Academic literature on the topic 'Enzyme artificiel'

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Journal articles on the topic "Enzyme artificiel"

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Dong, ZeYuan, JunYan Zhu, Quan Luo, and JunQiu Liu. "Understanding enzyme catalysis by means of supramolecular artificial enzymes." Science China Chemistry 56, no. 8 (2013): 1067–74. http://dx.doi.org/10.1007/s11426-013-4871-3.

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Wei, Hui, and Erkang Wang. "Nanomaterials with enzyme-like characteristics (nanozymes): next-generation artificial enzymes." Chemical Society Reviews 42, no. 14 (2013): 6060. http://dx.doi.org/10.1039/c3cs35486e.

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Mariz, Beatriz de Pina, Sara Carvalho, Iris L. Batalha, and Ana Sofia Pina. "Artificial enzymes bringing together computational design and directed evolution." Organic & Biomolecular Chemistry 19, no. 9 (2021): 1915–25. http://dx.doi.org/10.1039/d0ob02143a.

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Wu, Jiangjiexing, Xiaoyu Wang, Quan Wang, et al. "Nanomaterials with enzyme-like characteristics (nanozymes): next-generation artificial enzymes (II)." Chemical Society Reviews 48, no. 4 (2019): 1004–76. http://dx.doi.org/10.1039/c8cs00457a.

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Mirts, Evan N., Igor D. Petrik, Parisa Hosseinzadeh, Mark J. Nilges, and Yi Lu. "A designed heme-[4Fe-4S] metalloenzyme catalyzes sulfite reduction like the native enzyme." Science 361, no. 6407 (2018): 1098–101. http://dx.doi.org/10.1126/science.aat8474.

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Multielectron redox reactions often require multicofactor metalloenzymes to facilitate coupled electron and proton movement, but it is challenging to design artificial enzymes to catalyze these important reactions, owing to their structural and functional complexity. We report a designed heteronuclear heme-[4Fe-4S] cofactor in cytochromecperoxidase as a structural and functional model of the enzyme sulfite reductase. The initial model exhibits spectroscopic and ligand-binding properties of the native enzyme, and sulfite reduction activity was improved—through rational tuning of the secondary s
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Culp, Mary. "How to Construct an Artificial Stomach." American Biology Teacher 72, no. 7 (2010): 444–46. http://dx.doi.org/10.1525/abt.2010.72.7.10.

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Chemical digestion, the decomposition of macromolecules by the action of enzymes, begins in the mouth and stomach but occurs primarily in the small intestine. This exercise shows how to construct a simulated stomach and duodenum using common laboratory equipment and chemicals. The lab clearly demonstrates the effect of a gastric enzyme, pepsin, on proteins while leaving other food substances intact.
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Xiang, Heng-Fang, Jia-Kun Xu, Jiao Liu, et al. "Efficient biodegradation of malachite green by an artificial enzyme designed in myoglobin." RSC Advances 11, no. 26 (2021): 16090–95. http://dx.doi.org/10.1039/d1ra02202d.

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Wei, Hui, and Erkang Wang. "ChemInform Abstract: Nanomaterials with Enzyme-Like Characteristics (Nanozymes): Next-Generation Artificial Enzymes." ChemInform 44, no. 38 (2013): no. http://dx.doi.org/10.1002/chin.201338273.

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Frushicheva, Maria P., and Arieh Warshel. "Computational Enzyme Design: Refining Artificial Enzymes and Exploring Paths of Directed Evolution." Biophysical Journal 100, no. 3 (2011): 219a. http://dx.doi.org/10.1016/j.bpj.2010.12.1407.

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Gutte, B., and S. Klauser. "Design of catalytic polypeptides and proteins." Protein Engineering, Design and Selection 31, no. 12 (2018): 457–70. http://dx.doi.org/10.1093/protein/gzz009.

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Abstract The first part of this review article lists examples of complete, empirical de novo design that made important contributions to the development of the field and initiated challenging projects. The second part of this article deals with computational design of novel enzymes in native protein scaffolds; active designs were refined through random and site-directed mutagenesis producing artificial enzymes with nearly native enzyme- like activities against a number of non-natural substrates. Combining aspects of de novo design and biological evolution of nature’s enzymes has started and wi
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Dissertations / Theses on the topic "Enzyme artificiel"

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Puzio, Kinga. "Towards controlled release of Vanillin and bio-sensing of Adenosine monophosphate using molecularly imprinted polymers." Thesis, Orléans, 2012. http://www.theses.fr/2012ORLE2075.

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Ce mémoire présente une exploration des polymères à empreintes moléculaires (MIP) comme outils d’une libération contrôlée de bioactifs olfactifs ou pour le criblage/préselection de composés à activité antivirales ou anti-tumorales sur le site actif d’une enzyme. La première partie est une étude de la complexation de la vanilline sur des billes polymériques sphériques en vue d’une libération contrôlée (pH, salinité, …). Ces études portent sur les caractéristiques de l'absorption et la libération de la molécule d'intérêt dans le milieu aqueux sur les microsphères fonctionnalisées fourni par Merc
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Obrecht, Lorenz. "Artificial metalloenzymes in catalysis." Thesis, University of St Andrews, 2015. http://hdl.handle.net/10023/7248.

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This thesis describes the synthesis, characterisation and application of artificial metalloenzymes as catalysts. The focus was on two mutants of SCP-2L (SCP-2L A100C and SCP-2L V83C) both of which possess a hydrophobic tunnel in which apolar substrates can accumulate. The crystal structure of SCP-2L A100C was determined and discussed with a special emphasis on its hydrophobic tunnel. The SCP-2L mutants were covalently modified at their unique cysteine with two different N-ligands (phenanthroline or dipicolylamine based) or three different phosphine ligands (all based on triphenylphosphine) in
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Müller, Roger. "Artificial enzymes: from catalytic antibodies toward de novo enzyme design /." Zürich : ETH, 2008. http://e-collection.ethbib.ethz.ch/show?type=diss&nr=17897.

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Alonso, Cotchico Lur. "Computational design of artificial metalloenzymes." Doctoral thesis, Universitat Autònoma de Barcelona, 2018. http://hdl.handle.net/10803/664006.

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El diseño enzimático es el área basada en el descubrimiento y/o optimización de biomoléculas para el desarrollo de reacciones químicas no naturales. Es un área que se encuentra en su mayor crecimiento y constituye uno de los puntos clave en la transición de la química hacia alternativas más ecológicas. Una manera elegante de sintetizar nuevos biocatalizadores es mediante la inclusión de cofactores organometálicos en estructuras biológicas, dando lugar a lo que se conoce como Metaloenzimas Artificiales (ArMs). Estos híbridos combinan la versatilidad catalítica de los compuestos organometálicos
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Banaszczyk, Mariusz G. "Artificial hydrolytic enzymes." Thesis, McGill University, 1989. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=74289.

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The efficiencies of many rigidly held cis-aquahydroxotetraazacobalt(III) complexes in promoting the hydrolysis of phosphate esters (BDNPP, BNPP, NPP) have been compared. The phosphate diester bond in ((trpn)Co(OH)(BNPP)) $ sp{+}$ is hydrolyzed at about the same rate as BNPP bound to a real enzyme from Enterobacter aerogenes and about 10$ sp{10}$ times more rapidly than free BNPP. The dramatic increase in the activity of the Co(III) complex with change in the tetraamine ligand structure can be explained in terms of a detailed mechanism of the reaction.<br>Co(III) complexes, ((tren)Co(OH$ sb2)$(
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Smiljanic, E. "Some studies of artificial enzyme systems." Thesis, University College London (University of London), 2006. http://discovery.ucl.ac.uk/1445100/.

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This thesis describes a novel approach to the rational design of artificial esterases and aldolases. The Introduction provides a literature summary of the previous approaches that have been employed towards the design and synthesis of artificial enzyme systems. Chapter 2 describes the preparation and reactivity of a number of polymer based artificial enzymes, which are capable of catalysing ester hydrolysis. The study has involved the incorporation of a histidine catalytic group together with specifically designed peptide binding groups within a polymeric backbone. The binding groups were spec
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Muroni, Maurizio. "Rational design of artificial enzymes." Thesis, Cardiff University, 2011. http://orca.cf.ac.uk/55043/.

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Despite the endeavours of many decades, the design of artificial enzymes remains challenging. The work presented here investigates two known molecules as scaffolds for the design of artificial enzymes an 18 amino acids a helical peptide with two disulfide bridges - 'Apoxaldie' able to catalyse the decarboxylation of oxaloacetate, and the 86-amino acid colicin E9 immunity protein (Im9) with four a helices. Apoxaldie was modified such that the active site lysines were substituted by 2,4-diaminobutyric acid in order to increase the proximity of the enzyme active site to the chiral environment of
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Whetton, Stephen. "Novel imprinted polymers as artificial enzymes." Thesis, Aston University, 2001. http://publications.aston.ac.uk/9644/.

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Derivatives of L-histidine were investigated as suitable models for the Asp-His couple found in the catalytic triad of serine proteases. A combination of molecular dynamics and IH NMR spectroscopy suggested that the most populous conformations of N-acetyl-L-histidine and the N-acetyl-L-histidine anion were predominated by those in which the carboxylate group was gauche to the imidazole ring overcoming steric and electrostatic repulsion, suggesting there is an interaction between the carboxylate group and the imidazole ring. Kinetic studies, using imidazole, N-acetyl-L-histidine and the N-acety
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Ghach, Wissam. "Activité biologique et électrochimie de protéines membranes, de bactéries et de bactériophages dans un matériau sol-gel hybride." Thesis, Université de Lorraine, 2013. http://www.theses.fr/2013LORR0189/document.

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Le travail décrit dans cette thèse a été mené à l'interface entre trois disciplines: l'électrochimie, la science des matériaux et la microbiologie. L'objectif de cette recherche était tout d'abord d'étudier l'activité de bactéries immobilisées dans un film de silice déposé par le procédé sol-gel à la surface d'électrodes. Les applications potentielles de ce travail fondamental sont les biocapteurs, les bioréacteurs ou biopiles. L'encapsulation bactérienne assistée par électrochimie a été développée en utilisant l'électrolyse du sol de départ pour immobiliser la bactérie Escherichia Coli dans u
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Chevalier, Yoan. "Développement de flavo-enzymes artificielles pour la chimie radicalaire et l’activation du dioxygène dans l’eau." Thesis, université Paris-Saclay, 2020. http://www.theses.fr/2020UPASS061.

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Le sujet vise à développer des systèmes artificiels bio-inspirés capables de catalyser d'importantes réactions organiques dans l'eau, dans des conditions douces et en utilisant des réactifs inoffensifs tels que O2. Pour cela, nous envisageons de mimer les deux activités principales des flavoenzymes, qui sont capables de catalyser soit des réductions, en délivrant un flux monoélectronique à un partenaire biologique, soit des réactions d'oxydations, par activation réductrice du dioxygène, et ceci avec le même cofacteur flavinique, mais localisé dans différents échafaudages protéiques. Ce projet
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Books on the topic "Enzyme artificiel"

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Wang, Xiaoyu, Wenjing Guo, Yihui Hu, Jiangjiexing Wu, and Hui Wei. Nanozymes: Next Wave of Artificial Enzymes. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-53068-9.

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Breslow, Ronald. Artificial Enzymes. Wiley-VCH, 2005.

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Ronald, Breslow, ed. Artificial enzymes. Wiley-VCH, 2005.

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Breslow, Ronald. Artificial Enzymes. Wiley & Sons, Incorporated, John, 2006.

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Breslow, Ronald. Artificial Enzymes. Wiley-VCH Verlag GmbH, 2006.

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Breslow, Ronald, ed. Artificial Enzymes. Wiley, 2005. http://dx.doi.org/10.1002/3527606645.

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Wang, Xiaoyu, Hui Wei, Wenjing Guo, Yihui Hu, and Jiangjiexing Wu. Nanozymes: Next Wave of Artificial Enzymes. Springer, 2016.

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H, Schmid-Schönbein, Wurzinger L. J, Zimmermann R. E, and Commission of the European Communities. Committee on Medical and Public Health Research., eds. Enzyme activation in blood-perfused artificial organs: Proceedings of an interdisciplinary meeting. Nijhoff, 1985.

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Book chapters on the topic "Enzyme artificiel"

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Breslow, Ronald. "Artificial Enzymes and Enzyme Models." In Advances in Enzymology - and Related Areas of Molecular Biology. John Wiley & Sons, Inc., 2006. http://dx.doi.org/10.1002/9780470123041.ch1.

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Breslow, Ronald. "Artificial Enzymes." In Artificial Enzymes. Wiley-VCH Verlag GmbH & Co. KGaA, 2006. http://dx.doi.org/10.1002/3527606645.ch1.

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Chin, Jik, and Hae-Jo Kim. "Artificial Hydrolytic Metalloenzymes." In Artificial Enzymes. Wiley-VCH Verlag GmbH & Co. KGaA, 2006. http://dx.doi.org/10.1002/3527606645.ch6.

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Varfolomeev, Sergey, Bella Grigorenko, Sofya Lushchekina, et al. "Study and modeling of mechanisms of cholinesterasis reactions in order to improve their catalytic properties in the neutralization reactions of organophosphorus compounds." In ORGANOPHOSPHORUS NEUROTOXINS. Publishing Center RIOR, 2020. http://dx.doi.org/10.29039/23_140-180.

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“Biocleaners” or “bioscavengers” are biological objects (enzymes, catalytic antibodies) that are capable of binding and/or hydrolyzing organophosphorus compounds (OPC). Their use seems to be the most effective alternative to traditional antidotes to neutralize or detoxify OPC. The introduction of bioscavengers allows neutralizing toxicant molecules in the bloodstream before they reach their biological targets, thereby providing protection against poisoning. Bioscavengers of the first-generation neutralized OPC molecules by stoichiometrically binding to them. The safety and efficacy of human butyrylcholinesterase (BChE) for protecting against OPC poisoning has been shown. However, the stoichiometric neutralization of OPC requires the introduction of a huge amount of expensive biopharmaceuticals. Catalytic bioscavengers that hydrolytically neutralize OPC were introduced at a much lower dose to achieve the same degree of effectiveness. The most effective catalytic bioscavengers are enzymes. The most promising enzymes are artificial mammalian paraoxonase mutants and bacterial phosphotriesterases. However, studies of other enzymes, such as prolidases, oxidases, artificial mutants of cholinesterases and carboxyl esterases and catalytic antibodies are actively ongoing. Since OPC are pseudosubstrates of cholinesterases (ChEs), a detailed description of the mechanisms of inhibition, dealkylation, and spontaneous reactivation of phosphorylated ChEs is critical for the development of ChEs mutants with a high rate of hydrolysis of OPC. The review presents an analysis of different views on the mechanisms of interaction of ChEs with OPC, discusses the possible directions of creating effective catalytic biological traps based on BChE and changes in their mechanism of action as compared to the native enzyme. A separate section is devoted to the effect of mutations, both polymorphic and artificial, on the stability of the protein molecule of BChE.
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Varfolomeev, Sergey, Bella Grigorenko, Sofya Lushchekina, et al. "Study and modeling of mechanisms of cholinesterasis reactions in order to improve their catalytic properties in the neutralization reactions of organophosphorous compounds." In Organophosphorous Neurotoxins. Publishing Center RIOR, 2020. http://dx.doi.org/10.29039/chapter_5e4132b603bfc4.70818543.

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“Biocleaners” or “bioscavengers” are biological objects (enzymes, catalytic antibodies) that are capable of binding and/or hydrolyzing organophosphorus compounds (OPC). Their use seems to be the most effective alternative to traditional antidotes to neutralize or detoxify OPC. The introduction of bioscavengers allows neutralizing toxicant molecules in the bloodstream before they reach their biological targets, thereby providing protection against poisoning. Bioscavengers of the first-generation neutralized OPC molecules by stoichiometrically binding to them. The safety and efficacy of human butyrylcholinesterase (BChE) for protecting against OPC poisoning has been shown. However, the stoichiometric neutralization of OPC requires the introduction of a huge amount of expensive biopharmaceuticals. Catalytic bioscavengers that hydrolytically neutralize OPC were introduced at a much lower dose to achieve the same degree of effectiveness. The most effective catalytic bioscavengers are enzymes. The most promising enzymes are artificial mammalian paraoxonase mutants and bacterial phosphotriesterases. However, studies of other enzymes, such as prolidases, oxidases, artificial mutants of cholinesterases and carboxyl esterases and catalytic antibodies are actively ongoing. Since OPC are pseudosubstrates of cholinesterases (ChEs), a detailed description of the mechanisms of inhibition, dealkylation, and spontaneous reactivation of phosphorylated ChEs is critical for the development of ChEs mutants with a high rate of hydrolysis of OPC. The review presents an analysis of different views on the mechanisms of interaction of ChEs with OPC, discusses the possible directions of creating effective catalytic biological traps based on BChE and changes in their mechanism of action as compared to the native enzyme. A separate section is devoted to the effect of mutations, both polymorphic and artificial, on the stability of the protein molecule of BChE.
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Liu, Lei, and Ronald Breslow. "Vitamin B6 Enzyme Models." In Artificial Enzymes. Wiley-VCH Verlag GmbH & Co. KGaA, 2006. http://dx.doi.org/10.1002/3527606645.ch2.

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Bülow, Leif. "Artificial Bifunctional Enzymes." In ACS Symposium Series. American Chemical Society, 1993. http://dx.doi.org/10.1021/bk-1993-0516.ch014.

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Duckworth, Ben, and Mark D. Distefano. "Protein-based Artificial Enzymes." In Artificial Enzymes. Wiley-VCH Verlag GmbH & Co. KGaA, 2006. http://dx.doi.org/10.1002/3527606645.ch5.

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Klotz, Irving M., and Junghun Suh. "Evolution of Synthetic Polymers with Enzyme-like Catalytic Activities." In Artificial Enzymes. Wiley-VCH Verlag GmbH & Co. KGaA, 2006. http://dx.doi.org/10.1002/3527606645.ch3.

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Hilvert, Donald. "Mimicking Enzymes with Antibodies." In Artificial Enzymes. Wiley-VCH Verlag GmbH & Co. KGaA, 2006. http://dx.doi.org/10.1002/3527606645.ch4.

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Conference papers on the topic "Enzyme artificiel"

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Lee, Hyeseung, Dean Ho, Benjamin Chu, Karen Kuo, and Carlo Montemagno. "Reconstituting Membrane Proteins Into Artificial Membranes and Detection of Their Activities." In ASME 2004 3rd Integrated Nanosystems Conference. ASMEDC, 2004. http://dx.doi.org/10.1115/nano2004-46016.

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We have successfully purified BR from purple membrane of Halobacterium Salinarium and Cox from the genetically engineered plasmid inserted in Rhodobacter Sphaeroides. The activities of the purified enzymes have shown in lipid vesicles as well as in polymer vesicles and planar membranes. Phosphatidylcholine derived lipid vesicles created the most nature like environment for the enzymes. Triblock copolymer membrane was the alternative choice for membrane protein reconstitution since polymers are more durable, ideal for industrial applications and support enzyme activities better. We also demonst
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Liu, Jian. "ENZYME INSPIRED ARTIFICIAL PHOTOSYNTHESIS." In The 7th International Multidisciplinary Conference on Optofluidics 2017. MDPI, 2017. http://dx.doi.org/10.3390/optofluidics2017-04262.

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Liu, Jian. "Enzyme Inspired Artificial Photosynthesis." In The 7th International Multidisciplinary Conference on Optofluidics 2017. MDPI, 2017. http://dx.doi.org/10.3390/optofluidics2017-04263.

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Ibrahim, Hussam, Satyanarayana Moru, and Liang Dong. "A Biochemical Sensor with Artificial 3D Enzyme Network." In 2020 IEEE 33rd International Conference on Micro Electro Mechanical Systems (MEMS). IEEE, 2020. http://dx.doi.org/10.1109/mems46641.2020.9056232.

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Monti, Matteo, Tim Hutton, and Piet Hut. "Achieving Closure in Enzymes in Artificial Chemistries." In European Conference on Artificial Life 2015. The MIT Press, 2015. http://dx.doi.org/10.7551/978-0-262-33027-5-ch099.

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Virgo, Nathaniel, and Takashi Ikegami. "Autocatalysis Before Enzymes: The Emergence of Prebiotic Chain Reactions." In European Conference on Artificial Life 2013. MIT Press, 2013. http://dx.doi.org/10.7551/978-0-262-31709-2-ch036.

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Ochi, Anna, and Hiroyuki Hori. "Complex Formations between Artificial RNA-DNA Chimera Nucleic Acids and RNA Modification Enzyme." In 2007 International Symposium on Micro-NanoMechatronics and Human Science. IEEE, 2007. http://dx.doi.org/10.1109/mhs.2007.4420836.

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Klementeva, T. N., A. S. Artemchenko, M. V. Tyurin, et al. "EFFECT OF LARVAE NUTRITION WITH ANTIBIOTICS ON THE PHYSIOLOGICAL PARAMETERS OF WAX MOTH GALLERIA MELLONELLA (L.) IN A SERIES OF GENERATIONS." In V International Scientific Conference CONCEPTUAL AND APPLIED ASPECTS OF INVERTEBRATE SCIENTIFIC RESEARCH AND BIOLOGICAL EDUCATION. Tomsk State University Press, 2020. http://dx.doi.org/10.17223/978-5-94621-931-0-2020-16.

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The wax moth (Galleria mellonella; Lepidoptera: Pyralidae) lines have been obtained as a result of the artificial diet with broad-spectrum antibiotic selection. An influence of that diet on the insect’s physiological parameters was examined through several generations. A significant increase in the activity of a number of enzymatic and non-enzymatic antioxidants because of artificial diet with antibiotic has been observed in the midgut of the wax moth daughter generations. Observed changes in the midgut enzymes activity and increase of antioxidants level are denote a damage in the gut tissues.
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CAMPANELLA, LUIGI, ADRIANO NUCCILLI, MAURO TOMASSETTI, and STEFANO VECCHIO. "ORIGINAL TYROSINASE ORGANIC PHASE ENZYME ELECTRODE FOR THE KINETIC STUDY OF ARTIFICIAL RANCIDIFICATION OF EXTRA VIRGIN OLIVE OIL." In Proceedings of the 12th Italian Conference. WORLD SCIENTIFIC, 2008. http://dx.doi.org/10.1142/9789812833594_0002.

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Kitagawa, Teizo, and Takashi Ogura. "Resonance Raman spectra of transient species of a respiration enzyme detected with an artificial cardiovascular system and Raman/absorption simultaneous measurement system." In Moscow - DL tentative, edited by Sergei A. Akhmanov and Marina Y. Poroshina. SPIE, 1991. http://dx.doi.org/10.1117/12.57308.

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