PRODUCTIVITY ENHANCEMENT OF CORIANDRUM SATIVUM USING PLANT BIOLOGICALS

Authors

  • KAMAL JEET Research Scholar, I. K. G. Punjab Technical University, Jalandhar, Punjab, India 144603, I. S. F. College of Pharmacy, Moga, Punjab, India 142001
  • ALOK MALAVIYA Applied and Industrial Biotechnology Laboratory (AIBL), Department of Life Sciences, CHRIST (Deemed to be University), Hosur Road, Banglore, India 560029
  • ASHISH BALDI I. S. F. College of Pharmacy, Moga, Punjab, India 142001, Department of Pharmaceutical Sciences and Technology, Maharaja Ranjit Singh Punjab Technical University, Bathinda, Punjab, India 151001

DOI:

https://doi.org/10.22159/ijpps.2020v12i5.37374

Keywords:

Azotobacter chroococcum, Coriander, Emergence, Essential oil, Pseudomonas fluorescens, Sebacina vermifera

Abstract

Objective: The present study was designed to investigate phytopromotional effects of Sebacina vermifera on economically and medicinally important aromatic plant - Coriandrum sativum (coriander).

Methods: Phytopromotional effects of Sebacina vermifera were evaluated on coriander, under greenhouse and field conditions. The evaluations were carried out with reference to emergence, growth promotion and quantitative as well as the qualitative composition of essential oil. Beside this the overall effects were comparatively assessed with the effects of (a) Phosphate solubilizing bacteria (Pseudomonas fluorescens) (b) Nitrogen-fixing bacteria (Azotobacter chroococcum) on coriander using same parameters.

Results: Mycorrhizal fungus (Sebacina vermifera) was observed with the most significant effect in all aspects viz. emergence, growth promotion and quantitative as well as the qualitative composition of essential oil.

Conclusion: Based upon the observations, Sebacina vermifera is highly recommended as a potential biological agent that could be applied for phytopromotional effects and economic cultivation of aromatic plants.

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References

Small E. Culinary herbs. Ottawa: NRC Research Press; 1997.

Dyulgerov N, Dyulgerova B. Heritability and correlation coefficient analysis for fruit yield and its components in coriander (Coriandrum sativum L.). Turk J Agric Nat Sci 2014;1:618–22.

Nadeem M, Anjum FM, Khan MI, Tehseen S, El-Ghorab A, Sultan JI. Nutritional and medicinal aspects of Coriander (Coriandrum sativum L.) a review. Br Food J 2013;115:743–55.

Zheljazkov VD, Pickett KM, Caldwell CD, Pincock JA, Roberts JC, Mapplebeck L. Cultivar and sowing date effects on seed yield and oil composition of Coriander in Atlantic Canada. Ind Crops Prod 2008;28:88–94.

Diederichsen A. Coriander: Coriandrum Sativum L. Rome: Gatersleben/IPGRI; 1996.

Gray AM, Flatt PR. Insulin-releasing and insulin-like activity of the traditional anti-diabetic plant Coriandrum sativum (coriander). Br J Nutr 1999;81:203–9.

Carrubba A, la Torre R, Di Prima A, Saiano F, Alonzo G. Statistical analyses on the essential oil of Italian Coriander (Coriandrum sativum L.) fruits of different ages and origins. J Essential Oil Res 2002;14:389–96.

Wangensteen H, Samuelsen AB, Malterud KE. Antioxidant activity in extracts from coriander. Food Chem 2004;88:293–7.

Emamghoreishi M, Khasaki M, Aazam MF. Coriandrum sativum: evaluation of its anxiolytic effect in the elevated plus-maze. J Ethnopharmacol 2005;96:365–70.

Darughe F, Barzegar M, Sahari MA. Antioxidant and antifungal activity of Coriander (Coriandrum sativum L.) essential oil in cake. Int Food Res J 2012;19:1253–60.

Eidi M, Eidi A, Saeidi A, Molanaei S, Sadeghipour A, Bahar M, et al. Effect of coriander seed (Coriandrum sativum L) ethanol extract on insulin release from pancreatic beta cells in streptozotocin-induced diabetic rats. Phytother Res 2008;23:404–6.

Cortes Eslava J, Gomez Arroyo S, Villalobos Pietrini R, Espinosa Aguirrec JJ. Antimutagenicity of coriander (Coriandrum sativum) juice on the mutagenesis produced by plant metabolites of aromatic amines. Toxicol Lett 2004;153:283–92.

Sunil C, Agastian P, Kumarappan C, Ignacimuthu S. In vitro antioxidant, antidiabetic and antilipidemic activities of Symplocos cochinchinensis (Lour.) S. Moore bark. Food Chem Toxicol 2012;50:1547–53.

UNDESA. World population projected to reach 9.8 billion in 2050, and 11.2 billion in 2100. United Nations Department of Economic and Social Affairs. Available from: https://www.un.org/development/desa/en/news/population/world-population-prospects-2017.html. [Last accessed on 10 Sep 2017].

Smith SE, Read DJ. Mycorrhizal symbiosis. New York: Academic Press; 1995.

Ahmad F, Ahmad I, Khan MS. Screening of free-living rhizospheric bacteria for their multiple plant growth promoting activities. Microbiol Res 2008;63:173–81.

Gupta M, Kiran S, Gulati A, Singh B, Tewari R. Isolation and identification of phosphate solubilizing bacteria able to enhance the growth and aloin-a biosynthesis of Aloe barbadensis miller. Microbiol Res 2012;167:358–63.

Novozymes. The BioAg alliance advances new microbial solutions for agriculture: Strong pipeline of microbial products designed to boost crop yields in a sustainable way. Novozymes. Available from: https://www.novozymes.com/news/news-archive/2017/01/bioag-alliance-pipeline-2017. [Last accessed on 10 Sep 2017]

Mehrotra VS. Mycorrhiza: role and applications. New Delhi: Allied Publishers; 2005.

Allen MF. The ecology of mycorrhizae. USA: Cambridge University Press; 1991.

Baldi A, Farkya S, Jain A, Gupta N, Mehra R, Datta V, et al. Enhanced production of podophyllotoxins by co-culture of transformed Linum album cells with plant growth-promoting fungi. Pure Appl Chem 2010;82:227–41.

Saharan BS, Nehra V. Plant growth promoting rhizobacteria: a critical review. Life Sci Med Res 2011;2:1–30.

Bona E, Cantamessa S, Massa N, Manassero P, Marsano F, Copetta A, et al. Arbuscular mycorrhizal fungi and plant growth-promoting Pseudomonads improve yield, quality and nutritional value of tomato: a field study. Mycorrhiza 2017;27:1–11.

ISTA. International rules for seed testing. Seed Sci Technol 1985;13:299–513.

Association of Official Seed Analysis (AOSA). Seed vigor testing handbook. Contribution no. 32 to the handbook on Seed Testing; 1983.

Ellis RH, Roberts EH. The quantification of ageing and survival in orthodox seeds. Seed Sci Technol 1981;9:373–409.

Dezfuli PM, Sharif Zadeh F, Janmohammadi M. Influence of priming techniques on seed germination behavior of maize inbred lines (Zea mays L.). Arpn J Agric Biol Sci 2008;3:22–5.

Coolbear P, Francis A, Grierson D. The effect of low temperature pre-sowing treatment under the germination performance and membrane integrity of artificially aged tomato seeds. J Exp Bot 1984;35:1609–17.

Farooq M, Basra SMA, Ahmad N, Hafeez K. Thermal hardening: a new seed vigor enhancement tool in rice. J Integr Plant Biol 2005;47:187–93.

Farooq M, Basra SMA, Hafeez-ue-Rehman, Mehmood T. Germination and early seedling growth as affected by pre-sowing ethanol seed treatments in fine rice. Int J Agric Biol 2006;8:19–22.

Srinivasan K, Saxena S. Effect of dormancy breaking treatments on seed quality during storage of four acacia species. Indian J Forest 2007;30:233–40.

Abdul Baki AA, Anderson JD. Vigour determination in soybean seed by multiple criteria. Crop Sci 1973;13:630–3.

Phillip JM, Hayman DS. Improved procedures for clearing roots and staining parasitic and VAM fungi for rapid assessment of infection. T Br Mycol Soc 1970;55:158–61.

Giovannetti M, Mosse B. An evaluation of techniques for measuring vesicular-arbuscular mycorrhizal infection in roots. New Phytol 1980;84:489–500.

Tarraf W, Ruta C, Tagarelli A, De Cillis F, De Mastro G. Influence of arbuscular mycorrhizae on plant growth, essential oil production and phosphorus uptake of Salvia officinalis L. Ind Crops Prod 2017;102:144–53.

Dolatabadi HK, Goltapeh EM, Jaimand K, Rohani N, Varma A. Effects of Piriformospora indica and Sebacina vermifera on growth and yield of essential oil in Fennel (Foeniculum vulgare) under greenhouse conditions. J Basic Microbiols 2011;51:33–9.

Barazani O, Benderoth M, Groten K, Kuhlemeier C, Baldwin IT. Piriformospora indica and Sebacina vermifera increase growth performance at the expense of herbivore resistance in Nicotiana attenuata. Oecologia 2005;146:234–43.

Dolatabadi HK, Goltapeh EM, Moieni A, Jaimand K, Sardrood BP, Varma A. Effect of Piriformospora indica and Sebacina vermifera on plant growth and essential oil yield in Thymus vulgarisin vitro and in vivo experiments. Symbiosis 2011;53:29–35.

Ghimire SR, Craven KD. Enhancement of switchgrass (Panicum virgatum L.) biomass production under drought conditions by the ectomycorrhizal fungus Sebacina vermifera. Appl Environ Microbiol 2011;77:7063–7.

Ray P, Ishiga T, Decker SR, Turner GB, Craven KD. A novel delivery system for the root symbiotic fungus, Sebacina vermifera, and consequent biomass enhancement of low lignin COMT switchgrass lines. BioEnergy Res 2015;8:922–33.

Pirdashti H, Yaghoubian Y, Goltapeh E, Hosseini S. Effect of mycorrhiza-like endophyte (Sebacina vermifera) on growth, yield and nutrition of rice (Oryza sativa L.) under salt stress. J Agric Technol 2012;8:1651–61.

Harper SHT, Lynch JM. Effects of Azotobacter chroococcum on barley seed germination and seedling development. Microbiology 1979;112:45–51.

Gholami A, Shahsavani S, Nezarat S. The effect of plant growth promoting rhizobacteria (PGPR) on germination, seedling growth and yield of Maize. Int J Biol Bioml Agric Food Biotechnol Eng 2009;3:9–14.

Ardebili ZO, Ardebili NO, Hamdi SMM. Physiological effects of Pseudomonas fluorescens CHA0 on tomato (Lycopersicon esculentum Mill.) plants and its possible impact on Fusarium oxysporum f. sp. lycopersici. Aust J Crop Sci 2011;5:1631–8.

Ghimire SR, Charlton ND, Craven KD. The mycorrhizal fungus, Sebacina vermifera, enhances seed germination and biomass production in switchgrass (Panicum virgatum L) Bioenergy Res 2009;2:51–8.

Yousefi S, Kartoolinejad D, Bahmani M, Naghdi R. Effect of Azospirillum lipoferum and Azotobacter chroococcum on germination and early growth of hopbush shrub (Dodonaea viscosa L.) under salinity stress. J Sustainable Forest 2017;36:107–20.

Demissie S, Muleta D, Berecha G. Effect of phosphate solubilizing bacteria on seed germination and seedling growth of Faba Bean (Vicia faba L.). Int J Agric Res 2013;8:123–36.

Nandakumar R, Babua S, Viswanathan R, Raguchandera T, Samiyappan R. Induction of systemic resistance in rice against sheath blight disease by Pseudomonas fluorescens. Soil Biol Biochem 2001;33:603–12.

Abo Elyousr KAM, El-Hendawy HH. Integration of Pseudomonas fluorescens and acibenzolar-S-methyl to control bacterial spot disease of tomato. Crop Prot 2008;27:1118–24.

Sirrenberg A, Gobel C, Grond S, Czempinski N, Ratzinger A, Karlovsky P, et al. Piriformospora indica affects plant growth by auxin production. Physiol Plant 2007;131:581–9.

Vadassery J, Ritter C, Venus Y, Camehl I, Varma A, Shahollari B, et al. The role of auxins and cytokinins in the mutualistic interaction between Arabidopsis and Piriformospora indica. Mol Plant Microbe Interact 2008;21:1371–83.

Barazani O, Von Dahl CC, Baldwin IT. Sebacina vermifera promotes the growth and fitness of Nicotiana attenuata by inhibiting ethylene signaling. Plant Physiol 2007;144:1223–32.

Raven PH, Evert RF, Eichhorn SE. Biology of plants. New York: WH Freeman and Company Publishers; 2005.

Ananthanaik T, Earanna N, Suresh CK. Influence of Azotobacter chroococcum strains on growth and biomass of Adathoda vasica Nees. Karnataka J Agric Sci 2007;20:613–5.

Chaudhary D, Narula N, Sindhu SS, Behl RK. Plant growth stimulation of wheat (Triticum aestivum L.) by inoculation of salinity tolerant Azotobacter strains. Physiol Mol Biol Plants 2013;19:515–9.

Alemu F, Alemu T. Pseudomonas fluorescens isolates used as a plant growth promoter of Faba Bean (Vicia faba) in vitro as well as in vivo study in Ethiopia. Am J Life Sci 2015;3:100–8.

Otieno N, Lally RD, Kiwanuka S, Lloyd A, Ryan D, Germaine KJ, et al. Plant growth promotion induced by phosphate solubilizing endophytic Pseudomonas isolates. Front Microbiol 2015;6:745.

Dolatabadi HK, Goltapeh EM, Moieni A, Varma A. Evaluation of different densities of auxin and endophytic fungi (Piriformospora indica and Sebacina vermifera) on Mentha piperita and Thymus vulgaris growth. Afr J Biotechnol 2012;11:1644–50.

Karthikeyan A, Sakthivel KM. Efficacy of Azotobacter chroococcum in rooting and growth of Eucalyptus camaldulensis stem cuttings. Res J Microbiol 2011;6:618–24.

Xie H, Pastrnak JJ, Gilck BR. Isolation and characterization of mutants of plant growth promoting rhizobacteria Pseudomonas putida, GR12-2 that over produced indole acetic acid. Curr Microbiol 1966;32:67–71.

Glick BR, Patten CL, Holguin G, Penrose DM. Biochemical and genetic mechanisms used by plant growth promoting bacteria. London: Imperial College Press; 1999.

Lee YC, Johnson JM, Chien CT, Sun C, Cai DG, Lou BG, et al. Growth promotion of Chinese cabbage and Arabidopsis by Piriformospora indica is not stimulated by mycelium-synthesized auxin. Mol Plant Microbe Interact 2011;24:421–31.

Dong SQ, Tian ZH, Chen PJ, Kumar RS, Shen CH, Cai DG. The maturation zone is an important target of Piriformospora indica in Chinese cabbage roots. J Exp Bot 2013;64:4529–40.

Lakshminarayana K. Influence of Azotobacter on nitrogen nutrition of plants and crop productivity. Proc Indian Natn Sci Acad B 1993;59:303–8.

Kizilkaya R. Nitrogen fixation capacity of Azotobacter spp. strains isolated from soils in different ecosystems and relationship between them and the microbiological properties of soils. J Environ Biol 2009;30:73–82.

Levai L, Veres S, Bakonyi N, Gajdos E. Can wood ash and biofertilizer play a role in organic agriculture? Agronomski Glasnik 2008;70:263–72.

Rodrı́guez H, Fraga R. Phosphate solubilizing bacteria and their role in plant growth promotion. Biotechnol Adv 1999;17:319–39.

Di Simine CD, Sayer JA, Gadd GM. Solubilization of zinc phosphate by a strain of Pseudomonas fluorescens isolated from a forest soil. Biol Fertil Soils 1998;28:87–94.

Henri F, Laurette NN, Annette D, John Q, Wolfgang M, Franccedil E, et al. Solubilization of inorganic phosphates and plant growth promotion by strains of Pseudomonas fluorescens isolated from acidic soils of Cameroon. Afr J Microbiol Res 2008;2:171–8.

Goteti PK, Desai S, Emmanuel LDA, Taduri M, Sultana U. Phosphate solubilization potential of Fluorescent Pseudomonas spp. isolated from diverse agro-ecosystems of India. Int J Soil Sci 2014;9:101–10.

Nautiyal CS, Chauhan PS, DasGupta SM, Seem K, Varma A, Staddon WJ. Tripartite interactions among Paenibacillus lentimorbus NRRL B-30488, Piriformospora indica DSM 11827, and Cicer arietinum L. World J Microbiol Biotechnol 2010;26:1393–9.

Kumar V, Sarma MVRK, Saharan K, Srivastava R, Kumar L, Sahai Vikram, et al. Effect of formulated root endophytic fungus Piriformospora indica and plant growth promoting rhizobacteria fluorescent pseudomonads R62 and R81 on Vigna mungo. World J Microbiol Biotechnol 2012;28:595–603.

Sherameti I, Shahollari B, Venus Y, Altschmied L, Varma A, Oelmüller R. The endophytic fungus Piriformospora indica stimulates the expression of nitrate reductase and the starch-degrading enzyme glucan-water dikinase in tobacco and Arabidopsis roots through a homeodomain transcription factor that binds to a conserved motif in their promoters. J Biol Chem 2005;280:26241-7.

Yadav V, Kumar M, Deep DK, Kumar H, Sharma R, Tripathi T, et al. A phosphate transporter from the root endophytic fungus Piriformospora indica plays a role in phosphate transport to the host plant. J Biol Chem 2010;285:26532–44.

Kumar M, Yadav V, Kumar H, Sharma R, Singh A, Tuteja N, et al. Piriformospora indica enhances plant growth by transferring phosphate. Plant Signal Behav 2011;6:723–5.

Li Y, Hou L, Song B, Yang L, Li L. Effects of increased nitrogen and phosphorus deposition on offspring performance of two dominant species in a temperate steppe ecosystem. Sci Rep 2017;7:40951.

Satheesan J, Narayanan AK, Sakunthala M. Induction of root colonization by Piriformospora indica leads to enhanced asiaticoside production in Centella asiatica. Mycorrhiza 2012;22:195–202.

Gosal SK, Karlupia A, Gosal SS, Chhibba IM, Varma A. Biotization with Piriformospora indica and Pseudomonas fluorescens improves survival rate, nutrient acquisition, field performance and saponin content of micropropagated Chlorophytum sp. Indian J Biotechnol 2010;9:289–97.

Mahfouz SA, Sharaf-Eldin MA. Effect of mineral vs. biofertilizer on growth, yield, and essential oil content of fennel (Foeniculum vulgare Mill.). Int Agrophysics 2007;21:361–6.

Shirkhodaei M, Darzi MT, Hadi MHS. Influence of vermicompost and biostimulant on the growth and biomass of coriander (Coriandrum sativum L.). Int J Adv Biol Biomed Res 2014;2:706–14.

Darzi MT, Shirkhodaei M, Hadi MRHS. Effects of vermicompost and nitrogen fixing bacteria on seed yield, yield components of seed and essential oil content of coriander (Coriandrum sativum). J Med Plants By-Prod 2015;14:103–9.

Banchio E, Bogino PC, Zygadlo J, Giordano W. Plant growth promoting rhizobacteria improve growth and essential oil yield in Origanum majorana L. Biochem Syst Ecol 2008;36:766–71.

Hemavathi, Navi V, Sivakumr BS, Suresh CK, Earanna N. Effect of Glomus fasciculatum and plant growth promoting rhizobacteria on growth and yield of Ocimum basilicum. Karnataka J Agric Sci 2006;19:17–20.

Santoro MV, Zygadlo J, Giordano W, Banchio E. Volatile organic compounds from rhizobacteria increase biosynthesis of essential oils and growth parameters in peppermint (Mentha piperita). Plant Physiol Biochem 2011;49:1177–82.

Abdelaziz ME, Pokluda R, Abdelwahab MM. Influence of compost, microorganisms and NPK fertilizer upon growth, chemical composition and essential oil production of Rosmarinus officinalis L. Not Bot Horti Agrobot Cluj Napoca 2007;35:86–90.

Floß DS, Hause B, Lange PR, Kuester H, Strack D, Walter MH. Knock-down of the MEP pathway isogene 1-deoxy-d-xylulose 5-phosphate synthase 2 inhibits formation of arbuscular mycorrhiza-induced apocarotenoids, and abolishes normal expression of mycorrhiza-specific plant marker genes. Plant J 2008;56:86–100.

Mandal S, Upadhyay S, Singh VP, Kapoor R. Enhanced production of steviol glycosides in mycorrhizal plants: a concerted effect of arbuscular mycorrhizal symbiosis on transcription of biosynthetic genes. Plant Physiol Biochem 2015;89:100–6.

Torelli A, Trotta A, Acerbi L, Arcidiacono G, Berta G, Branca C. IAA and ZR content in leek (Allium porrum L.), as influenced by P nutrition and arbuscular mycorrhizae, in relation to plant development. Plant Soil 2000;226:29–35.

Kapoor R, Giri B, Mukerji KG. Glomus macrocarpum: a potential bioinoculant to improve essential oil quality and concentration in dill (Anethum graveolens L.) and Carum (Trachyspermum ammi (Linn.) Sprague). World J Microbiol Biotechnol 2002;18:459–63.

Strack D, Fester T, Hause B, Schliemann W, Walter MH. Review paper: arbuscular mycorrhiza: biological, chemical, and molecular aspects. J Chem Ecol 2003;29:1955–79.

Krishna H, Singh SK, Sharma RR, Khawale RN, Grover M, Patel VB. Biochemical changes in micropropagated grape (Vitis vinifera L.) plantlets due to arbuscular-mycorrhizal fungi (AMF) inoculation during ex vitro acclimatization. Sci Hort 2005;106:554–67.

Sailo GL, Bagyaraj DJ. Influence of different AM-fungi on the growth, nutrition and forskolin content of Coleus forskohlii. Mycol Res 2005;109:795–8.

Prasad A, Kumar S, Pandey A, Chand S. Microbial and chemical sources of phosphorus supply modulate the yield and chemical composition of essential oil of rose-scented geranium (Pelargonium species) in sodic soils. Biol Fertil Soils 2012;48:117–22.

Loomis WD, Corteau R. Biochemistry and physiology of lower terpenoids. Recent Adv Phytochem 1973;6:147–85.

Vafadar F, Amooaghaie R, Otroshy M. Effects of plant-growth-promoting rhizobacteria and arbuscular mycorrhizal fungus on plant growth, stevioside, NPK, and chlorophyll content of Stevia rebaudiana. J Plant Interact 2014;9:128–36.

Kilam D, Saifi M, Abdin MZ, Agnihotri A, Varma A. Combined effects of Piriformospora indica and Azotobacter chroococcum enhance plant growth, antioxidant potential and steviol glycoside content in Stevia rebaudiana. Symbiosis 2015;66:149–56.

Ghorbanpour M, Hatami M, Khavazi K. Role of plant growth promoting rhizobacteria on antioxidant enzyme activities and tropane alkaloid production of Hyoscyamus niger under water deficit stress. Turk J Biol 2013;37:350–60.

Baldi A. Production of anticancer drug, podophyllotoxin, by plant cell cultivation of Linum album. India, New Delhi: Dissertation, Indian Institute of Technology Delhi; 2008.

Baldi A, Jain A, Gupta N, Srivastava AK, Bisaria VS. Co-culture of arbuscular mycorrhiza-like fungi (Piriformospora indica and Sebacina vermifera) with plant cells of Linum album for enhanced production of podophyllotoxins: a first report. Biotechnol Lett 2008;30:1671–7.

Farkya S, Baldi A, Kumar V, Datta V, Mehra R, Gupta N, et al. Impact of symbiotic fungi on production of secondary metabolites by plant cell culture. AsPac J Mol Biol Biotechnol 2010;18:51–3.

Sangwan NS, Farooqi AHA, Shabih F, Sangwan RS. Regulation of essential oil production in plants. Plant Growth Regul 2001;34:3–21.

Lima HRP, Kaplan MAC, Cruz AVM. Influence of abiotic factors on terpenoids production and variability in the plants. Florestae Ambiente 2003;10:71–7.

Gobbo Neto L, Lopes NP. Medicinal plants: factors of influence on the content of secondary metabolites. Quim Nova 2007;30:374–81.

Bisaria VS, Baldi A, Kumar V, Gupta N, Jain A, Farkya S, et al. Interaction of phytopromotional fungi and plant cells on synthesis of plant-derived metabolites. J Biotechnol 2008;136:S11.

Baldi A, Jain A, Gupta N, Srivastava AK, Bisaria VS. Co-culture of Linum album cells and Piriformospora indica for improved production of phytopharmaceuticals. In: Varma A, Kharkwal AC. (ed) Symbiotic fungi. Berlin Heidelberg: Springer; 2009. p. 361–72.

Baldi A, Srivastava AK, Bisaria VS. Fungal elicitors for enhanced production of secondary metabolites in plant cell suspension cultures. In: Varma A, Kharkwal AC. (ed) Symbiotic fungi. Berlin Heidelberg: Springer; 2009. p. 373–80.

Baldi A, Dixit VK. Yield enhancement strategies for artemisinin production by suspension cultures of Artemisia annua. Bioresour Technol 2008;99:4609–14.

Baldi A, Singh D, Dixit VK. Dual elicitation for improved production of withaferin A by cell suspension cultures of Withania somnifera. Appl Biochem Biotechnol 2008; 151:556–64.

Published

01-05-2020

How to Cite

JEET, K., A. MALAVIYA, and A. BALDI. “PRODUCTIVITY ENHANCEMENT OF CORIANDRUM SATIVUM USING PLANT BIOLOGICALS”. International Journal of Pharmacy and Pharmaceutical Sciences, vol. 12, no. 5, May 2020, pp. 60-72, doi:10.22159/ijpps.2020v12i5.37374.

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