Analysis of the differential effects of methyl jasmonate on induction of adventitious roots and antioxidant potential in Artimisia scoparia

Paper Details

Research Paper 01/08/2019
Views (327) Download (15)
current_issue_feature_image
publication_file

Analysis of the differential effects of methyl jasmonate on induction of adventitious roots and antioxidant potential in Artimisia scoparia

Asghar Khan, Mubarak Ali Khan, Maqsood Alam, Raj Akbar, Amir Ali, Sher Mohammad, Ijaz Naeem, Mamoona Rauf
Int. J. Biosci.15( 2), 547-558, August 2019.
Certificate: IJB 2019 [Generate Certificate]

Abstract

Artemisia scoparia is an important medicinal plant, having plenty of pharmacological applications. In this study the comparative effects of auxins and elicitors were investigated on the induction, biomass formation and antioxidant potential of adventitious roots (AR) in leaf explants on solid MS media, followed by studying the growth kinetics in suspension cultures. It was observed that among the different auxins employed in vitro, NAA showed highest induction frequency (57%) when employed at 1.0mg/L on solid MS media. Within the elicitors, 0.5mg/L Me-J inducted maximum roots induction frequency (58%), while 1.0mg/LPAA resulted in 43% induction frequency. During AR suspension cultures, in response to 1.0mg/L NAA, shorter lag and stationary phases of 8 and 4 days respectively were observed in the growth curve. The log phase was quite longer consisting of 24 days, wherein highest biomass (7.36g/L; DW) was accumulated on 28 day of the growth curve. Within the different growth phases, day 20 (log phase) was observed to accumulate higher antioxidant activity in the AR suspension cultures than other growth stages. Lesser antioxidant activity was determined in the stationary phase of cell cycle. Highest antioxidant potential (87%) was recorded in the AR suspension cultures raised in presence of 0.5mg/L Me-J. This protocol has the potential for commercial production of antioxidants enriched biomass of A. scoparia.

VIEWS 24

Ali A, Mohammad S, Khan MA, Raja NI, Arif M, Kamil A, Mashwani ZUR. 2019. Silver nanoparticles elicited in vitro callus cultures for accumulation of biomass and secondary metabolites in Caralluma tuberculata. Artificial cells nanomedicine and biotechnology 47(1), 715-724.

Ali H, Khan MA, Kayani WK, Dilshad R, Rani R, Khan RS. 2019. Production of biomass and medicinal metabolites through adventitious roots in Ajuga bracteosa under different spectral lights. Journal of Photochemistry and Photobiology B: Biology 193, 109-117. https:// doi.org%2F10.1016% 2Fj.jphotobiol.2019.02.010

Ali H, Khan MA, Kayani WK, Khan T, Khan RS. 2018a. Thidiazuron regulated growth, secondary metabolism and essential oil profiles in shoot cultures of Ajuga bracteosa. Industrial Crops and Products 121, 418-427. https://doi.org/10.1016j.indcrop.201

Ali H, Khan MA, Ullah N, Khan RS. 2018b. Impacts of hormonal elicitors and photoperiod regimes on elicitation of bioactive secondary volatiles in cell cultures of Ajuga bracteosa. Journal of Photochemistry and Photobiology B: Biology 183, 242-250. https://doi.org/10.1016/j.jphotobiol.2018.

Ashraf M, Hayat MQ, Jabeen S, Shaheen N, Khan MA, Yasmin G. 2010. Artemisia L. species recognized by the local community of the northern areas of Pakistan as folk therapeutic plants. Journal of Medicinal Plants Research 4, 112-119.

Chao W, Anderson J, Horvath D. 2006. Sugars, Hormones, environment affect the dormancy status in underground adventitious buds of leaf spurge (Euphorbia esula). Weed Sci 54, 5968. https:// doi.org/10.1614/WS-05-088R.1

Fang Y, Li Z, Watanabe Y. 2003. Pharmacokinetics of a novel anti-asthmatic, scoparone, in the rabbit serum assessed by a simple HPLC method. Journal of ethnopharmacology 86, 127-130. https://doi.org/10.1016/S0378-8741(03) 00

Kaur S, Singh HP, Batish DR, Kohli RK. 2012. Artemisia scoparia essential oil inhibited root growth involves reactive oxygen species (ROS)-mediated disruption of oxidative metabolism: In vivo ROS detection and alterations in antioxidant enzymes. Biochemical systematics and ecology 44, 390-399.

Kazmi A, Khan MA, Ali H. 2019a. Biotechnological approaches for production of bioactive secondary metabolites in Nigella sativa: an up-to-date review. International Journal of Secondary Metabolite 6(2), 172-195. https://doi.org/10.21448/ij

Kazmi A, Khan MA, Mohammad S, Ali A, Kamil A, Arif M, Ali H. 2019b. Elicitation directed growth and production of steviol glycosides in the adventitious roots of Stevia rebaudiana Bertoni. Industrial Crops and Products 139, 111530. https:doi.org%2F10.1016%2Fj.indcrop.2019.111530

Khan MA, Abbasi BH, Ahmed N, Ali H. 2013. Effects of light regimes on in vitro seed germination and silymarin content in Silybum marianum. Industrial Crops and Products 46, 105-110 DOI:10.1016/j.indcrop.2012.12.035

Khan MA, Abbasi BH, Ali H, Ali M, Adil M, Hussain I. 2015a. Temporal variations in metabolite profiles at different growth phases during somatic embryogenesis of Silybum marianum L. Plant Cell, Tissue and Organ Culture (PCTOC) 120, 127-139.

Khan MA, Abbasi BH, Shah NA, Yücesan B, Ali H. 2015b. Analysis of metabolic variations throughout growth and development of adventitious roots in Silybum marianum L.(Milk thistle), a medicinal plant. Plant Cell, Tissue and Organ Culture (PCTOC) 123, 501-510. DOI: 10.1007/s11240-015-0

Khan MA, Khan T, Ali H. 2019a. Plant cell culture strategies for the production of terpenes as green solvents. Ind. Appl. Green Solvents 50, 1-20. https://doi.org/10. 21741/9781644900239-1

Khan MA, Khan T, Riaz MS, Ullah N, Ali H, Nadhman A. 2019b. Plant cell nanomaterials interaction: growth, physiology and secondary metabolism. Compr. Anal. Chem 84, 23-54. https://doi.org/10.1016/bs.coac.2019.04.005

Khan T, Abbasi BH, Khan MA, Azeem M. 2017. Production of biomass and useful compounds through elicitation in adventitious root cultures of Fagonia indica. Industrial crops and products 108, 451-457. DOI: 10.1016/j.indcrop.2017.07.019

Kollarova K, Liskova D, Kakoniova D, Lux A. 2004. Effect of auxins on Karwinskia humboldtiana root cultures. Plant Cell Tiss. Org. Cult 79, 213-21. https://doi.org/10.1007/s11240-004-0662-z

Mohammad S, Khan MA, Ali A, Khan L, Khan MS. 2019. Feasible production of biomass and natural antioxidants through callus cultures in response to varying light intensities in olive (Olea europaea L) cult. Arbosana. Journal of Photochemistry and Photobiology B: Biology 193, 140-147. https:// doi.org%2F10.1016%2Fj.jphotobiol

Movafeghi A, Djozan DJ. Torbati S. 2010. Solid-phase microextraction of volatile organic compounds released from leaves and flowers of Artemisia fragrans, followed by GC and GC/MS analysis. Natural product research 24(13), 1235-1242. https://doi.org/10.1080/14786410903108951

Murashige T, Skoog F. 1962. A revised medium for rapid growth and bio assays with tobacco tissue cultures. Physiologia plantarum 15, 473-497. https://doi.org/10.1111/j.1399-3054.1962.tb08052.x

Praveen N, Manohar SH, Naik PM, Nayeem A, Jeong JH, Murthy HN. 2009. Production of and roghrapholide from adventitious root cultures of Andrographis paniculata. Curr Sci 96, 510.

Rani R, Khan MA, Kayani WK, Ullah S, Naeem I, Mirza B. 2017. Metabolic signatures altered by in vitro temperature stress in Ajuga bracteosa Wall. ex. Benth. Acta physiologiae plantarum 39, 97. DOI 10.1007/s11738-017-2394-9

Saeed S, Ali H, Khan T, Kayani W, Khan MA. 2017. Impacts of methyl jasmonate and phenyl acetic acid on biomass accumulation and antioxidant potential in adventitious roots of Ajuga bracteosa Wall ex Benth., a high valued endangered medicinal plant. Physiology and Molecular Biology of Plants 23, 229-237. https://doi.org/10.1007/s12298-016-0406-

Sharma S, Ali M. 1998. New compounds from roots of Artemisia scoparia. Journal of herbs, spices and medicinal plants 5, 77-86. https://doi.org/10.1300/J

Singh HP, Kaur S, Mittal S, Batish DR, Kohli RK. 2009. Essential oil of Artemisia scoparia inhibits plant growth by generating reactive oxygen species and causing oxidative damage. Journal of chemical ecology 35, 154-162. https://doi.org/10.1007/s10886

Sivanesan I, Jeong BR. 2009. Induction and establishment of adventitious and hairy root cultures of Plumbago zeylanica L. Afr J Biotechnol 8, 52945300.

Tan RX, Zheng W, Tang H. 1998. Biologically active substances from the genus Artemisia. Planta medica 64, 295-302. https://doi.org/10.1055/s-2006

Weathers PJ, Bunk G, Mccoy MC. 2005. The effect of phytohormones on growth and artemisinin production in Artemisia annua L. hairy roots. In vitro Cell Dev. Biol.-Plant 41, 47-53.

Yan YH, Li JL, Zhang XQ, Yang WY, Wan Y, M YM, Zhu YQ, Peng Y, Huang LK. 2014. Effect of naphthalene acetic acid on adventitious root development and associated physiological changes in stem cutting of Hemarthria compressa. PLoS One 9, e90700. https://doi.org/10.1371/journal.pone.0090

Yousaf R, Khan MA, Ullah N, Khan I, Hayat O, Shehzad MA, Naeem I. 2019. Biosynthesis of anti-leishmanial natural products in callus cultures of Artemisia scoparia. Artificial cells, nanomedicine, and biotechnology 47(1), 1122-1131. https://doi.org/10.1