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JOURNAL OF NATURAL PRODUCTS · 2024 · IF 3.3

Nonenzymatic Sequestering of Formaldehyde into the Antibiotic Methylene-Bridged Dimer Phaeochromycin F by Streptomyces sp. OUCMDZ-4982 as a Possible Multipronged Chemical Defense Mechanism

Weihong Wang,Jiaxu Shang,Shupeng Yin,Kunyu Xia,Rui Ma,Weiming Zhu,Peng Fu

Metabolites with high chemical reactivity serve important roles in chemical defenses of organisms. Formaldehyde, as a simple and highly reactive small molecule, can be produced by microorganisms, plants, and animals. Its toxicity is well known, but information about its other biological functions remains scarce. Here, we report that the natural product SEK34b produced by Streptomyces species can react nonenzymatically with formaldehyde in water to yield the methylene-bridged dimer phaeochromycin F. This process can eliminate the toxic substance formaldehyde produced by Staphylococcus aureus. Furthermore, there is a substantial inhibitory impact of phaeochromycin F on S. aureus. We hypothesize that these constitute an integrated system of defense and attack of Streptomyces species against competitors. Our study indicates that formaldehyde can react with vancomycin and tigecycline under mild conditions to generate the derivatives bearing an imidazolidin-4-one moiety, thereby reducing the antibacterial activity of these antibiotics. These data provide a possible chemical interaction mechanism of bacteria involving the nonenzymatic reactions of formaldehyde with highly reactive natural products.

研究领域: 微生物学 · 生物化学 · 药理学
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SENSORS AND ACTUATORS B-CHEMICAL · 2015 · IF 4.097

Dual-functional cubic cuprous oxide for non-enzymatic and oxygen-sensitive photoelectrochemical sensing of glucose

Hongbo Li,Jing Li,Daye Chen,Yanxia Qiu,Wei Wang

A novel non-enzymatic and oxygen-sensitive photoelectrochemical (PEC) sensor for glucose was first constructed based on dual-functional cubic cuprous oxide. Herein, cuprous oxide acts both as an excellent catalyst for the preoxidation of glucose and as a photocathode for the PEC non-enzymatic glucose sensing. The fabricated cuprous oxide was characterized by scanning electron microscopy, X-ray diffractometry, X-ray photoelectron spectrometry, and UV–vis spectrophotometry. Under the optimized conditions, the PEC sensing was linear in its response to the logarithm of concentration of glucose in the range of 0.0005 to 6   mmol   L −1 with a detection limit of 0.3   μmol   L −1 . The same concentration of other common species did not interfere with the detection of glucose, and the results of the PEC sensor corresponded well with those obtained by the commercially available enzymatic glucose sensor. This novel non-enzymatic and oxygen-sensitive PEC sensor exhibited good performance with its high sensitivity, good selectivity, wide linear range, low cost, and portable features. Also it provides an alternative way for improving non-enzymatic PEC sensor of glucose.

研究领域: 生物传感器 · 材料科学 · 分析化学
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EUROPEAN JOURNAL OF INORGANIC CHEMISTRY · 2023 ·Vol. 26 ·期 11 ·e202200640 · IF 2.3

An Effective Non-Enzymatic Glucose Biosensor Based on Nanostructured CuxO/Cu Electrodes Synthesized in Situ by Copper Anodization

Chen Wang,Nan Gao,Zhaoqing Gao,Ruofan Li,Yunpeng Wang,Weitao Gong

Graphical CuO/Cu glucose catalytic electrode is fabricated by copper anodization which can construct nanostructure in situ on copper substrates and regulate the chemical composition and morphology of the anodized films. The anodized CuO/Cu sample can be used as catalytic electrode directly and presents a high catalytic performance towards glucose oxidation. Potentiostatic anodization was developed to synthesize copper oxide/copper (Cu x O/Cu, x=1,2) electrode with nano structure for sensitive non-enzymatic glucose detection. At a catalytic potential of 0.55 V, the CuO/Cu electrode presented a high sensitivity of 2954.38 μA mM −1 cm −2 to glucose and a linear range of 0.1 mM to 1.3 mM. The response time is less than 3 s with addition of 0.1 mM glucose. The CuO/Cu electrode above was anodized in 1M KOH solution at −100 mV and the morphology was compact nanoparticles and sparsely dispersed nanosheets, which enlarged the surface area and provided abundant electrocatalytic active sites. Compared the sensing property of electrodes with different morphologies, it indicated that nanostructure was significant to the efficient glucose catalytic oxidation process and it could be regulated by changing the potential and electrolyte concentration during anodization.

CAS / MDL: 50-99-7 1310-73-2
研究领域: 生物化学 · 材料科学
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TALANTA · 2018 · IF 4.244

Layer-by-layer chitosan-decorated pristine graphene on screen-printed electrodes by one-step electrodeposition for non-enzymatic hydrogen peroxide sensor

Qin Zhu,Bo Liang,Yu Cai,Qingpeng Cao,Tingting Tu,Bobo Huang,Lu Fang,Xuesong Ye

Layer-by-layer chitosan-decorated pristine graphene on screen-printed electrodes was achieved by one-step electrodeposition method and an enzyme-free hydrogen peroxide electrochemical biosensor was fabricated for its application. Negatively charged pristine graphene absorbed with positively charged chitosan by electrostatic interactions was electrodeposited on the electrodes. The successful immobilization of pristine graphene was confirmed by scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS) and electrochemical characterizations. The graphene-chitosan volume ratio and cyclic voltammetry scan cycles during the electrodeposition process were optimized. The resulting hydrogen peroxide biosensors showed a 178 times improved sensitivity and exhibited two wide linear detection ranges from 20 μM to 20 mM and from 20 mM to 60 mM. The biosensors also showed a good reproducibility, stability, selectivity and could be used in real samples detection. The superior electrochemical performance of graphene-chitosan was attributed to the preservation of excellent properties of pristine graphene, and the formation of layer-by-layer structure with high surface area. The proposed strategy of direct immobilization of pristine graphene can be extended for the immobilization of other nanomaterials and biomolecules.

CAS / MDL: 872-50-4
研究领域: 材料科学 · 生物传感技术 · 电化学分析
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APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY · 2020 ·Vol. 191 ·期 4 ·1533-1544 · IF 2.277

A Sensitive Electrochemical Ascorbic Acid Sensor Using Glassy Carbon Electrode Modified by Molybdenite with Electrodeposited Methylene Blue

Zhang Yan,Wang Yue,Hasebe Yasushi,Zhang Zhiqiang,Tao Dongping

A non-enzymatic amperometric sensor using natural molybdenite (MLN) electrodeposited with methylene blue (MB) has been fabricated and characterized and its analytical performances were investigated for the determination of ascorbic acid (AA). The surface morphology of the electrode modified by electrodeposited MB was studied by use of the Advanced Mineral Identification and Characterization System (AMICS) and laser confocal high-temperature scanning microscope (LCSM). The poly(MB) and MLN immobilized sensor showed good stability, reproducibility, sensitivity, and selectivity. It exhibited a linear performance range from 3 to 1000 μM, with a lower detection limit of 0.083 μM (signal/noise = 3) and short response time (< 5 s). No obvious decrease in the current was observed after 20 days storage. The methodology reproducibility of this sensor was 2.6%. It showed good anti-interference ability for the potential interfering compounds. The poly(MB) film not only can enhance the electron-transfer rate but also increase the lifetime of the sensor. This study demonstrated the applicability of natural molybdenite for the fabrication of non-enzymatic electrochemical AA sensor.

研究领域: 分析化学 · 材料科学 · 电化学
✓ 已验证 DOI PubMed 高影响因子
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ANALYTICAL SCIENCES · 2024 ·Vol. 40 ·期 8 ·1437-1448 · IF 1.8

Construction of Pt/Ni/NiFe2O4/C nanocomposite with one dimensional hollow structure for portable glucose sensing application

Feng Chengqi,Chen Zhiyuan,Yin Haoyong,Gong Jianying,Wang Hui,Wu Shengji,Wang Ling

Designing portable electrochemical sensors combined with highly efficient glucose oxidation electrodes offers a significant opportunity for convenient glucose detection. In this report, we present the design and preparation of platinum deposited Ni/NiFe 2 O 4 /Carbon composite (Pt/Ni/NiFe 2 O 4 /C) derived from Ni/Fe metal–organic frameworks (MOFs) followed by Pt deposition. Energy-dispersive X-ray spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), and electron microscopy (EM) were utilized to analyze the crystal structure, morphology, and chemical composition of the resulting materials. The glucose sensing capabilities of the optimal Pt/Ni/NiFe 2 O 4 /C-3 were assessed using amperometry methods on a smartphone-based portable device. Acting as a nonenzymatic glucose sensor, the Pt/Ni/NiFe 2 O 4 /C-3 electrode demonstrated notable sensitivity and a low limit of detection for glucose. The portable sensor exhibits high sensitivities of 131.88 μM mM cm −2 at low glucose concentration (3–500 μM) and 29.52 μA mM cm −2 at high glucose concentration (700–4000 μM), achieving a low detection limit of 1.1 μM (S/N = 3). The sensor also demonstrates enhanced selectivity and stability for detecting glucose. Furthermore, the portable sensor exhibits a clear step-ampere response in the detection of serum samples with satisfactory recovery ranging from 99.30 to 101.32%. This suggests the significant potential of portable glucose sensing applications. Graphical abstract

研究领域: 材料科学 · 生物医学工程 · 分析化学
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FOOD CHEMISTRY · 2018 · IF 4.946

Galangin inhibits α-glucosidase activity and formation of non-enzymatic glycation products

Li Zeng,Huafang Ding,Xing Hu,Guowen Zhang,Deming Gong

Inhibition of α-glucosidase and non-enzymatic glycation is considered as an effective approach to treat type 2 diabetes. Herein, multispectroscopic techniques and molecular docking analysis were used to investigate the inhibition of galangin on α-glucosidase and non-enzymatic glycation. Galangin showed a reversible inhibition on α-glucosidase activity in a mixed-type manner through a monophasic kinetic process, and induced the fluorescence quenching and conformational changes of α-glucosidase by forming α-glucosidase-galgangin complex. Molecular docking revealed that galangin primarily interacted with the amino acid residues within the active site of α-glucosidase, which may prevent the entrance of substrate resulting in a decrease in catalytic efficiency of α-glucosidase. Moreover, galangin moderately inhibited the formation of intermediates of non-enzymatic glycation, fructosamine and α-dicarbonyl compounds and strongly inhibited the formation of advanced glycation end products.

研究领域: 生物化学 · 药理学 · 糖尿病研究
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APPLIED SURFACE SCIENCE · 2020 · IF 6.182

Cu3Pt/Cu2O nanorod array prepared by a facile method for glucose detection

Bingwang Yang,Ning Han,Liying Zhang,Shasha Yi,Zongtao Zhang,Yu Wang,Ying Zhou,Deliang Chen,Yanfeng Gao

The combination of noble metal and transition metal oxide (TMO) can effectively expand their application in electrochemistry. However, rational design and convenient fabrication of the noble metal/TMO nanoarray is rarely reported. Here, Cu 3 Pt/Cu 2 O nanorod array was constructed on copper substrate by a convenient method and used as non-enzymatic glucose detector. In the nanorod, Moreover, the glycol ligand acted as a bridge for electron transfer from Cu 2 O at surface to Cu 3 Pt and the nanorod structure of Cu 3 Pt could serve as a highway for electron transfer, hence, when the Cu 3 Pt/Cu 2 O nanorod array was used as glucose detector, it delivered enhanced linear detection range (0.005–0.1 mM, 0.1–1.5 mM and 1.5–10 mM), high corresponding sensitivity (5082 μA mM −1 cm −2 , 3331 μA mM −1 cm −2 and 118 μA mM −1 cm −2 ), fast response time (<6 s), low detection limit (1.759 μM, S/N = 3) and high selectivity.

研究领域: 材料科学 · 电化学 · 生物传感
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JOURNAL OF ALLOYS AND COMPOUNDS · 2025 · IF 6.3

1D/2D SnO2/rGO composites-modified GCE for highly sensitive nonenzymatic electrochemical determination of chloramphenicol

Yongkang Li,Feitong Ren,Jiayin Li,Yao Chen,Jun Liu,Chun Yang

Chloramphenicol (CAP) has demonstrated favorable therapeutic effects against various bacteria and is widely utilized in the aquaculture industry. However, CAP has recently been classified as a carcinogen, emphasizing the importance of developing effective methods to monitor its concentration. In this study, one-dimensional/two-dimensional (1D/2D) SnO 2 /reduced graphene oxide (rGO) composites were employed to modify a glassy carbon electrode (GCE) for the electrochemical detection of CAP. The SnO 2 /rGO composite materials were synthesized via a solution reaction and calcination method. Optimal electrochemical sensing conditions, including pH values, scan rates, and accumulation parameters, were systematically investigated to demonstrate feasibility. The resulting SnO 2 /rGO/GCE achieved a current density of 154.56   µA/cm², up to 75 times higher than other modified electrodes. Furthermore, the SnO 2 /rGO/GCE exhibited a strong linear relationship within a detection range of 0.001–100   μM and an excellent limit of detection of 0.315   nM for CAP. Finally, the electrodes with optimized modifications were successfully applied to determine CAP concentrations in real lake water and milk samples. These promising results suggest that the as-fabricated SnO 2 /rGO electrode presents a novel and highly effective approach for CAP detection.

CAS / MDL: 12167-74-7
研究领域: 分析化学 · 环境科学 · 食品科学
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MICROCHIMICA ACTA · 2012 ·Vol. 177 ·期 3 ·485-490 · IF 3.033

Facile one-step electrochemical fabrication of a non-enzymatic glucose-selective glassy carbon electrode modified with copper nanoparticles and graphene

Luo Jing,Zhang Hongyan,Jiang Sisi,Jiang Jinqiang,Liu Xiaoya

We have developed a non-enzymatic glucose sensor by using a composite prepared from copper nanoparticles (CuNPs) and graphene which can be prepared by simple 1-step electrochemical reduction using graphene oxide (GO) and copper ion as the starting materials. The GO is electrochemically reduced to graphene at a voltage of −1.5 V, and this is accompanied by the simultaneous formation of CuNPs on the surface of the graphene. This novel nanocomposite combines the advantages of graphene and of CuNPs and displays good electrocatalytic activity toward glucose in alkaline media. The performance of the respective glucose electrode was evaluated by amperometric experiments and revealed a fast response (<2 s), a low detection limit (200 nM), and high sensitivity (607 μA mM −1 ). The sensor also exhibits good reproducibility and very good specificity for glucose over ascorbic acid, dopamine, uric acid, fructose, lactose and sucrose. (A) CVs of Cu NPs/graphene electrode (a), graphene electrode (b),and Cu/GC electrode (c) in 0.1 M NaOH solution with 0.5 mM glucose; (B) The response of the Cu NPs/graphene electrode to successive addition of glucose from 5 μM to 0.2 mM.

研究领域: 生物化学 · 材料科学 · 分析化学
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JOURNAL OF THE ELECTROCHEMICAL SOCIETY · 2014 ·Vol. 162 ·期 1 ·B36 · IF 2.859

Highly-Sensitive Electrochemical Sensor for Glucose based on the Ordered Macroporous Polycysteine/Cu Film

Jinshou Wang,Zhen Shi,Jing Jin,Yuanbin Tan,Shenghui Zhang

A novel ordered macroporous polycysteine/Cu composite film (DOM PCE/Cu) was successfully prepared by electrochemical deposition method using polystyrene spheres as templates on a bare glassy carbon electrode (GCE). The structure and electrochemical properties of DOM PCE/Cu film were characterized. The DOM PCE/Cu composite film modified electrode exhibits good electrochemical catalytic activity toward the oxidation of glucose, which may be related to the structure of DOM PCE/Cu film. The non-enzymatic glucose sensor has a wide linear range from 2 μM to 2.9 mM, with a low detection limit of 0.8 μM. The modified electrode also has highly sensitive and fast amperometric (within 3 s) sensing of glucose, thus it can be used for the future development of non-enzymatic glucose sensor.

研究领域: 生物化学 · 分析化学 · 材料科学
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APPLIED SURFACE SCIENCE · 2020 · IF 6.182

Hierarchical α-Fe2O3 microcubes supported on Ni foam as non-enzymatic glucose sensor

Yuejia Liu,Wenqiang Zhao,Xianliang Li,Jiaqiang Liu,Yide Han,Junbiao Wu,Xia Zhang,Yan Xu

Hierarchical α-Fe 2 O 3 microcubes supported on Ni foam (NF) have been successfully prepared using Fe-MOF as a precursor combined with a hydrolysis process, which can be used as the electrodes directly for effective non-enzymatic glucose sensing. The structures and compositions of the as-prepared α-Fe 2 O 3 /NF electrode materials were carefully characterized by scanning electron microscopy (SEM), X-ray powder diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and energy dispersive spectroscopy (EDS), respectively. The α-Fe 2 O 3 /NF electrodes exhibit excellent glucose oxidation performance with a response time < 3 s and a sensitivity of 10,356 μA mM −1 cm −2 . Additionally, the material shows good anti-interference sensing performance and stability for glucose detection in the presence of ascorbic acid (AA), dopamine (DA), cysteine (Cys), uric acid (UA), NaCl and other interferences. It is believed that α-Fe 2 O 3 /NF composite can act as a promising electrode material for non-enzymatic glucose sensing applications, and the materials design strategy can be also expanded for other functional systems.

研究领域: 材料科学 · 电化学 · 生物传感
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