Academic literature on the topic 'Bacterial motility; Motor; Chemotaxis'

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Journal articles on the topic "Bacterial motility; Motor; Chemotaxis"

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Lux, Renate, and Wenyuan Shi. "Chemotaxis-guided Movements in Bacteria." Critical Reviews in Oral Biology & Medicine 15, no. 4 (2004): 207–20. http://dx.doi.org/10.1177/154411130401500404.

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Motile bacteria often use sophisticated chemotaxis signaling systems to direct their movements. In general, bacterial chemotactic signal transduction pathways have three basic elements: (1) signal reception by bacterial chemoreceptors located on the membrane; (2) signal transduction to relay the signals from membrane receptors to the motor; and (3) signal adaptation to desensitize the initial signal input. The chemotaxis proteins involved in these signal transduction pathways have been identified and extensively studied, especially in the enterobacteria Escherichia coli and Salmonella enterica
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Quax, Tessa E. F., Florian Altegoer, Fernando Rossi, et al. "Structure and function of the archaeal response regulator CheY." Proceedings of the National Academy of Sciences 115, no. 6 (2018): E1259—E1268. http://dx.doi.org/10.1073/pnas.1716661115.

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Motility is a central feature of many microorganisms and provides an efficient strategy to respond to environmental changes. Bacteria and archaea have developed fundamentally different rotary motors enabling their motility, termed flagellum and archaellum, respectively. Bacterial motility along chemical gradients, called chemotaxis, critically relies on the response regulator CheY, which, when phosphorylated, inverses the rotational direction of the flagellum via a switch complex at the base of the motor. The structural difference between archaellum and flagellum and the presence of functional
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Rosko, Jerko, Vincent A. Martinez, Wilson C. K. Poon, and Teuta Pilizota. "Osmotaxis inEscherichia colithrough changes in motor speed." Proceedings of the National Academy of Sciences 114, no. 38 (2017): E7969—E7976. http://dx.doi.org/10.1073/pnas.1620945114.

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Bacterial motility, and in particular repulsion or attraction toward specific chemicals, has been a subject of investigation for over 100 years, resulting in detailed understanding of bacterial chemotaxis and the corresponding sensory network in many bacterial species. ForEscherichia colimost of the current understanding comes from the experiments with low levels of chemotactically active ligands. However, chemotactically inactive chemical species at concentrations found in the human gastrointestinal tract produce significant changes inE. coli’sosmotic pressure and have been shown to lead to t
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Wei, Xueming, and Wolfgang D. Bauer. "Starvation-Induced Changes in Motility, Chemotaxis, and Flagellation of Rhizobium meliloti." Applied and Environmental Microbiology 64, no. 5 (1998): 1708–14. http://dx.doi.org/10.1128/aem.64.5.1708-1714.1998.

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ABSTRACT The changes in motility, chemotactic responsiveness, and flagellation of Rhizobium meliloti RMB7201, L5-30, and JJ1c10 were analyzed after transfer of the bacteria to buffer with no available C, N, or phosphate. Cells of these three strains remained viable for weeks after transfer to starvation buffer (SB) but lost all motility within just 8 to 72 h after transfer to SB. The rates of motility loss differed by severalfold among the strains. Each strain showed a transient, two- to sixfold increase in chemotactic responsiveness toward glutamine within a few hours after transfer to SB, ev
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Spormann, Alfred M. "Gliding Motility in Bacteria: Insights from Studies ofMyxococcus xanthus." Microbiology and Molecular Biology Reviews 63, no. 3 (1999): 621–41. http://dx.doi.org/10.1128/mmbr.63.3.621-641.1999.

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SUMMARY Gliding motility is observed in a large variety of phylogenetically unrelated bacteria. Gliding provides a means for microbes to travel in environments with a low water content, such as might be found in biofilms, microbial mats, and soil. Gliding is defined as the movement of a cell on a surface in the direction of the long axis of the cell. Because this definition is operational and not mechanistic, the underlying molecular motor(s) may be quite different in diverse microbes. In fact, studies on the gliding bacterium Myxococcus xanthus suggest that two independent gliding machineries
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Eisenbach, Michael, Amnon Wolf, Martin Welch, et al. "Pausing, switching and speed fluctuation of the bacterial flagellar motor and their relation to motility and chemotaxis." Journal of Molecular Biology 211, no. 3 (1990): 551–63. http://dx.doi.org/10.1016/0022-2836(90)90265-n.

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Trachtenberg, Shlomo, S. Brian Andrews, and Richard D. Leapman. "Mass Distribution and Spatial Organization of the Linear Bacterial Motor of Spiroplasma citri R8A2." Journal of Bacteriology 185, no. 6 (2003): 1987–94. http://dx.doi.org/10.1128/jb.185.6.1987-1994.2003.

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ABSTRACT In the simple, helical, wall-less bacterial genus Spiroplasma, chemotaxis and motility are effected by a linear, contractile motor arranged as a flat cytoskeletal ribbon attached to the inner side of the membrane along the shortest helical line. With scanning transmission electron microscopy and diffraction analysis, we determined the hierarchical and spatial organization of the cytoskeleton of Spiroplasma citri R8A2. The structural unit appears to be a fibril, ∼5 nm wide, composed of dimers of a 59-kDa protein; each ribbon is assembled from seven fibril pairs. The functional unit of
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Belas, Robert, Eiko Horikawa, Shin-Ichi Aizawa, and Rooge Suvanasuthi. "Genetic Determinants of Silicibacter sp. TM1040 Motility." Journal of Bacteriology 191, no. 14 (2009): 4502–12. http://dx.doi.org/10.1128/jb.00429-09.

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ABSTRACT Silicibacter sp. TM1040 is a member of the marine Roseobacter clade of Alphaproteobacteria that forms symbioses with unicellular eukaryotic phytoplankton, such as dinoflagellates. The symbiosis is complex and involves a series of steps that physiologically change highly motile bacteria into cells that readily form biofilms on the surface of the host. The initial phases of symbiosis require bacterial motility and chemotaxis that drive the swimming bacteria toward their planktonic host. Cells lacking wild-type motility fail to establish biofilms on host cells and do not produce effectiv
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Horváth, Péter, Takayuki Kato, Tomoko Miyata, and Keiichi Namba. "Structure of Salmonella Flagellar Hook Reveals Intermolecular Domain Interactions for the Universal Joint Function." Biomolecules 9, no. 9 (2019): 462. http://dx.doi.org/10.3390/biom9090462.

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The bacterial flagellum is a motility organelle consisting of a rotary motor and a long helical filament as a propeller. The flagellar hook is a flexible universal joint that transmits motor torque to the filament in its various orientations that change dynamically between swimming and tumbling of the cell upon switching the motor rotation for chemotaxis. Although the structures of the hook and hook protein FlgE from different bacterial species have been studied, the structure of Salmonella hook, which has been studied most over the years, has not been solved at a high enough resolution to all
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Kihara, May, Gabriele U. Miller, and Robert M. Macnab. "Deletion Analysis of the Flagellar Switch Protein FliG of Salmonella." Journal of Bacteriology 182, no. 11 (2000): 3022–28. http://dx.doi.org/10.1128/jb.182.11.3022-3028.2000.

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ABSTRACT The flagellar motor/switch complex, consisting of the three proteins FliG, FliM, and FliN, plays a central role in bacterial motility and chemotaxis. We have analyzed FliG, using 10-amino-acid deletions throughout the protein and testing the deletion clones for their motility and dominance properties and for interaction of the deletion proteins with the MS ring protein FliF. Only the N-terminal 46 amino acids of FliG (segments 1 to 4) were important for binding to FliF; consistent with this, an N-terminal fragment consisting of residues 1 to 108 bound FliF strongly, whereas a C-termin
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Dissertations / Theses on the topic "Bacterial motility; Motor; Chemotaxis"

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Edge, Matthew James. "Analysis of flagellar switch proteins in Rhodobacter sphaeroides." Thesis, University of Nottingham, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.342030.

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Rosko, Jerko. "Osmotaxis in Escherichia coli." Thesis, University of Edinburgh, 2017. http://hdl.handle.net/1842/28947.

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Bacterial motility, and in particular repulsion or attraction towards specific chemicals, has been a subject of investigation for over 100 years, resulting in detailed understanding of bacterial chemotaxis and the corresponding sensory network in many bacterial species including Escherichia coli. E. Coli swims by rotating a bundle of flagellar filaments, each powered by an individual rotary motor located in the cell membrane. When all motors rotate counter-clockwise (CCW), a stable bundle forms and propels the cell forward. When one or more motors switch to clock-wise (CW) rotation, their resp
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Foynes, Susan. "Motility and chemotaxis studies in Helicobacter pylori." Thesis, University College London (University of London), 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.322447.

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Broadway, Katherine Marie. "Novel Perspectives on the Utilization of Chemotactic Salmonella Typhimurium VNP20009 as an Anticancer Agent." Diss., Virginia Tech, 2018. http://hdl.handle.net/10919/84898.

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Attenuated bacterial strains have been investigated on the premise of selective tumor colonization and drug delivery potential for decades. Salmonella Typhimurium VNP20009 was derived from the parental strain 14028 through genetic modification and tumor targeting ability, being well studied for anticancer effects in mice. In 2001 Phase 1 Clinical Trials, patients diagnosed with melanoma were introduced with VNP20009, resulting in safe delivery of the strain and targeting to the tumor, however no anticancer effects were observed. Recently, it was discovered that VNP20009 contains a SNP in cheY,
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Rosser, Gabriel A. "Mathematical modelling and analysis of aspects of bacterial motility." Thesis, University of Oxford, 2012. http://ora.ox.ac.uk/objects/uuid:1af98367-aa2f-4af3-9344-8c361311b553.

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The motile behaviour of bacteria underlies many important aspects of their actions, including pathogenicity, foraging efficiency, and ability to form biofilms. In this thesis, we apply mathematical modelling and analysis to various aspects of the planktonic motility of flagellated bacteria, guided by experimental observations. We use data obtained by tracking free-swimming Rhodobacter sphaeroides under a microscope, taking advantage of the availability of a large dataset acquired using a recently developed, high-throughput protocol. A novel analysis method using a hidden Markov model for the i
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Altinoglu, Ipek. "Organization of Bacterial Cell Pole." Thesis, Université Paris-Saclay (ComUE), 2018. http://www.theses.fr/2018SACLS367/document.

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Chez les bactéries, les pôles cellulaires servent de domaines subcellulaires impliqués dans plusieurs processus cellulaires. Chez l’agent pathogène du choléra, Vibrio cholerae, en forme de bâtonnet incurvé, le pole contenant l’unique flagelle est impliqué dans la virulence. La protéine d’ancrage polaire HubP interagit avec plusieurs ATPases telles que ParA1 (ségrégation des chromosomes), ParC (localisation polaire du système de chimiotaxie) et FlhG (biosynthèse des flagelles), organisant ainsi l'identité polaire de V. cholerae. Cependant, les mécanismes moléculaires exacts de cet ancrage polai
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Faure, Laura. "La machinerie de motilité de Myxococcus xanthus : caractérisation d'une nouvelle famille de moteurs moléculaires dans l'enveloppe bactérienne." Thesis, Aix-Marseille, 2017. http://www.theses.fr/2017AIXM0011/document.

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Dans les cellules il existe deux grandes sources d’énergie : l’ATP et la force proton-motrice, produites au niveau du cytoplasme et de la membrane interne respectivement. La mise en place de processus actifs dans la membrane externe ou à la surface des bactéries à Gram négatif requière la présence de machineries protéiques transmettant les forces de leur lieu de production à leur lieu d’utilisation. Durant ma thèse j’ai étudié une de ces machines : la machinerie de motilité (Agl-Glt) de Myxococcus xanthus. Plus précisément, j’ai cherché à comprendre comment les composants de cette machine s’or
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"Bacterial motility and chemotaxis in geometrically restrictive environments." Tulane University, 1996.

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Motile bacteria swim by rotating their helical flagella. In the absence of any chemical concentration gradients in their surrounding medium, the swimming behavior of motile bacteria is referred to as random motility. At population level, bacterial swimming can be characterized by the random motility coefficient, whereas at individual cell level, swimming speed, tumbling frequency and the index of directional persistence are used to describe bacterial swimming. In the presence of chemical concentration gradients, bacteria move toward favorable substances termed chemoattractants and away from re
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Olson, Mira Beth Stone. "Quantification of bacterial motility and chemotaxis in porous media using magnetic resonance imaging (MRI) /." 2004. http://wwwlib.umi.com/dissertations/fullcit/3144649.

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Book chapters on the topic "Bacterial motility; Motor; Chemotaxis"

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Koch, Arthur L. "Gliding Motility, Protonmotive Force Motor, and Flagellar Rotation." In Bacterial Growth and Form. Springer Netherlands, 2001. http://dx.doi.org/10.1007/978-94-017-0827-2_15.

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Erhardt, Marc. "Strategies to Block Bacterial Pathogenesis by Interference with Motility and Chemotaxis." In Current Topics in Microbiology and Immunology. Springer International Publishing, 2016. http://dx.doi.org/10.1007/82_2016_493.

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Manson, Michael D. "Bacterial Motility and Chemotaxis." In Advances in Microbial Physiology Volume 33. Elsevier, 1992. http://dx.doi.org/10.1016/s0065-2911(08)60219-2.

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NEWTON, AUSTIN. "Differentiation in Caulobacter: Flagellum Development, Motility and Chemotaxis." In Genetics of Bacterial Diversity. Elsevier, 1989. http://dx.doi.org/10.1016/b978-0-12-355574-8.50018-5.

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NEWTON, AUSTIN. "Differentiation in Caulobacter: Flagellum Development, Motility and Chemotaxis." In Genetics of Bacterial Diversity. Elsevier, 1989. http://dx.doi.org/10.1016/b978-0-12-355575-5.50017-4.

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Barak, Rina, and Michael Eisenbach. "Regulation of interaction between signaling protein CheY and flagellar motor during bacterial chemotaxis." In Current Topics in Cellular Regulation. Elsevier, 1996. http://dx.doi.org/10.1016/s0070-2137(96)80005-7.

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Maynard Smith, John, and Eors Szathmary. "The origin of eukaryotes." In The Major Transitions in Evolution. Oxford University Press, 1997. http://dx.doi.org/10.1093/oso/9780198502944.003.0012.

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The basic structures of a bacterial and a eukaryotic cell are shown in Fig. 8.1. The differences whose origins call for an explanation are as follows: • The bacterial cell has a rigid outer cell wall, usually made of the peptidoglycan, murein. In eukaryotes, the rigid cell wall is not universal, and cell shape is maintained primarily by an internal cytoskeleton of filaments and microtubules. • Eukaryotic cells have a complex system of internal membranes, including the nuclear envelope, endoplasmic reticulum and lysosomes. • Bacteria have a single circular chromosome, attached to the rigid outer cell wall. In eukaryotes, linear chromosomes are contained within a nuclear envelope, which separates transcription from translation: communication between nucleus and cytoplasm is via pores in the nuclear envelope. • Eukaryotes have a complex cytoskeleton. The actomyosin system powers cell division, phagocytosis, amoeboid motion and the overall contractility to resist osmotic swelling. Microtubules and the associated motor proteins (kinesin, dynein and dynamin) ensure the accurate segregation of chromosomes in mitosis, ciliary motility and the movement of transport vesicles. Intermediate filaments form the structural basis for the association of the endomembranes and nuclear-pore complexes with the chromatin to form the nuclear envelope, while other intermediate filaments help to anchor the nucleus in the cytoplasm. One crucial difference between prokaryotes and most eukaryotes has been omitted from Fig. 8.1: this is the presence of mitochondria, and, in plants and algae, of chloroplasts. The reason for the omission is that, on the scenario for eukaryote origins that seems to us most plausible, these intracellular organelles originated later in time than the structures shown in the figure. The differences between these cell types justifies the recognition of two empires of life (above the kingdom level): Bacteria and Eukaryota (Cavalier-Smith, 199la; Table 8.1). (It is interesting that this taxonomic rank was recognized by Linnaeus.) Within each of the empires, there are two major categories: Bacteria consist of the kingdoms Eubacteria and Archaebacteria, and Eukaryota are divided into the superkingdoms Archaezoa and Metakaryota. The justification for these divisions is as follows. The Archaebacteria, in contrast to the Eubacteria, never have murein cell walls, and their single cell membrane contains isoprenoidal ether rather than acyl ester lipids.
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Conference papers on the topic "Bacterial motility; Motor; Chemotaxis"

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Wang, Zhiyu, MinJun Kim, and Gail Rosen. "Validating models of bacterial chemotaxis by simulating the random motility coefficient." In 2008 8th IEEE International Conference on Bioinformatics and BioEngineering (BIBE). IEEE, 2008. http://dx.doi.org/10.1109/bibe.2008.4696658.

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Traore, Mahama A., and Bahareh Behkam. "Autonomous Sorting of Micro-Particles Using Bacterial Chemotaxis." In ASME 2012 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/sbc2012-80827.

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The autonomous manipulation and assembly at the micro and nanoscale continues to be one of the main challenges in the field of micro/nanorobotics. On the other hand, biomotors are increasingly being considered as robust, versatile and cost-effective choices for a variety of micro/nanorobotic tasks. Here we propose the utilization of the motility and chemotaxis in flagellated bacteria to autonomously sort spherical particles with 6 μm and 10 μm in diameter within a microfluidic platform. Surface chemistry methods are utilized to selectively self-assemble bacteria onto the 6 μm diameter particle
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Vourc’h, Thomas, Julien Léopoldès, and Hassan Peerhossaini. "Phototactic Behaviour of Active Fluids: Effects of Light Perturbation on Diffusion Coefficient of Bacterial Suspensions." In ASME-JSME-KSME 2019 8th Joint Fluids Engineering Conference. American Society of Mechanical Engineers, 2019. http://dx.doi.org/10.1115/ajkfluids2019-4904.

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Abstract Active fluids refer to the fluids that contain self-propelled particles such as bacteria or micro-algae, whose properties differ fundamentally from the passive fluids. Such particles often exhibit an intermittent motion; with high-motility “run” periods separated by low-motility “tumble” periods. The average motion can be modified with external stresses, such as nutrient or light gradient, leading to a directed movement called chemotaxis and phototaxis, respectively. Using cyanobacterium Synechocystis sp.PCC 6803, a model micro-organism to study photosynthesis, we track the bacterial
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