Academic literature on the topic 'Hyphal branching'

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Journal articles on the topic "Hyphal branching"

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Falloon, Richard E., Paul W. Sutherland, and Ian C. Hallett. "Morphology of Erysiphe pisi on leaves of Pisum sativum." Canadian Journal of Botany 67, no. 11 (1989): 3410–16. http://dx.doi.org/10.1139/b89-415.

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Morphological details of conidium germination, hyphae, appressoria, conidiophores, and organisation within colonies of Erysiphe pisi on leaves of Pisum sativum were studied in frozen, hydrated specimens with a scanning electron microscope. The pathogen has several adaptations to enable efficient colonisation of host leaf surfaces, including production of several hyphae from each germinated conidium, unidirectional growth of individual hyphae, prolific hyphal branching at obtuse angles to lines of hyphal growth, and rapid and prolific development of appressoria and conidiophores. Hyphal cells o
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Barelle, Caroline J., Mathias L. Richard, Claude Gaillardin, Neil A. R. Gow, and Alistair J. P. Brown. "Candida albicans VAC8 Is Required for Vacuolar Inheritance and Normal Hyphal Branching." Eukaryotic Cell 5, no. 2 (2006): 359–67. http://dx.doi.org/10.1128/ec.5.2.359-367.2006.

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ABSTRACT Hyphal growth is prevalent during most Candida albicans infections. Current cell division models, which are based on cytological analyses of C. albicans, predict that hyphal branching is intimately linked with vacuolar inheritance in this fungus. Here we report the molecular validation of this model, showing that a specific mutation that disrupts vacuolar inheritance also affects hyphal division. The armadillo repeat-containing protein Vac8p plays an important role in vacuolar inheritance in Saccharomyces cerevisiae. The VAC8 gene was identified in the C. albicans genome sequence and
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Tan, Yong Y., Martin J. Spiering, Vicki Scott, Geoffrey A. Lane, Michael J. Christensen, and Jan Schmid. "In Planta Regulation of Extension of an Endophytic Fungus and Maintenance of High Metabolic Rates in Its Mycelium in the Absence of Apical Extension." Applied and Environmental Microbiology 67, no. 12 (2001): 5377–83. http://dx.doi.org/10.1128/aem.67.12.5377-5383.2001.

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ABSTRACT The fungus Neotyphodium lolii is an endophytic symbiont. It grows in the intercellular spaces of the perennial ryegrass Lolium perenne, producing secondary metabolites which enhance the fitness of the association over that of uninfectedL. perenne. We report that the average number of hyphal strands in a given section of a leaf remains constant during the life of a leaf, indicating synchrony of leaf and hyphal extension, including cessation of hyphal extension when leaf extension ceases. We used a constitutively expressed reporter gene as an indicator of the mycelium's metabolic activi
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Wilson, Duncan, François L. Mayer, Pedro Miramón, et al. "Distinct Roles of Candida albicans-Specific Genes in Host-Pathogen Interactions." Eukaryotic Cell 13, no. 8 (2014): 977–89. http://dx.doi.org/10.1128/ec.00051-14.

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ABSTRACTHuman fungal pathogens are distributed throughout their kingdom, suggesting that pathogenic potential evolved independently.Candida albicansis the most virulent member of the CUG clade of yeasts and a common cause of both superficial and invasive infections. We therefore hypothesized thatC. albicanspossesses distinct pathogenicity mechanisms.In silicogenome subtraction and comparative transcriptional analysis identified a total of 65C.albicans-specificgenes (ASGs) expressed during infection. Phenotypic characterization of six ASG-null mutants demonstrated that these genes are dispensab
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Harris, Steven D. "Hyphal branching in filamentous fungi." Developmental Biology 451, no. 1 (2019): 35–39. http://dx.doi.org/10.1016/j.ydbio.2019.02.012.

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Suryanarayanan, T. S., V. Muruganandam, and G. Sampath. "Effect of Congo red on hyphal morphogenesis and sporulation of Botryodiplodia theobromae." Canadian Journal of Botany 65, no. 5 (1987): 815–16. http://dx.doi.org/10.1139/b87-110.

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The effect of Congo red, a dye which inhibits crystallization of cell wall polysaccharides, on hyphal differentiation and sporulation of Botryodiplodia theobromae Pat. was studied. The fungus has an obligate requirement for light to fruit in culture. The dye replaced the light requirement for formation of pycnidia. It also affected the structural integrity of the hyphal wall and the branching frequency of the hypha.
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Youatt, Jean. "DNA Synthesis in Relation to Hyphal Branching and Wall Composition in Allomyces macrogynus." Australian Journal of Biological Sciences 38, no. 1 (1985): 67. http://dx.doi.org/10.1071/bi9850067.

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In A. macrogynus the first replication of DNA occurred after germination, at the time of the first branching of rhizoids. Before the second replication galactan in the wall exceeded the glucan content and was not firmly attached. After the second DNA replication hyphallengthening commenced with an increase in the content of glucan but the walls lacked rigidity. At the time of the third replication walls underwent a change which commenced at the hyphal tip and worked back to the rhizoids, converting the hyphae to a rigid, cylindrical shape. Branching commenced after the fourth replication of DN
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Bauer, Yasmina, Philipp Knechtle, Jürgen Wendland, Hanspeter Helfer, and Peter Philippsen. "A Ras-like GTPase Is Involved in Hyphal Growth Guidance in the Filamentous Fungus Ashbya gossypii." Molecular Biology of the Cell 15, no. 10 (2004): 4622–32. http://dx.doi.org/10.1091/mbc.e04-02-0104.

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Characteristic features of morphogenesis in filamentous fungi are sustained polar growth at tips of hyphae and frequent initiation of novel growth sites (branches) along the extending hyphae. We have begun to study regulation of this process on the molecular level by using the model fungus Ashbya gossypii. We found that the A. gossypii Ras-like GTPase Rsr1p/Bud1p localizes to the tip region and that it is involved in apical polarization of the actin cytoskeleton, a determinant of growth direction. In the absence of RSR1/BUD1, hyphal growth was severely slowed down due to frequent phases of pau
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Ajme, Gufran Moneam, and Ali Hussein Shuaa. "Mathematical Model of Tip-hypha Anastomosis and Dichotomous Branching with Hyphal Death." Journal of Physics: Conference Series 1963, no. 1 (2021): 012087. http://dx.doi.org/10.1088/1742-6596/1963/1/012087.

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Kornitzer, Daniel. "Regulation of Candida albicans Hyphal Morphogenesis by Endogenous Signals." Journal of Fungi 5, no. 1 (2019): 21. http://dx.doi.org/10.3390/jof5010021.

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Candida albicans is a human commensal fungus that is able to assume several morphologies, including yeast, hyphal, and pseudohyphal. Under a range of conditions, C. albicans performs a regulated switch to the filamentous morphology, characterized by the emergence of a germ tube from the yeast cell, followed by a mold-like growth of branching hyphae. This transition from yeast to hyphal growth has attracted particular attention, as it has been linked to the virulence of C. albicans as an opportunistic human pathogen. Signal transduction pathways that mediate the induction of the hyphal transcri
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Dissertations / Theses on the topic "Hyphal branching"

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McNaughton, Fergus Samuel. "The Role of F-actin in Hyphal Branching." Thesis, University of Canterbury. Biological Sciences, 2005. http://hdl.handle.net/10092/1288.

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Hyphal organisms are a commonly used model system for studies of polarised growth. While growing hyphal tips offer a good example of polarised growth, little detail of the process of polarisation can be determined from them. Hyphal branching offers a good example of the development of polarity, however to date it has been largely impractical to study hyphal branching, due to the irregular timing and location along the hypha of natural branch formation. Chemical induction of branches circumnavigates this problem, using a localised concentration of nutrients adjacent to the growing hypha to stim
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Pollerman, Sarah Elizabeth. "An analysis of the molecular biology of hyphal branching in Aspergillus." Thesis, University of Sheffield, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.484208.

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Swadel, Emma Kate. "An Investigation into the Underlying Mechanisms of Hyphal Branching in Filamentous Microorganisms." Thesis, University of Canterbury. Biological Sciences, 2013. http://hdl.handle.net/10092/8558.

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Understanding how hyphal organisms grow and develop is essential in order to manipulate mycelial colonies for purposes such as disease prevention and food production. One aspect of hyphal development that is not well understood is hyphal branching. Hyphal organisms branch as a way of creating new hyphal tips required for the search for nutrients, the acquisition of these nutrients and for hyphal fusion events that facilitate communication of signals within a mycelial colony. This investigation focused on the branching process occurring in the fungus N. crassa and in the oomycete A. bisexualis.
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Kyriakopoulou, Garyfallia. "Molecular cloning of three different Achlya ambisexualis hsp70 cDNAs, and changes in the accumulation of hsp70 transcript populations during hyphal branching." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp02/NQ35215.pdf.

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Books on the topic "Hyphal branching"

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Kyriakopoulou, Garyfallia. Molecular cloning of three different Achlya ambisexualis hsp70 cDNAs, and changes in the accumulation of hsp70 transcript populations during hyphal branching. 1998.

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Book chapters on the topic "Hyphal branching"

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Nagahashi, Gerald, and David D. Douds. "Environmental Factors That Affect Presymbiotic Hyphal Growth and Branching of Arbuscular Mycorrhizal Fungi." In Soil Biology. Springer Berlin Heidelberg, 2005. http://dx.doi.org/10.1007/3-540-27331-x_6.

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Rogosa, Morrison, Micah I. Krichevsky, and Rita R. Colwell. "Branching, Hyphae, and Production of Asexual Spores." In Springer Series in Microbiology. Springer New York, 1986. http://dx.doi.org/10.1007/978-1-4612-4986-3_10.

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Smith, Stephanie J., and Rohini J. Manuel. "The Biology of Fungi." In Tutorial Topics in Infection for the Combined Infection Training Programme. Oxford University Press, 2019. http://dx.doi.org/10.1093/oso/9780198801740.003.0009.

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Fungi are found ubiquitously in the environment such as soil, water, and food. There are an estimated 1.5 million fungal species worldwide, although this number is felt to be grossly underestimated and is regularly updated. Of these vast numbers, around 500 fungi to date have been implicated in human disease. As opposed to bacteria, which are prokaryotes, fungi are eukaryotes, meaning they have a well-defined nucleus and have membrane- bound organelles in the cytoplasm, including an endoplasmic reticulum and a golgi apparatus. In 1969, the scientist R. H. Whittaker first proposed that organisms be classified into five kingdoms: Monera (Bacteria), Protista (Algae and Protozoans), Plantae (Plants), Mycetae (Fungi), and Animalia (Animals). Since then, there have been dramatic changes to the classifications of fungi, largely due to the appliance of phylogenetic molecular techniques. This has resulted in variances to the number of phylums, and the species assigned to them. Table 3.1 shows the seven phyla of the Fungi Kingdom. The majority of fungi pathogenic to humans inhabit the Ascomycota and Basidiomycota phyla. Fungi used to be dually named if they had a pleomorphic life cycle with sexual/ asexual stages (teleomorph/ anamorph, respectively), which meant that fungi often had two names and were classed differently. This practice was discontinued in January 2013 after the International Commission on the Taxonomy of Fungi decided that a ‘one fungus, one name’ approach should be followed. Fungi can be unicellular (yeast) or multicellular (fungi). Yeasts may look globose in nature when grown, whereas multicellular fungi grow as tubular, filamentous material called hyphae that can create a branching, hyphal network called a mycelium. Hyphae may have septa that cross their walls or be nonseptate, which is a method of differentiating fungi. An early hyphal outgrowth from a spore is called a germ tube. The germ tube test can be used to differentiate the yeasts Candida albicans and Candida dubliniensis from other Candida species. The fungal cell wall is composed of chitin and glucans, which are different components to the human cell wall. This means that they can be an effective target for antifungal therapy.
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