AMB Express
·
2019
·Vol. 9
·期 1
·1-9
·
IF 2.226
Zhao Shuxue,Hu Chunhui,Guo Lizhong,Li Kuiran,Yu Hao
A 3-hydroxypyridine degrading bacterium, designated strain DW-1, was isolated from petroleum contaminated soil in Liao River China. 16S rRNA-based phylogenetic analysis indicates that strain DW-1 belongs to genus Agrobacterium. The optimal cultivation temperature and pH for strain DW-1 with 3-hydroxypyridine were 30 °C and 8.0, respectively. Under optimal conditions, strain DW-1 could completely degrade up to 1500 mg/L of 3-hydroxypyridine in 66 h. The 3-hydroxypyridine degradation pathway of strain DW-1 was suggested by HPLC and LC–MS analysis. The first reaction of 3-hydroxypyridine degradation in strain DW-1 was α-hydroxylation so that the major metabolite 2,5-dihydroxypyridine was produced, and then 2,5-dihydroxypyridine was transformed by a Fe2+-dependent dioxygenase to form N-formylmaleamic acid. N-Formylmaleamic acid will be transformed to maleic acid and fumaric acid through maleamic acid. This is the first report of the 3-hydroxypyridine degradation pathway and the utilization of 3-hydroxypyridine by a Agrobacterium sp. It may be potentially used for the bioremediation of environments polluted with 3-hydroxypyridine.
研究领域:
微生物学
·
环境科学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
Biomass Conversion and Biorefinery
·
2021
·Vol. 13
·期 9
·8115-8121
·
IF 4.987
Ren Dezhang,Jiang Xuelei,Zhang Nahui,Duo Jia,Norinaga Koyo,Huo Zhibao
Production of pyridine derivatives from bio-based feedstocks instead of fossil fuels is a promising strategy. The development of effective heterogeneous catalysts and mild reaction systems for pyridinization of renewable biomass derivatives remains a huge challenge. In this article, a direct and environment-friendly method was reported to produce 3-hydroxypyridine from bio-based furfural in water over a Raney Fe catalyst. Raney Fe exhibited an efficient catalytic performance for activation of the aldehyde group of furfural and afforded an 18.2% yield of 3-hydroxypyridine at 120 °C with ammonia as N source. The polymerization of furfural on the catalyst in hot water was the main cause of deactivation, which was verified by the scanning electron microscope (SEM), X-ray diffraction (XRD), and N 2 adsorption and desorption analysis. A possible mechanism for this reaction was also proposed. This study provides a new way for academia and industry to realize the synthesis of nitrogen-containing chemicals from biomass and its derivatives.
研究领域:
催化化学
·
绿色化学
·
可再生资源转化
✓ 已验证
产品关联
DOI
高影响因子
Journal of Materials Chemistry C
·
2022
·Vol. 11
·期 1
·151-160
·
IF 8.067
Wentao Chen,Kuo Su,Yuqiong Huang,Keith Gregory Brooks,Sachin Kinge,Bao Zhang,Yaqing Feng,Mohammad Khaja Nazeeruddin,Yi Zhang
Tin–lead (Sn–Pb) mixed perovskite has received widespread attention due to its suitable band gap width and high optical absorption coefficients. However, the power conversion efficiency (PCE) of Sn–Pb mixed perovskite solar cells (PSCs) is still low due to the fact that Sn2+ could be easily oxidized to Sn4+ and an excessively rapid crystallization rate was observed for the Sn–Pb mixed perovskite materials. Herein, we introduced 2-amino-3-hydroxypyridine (AHPD), which contains a pyridine nitrogen and an –NH2 group in the molecule, as a bidentate anchoring additive in the FA0.7MA0.3Pb0.5Sn0.5I3 precursor solution to improve device performance. Incorporation of AHPD into the FA0.7MA0.3Pb0.5Sn0.5I3 precursor solution was found to effectively suppress the Sn2+ oxidation and thus the p-doping level defects. Furthermore, the pyridine nitrogen and the enamine-like –NH2 could retard the nucleation and crystallization rate by forming a coordinating interaction with PbI2/SnI2, forming compact large-grained films and also improving the carrier transport by passivation of the grain boundaries. Overall, compared with the control device (a PCE of 15.72%), an optimized device incorporating 2 mol% AHPD exhibited a PCE of 19.18% for narrow band gap perovskite solar cells, an increase of nearly 22%, with a high level of reproducibility.
研究领域:
材料科学
·
能源科学
✓ 已验证
产品关联
DOI
高影响因子
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
·
2023
·
IF 6.7
Yong-Jun Huang,Xiao-Lin Zhong,Yi-Peng Zang,Ming-Han Yang,Jing Lin,Wei-Min Chen
The natural prenylated chalcone isobavachalcone ( IBC ) shows good antibacterial activity against Gram-positive bacteria but is ineffective against Gram-negative bacteria, most likely due to the outer membrane barrier of Gram-negative bacteria. The Trojan horse strategy has been shown to be an effective strategy to overcome the reduction in the permeability of the outer membrane of Gram-negative bacteria. In this study, eight different 3-hydroxy-pyridin-4(1 H )-one-isobavachalcone conjugates were designed and synthesized based on the siderophore Trojan horse strategy. The conjugates exhibited 8- to 32-fold lower minimum inhibitory concentrations (MICs) and 32- to 177-fold lower half-inhibitory concentrations (IC 50 s) against Pseudomonas aeruginosa PAO1 as well as clinical multidrug-resistant (MDR) strains compared to the parent IBC under iron limitation. Further studies showed that the antibacterial activity of the conjugates was regulated by the bacterial iron uptake pathway under different iron concentration conditions . Studies on the antibacterial mechanism of conjugate 1b showed that it exerts antibacterial activity by disrupting cytoplasmic membrane integrity and inhibiting cell metabolism. Finally, conjugate 1b showed a lower cytotoxic effects on Vero cells than IBC and a positive therapeutic effect in the treatment of bacterial infections caused by Gram-negative bacteria PAO1. Overall, this work demonstrates that IBC can be delivered to Gram-negative bacteria when combined with 3-hydroxy-pyridin-4(1H)-ones as siderophores and provides a scientific basis for the development of effective antibacterial agents against Gram-negative bacteria.
研究领域:
微生物学
·
药物化学
·
感染病学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
·
2024
·
IF 6
Yong-Jun Huang,Yi-Peng Zang,Li-Jun Peng,Ming-Han Yang,Jing Lin,Wei-Min Chen
The low permeability of the outer membrane of Gram-negative bacteria is a serious obstacle to the development of new antibiotics against them. Conjugation of antibiotic with siderophore based on the “Trojan horse strategy” is a promising strategy to overcome the outer membrane obstacle. In this study, series of antibacterial agents were designed and synthesized by conjugating the 3-hydroxypyridin-4(1 H )-one based siderophores with cajaninstilbene acid ( CSA ) derivative 4 which shows good activity against Gram-positive bacteria by targeting their cell membranes but is ineffective against Gram-negative bacteria. Compared to the inactive parent compound 4 , the conjugates 45c or 45d exhibits significant improvement in activity against Gram-negative bacteria, including Escherichia coli , Klebsiella pneumoniae and especially P. aeruginosa (minimum inhibitory concentrations, MICs = 7.8–31.25 μM). The antibacterial activity of the conjugates is attributed to the CSA derivative moiety, and the action mechanism is by disruption of bacterial cell membranes. Further studies on the uptake mechanisms showed that the bacterial siderophore-dependent iron transport system was involved in the uptake of the conjugates. In addition, the conjugates 45c and 45d showed a lower cytotoxic effects in vivo and in vitro and a positive therapeutic effect in the treatment of C. elegans infected by P. aeruginosa . Overall, our work describes a new class and a promising 3-hydroxypyridin-4(1 H )-one- CSA derivative conjugates for further development as antibacterial agents against Gram-negative bacteria.
研究领域:
微生物学
·
药理学
·
传染病学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
CATALYSIS LETTERS
·
2025
·Vol. 156
·期 1
·4
·
IF 2.4
Zhang Baoyu,Cui Xuchao,Liu Peng,Lv Shuheng,Zhao Jiquan,Zhang Hong-Yu,Zhang Yuecheng
Achieving cost-effective hydrogenation of 3-hydroxypyridine to 3-hydroxypiperidine is still a challenge issue. Herein, a non-noble metal core–shell structured catalyst Ni 8.0 -Co 2.0 @SiO 2 -5.0–0.10 has been prepared for the hydrogenation of 3-hydroxypyridine with a yield of 95.0%. In this study, a membrane dispersion reactor was used to prepare the core of the catalyst, followed by a hydrolysis process to construct the SiO 2 shell. This semi-continuous method enables the efficient production of core–shell catalysts, not only overcoming the low efficiency of traditional preparation methods but also enhancing catalytic performance. Characterization results indicate that the metal cores synthesized using the membrane dispersion reactor exhibit smaller particle sizes, while the SiO 2 shell effectively prevents agglomeration of the core nanoparticles. This ensures that the catalyst simultaneously achieves a minimum particle size of 9.17 nm and a maximum specific surface area of 110.31 m 2 /g. Graphical By using membrane dispersion reactor, a large number of non-noble metal nanoparticles can be prepared quickly, and then coated with a SiO2 shell exhibits remarkable hydrogenation activity, resulting in a 97.5% selectivity and 95% yield of 3-hydroxypiperidine.
✓ 已验证
产品关联
DOI
高影响因子
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
·
2023
·
IF 6.7
Changjun Zhang,Yi Lu,Jingqi Zhang,Anjie Zang,Jinhui Ren,Zhiyuan Zheng,Miaoliang Fan,Yuanyuan Xie
Recent advances in understanding the role of iron and ROS in cell death suggest new therapeutic avenues to treat organ damage including acute kidney injury (AKI). Inhibiting ferroptosis was expected to have great potential for the treatment of this disease. Ferroptosis is characterized by iron-dependent lipid peroxidation and currently, a majority of reported ferroptosis inhibitors belong to either radical-trapping antioxidants or iron chelators . However, clinically used iron chelators such as deferoxamine and deferiprone have limited efficacy against ferroptosis (generally with EC 50 > 100 μM), despite their proven safety. Herein, we present the rational design of novel ferroptosis inhibitors by incorporating the naturally occurring cinnamic acid scaffold and the 3-hydroxypyridin-4(1 H )-one iron-chelating pharmacophore . Through ABTS ˙ + radical-scavenging assay, oxygen radical absorbance capacity (ORAC) measurement, Fe 3+ affinity evaluation, and anti-erastin-induced HT22 cell ferroptosis assays, we identified compound 9c as the most prospective ferroptosis inhibitor (ABTS ˙ + , IC 50 = 4.35 ± 0.05 μM; ORCA = 23.79 ± 0.56 TE; pFe 3+ = 18.59; EC 50 = 14.89 ± 0.08 μM, respectively). Notably, 9c dose-dependently alleviated cell death in cisplatin-induced AKI model. Our results provide insight into the development of new ferroptosis inhibitors through rational incorporation of pharmacophores from existing ferroptosis inhibitors, and compound 9c could be a promising lead compound worth further investigation.
研究领域:
药理学
·
医学
·
分子生物学
✓ 已验证
DOI
PubMed
高影响因子
BIOLOGICAL TRACE ELEMENT RESEARCH
·
2016
·Vol. 174
·期 1
·142-149
·
IF 1.798
Feng Tong,Liu Ping,Zhang Zhen,Hu Jinyu,Kong Zhengqiao
The study investigated the combined effect of 1,2-dimethyl-3-hydroxypyrid-4-one (DFP) and taurine on aluminum (Al) toxicity in cortex and blood of rats. The control group received 1 ml/kg/day saline solution for 8 weeks. Other animals were exposed to Al at a dose of 281.40 mg/kg/day orally for 4 weeks. Then, they were administered with 1 ml/kg/day saline solution, 400 mg/(kg·day) taurine, 13.82 mg/(kg·day) DFP, 27.44 mg/(kg·day) DFP, 400 mg/(kg·day) taurine +13.82 mg/(kg·day) DFP, and 400 mg/(kg·day) taurine +27.44 mg/(kg·day) DFP for 4 weeks. The changes in markers of oxidative stress, activities of antioxidant enzymes, and triphosphatase (ATPase) in the cortex and blood were determined. Administration of Al led to significant increase in the malondialdehyde (MDA) level and decrease in the activities of antioxidant enzymes, Na + K + -ATPase, Mg 2+ -ATPase, and Ca 2+ -ATPase in the cortex and blood, compared with the control group. DFP was observed to reverse alteration of these parameters except for Ca 2+ -ATPase activity. Treatment with taurine caused significant increase of GSH-Px activity and decrease of the MDA level in the cortex and serum and rise of Na + K + -ATPase in the blood. Effects of DFP combined with taurine were investigated and found to provide a more significant benefit than either drug alone. Combined intake of taurine and DFP could achieve an optimum effect of therapy for Al exposure.
研究领域:
药理学
·
毒理学
·
神经科学
✓ 已验证
DOI
PubMed
高影响因子
APPLIED AND ENVIRONMENTAL MICROBIOLOGY
·
2020
·Vol. 86
·期 19
·
IF 4.016
Haixia Wang,Xiaoyu Wang,Hao Ren,Xuejun Wang,Zhenmei Lu
3-Hydroxypyridine (3HP) is an important natural pyridine derivative. Ensifer adhaerens HP1 can utilize 3HP as its sole sources of carbon, nitrogen, and energy to grow, but the genes responsible for the degradation of 3HP remain unknown. In this study, we predicted that a gene cluster, designated 3hpd, might be responsible for the degradation of 3HP. The analysis showed that the initial hydroxylation of 3HP in E. adhaerens HP1 was catalyzed by a four-component dehydrogenase (HpdA1A2A3A4) and led to the formation of 2,5-dihydroxypyridine (2,5-DHP). In addition, the SRPBCC component in HpdA existed as a separate subunit, which is different from other SRPBCC-containing molybdohydroxylases acting on N-heterocyclic aromatic compounds. Moreover, the results demonstrated that the phosphoenolpyruvate (PEP)-utilizing protein and pyruvate-phosphate dikinase were involved in the HpdA activity, and the presence of the gene cluster 3hpd was discovered in the genomes of diverse microbial strains. Our findings provide a better understanding of the microbial degradation of pyridine derivatives in nature and indicated that further research on the origin of the discovered four-component dehydrogenase with a separate SRPBCC domain and the function of PEP-utilizing protein and pyruvate-phosphate dikinase might be of great significance.IMPORTANCE 3-Hydroxypyridine is an important building block for the synthesis of drugs, herbicides, and antibiotics. Although the microbial degradation of 3-hydroxypyridine has been studied for many years, the molecular mechanisms remain unclear. Here, we show that 3hpd is responsible for the catabolism of 3-hydroxypyridine. The 3hpd gene cluster was found to be widespread in Actinobacteria, Rubrobacteria, Thermoleophilia, and Alpha-, Beta-, and Gammaproteobacteria, and the genetic organization of the 3hpd gene clusters in these bacteria shows high diversity. Our findings provide new insight into the catabolism of 3-hydroxypyridine in bacteria.
研究领域:
微生物学
·
生物化学
·
分子生物学
·
环境科学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2024
·
IF 13.3
Jiaming Mao,Yuhui Ci,Jia Liu,Chang Li,Wenjuan Yang,Yanbin Yun,Guicheng Liu,Meng Li,Manxiang Wang
To break through the “trade-off” effect of biphasic solvents between rich-phase viscosity and CO 2 loading, we synthesized a novel ionic liquid (diethylenetriamine-3-hydroxypyridine, [DETA][3HPyr]) with multiple active sites and combined it with the organic solvent diethylene glycol monobutyl ether (DGME) and water to prepare a biphasic solvent for CO 2 absorption, the best absorption condition was optimized. The results demonstrated that after absorption, the solvent transformed from homogeneous to biphasic with highly self-concentrated absorption products in the rich phase. The volume of the rich phase accounted for only 36.3 % of the total solvent, while its viscosity decreased significantly to 28.1 mPa·s, with a high blend absorption capacity of 2.67 mol·kg −1 . The species of absorption product and absorption mechanism was investigated using 13 C NMR. The stable presence of carbamic acid in the system was confirmed, contributing to enhanced absorption capacity. Density functional theory calculations revealed that DGME stabilized carbamic acid through intermolecular hydrogen bonding interactions, and highly polar ions generated during absorption and uneven charge distribution between ions dominated the phase-change process and increased the water content in the rich phase. Thermodynamic energy barrier calculation showed that the solvent effect of DGME reduced the Gibbs free energy barriers of proton transfer and facilitated reaction progress. 3IL4D3H exhibited excellent cyclic performance with low regeneration energy consumption at 1.77 GJ·t −1 . This is the first work to revealing the intrinsic dynamics of carbamic acid formation, and provides a new perspective for the phase-change mechanism of ionic liquid-based biphasic solvent.
研究领域:
化学工程
·
环境科学
·
材料科学
✓ 已验证
产品关联
DOI
高影响因子
Journal of Environmental Chemical Engineering
·
2024
·
IF 7.4
Xiao Zhu,Shuhui Liu,Ruhui Shang,Xin Chen,Yingjie Xu,Yujun Guo,Baoping Ling
Three novel anion-functionalized proton ionic liquids (ILs) were prepared from superbase 1,5-diazabicyclic [4.3.0]non-5-nonene (DBN) and 2-hydroxypyridine (2-OP), 3-hydroxypyridine (3-OP) and 4-hydroxypyridine (4-OP). Then application of ILs in the CO 2 absorption have been investigated and the effects of temperature, pressure and humidity on the absorption properties of ILs were also studied. Experimental results demonstrated that such ionic liquids can exhibit outstanding reversibility and high CO 2 capacity at room temperature . In order to reveal the influence of position of substituents in anion on the absorption behavior, the physicochemical properties including density ( ρ ), viscosity( η ), and speed of sound ( u ) were measured at T = 298.15–328.15 K, which were used to calculate the molecular volume ( V m ), standard entropy ( S 0 ), lattice energy ( U POT ), isentropic compressibility coefficient ( κ s ) and thermal expansion coefficient ( α p ) of the pure ionic liquids at different temperatures. The results showed that [DBNH][2-OP] with O atom located in the ortho position of N atom appeared lower viscosity and larger free volumes as well as stronger alkalinity , which can endow it excellent CO 2 capture capacity of about 1.4 mol CO 2 /mol IL (about 0.3 g CO 2 /g IL) at 30 ºC. Based on quantum chemical calculation and 13 C NMR as well as FT-IR spectra, the chemical absorption mechanisms of the two active sites was proposed. These results provide important insights into effective strategies for CO 2 capture.
研究领域:
化学
·
环境科学
✓ 已验证
产品关联
DOI
高影响因子
Catalysis Science & Technology
·
2024
·
IF 4.4
Peng Zhang,Liying An,Chunqiu Zhao,Qiang Chang,Fei Wang,Chenghua Zhang,Yulei Zhu,Yong Yang,Yongwang Li
For catalytic carbonylation reactions, the high-cost catalyst recovery process is a huge challenge in industrial applications. Herein, the “honeycomb catalytic strategy” based on the structural evolution of supported cobalt catalysts successfully implements a facile and efficient catalyst recovery in the methoxycarbonylation of propylene oxide. In this strategy, cobalt species mainly exist in the form of homogeneous cobalt carbonyl species and supported cobalt nanoparticles in the reaction and product/catalyst separation stage, respectively, for reconciling catalytic efficiency and metal recovery. Our results demonstrate that catalytic behaviors of supported cobalt catalysts strongly depend on the support materials and the in situ generated cobalt carbonyls. And higher CO partial pressure and lower temperature are conducive to the conversion of metallic cobalt into cobalt carbonyls, while additional post-treatment procedures (removing CO and introducing high temperature) can recover the dissolved cobalt species in the product mixture onto the support. ICP testing proved that the optimal post-treatment process can increase the Co retention ratio of the Co/C catalyst from 45.3% to 98.9%. After four honeycomb catalytic cycles, the Co retention ratio remained at 95.2% with a slight loss of productivity. Meanwhile, for the cobalt-based catalysts with different supports and higher loadings, the post-treatment process also significantly enhanced the Co retention ratio, thereby demonstrating the effectiveness and universality of the “honeycomb catalytic strategy”.
研究领域:
化学工程
·
催化化学
✓ 已验证
产品关联
DOI
高影响因子
危险品化学品经营许可证（带存储）