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In vitro regeneration of Ugandan passion fruit cultivars from leaf discs

OBJECTIVE: Passion fruit improvement efforts by conventional breeding have had limited success calling for research into alternative approaches such as tissue culture and genetic engineering. An efficient and reproducible regeneration system is a prerequisite for successful genetic engineering. Curr...

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Autores principales: Tuhaise, Samuel, Nakavuma, Jesca L., Adriko, John, Ssekatawa, Kenneth, Kiggundu, Andrew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6636056/
https://www.ncbi.nlm.nih.gov/pubmed/31311592
http://dx.doi.org/10.1186/s13104-019-4469-8
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author Tuhaise, Samuel
Nakavuma, Jesca L.
Adriko, John
Ssekatawa, Kenneth
Kiggundu, Andrew
author_facet Tuhaise, Samuel
Nakavuma, Jesca L.
Adriko, John
Ssekatawa, Kenneth
Kiggundu, Andrew
author_sort Tuhaise, Samuel
collection PubMed
description OBJECTIVE: Passion fruit improvement efforts by conventional breeding have had limited success calling for research into alternative approaches such as tissue culture and genetic engineering. An efficient and reproducible regeneration system is a prerequisite for successful genetic engineering. Currently, there is no reliable regeneration system for Uganda’s passion fruit varieties owing to the high heterogeneity of the Passiflora genus. Therefore, this study aimed at establishing an efficient and reproducible regeneration system for Uganda’s Passiflora edulis f. flavicarpa (yellow passion fruit) and Passiflora edulis f. edulis (purple passion fruit) for routine utilization with an ultimate goal of improving its agronomic value. RESULTS: The study successfully induced shoots by both direct and indirect organogenesis for the yellow passion fruit variety. Highest shoot induction frequency (14.85%) was achieved on 8.9 μM BAP while 7.9 μM BAP did not initiate any shoots. Optimal shoot elongation and rooting was achieved on 0.44 μM BAP and 5.37 µM α-naphthaleneacetic (NAA) respectively. Rooted yellow passion fruit plantlets were successfully weaned with over 65% survival rates. It took approximately 6 months to produce a weaned healthy passion fruit plant. The purple passion fruit variety proved to be recalcitrant to tissue culture with no successful shoot or callus induction. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13104-019-4469-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-66360562019-07-25 In vitro regeneration of Ugandan passion fruit cultivars from leaf discs Tuhaise, Samuel Nakavuma, Jesca L. Adriko, John Ssekatawa, Kenneth Kiggundu, Andrew BMC Res Notes Research Note OBJECTIVE: Passion fruit improvement efforts by conventional breeding have had limited success calling for research into alternative approaches such as tissue culture and genetic engineering. An efficient and reproducible regeneration system is a prerequisite for successful genetic engineering. Currently, there is no reliable regeneration system for Uganda’s passion fruit varieties owing to the high heterogeneity of the Passiflora genus. Therefore, this study aimed at establishing an efficient and reproducible regeneration system for Uganda’s Passiflora edulis f. flavicarpa (yellow passion fruit) and Passiflora edulis f. edulis (purple passion fruit) for routine utilization with an ultimate goal of improving its agronomic value. RESULTS: The study successfully induced shoots by both direct and indirect organogenesis for the yellow passion fruit variety. Highest shoot induction frequency (14.85%) was achieved on 8.9 μM BAP while 7.9 μM BAP did not initiate any shoots. Optimal shoot elongation and rooting was achieved on 0.44 μM BAP and 5.37 µM α-naphthaleneacetic (NAA) respectively. Rooted yellow passion fruit plantlets were successfully weaned with over 65% survival rates. It took approximately 6 months to produce a weaned healthy passion fruit plant. The purple passion fruit variety proved to be recalcitrant to tissue culture with no successful shoot or callus induction. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13104-019-4469-8) contains supplementary material, which is available to authorized users. BioMed Central 2019-07-16 /pmc/articles/PMC6636056/ /pubmed/31311592 http://dx.doi.org/10.1186/s13104-019-4469-8 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Note
Tuhaise, Samuel
Nakavuma, Jesca L.
Adriko, John
Ssekatawa, Kenneth
Kiggundu, Andrew
In vitro regeneration of Ugandan passion fruit cultivars from leaf discs
title In vitro regeneration of Ugandan passion fruit cultivars from leaf discs
title_full In vitro regeneration of Ugandan passion fruit cultivars from leaf discs
title_fullStr In vitro regeneration of Ugandan passion fruit cultivars from leaf discs
title_full_unstemmed In vitro regeneration of Ugandan passion fruit cultivars from leaf discs
title_short In vitro regeneration of Ugandan passion fruit cultivars from leaf discs
title_sort in vitro regeneration of ugandan passion fruit cultivars from leaf discs
topic Research Note
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6636056/
https://www.ncbi.nlm.nih.gov/pubmed/31311592
http://dx.doi.org/10.1186/s13104-019-4469-8
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