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Relevant bibliographies by topics / Agrobacterium tumefaciens-mediated transformation of fungi

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Academic literature on the topic 'Agrobacterium tumefaciens-mediated transformation of fungi'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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Dissertations / Theses on the topic "Agrobacterium tumefaciens-mediated transformation of fungi"

1

Knight, Claire Jane. "Investigation into agrobacterium-mediated transformation of fungi in nauture." Thesis, University of Bristol, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.500434.

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2

Zemska, Olga. "Discovery Of Intracellular Growth Requirements of the Fungal Pathogen Histoplasma capsulatum." The Ohio State University, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=osu1343803044.

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3

Meyer, Tania. "Agrobacterium tumefaciens-mediated transformation of Fusarium oxysporum f. sp. cubense for pathogenicity gene analysis." Pretoria : [s.n.], 2009. http://upetd.up.ac.za/thesis/available/etd-06122009-132700/.

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4

Meyer, Tanja. "Agrobacterium tumefaciens-mediated transformation of Fusarium oxysporum f. sp. cubense for pathogenicity gene analysis." Diss., University of Pretoria, 2008. http://hdl.handle.net/2263/25473.

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Fusarium wilt of banana, caused by Fusarium oxysporum f. sp. cubense (Foc), is one of the most destructive plant diseases in recorded history. The disease was first discovered in Australia in 1874 but became renowned for the severe losses it caused to export banana plantations during the 1960s in Central America. The banana export industry was saved only by replacing Gros Michel bananas, the dessert banana grown for the export market, with highly resistant Cavendish banana cultivars. Despite this apparent solution, the fungus was found to attack Cavendish bananas in the sub-tropics, where plan

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5

Celikkol, Akcay Ufuk. "Regeneration Of Lentil (lens Culinaris Medik) And Genetic Transformation By Using Agrobacterium Tumefaciens-mediated Gene Transfer." Phd thesis, METU, 2008. http://etd.lib.metu.edu.tr/upload/3/12609425/index.pdf.

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In this study, the effects of different plant growth regulators on regeneration responses of various lentil explants through direct and indirect organogenesis and through somatic embryogenesis from calli and cell suspension cultures were investigated. Shoot regeneration was obtained in low frequencies from longitudinal embryonic axis explants and nodal buds of epicotyls, however whole plant regeneration was unsuccessful. Conditions provided for indirect organogenesis resulted only in swelling of hypocotyls and root directed ends of internodes and weak callus formation on leaves which were foll

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6

Dube, Thabani. "The use of the broad-host-range plasmid, pTF-FC2, in Agrobacterium tumefaciens mediated plant transformation." Doctoral thesis, University of Cape Town, 2002. http://hdl.handle.net/11427/4255.

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Bibliography: leaves 165-195.<br>The transfer of T-DNA from Agrobacterium tumefaciens to eukaryotic cells is on of the most extensively studied examples of interkingdom DNA transfer. This transfer system has revolutionized plant molecular biology to the extent that the introduction of foreign genes into plant genomes is now a basic technique. Apart from the finding that a defined segment (T-DNA) of the A. tumefaciens Ti plasmid can be transferred to plant DNA, the discovery that the mobilization functions of the IncQ plasmid, RSF1010, can mediate its transfer from A. tumefaciens into plant ce

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7

Akpadock, Evelyn. "Analysis of a ufdB Penicillium marneffei Mutant Generated by Agrobacterium tumefaciens-Mediated Transformation." Youngstown State University / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1377083669.

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8

Demirbas, Didem. "Optimization Of Regeneration And Agrobacterium Mediated Transformation Of Wheat (triticum Aestivum L.cv. Yuregir 89)." Master's thesis, METU, 2004. http://etd.lib.metu.edu.tr/upload/3/12605454/index.pdf.

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The objective of this study was to optimize regeneration parameters of immature inflorescence culture of Triticum aestivum cv. Y&uuml<br>regir-89. The effects of dark incubation period and explant region on regeneration success were tested. Immature inflorescences were cut into 3 pieces as tip, mid, base and put onto 2mg /L 2,4-dichlorophenoxyacetic acid containing callus induction medium. These explants were taken to regeneration after 6, 9, 13 weeks of dark incubation period. The regeneration capacities of calli were determined as rooting and shooting percentages. Shooting percentages were f

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9

Baloglu, Cengiz Mehmet. "Optimization Of Regeneration And Agrobacterium Mediated Transformation Of Sugar Beet (beta Vulgaris L.)." Master's thesis, METU, 2005. http://etd.lib.metu.edu.tr/upload/3/12606476/index.pdf.

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In this study, optimization of a transformation and regeneration system via indirect and direct organogenesis in cotyledon, hypocotyl, petiole, leaf and shoot base tissues of sugar beet (Beta vulgaris L. cv. ELK 345 and 1195) was investigated. Two different germination, three different callus induction and shoot induction medium was used for indirect organogenesis of sugar beet cultivar ELK 345. Except cotyledon, other explants (hypocotyl, petiole and leaf) produced callus. However no shoot development was observed from callus of these explants. Shoot base tissue of sugar beet cultivar 1195 wa

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10

Oz, M. Tufan. "Optimization Of Selection Conditions And Agrobacterium Mediated Transformation Of Chickpea (cicer Arietinum L. Cv. Gokce)." Master's thesis, METU, 2005. http://etd.lib.metu.edu.tr/upload/3/12605842/index.pdf.

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The objective of this study was to optimize an efficient selection system and Agrobacterium mediated transformation of chickpea (Cicer arietinum L.). Cotyledonary node explants of Turkish chickpea cultivar G&ouml<br>k&ccedil<br>e were used to determine the effects of selective agents, two antibiotics (Kanamycin, Hygromycin) and two herbicides (PPT, Glyphosate) as well as four antibiotics (Augmentin, Carbenicillin, Cefotaxime, Timentin) for eliminating Agrobacterium on multiple shoot and root induction. Selective agents and antibiotics were applied to explants at different concentrations for

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