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dc.contributor.advisorPatil, Bhimanagouda S.
dc.contributor.advisorCrosby, Kevin M.
dc.creatorRen, Yan
dc.date.accessioned2012-02-14T22:20:57Z
dc.date.accessioned2012-02-16T16:18:12Z
dc.date.available2014-01-15T07:05:32Z
dc.date.created2011-12
dc.date.issued2012-02-14
dc.date.submittedDecember 2011
dc.identifier.urihttps://hdl.handle.net/1969.1/ETD-TAMU-2011-12-10707
dc.description.abstractGenetic transformation is a useful tool to incorporate novel genes, potentially allowing sexual incompatibility and interspecific barriers to be circumvented. The purpose of this study was to improve beta-carotene levels in melon fruits by transferring a phytoene synthase (PSY) gene. At present, there are not sufficient regeneration and transformation studies reported on two commercially important melon types - western shipper cantaloupe and honeydew. To establish a high efficiency shoot regeneration system, we evaluated three types of explants in our elite breeding lines. A shoot tip with a hypocotyl and cotyledon fragments, regenerated shoots whereas a shoot tip with a hypocotyl without cotyledon, did not produce regenerants. Murashige & Skoog (MS) basal medium with 1 mg 1⁻¹ benzyladenine (BA), 0.26 mg 1⁻¹ abscisic acid (ABA) and 0.8 mg 1⁻¹ indole-3-acetic acid (IAA) was the best for regeneration from cotyledon explants in cantaloupe 'F39'. MS basal medium with 1 mg 1⁻¹ BA and 0.26 mg 1⁻¹ ABA was chosen for honeydew '150' to solve a curving-up problem of explants. Fifty to sixty percent of regenerants were found to be polyploids. To establish a reliable Agrobacterium-mediated transformation protocol, kanamycin sensitivity as well as Timentin[trademark] and Clavamox® were evaluated. Kanamycin 200 and 150 mg 1⁻¹ were chosen as the threshold levels for 'F39' and '150' respectively. No significant differences were found between Timentin[trademark] and Clavamox® in 'F39'; however, Clavamox® reduced the incidence of vitrification and increased the frequency of shoot elongation in '150'. A. tumefaciens strain EHA105, harboring pCNL56 carrying nptII and gusA genes, was used to establish a transformation protocol. The transformation efficiency was 0.3% from 'F39' and 0.5% from '150'. We introduced a watermelon PSY-C gene under the control of a fruit-specific promoter of a polygalacturonase gene into '150'. All the transgenic plants were tetraploids based on flow cytometry assays. Up to 32-fold of beta-carotene was elevated in the rind tissue of transgenic honeydew including phytoene increase. This is a very promising result for a further investigation to increase beta-carotene level in flesh tissue using the PSY-C gene with an appropriate promoter.en
dc.format.mimetypeapplication/pdf
dc.language.isoen_US
dc.subjectMelonen
dc.subjecttransformationen
dc.subjectbeta-caroteneen
dc.subjectPSY-Cen
dc.titleGenetic Engineering of Beta-Carotene Production in Honeydew Melons (Cucumis melo L. inodorus)en
dc.typeThesisen
thesis.degree.departmentHorticultural Sciencesen
thesis.degree.disciplineHorticultureen
thesis.degree.grantorTexas A&M Universityen
thesis.degree.nameDoctor of Philosophyen
thesis.degree.levelDoctoralen
dc.contributor.committeeMemberGould, Jean H.
dc.contributor.committeeMemberRathore, Keerti S.
dc.type.genrethesisen
dc.type.materialtexten
local.embargo.terms2014-01-15


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