Published June 30, 2021
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Impact of potential stimulants on asiaticoside and madecassoside levels and expression of triterpenoid-related genes in axenic shoot cultures of Centella asiatica (L.) Urb
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- 1. * & Division of Biotechnology and Bioinformatics, Jawaharlal Nehru Tropical Botanic Garden and Research Institute, Thiruvananthapuram, 695562, Kerala, India
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Ranjith, Gouri Priya, Jisha, S., Hemanthakumar, Achutan Sudarsanan, Saji, Chinthu V., Shenoi, Rajesh A., Sabu, Kallevettankuzhy Krishnannair (2021): Impact of potential stimulants on asiaticoside and madecassoside levels and expression of triterpenoid-related genes in axenic shoot cultures of Centella asiatica (L.) Urb. Phytochemistry (112735) 186: 1-10, DOI: 10.1016/j.phytochem.2021.112735, URL: http://dx.doi.org/10.1016/j.phytochem.2021.112735
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- urn:lsid:plazi.org:pub:FFE1FFECBF43FFEBFFB5FF8CFFCCFFAA
References
- James, J.T., Dubery, I.A., 2009. Pentacyclic triterpenoids from the medicinal herb.
- James, J.T., Tugizimana, F., Steenkamp, P.A., Dubery, I.A., 2013. Metabolomic analysis of methyl jasmonate-induced triterpenoid production in the medicinal herb centella asiatica (L.) urban. Molecules 18, 4267-4281. https://doi.org/10.3390/ molecules18044267.
- Jung, E., Lee, J.A., Shin, S., Roh, K.B., Kim, J.H., Park, D., 2013. Madecassoside inhibits melanin synthesis by blocking ultraviolet-induced inflammation. Molecules 18, 15724-15736. https://doi.org/10.3390/molecules181215724.
- Kalita, R., Patar, L., Shasany, A.K., Modi, M.K., Sen, P., 2015. Molecular cloning, characterization and expression analysis of 3-hydroxy-3-methylglutaryl coenzyme A reductase gene from Centella asiatica L. Mol. Biol. Rep. 42, 1431-1439. https://doi. org/10.1007/s11033-015-3922-6.
- Kim, O.-T., Bang, K.-H., Shin, Y.-S., Lee, M.-J., Jung, S.-J., Hyun, D.-Y., Kim, Y.-C., Seong, N.-S., Cha, S.-W., Hwang, B., 2007. Enhanced production of asiaticoside from hairy root cultures of Centella asiatica (L.) Urban elicited by methyl jasmonate. Plant Cell Rep. 26, 1941-1949. https://doi.org/10.1007/s00299-007-0400-1.
- Kim, O.T., Jin, M.L., Lee, D.Y., Jetter, R., 2017. Characterization of the asiatic acid glucosyltransferase, UGT73AH1, involved in asiaticoside biosynthesis in Centella asiatica (L.) urban. Int. J. Mol. Sci. 18 https://doi.org/10.3390/ijms18122630.
- Kim, O.T., Kim, M.Y., Hong, M.H., Ahn, J.C., Hwang, B., 2004. Stimulation of asiaticoside accumulation in the whole plant cultures of Centella asiatica (L.) Urban by elicitors. Plant Cell Rep. 23, 339-344. https://doi.org/10.1007/s00299-004- 0826-7.
- Kim, O.T., Um, Y., Jin, M.L., Kim, Y.C., Bang, K.H., Hyun, D.Y., Lee, H.S., Lee, Y., 2014. Analysis of expressed sequence tags from Centella asiatica (L.) Urban hairy roots elicited by methyl jasmonate to discover genes related to cytochrome P450s and glucosyltransferases. Plant Biotechnol. Rep. 8, 211-220. https://doi.org/10.1007/ s11816-013-0311-2.
- Kim, Y.S., Cho, J.H., Park, S., Han, J.-Y., Back, K., Choi, Y.-E., 2011. Gene regulation patterns in triterpene biosynthetic pathway driven by overexpression of squalene synthase and methyl jasmonate elicitation in Bupleurum falcatum. Planta 233, 343-355. https://doi.org/10.1007/s00425-010-1292-9.
- Franklin, G., 2020. Silver nanoparticles affect phenolic and phytoalexin composition of Arabidopsis thaliana. Sci. Total Environ. 716, 135361. https://doi.org/10.1016/j. scitotenv.2019.135361.
- Kumari, S., Deori, M., Elancheran, R., Kotoky, J., Devi, R., 2016. In vitro and in vivo antioxidant, anti-hyperlipidemic properties and chemical characterization of Centella asiatica (L.) extract. Front. Pharmacol. 7, 400. https://doi.org/10.3389/ fphar.2016.00400.
- Li, B., Wang, B., Li, H., Peng, L., Ru, M., Liang, Z., Yan, X., Zhu, Y., 2016. Establishment of Salvia castanea Diels f. tomentosa Stib. hairy root cultures and the promotion of tanshinone accumulation and gene expression with Ag+, methyl jasmonate, and yeast extract elicitation. Protoplasma 253, 87-100. https://doi.org/10.1007/ s00709-015-0790-9.
- Liu, J., He, T., Lu, Q., Shang, J., Sun, H., Zhang, L., 2010. Asiatic acid preserves beta cell mass and mitigates hyperglycemia in streptozocin-induced diabetic rats. Diabetes.
- Metab. Res. Rev. 26, 448-454. https://doi.org/10.1002/dmrr.1101.
- Livak, K.J., Schmittgen, T.D., 2001. Analysis of relative gene expression data using real-time quantitative PCR and the 2 ΔΔCT method. Methods 25, 402-408. https://doi. org/10.1006/meth.2001.1262.
- Loc, N.H., Giang, N.T., 2012. Effects of elicitors on the enhancement of asiaticoside biosynthesis in cell cultures of centella (Centella asiatica L. Urban). Chem. Pap. 66, 642-648. https://doi.org/10.2478/s11696-012-0168-9.
- Loc, N.H., Giang, N.T., Huy, N.D., Lan, T.T.P., 2017. Accumulation of madecassoside - a major component of centelloside - in centella (Centella asiatica (L.) Urban) cells elicited by salicylic acid. Period. Biol. 119, 81-85. https://doi.org/10.18054/pb.
- Mangas, S., Moyano, E., Osuna, L., Cusido, R.M., Bonfill, M., Palaz´on, J., 2008a.
- Triterpenoid saponin content and the expression level of some related genes in calli of Centella asiatica. Biotechnol. Lett. 30, 1853-1859. https://doi.org/10.1007/ s10529-008-9766-6.
- Mangas, S., Moyano, E., Osuna, L., Cusido, R.M., Bonfill, M., Palaz´on, J., 2008b.
- Triterpenoid saponin content and the expression level of some related genes in calli of Centella asiatica. Biotechnol. Lett. 30, 1853. https://doi.org/10.1007/s10529- 008-9766-6.
- Mao, J., He, Z., Hao, J., Liu, T., Chen, J., Huang, S., 2019. Identification, expression, and phylogenetic analyses of terpenoid biosynthesis-related genes in secondary xylem of loblolly pine (Pinus taeda L.) based on transcriptome analyses. PeerJ 7, e6124. https://doi.org/10.7717/peerj.6124.
- Matthews, D.G., Caruso, M., Murchison, C.F., Zhu, J.Y., Wright, K.M., Harris, C.J., Gray, N.E., Quinn, J.F., Soumyanath, A., 2019. Centella asiatica improves memory and promotes antioxidative signaling in 5XFAD mice. Antioxidants 8. https://doi.
- Monton, C., Luprasong, C., Suksaeree, J., Songsak, T., 2018. Validated high performance liquid chromatography for simultaneous determination of stability of madecassoside and asiaticoside in film forming polymeric dispersions. Brazilian J. Pharmacogn. 28, 289-293. https://doi.org/10.1016/j.bjp.2018.04.003.
- Murashige, T., Skoog, F., 1962. A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiol. Plantarum 15, 473-497. https://doi.org/10.1111/ j.1399-3054.1962.tb08052.x.
- Nasution, M.Y., Restuati, M., Pulungan, A.S.S., Pratiwi, N., Diningrat, D.S., 2018. Antimicrobial activities of Centella asiatica leaf and root extracts on selected pathogenic micro-organisms. J. Med. Sci. 18, 198-204. https://doi.org/10.3923/ jms.2018.198.204.
- Oyedeji, O.A., Afolayan, A.J., 2005. Chemical composition and antibacterial activity of the essential oil of Centella asiatica. Growing in South Africa. Pharm. Biol. 43, 249-252. https://doi.org/10.1080/13880200590928843.
- Paeizi, M., Karimi, F., Razavi, K., 2018. Changes in medicinal alkaloids production and expression of related regulatory and biosynthetic genes in response to silver nitrate combined with methyl jasmonate in Catharanthus roseus in vitro propagated shoots. Plant Physiol. Biochem. 132, 623-632. https://doi.org/10.1016/j. plaphy.2018.10.015.
- Park, J.H., Choi, J.Y., Son, D.J., Park, E.K., Song, M.J., Hellstrom, M., Hong, J.T., 2017. Anti-Inflammatory effect of titrated extract of Centella asiatica in phthalic anhydride-induced allergic dermatitis animal model. Int. J. Mol. Sci. 18 https://doi. org/10.3390/ijms18040738.
- Park, W.T., Arasu, M.V., Al-Dhabi, N.A., Yeo, S.K., Jeon, J., Park, J.S., Lee, S.Y., Park, S. U., 2016. Yeast extract and silver nitrate induce the expression of phenylpropanoid biosynthetic genes and induce the accumulation of rosmarinic acid in Agastache rugosa cell culture. Molecules 21, 426. https://doi.org/10.3390/ molecules21040426.
- Patel, N., Patel, P., Kendurkar, S.V., Thulasiram, H.V., Khan, B.M., 2015. Overexpression of squalene synthase in Withania somnifera leads to enhanced withanolide biosynthesis. Plant Cell Tissue Organ Cult. 122, 409-420. https://doi.org/10.1007/ s11240-015-0778-3.
- Prasad, A., Kumari, M., Srivastava, N.K., Mathur, A.K., Mathur, A., 2018. Copper-induced modulation of biomass growth, physiological parameters, bioactive centellosides, and expression of biosynthetic pathway genes in an important medicinal herb, Centella asiatica. J. Plant Growth Regul. 37, 471-480. https://doi.org/10.1007/ s00344-017-9745-z.
- Prasad, A., Mathur, A., Kalra, A., Gupta, M.M., Lal, R.K., Mathur, A.K., 2013. Fungal elicitor-mediated enhancement in growth and asiaticoside content of Centella asiatica L. shoot cultures. Plant Growth Regul. 69, 265-273. https://doi.org/ 10.1007/s10725-012-9769-0.
- Prasad, A., Mathur, A.K., Mathur, A., 2019. Advances and emerging research trends for modulation of centelloside biosynthesis in Centella asiatica (L.) Urban- A review. Ind. Crop. Prod. https://doi.org/10.1016/j.indcrop.2019.111768.
- Putri, S.P., Nakayama, Y., Matsuda, F., Uchikata, T., Kobayashi, S., Matsubara, A., Fukusaki, E., 2013. Current metabolomics: practical applications. J. Biosci. Bioeng. 115, 579-589. https://doi.org/10.1016/j.jbiosc.2012.12.007.
- Saito, K., Hirai, M.Y., Yonekura-Sakakibara, K., 2008. Decoding genes with coexpression networks and metabolomics-'majority report by precogs. Trends Plant Sci. 13, 36-43. https://doi.org/10.1016/j.tplants.2007.10.006.
- Sangwan, R.S., Tripathi, S., Singh, J., Narnoliya, L.K., Sangwan, N.S., 2013. De novo sequencing and assembly of Centella asiatica leaf transcriptome for mapping of structural, functional, and regulatory genes with special reference to secondary metabolism. Gene 525, 58-76. https://doi.org/10.1016/j.gene.2013.04.057.
- Seo, J.-W., Jeong, J.-H., Shin, C.-G., Lo, S.-C., Han, S.-S., Yu, K.-W., Harada, E., Han, J.- Y., Choi, Y.-E., 2005. Overexpression of squalene synthase in Eleutherococcus senticosus increases phytosterol and triterpene accumulation. Phytochemistry 66, 869-877. https://doi.org/10.1016/j.phytochem.2005.02.016.
- Sh Ahmed, A., Taher, M., Mandal, U.K., Jaffri, J.M., Susanti, D., Mahmood, S., Zakaria, Z. A., 2019. Pharmacological properties of Centella asiatica hydrogel in accelerating wound healing in rabbits. BMC Compl. Alternative Med. 19, 213. https://doi.org/ 10.1186/s12906-019-2625-2.
- Sirisom, Y., Te-chato, S., 2012. The effect of peptone and silver nitrate on in vitro shoot formation in Hevea brasiliensis Muell Arg. J Agric Technol 8, 1509-1516. http://www.ijat-aatsea.comISSN1686-9141.
- Suh, H.W., Hyun, S.-H., Kim, S.-H., Lee, S.-Y., Choi, H.-K., 2013. Metabolic profiling and enhanced production of phytosterols by elicitation with methyl jasmonate and silver nitrate in whole plant cultures of Lemna paucicostata. Process Biochem. 48, 1581-1586. https://doi.org/10.1016/j.procbio.2013.06.032.
- Szkopinska ´, A., Plochocka, D., 2005. Farnesyl diphosphate synthase; regulation of product specificity. Acta Biochim. Pol. 52, 45-55. https://doi.org/10.18388/ abp.2005_3485.
- Thimmappa, R., Geisler, K., Louveau, T., O' Maille, P., Osbourn, A., 2014. Triterpene biosynthesis in plants. Annu. Rev. Plant Biol. 65, 225-257. https://doi.org/10.1146/ annurev-arplant-050312-120229.
- Yang, D., Fang, Y., Xia, P., Zhang, X., Liang, Z., 2018. Diverse responses of tanshinone biosynthesis to biotic and abiotic elicitors in hairy root cultures of Salvia miltiorrhiza and Salvia castanea Diels f. tomentosa. Gene 643, 61-67. https://doi.org/10.1016/j. gene.2017.11.067.
- Yonekura-Sakakibara, K., Saito, K., 2009. Functional genomics for plant natural product biosynthesis. Nat. Prod. Rep. 26, 1466-1487. https://doi.org/10.1039/B817077K.
- Yoo, N.H., Kim, O.T., Kim, J.B., Kim, S.H., Kim, Y.C., Bang, K.H., Hyun, D.Y., Cha, S.W., Kim, M.Y., Hwang, B., 2011a. Enhancement of centelloside production from cultured plants of Centella asiatica by combination of thidiazuron and methyl jasmonate. Plant Biotechnol. Rep. 5, 283-287. https://doi.org/10.1007/s11816-011-0173-4.
- Yoo, N.H., Kim, O.T., Kim, J.B., Kim, S.H., Kim, Y.C., Bang, K.H., Hyun, D.Y., Cha, S.W., Kim, M.Y., Hwang, B., 2011b. Enhancement of centelloside production from cultured plants of Centella asiatica by combination of thidiazuron and methyl jasmonate. Plant Biotechnol. Rep. 5, 283-287. https://doi.org/10.1007/s11816-011-0173-4.
- Zhang, L., Li, H.-Z., Gong, X., Luo, F.-L., Wang, B., Hu, N., Wang, C.-D., Zhang, Z., Wan, J.-Y., 2010. Protective effects of Asiaticoside on acute liver injury induced by lipopolysaccharide/D-galactosamine in mice. Phytomedicine 17, 811-819. https:// doi.org/10.1016/j.phymed.2010.01.008.
- Zhou, J.-S., Ji, S.-L., Ren, M.-F., He, Y.-L., Jing, X.-R., Xu, J.-W., 2014. Enhanced accumulation of individual ganoderic acids in a submerged culture of Ganoderma lucidum by the overexpression of squalene synthase gene. Biochem. Eng. J. 90, 178-183. https://doi.org/10.1016/j.bej.2014.06.008.