In-vitro propagation, callus culture and bioactive lignan production in Phyllanthus tenellus Roxb: a new source of phyllanthin, hypophyllanthin and phyltetralin
This is the first report on identification and quantification of important hepatoprotective and anticancer polyphenolic lignans such as phyllanthin (PH), hypophyllanthin (HPH), niranthin (NH) and phyltetralin (PT) in natural plant and in vitro cultures of Phyllanthus tenellus Roxb. The identificatio...
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description | This is the first report on identification and quantification of important hepatoprotective and anticancer polyphenolic lignans such as phyllanthin (PH), hypophyllanthin (HPH), niranthin (NH) and phyltetralin (PT) in natural plant and in vitro cultures of
Phyllanthus tenellus
Roxb. The identification of lignans was carried out by Liquid Chromatography–High Resolution Mass Spectrometry (LC–HRMS) and quantified using High-Performance Liquid Chromatography (HPLC). In addition, an efficient protocol has been developed for multiple shoot induction in nodal explants of in vitro derived shoots of
P. tenellus
. Maximum number of shoot regeneration (7.83 ± 0.15) was achieved on medium incorporated with 1.0 mg/l 6-Benzylaminopurine (BAP). The medium containing Indole-3-acetic acid (IAA) 2 mg/l was superior for induction of rooting in in vitro raised shoots. The plantlets were acclimatized to the field condition with 100% survival. The quantitative HPLC analysis showed that the lignan content was variable with the auxins and cytokinins incorporated in the medium. The lignan content was higher in callus grown on Murashige and Skoog (MS) medium + 2.0 mg/l Naphthaleneacetic acid (NAA). The reported protocol can be used for mass propagation and application of biotechnological approaches for improvement of
P. tenellus
. The results indicate intriguing possibilities for the utilization of
P. tenellus
plant parts as an alternative source and of callus culture to scale up bioactive lignan production for pharmaceutical applications. |
doi_str_mv | 10.1038/s41598-020-67637-8 |
format | Article |
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Phyllanthus tenellus
Roxb. The identification of lignans was carried out by Liquid Chromatography–High Resolution Mass Spectrometry (LC–HRMS) and quantified using High-Performance Liquid Chromatography (HPLC). In addition, an efficient protocol has been developed for multiple shoot induction in nodal explants of in vitro derived shoots of
P. tenellus
. Maximum number of shoot regeneration (7.83 ± 0.15) was achieved on medium incorporated with 1.0 mg/l 6-Benzylaminopurine (BAP). The medium containing Indole-3-acetic acid (IAA) 2 mg/l was superior for induction of rooting in in vitro raised shoots. The plantlets were acclimatized to the field condition with 100% survival. The quantitative HPLC analysis showed that the lignan content was variable with the auxins and cytokinins incorporated in the medium. The lignan content was higher in callus grown on Murashige and Skoog (MS) medium + 2.0 mg/l Naphthaleneacetic acid (NAA). The reported protocol can be used for mass propagation and application of biotechnological approaches for improvement of
P. tenellus
. The results indicate intriguing possibilities for the utilization of
P. tenellus
plant parts as an alternative source and of callus culture to scale up bioactive lignan production for pharmaceutical applications.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-020-67637-8</identifier><identifier>PMID: 32606305</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/449 ; 631/449/1736 ; 631/449/447 ; Acetic acid ; Auxins ; Benzyl Compounds - metabolism ; Benzyladenine ; Biotechnology ; Callus ; Callus culture ; Chromatography ; Culture Media - metabolism ; Cytokinins ; Cytokinins - metabolism ; Explants ; High-performance liquid chromatography ; Humanities and Social Sciences ; Indoleacetic acid ; Indoleacetic Acids - metabolism ; Lignans - metabolism ; Liquid chromatography ; Mass spectrometry ; Mass spectroscopy ; multidisciplinary ; Naphthaleneacetic acid ; Phyllanthus - metabolism ; Phyllanthus tenellus ; Plant propagation ; Plant Roots - metabolism ; Plant Shoots - metabolism ; Plantlets ; Propagation ; Purines - metabolism ; Rooting ; Science ; Science (multidisciplinary) ; Shoots</subject><ispartof>Scientific reports, 2020-06, Vol.10 (1), p.10668-10668, Article 10668</ispartof><rights>The Author(s) 2020</rights><rights>The Author(s) 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c511t-bbb8eeb21e3a56952bcbe19d7c1a54f30ed49e593ae742a15e52b939f15cd64a3</citedby><cites>FETCH-LOGICAL-c511t-bbb8eeb21e3a56952bcbe19d7c1a54f30ed49e593ae742a15e52b939f15cd64a3</cites><orcidid>0000-0002-9578-0622 ; 0000-0003-1272-9862</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7327055/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7327055/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27924,27925,41120,42189,51576,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32606305$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nikule, Harichandra A.</creatorcontrib><creatorcontrib>Nitnaware, Kirti M.</creatorcontrib><creatorcontrib>Chambhare, Mahadev R.</creatorcontrib><creatorcontrib>Kadam, Nitin S.</creatorcontrib><creatorcontrib>Borde, Mahesh Y.</creatorcontrib><creatorcontrib>Nikam, Tukaram D.</creatorcontrib><title>In-vitro propagation, callus culture and bioactive lignan production in Phyllanthus tenellus Roxb: a new source of phyllanthin, hypophyllanthin and phyltetralin</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>This is the first report on identification and quantification of important hepatoprotective and anticancer polyphenolic lignans such as phyllanthin (PH), hypophyllanthin (HPH), niranthin (NH) and phyltetralin (PT) in natural plant and in vitro cultures of
Phyllanthus tenellus
Roxb. The identification of lignans was carried out by Liquid Chromatography–High Resolution Mass Spectrometry (LC–HRMS) and quantified using High-Performance Liquid Chromatography (HPLC). In addition, an efficient protocol has been developed for multiple shoot induction in nodal explants of in vitro derived shoots of
P. tenellus
. Maximum number of shoot regeneration (7.83 ± 0.15) was achieved on medium incorporated with 1.0 mg/l 6-Benzylaminopurine (BAP). The medium containing Indole-3-acetic acid (IAA) 2 mg/l was superior for induction of rooting in in vitro raised shoots. The plantlets were acclimatized to the field condition with 100% survival. The quantitative HPLC analysis showed that the lignan content was variable with the auxins and cytokinins incorporated in the medium. The lignan content was higher in callus grown on Murashige and Skoog (MS) medium + 2.0 mg/l Naphthaleneacetic acid (NAA). The reported protocol can be used for mass propagation and application of biotechnological approaches for improvement of
P. tenellus
. The results indicate intriguing possibilities for the utilization of
P. tenellus
plant parts as an alternative source and of callus culture to scale up bioactive lignan production for pharmaceutical applications.</description><subject>631/449</subject><subject>631/449/1736</subject><subject>631/449/447</subject><subject>Acetic acid</subject><subject>Auxins</subject><subject>Benzyl Compounds - metabolism</subject><subject>Benzyladenine</subject><subject>Biotechnology</subject><subject>Callus</subject><subject>Callus culture</subject><subject>Chromatography</subject><subject>Culture Media - metabolism</subject><subject>Cytokinins</subject><subject>Cytokinins - metabolism</subject><subject>Explants</subject><subject>High-performance liquid chromatography</subject><subject>Humanities and Social Sciences</subject><subject>Indoleacetic acid</subject><subject>Indoleacetic Acids - metabolism</subject><subject>Lignans - metabolism</subject><subject>Liquid chromatography</subject><subject>Mass spectrometry</subject><subject>Mass spectroscopy</subject><subject>multidisciplinary</subject><subject>Naphthaleneacetic acid</subject><subject>Phyllanthus - 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metabolism</topic><topic>Benzyladenine</topic><topic>Biotechnology</topic><topic>Callus</topic><topic>Callus culture</topic><topic>Chromatography</topic><topic>Culture Media - metabolism</topic><topic>Cytokinins</topic><topic>Cytokinins - metabolism</topic><topic>Explants</topic><topic>High-performance liquid chromatography</topic><topic>Humanities and Social Sciences</topic><topic>Indoleacetic acid</topic><topic>Indoleacetic Acids - metabolism</topic><topic>Lignans - metabolism</topic><topic>Liquid chromatography</topic><topic>Mass spectrometry</topic><topic>Mass spectroscopy</topic><topic>multidisciplinary</topic><topic>Naphthaleneacetic acid</topic><topic>Phyllanthus - metabolism</topic><topic>Phyllanthus tenellus</topic><topic>Plant propagation</topic><topic>Plant Roots - metabolism</topic><topic>Plant Shoots - metabolism</topic><topic>Plantlets</topic><topic>Propagation</topic><topic>Purines - metabolism</topic><topic>Rooting</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><topic>Shoots</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nikule, Harichandra A.</creatorcontrib><creatorcontrib>Nitnaware, Kirti M.</creatorcontrib><creatorcontrib>Chambhare, Mahadev R.</creatorcontrib><creatorcontrib>Kadam, Nitin S.</creatorcontrib><creatorcontrib>Borde, Mahesh Y.</creatorcontrib><creatorcontrib>Nikam, Tukaram D.</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nikule, Harichandra A.</au><au>Nitnaware, Kirti M.</au><au>Chambhare, Mahadev R.</au><au>Kadam, Nitin S.</au><au>Borde, Mahesh Y.</au><au>Nikam, Tukaram D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In-vitro propagation, callus culture and bioactive lignan production in Phyllanthus tenellus Roxb: a new source of phyllanthin, hypophyllanthin and phyltetralin</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2020-06-30</date><risdate>2020</risdate><volume>10</volume><issue>1</issue><spage>10668</spage><epage>10668</epage><pages>10668-10668</pages><artnum>10668</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>This is the first report on identification and quantification of important hepatoprotective and anticancer polyphenolic lignans such as phyllanthin (PH), hypophyllanthin (HPH), niranthin (NH) and phyltetralin (PT) in natural plant and in vitro cultures of
Phyllanthus tenellus
Roxb. The identification of lignans was carried out by Liquid Chromatography–High Resolution Mass Spectrometry (LC–HRMS) and quantified using High-Performance Liquid Chromatography (HPLC). In addition, an efficient protocol has been developed for multiple shoot induction in nodal explants of in vitro derived shoots of
P. tenellus
. Maximum number of shoot regeneration (7.83 ± 0.15) was achieved on medium incorporated with 1.0 mg/l 6-Benzylaminopurine (BAP). The medium containing Indole-3-acetic acid (IAA) 2 mg/l was superior for induction of rooting in in vitro raised shoots. The plantlets were acclimatized to the field condition with 100% survival. The quantitative HPLC analysis showed that the lignan content was variable with the auxins and cytokinins incorporated in the medium. The lignan content was higher in callus grown on Murashige and Skoog (MS) medium + 2.0 mg/l Naphthaleneacetic acid (NAA). The reported protocol can be used for mass propagation and application of biotechnological approaches for improvement of
P. tenellus
. The results indicate intriguing possibilities for the utilization of
P. tenellus
plant parts as an alternative source and of callus culture to scale up bioactive lignan production for pharmaceutical applications.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>32606305</pmid><doi>10.1038/s41598-020-67637-8</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-9578-0622</orcidid><orcidid>https://orcid.org/0000-0003-1272-9862</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 631/449 631/449/1736 631/449/447 Acetic acid Auxins Benzyl Compounds - metabolism Benzyladenine Biotechnology Callus Callus culture Chromatography Culture Media - metabolism Cytokinins Cytokinins - metabolism Explants High-performance liquid chromatography Humanities and Social Sciences Indoleacetic acid Indoleacetic Acids - metabolism Lignans - metabolism Liquid chromatography Mass spectrometry Mass spectroscopy multidisciplinary Naphthaleneacetic acid Phyllanthus - metabolism Phyllanthus tenellus Plant propagation Plant Roots - metabolism Plant Shoots - metabolism Plantlets Propagation Purines - metabolism Rooting Science Science (multidisciplinary) Shoots |
title | In-vitro propagation, callus culture and bioactive lignan production in Phyllanthus tenellus Roxb: a new source of phyllanthin, hypophyllanthin and phyltetralin |
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