Corralarenes: A Family of Conjugated Tubular Hosts.

Despite the advances in host-guest chemistry, macrocyclic hosts with deep cavities are far from abundant among the large number of wholly synthetic hosts described in the literature. Herein, we describe the design and synthesis of two new tubular hosts, namely, corral[4]arene and corral[5]arene. The former has been isolated and characterized as two conformational diastereoisomers, one is centrosymmetric and the other asymmetric. The latter, a fivefold symmetrical and flexible host, has also been investigated in detail. It is composed of five 4,4'-dimethoxybiphenyl units bridged by ethynylene linkers at their 2,2'-positions and adopts a pentagonal conformation with a tubular-shaped cavity in the presence of guests. This structure endows corral[5]arene not only with a conjugated backbone, capable of bright fluorescent emission (quantum yield, 56%), but also a deep π-electron-rich aromatic cavity with remarkable conformational flexibility. The adaptive cavity of corral[5]arene allows it to accommodate a wide range of neutral and positively charged electron-deficient guests with different molecular sizes and shapes. Binding constants between this host and these guests in three different nonpolar organic solvents lie in the range of 103 to 107 M-1. Moreover, corral[5]arene exhibits dynamic chirality on account of the axes of chirality associated with each of the five biphenyl units and displays first-order transformation as exhibited by circular dichroism in response to the addition of chiral guests. All these stereochemical features render corral[5]arene an attractive host for a variety of supramolecular and nanotechnological applications.

Stereodynamics Observed in the Reactive Collisions of Low-Energy Ar+ with Randomly Oriented O2.

Stereodynamics of the collisional reaction between mutually aligned or oriented reactants has been a striking topic of chemical dynamics for decades. However, the stereodynamic aspects are scarcely revealed for the low-energy collision with a randomly oriented target. Here in the dissociative charge-exchange reaction between randomly oriented O2 and low-energy Ar+, we, using the three-dimensional ion velocity map imaging technique, clearly observe a linear alignment and a nearly isotropic distribution of the O+ yields along the collision axis. These observations are rationalized with the Doppler kinetic models in which the O2 bond is assumed to be parallel or unparallel to the collision axis of the large impact parameter collision. The linearly aligned O+, as the predominant yield, is produced in the parallel collision, while a rotating O2+, as the intermediate in the unparallel collision, leads to the isotropic distribution of O+.

Collision-Energy Dependence of the Ion-Molecule Charge-Exchange Reaction Ar+ + CO → Ar + CO.

Ion-molecule charge-exchange reactions Ar+ + CO → Ar + CO+ at the center-of-mass collision energies of 4.40, 6.40, and 8.39 eV are investigated using ion velocity map imaging technique. Although multiple electronically excited states of CO+ are accessed, the population of CO+ at the A2Π state is predominant in the present collision-energy range. In contrast to our previous study for NO, but similar to the case of O2, the forward-scattered CO+ yields show a broader angular distribution at the higher collision energy. Typically, the Franck-Condon-region charge transfer, energy resonant charge transfer, and intimate collision are three different mechanisms in which the intimate collision experiences an intermediate complex, and this mechanism usually plays an essential role in the thermal-energy reactions. However, the present observations indicate that this mechanism, concerning the intermediate (Ar-CO)+, is still of utmost importance in a relatively high collision-energy range.

Ion momentum imaging study of the ion-molecule reaction Ar+ + O2→ Ar + O2.

Charge exchange reactions between Ar+(2P) and O2 (X3Σ) are investigated in the collision energy range of 3.40-9.24 eV within the center-of-mass coordinate, by using the ion momentum imaging technique. The internal energy of the product O2+ is enhanced gradually with the increase of collision energy, and the forward-scattered O2+ ions are distributed in the broader range of scattering angle at higher collision energies. At the low collision energy of 3.40 eV, the resonant charge transfer, similar to a photon ionization process, leads to the Franck-Condon-like vibrational state population of O2+ at the a4Πu state. At the higher collision energies, besides a4Πu and the high-lying states that are visible in the photoionization process, the O2+ products could be populated at some electronically bound states in the non-Franck-Condon region. The present observations indicate again the strong collision-energy dependences of the charge exchange reactions, but distinctly different from our previous findings for Ar+ + NO → Ar + NO+.

Cloning and characterization of a glycosyltransferase from Catharanthus roseus for glycosylation of cardiotonic steroids and phenolic compounds.

OBJECTIVES: To characterize a glycosyltransferase (UGT74AN3) from Catharanthus roseus and investigate its specificity toward cardiotonic steroids and phenolic compounds. RESULTS: UGT74AN3, a novel permissive GT from C. roseus, displayed average high conversion rate (> 90%) toward eight structurally different cardiotonic steroids. Among them, resibufogenin, digitoxigenin, and uzarigenin gave 100% yield. Based on LC-MS, 1H-NMR and 13C-NMR analysis, structure elucidation of eight glycosides was consistent with 3-O-ß-D-glucosides. We further confirmed UGT74AN3 was permissive enough to glycosylate curcumin, resveratrol, and phloretin. The cDNA sequence of UGT74AN3 contained an ORF of 1,425 nucleotides encoding 474 amino acids. UGT74AN3 performed the maximum catalytic activity at 40 °C, pH 8.0, and was divalent cation-independent. Km values of UGT74AN3 toward resibufogenin, digitoxigenin, and uzarigenin were 7.0 µM, 12.3 µM, and 17.4 µM, respectively. CONCLUSIONS: UGT74AN3, a glycosyltransferase from a noncardenolide-producing plant, displayed catalytic efficiency toward cardiotonic steroids and phenolic compounds, which would make it feasible for glycosylation of bioactive molecules.

Ion Momentum Imaging Study of the Ion-Molecule Charge Exchange Reaction of Ar+ + CO2.

Three-dimensional ion momentum imaging is developed in a combination of ion velocity map imaging technique and delay-line anode ion detection, and it is applied for the ion-molecule charge exchange reaction between Ar+ and CO2. In a center-of-mass collision energy range of 7.23-15.96 eV, CO2+ products are primarily populated at the ground state X2Πg and the single-electron excited states A2Πu, B2Σu+, and C2Σg+; the multielectron excited states of CO2+ are also found at the higher collision energies. The production efficiency profiles of CO2+ are distinctly different from the photoionization electron spectrum of CO2, implying that the charge transfer from Ar+ would be not fast as expected. The strong electron correlations in the short-lived intermediate (Ar-CO2)+ should be responsible for the CO2+ yields at the multielectron excited states.

Anammox granule as new inoculum for start-up of anaerobic sulfide oxidation (ASO) process and its reverse start-up.

The feasibility of implementing anaerobic ammonium oxidation (anammox) granules to start up high-loading anaerobic sulfide oxidation (ASO) in an upflow anaerobic sludge bed (UASB) reactor was investigated. An innovation method of the reverse start-up of anammox was also validated. Firstly, the reactor was operated to treat sulfide-rich wastewaters into which nitrite was introduced as an electron acceptor. An high-rate performance with sulfide and nitrate removal rates of 105.5 ±â€¯0.11 kg S m-3 d-1 and 28.45 ±â€¯3.40 kg N m-3 d-1, respectively, was accomplished. Sulfurovum were enriched with the increase of the substrate load and then conquered Candidatus Kuenenia to be the predominant bacteria. Excitation-emission matrix (EEM) spectroscopy showed that the intensities of fluorescence decreased and protein-like substrates were the main components associated with the process of start-up. FT-IR analysis found that the main functional groups indicator were O-H groups. Secondly, the reverse start-up of anammox (achieving 90% TN removal) was achieved immediately when the substrate changed. 16S rRNA analysis indicated the successfully enrichment of anammox bacteria (Candidatus Kuenenia). These results suggest that anammox granules can act as inoculum of high-loading ASO process and the reverse start-up provides a new perspective for the fast initiation of anammox process.

Targeting of AML1-ETO in t(8;21) leukemia by oridonin generates a tumor suppressor-like protein.

Nearly 60% of acute myeloid leukemia (AML) patients with the t(8;21)(q22;q22) translocation fail to achieve long-term disease-free survival. Our previous studies demonstrated that oridonin selectively induces apoptosis of t(8;21) leukemia cells and causes cleavage of AML1-ETO oncoprotein resulting from t(8;21), but the underlying mechanisms remain unclear. We show that oridonin interacted with glutathione and thioredoxin/thioredoxin reductase to increase intracellular reactive oxygen species, which in turn activated caspase-3 in t(8;21) cells. Moreover, oridonin bound AML1-ETO, directing the enzymatic cleavage at aspartic acid 188 via caspase-3 to generate a truncated AML1-ETO (ΔAML1-ETO) and preventing the protein from further proteolysis. ΔAML1-ETO interacted with AML1-ETO and interfered with the trans-regulatory functions of remaining AML1-ETO oncoprotein, thus acting as a tumor suppressor that mediates the anti-leukemia effect of oridonin. Furthermore, oridonin inhibited the activity of c-Kit(+) leukemia-initiating cells. Therefore, oridonin is a potential lead compound for molecular target-based therapy of leukemia.

[Genomic distribution of AML1-ETO fusion protein binding sites].

This study was purposed to characterize the genomic distribution of the binding sites for AML1-ETO fusion protein on chromosome 2, 9 and 19, and to further gain insights into the characteristics of transcriptional regulation by AML1-ETO in acute myeloid leukemia so as to provide theoretical basis for the development of targeted therapy and optimization for treatment. Chromatin immunoprecipitation (ChIP) coupled with high density tiling arrays (chip), also known as ChIP-chip, was utilized in this study. ChIP-DNA enriched by an anti-ETO antibody and total genomic DNA of Kasumi cells were hybridized to tiling arrays, tiled through chromosome 2, 9 and 19. The ChIP enriched regions were identified using a model based analytical tool (MAT). Genomic distribution of the ChIP regions was analyzed using publicly available CEAS web server. The Gene Ontology (GO) enrichment analysis was performed to excavated the biological significance. The results indicated that a total of 588 enriched regions were identified on chromosome 2, 9 and 19 by the anti-ETO antibody. A number of the identified regions were located within enhancers (48.86%) or introns (37.35%), much smaller fractions were within proximal promoters (5.96%) or exons (5.49%). Functional enrichment analysis showed that cell proliferation and signal transduction biological pathways were enriched in potential genes of AML-ETO. It is concluded that half of the AML1-ETO binding sites are located within known transcriptional regulatory regions (promoter, 5' UTR and enhancer), while almost another half were within the sequences which were not previously reported as regulatory regions. The potential target molecular network of AML1-ETO is involved in several essential biological processes.

Phytotoxicity and speciation of copper, zinc and lead during the aerobic composting of sewage sludge.

The content and speciation of heavy metals in composted sewage sludge is the main cause of negative impacts on environment and health of animal and human. An aerobic composting procedure was conducted to investigate the influences of some key parameters on phytotoxicity and speciation of Cu, Zn and Pb during sewage sludge composting. The pH value reached the optimal range for development of microorganisms, and content of organic matter (OM) and dissolved organic carbon (DOC) decreased with the composting age. The total amounts of Cu, Zn and Pb were much lower in the final compost. The results from sequential extraction procedure of heavy metals showed that composting process changed the distribution of five fractions of Cu, Zn and Pb, and reduced the total contents and sum percentages of four mobile fractions (exchangeable (EXCH), carbonate (CAR), reducible iron and manganese (FeMnOX), and organic matter bound (OMB)), indicating that the metal mobility and phytotoxicity decreased after aerobic composting. The seed germination and root growth of Pakchoi (Brassica Chinensis L.) were enhanced with composting age and reached the highest value at the end of compost. The decrease of OM and DOC was significantly correlated to changes of metal distribution and germination index (GI) of Pakchoi. Only for Cu in the compost, the GI could be predictable from the sum mobile metal fractions (EXCH+CAR+FeMnOX+OMB) (R=-0.814(*)). For Zn and Pb, R value was significantly increased by use of other components, such as pH, OM and DOC, which suggested that the transformation of heavy metal speciation and phytotoxicity of sewage sludge during an aerobic composting was rather strongly dependent on multiple components than a single element.

Nitrogen loss through lateral seepage in near-trench paddy fields.

A near-trench paddy field experiment with five urea application rates (0-360 kg N ha(-1) in 90-kg increments) was conducted on a paddy soil in the Taihu Lake Region of China to elucidate N losses through lateral seepage during three rice (Oryza sativa L.) growing seasons. The total N (Nt), NH4(+) -N, and NO3(-) -N concentrations in the lateral seepage water increased with increasing N rates. The seasonal Nt fluxes by lateral seepage varied from 6.8 to 25.6 kg N ha(-1) for urea application rates of 90 to 360 kg N ha(-1). Lateral seepage accounted for 4.7 to 6.6% of the Nt applied, implying that lateral seepage was an important pathway of N loss from near-trench paddy fields. The cumulative N loss via lateral seepage was significantly related to N fertilization rate (P = 0.05). Floodwater level was also identified as a main factor affecting N losses via lateral seepage from paddy fields, as indicated by a positive linear relationship (R2 = 0.43) between floodwater level and daily lateral flow during the flooded period (P = 0.05). Under the conditions of these experiments, a shallow floodwater depth of 50 mm, urea application rates of 90 kg N ha(-1) or less, and no rainfall within 1 wk after N application reduced N losses by lateral seepage from paddy fields.

Effects of two sludge application on fractionation and phytotoxicity of zinc and copper in soil.

The potential harm of heavy metals is a primary concern in application of sludge to the agricultural land. A pot experiment was conducted to evaluate the effect of two sludges on fractionation of Zn and Cu in soil and their phytotoxicity to pakchoi. The loamy soil was mixed with 0%, 20%, 40%, 60% and 80% (by weight) of digested sewage sludge (SS) and composted sludge (SC). The additions of the both sludges caused a significant raise in all fractions, resulting in that exchangeable (EXCH) and organic matter (OM) became predominance for Zn and organic bound Cu occupied the largest portion. There was more available amount for Zn and Cu in SS treatments than SC treatments. During the pot experiment, the concentration of Zn in EXCH, carbonate (CAR) and OM and Cu in EXCH and OM fractions decreased in all treatments, so their bioavailability reduced. Germination rate and plant biomass decreased when the addition rate was high and the best yield appeared in 20% mixtures at the harvest of pakchoi. The two sludges increased tissue contents of Zn and Cu especially in the SS treatments. Zn in pakchoi was not only in relationship to deltaEXCH and deltaCAR forms but also in deltaOM forms in the sludge-soil mixtures. Tissue content of Cu in pakchoi grown on SC-soils could not be predicted by deltaEXCH. These correlation rates between Zn and Cu accumulation in pakchoi and variation of different fractions increased with time, which might indicate that sludges represented stronger impacts on the plant in long-term land application.

Nitrogen interception in floodwater of rice field in Taihu region of China.

A field experiment located in Taihu Lake Basin of China was conducted, by application of urea or a mixture of urea with manure, to elucidate the interception of nitrogen (N) export in a typical rice field through "zero-drainage water management" combined with sound irrigation, rainfall forecasting and field drying. N concentrations in floodwater rapidly declined before the first event of field drying after three split fertilizations, and subsequently tended to return to the background level. Before the first field drying, total particulate nitrogen (TPN) was the predominant N form in floodwater of plots with no N input, dissolved inorganic nitrogen (DIN) on plots that received urea only, and dissolved organic nitrogen (DON) on plots treated with the mixture of urea and manure. Thereafter TPN became the major form. No N export was found from the rice field, but total nitrogen (TN) of 15.8 kg/hm2 was remained, mainly due to soil N sorption. The results recommended the zero-drainage water management for full-scale areas for minimizing N export.