ARCHIVES OF MICROBIOLOGY
·
2022
·Vol. 204
·期 3
·1-14
·
IF 2.667
Chen Sha,Ding Zhexu,Chen Jinyuan,Luo Jun,Ruan Xiaofang,Li Zongpei,Liao Fengfeng,He Jing,Li Ding
Bacterial non-enzymatic Mn(II) oxidation involving reactive oxygen species (ROS) (i.e., indirect oxidation), initially discovered from a marine alpha-proteobacterium, is believed to be of importance in controlling biogeochemical cycles. For soil-borne bacteria, however, evidence of indirect Mn(II) oxidation remains unclear. In this study, the indirect Mn(II) oxidation was evidenced in a soil-borne bacterium, Providencia sp. LLDRA6. First, with and without 50 mM of Mn(II) exposure for LLDRA6, 300 differentially expressed genes were found to be linked to Mn(II) exposure via transcriptome sequencing. Among them, an operon, responsible for phenylacetic acid catabolism, was sharply upregulated in transcription, drawing us a special attention, since its transcriptional upregulation has recently shown to be important for withstanding ROS. Next, a fluorometric probe, 2′,7′-Dichlorofluorescin diacetate (DCFDA), was used to qualitatively detect ROS from cells, showing a distinct increase in fluorescence intensities of ROS during Mn(II) exposure. Furthermore, concentrations of superoxide and hydrogen peroxide from cells were detected, respectively, with and without Mn(II) exposure, exhibiting that when Mn(II) oxidation occurred, superoxide concentration significantly increased but hydrogen peroxide concentration significantly decreased. Particularly, superoxide produced by LLDRA6 was proven to be the oxidant for Mn(II) in the formation of Mn oxides. Finally, we predicted links between phenylacetic acid metabolism pathway and ROS during Mn(II) exposure, proposing that the excessive ROS, generated in response to Mn(II) exposure, transcriptionally activate phenylacetic acid catabolism presumably by increasing concentrations of highly reactive oxepins.
研究领域:
微生物学
·
环境科学
·
生物地球化学
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DOI
PubMed
高影响因子
JOURNAL OF COORDINATION CHEMISTRY
·
2024
·
IF 2.2
Ying Zhou,Xiao-Tong Song,Hui-Chao Guan,Shu-Mei Yue
In this investigation, six new metal complexes with 2-(pyridin-2-yl)benzo[d]imidazole (bpm) were synthesized and analyzed by single-crystal X-ray diffraction (XRD), including catena-bis[(µ-2,2-bis(4-carobxyphenyl)hexafluoropropane)-(2-(pyidin-2-yl)-1H-benzimidazole)-aqua-zinc] (1), catena-[(µ-2,2-bis(4-carobxyphenyl)hexafluoropropane)-(2-(pyidin-2-yl)-1H-benzimidazole)-aqua-cadmium] (2), aqua-[2,2-bis(4-carobxyphenyl)hexafluoropropane]-bis[2-(pyridin-2-yl)-1H-benzimidazole]-manganese (3), μ-[2-nitrobenzene-1,4-dicarboxylato]-μ-[2-nitrobenzene-1,4-dicarboxylato]-bis[2-(pyridin-2-yl)-1H-benzimidazole]-di-zinc (4), catena-[bis(µ-2-nitrobenzene-1,4-dicarboxylato)-diaqua-bis(2-(pyridin-2-yl)-1H-benzimidazole)-di-cadmium] (5), aqua-[pyridine-2,6-dicarboxylato]-[2-(pyridin-2-yl)-1H-benzimidazole]-copper hydrate (6) (H2hfipbb = 2,2-bis(4-carboxyphenyl)hexafluoropropane, H2nbdc acid = Nitroterephthalic acid, and H2pda = 2,6-pyridinedicarboxylic acid). Complex 1 crystallized in a monoclinic system with space group P21/n; 2 crystallized in a monoclinic system with space group C2/c; 3 crystallized in an orthorhombic system with space group Pna21; 5 crystallized in a monoclinic system with space group P21/c; 4 and 6 crystallized in triclinic systems with space group P-1. The DNA-binding modes of the complexes were investigated by several analysis methods (e.g. viscosity analysis, circular dichroism spectroscopy, fluorescent spectroscopic analysis, as well as UV spectroscopic analysis). Complexes 1-6 bind to calf thymus DNA via an intercalative mode. The results of this study provide insights into the mechanism of DNA binding and provide a basis for rationally designing new powerful reagents for DNA detection and targeting.
研究领域:
化学
·
生物化学
·
材料科学
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产品关联
DOI
高影响因子
JOURNAL OF COORDINATION CHEMISTRY
·
2023
·
IF 1.9
Xiao-Tong Song,Ying Zhou,Gui-Bao Liu,Hui-Chao Guan,Shu-Mei Yue
By single-crystal X-ray diffraction (XRD) analysis, five complexes, catena-[(µ-2,2-bis(4-carboxyphenyl)hexafluoropropane)-(2-(pyidin-2-yl)-1,3-benzothiazole)-aqua-zinc(II)] (1), catena-[(µ-2,2-bis(4-carboxyphenyl)hexafluoropropane)-(2-(pyidin-2-yl)1,3-benzothiazole)-aqua-cadmium(II)] (2), catena-[hepta(µ-2,2-bis(4carboxyphenyl)hexafluoropropane)-diaqua-bis(2-(pyidin-2-yl)-1,3-benzothiazole)-tri-manganes(II)] (3), catena-[(µ-benzene-1,2,4,5-tetracarboxylato)-(2-(pyidin-2-yl)-1,3benzothiazole)copper(II)] (4) and catena-[(µ-3-nitrobenzene-1,2-dicarboxylato)-(2-(pyidin-2-yl)1,3-benzothiazole)-aqua-zinc(II)] (5), were characterized in this research. In these five complexes, H2hfipbb = 2,2-bis(4-carboxyphenyl)hexafluoropropane, H4btec = 1,2,4,5-benzenetetracarboxylic acid, H2NPTA = 3-nitrophthalic acid and bpt = 2-(pyridin-2-yl)benzo[d]thiazole). Complexes 1 and 2 occur in the monoclinic system with space group C2/c, 4 and 5 occur in the monoclinic system with space group P21/c, and 3 occurs in the triclinic system with space group P-1. The interaction between CT-DNA (calf thymus DNA) and those complexes was examined using UV spectroscopic analysis, fluorescent spectroscopic analysis, circular dichroism spectroscopy (CD) and viscosity analysis. This research reveals that those complexes have strong ability to interact with DNA, and they all bind to DNA in an intercalation mode, thus affecting the structure of DNA. This binding mode can arise from the interaction between the benzothiazole metal complexes and DNA. Hence, we hope to provide some scientific research bases for studying benzothiazole complexes and designing new thiazole anticancer drugs.
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DOI
高影响因子
Food Analytical Methods
·
2013
·Vol. 7
·期 2
·291-297
·
IF 1.969
Wen Shengping,Zhu Xiashi
A simple and rapid method based on dispersive liquid–liquid microextraction with room temperature ionic liquid 1,3-dibutylimidazolium hexafluorophosophate ([BBIM][PF 6 ]) coupled to flame atomic absorption spectrometry was developed for the speciation of Mn(II)/Mn(VII) in tea samples. The main factors affecting dispersive liquid–liquid microextraction were investigated in detail. Mn(II) and total manganese [Mn(II)+Mn(VII)] were quantitatively extracted after adjusting aqueous sample solution to pH 10.0 and 7.0, respectively. Mn(VII) was calculated by subtraction of Mn(II) from total manganese. Under the optimized conditions, the limits of detection (3 σ ) for Mn(II) and Mn(VII) were 0.26 and 1.86 ng/mL, and their relative standard deviations were 2.6 and 4.8 % ( n = 7, c = 25.00 ng/mL). The proposed method was validated by the determination of Mn(II) and Mn(VII) in the certified reference material [GBW(E)08513] of tea sample and different local tea samples with satisfactory results.
研究领域:
分析化学
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环境科学
✓ 已验证
产品关联
DOI
高影响因子
POLYHEDRON
·
2024
·
IF 2.4
Gao-Sheng Zhu,Yu-Meng Wei,Dan Wang,Xuan-Zu Guo,Long Li,Yan-Ying Zheng,Yi Jia,Bao-Yi Yu,Qiao-Xia Shang
Four new Zn(II)-, Cd(II)-, Mn(II)-, and Co(II) - based 1D to 2D coordination polymers (CPs) were synthesized from metal salts and 1,4-di(1-imidazol-1-yl)naphthalene (DIN) ligand via the coordination reaction under hydrothermal conditions with quantitative yields , namely, [Zn(SO 4 )(DIN)(H 2 O)] ( CP-1 ), [Cd(NO 3 ) 2 (DIN)] ( CP-2 ), [Mn(SO 4 )(DIN)(H 2 O) 3 ] ( CP-3 ), and [Co(NO 3 ) 2 (DIN) 2 (H 2 O) 4 ] ( CP-4 ). The CPs were analyzed and characterized using FT-IR, Elemental Analysis , TGA , SC-XRD, and PXRD . CP-1 was selected as a model sensor for fluorescence detection , and the sensor exhibited high quenching rates at two excitation wavelengths of λ ex = 230 and 290 nm, and at a single emission wavelength of λ em = 350 nm. At these two different excitation wavelengths, CP-1 behaved differently during the sensing of pesticides, and the highest quenching rate was achieved by the sensor for nitenpyram ( λ ex = 230 nm) and imidacloprid ( λ ex = 290 nm). Furthermore, during the sensing of vitamins, CP-1 encountered a strong quenching effect toward vitamin B2 . During the sensing processes, the inner filter effect (for nitenpyram , imidacloprid , and vitamin B2), fluorescence resonance energy transfer (for nitenpyram, imidacloprid, and vitamin B2), and photo-induced electron transfer (for vitamin B2) were the mechanisms responsible for fluorescence quenching .
研究领域:
化学
·
材料科学
·
环境科学
✓ 已验证
产品关联
DOI
高影响因子
RSC Advances
·
2015
·Vol. 5
·期 36
·28762-28768
·
IF 3.84
Yuan Su,Xiaoyu Mu,Li Qi
L-Alanine (L-Ala) derived amino acid ionic liquids (AAILs) were synthesized successfully and applied as new chiral ligands in a chiral ligand exchange capillary electrophoresis (CLE-CE) system. With Mn(II)–AAIL complexes and β-cyclodextrin (β-CD) as the dual chiral selectors, a CLE-CE system was further developed for enantioseparation of dansyl D,L-amino acids (Dns-D,L-AAs). The influence of different separation parameters in CLE-CE, including the different kinds of AAILs, pH of the running buffer, the ratio of Mn(II) to AAILs, the concentration of complexes and β-CD were investigated and the optimum buffer was obtained: 100.0 mM boric acid, 5.0 mM ammonium acetate, 2.5 mM Mn(II), 5.0 mM [1-butyl-3-methylimidazolium][L-Ala] and 5.0 mM β-CD at pH 8.3. Under the optimum conditions, twelve pairs of Dns-D,L-AAs could be baseline separated and six pairs were partly separated. Additionally, a control study between the performance of Mn(II)–L-Ala and Mn(II)–[1-butyl-3-methylimidazolium][L-Ala] complexes was conducted to prove the unique behavior of AAILs in CLE-CE. Moreover, the proposed CLE-CE method was applied in screening tyrosinase inhibitors with benzoic acid and its derivatives as the typical compounds. The results illustrated that the CDs acting synergistically with the CLE-CE system could produce better performance on enantioseparation, and the novel CLE-CE method has great application potential in enzyme analysis.
研究领域:
分析化学
·
生物化学
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产品关联
DOI
高影响因子
Biomass Conversion and Biorefinery
·
2020
·Vol. 12
·期 9
·3933-3942
·
IF 2.602
Xu Lu,Wang Aili,Li Siqiang,Zhang Liya,Pan Ruiyu,Guo Peng,Yi Ming,Liu Jie
Biomass residue cellulose-based poly-(ionic liquid)s (ILs) were in situ synthesized via activators generated by electron transfer for atom transfer radical polymerization in ionic liquid microemulsions. These biomass residues, including apple residue, citrus residue, and ginkgo leaf, were started with pretreatment and modification in ionic liquid microemulsions, and their structure and thermal stability were significantly altered before and after modification as confirmed by scanning electron microscopy and thermogravimetric analysis. Fourier-transform infrared spectroscopy and 31 P nuclear magnetic resonance spectroscopy were used to investigate the molecular structure of the biomass residue cellulose-based poly-ILs. In addition, the adsorption performance of the biomass residue cellulose-based poly-IL adsorbents for heavy metal ions, such as Cd(II), Zn(II), Cr(IV), Cu(II), Mn(II), Ni(II), and Pb(II), in water were investigated. Results show that the prepared adsorbent possesses good thermal stability and certain adsorption capacity for metal ions in water, especially for nickel ions (93.91 mg/g). The prepared adsorbent also exhibits remarkable performance in the field of biomass residue utilization and novel poly-IL adsorbents.
研究领域:
材料科学
·
环境科学
·
化学工程
✓ 已验证
产品关联
DOI
高影响因子
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