X-ray structure and photoluminescence of copper(I) 2,6-bis(trifluoromethyl)benzoate

This report describes synthesis, X-ray crystallographic characterization, and photoluminescence of copper(I) 2,6-bis(trifluoromethyl)benzoate, [Cu(O₂C(2,6-CF₃)₂C₆H₃)] (1). Complex 1 has a polymeric structure comprised of axially bound dinuclear [Cu₂(O₂C(2,6-CF₃)₂C₆H₃)₂] units that is reminiscent of the well-known structure of copper(I) acetate, [Cu₂(O₂CMe)₂] (2). However, a close comparison of two analogues revealed a non-planarity of 1D chains and their orthogonal disposition in the crystal structure of 1 versus parallel alignment of planar chains in 2. Complex 1 exhibits green photoluminescence at ca. 560 nm upon UV-radiation (λ_ex = 350 nm) in the solid state.     

Catabolic pathways and cellular responses of Pseudomonas putida P8 during growth on benzoate with a proteomics approach

The catabolic pathways and cellular responses of Pseudomonas putida P8 during growth on benzoate were studied through proteomics approach. Two-dimensional gel electrophoresis (2-DE) gel profiles of P. putida cells grown on 100 and 800 mg/L benzoate were quantitatively compared using threshold criteria and statistical tools. Protein spots of interest were identified through database searching based on peptide mass fingerprints (PMFs) obtained using matrix assisted laser desorption/ionization-time of flight mass spectrometry (MALDI-TOF MS). Eight catabolic enzymes involved in both the ortho-cleavage (CatB, PcaI, and PcaF) and the meta-cleavage (DmpC, DmpD, DmpE, DmpF, and DmpG) pathways for benzoate biodegradation were identified in P. putida grown on 800 mg/L of benzoate while no meta-cleavage pathway enzymes were observed in the 2-DE gel profiles of P. putida grown on 100 mg/L of benzoate. The activation of both the ortho- and the meta-cleavage pathways in P. putida P8 grown on high benzoate concentration was confirmed directly at the protein level. In addition, another 28 differentially expressed proteins were also identified, including proteins involved in (i) detoxification and stress response (AhpC, ATPase-like ATP-binding region, putative DNA-binding stress protein, SodB and catalase/peroxidase HPI); (ii) carbohydrate, amino acid/protein and energy metabolism (isocitrate dehydrogenase, SucC, SucD, AcnB, GabD, ArcA, ArgI, Efp and periplasmic binding proteins of several ABC-transporters); and (iii) cell envelope and cell division (bacterial surface antigen family protein and MinD). Based on the data obtained, physiological changes of P. putida in response to growth on benzoate at different concentrations were discussed.     

甲维盐·毒死蜱及其复配对小菜蛾的毒力分析

以小菜蛾（Plutella xylostellar） 3龄幼虫为试虫测定了甲胺基阿维菌素苯甲酸盐、毒死蜱及两者5种不同配比的复配剂的毒力,测定结果建立了“时间-剂量-死亡率”模型.根据模型分析结果,甲胺基阿维菌素苯甲酸盐与毒死蜱混配后增效显著.在5种配比中以甲氨基阿维菌素苯甲酸盐∶毒死蜱 =1∶ 74为最佳配比,其24-60 h 4个时段的共毒系数在334到550之间;与单剂相比,该配比明显提高了24 h时段内和48-60 h时段的杀虫率.     

3.2%高效氯氰菊酯·甲氨基阿维菌素苯甲酸盐微乳剂对十字花科蔬菜主要害虫的控制作用

田间药效试验结果表明,3.2%高效氯氰菊酯·甲氨基阿维菌素苯甲酸盐微乳剂对十字花科蔬菜主要害虫甜菜夜蛾Spodoptera exigua(Hbner)、小菜蛾Plutella xylostella(L.)、菜青虫Pieris rapae(L.)和斜纹夜蛾Spodoptera litura(Fabricius)均具有优良的防治效果,并有较好的速效性和持效性。3.2%高效氯氰菊酯.甲氨基阿维菌素苯甲酸盐微乳剂20,25和30g/667m23个处理药后1d对甜菜夜蛾、小菜蛾、菜青虫和斜纹夜蛾的防治效果为60.67%～77.41%,药后3d的防治效果达81.82%～97.77%,药后7d的防治效果达83.74%～99.25%。3.2%高效氯氰菊酯.甲氨基阿维菌素苯甲酸盐微乳剂可以作为防治蔬菜主要害虫的有效药剂推广使用,推荐使用剂量为25～30g/667m2(12～14.4gai/hm2)。     

Effects of 5-Aminolevulinic Acid on Oilseed Rape Seedling Growth under Herbicide Toxicity Stress

Weeds are one of the major constraints in oilseed Brassica production. Use of effective herbicides to control weeds in the fields is one of the major objectives of agronomists. To improve weed control efficacy and minimize the application costs, complex combinations of 5-aminolevulinic acid (ALA) and a new postemergence herbicide, propyl 4-(2-(4,6-dimethoxypyrimidin-2-yloxy)benzylamino)benzoate (ZJ0273), were used to investigate their combined effects in relation to seedling growth and development of oilseed rape (Brassica napus cv. ZS 758). Brassica seeds were treated with different concentrations of ZJ0273 [100 (normal dose for rape), 200, 500, and 1000 mg/L] and ALA (0.1, 1, 10, and 50 mg/L). ALA was applied as pre- and post-treatment alone and in combination with ZJ0273. We found that ZJ0273 stress imposed negative effects on rape seedling growth. Shoot fresh weight, shoot length, and root fresh weight were inhibited significantly under ZJ0273 stress, and the rate of decline increased consistently with increased ZJ0273 concentration. Root oxidizability was also inhibited significantly under ZJ0273 stress conditions, and the higher the concentration of the herbicide ZJ0273, the lower the oxidizability. Herbicide ZJ0273 treatment produced a gradual decrease in antioxidant enzymes (peroxidase, superoxide dismutase, and ascorbate peroxidase) and an increase in peroxidation substance (malondialdehyde accumulation). The increase and decrease were consistent with the ZJ0273 dosage. Our results indicated that pre- and post-treatments with a lower dosage of ALA (1 mg/L) improved rape seedling growth and root oxidizability parameters, whereas a higher concentration of ALA (50 mg/L) depressed growth. We also found that plants treated with 1 mg/L ALA produced the highest shoot fresh weights, shoot lengths, root fresh weights, and root oxidizability when the seeds were treated with different concentrations of ZJ0273. Lower dosages of ALA improved the activities of antioxidant enzymes, whereas the highest dosage of ALA increased the accumulation of peroxidation substance. These results indicate that ALA has promotive effects in the recovery of growth and development of rape seedlings under herbicide ZJ0273 toxicity stress.     

Phenolic and other constituents of fresh water fern Salvinia molesta

Two glycosides, 6'-O-(3,4-dihydroxy benzoyl)-beta-D-glucopyranosyl ester (1), and 4-O-beta-d-glucopyranoside-3-hydroxy methyl benzoate (2), along with five known compounds methyl benzoate (3), hypogallic acid (4), caffeic acid (5), paeoniflorin (6) and pikuroside (7) were isolated for the first time from a fresh water fern Salvinia molesta D.S. Mitch. These compounds showed a potent antioxidant radical scavenging activity in a non-physiological assay. Their structures were determined by NMR spectroscopic and CID mass spectrometry techniques.     

Energetic domains and conformational analysis of human serum albumin upon co-incubation with sodium benzoate and glucose

Sodium benzoate (SB), a powerful inhibitor of microbial growth, is one of the most commonly used food preservative. Here, we determined the effects of SB on human serum albumin (HSA) structure in the presence or absence of glucose after 35?days of incubation under physiological conditions. The biochemical, biophysical, and molecular approaches including free amine content assay (TNBSA assay), fluorescence, and circular dichroism spectroscopy (CD), differential scanning calorimetry (DSC), and molecular docking and LIGPLOT studies were utilized for structural studies. The TNBSA results indicated that SB has the ability to bind Lys residues in HSA through covalent bonds. The docking and LIGPLOT studies also determined another specific site via hydrophobic interactions. The CD results showed more structural helicity for HSA incubated with SB, while HSA incubated with glucose had the least, and HSA incubated with glucose?+?SB had medium helicity. Fluorescence spectrophotometry results demonstrated partial unfolding of HSA incubated with SB in the presence or absence of glucose, while maximum partial unfolding was observed in HSA incubated with glucose. These results were confirmed by DSC and its deconvoluted thermograms. The DSC results also showed significant changes in HSA energetic structural domains due to HSA incubation with SB in the presence or absence of glucose. Together, our studies showed the formation of three different intermediates and indicate that biomolecular investigation are effective in providing new insight into safety determinations especially in health-related conditions including diabetes.     

Interference of gonadotropin-receptor interaction by synthetic estrogens.

In in vitro studies, the synthetic estrogens diethylstilbestrol and diethylstilbestrol sodium phosphate inhibited the binding of ¹²⁵I ovine lutropin to the rat ovarian receptor and ¹²⁵I ovine follitropin to the bovine testicular receptor. As the lutropin binding to receptor is affected to a greater extent, a preferential inhibitory effect may be suggested. Removal of the estrogens from the incubation medium by washing does not restore gonadotropin binding ability, indicating a strong effect. The two compounds were effective in displacing the labeled gonadotropin from the preformed receptor-hormone complex. This effect increased with time of incubation. It appears unlikely that the interference of gonadotropin-receptor interaction may be because of increased hormone and/or receptor degradation by the two compounds.