The effectiveness of light emitting diodes on shoot regeneration in vitro from shoot tip tissues of Limnophila aromatica (Lamk.) Merr. and Rotala rotundifolia (Buch-Ham. ex Roxb) Koehne

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Taylor & Francis Ltd

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info:eu-repo/semantics/closedAccess

Özet

Light emitting diodes (LEDs) have become a promising technology for agriculture and horticulture. I investigated the effects of white (W), red (R) and blue (B) LED lights on the propagation of Limnophila aromatica (Lamk.) Merr. and Rotala rotundifolia (Buch-Ham. ex Roxb) Koehne using tissue culture. The shoot tip explants of L. aromatica and R. rotundifolia under different light environments were cultured in Murashige and Skoog (MS) basic nutrient medium with 6-benzylaminopurine (BAP) (0.05, 0.10 and 0.20 mg/l) and gibberellic acid (GA(3)) 0.25 mg/l) + kinetin (KIN) 0.25, 0.50 and 0.75 mg/l. The explants grown under combinations of white, red and blue LEDs were more effective for propagation of the plants in vitro. In L. aromatica, the maximum number of shoots/explant and the longest shoot lengths were obtained using the combination of white, red and blue LED lights in a 1:2:1 ratio in MS medium supplemented with 0.10 and 0.20 mg/l BAP. In R. rotundifolia, the maximum shoots/explant and shoot lengths were obtained in the explants using the combination of white, red and blue LED lights in a 1:2:1 ratio in the MS culture media fortified with 0.25 mg/l GA(3) + 0.25 and 0.75 mg/l KIN. After the regenerated shoots were rooted, they were adapted successfully to external conditions. LEDs have significant advantages over fluorescent lights.

Açıklama

WOS:000492505200001
PubMed:31650867

Anahtar Kelimeler

LEDs, Limnophila Aromatica, Propagation, Rotala Rotundifolia, Shoot Tip, Tissue Culture

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WoS Q Değeri

Q4

Scopus Q Değeri

Q2

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Doğan, M. (2020). The effectiveness of light emitting diodes on shoot regeneration in vitro from shoot tip tissues of Limnophila aromatica (Lamk.) Merr. and Rotala rotundifolia (Buch-Ham. ex Roxb) Koehne. Biotechnic & Histochemistry : Official Publication of the Biological Stain Commission, 95, 3, 225-232.