Development of an Efficient <i>Agrobacterium</i> Mediated Transformation Protocol for Sri Lankan Rice Variety - Bg 250
Experiments were conducted to establish an efficient and simple protocol for regeneration and <em>Agrobacterium</em> mediated genetic transformation of an agronomically important <em>indica</em> rice variety Bg 250. Callus induction was achieved on modified N6B5 medium supple...
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Postgraduate Institute of Agriculture, University of Peradeniya
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doaj-311c21c503d5441ab647025942a1689b2020-11-25T02:22:44ZengPostgraduate Institute of Agriculture, University of PeradeniyaTropical Agricultural Research1016-14222011-01-01221455310.4038/tar.v22i1.26692259Development of an Efficient <i>Agrobacterium</i> Mediated Transformation Protocol for Sri Lankan Rice Variety - Bg 250RMLK Ratnayake0GHCM Hettiarachchi1Department of Chemistry Faculty of Science, University of ColomboDepartment of Chemistry Faculty of Science, University of ColomboExperiments were conducted to establish an efficient and simple protocol for regeneration and <em>Agrobacterium</em> mediated genetic transformation of an agronomically important <em>indica</em> rice variety Bg 250. Callus induction was achieved on modified N6B5 medium supplemented with 2,4 –D (2.0 mg/L), BAP (1.0 mg/L) and NAA (1.0 mg/L). The maximum callusing frequency of 90% was observed after 21 days followed by 4 days of incubation on callus induction medium under dark. The highly prolific, nodular, compact yellowish large calli produced after 25 days were first checked for regeneration ability. Ninety five percent of regeneration frequency was observed with N<sub>6</sub>B<sub>5</sub> medium supplemented with 3.0 mg/L BAP and 1.5 mg/L NAA. Therefore, embryonic calli induced after 25 days were used for genetic transformation in subsequent experiments. <em>Agrobacterium tumefaciens</em> strain GV 3101 was transformed with pCAMBIA 1303 binary vector which contains hygromycin marker and GUS reporter gene. The transformed colonies were selected on 50 mg/L kanamycin and 25 mg/L rifampicin and confirmed by colony PCR. The PCR positive colonies were used to transform Bg 250 rice calli. The maximum transformation efficiency of 20% was obtained using 500 mg/L cefotaxime as a bacteriostatic agent to inhibit growth of <em>Agrobacterium</em>. 100 μM acetosyringone in co-cultivation medium and cocultivation for 3 days were the optimum conditions for maximum transformation. The expression of GUS gene revealed that the calli were successfully transformed. <br /><br /><strong>Key words: </strong><em>Agrobacterium</em>; Bg 250; Callus induction; Rice transformation. <br /><br />DOI: 10.4038/tar.v22i1.2669<br /><br /><em>Tropical Agricultural Research </em>Vol. 22 (1): 45-53 (2010)https://tar.sljol.info/articles/2669agrobacteriumbg 250callus inductionrice transformation |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
RMLK Ratnayake GHCM Hettiarachchi |
spellingShingle |
RMLK Ratnayake GHCM Hettiarachchi Development of an Efficient <i>Agrobacterium</i> Mediated Transformation Protocol for Sri Lankan Rice Variety - Bg 250 Tropical Agricultural Research agrobacterium bg 250 callus induction rice transformation |
author_facet |
RMLK Ratnayake GHCM Hettiarachchi |
author_sort |
RMLK Ratnayake |
title |
Development of an Efficient <i>Agrobacterium</i> Mediated Transformation Protocol for Sri Lankan Rice Variety - Bg 250 |
title_short |
Development of an Efficient <i>Agrobacterium</i> Mediated Transformation Protocol for Sri Lankan Rice Variety - Bg 250 |
title_full |
Development of an Efficient <i>Agrobacterium</i> Mediated Transformation Protocol for Sri Lankan Rice Variety - Bg 250 |
title_fullStr |
Development of an Efficient <i>Agrobacterium</i> Mediated Transformation Protocol for Sri Lankan Rice Variety - Bg 250 |
title_full_unstemmed |
Development of an Efficient <i>Agrobacterium</i> Mediated Transformation Protocol for Sri Lankan Rice Variety - Bg 250 |
title_sort |
development of an efficient <i>agrobacterium</i> mediated transformation protocol for sri lankan rice variety - bg 250 |
publisher |
Postgraduate Institute of Agriculture, University of Peradeniya |
series |
Tropical Agricultural Research |
issn |
1016-1422 |
publishDate |
2011-01-01 |
description |
Experiments were conducted to establish an efficient and simple protocol for regeneration and <em>Agrobacterium</em> mediated genetic transformation of an agronomically important <em>indica</em> rice variety Bg 250. Callus induction was achieved on modified N6B5 medium supplemented with 2,4 –D (2.0 mg/L), BAP (1.0 mg/L) and NAA (1.0 mg/L). The maximum callusing frequency of 90% was observed after 21 days followed by 4 days of incubation on callus induction medium under dark. The highly prolific, nodular, compact yellowish large calli produced after 25 days were first checked for regeneration ability. Ninety five percent of regeneration frequency was observed with N<sub>6</sub>B<sub>5</sub> medium supplemented with 3.0 mg/L BAP and 1.5 mg/L NAA. Therefore, embryonic calli induced after 25 days were used for genetic transformation in subsequent experiments. <em>Agrobacterium tumefaciens</em> strain GV 3101 was transformed with pCAMBIA 1303 binary vector which contains hygromycin marker and GUS reporter gene. The transformed colonies were selected on 50 mg/L kanamycin and 25 mg/L rifampicin and confirmed by colony PCR. The PCR positive colonies were used to transform Bg 250 rice calli. The maximum transformation efficiency of 20% was obtained using 500 mg/L cefotaxime as a bacteriostatic agent to inhibit growth of <em>Agrobacterium</em>. 100 μM acetosyringone in co-cultivation medium and cocultivation for 3 days were the optimum conditions for maximum transformation. The expression of GUS gene revealed that the calli were successfully transformed. <br /><br /><strong>Key words: </strong><em>Agrobacterium</em>; Bg 250; Callus induction; Rice transformation. <br /><br />DOI: 10.4038/tar.v22i1.2669<br /><br /><em>Tropical Agricultural Research </em>Vol. 22 (1): 45-53 (2010) |
topic |
agrobacterium bg 250 callus induction rice transformation |
url |
https://tar.sljol.info/articles/2669 |
work_keys_str_mv |
AT rmlkratnayake developmentofanefficientiagrobacteriumimediatedtransformationprotocolforsrilankanricevarietybg250 AT ghcmhettiarachchi developmentofanefficientiagrobacteriumimediatedtransformationprotocolforsrilankanricevarietybg250 |
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