PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY
·
2025
·
IF 4
Jing Liu,Zhengjie Wang,Shuo Yin,Zhonghao Wang,Meng Wu,Jianhua Qin,Junlong Liu,Chuanwen Wang
Dermanyssus gallinae is a significant haematophagous ectoparasite of laying hens. Despite the worldwide application of beta-cypermethrin for mite control, resistance to this compound has been developed by D. gallinae . P450s, as key detoxification enzymes involved in the metabolism of exogenous and endogenous chemical substances, have not been functionally characterized in D. gallinae . Here, the role of the P450s gene (Deg-CYP-3) of D. gallinae in acaricide resistance was studied. Firstly, P450s activities of the five beta-cypermethrin resistant strains (RR) against p-nitroanisole were significantly higher than that of the susceptible strain (RS), suggesting enhanced enzymatic activities might contribute to mite beta-cypermethrin resistance. Both mRNA expression level and DNA copy number of Deg-CYP-3 were significantly higher in RR than in RS, except for DK RR strain. Moreover, recombinant Deg-CYP-3 (rCYP-3) expressed in Escherichia coli displayed high enzymatic activity against p-nitroanisole, while Qulaton-100, acetone, isoacetone, avermectin, and ivermectin were found to inhibit this activity. Immunohistochemical analysis revealed the presence of Deg-CYP-3 protein in the digestive tract and Malpighian tubules. Finally, silencing of Deg-CYP-3 via RNAi resulted in decreased enzyme activity and increased susceptibility of PG RR strain to beta-cypermethrin, confirming that Deg-CYP-3 is crucial for beta-cypermethrin detoxification. RNAi also resulted in enhanced mortality, as well as reduced oviposition and fecundity in the PG RR strain. Collectively, these findings indicate that resistance of D. gallinae to beta-cypermethrin is associated with elevated P450s protein activity and increased Deg-CYP-3 expression levels. The results provide insights into the metabolic resistance mechanisms of D. gallinae and offer scientific guidance for the management and control of mite.
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RSC Advances
·
2025
·Vol. 15
·期 42
·35109-35114
·
IF 4.6
Xiaoyan Zhang,Qisheng Zhang,Yunshu Zhao,Guiying Li,Tiying Jiang,Zhirong Suo,Shanhu Sun,Li Su
The oxygen balance (OB) of energetic materials plays a critical role in determining the efficiency and effectiveness of energy release during combustion or detonation. To enhance the OB and comprehensive properties of 3-picrylamino-1,2,4-triazole (PATO), which is a high-energy and low-sensitivity explosive, this study employed a self-assembly strategy to combine nitric acid with PATO, resulting in a novel 3-picrylamino-1,2,4-triazole-nitric acid self-assembled energetic material (PATO-N). Its structure was characterized by single crystal X-ray diffraction, and the thermal decomposition properties and impact sensitivity were measured. The detonation performances were predicted by EXPLO5 and the OB was calculated based on its molecular formula. The results indicate that the self-assembly of PATO and HNO3 effectively enhanced the explosive's OB (−67.7% to −44.6%)and promoted the completeness of the detonation reaction. PATO-N exhibits good thermal stability with an improved decomposition temperature of 315.9 °C. Its theoretical detonation velocity is 7.8 km s−1, while the detonation pressure is 25.2 Gpa. PATO-N exhibited an impact sensitivity (H50) exceeding 112.2 cm, classifying it as an insensitive energetic material.
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ADVANCED FUNCTIONAL MATERIALS
·
2021
·Vol. 31
·期 28
·2101476
·
IF 18.808
Yanlin Pan,Xiaobo Hu,Yixin Guo,Xingyu Pan,Fei Zhao,Guoen Weng,Jiahua Tao,Chunhu Zhao,Jinchun Jiang,Shaoqiang Chen,Pingxiong Yang,Junhao Chu
The vapor transport deposition of quasi-one-dimensional antimony selenosulfide (Sb 2 (S,Se) 3 ) has recently attracted increasing research interest for the inexpensive, high-throughput production of thin film photovoltaic devices. Further improvements in Sb 2 (S,Se) 3 solar cell performance urgently require the identification of processing strategies to control the orientation, however the growth mechanism of high quality absorbers is still not completely clear. Herein, a facile and general vapor transport deposition approach to precisely control the growth of large-grained dense Sb 2 (S,Se) 3 films with good crystallization and preferred orientation via the source vapor speed is utilized. It is found that defect activation energy rather than the defect concentration plays a decisive role in the Sb 2 (S,Se) 3 photovoltaic performance. Admittance spectroscopy analysis is used to obtain efficient Sb 2 (S,Se) 3 solar cells. By employing dual-source coordinations to optimize the absorber layer a power conversion efficiency of 8.17% is obtained which is the highest efficiency for Sb 2 (S,Se) 3 solar cells fabricated by vapor transport technology. This study suggests that there are other opportunities for gaining deeper a understanding of the defect physics and carrier recombination mechanisms in other highly oriented low-dimensional materials to achieve improved device performance.
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PLANT CELL AND ENVIRONMENT
·
2018
·Vol. 42
·期 4
·1352-1367
·
IF 5.415
Tingting Jing,Na Zhang,Ting Gao,Mingyue Zhao,Jieyang Jin,Yongxian Chen,Miaojing Xu,Xiaochun Wan,Wilfried Schwab,Chuankui Song
Plants emit a variety of volatiles in response to herbivore attack, and (Z)-3-hexenol and its glycosides have been shown to function as defence compounds. Although the ability to incorporate and convert (Z)-3-hexenol to glycosides is widely conserved in plants, the enzymes responsible for the glycosylation of (Z)-3-hexenol remained unknown until today. In this study, uridine-diphosphate-dependent glycosyltransferase ( UGT ) candidate genes were selected by correlation analysis and their response to airborne (Z)-3-hexenol, which has been shown to be taken up by the tea plant. The allelic proteins UGT85A53-1 and UGT85A53-2 showed the highest activity towards (Z)-3-hexenol and are distinct from UGT85A53-3, which displayed a similar catalytic efficiency for (Z)-3-hexenol and nerol. A single amino acid exchange E59D enhanced the activity towards (Z)-3-hexenol, whereas a L445M mutation reduced the catalytic activity towards all substrates tested. Transient overexpression of CsUGT85A53-1 in tobacco significantly increased the level of (Z)-3-hexenyl glucoside. The functional characterization of CsUGT85A53 as a (Z)-3-hexenol UGT not only provides the foundation for the biotechnological production of (Z)-3-hexenyl glucoside but also delivers insights for the development of novel insect pest control strategies in tea plant and might be generally applicable to other plants.
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Materials Science & Engineering C-Materials for Biological Applications
·
2020
·
IF 5.88
Zetao Wang,Ke Ma,Xianfang Jiang,Jiali Xie,Peian Cai,Fuxin Li,Ruiming Liang,Jinmin Zhao,Li Zheng
Membranes used in guided bone regeneration (GBR) are required to exhibit high mechanical strength, biocompatibility, biodegradation, osteogenic and osteoinductive potential. In our study, poly(3-hydroxybutyrate- co -4-hydroxybutyrate)(P(3HB-co-4HB))/octacalcium phosphate (OCP) (P(3HB-co-4HB)/OCP) nanofibrous membranes were fabricated by electrospinning with two different P(3HB-co-4HB) to OCP ratios (P(3HB-co-4HB):OCP = 95:5 wt% and 90:10 wt%, termed P(3HB-co-4HB)/OCP(5)and P(3HB-co-4HB)/OCP (10), respectively) for GBR. The developed P(3HB-co-4HB)/OCP nanofibrous membranes were analysed for their osteogenic and osteoinductive properties using mesenchymal stem cells (MSCs) in vitro and in a calvarial bone defect rat model. The composite P(3HB-co-4HB)/OCP nanofibrous membranes showed decreased fibre size and enhanced tensile strength compared with those of P(3HB-co-4HB) nanofibrous membranes. In the in vitro studies, the P(3HB-co-4HB)/OCP membranes facilitated cell growth and osteoblastic differentiation of MSCs and were superior to P(3HB-co-4HB) membranes. After covered on the calvarial bone defects, P(3HB-co-4HB)/OCP membranes facilitated greater neobone formation than P(3HB-co-4HB) membranes did, as the result of histological evaluation and micro-CT analysis with higher bone volume/total volume (BV/TV) ratio and bone mineral density (BMD). P(3HB-co-4HB)/OCP(10) membranes with higher OCP content showed greater stiffness and osteoinductivity than P(3HB-co-4HB)/OCP (5)membranes, demonstrating the role of OCP in the composite membranes. These results indicated that electrospun P(3HB-co-4HB)/OCP nanofibrous membranes hold promise for the clinical application of GBR.
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CARBOHYDRATE POLYMERS
·
2021
·
IF 9.381
Junwei Yao,Jingxia Liu,Heng Zhi,Hongbing Tao,Xiaobao Xie,Qingshan Shi
The primary purpose of this study was to develop an innovative chitosan (CS) modified polylactic acid (PLA) nanospheres for enhancing the bioavailability of 1, 2-benzisothiazolin-3-one (BIT). The cellular uptake efficiency was corresponded positively to the quantity of CS coated on BIT-PLA nanospheres against E. coli and S. aureus . The membrane potentials of E.coli and S. aureus treated with BIT-PLA, BIT-PLA-0.1%CS and BIT-PLA-0.5%CS were reduced with the extension of incubation time and the ratio of coated CS. The enhancement of CS modified on BIT-PLA nanospheres was reduced antioxidase activities and generated excessive reactive oxygen species . The lowest EC 50 value of the modified BIT-PLA-0.5%CS suggested that its toxicity index was around 2.95-fold and 2.11-fold that of non-modified BIT-PLA against E. coli and S. aureus , respectively. These results revealed that the CS modified BIT-PLA nanospheres had a bright prospect in antibacterial formulation delivery system and improving the bioavailability.
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JOURNAL OF MOLECULAR LIQUIDS
·
2021
·
IF 6.165
Yannan Du,Hongjun Zang,Yimo Feng,Kai Wang,Yaxin Lv,Zhipeng Liu
This paper briefs the emerging strategies for the designing of catalytic systems, which direct conversion of chitin biomass monomer N -acetyl- d -glucosamine (NAG) to 3-acetylamino-5-acetylfuran was studied systemically. Twelve catalysts were investigated, and pyrazine hydrochloride ([Pyz]Cl) ionic liquid exhibited the good performance-achieving 3A5AF with yields of 36.94% from NAG . Further adding boric acid and CaCl 2 , treating at 190 °C for 60 min, the conversion rate of NAG is 100%, and the yield of 3A5AF can be increased to 69.54% in DMA. Furthermore, functional group changes before and after the reaction have been characterized by FTIR, HPLC-MS and 13 C NMR were applied to monitor the reaction process with [Pyz]Cl as the catalyst. The reactive intermediate was clearly detected by these techniques. Accordingly, a possible reaction pathway was proposed. The results of this experiment provide a mild and efficient reaction route for the degradation of biomass, and enrich the theoretical research of quaternary amine catalysts in the conversion of biomass waste into high value-added chemicals.
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ORGANIC & BIOMOLECULAR CHEMISTRY
·
2019
·Vol. 17
·期 4
·930-938
·
IF 3.49
Yue-Wei Sun,Yue-Ming Bei,Lan-Zhi Wang
Various functional 3-acyl-1,5-benzodiazepines containing carboxyl, ester and acyl groups at the 2-position were synthesized via an efficient, sustainable and catalyst-free domino reaction. During the synthesis process, one new cycle and four new bonds (one C–C, two C–N and one CC) were constructed by the nucleophilic substitution, nucleophilic addition, dehydration and cyclization reaction by the H+ shift. Furthermore, a total of 26 examples were examined by reacting inexpensive starting materials of N,N-dimethylformamide dimethyl acetal, aromatic ketones, 1,2-phenylenediamine compounds and aldehyde derivatives. Therefore, it displayed a broad substrate scope, good functional group tolerance, high yields (77–97%) and the ease of obtaining target compounds without the involvement of toxic solvents and column chromatography, which provided a novel method for the synthesis of a wide variety of biologically relevant 1,5-benzodiazepines.
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COMBINATORIAL CHEMISTRY & HIGH THROUGHPUT SCREENING
·
2022
·Vol. 25
·期 6
·1031-1039
·
IF 1.714
Chen Genqiang,Zhu Lina,Xia Yanfei,Yang Jinming,Zhang Song,Li Yuanhao,Guo Xiaolong,Sun Di,He Jiaxuan,Tian Yuee,Liu Shengming,Jiang Jia,Che Zhiping
Background: Developing the high-efficiency and low-risk small-molecule greennematocide is the key of effective control of the nematodes. Paeonol, is a naturally occurring phenolic compound, isolated from the root bark of Paeonia suffruticosa and the whole plant of Cynanchum paniculatum.
Due to its crucial phenolic ketone skeleton, modern biological science research has indicated that paeonol has a wide range of biological activities. Methods: The structural modification of paeonol into paeonol carbonyl hydrazone derivatives is a potential approach for the development
of novel nematodes, which showed more toxicity than paeonol. However, there are no reports on the nematicidal activity of paeonol carbonyl hydrazone derivatives to control Heterodera glycines. Results: We always endeavor to discover and develop biorational natural products-based pesticidal
agents, 4 significant intermediates and 21 novel 3/5(3,5)-(di)nitro/chloropaeonol carbonyl hydrazone derivatives were prepared, and their structures well characterized by 1H NMR, HRMS, MS, and mp. Due to the steric hindrance, the substituents on the C=N double bond of
all hydrazine compounds adopted E configuration. Results of nematicidal activity revealed that, among all compounds, especially 5-nitropaeonol (5) and 3,5-dinitropaeonol (7) displayed the most potent nematicidal activity H. glycines in vivo with LC50 values of 0.0323
and 0.0367 mg/mL, respectively. Conclusion: It suggested that for the 3/5(3,5)-(di)nitro/chloropaeonol carbonyl hydrazone derivatives, a nitro group introduced at C5 position of 1 was necessary for obtaining the potent compound as nematicidal agents. These preliminary results will pave
the way for further modification of paeonol in the development of potential new nematicides.
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JOURNAL OF SOLID STATE CHEMISTRY
·
2022
·
IF 3.656
Hui Yang,Ziyu Wang,Cuixia Xu,Yuan Lin,Guoliang Liu
The first example of lanthanide borate-sulfate compound, namely, La 2 B 3 O 4 (OH) 3 (SO 4 ) 2 has been obtained through hydrothermal synthesis , which belongs to polar space group Pna 2(1) (No. 33). Its structure possesses double lanthanum sulfate layers in the ab plane in which the lanthanide ions are bridged by SO 4 tetrahedra. These layers are further cross-linked by borate chains into the final 3D framework. It is noteworthy that this compound is the first lanthanide borate-sulfate which crystalizes in polar space group and it displays second-harmonic generation (SHG) signal of about 0.1 times that of KH 2 PO 4 . The SHG coefficient of the compound is ascribed to the synergistic effect of SO 4 units and borate units. Meanwhile, distorted LaO x polyhedra also play an important role in the contribution to SHG response.
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JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY
·
2019
·Vol. 19
·期 12
·7840-7845
·
IF 1.093
Cheng Zi-Qiang,Yu Ping,Shi Hai-Quan,Liu Zhi-Min,Cheng Guang-Ling,Cheng Hong-Bo,Liang Shan
In this study, In(OH)3 nanocrystals with three morphologies including rods, cubes and spheres were synthesized through a hydrothermal method. The morphology and crystalline were manipulated by controlling the growth speed and the addition of ascorbic acid. The InVO4
nanocrystals were obtained by a process sacrificing In(OH)3 templates. The phase transformation of rods and cubes generated size-controllable products, whereas that of nanospheres formed hollow micro-spheres. InVO4 nanocrystals display a brilliant yellow emission band
with the peak at 517 nm. Intriguingly, luminescent rare-earth Eu ions with red emission could be doped into InVO4 nanocrystals during the phase transformation. Excitation and the emission spectra indicated an excitation energy transfer from the vanadate to the rare-earth ions.
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JOURNAL OF ORGANIC CHEMISTRY
·
2019
·
IF 4.745
Erbao Zhao,Feilong Zhou,Yujun Zhao
Syntheses of isoxazolidines through the carbonyl imine intermediates are currently limited to monosubstituted olefin substrates. Herein, we reported syntheses of novel bicyclic isoxazolidine-containing compounds through 1,3-dipolar cycloaddition reactions using cyclic allylic alcohols as substrates, which proved challenging in previous reports. Generally, the reaction yields range from good to high, and the reaction substrates tolerate various functional groups, including the cyclopropyl and amine groups. Mechanistic studies suggest that an allylic cation and a carbonyl imine intermediate are involved and responsible for the observed stereochemistry and diastereoselectivity.
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