1 : 1 host-guest species are present, while the cation does not influence their selfassembly in solution. The folded conformations observed in the solid-state X-ray single-crystal structures shed light on the constitutional adaptivity of flexible chains to environmental factors. Futhermore, a comprehensive screening of 30 single crystal structures helped to understand the in situ conformational fixation and accurate determination of the folded structures of the confined guest molecules, with a compression up to 40 % compared with their linear conformations.

A chiral CpRhIII-catalyzed asymmetric C–H activation reaction of N-methoxybenzamides with quinones has been developed to efficiently forge chiral tricyclic hydrophenanthridinone scaffolds in ≤88% y...

A C2-symmetric chiral spirocyclic diol aza-SPINOL containing a spirooxindole scaffold has been designed, synthesized, and optically resolved. The product could be synthesized on gram scale in an ov...

Gastric cancer is one of the most common malignant tumors in the world, and prevention through diet is one of the ways to control. Houttuynia cordata thunb.(HCT) is a plant having medicine and food function, has many biological properties. However, the effect of food style on the anticancer activity of HCT is not clear. So, we investigate the effect of heat treatment on anticancer activity of HCT. HCT extracts (heated aerial stem, heated subterraneous stem, heated leaves defined as HAS, HSS, HL, respectively, and not heated defined as NAS, NSS, NL, respectively) were obtained, and their inhibited activity were detected by alamar blue assay. The cell apoptosis was detected by DAPI staining and flow cytometry analysis. Western blot was performed to test the expression of apoptotic related protein. HCT showed the anticancer activity in four human tumor cell lines. Interestingly, heat treatment could increase the anticancer activity. In SCG-7901 cells, heat treatment increased anticancer activity of AS by 2-14 folds and induced apoptosis through regulating the intrinsic signaling pathways. Intriguingly, the caspase nine specific inhibitor blocked AS-reduced cell viability. Heat treatment increased the anticancer activity of HCT, and can be used as a dietary style for prevention of gastric cancer.

A Gram-stain-positive, aerobic actinomycete, designated strain BMP B8144T, was isolated from desert soil, in Xinjiang province, northwest China. The isolate produced scanty aerial mycelium and fragmented substrate mycelium on most tested media. Cell-wall hydrolysates contained meso-diaminopimelic acid, galactose and mannose. The diagnostic phospholipids were diphosphatidylglycerol, phosphatidylethanolamine, phosphatidylhydroxylethanolamine, phosphatidylinositol, and phosphatidylinositol mannosides. The major fatty acids included iso-C16 : 0, C17 : 1 ω8c and iso-C15 : 0. The predominant menaquinones were MK-9(H4) and MK-10(H4). The DNA G+C content was 70.4 mol% (genome). Based on the 16S rRNA gene sequence analysis on EzBioCloud server, strain BMP B8144T showed the closest similarities to Saccharothrix lopnurensis YIM LPA2hT (98.9 %) and ‘ Saccharothrix yanglingensis ’ Hhs.015 (98.6 %). However, it can be distinguished from the closest strains based on the low levels of DNA–DNA relatedness (59.3±1.8 and 47.9±2.3 %, respectively). A combination of morphological, chemotaxonomic and phylogenetic characteristics, strain BMP B8144T represents a novel species of the genus Saccharothrix , for which the name Saccharothrix deserti sp. nov. is proposed. The type strain is BMP B8144T (=CGMCC 4.7490T=KCTC 49001T).

In the field of transition-metal-catalyzed C-H activation, N-methoxyamides are widely used as C-H activation substrate. Unexpectedly, in this work N-methoxyamides were found to work as efficient amidation reagents in the rhodium(III)-catalyzed C-H activation with boric acid as a cocatalyst. This reaction features broad substrate scope and good yields.

International audience; The self-assembly of triazole amphiphiles was examined in solution, the solid state, and in bilayer membranes. Single-crystal X-ray diffraction experiments show that stacked protonated triazole quartets (T-4) are stabilized by multiple strong interactions with two anions. Hydrogen bonding/ion pairing of the anions are combined with anion-pi recognition to produce columnar architectures. In bilayer membranes, low transport activity is observed when the T-4 channels are operated as H+/X- translocators, but higher transport activity is observed for X- in the presence of the K+-carrier valinomycin. These self-assembled superstructures, presenting intriguing structural behaviors such as directionality, and strong anion encapsulation by hydrogen bonding supported by vicinal anion-pi interactions can serve as artificial supramolecular channels for transporting anions across lipid bilayer membranes.

A zirconium-based metal–organic framework (Zr-MOF) with a 2-fold catenated breathing structure is designed, whose framework contracts in a similarly consecutive manner responsive to solvent (S), te...

Five transition metal coordination polymers, {[Cu(4-pmntd)2(NO3)2]∙2CHCl3}n (1), {[Cu(4-pmntd)2(NO3)2]·3C7H8}n (2), {[Cu(4-pmntd)2(CF3SO3)(H2O)]·CF3SO3·H2O·CH3OH}n (3), [Cd(4-pmntd)2]n·nSiF6·x(CH3OH)·y(CHCl3) (4), and [Zn(4-pmntd)2(CF3SO3)2]n·x(solvent) (5), have been obtained from a ditopic ligand, N,N'-bis(4-pyridylmethyl)naphthalene diimide (4-pmntd). Either sql- or dia- structures are generated from four connecting coordination nodes of the metal centers. While delicate interpenetration and structural tuning in these complexes is achieved by the different conformations and spatially extending geometries adopted by the ligand and “secondary building process” induced by pillar-like anions.

Much of the efficient efforts have been largely devoted to enhancing the CO2 binding affinity in MOFs. In this paper, three isoreticular triazolate frameworks with the formula LIFM-1(TAZ).solvents, LIFM-1(MTAZ).solvents and LIFM-1(AmTAZ).solvents (TAZ = 1,2,4-triazole; MTAZ = 3-methyl-1H-1,2,4-triazole; AmTAZ = 3-amino-1H-1,2,4-triazole) have been prepared by using divalent zinc ions with the ligands of TAZ and its amino and methyl substituted derivatives for comparison of their sorption properties. High thermal stability and phase purity of the three MOFs were verified by thermogravimetric analysis and powder X-ray diffraction, respectively. Single component adsorption isotherms of N2, CO2 and H2 were also measured experimentally. Virial method shows that the porous frameworks of LIFM-1(AmTAZ) display high selectivity of CO2 over N2.

The chiral transient directing group (TDG) strategy has been successfully introduced to the rhodium(III)-catalyzed asymmetric C-H activation. In the presence of a catalytic amount of a chiral amine and an achiral rhodium catalyst, various chiral phthalides were synthesized from simple aldehydes with high chemoselectivity, regioselectivity, and enantioselectivity (53 examples, up to 73 % yield and >99 % ee). It is noteworthy that the chiral induction model is different from the previously reported chiral TDG system using amino acid derivatives and palladium salts. The imino group generated in situ from chiral amine and aldehyde acts as the monodentate TDG to promote the C-H activation, stereoselectively generating the chiral rhodacycle bearing a chiral metal center. Moreover, the stereogenic center of the product is created and stereocontrolled during the Grignard-type addition of the C-Rh bond to aldehyde, rather than during the C-H activation step.

A flexible and robust microporous copper(II) metal-organic framework (MOF) based on a methyl-functionalized ligand, namely, [Cu3(μ3-OH)2(L)2(DMF)] (LIFM-ZZ-1; L = 2,2'-dimethyl-4,4'-biphenyldicarboxylic acid and DMF = N,N-dimethylformamide), was constructed. Its sorption performance for the separation of CH4, C2H6, and C3H8 was investigated. LIFM-ZZ-1 showed a breathing behavior that led to a transition between large- and narrow-pore states. The sample also showed outstanding water stability. Gas adsorption experiments revealed that desolvated LIFM-ZZ-1 exhibited higher adsorption capacities for C2H6 and C3H8 (2.80 and 4.06 mmol·g-1) than for CH4 (0.39 mmol·g-1) at 298 K and 1 bar. Breakthrough experiments showed that a CH4/C2H6/C3H8 mixture was completely separated at 298 K, demonstrating the promising potential applications of this material for separating low contents of C2/C3 hydrocarbons from natural gas.

Background Allium sativum (garlic) is an economically important food source and medicinal plant rich in sulfides and other protective substances such as alliin, the precursor of allicin biosynthesis. Cysteine, serine and sulfur is the precursor of alliin biosynthesis. However, little is known about the alliin content under abiotic stress or the mechanism by which it is synthesized. Results The findings revealed that the content of alliin was lowest in the garlic roots, and highest in the buds. Furthermore, alliin levels decreased in mature leaves following wounding. Transcriptome data generated over time after wounding further revealed significant up-regulation of genes integral to the biosynthetic pathways of cysteine and serine in mature garlic leaves. Conclusions The findings suggest that differential expression of cysteine, serine and sulfide-related genes underlies the accumulation of alliin and its precursors in garlic, providing a basis for further analyses of alliin biosynthesis.

We present optical and near-infrared observations of SN 2019ehk, which was initially reported as a Type Ib supernova (SN). We show that it evolved to a Ca-rich transient according to its spectral properties and evolution in late phases. However, it shows a few properties distinct from those of the canonical Ca-rich transients: a short-duration first peak in the light curve, high peak luminosity, and association with a star-forming environment. Indeed, some of these features are shared with iPTF14gqr and iPTF16hgs, which are candidates for a special class of core-collapse SNe: the so-called ultra-stripped envelope SNe, i.e., a relatively low-mass He (or C+O) star explosion in a binary as a precursor of short-period double neutron star (NS) binaries. The estimated ejecta mass (0.4M (circle dot)) and explosion energy (1.7 x 10(50) erg) are consistent with this scenario. The analysis of the first peak suggests the existence of dense circumstellar material in the vicinity of the progenitor, implying a CCSN origin. Based on this analysis, we suggest SN 2019ehk is another candidate for a low-mass He star explosion. It might create a double NS binary, but with a wide separation. These candidates for low-mass stripped envelope SNe, including ultra-stripped envelope SN candidates, seem to form a subpopulation among Ca-rich transients, associated with young population. We propose that the key to distinguishing this population is the early first peak in their light curves., Japan Society for the Promotion of Science (JSPS) through KAKENHI [JP17H02864, JP18H04585, JP18H05223, JP20H00174, JP20H04737, JP18H03720, JP16H02158]; Japan Society for the Promotion of Science [JP17K14253]; Turkish Scientific and Technical Research Council [TuBTAK-2211C, TuBTAK-2214A]; National Aeronautics and Space Administration, The authors acknowledge Raffaella Margutti, Dan Milisavljevic, and Wynn Jacobson-Galan for stimulating discussion, after their manuscript and this manuscript on SN 2019ehk were both posted on arXiv. The GMOS observation, S19A-051, was conducted via the time exchange program between Gemini and the Subaru Telescope. The FOCAS observation, S19B-055, was conducted at the Subaru Telescope, and the authors thank Kentaro Aoki and the Subaru telescope staff for the observation. This research has made use of the NASA/IPAC Extragalactic Database (NED), which is operated by the Jet Propulsion Laboratory, California Institute of Technology, under contract with the National Aeronautics and Space Administration. This research has made use of the NASA/ IPAC Infrared Science Archive, which is operated by the Jet Propulsion Laboratory, California Institute of Technology, under contract with the National Aeronautics and Space Administration. Keiichi Maeda acknowledges support provided by the Japan Society for the Promotion of Science (JSPS) through KAKENHI Grants JP17H02864, JP18H04585, JP18H05223, JP20H00174, and JP20H04737. Masayuki Yamanaka is supported by the Grants-in-Aid for Young Scientists of the Japan Society for the Promotion of Science (JP17K14253). Koji S. Kawabata acknowledges support provided by the Japan Society for the Promotion of Science (JSPS) through KAKENHI Grant JP18H03720. Umut Burgaz acknowledges support provided by the Turkish Scientific and Technical Research Council (TuBTAK-2211C and 2214A) Tomoki Morokuma acknowledges support provided by the Japan Society for the Promotion of Science (JSPS) through KAKENHI Grants JP16H02158 and JP18H05223.

Tissue engineering is considered highly promising for the repair of traumatic brain injury (TBI), and accumulating evidence has proved the efficacy of biomaterials and 3D printing. Although collagen is famous for its natural properties, some defects still restrict its potential applications in tissue repair. In this experimental study, we fabricated a kind of scaffold with collagen and heparin sulfate via 3D printing, which possesses favorable physical properties and suitable degradation rate along with satisfactory cytocompatibility. After implantation, the results of motor evoked potentials (MEPs) showed that the latency and amplitude can both be improved in hemiplegic limbs, and the structural integrity of the cerebral cortex and corticospinal tract can be enhanced significantly under magnetic resonance imaging (MRI) evaluation. Additionally, the results of in situ hybridization (ISH) and immunofluorescence staining also revealed the facilitating role of 3D printing collagen/heparin sulfate scaffolds on vascular and neural regeneration. Moreover, the individuals implanted with this kind of scaffold present better gait characteristics and preferable electromyography and myodynamia. In general, 3D printed collagen/heparin sulfate scaffolds have superb performance in both structural repair and functional improvement and may offer a new strategy for the repair of TBI.

Endophytes play an important role in plant growth and development. Some one can produce auxins, ACCs, iron carriers, and so on to help plants grow and resist unhealthy growth environments. In addition, they can produce certain antimicrobial substances to resist pests and diseases. Among them, Bacillus is the most common beneficial endophytic bacterium in plants. In this paper, 20 IAA-producing strains were screened from endophytic bacteria isolated from Taxus chinensis var. mairei plant tissues by high-performance liquid-chromatography (HPLC). Based on the 20 IAA-producing strains, LC-TOF-MS technology was used to screen lipopeptide-producing Bacillus sp. As a result, three strains (KLBMPTC01, KLBMPTC10, and KLBMPTC29) of Bacillus-producing lipopeptides with abundant contents and species were obtained. According to the situation of the IAA and lipopeptides produced by these strains, KLBMPTC10 was selected as the experimental strain for later toxicological tests. In an Ames test and oral toxicity experiments in mice, we did not detect mutagenicity and other physiological toxicity. This is hoping to provide a theoretical basis for forest resource protection and biofertiliser production therewith.

We demonstrate herein a facile strategy to engineer versatile catalytically active coordination interspace in the same primitive metal-organic framework (MOF) for variable heterogeneous catalysis. Different functional ligands can be reversibly inserted into and removed from proto-LIFM-28 individually or successively to bring in single or binary catalytic sites for specific reactions and switch the parent MOF to multipurpose catalysts. Alcohol-oxidation, Knoevenagel-condensation, click, acetal, and Baylis-Hillman reactions are achievable through simple exchange of a single catalytic spacer, while sequential or stepwise reactions are designable via selective combination of two catalytic spacers with different functionalities, thus making proto-LIFM-28 a multivariate MOF for multiuse and economic catalysis.

It is of significant importance to capture and separate organic pollutants from water sources to combat the growing environmental problems. Advanced sorbent materials with rapid, high-capacity and selective sorption performances are desirable. Herein, a coordination framework (LIFM-WZ-4) containing micro-channels with a large percentage (70%) of “naked” nitrogens is reported, affording donor–acceptor (D–A) interaction abilities with specific selectivity for electron-deficient CO2 gases or cationic dyes. Especially, although with a neutral network, exclusively selective, fast and large adsorption capacities for cationic dyes from aqueous solutions were achieved, with a record high value of 1492.0 mg g−1 for MB+ among the materials reported to date. The underlying adsorption mechanism was probed from both kinetic and thermodynamic considerations, revealing a pseudo-second-order kinetic model and a D–A inducing chemisorption process accounting for the unique selectivity. The saturated sorbent can then be readily recovered by dye release in CH3CN. This easy recyclability provides potential for practical applications in water sanitation and dye separation.

The effect of framework (pore) disorder on gas sorption of azole-based isoreticular Cu(II) MOFs with rtl (rutile) topology and characteristic 1D tubular pore channels is investigated for the first time., Metal–organic frameworks with highly ordered porosity have been studied extensively. In this paper, the effect of framework (pore) disorder on the gas sorption of azole-based isoreticular Cu(II) MOFs with rtl topology and characteristic 1D tubular pore channels is investigated for the first time. In contrast to other isoreticular rtl metal–organic frameworks, the Cu(II) metal–organic framework based on 5-(1H-imidazol-1-yl)isophthalate acid has a crystallographically identifiable disordered framework without open N-donor sites. The framework provides a unique example for investigating the effect of pore disorder on gas sorption that can be systematically evaluated. It exhibits remarkable temperature-dependent hysteretic CO2 sorption up to room temperature, and shows selectivity of CO2 over H2, CH4 and N2 at ambient temperature. The unique property of the framework is its disordered structure featuring distorted 1D tubular channels and DMF-guest-remediated defects. The results imply that structural disorder (defects) may play an important role in the modification of the performance of the material.

To observe the effectiveness and complications of inverted internal limiting membrane insertion through 25-G minimally invasive vitrectomy assisted with autologous blood adhesion fixation and combined with gas tamponade type-II macular hole retinal detachment in pathologic myopia. This was a retrospective study. The best-corrected visual acuity, intraocular pressure, macular hole closure, retinal reattachment, and systemic and ocular adverse events were observed. Twenty-three eyes were operated. Best-corrected visual acuity before surgery and at 3 and 6 months were 2.25 ± 0.47, 1.85 ± 0.32, and 1.32 ± 0.36 LogMAR (P

An asymmetric Rh(I)-catalyzed functionalization of the 3-C(sp3)–H bond of benzofuranones with α-diazoesters has been developed, providing a new strategy for the stereoselective 3-alkylation of benzofuranones. With low catalyst loadings (low to 0.02 mol % Rh), a number of benzofuranones bearing consecutive quaternary and tertiary stereogenic centers have been synthesized (up to 94% yield, 95:5 dr, and >99% ee). The synthetic utilities of this methodology have been demonstrated by elaborating the model product 3aa to a series of enantiopure compounds with similarities to natural products and drug candidates.

Anthocyanin accumulation specifically depends on sucrose (Suc) signaling. However, the molecular basis of this process remains unknown. In this study, in vitro pull-down assays identified ETHYLENE-INSENSITIVE3 (EIN3), a component of both sugar signaling or/and metabolism. This protein interacted with YDA, and the physiological relevance of this interaction was confirmed by in planta co-immunoprecipitation, yeast two-hybrid (Y2H) assay, and bimolecular fluorescence complementation. Ethylene insensitive3-like 1 (eil1) ein3 double-mutant seedlings, but not ein3-1 seedlings, showed anthocyanin accumulation. Furthermore, ein3-1 suppressed anthocyanin accumulation in yda-1 plants. Thus, EMB71/YDA-EIN3-EIL1 may form a sugar-mediated gene cascade integral to the regulation of anthocyanin accumulation. Moreover, the EMB71/YDA-EIN3-EIL1 gene cascade module directly targeted the promoter of Transparent Testa 8 (TT8) by direct EIN3 binding. Collectively, our data inferred a molecular model where the signaling cascade of the YDA-EIN3-TT8 appeared to target TT8 via EIN3, thereby modulating Suc signaling–mediated anthocyanin accumulation.

Traditional composting processes must be conducted with a bulking agent to ensure adequate air space for aeration. The bulking agent and composting materials are always completely mixed. A novel layered structure was introduced in sewage sludge composting, in which no bulking agent was used and bamboo charcoal was used as a separating material. Three lab-scale composting reactors (A: sawdust and sludge; B: bamboo charcoal and sludge; and C: sawdust, bamboo charcoal, and sludge) were continuously operated for 29 days. Several physicochemical parameters were investigated to evaluate the feasibility of layered composting with bamboo charcoal. The results indicated that the maximum temperatures during the thermophilic stage in treatments A, B, and C were 51.4, 50.9, and 51 °C, respectively. Layered composting with bamboo charcoal decreased the pH of the thermophilic stage from 8.98 in A to 8.75 in C, and delayed the peaks by about 120 h. The degradation rates of dissolve organic carbon (DOC) and dissolved nitrogen (DN) were 75 and 71.5% in treatment B, respectively, which were significantly higher than those of control group A (60 and 59.1%, respectively). The total NH3 emissions of treatment C (2127.8 mg) were significantly lower than those of A (2522.8 mg). Our results suggested that layered composting using bamboo charcoal as a separating material could be an alternative strategy to the traditional composting method. Moreover, layered composting combined with sawdust could effectively reduce NH3 emissions and N loss.

A new copper (II) metal-organic framework Cu-MOF based on the ligand of 5-aminoisophthalic acid (AIPA) has been synthesized. Single-crystal X-ray structural analysis confirmed the formation of this compound, namely [Cu(AIPA)·DMF]n. The crystal structure exhibits a 2D sheet, which generate a 3D framework through non-classical hydrogen bond interactions. TGA, IR and VT-PXRD have been carried out to characterize the compound's thermal stability and purity. The as-synthesized sample was activated by removal of the coordination DMF solvent to afford porous framework Cu-MOF (1) without degradation of the original crystallinity. As the model of volatile organic compounds (VOCs), formaldehyde capture studies have shown that Cu-MOF (1) exhibits a versatile behavior for toxic gas accumulation.

Radioactive cesium pollution have received considerable attention due to the increasing risks in development of the nuclear power plants in the world. Although various functional porous materials are utilized to adsorb Cs+ ions in water, Prussian blue analogues (PBAs) are an impressive class of candidates because of their super affinity of Cs+ ions. The adsorption ability of the PBAs strongly relate to the mesostructure and interstitial sites. To design a hollow PBA with large number of interstitial sites, the traditional hollowing methods are not suitable owing to the difficulty in processing the specific PBAs with large number of interstitial sites. In this work, we empolyed a rational strategy which was to form a "metal oxide"@"PBA" core-shell structure via coordination replication at first, then utilized a mild etching to remove the metal oxide core, led to hollow PBA finally. The obtained hollow PBAs were of high crystallinity and large number of interstitial sites, showing a super adsorption performance for Cs+ ions (221.6 mg/g) within a short period (10 min).

An actinomycete strain, designated KLBMP S0039T, was isolated from the rhizosphere soil of Lycium Linn., collected from the coastal region in Lianyungang, Jiangsu Province, eastern PR China, and was studied to determine its taxonomic position. The isolate showed a combination of morphological and chemotaxonomic properties typical of the members of the genus Nocardia . The cell wall contained meso-diaminopimelic acid as the diagnostic diamino acid and the whole-cell sugars were galactose, arabinose, glucose and ribose. The predominant menaquinone was identified as MK-8(H4ω-cycl). The diagnostic phospholipids were found to be diphosphatidylglycerol, phosphatidylglycerol, phosphatidylethanolamine, phosphatidylinositol and unknown lipids. The predominant cellular fatty acids were identified as C16 : 0, C18 : 0, C18 : 1ω9c, and 10-methyl C18 : 0 [tuberculostearic acid (TBSA)]. The G+C content of the genomic DNA was determined to be 68.2 mol%. The 16S rRNA gene sequence similarity indicated that KLBMP S0039T was most closely related to Nocardia neocaledoniensis NBRC 108232T (99.4 % 16S rRNA gene sequence similarity) and Nocardia asteroides NBRC 15531T (99.2 %), similarities to other type strains of species of the genus Nocardia were found to be less than 98.6 %. However, DNA–DNA relatedness values and phenotypic data indicated that KLBMP S0039T could be clearly distinguished from the closely related species of the genus Nocardia . On the basis of polyphasic taxonomic data, it is concluded that KLBMP S0039T represents a novel species of the genus Nocardia , for which the name Nocardia rhizosphaerihabitans sp. nov. is proposed. The type strain is KLBMP S0039T (=KCTC 39693T=CGMCC 4.7329T).

A metalloporphyrin Cu5-cluster based MOF (metal–organic framework), [Cu4.5((H4TZPP)(TZPP)Cl2)(H2O)0.5]·CH3NH2CH3·7EtOH·8H2O (LIFM-WZ-3) was synthesized from the tetrapodal ligand 5,10,15,20-tetrakis[4-(2,3,4,5-tetrazolyl)phenyl]porphyrin (H6TZPP) and copper chloride. LIFM-WZ-3 exhibits a rare 2D + 3D → 3D interpenetration topology, of which the frl-type 3D MOF and a layered 2D HOF (hydrogen bond organic framework) are intertwined, leading to an anionic framework with 1D spindle-like channels. Powder X-ray diffraction analysis reveals that the framework is stable in acid, base and various organic solvent environments. LIFM-WZ-3 exhibits moderately high separation performances for CO2/CH4, CO2/N2, C3H6/CH4, C2H6/CH4, and C2H4/CH4 at room temperature. Specifically, the anionic framework in LIFM-WZ-3 containing dimethylamine cations can selectively adsorb cationic organic dyes from aqueous pollutants for recycle purpose. The high adsorption capacity for methylene-blue (MB+, 983 mg g−1) and crystal violet (CV+, 713.5 mg g−1) ranks the highest among those MOFs ever reported.

2D graphitic carbon nitride (g-C3N4) has attracted great attention as one of the rising-star candidates for prominent water-splitting photocatalysts. Here, we report an extremely facile one-step, template-free method to synthesize ultrathin g-C3N4 nanosheets (CN-UMF) by thermal polycondensation of urea simply covered with kitchen-available melamine foam (MF). Compared with g-C3N4 agglomerates (CN-U) prepared without the covering of MF, the as-synthesized CN-UMF has an average thickness of about 4.5 nm and an enlarged surface area of 150.3 m2 g−1, leading to enhanced visible light absorption and charge carrier separation abilities. Therefore, it is able to serve as an efficient water-splitting photocatalyst to result in an outstanding hydrogen production rate of 5498 μmol g−1 h−1. This work provides a new facile strategy for the scalable synthesis of 2D g-C3N4 photocatalysts and paves the way for batch and green production of other 2D materials with good performance.

A LC-Q-Orbitrap HRMS analytical method for both qualitative screening and quantitative determination of 90 synthetic dyes including ten groups of isomers in foods has been established. An in-house synthetic dyes database and characteristic ions were also developed. Based on Q-Orbitrap HRMS, mass spectrum and fragmentation patterns of synthetic dyes were studied, which indicated that double charged ions were usually the main precursor ions. Matrix effects were successfully eliminated by the C18 d-SPE clean-up coupled with dilute and shoot approach with methanol–water (1:4, v/v) in 100-fold. For most of the compounds, mean recoveries were satisfactory between 70% and 120% with RSD

Euphorbia pekinensis Radixz (EPR) is a commonly used Chinese herbal medicine prepared from the dried roots of E. pekinensis Rupr. It has been revealed in chemical analysis that diterpenoids are the primary component of EPR bestowing toxicity and bioactivity; however, little is known about these bioactive and toxic diterpenoid biosynthesis pathways and diterpene diversity in E. Pekinensis. In this study, we sequenced root, stem, and leaf transcriptomes of E. pekinensis, and conducted de novo assembly using 429 million clean reads with Trinity software. Then, 157,491 unigenes were generated whose N50 contained 1826 bp. All of the unigenes were interpreted using Nt, Nr, COGs, SwissProt, GO, and KEGG databases. The expression profiling based on FPKM showed 665 genes up-regulated in roots were enrichment pathways for CYP450s and transcript factors. There are extremely diverse specialised diterpene pathways therein, and most specialised diterpenes are limited to several plant genera, species, or special tissues according to their taxonomy. Using homology, we identified 26 diterpenoid synthase candidates which comprised 25 class I proteins, and only one class II protein, in TPS-a and TPS-c sub-families, among which five class I proteins were highly expressed in root. Additionally, 23 CYP450 enzymes from sub-families of CYP71D and CYP726 were identified, and three were highly expressed in root, for which expression patterns were similar to the aforementioned five class I diTPSs expressed in root and may be involved in macroditerpenoid biosynthesis in EPR. Our results provided a beneficial genomic resource which is able to be used for future functional genomics research on E. pekinensis.

Ionic liquids (ILs) with catalysts have been widely investigated in the production of 5-hydroxymethylfurfural (5-HMF) from biomass, in particular those which are high in cellulose. In this study, a series of hydrophobic imidazolium ionic liquids and magnetic-chitosan metallo-porphyrin particles (MCMP-M) were designed and their abilities to convert 5-hydroxymethylfurfural (5-HMF) and total reducing sugars (TRS) from the corncob were evaluated. The results showed that [moMIM][PF6] and MCMP-Al were suitable solvents and both the catalysts were effective for the 5-HMF and TRS conversion (52.47 and 31.06, respectively). The mixed catalysts (MCMP-Al, Cr and Mg) coupled with [moMIM][PF6] could increase the conversion yield of 5-HMF and TRS (66.58% and 43.68% in 50 min, respectively) with infrared radiation heating during distillation under reduced pressure for a short time (50 min). More importantly, the products could be separately recovered through the aqueous phase and the ILs and catalysts could be reused up to 40 times despite the slight loss of its catalytic activity. Moreover, the catalyst system also could be used for other carbon sources to produce the 5-HMF.

A novel Gram-stain-positive, aerobic bacterium, designated strain DHS C021T, was isolated from a limestone sample collected from the Puding Karst Ecosystem Research Station of Guizhou Province, southwest China. This strain developed branched vegetative mycelia, and its aerial mycelia fragmented into rod-shaped spores. The cell-wall peptidoglycan contained meso-diaminopimelic acid and the whole-cell sugars comprised galactose, ribose and mannose. The respiratory quinone was identified as menaquinone MK-9(H4). The major cellular fatty acids were iso-C14 : 0 and iso-C16 : 0. The phospholipids detected were diphosphatidylglycerol, phosphatidylethanolamine, hydroxyl-phosphatidyethanolamine, phosphatidylinositol, phosphotidylinositolmannosides and one unidentified phospholipid. The genomic DNA G+C content was 69.8 mol% and 16S rRNA gene sequence analysis showed that the strain belonged to the genus Lentzea and shared highest sequence similarity with Lentzea albida CGMCC 4.1727T (98.8 %) and Lentzea waywayandensis CGMCC 4.1646T (98.5 %). However, it could be distinguished from these reference strains based on the low levels of DNA–DNA relatedness (54.5±2.7 and 41.7±3.2 %, respectively). On the basis of morphological, chemotaxonomic and phylogenetic characteristics, and DNA–DNA hybridization data, strain DHS C021T represents a novel species of the genus Lentzea , for which the name Lentzea pudingi sp. nov. is proposed. The type strain is DHS C021T (=CGMCC 4.7319T=KCTC 39694T).

Dye dispersion and the interaction efficiency between azoreductases and dye molecules are rate-limiting steps for the decolorization of azo dyes. In this study, a biosurfactant-producing strain, Pseudomonas taiwanensis L1011, was isolated from crude oil. To increase the yield of the biosurfactant BS-L1011 from P. taiwanensis L1011, culture conditions were optimized including temperature, initial pH, carbon source, nitrogen source and C/N ratio. A maximum yield of 1.12g/L of BS-L1011 was obtained using D-mannitol as carbon source and yeast extract/urea as compound nitrogen source with C/N ratio of 10/4, pH 7.0 and 28°C. BS-L1011 exhibited a low critical micelle concentration (CMC) of 10.5mg/L and was able to reduce the surface tension of water to 25.8±0.1 mN/m. BS-L1011 was stable over a wide range of temperatures, pH values and salt concentrations. The biosurfactant is reported for the first time to accelerate chemical decolorization of Congo red by sodium hypochlorite, and biological decolorization of Amaranth by Bacillus circulans BWL1061, thus showing a potential in the treatment of dyeing wastewater.

The co-existence of dyes, Cr(VI) and high concentration of salt in dyeing wastewater causes serious and complex environmental problems. In this study, a salt-tolerant strain Bacillus circulans BWL1061 was reported to simultaneously remove 50mg/L methyl orange and 50mg/L Cr(VI) under the anaerobic condition with 60g/L NaCl. During the decolorization process, the Cr(VI) reduction occurred preferentially over the dye decolorization due to the dominate utilization of electron by Cr(VI). The analysis of enzyme activities suggested that azoreductase, NADH-DCIP reductase, and laccase were associated with decolorization of methyl orange. A possible degradation pathway was proposed based on the metabolites analysis. The decolorization of methyl orange is involved in the symmetric cleavage of azo bond, which formed N,N-dimethyl p-phenylenediamine and 4-amino sulfonic acid, or the asymmetric cleavage of azo bond, which formed 4-(dimethylamino) phenol and 4-diazenylbenzene sulfonic acid. Phytotoxicity assays showed that strain BWL1061 could decrease the toxicity of methyl orange to Triticum aestivum, Pogostemon cablin and Isatis indigotica Fort during the decolorization process. In this study, Bacillus circulans is reported for the first time that could simultaneously remove azo dyes and Cr (VI) under high salt condition.

In higher plants, seed size is central to many aspects in evolutionary fitness and is a crucial agricultural trait. In this study, Arabidopsis an3 (angustifolia3) mutants present with increased seed size. Target-gene analysis revealed that YDA, which encodes a mitogen-activated protein kinase kinase kinase, is a target gene of AN3. Indeed, the loss of YDA function decreases seed size. Furthermore, AN3 and YDA mutations both disrupt normal sucrose and glucose contents and cause altered seed size in an3 or yda mutants. With these results, we provide a molecular model in which soluble sugar accumulation might affect seed size regulation via the AN3-YDA gene cascade. Our findings guide the synthesis of a model that predicts the integration of soluble sugar accumulation at AN3 to control the establishment of seed size.

A novel actinobacterium, designated KLBMP 5180T, was isolated from the surface-sterilized root of a coastal halophyte, Limonium sinense, collected from the city of Lianyungang, Jiangsu Province, eastern China. The isolate was Gram-stain-positive, aerobic and non-motile. The components of the cell-wall peptidoglycan were lysine, glutamic acid and alanine. The predominant menaquinone was MK-9. The polar lipids were diphosphatidylglycerol, phosphatidylglycerol, phosphatidylinositol, one unknown phospholipid, one unidentified glycolipid and two unidentified lipids. anteiso-C15 : 0 and iso-C16 : 0 were the major cellular fatty acids. The DNA G+C content of strain KLBMP 5180T was 60.0 mol%. Phylogenetic analysis based on 16S rRNA gene sequences showed that strain KLBMP 5180T belongs to the genus Glutamicibacter and was related most closely to Glutamicibacter nicotianae DSM 20123T (99.3 % similarity), Glutamicibacterarilaitensis Re117T (99.3 %) and Glutamicibacter mysorens LMG 16219T (99.1 %); similarity to other type strains of the genus Glutamicibacter was lower than 98.5 %. However, DNA–DNA relatedness values between strain KLBMP 5180T, G . nicotianae DSM 20123T, G. arilaitensis Re117T and G. mysorens LMG 16219T were 47.5±2.6, 51.3±3.1 and 41.2±4.3 %, respectively. The combination of DNA–DNA hybridization, phylogenetic, phenotypic and chemotaxonomic data supported the suggestion that strain KLBMP 5180T represents a novel species of the genus Glutamicibacter, for which the name Glutamicibacter halophytocola sp. nov. is proposed. The type strain is KLBMP 5180T (=DSM 101718T=KCTC 39692T).