unsuccessful in vitro regeneration from phalaenopsis (orchidaceae) flowers

Clicks: 182
ID: 148128
2014
Article Quality & Performance Metrics
Overall Quality
Not rated
Combines reader engagement with the AI quality analysis. This article has not been analysed, so there is no overall score — reader engagement is measured and shown alongside.
AI Quality Assessment
Not analyzed
Mint this article as an NFT
Not yet minted

Create a permanent, verifiable on-chain record of this article on the Scimatic Network. The NFT is held in your Journament account, and you can withdraw it to your own wallet at any time.

5 SUSD one-off · no wallet required
Abstract
Regeneration in vitro has never been achieved from flower parts from members of the Orchidaceae and no report exists for Phalaenopsis. Studies that do exist all used immature (unopened) flower buds. In a bid to overcome this hurdle, in vitro organogenesis was attempted with various parts (dorsal sepal (base + center + tip); petal (base + center + tip); lateral sepal (base + center + tip); labellum (base + center + tip); pedicel (outer + inner tissue); column; anther cap; stigmatic surface) of immature and fully opened Phalaenopsis Gallant Beau ‘George Vazquez’ flowers. Despite the use of an extremely wide selection of plant growth regulators in Vacin and Went basal medium, and their concentrations, in both darkness and light conditions, no organogenesis could be achieved from any of the flower parts tested. Some callus was obtained on the column in response to 2 or 4 mg/l TDZ in the light, or to 1 mg/l 2,4-D and 1 mg/l dicamba in the dark, but the callus was hard and could not be further proliferated or induced to form organs. Although negative, these trials provide encouraging signs that organogenesis may be possible from flower parts with a little more insistence. To be able to achieve such regeneration would potential allow for the generation of haploid or polyploidy plants which may have practical use in orchid breeding and biotechnology if such plants (or plant parts) can be clonally propagated.
Reference Key
silva2014allunsuccessful Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors ;Jaime Teixeira da Silva
Journal all results journals: biol
Year 2014
DOI
DOI not found
URL
Keywords

Citations

No citations found. To add a citation, contact the admin at info@scimatic.org

No comments yet. Be the first to comment on this article.