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Multiple shoot induction from axillary bud cultures of the medicinal orchid, Dendrobium longicornu
BACKGROUND AND AIMS: Dendrobium longicornu, commonly known as the ‘Long-horned Dendrobium’, is an endangered and medicinally important epiphytic orchid. Over-exploitation and habitat destruction seriously threaten this orchid in Northeast India. Our objective was to develop an efficient protocol for...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3491754/ https://www.ncbi.nlm.nih.gov/pubmed/23136638 http://dx.doi.org/10.1093/aobpla/pls032 |
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author | Dohling, Stadwelson Kumaria, Suman Tandon, Pramod |
author_facet | Dohling, Stadwelson Kumaria, Suman Tandon, Pramod |
author_sort | Dohling, Stadwelson |
collection | PubMed |
description | BACKGROUND AND AIMS: Dendrobium longicornu, commonly known as the ‘Long-horned Dendrobium’, is an endangered and medicinally important epiphytic orchid. Over-exploitation and habitat destruction seriously threaten this orchid in Northeast India. Our objective was to develop an efficient protocol for the mass propagation of D. longicornu using axillary bud segments. METHODOLOGY AND PRINCIPAL RESULTS: Axillary buds cultured in Murashige and Skoog semi-solid medium supplemented with α-naphthalene acetic acid (NAA), 2,4-dichlorophenoxy acetic acid (2,4-D) and 6-benzylaminopurine (BAP) readily developed into plantlets. These formed either directly from shoot buds or from intermediary protocorm-like bodies (PLBs). The maximum explant response (86.6 %) was obtained in medium supplemented with NAA at 30 µM, while the maximum number of shoots (4.42) and maximum bud-forming capacity (3.51) were observed in medium containing 15 µM BAP and 5 µM NAA in combination. Protocorm-like bodies were obtained when the medium contained 2,4-D. The maximum number of explants forming PLBs (41.48 %) was obtained in medium containing 15 µM BAP and 15 µM 2,4-D. Well-developed plantlets obtained after 20–25 weeks of culture were acclimatized and eventually transferred to the greenhouse. Over 60 % of these survived to form plants ∼3–4 cm tall after 90 days in glasshouse conditions using a substrate of crushed brick and charcoal, shredded bark and moss. CONCLUSIONS: The method described can readily be used for the rapid and large-scale regeneration of D. longicornu. Its commercial adoption would reduce the collection of this medicinally important and increasingly rare orchid from the wild. |
format | Online Article Text |
id | pubmed-3491754 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-34917542012-11-07 Multiple shoot induction from axillary bud cultures of the medicinal orchid, Dendrobium longicornu Dohling, Stadwelson Kumaria, Suman Tandon, Pramod AoB Plants Technical Articles BACKGROUND AND AIMS: Dendrobium longicornu, commonly known as the ‘Long-horned Dendrobium’, is an endangered and medicinally important epiphytic orchid. Over-exploitation and habitat destruction seriously threaten this orchid in Northeast India. Our objective was to develop an efficient protocol for the mass propagation of D. longicornu using axillary bud segments. METHODOLOGY AND PRINCIPAL RESULTS: Axillary buds cultured in Murashige and Skoog semi-solid medium supplemented with α-naphthalene acetic acid (NAA), 2,4-dichlorophenoxy acetic acid (2,4-D) and 6-benzylaminopurine (BAP) readily developed into plantlets. These formed either directly from shoot buds or from intermediary protocorm-like bodies (PLBs). The maximum explant response (86.6 %) was obtained in medium supplemented with NAA at 30 µM, while the maximum number of shoots (4.42) and maximum bud-forming capacity (3.51) were observed in medium containing 15 µM BAP and 5 µM NAA in combination. Protocorm-like bodies were obtained when the medium contained 2,4-D. The maximum number of explants forming PLBs (41.48 %) was obtained in medium containing 15 µM BAP and 15 µM 2,4-D. Well-developed plantlets obtained after 20–25 weeks of culture were acclimatized and eventually transferred to the greenhouse. Over 60 % of these survived to form plants ∼3–4 cm tall after 90 days in glasshouse conditions using a substrate of crushed brick and charcoal, shredded bark and moss. CONCLUSIONS: The method described can readily be used for the rapid and large-scale regeneration of D. longicornu. Its commercial adoption would reduce the collection of this medicinally important and increasingly rare orchid from the wild. Oxford University Press 2012 2012-11-05 /pmc/articles/PMC3491754/ /pubmed/23136638 http://dx.doi.org/10.1093/aobpla/pls032 Text en Published by Oxford University Press on behalf of the Annals of Botany Company. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Technical Articles Dohling, Stadwelson Kumaria, Suman Tandon, Pramod Multiple shoot induction from axillary bud cultures of the medicinal orchid, Dendrobium longicornu |
title | Multiple shoot induction from axillary bud cultures of the medicinal orchid,
Dendrobium longicornu |
title_full | Multiple shoot induction from axillary bud cultures of the medicinal orchid,
Dendrobium longicornu |
title_fullStr | Multiple shoot induction from axillary bud cultures of the medicinal orchid,
Dendrobium longicornu |
title_full_unstemmed | Multiple shoot induction from axillary bud cultures of the medicinal orchid,
Dendrobium longicornu |
title_short | Multiple shoot induction from axillary bud cultures of the medicinal orchid,
Dendrobium longicornu |
title_sort | multiple shoot induction from axillary bud cultures of the medicinal orchid,
dendrobium longicornu |
topic | Technical Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3491754/ https://www.ncbi.nlm.nih.gov/pubmed/23136638 http://dx.doi.org/10.1093/aobpla/pls032 |
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