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1.
甲酸脱氢酶用于辅酶NADH再生的研究进展   总被引:8,自引:0,他引:8  
NADH依赖型氧化还原酶广泛应用于精细化学品和手性化合物的生物合成,其中辅酶NADH作为还原当量起着关键的作用,NADH的再生关系到生物氧化还原过程能否进行. 甲酸脱氢酶在辅酶NADH再生中的应用是目前代谢工程领域研究的热点之一. 本工作回顾了甲酸脱氢酶的来源和氨基酸序列、酶的理化性质和催化机理等方面的研究进展,从化学稳定性、热稳定性和成本等方面阐述了甲酸脱氢酶在辅酶再生系统中的应用,讨论了甲酸脱氢酶用于辅酶再生的代谢工程平台的发展趋势,并对研究发展方向提出了一些设想.  相似文献   

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Polydimethylsiloxane (PDMS) is hailed as one of the foundational materials for microfluidics. Though a silicone-based elastomer of many desirable properties, the emergence of microfluidic fabrication techniques, especially soft lithography, has elevated its status to an exceptional one. In this mini review, we look at the salient aspects that make PDMS so special in achieving such a coveted status in the microfluidics community. A methodical approach is followed to touch upon the application of PDMS in various aspects of microfluidics with the advantages, limitations, and some future directions. © 2020 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48958.  相似文献   

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Metal organic frameworks (MOFs) are porous crystalline materials of one-, two-, or three-dimensional networks constructed from metal ions/clusters and multidentate organic linkers via coordination bonding, which are emerging as an important group of materials for energy storage, CO2 adsorption, alkane/alkene separation, and catalysis. To introduce newcomers in chemical engineering discipline to the rapidly expanding MOF research works, this review presents a brief introduction to the currently available MOFs synthesis methods. Starting from the conventional solvothermal/hydrothermal synthesis, microwave-assisted, sonochemical, electrochemical, mechanochemical, ionothermal, drygel conversion, and microfluidic synthesis methods will be presented. Examples will be limited to those representative MOF structures that can be synthesized using common organic ligands of 1,4-benzenedicarboxylic acid (and its functionalized forms) and 1,3,5-benzenetricarboxylic acid, in conjunction with metal nodes of Zn2+, Cu2+, Cr3+, Al3+, Fe3+ and Zr4+. Synthesis of widely-investigated zeolitic imidazolate framework (ZIF) structure, ZIF-8 is also included.  相似文献   

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Poly (vinyl alcohol) (PVA) is a hydrophilic polymer with excellent biocompatibility and has been applied in various biomedical areas due to its favorable properties. PVA-based hydrogels have been recognized as promising biomaterials and suitable candidates for tissue engineering applications and can be manipulated to act various critical roles. However, due to some disadvantages (i.e., lack of cell-adhesive property), they needs further modification for desired and targeted applications. This review highlights recent progress in the design and fabrication of PVA-based hydrogels, including crosslinking and processing techniques. Finally, major challenges and future perspectives in tissue engineering are briefly discussed.  相似文献   

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Bioceramic scaffolds have a promising application in bone-tissue engineering field. However, bioceramic scaffolds exhibit low fracture toughness; hence, to overcome this problem, hierarchical bioceramic scaffold or bioceramic scaffolds coated with polymer are produced. Starting with the fundamental requirements for bioceramic scaffold, this article provides detailed information on recent developments of method to produce porous bioceramics scaffold and hierarchical bioceramic scaffold. Chemical modifications to enhance interfacial adhesion and formation of interpenetrating network structures between the bioceramic scaffold and the natural polymer layer are discussed in this article. Areas of future research are highlighted at the end of this review.  相似文献   

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Nanostructures have drawn great attentions for functional device applications. Among the various techniques developed for fabricating arrayed nanostructures of functional materials, nanostructuring technique with porous anodic aluminum oxide (AAO) membrane as templates becomes more attractive owing to the superior geometrical characteristics and low-cost preparation process. In this mini review, we summarize our recent progress about functional nanostructuring based on perfectly-ordered AAO membrane to prepare perfectly-ordered nanostructure arrays of functional materials toward constructing high-performance energy conversion and storage devices. By employing the perfectly-ordered AAO membrane as templates, arrayed nanostructures in the form of nanodot, nanorod, nanotube and nanopore have been synthesized over a large area. These as-obtained nanostructure arrays have large specific surface area, high regularity, large-scale implementation, and tunable nanoscale features. All these advanced features enable them to be of great advantage for the performance improvement of energy conversion and storage devices, including photoelectrochemical water splitting cells, supercapacitors, and batteries, etc.
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In this article, we present our research results on chemical fixation of CO2 using organobismuth compounds. We fabricated bismuth biphenoate complex, Zn-Mg-Al composite oxides, and SBA-15 or Al-SBA-15 immobilized hydroxyl ionic liquid for CO2 cycloaddition onto epoxides. The hypervalent bismuth compounds show good ability for association and dissociation with CO2. The bismuth biphenolate complexes are catalytically effective for the cycloaddition reaction. The heterogeneous catalysts, viz. Zn-Mg-Al oxides and SBA-15 or Al-SBA-15 immobilized ionic liquid, are efficient for the synthesis of cyclic carbonate from CO2 and epoxide. It is found that the presence of a trace amount of water can improve the catalytic activity of the immobilized ionic liquid.  相似文献   

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Coal combustion in thermal power plants throughout the world produces large amounts of fly ash. Disposal of fly ash is a serious threat to the environment and hence is a worldwide concern for conversion of these wastes into useful products. Synthesis of mesoporous silica materials from coal fly ash has already been proposed as an option which can be utilized as an adsorbent. Adsorption is considered to be one of the more promising technologies for capturing CO2 from flue gases. This paper reviews the recent development of solid adsorbents from industrial waste materials with special reference to fly ash for post-combustion capture of CO2.  相似文献   

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Artemisinins are proposed to act in the malaria parasite cytosol by oxidizing dihydroflavin cofactors of redox‐active flavoenzymes, and under aerobic conditions by inducing their autoxidation. Perturbation of redox homeostasis coupled with the generation of reactive oxygen species (ROS) ensues. Ascorbic acid–methylene blue (MB), N‐benzyl‐1,4‐dihydronicotinamide (BNAH)–MB, BNAH–lumiflavine, BNAH–riboflavin (RF), and NADPH–FAD–E. coli flavin reductase (Fre) systems at pH 7.4 generate leucomethylene blue (LMB) and reduced flavins that are rapidly oxidized in situ by artemisinins. These oxidations are inhibited by the 4‐aminoquinolines piperaquine (PPQ), chloroquine (CQ), and others. In contrast, the arylmethanols lumefantrine, mefloquine (MFQ), and quinine (QN) have little or no effect. Inhibition correlates with the antagonism exerted by 4‐aminoquinolines on the antimalarial activities of MB, RF, and artemisinins. Lack of inhibition correlates with the additivity/synergism between the arylmethanols and artemisinins. We propose association via π complex formation between the 4‐aminoquinolines and LMB or the dihydroflavins; this hinders hydride transfer from the reduced conjugates to the artemisinins. The arylmethanols have a decreased tendency to form π complexes, and so exert no effect. The parallel between chemical reactivity and antagonism or additivity/synergism draws attention to the mechanism of action of all drugs described herein. CQ and QN inhibit the formation of hemozoin in the parasite digestive vacuole (DV). The buildup of heme–FeIII results in an enhanced efflux from the DV into the cytosol. In addition, the lipophilic heme–FeIII complexes of CQ and QN that form in the DV are proposed to diffuse across the DV membrane. At the higher pH of the cytosol, the complexes decompose to liberate heme–FeIII. The quinoline or arylmethanol reenters the DV, and so transfers more heme–FeIII out of the DV. In this way, the 4‐aminoquinolines and arylmethanols exert antimalarial activities by enhancing heme–FeIII and thence free FeIII concentrations in the cytosol. The iron species enter into redox cycles through reduction of FeIII to FeII largely mediated by reduced flavin cofactors and likely also by NAD(P)H–Fre. Generation of ROS through oxidation of FeII by oxygen will also result. The cytotoxicities of artemisinins are thereby reinforced by the iron. Other aspects of drug action are emphasized. In the cytosol or DV, association by π complex formation between pairs of lipophilic drugs must adversely influence the pharmacokinetics of each drug. This explains the antagonism between PPQ and MFQ, for example. The basis for the antimalarial activity of RF mirrors that of MB, wherein it participates in redox cycling that involves flavoenzymes or Fre, resulting in attrition of NAD(P)H. The generation of ROS by artemisinins and ensuing Fenton chemistry accommodate the ability of artemisinins to induce membrane damage and to affect the parasite SERCA PfATP6 Ca2+ transporter. Thus, the effect exerted by artemisinins is more likely a downstream event involving ROS that will also be modulated by mutations in PfATP6. Such mutations attenuate, but cannot abrogate, antimalarial activities of artemisinins. Overall, parasite resistance to artemisinins arises through enhancement of antioxidant defense mechanisms.  相似文献   

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Bacterial adhesion to surfaces and subsequent biofilm formation are a leading cause of chronic infections and biofouling. These processes are highly sensitive to environmental factors and present a challenge to research using traditional approaches with uncontrolled surfaces. Recent advances in materials research and surface engineering have brought exciting opportunities to pattern bacterial cell clusters and to obtain synthetic biofilms with well-controlled cell density and morphology of cell clusters. In this article, we will review the recent achievements in this field and comment on the future directions.  相似文献   

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It is of importance to convert glycerol, the primary by-product from biodiesel manufacturing, to various valuable C_3 chemicals, such as acrolein via dehydration, lactic acid, 1,3-dihydroxyacetone via oxidation,and 1,3-propanediol, allyl alcohol via hydrogenolysis. As compared to petroleum-based resources, C_3 chemicals from glycerol provide a benign, sustainable and atomically economic feature. Extensive heterogeneous catalysts have been designed, prepared and tested for these transformations. In recent five years,great progress, including high yields to target products over appropriate catalysts, insight into reaction mechanism and network, has been achieved. The present review systematically covers recent research progress on sustainable C_3 chemical production from catalytic glycerol transformations. We hope that it will benefit future research on transformations of glycerol as well as other polyols.  相似文献   

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Low thermal conductivity is the key property dominating the heat insulation ability of thermal barrier coatings (TBC). Reducing the intrinsic thermal conductivity is the major topic for developing advanced TBCs. Defect engineering has attracted much attention in seeking better TBC materials since lattice defects play a crucial role in phonon scattering and thermal conductivity reduction. Oxygen vacancies and substitutions are proven to be the most effective, while the accompanying lattice distortion is also of great importance. In this paper, recent advances of reducing the thermal conductivity of potential thermal barrier coating materials by defect engineering are comprehensively reviewed. Effects of the mass and size mismatch between the defects and the host lattice are quantitatively estimated and unconventional thermal conductivity reduction caused by the lattice distortions is also discussed. Finally, challenges and potential opportunities are briefly assessed to further minimize the thermal conductivity of TBC materials in the future.  相似文献   

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In recent years, organoid technology, i.e., in vitro three-dimensional (3D) tissue culture, has attracted increasing attention in biomedical engineering. Organoids are cell complexes induced by differentiation of stem cells or organ-progenitor cells in vitro using 3D culture technology. They can replicate the key structural and functional characteristics of the target organs in vivo. With the opening up of this new field of health engineering, there is a need for engineering-system approaches to the production, control, and quantitative analysis of organoids and their microenvironment. Traditional organoid technology has limitations, including lack of physical and chemical microenvironment control, high heterogeneity, complex manual operation, imperfect nutritional supply system, and lack of feasible online analytical technology for the organoids. The introduction of microfluidic chip technology into organoids has overcome many of these limitations and greatly expanded the scope of applications. Engineering organoid microfluidic system has become an interdisciplinary field in biomedical and health engineering. In this review, we summarize the development and culture system of organoids, discuss how microfluidic technology has been used to solve the main technical challenges in organoid research and development, and point out new opportunities and prospects for applications of organoid microfluidic system in drug development and screening, food safety, precision medicine, and other biomedical and health engineering fields.  相似文献   

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As an eco-friendly, efficient, and low-cost technique, photoelectrochemical water splitting has attracted growing interest in the production of clean and sustainable hydrogen by the conversion of abundant solar energy. In the photoelectrochemical system, the photoelectrode plays a vital role in absorbing the energy of sunlight to trigger the water splitting process and the overall efficiency depends largely on the integration and design of photoelectrochemical devices. In recent years, the optimization of photoelectrodes and photoelectrochemical devices to achieve highly efficient hydrogen production has been extensively investigated. In this paper, a concise review of recent advances in the modification of nanostructured photoelectrodes and the design of photoelectrochemical devices is presented. Meanwhile, the general principles of structural and morphological factors in altering the photoelectrochemical performance of photoelectrodes are discussed. Furthermore, the performance indicators and first principles to describe the behaviors of charge carriers are analyzed, which will be of profound guiding significance to increasing the overall efficiency of the photoelectrochemical water splitting system. Finally, current challenges and prospects for an in-depth understanding of reaction mechanisms using advanced characterization technologies and potential strategies for developing novel photoelectrodes and advanced photoelectrochemical water splitting devices are demonstrated.  相似文献   

18.
The use of the electronic spreadsheet to carry out a variety of routine chemical engineering calculations in process design and project engineering is reviewed. Some possible formats for carrying out these calculations are demonstrated. The limitations and advantages of the spreadsheet are discussed with respect to a variety of its potential uses.  相似文献   

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