Agrobacterium-mediated transformation of Melastoma malabathricum and Tibouchina semidecandra with sense and antisense dihydroflavonol-4-reductase (DFR) genes

被引:11
|
作者
Yong, Wilson Thau Lym [1 ]
Abdullah, Janna Ong [2 ]
Mahmood, Maziah [3 ]
机构
[1] Univ Malaysia Sabah, Biotechnol Res Inst, Kota Kinabalu 88999, Sabah, Malaysia
[2] Univ Putra Malaysia, Fac Biotechnol & Biomol Sci, Dept Microbiol, Serdang 43400, Malaysia
[3] Univ Putra Malaysia, Fac Biotechnol & Biomol Sci, Dept Biochem, Serdang 43400, Malaysia
关键词
Agrobacterium-mediated transformation; Melastoma malabathricum; Tibouchina semidecandra; Dihydroflavonol-4-reductase gene; Colour; CELL-SUSPENSIONS; WATER RELATIONS; PLANTS; BIOSYNTHESIS; BOMBARDMENT; EXPRESSION; GFP; OPTIMIZATION; REGENERATION; TUMEFACIENS;
D O I
10.1007/s11240-008-9460-3
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Genetic engineering of a wide variety of plant species has led to the improvement of plant traits. In this study, the genetic transformation of two potentially important flowering ornamentals, Melastoma malabathricum and Tibouchina semidecandra, with sense and antisense dihydroflavonol-4-reductase (DFR) genes using the Agrobacterium-mediated method was carried out. Plasmids pBETD10 and pBETD11, each harbouring the DFR gene at different orientations (sense and antisense) and selectable marker nptII for kanamycin resistance, were used to transform M. malabathricum and T. semidecandra under the optimized transformation protocol. Putative transformants were selected in the presence of kanamycin with their respective optimized concentration. The results indicated that approximately 4.0% of shoots and 6.7% of nodes for M. malabathricum regenerated after transforming with pBETD10, whereas only 3.7% (shoots) and 5.3% (nodes) regenerated with pBETD11 transformation. For the selection of T. semidecandra, 5.3% of shoots and 9.3% of nodes regenerated with pBETD10 transformation, while only 4.7% (shoots) and 8.3% (nodes) regenerated after being transformed with pBETD11. The presence and integration of the sense and antisense DFR genes into the genome of M. malabathricum and T. semidecandra were verified by polymerase chain reaction (PCR) and nucleotide sequence alignment and confirmed by southern analysis. The regenerated putative transformants were acclimatized to glasshouse conditions. Approximately 31.0% pBETD10-transformed and 23.1% pBETD11-transformed M. malabathricum survived in the glasshouse, whereas 69.4% pBETD10-transformed and 57.4% pBETD11-transformed T. semidecandra survived. The colour changes caused by transformation were observed at the budding stage of putative T. semidecandra transformants where greenish buds were produced by both T. semidecandra harbouring the sense and antisense DFR transgenes. Besides that, the production of four-petal flowers also indicated another morphological difference of putative T. semidecandra transformants from the wild type plants which produce five-petal flowers.
引用
收藏
页码:59 / 67
页数:9
相关论文
共 4 条
  • [1] Agrobacterium-mediated transformation of Melastoma malabathricum and Tibouchina semidecandra with sense and antisense dihydroflavonol-4-reductase (DFR) genes
    Wilson Thau Lym Yong
    Janna Ong Abdullah
    Maziah Mahmood
    Plant Cell, Tissue and Organ Culture, 2009, 96 : 59 - 67
  • [2] Enhancers of Agrobacterium-mediated Transformation of Tibouchina semidecandra Selected on the Basis of GFP Expression
    Yong, Wilson Thau Lym
    Henry, Erle Stanley
    Abdullah, Janna Ong
    TROPICAL LIFE SCIENCES RESEARCH, 2010, 21 (02) : 115 - 130
  • [3] Transformation of Antisense Dihydroflavonal 4-Reductase (DFR) into Sacred Lotus 'Buntharik' Using Agrobacterium-Mediated Gene Transfer
    Saetiew, K.
    Leethaweesup, W.
    Parinthawong, N.
    Arunyanart, S.
    INTERNATIONAL SYMPOSIUM ON ORCHIDS AND ORNAMENTAL PLANTS, 2014, 1025 : 99 - 106
  • [4] Isolation and location of three homoeologous dihydroflavonol-4-reductase (DFR) genes of wheat and their tissue-dependent expression
    Himi, E
    Noda, K
    JOURNAL OF EXPERIMENTAL BOTANY, 2004, 55 (396) : 365 - 375