Literatura académica sobre el tema "Recombinase RecA"
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Artículos de revistas sobre el tema "Recombinase RecA"
del Val, Elsa, William Nasser, Hafid Abaibou y Sylvie Reverchon. "RecA and DNA recombination: a review of molecular mechanisms". Biochemical Society Transactions 47, n.º 5 (18 de octubre de 2019): 1511–31. http://dx.doi.org/10.1042/bst20190558.
Texto completoLuisi-DeLuca, C., S. T. Lovett y R. D. Kolodner. "Genetic and physical analysis of plasmid recombination in recB recC sbcB and recB recC sbcA Escherichia coli K-12 mutants." Genetics 122, n.º 2 (1 de junio de 1989): 269–78. http://dx.doi.org/10.1093/genetics/122.2.269.
Texto completoChittela, Rajani Kant y Jayashree K. Sainis. "Plant DNA Recombinases: A Long Way to Go". Journal of Nucleic Acids 2010 (2010): 1–10. http://dx.doi.org/10.4061/2010/646109.
Texto completoHaldenby, Sam, Malcolm F. White y Thorsten Allers. "RecA family proteins in archaea: RadA and its cousins". Biochemical Society Transactions 37, n.º 1 (20 de enero de 2009): 102–7. http://dx.doi.org/10.1042/bst0370102.
Texto completoGarcía-Vázquez, Francisco A., Salvador Ruiz, Carmen Matás, M. José Izquierdo-Rico, Luis A. Grullón, Aitor De Ondiz, Luis Vieira, Karen Avilés-López, Alfonso Gutiérrez-Adán y Joaquín Gadea. "Production of transgenic piglets using ICSI–sperm-mediated gene transfer in combination with recombinase RecA". REPRODUCTION 140, n.º 2 (agosto de 2010): 259–72. http://dx.doi.org/10.1530/rep-10-0129.
Texto completoHofstatter, Paulo G., Alexander K. Tice, Seungho Kang, Matthew W. Brown y Daniel J. G. Lahr. "Evolution of bacterial recombinase A ( recA ) in eukaryotes explained by addition of genomic data of key microbial lineages". Proceedings of the Royal Society B: Biological Sciences 283, n.º 1840 (12 de octubre de 2016): 20161453. http://dx.doi.org/10.1098/rspb.2016.1453.
Texto completoLiu, Yu-Tien, Chia-Geun Chen, Der-Chiang Chao, Fan Lee, Ching-Len Liao, Huey-Kang Sytwu, Chi-Fu Chou y Dar-Der Ji. "Sequence analysis of theGluconobacter oxydansRecA protein and construction of arecA-deficient mutant". Canadian Journal of Microbiology 45, n.º 4 (1 de abril de 1999): 347–51. http://dx.doi.org/10.1139/w99-009.
Texto completoInagaki, Satoko, Kazuyo Fujita, Yukiko Takashima, Kayoko Nagayama, Arifah C. Ardin, Yuki Matsumi y Michiyo Matsumoto-Nakano. "Regulation of Recombination betweengtfB/gtfCGenes inStreptococcus mutansby Recombinase A". Scientific World Journal 2013 (2013): 1–7. http://dx.doi.org/10.1155/2013/405075.
Texto completoPan, Yue, Ningkang Xie, Xin Zhang, Shuo Yang y Shaowu Lv. "Computational Insights into the Dynamic Structural Features and Binding Characteristics of Recombinase UvsX Compared with RecA". Molecules 28, n.º 8 (11 de abril de 2023): 3363. http://dx.doi.org/10.3390/molecules28083363.
Texto completoRamos, Cristina, Rogelio Hernández-Tamayo, María López-Sanz, Begoña Carrasco, Ester Serrano, Juan C. Alonso, Peter L. Graumann y Silvia Ayora. "The RecD2 helicase balances RecA activities". Nucleic Acids Research 50, n.º 6 (2 de marzo de 2022): 3432–44. http://dx.doi.org/10.1093/nar/gkac131.
Texto completoTesis sobre el tema "Recombinase RecA"
Mah, Wayne. "Single molecule study of RecA recombinase enzyme activity". Thesis, McGill University, 2008. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=18743.
Texto completoLa recombinaison Homologue est un chemin essentiel dans la réparation de dommages d'ADN pendant le procédé de réplication d'ADN. La protéine de RecA promeut les étapes centrales dans la recombinaison homologue, après avoir revêtu ADN seul-abandonné (ssDNA), RecA exécute un mettre et la réaction d'échange de brin impliquant ADN homologue. Ce projet de recherche vise à caractériser la fonction de RecA dans la recombinaison homologue utilisant la molécule seule mouvement de particule attaché (TPM). TPM d'utilisation pour observer l'extension de RecA le long d'ADN, le taux d'extension de RecA sur ssDNA a été déterminé pour la première fois. Le taux obtenu pour dsDNA était similaire, impliquant ce RecA polymerizes le long de seulement un brin d'un substrat d'ADN. Le comportement de nucleation de RecA sur ADN a été aussi obtenu de la trace d'extension, confirmant l'hypothèse ce nucleation rapide sur ssDNA est indépendant du pH, pendant que nucleation sur dsDNA est dépendant du pH. Plusieurs pilote plusieurs expériences de molécule seules ont visé à contrôlant le mettre et la réaction d'échange de brin a été tentée en temps réel. Bien que ces expériences étaient les ensembles infructueuses et réussies analogues biochimiques de ces expériences ont prouvé la possibilité des expériences de molécule seules. Ces tentatives ont donné de l'aux perspicacités dans les facteurs possibles freinant le succès et a mené à l'élément essentiel de suggestions expérimental au succès d'expériences futures
Perry, Thomas. "Étude structurale et fonctionnelle de l'appareil de recombinaison homologue chez Streptococcus pneumoniae". Electronic Thesis or Diss., Sorbonne université, 2019. http://www.theses.fr/2019SORUS300.
Texto completoNatural transformation is the ability of some bacteria to incorporate and actively integrate extracellular DNA. This major process increases the plasticity and adaptability of gram positive and negative bacteria by performing intra- and inter-species genetic exchanges. S. pneumoniae is a major human pathogen and is found commensally in the mucous membranes of the nasopharynx. This bacterium is responsible for severe infections such as pneumonia, meningitis and sepsis. In this species, the natural transformation is correlated with the phenomenon of capsule change and the decrease of vaccine efficacy, as well as the obtaining of genes for antibiotic resistance. During the transformation, the extracellular DNA will be supported in the cytoplasm by different proteins, which will eventually integrate this gene into the bacterial genome by homologous recombination. The search for homology and the integration of the gene is under the control of the universal recombinase RecA. For this, RecA will form a helical filament with exogenous ssDNA and endogenous dsDNA, and those in ATP dependent manner. However, the atomic structure of such filaments has never been observed in S. pneumoniae. Using biochemical characterization techniques and electron cryomicroscopy, we succeeded in solving the structure of the two types of filaments at resolutions of 3.8 Å and 3.9 Å. This allowed us to better characterize the interaction of RecA with DNA. By comparing our structures with those obtained by crystallography of RecA filaments observed in E. coli, we partly explained the reasons for the 3-fold recombination efficiency of S. pneumoniae. In a second step, we demonstrated in vitro a link between the RecA filamentation along the DNA and the helicase activity of RadA. RadA is a protein necessary for homologous recombination and whose helicase activity seems to promote and extend D-loop at the level of endogenous dsDNA. We have also characterized, by NMR, the structure of the zinc finger motif of RadA and its interaction with DNA, a motif that could not be solved in the RadA structure in crystallography and which seems essential for its helicase activity
Kobir, Ahasanul. "Physiological roles of Eukaryotic Hanks type Ser/Thr kinase in transition to stationary phase in Bacillus subtilis". Phd thesis, Université Paris Sud - Paris XI, 2012. http://tel.archives-ouvertes.fr/tel-00911812.
Texto completoDulermo, Rémi. "Etude des mécanismes de l'extrême tolérance aux radiations de la bactérie Deinococcus deserti par une approche de génomique fonctionnelle". Aix-Marseille 2, 2009. http://theses.univ-amu.fr.lama.univ-amu.fr/2009AIX22100.pdf.
Texto completoThe genome of Deinococcus deserti, a highly radiation-tolerant bacterium, was analyzed and compared to those of D. Radiodurans and D. Geothermalis. About 230 proteins are specifically conserved in these 3 species, including IrrE, a regulator protein essential for radiotolerance. D. Deserti has several supplementary DNA repair genes, like imuY and dnaE2 (translesion DNA polymerases). Moreover, D. Deserti has 3 recA that code for 2 different RecA proteins (RecAC et RecAP). To study these genes, genetic tools were developed for D. Deserti. Different results suggest that IrrE, required for the induction of several genes after irradiation, has peptidase activity. The 2 RecA proteins are functional for DNA repair. D. Deserti is mutable by UV, which requires ImuY, DnaE2 and RecAC, but not RecAP
Chen, Zhucheng. "Mechanism of homologous recombination : from crystal structures of RecA-single stranded DNA and RecA-double stranded DNA filaments /". Access full-text from WCMC, 2009. http://proquest.umi.com/pqdweb?did=1619205721&sid=8&Fmt=2&clientId=8424&RQT=309&VName=PQD.
Texto completoRamdas, Jyoti. "Functions Of Nucleosomes And Other Regulatory Factor(S) In Homologous Recombination Promoted By RecA Protein". Thesis, Indian Institute of Science, 1994. https://etd.iisc.ac.in/handle/2005/99.
Texto completoRamdas, Jyoti. "Functions Of Nucleosomes And Other Regulatory Factor(S) In Homologous Recombination Promoted By RecA Protein". Thesis, Indian Institute of Science, 1994. http://hdl.handle.net/2005/99.
Texto completoSaladin, Adrien. "Macromolecular Docking : applications to the RecA nucleofilament". Paris 7, 2009. http://www.theses.fr/2009PA077098.
Texto completoProteins play a central role in various cellular processes with various interactions with other proteins, DNA, lipids or small ligands. Because the determination of these interactions is fundamental for understanding key biological processes, several experimental methods have been developed to characterize them. Experimental studies can take a long time and an expensive. Computational methods can therefore be of great help to guide future biochemical experiments. Development of docking software is a long process involving cycles of algorithm conception, programming and tests. During my thesis, I developed an object oriented library to help and speed-up development and tests of docking methods. This library was programmed in C++ with Python bindings, and has been used to test new methods applied to protein-DNA docking and multicomponent docking. Programs made with the help of this library are presently used to study the binding of DNA to the RecA complex, responsible of homologous recombination
黃楚華 y Choi-wah Brian Wong. "In vitro studies on the mechanism of homologous DNA recombination promoted by Escherichia coli RecA protein". Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1993. http://hub.hku.hk/bib/B31233284.
Texto completoWong, Choi-wah Brian. "In vitro studies on the mechanism of homologous DNA recombination promoted by Escherichia coli RecA protein /". [Hong Kong : University of Hong Kong], 1993. http://sunzi.lib.hku.hk/hkuto/record.jsp?B13408902.
Texto completoLibros sobre el tema "Recombinase RecA"
Suzuki. Genetic Analysis, 4/E and Reco: Beyond the Myth of. W.H. Freeman & Company, 1992.
Buscar texto completoOrganisation for economic co-operation and development. Recombinant DNA Safety Considerations (Safety Considerations for Industrial, Agricultural and Environmental Applications of Organisms Derived By Reco). Organization for Economic, 1986.
Buscar texto completoActas de conferencias sobre el tema "Recombinase RecA"
Duarte, Gabriela Alves Carvalho, Vanessa Bridi, Dhullya Eduarda Resende Santos y Hanstter Hallison Alves Rezende. "TECNOLOGIA DO DNA RECOMBINANTE NA PRODUÇÃO DE INSULINA". En I Congresso de Engenharia de Biotecnologia. Revista Multidisciplinar de Educação e Meio Ambiente, 2021. http://dx.doi.org/10.51189/rema/1377.
Texto completoHirschberg, M., A. Manoutchei, B. Klemens y B. Hofferberth. "CEREBRAL THROMBOLYSIS WITH INTRAVENOUSLY ADMINISTERED RECOMBINANT LOW- MOLECULAR-WEIGHT-UROKINASE AND RECOMBINANT PRO-UROKINASE IN A DOG MODEL". En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643571.
Texto completoDuarte, Amanda Alves, Renata Andrade De Oliveira, Eliane Pereira Cipolatti, Evelin Andrade Manoel y Martina Costa Cerqueira. "COMPARAÇÃO DO DESEMPENHO DE LIPASE COMERCIAL E RECOMBINANTE DE CANDIDA ANTARCTICA FRAÇÃO B EM PARTÍCULAS DE PMMA". En I Congresso de Engenharia de Biotecnologia. Revista Multidisciplinar de Educação e Meio Ambiente, 2021. http://dx.doi.org/10.51189/rema/1356.
Texto completoCamargo, Luiza Helena Angarten Ferraz de, Thalita Barcelos Silva, Lysandra De Queiroz Cunha Barradas, Dhullya Eduarda Resende Santos y Hanstter Hallison Alves Rezende. "O USO DA BIOTECNOLOGIA NO CONTEXTO DOS ALIMENTOS FUNCIONAIS". En I Congresso de Engenharia de Biotecnologia. Revista Multidisciplinar de Educação e Meio Ambiente, 2021. http://dx.doi.org/10.51189/rema/1368.
Texto completoBridi, Vanessa, Gabriela Alves Carvalho Duarte, Dhullya Eduarda Resende Santos y Hanstter Hallison Alves Rezende. "BIOFÁRMACOS: DESAFIOS ENFRENTADOS NA PRODUÇÃO NACIONAL". En I Congresso de Engenharia de Biotecnologia. Revista Multidisciplinar de Educação e Meio Ambiente, 2021. http://dx.doi.org/10.51189/rema/1376.
Texto completoGonçalves, Thalita Carvalho de, Dayane Silva Cavalcante, Martina Cerqueira Pinto, Eliane Pereira Cipolatti y Evelin Andrade Manoel. "APLICAÇÕES INDUSTRIAIS DE LIPASES IMOBILIZADAS: UM ESTUDO QUANTITATIVO". En I Congresso de Engenharia de Biotecnologia. Revista Multidisciplinar de Educação e Meio Ambiente, 2021. http://dx.doi.org/10.51189/rema/1392.
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