Please use this identifier to cite or link to this item:
http://nopr.niscpr.res.in/handle/123456789/17173Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Chaturvedi, H C | - |
| dc.contributor.author | Agnihotri, S | - |
| dc.contributor.author | Sharllla, M | - |
| dc.contributor.author | Sharma, A K | - |
| dc.contributor.author | Jain, M | - |
| dc.contributor.author | Chourasia, A | - |
| dc.date.accessioned | 2013-04-20T14:35:07Z | - |
| dc.date.available | 2013-04-20T14:35:07Z | - |
| dc.date.issued | 2003-11 | - |
| dc.identifier.issn | 0975-1009 (Online); 0019-5189 (Print) | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/17173 | - |
| dc.description | 1311-1316 | en_US |
| dc.description.abstract | Nucellar tissue contained in ovular halves of young fruits of Mangifera indica L. totapari red small, a dwarfing rootstock, differentiated fasciated embryonal structures in presence of 6-benzylaminopurine [BA P(0.15 mg l-1)] 1, 6-(γ-γ-dimethylallylamino) purine [2iP(0.15 mg l-1)] and indole-3- acetic acid [(IAA(0.5 mg l-1)] incorporated in the semisolid medium during 50-60 days. Due to embryonal fasciation, hardly 2-3 well-formed embryos could be obtained per culture of proliferating embryos. Of the 3 ethylene inhibitors [ L-α-(2-aminoethoxyvinyl)-glycine-HCl (AVG), AgNO3, and salicylic acid (SA)]used, embryonal fasciation and necrosis of intervening tissue was completely control led by 3-4 subcultures of fasciated mass of embryos under the influenee of AVG (0.05 mg l‑1) in presence of adenine sulphate [AdS (50mg l-1)] incorporated in the same medium. Almost synchronized development of isolated embryos, measuring ca 2 cm in length, was observed in a different medium used in liquid stationary state and supplemented. particularly with stress-producing substances [abscisic acid (ABA 0.01 mgl-1) : and polyethylene glycol (PEG, 100 mg l-1) besides certain other modifications, About 34% convertibility of processed embryos was obtained during a period of 90 days. The plantlets had well -developed roots along with laterals which were longer than leafy shoots. In vitro raised plants survived ex vitro for about 2 months. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | NISCAIR-CSIR, India | en_US |
| dc.rights | CC Attribution-Noncommercial-No Derivative Works 2.5 India | en_US |
| dc.source | IJEB Vol.41(11) [November 2003] | en_US |
| dc.subject | Convertibility of embryos | en_US |
| dc.subject | Dwarfing rootstock | en_US |
| dc.subject | Ethylene inhibitors | en_US |
| dc.subject | Fasciation of embryos | en_US |
| dc.subject | Mangifera indica totaparired small | en_US |
| dc.subject | Nucellar embryos | en_US |
| dc.title | In vitro control of fasciation in proliferating nucel1ar embryos of Mangifera indica L.var totapari red small for cloning | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJEB Vol.41(11) [November 2003] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJEB 41(11) 1311-1316.pdf | 1.39 MB | Adobe PDF | View/Open |
Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.