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Please use this identifier to cite or link to this item:
http://krishi.icar.gov.in/jspui/handle/123456789/51344
Title: | In vitro regeneration of coconut plantlets from immature inflorescence. |
Other Titles: | Not Available |
Authors: | Shareefa, M., Thomas, R.J., Sreelekshmi, J.S., Rajesh, M. K. and Anitha Karun |
ICAR Data Use Licennce: | http://krishi.icar.gov.in/PDF/ICAR_Data_Use_Licence.pdf |
Author's Affiliated institute: | ICAR::Central Plantation Crops Research Institute |
Published/ Complete Date: | 2019-09-10 |
Project Code: | 1000761031 |
Keywords: | clonal fidelity, coconut, in vitor regeneration, rachillae |
Publisher: | Current Science Association |
Citation: | Shareefa, M., Thomas, R.J., Sreelekshmi, J.S., Rajesh, M. K. and Anitha Karun. 2019. In vitro regeneration of coconut plantlets from immature inflorescence. Current Science 117 (5): 813-820 Not Available |
Series/Report no.: | Not Available; |
Abstract/Description: | Clonal propagation of elite, disease-free coconut palms is a promising technique for producing uniform planting material with high yield and disease resistance. Over the past few decades cloning of coconut has been attempted in a number of laboratories worldwide; however, success has been limited. In the present study, immature inflorescences of 2–12 cm size were collected from West Coast Tall variety and the rachilla segments were cultured on four different media combinations in dark condition. White translucent outgrowths were maximum in Y3 medium supplemented with 4.54 μM 2,4-dichlorophenoxyacetic acid (92%) followed by medium 72 with 41.4 μM picloram, 61.8 μM putrescine and 4.54 μM thidiazuron (TDZ) (87%). After eight weeks in dark, shoot-like outgrowth was noticed more in Y3 III (65%) followed by Y3 I. After eight months dark incubation, the cultures were transferred to 1/2 Murashige and Skoog (MS) with two hormone combinations and high frequency of multiple shoot formation was noticed in 1/2 MS with 5.37 μM naphthalene acetic acid (NAA) and 4.44 μM 6-benzylaminopurine (BAP). Maximum shoot development was observed Y3 medium fortified with 5 μM 2-isopentenyl adenine (2ip) and 5 μM BAP. The individual shoots after development of 3–4 leaves were transferred to 1/2 Y3 medium supplemented with 5.37 μM NAA and 24.6 μM indole-3-butyric acid (IBA), and root initiation was observed in 39.28% plantlets. Start codon targeted (SCoT) profiling based on banding pattern of PCR-amplified products confirmed the clonal fidelity of in vitro regenerated coconut plantlets. The study indicates the possibility of developing an in vitro regeneration protocol for coconut using immature inflorescence explants. |
Description: | Not Available |
ISSN: | Not Available |
Type(s) of content: | Journal |
Sponsors: | Not Available |
Language: | English |
Name of Journal: | Current Science |
Journal Type: | Fortnightly Multidisciplinary Research Journal |
NAAS Rating: | 6.73 |
Impact Factor: | 0.756 |
Volume No.: | 117 (5) |
Page Number: | 813-820 |
Name of the Division/Regional Station: | Crop Improvement |
Source, DOI or any other URL: | doi: 10.18520/cs/v117/i5/813-820 |
URI: | http://krishi.icar.gov.in/jspui/handle/123456789/51344 |
Appears in Collections: | HS-CPCRI-Publication |
Files in This Item:
File | Description | Size | Format | |
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In vitro current science.pdf | 4.96 MB | Adobe PDF | View/Open |
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