Green fluorescent protein as a visual selection marker for coffee transformation |
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Authors: | Manoj K Mishra Santosini Devi Alex McCormac Nigel Scott DongFang Chen Malcolm Elliott Adrian Slater |
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Institution: | 1.The Norman Borlaug Institute for Plant Science Research,De Montfort University,Leicester,UK;2.Central Coffee Research Institute,Coffee Research Station,Karnataka,India;3.The Biomolecular Technology Group, Faculty of Health and Life Sciences,De Montfort University,Leicester,UK |
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Abstract: | The green fluorescent protein (GFP) was used as a visual selectable marker to produce transgenic coffee (Coffea canephora) plants following Agrobacterium-mediated transformation. The binary vector pBECKS 2000.7 containing synthetic gene for GFP (sgfp) S65T and the hygromycin phosphotransferase gene hph both controlled by 35S cauliflower mosaic virus CaMV35S promoters was used for transformation. Embryogenic cultures were initiated from hypocotyls and cotyledon leaves of in vitro grown seedlings and used as target material. Selection of transformed tissue was carried out using GFP visual selection as
the sole screen or in combination with a low level of antibiotics (hygromycin 10 mg/L), and the efficiency was compared with
antibiotics selection alone (hygromycin 30 mg/L). GFP selection reduced the time for transformed somatic embryos formation
from 18 weeks on a hygromycin (30 mg/L) antibiotics containing medium to 8 weeks. Moreover, visual selection of GFP combined
with low level of antibiotics selection improved the transformation efficiency and increased the number of transformed coffee
plants compared to selection in the presence of antibiotics. Molecular analysis confirmed the presence of the sgfp-S65T coding region in the regenerated plants. Visual screening of transformed cells using GFP by Agrobacterium-mediated transformation techniques was found to be efficient and therefore has the potential for development of selectable
marker-free transgenic coffee plants. |
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