Relationship of light intensity and quality with callus biomass and antioxidant potential in Ajuga bracteosa

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Research Paper 01/07/2019
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Relationship of light intensity and quality with callus biomass and antioxidant potential in Ajuga bracteosa

Nizam Ud Din, Huma Ali, Syeda Kokab Shah, Syeda Faryal Israr, Amir Ali, Sher Mohammad, Raham Sher Khan, Mubarak Ali Khan
Int. J. Biosci.15( 1), 507-517, July 2019.
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Abstract

In the current study, effects of different light regimes and spectral lights were evaluated on the callus induction frequency, callus biomass and free radical scavenging activity in Ajuga Bracteosa. The hypocotyl explants derived from wild grown plants were used for callus culture establishment on MS solid media fortified with 1.0mg/L TDZ in combination with 0.5mg/L NAA. Among the different light regimes applied in this study, higher growth characteristics in callus cultures (maximum callus induction frequency: 90%) and biomass formation (5.6g/L FBM) were observed in the explants grown under continuous dark for two weeks culture period followed by transference into light (16h light & 8 h dark) for two weeks. The monochromatic lights were found most effective in terms of enhancement of biomass and antioxidant activity. Yellow light was found to influence maximum callus biomass (FW: 28g/L). Comparatively higher antioxidant activity (88%) was observed in yellow light grown callus tissues, followed by red light (80%). Hence, the findings of the current study emphasized the important role of different photoperiod regimes and monochromatic lights on callus induction, biomass accumulation and antioxidant activity in A. bracteosa.

VIEWS 6

Abbasi BH, Ali H, Yucesan B, Saeed S, Rehman K, Khan MA. 2016. Evaluation of biochemical markers during somatic embryogenesis in Silybum marianum L. 3 Biotech 6, 71. https://doi.org/10.1007/s13205-016-0366-1

Abbasi BH, Khan MA, Mahmood T, Ahmad M, Chaudhary MF, Khan MA. 2010. Shoot regeneration and free-radical scavenging activity in Silybum marianum L. Plant Cell, Tissue and Organ Culture (PCTOC) 101, 371-376. https://doi.org /10.1007/s11240-010-9692-x

Ahmad N, Abbasi BH, Fazal H, Khan MA. Afridi MS. 2014. Effect of reverse photoperiod on in vitro regeneration and piperine production in Piper nigrum L. Comptes Rendus Biologies 337(1), pp.19-28. http://dx.doi.org/10.1016/j.crvi.2013.10.011

Ali H, Khan MA, Kayani WK, Dilshad R, Rani R, Khan RS, Khan T. 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, Ullah N, Khan RS. 2018. 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.crvi.2013.10.011

Ali M, Abbasi BH. 2014. Light-induced fluctuations in biomass accumulation, secondary metabolites production and antioxidant activity in cell suspension cultures of Artemisia absinthium L. Journal of Photochemistry and Photobiology B Biology 140C, 223-227. https://doi.org/10.1016/j.jphotobiol.2014.

Almagro L, Sabater-Jara AB, Belchí-Navarro S, Fernández-Pérez F, Bru R, Pedreño MA. 2011. Effect of UV light on secondary metabolite biosynthesis in plant cell cultures elicited with cyclodextrins and methyl jasmonate. In Plants and Environment. InTech.

Chandel S, Bagai U. 2010. Antiplasmodial activity of Ajuga bracteosa against Plasmodium berghei infected BALB/c mice.

Chopra RN, Nayar SL. 1956. Glossary of Indian medicinal plants, Council of Scientific And Industrial Research; New Delhi.

da Silva MM, Debergh PC. 1997. The effect of light quality on the morphogenesis of in vitro cultures of Azorina vidalii (Wats.) Feer. Plant cell, tissue and organ culture 51(3), pp. 187-193. https://doi.org /10.1023/A:1005988621036

Evans P, Halliwell B. 2001. Micronutrients: oxidant/antioxidant status. British Journal of Nutrition 85(S2), pp. S67-S74. https://doi.org /10.1049/ BJN2000296

Fazal H, Abbasi BH, Ahmad N, Ali M. 2016. Elicitation of medicinally important antioxidant secondary metabolites with silver and gold nanoparticles in callus cultures of Prunella vulgaris L. Applied biochemistry and biotechnology 180, 1076-1092. https://doi.org/10.1007/s12010-016-2153-1

Ganaie H, Ali M, Ganai B, Kaur J, Ahmad M. 2016. GC-MS analysis and evaluation of mutagenic and antimutagenic activity of ethyl acetate extract of Ajuga bracteosa Wall ex. Benth: An endemic medicinal plant of Kashmir Himalaya, India. Journal of Clinical Toxicology 6, 288. 10.4172/2161

Gautam R, Jachak SM, Saklani A. 2011. Anti-inflammatory effect of Ajuga bracteosa Wall Ex Benth. mediated through cyclooxygenase (COX) inhibition. Journal of ethnopharmacology 133, 928-930. DOI: 10.1016/j.jep.2010.11.003.

Ghasemzadeh A, Jaafar HZ, Rahmat A. 2010. Antioxidant activities, total phenolics and flavonoids content in two varieties of Malaysia young ginger (Zingiberofficinale Roscoe). Molecules 15(6), pp. 4324-4333. https://doi.org/10.3390/molecules1506

Hare C. 2007. Indian Medicinal Plants-An Illustrated Dictionary. 1st Indian Reprint Springer (India) Pvt. Ltd., New Delhi, India 28.

Ibrar M, Hussain F. 2009. Ethnobotanical studies of plants of Charkotli hills, Batkhela district, Malakand, Pakistan. Frontiers of Biology in China 4, 539. https://doi.org/10.1007/s11515-009-0045-2

Jan M, Singh S, Kaloo ZA, Maqbool F. 2014. Callus induction and multiple shoot regeneration in Ajuga bracteosa Wall. ex Benth. An important medicinal plant growing in Kashmir Himalaya. J Sci Innov Res 3, 319-324.

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

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. www.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. http://dx.doi.org/10.1016/j.indcrop.2012.12.035

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.DOI:10.1007/s11240-014-0587-0

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

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

Khan T, Abbasi BH, Khan MA, Shinwari ZK. 2016. Differential effects of thidiazuron on production of anticancer phenolic compounds in callus cultures of Fagonia indica. Applied biochemistry and biotechnology 179, 46-58. https://doi.org/ 10.1007/ s12010-016-1978-y

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. 2019.03.001

Nagella P, Murthy HN. 2011. Effects of macroelements and nitrogen source on biomass accumulation and withanolide-A production from cell suspension cultures of Withania somnifera (L.) Dunal. Plant Cell, Tissue and Organ Culture (PCTOC) 104, 119-124. DOI: 10.1007/s11240-010-9799-0

Nikolaeva TN, Zagoskina NV, Zaprometov MN. 2009. Production of phenolic compounds in callus cultures of tea plant under the effect of 2,4-D and NAA. Russian Journal of Plant Physiology 56, 45-49. https://doi.org/10.1134/S10214437090100

Pala A, Jadona M, Katarea Y, Singoura P, Rajakb H, Chaurasiyaa P, Patila U, Pawar R. 2011. Ajuga bracteosa wall: a review on its ethn opharmacological and phytochemical studies. Der Pharmacia Sinica 2, 1-10.

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

Rastogi R, Merhotra B. 1990. Compendium of Indian Medicinal Plants published by Central Drug Research Institute. Lucknow and National Institute of Sciences Communication and Information Resources, New Delhi 1994, 395-398.

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/s12298-016-0406-7

Senger H. 1982. The effect of blue light on plants and microorganisms. Photochemistry and Photobiology 35(6), pp.911-920. https://doi.org /10.1111/j.1751-1097.1982.tb02668.x

Sharma P, Mohan L, Srivastava C. 2004. Larval susceptibility of Ajuga remota against anopheline and culicine mosquitos.

Shin KS, Murthy HN, Heo JW, Hahn EJ, Paek KY. 2008. The effect of light quality on the growth and development of in vitro cultured Doritaenopsis plants. Acta Physiologiae Plantarum 30, 339-343. DOI: 10.1007/s11738-007-0128-0

Shohael A, Ali M, Yu K, Hahn E, Islam R, Paek K. 2006. Effect of light on oxidative stress, secondary metabolites and induction of antioxidant enzymes in Eleutherococcus senticosus somatic embryos in bioreactor. Process Biochemistry 41. DOI: 10.1016 /j.procbio.2005.12.015

Tariq U, Ali M, Abbasi BH. 2014. Morphogenic and biochemical variations under different spectral lights in callus cultures of Artemisia absinthium L. Journal of Photochemistry and Photobiology B: Biology 130, pp. 264-271. https://doi.org /10.1016 /j.jphotobiol.2013.11.026

Wang YZhang HZhao B, Yuan X. 2001. Improved growth of Artemisia annua L hairy roots and artemisinin production under red light conditions. Biotechnology Letters 23, 1971-1973. DOI: 10.1023/A:1013786332363

Wu CH, Murthy HN, Hahn EJ, Paek KY. 2007. Enhanced production of caftaric acid, chlorogenic acid and cichoric acid in suspension cultures of Echinacea purpurea by the manipulation of incubation temperature and photoperiod. Biochemical Engineering Journal 36(3), pp.301-303. DOI: 10.1016/j.bej.2007.02.024

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/10.1080/21691401.2019.1593856