Somatic embryogenesis of Artemisia Annua L.


Citation

Boey P. L., . and Abu Hassan A., . and Chan L. K., . and Ku Nornadia K. R., . and Tran VM., . (2010) Somatic embryogenesis of Artemisia Annua L. [Proceedings Paper]

Abstract

Artemisia annua L. is one of the most important medicinal plants in the world for its artemisinin an anti-malarial drug. Commercially available artemisinin is mainly extracted from the wild plants hence subjected to seasonal and other environmental limitations. Somatic embryogenesis an in vitro culture technology provides an alternative to overcome these limitations. Somatic embryos could be induced from the leaf-derived callus of A. annua. Callus was initiated from the leaf pieces on callus induction medium Murashige and Skoog MS medium supplemented with 0.5 mg/I naphathaleneacetic acid NAA and 0.5 mg/I 6- benzylaminopurine BA 0.5 g casein hyrolysate and 30 g/l sucrose. Optimum callus production and variations in dallus morphology colour and texture were observed and evaluated. After one week of transferring the callus tissues onto basic MS medium without any plant growth regulator the callus that were pre-treated with various concentration of 2 4-dichlorophenoxyacetic acid formed somatic embryos. Histological studies confirmed the formation of somatic embryos. Somatic embryos that contained artemisinin will be tested against mosquito larvae in subsequent study.


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Abstract

Artemisia annua L. is one of the most important medicinal plants in the world for its artemisinin an anti-malarial drug. Commercially available artemisinin is mainly extracted from the wild plants hence subjected to seasonal and other environmental limitations. Somatic embryogenesis an in vitro culture technology provides an alternative to overcome these limitations. Somatic embryos could be induced from the leaf-derived callus of A. annua. Callus was initiated from the leaf pieces on callus induction medium Murashige and Skoog MS medium supplemented with 0.5 mg/I naphathaleneacetic acid NAA and 0.5 mg/I 6- benzylaminopurine BA 0.5 g casein hyrolysate and 30 g/l sucrose. Optimum callus production and variations in dallus morphology colour and texture were observed and evaluated. After one week of transferring the callus tissues onto basic MS medium without any plant growth regulator the callus that were pre-treated with various concentration of 2 4-dichlorophenoxyacetic acid formed somatic embryos. Histological studies confirmed the formation of somatic embryos. Somatic embryos that contained artemisinin will be tested against mosquito larvae in subsequent study.

Additional Metadata

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Item Type: Proceedings Paper
Additional Information: 5 ref. SB 293 S471 2010
AGROVOC Term: Somatic embryogenesis
AGROVOC Term: Artemisia annua
AGROVOC Term: Medicinal plants
AGROVOC Term: Artemisinin
AGROVOC Term: Callus culture
AGROVOC Term: Asteraceae
Geographical Term: MALAYSIA
Depositing User: Ms. Suzila Mohamad Kasim
Last Modified: 24 Apr 2025 05:14
URI: http://webagris.upm.edu.my/id/eprint/11546

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