Agrobacterium-mediated transformation of oil palm (Elaeis guineensis jacq.) suspension culture
The life cycle of flowering plants in general can be divided into two growth phases: vegetative and reproductive. The reproductive phase can be subdivided into the development of the inflorescence meristem and floral meristems. Control of flowering and the regulation of plant architecture has bee...
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my-upm-ir.87262024-01-23T07:30:09Z Agrobacterium-mediated transformation of oil palm (Elaeis guineensis jacq.) suspension culture 2003-06 Roowi, Siti Habsah The life cycle of flowering plants in general can be divided into two growth phases: vegetative and reproductive. The reproductive phase can be subdivided into the development of the inflorescence meristem and floral meristems. Control of flowering and the regulation of plant architecture has been thoroughly investigated in a number of wellstudied dicot plants such as Arabidopsis, Antirrhinum, tomato and tobacco. However, in monocot plants, molecular information related to plant reproduction is still limited. In A rabidopsis , the Terminal Flowering I(TFLI) gene, LEAFY, and the target genes of CONSTANS (CO) including the FLOWERING LOCUS T (FI) and SUPPRESSOR OF OVEREXPRESSION OF COI (SOCI) genes, have a major role in promoting flowering and thus controlling flowering time. To investigate the regulation of meristem identity as well as the control of floral transition in oil palm, we transferred genes pCAMBIA/TFL1, pCAMBIA/JIT60, pCAMBIA/LFY, pGA/LFY and pCAMBIA/SOCl into oil palm embryogenic callus. This present study focuses on the optimization of Agrobacterium-mediated transformation and the analysis of transgenic plants. The objective of this study was also to clone the putative oil palm (OPSOCI and OPLFy) genes into a plasmid binary vector system, so as to transform these genes into oil palm embryogenic callus and to determine their effect on expression driven by a cauliflower mosaic virus (CaMV) 35S promoter in oil palm. The success of gene delivery using Agrobacterium into the plant genome is often based on several factors including temperature used during co-cultivation, the binary vector and promoters used, and the plant genotype itself. The most important factors contributing to the success of T -DNA transfer is the type of plant material used. We used embryogenic suspension cells as starting material for the transformation of oil palm because of the large numbers of totipotent cells found in these cultures. Agrobacterium Angiosperms Oil palm 2003-06 Thesis http://psasir.upm.edu.my/id/eprint/8726/ http://psasir.upm.edu.my/id/eprint/8726/1/FSMB_2003_19%20IR.pdf text en public masters Universiti Putra Malaysia Agrobacterium Angiosperms Oil palm Faculty of Food Science and Technology Harikrishna, K. English |
institution |
Universiti Putra Malaysia |
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PSAS Institutional Repository |
language |
English English |
advisor |
Harikrishna, K. |
topic |
Agrobacterium Angiosperms Oil palm |
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Agrobacterium Angiosperms Oil palm Roowi, Siti Habsah Agrobacterium-mediated transformation of oil palm (Elaeis guineensis jacq.) suspension culture |
description |
The life cycle of flowering plants in general can be divided into two growth phases:
vegetative and reproductive. The reproductive phase can be subdivided into the
development of the inflorescence meristem and floral meristems. Control of flowering and
the regulation of plant architecture has been thoroughly investigated in a number of wellstudied
dicot plants such as Arabidopsis, Antirrhinum, tomato and tobacco. However, in
monocot plants, molecular information related to plant reproduction is still limited. In A rabidopsis , the Terminal Flowering I(TFLI) gene, LEAFY, and the target genes of
CONSTANS (CO) including the FLOWERING LOCUS T (FI) and SUPPRESSOR OF
OVEREXPRESSION OF COI (SOCI) genes, have a major role in promoting flowering
and thus controlling flowering time.
To investigate the regulation of meristem identity as well as the control of floral
transition in oil palm, we transferred genes pCAMBIA/TFL1, pCAMBIA/JIT60,
pCAMBIA/LFY, pGA/LFY and pCAMBIA/SOCl into oil palm embryogenic callus. This
present study focuses on the optimization of Agrobacterium-mediated transformation and
the analysis of transgenic plants. The objective of this study was also to clone the putative
oil palm (OPSOCI and OPLFy) genes into a plasmid binary vector system, so as to
transform these genes into oil palm embryogenic callus and to determine their effect on
expression driven by a cauliflower mosaic virus (CaMV) 35S promoter in oil palm.
The success of gene delivery using Agrobacterium into the plant genome is often
based on several factors including temperature used during co-cultivation, the binary
vector and promoters used, and the plant genotype itself. The most important factors
contributing to the success of T -DNA transfer is the type of plant material used. We used
embryogenic suspension cells as starting material for the transformation of oil palm
because of the large numbers of totipotent cells found in these cultures. |
format |
Thesis |
qualification_level |
Master's degree |
author |
Roowi, Siti Habsah |
author_facet |
Roowi, Siti Habsah |
author_sort |
Roowi, Siti Habsah |
title |
Agrobacterium-mediated transformation of oil palm (Elaeis guineensis jacq.) suspension culture |
title_short |
Agrobacterium-mediated transformation of oil palm (Elaeis guineensis jacq.) suspension culture |
title_full |
Agrobacterium-mediated transformation of oil palm (Elaeis guineensis jacq.) suspension culture |
title_fullStr |
Agrobacterium-mediated transformation of oil palm (Elaeis guineensis jacq.) suspension culture |
title_full_unstemmed |
Agrobacterium-mediated transformation of oil palm (Elaeis guineensis jacq.) suspension culture |
title_sort |
agrobacterium-mediated transformation of oil palm (elaeis guineensis jacq.) suspension culture |
granting_institution |
Universiti Putra Malaysia |
granting_department |
Faculty of Food Science and Technology |
publishDate |
2003 |
url |
http://psasir.upm.edu.my/id/eprint/8726/1/FSMB_2003_19%20IR.pdf |
_version_ |
1794018777568903168 |