Mass propagation of Juniperus procera Hoechst. Ex Endl. From seedling and screening of bioactive compounds in shoot and callus extract.


Journal

BMC plant biology
ISSN: 1471-2229
Titre abrégé: BMC Plant Biol
Pays: England
ID NLM: 100967807

Informations de publication

Date de publication:
21 Apr 2021
Historique:
received: 26 01 2021
accepted: 24 03 2021
entrez: 22 4 2021
pubmed: 23 4 2021
medline: 22 5 2021
Statut: epublish

Résumé

Juniperus procera Hoechst. ex Endl. is a medicinal tree in Saudi Arabia, primarily in the Enemas region, but it is locally threatened due to die-back disease and difficulties regarding seed reproduction (seed dormancy and underdeveloped embryonic anatomy, and germination rate < 40%). Hence, the alternative methods for reproduction of Juniperus procera are really needed for conservation and getting mass propagation for pharmaceutical uses. In this manuscript, we articulated the successful in vitro shoot multiplication and callus induction of J. procera by using young seedling as explants and detected an important antibacterial and antitumor product. Explants were grown on different types of media with the supplement of different combinations of Plant Growth Regulators (PGRs) at different concentrations. The best media for shoot multiplication was Woody Plant Media (WPM) supplemented with PGRs (0.5 μM of IAA and 0.5 μM BAP or 0.5 μM IBA and 0.5 μM BAP). Whereas for callus induction and formation Woody Plant Media (WPM) with the addition of PGRs (0.5 μM 2,4-D and 0.5 μM BAP) was better than the Chu Basal Salt Mixture (N6), Gamborg's B-5 Basal Medium (B5), and Murashige and Skoog media. The possibility of multiplication of J. procera in vitro creates significant advantages to overcome the difficulties of seeds dormancy for the reproduction of plants, conservation of trees, and getting mass propagation material for pharmaceutical studies. The shoot and callus extract of J. procera was detected using gas chromatography-mass spectrometry analysis and revealed more than 20 compounds related to secondary metabolites, which contained antibacterial and antitumor agents, such as ferruginol, Retinol, and Quinolone as well as confirmed by Direct Analysis in Real Time, Time of Flight Mass Spectrometry (DART-ToF-MS). Podophyllotoxin (PTOX) was detected in callus material by HPLC with sigma standard and confirmed by DART-ToF-MS and UV spectra. We successfully conducted in vitro shoot multiplication and callus induction from J. procera seedlings using WPM and a different combination of PGRs and, detected an important antibacterial and antitumor product such as ferruginol and podophyllotoxin. According to our findings, J. procera has become a new natural source of novel bioactive compounds.

Sections du résumé

BACKGROUND BACKGROUND
Juniperus procera Hoechst. ex Endl. is a medicinal tree in Saudi Arabia, primarily in the Enemas region, but it is locally threatened due to die-back disease and difficulties regarding seed reproduction (seed dormancy and underdeveloped embryonic anatomy, and germination rate < 40%). Hence, the alternative methods for reproduction of Juniperus procera are really needed for conservation and getting mass propagation for pharmaceutical uses.
RESULTS RESULTS
In this manuscript, we articulated the successful in vitro shoot multiplication and callus induction of J. procera by using young seedling as explants and detected an important antibacterial and antitumor product. Explants were grown on different types of media with the supplement of different combinations of Plant Growth Regulators (PGRs) at different concentrations. The best media for shoot multiplication was Woody Plant Media (WPM) supplemented with PGRs (0.5 μM of IAA and 0.5 μM BAP or 0.5 μM IBA and 0.5 μM BAP). Whereas for callus induction and formation Woody Plant Media (WPM) with the addition of PGRs (0.5 μM 2,4-D and 0.5 μM BAP) was better than the Chu Basal Salt Mixture (N6), Gamborg's B-5 Basal Medium (B5), and Murashige and Skoog media. The possibility of multiplication of J. procera in vitro creates significant advantages to overcome the difficulties of seeds dormancy for the reproduction of plants, conservation of trees, and getting mass propagation material for pharmaceutical studies. The shoot and callus extract of J. procera was detected using gas chromatography-mass spectrometry analysis and revealed more than 20 compounds related to secondary metabolites, which contained antibacterial and antitumor agents, such as ferruginol, Retinol, and Quinolone as well as confirmed by Direct Analysis in Real Time, Time of Flight Mass Spectrometry (DART-ToF-MS). Podophyllotoxin (PTOX) was detected in callus material by HPLC with sigma standard and confirmed by DART-ToF-MS and UV spectra.
CONCLUSION CONCLUSIONS
We successfully conducted in vitro shoot multiplication and callus induction from J. procera seedlings using WPM and a different combination of PGRs and, detected an important antibacterial and antitumor product such as ferruginol and podophyllotoxin. According to our findings, J. procera has become a new natural source of novel bioactive compounds.

Identifiants

pubmed: 33882830
doi: 10.1186/s12870-021-02946-2
pii: 10.1186/s12870-021-02946-2
pmc: PMC8059214
doi:

Substances chimiques

Phytochemicals 0
Plant Extracts 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

192

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Auteurs

Abdalrhaman M Salih (AM)

Botany and Microbiology Department, College of Science King Saud University, P. O. BOX 2455, Riyadh, 11451, Saudi Arabia. aabdalmola@ksu.edu.sa.

Fahad Al-Qurainy (F)

Botany and Microbiology Department, College of Science King Saud University, P. O. BOX 2455, Riyadh, 11451, Saudi Arabia.

Salim Khan (S)

Botany and Microbiology Department, College of Science King Saud University, P. O. BOX 2455, Riyadh, 11451, Saudi Arabia.

Mohamed Tarroum (M)

Botany and Microbiology Department, College of Science King Saud University, P. O. BOX 2455, Riyadh, 11451, Saudi Arabia.

Mohammad Nadeem (M)

Botany and Microbiology Department, College of Science King Saud University, P. O. BOX 2455, Riyadh, 11451, Saudi Arabia.

Hassan O Shaikhaldein (HO)

Botany and Microbiology Department, College of Science King Saud University, P. O. BOX 2455, Riyadh, 11451, Saudi Arabia.

Nadiyah M Alabdallah (NM)

Department of Biology, College of Science, Imam Abdulrahman Bin Faisal University, P.O. Box 383, Dammam, Saudi Arabia.

Saleh Alansi (S)

Botany and Microbiology Department, College of Science King Saud University, P. O. BOX 2455, Riyadh, 11451, Saudi Arabia.

Aref Alshameri (A)

Botany and Microbiology Department, College of Science King Saud University, P. O. BOX 2455, Riyadh, 11451, Saudi Arabia.

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