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In Vitro Propagation of “Jarilla” (Larrea divaricata CAV.) and Secondary Metabolite Production
An efficient protocol for the in vitro germination and propagation of Larrea divaricata CAV. (Jarilla) was established. To determine the effect of different growth regulators on the growth rates and phenol production, apical-node microshoots from in vitro germinated plantlets were incubated on the f...
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Published in: | Biological & Pharmaceutical Bulletin 2008/12/01, Vol.31(12), pp.2321-2325 |
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description | An efficient protocol for the in vitro germination and propagation of Larrea divaricata CAV. (Jarilla) was established. To determine the effect of different growth regulators on the growth rates and phenol production, apical-node microshoots from in vitro germinated plantlets were incubated on the following media: 1) full-strength MS (Murashige and Skoog) salt medium with different ratios of α-naphthaleneacetic acid (NAA) and N6-benzyladenine (BA); 2) after pre-treatment with indolebutyric acid (IBA), transfer to MS medium of different inorganic salt strengths; and 3) full-strength MS salt medium with different ratios of sucrose and IBA. Successful microshoot rooting percentages were achieved by the second and third strategies, the highest being 87.5—100%. The maximum principal shoot length and node number obtained by the second strategy corresponded to the plantlets previously induced with 50 μM IBA, and grown on half- or full-strength MS salt media (7.03±0.93 and 9.86±1.07 cm, respectively) while in the third strategy the most efficient micropropagation medium was full-strength MS salt medium supplemented with 7.5 μM IBA: 3% (w/v) sucrose (7.05±1.08 and 7.0±1.51 cm, respectively). The phenol concentration was determined by analytical HPLC. The highest content of nordihydroguiaretic acid (NDGA) accumulated in microplants of L. divaricata cultivated on half-strength MS salt medium (35.90±3.82 mg/g DW). Reducing the MS medium salt concentration by half, in the absence of IBA, it resulted in a higher NDGA production. NDGA production was not sensitive to the variation of IBA concentration. The medium supplemented with 5% (w/v) sucrose and 2.5 μM IBA induced not only a higher NDGA production but also a higher quercetin production. |
doi_str_mv | 10.1248/bpb.31.2321 |
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(Jarilla) was established. To determine the effect of different growth regulators on the growth rates and phenol production, apical-node microshoots from in vitro germinated plantlets were incubated on the following media: 1) full-strength MS (Murashige and Skoog) salt medium with different ratios of α-naphthaleneacetic acid (NAA) and N6-benzyladenine (BA); 2) after pre-treatment with indolebutyric acid (IBA), transfer to MS medium of different inorganic salt strengths; and 3) full-strength MS salt medium with different ratios of sucrose and IBA. Successful microshoot rooting percentages were achieved by the second and third strategies, the highest being 87.5—100%. The maximum principal shoot length and node number obtained by the second strategy corresponded to the plantlets previously induced with 50 μM IBA, and grown on half- or full-strength MS salt media (7.03±0.93 and 9.86±1.07 cm, respectively) while in the third strategy the most efficient micropropagation medium was full-strength MS salt medium supplemented with 7.5 μM IBA: 3% (w/v) sucrose (7.05±1.08 and 7.0±1.51 cm, respectively). The phenol concentration was determined by analytical HPLC. The highest content of nordihydroguiaretic acid (NDGA) accumulated in microplants of L. divaricata cultivated on half-strength MS salt medium (35.90±3.82 mg/g DW). Reducing the MS medium salt concentration by half, in the absence of IBA, it resulted in a higher NDGA production. NDGA production was not sensitive to the variation of IBA concentration. The medium supplemented with 5% (w/v) sucrose and 2.5 μM IBA induced not only a higher NDGA production but also a higher quercetin production.</description><identifier>ISSN: 0918-6158</identifier><identifier>EISSN: 1347-5215</identifier><identifier>DOI: 10.1248/bpb.31.2321</identifier><identifier>PMID: 19043220</identifier><language>eng</language><publisher>Japan: The Pharmaceutical Society of Japan</publisher><subject>Acclimatization ; apical-double node microshoot ; Culture Media ; Germination ; Larrea - growth & development ; Larrea - metabolism ; micropropagation ; nordihydroguaiaretic acid ; plant growth regulator ; Plant Roots - growth & development ; Plant Roots - metabolism ; Quercetin - biosynthesis ; Quercetin - chemistry ; rooting ; Seeds - chemistry ; shoot elongation ; Solvents ; Tissue Culture Techniques - methods</subject><ispartof>Biological and Pharmaceutical Bulletin, 2008/12/01, Vol.31(12), pp.2321-2325</ispartof><rights>2008 The Pharmaceutical Society of Japan</rights><rights>Copyright Japan Science and Technology Agency 2008</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c574t-49074b05ddd853563af0c8bb73ec6bfb0043a0ca2f2fc512da8a58be9d40c4b3</citedby><cites>FETCH-LOGICAL-c574t-49074b05ddd853563af0c8bb73ec6bfb0043a0ca2f2fc512da8a58be9d40c4b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19043220$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Palacio, Lorena</creatorcontrib><creatorcontrib>Baeza, María Cecilia</creatorcontrib><creatorcontrib>Cantero, Juan José</creatorcontrib><creatorcontrib>Cusidó, Rosa</creatorcontrib><creatorcontrib>Goleniowski, Marta Ester</creatorcontrib><creatorcontrib>aMinisterio de Ciencia y Tecnologia Unidad CEPROCOR</creatorcontrib><creatorcontrib>bCatedra de Fisiologia Vegetal Facultad de Farmacia Universidad de Barcelona</creatorcontrib><title>In Vitro Propagation of “Jarilla” (Larrea divaricata CAV.) and Secondary Metabolite Production</title><title>Biological & Pharmaceutical Bulletin</title><addtitle>Biol Pharm Bull</addtitle><description>An efficient protocol for the in vitro germination and propagation of Larrea divaricata CAV. (Jarilla) was established. To determine the effect of different growth regulators on the growth rates and phenol production, apical-node microshoots from in vitro germinated plantlets were incubated on the following media: 1) full-strength MS (Murashige and Skoog) salt medium with different ratios of α-naphthaleneacetic acid (NAA) and N6-benzyladenine (BA); 2) after pre-treatment with indolebutyric acid (IBA), transfer to MS medium of different inorganic salt strengths; and 3) full-strength MS salt medium with different ratios of sucrose and IBA. Successful microshoot rooting percentages were achieved by the second and third strategies, the highest being 87.5—100%. The maximum principal shoot length and node number obtained by the second strategy corresponded to the plantlets previously induced with 50 μM IBA, and grown on half- or full-strength MS salt media (7.03±0.93 and 9.86±1.07 cm, respectively) while in the third strategy the most efficient micropropagation medium was full-strength MS salt medium supplemented with 7.5 μM IBA: 3% (w/v) sucrose (7.05±1.08 and 7.0±1.51 cm, respectively). The phenol concentration was determined by analytical HPLC. The highest content of nordihydroguiaretic acid (NDGA) accumulated in microplants of L. divaricata cultivated on half-strength MS salt medium (35.90±3.82 mg/g DW). Reducing the MS medium salt concentration by half, in the absence of IBA, it resulted in a higher NDGA production. NDGA production was not sensitive to the variation of IBA concentration. The medium supplemented with 5% (w/v) sucrose and 2.5 μM IBA induced not only a higher NDGA production but also a higher quercetin production.</description><subject>Acclimatization</subject><subject>apical-double node microshoot</subject><subject>Culture Media</subject><subject>Germination</subject><subject>Larrea - growth & development</subject><subject>Larrea - metabolism</subject><subject>micropropagation</subject><subject>nordihydroguaiaretic acid</subject><subject>plant growth regulator</subject><subject>Plant Roots - growth & development</subject><subject>Plant Roots - metabolism</subject><subject>Quercetin - biosynthesis</subject><subject>Quercetin - chemistry</subject><subject>rooting</subject><subject>Seeds - chemistry</subject><subject>shoot elongation</subject><subject>Solvents</subject><subject>Tissue Culture Techniques - methods</subject><issn>0918-6158</issn><issn>1347-5215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNpdkF1rFDEUhoModq1eeS8BQRSZ9eRrJnNZl6qVFQVLb0O-pmaZnWyTWcG7_hD9c_0lZjpbC96cQM5z3vOeF6HnBJaEcvnO7MySkSVllDxAC8J4UwlKxEO0gJbIqiZCHqEnOW8AoAHKHqMj0gJnlMICmbMBX4QxRfwtxZ2-1GOIA44dvrn-_Vmn0Pf65voPfr3WKXmNXfhZPq0eNV6dXCzfYD04_N3bODidfuEvftQm9mH0k5zb20ntKXrU6T77Z4f3GJ1_OD1ffarWXz-erU7WlRUNHyveQsMNCOecFEzUTHdgpTEN87Y2nYFiWYPVtKOdFYQ6LbWQxreOg-WGHaNXs-wuxau9z6Pahmx9OWDwcZ9V3UoOvOEFfPkfuIn7NBRrinDeslo0khTq7UzZFHNOvlO7FLblSEVATbmrkrtiRE25F_rFQXNvtt7ds4egC3A6A6Vb8uvj0IfB32-2uTEh9lFRAKkAGCFUAa1v5acimpoJWnTezzqbPOpL_2-RTmOwvb8zVYbnejt-17Q_dFJ-YH8BrRmsSQ</recordid><startdate>20081201</startdate><enddate>20081201</enddate><creator>Palacio, Lorena</creator><creator>Baeza, María Cecilia</creator><creator>Cantero, Juan José</creator><creator>Cusidó, Rosa</creator><creator>Goleniowski, Marta Ester</creator><general>The Pharmaceutical Society of Japan</general><general>Pharmaceutical Society of Japan</general><general>Japan Science and Technology Agency</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7U9</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20081201</creationdate><title>In Vitro Propagation of “Jarilla” (Larrea divaricata CAV.) and Secondary Metabolite Production</title><author>Palacio, Lorena ; Baeza, María Cecilia ; Cantero, Juan José ; Cusidó, Rosa ; Goleniowski, Marta Ester</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c574t-49074b05ddd853563af0c8bb73ec6bfb0043a0ca2f2fc512da8a58be9d40c4b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Acclimatization</topic><topic>apical-double node microshoot</topic><topic>Culture Media</topic><topic>Germination</topic><topic>Larrea - growth & development</topic><topic>Larrea - metabolism</topic><topic>micropropagation</topic><topic>nordihydroguaiaretic acid</topic><topic>plant growth regulator</topic><topic>Plant Roots - growth & development</topic><topic>Plant Roots - metabolism</topic><topic>Quercetin - biosynthesis</topic><topic>Quercetin - chemistry</topic><topic>rooting</topic><topic>Seeds - chemistry</topic><topic>shoot elongation</topic><topic>Solvents</topic><topic>Tissue Culture Techniques - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Palacio, Lorena</creatorcontrib><creatorcontrib>Baeza, María Cecilia</creatorcontrib><creatorcontrib>Cantero, Juan José</creatorcontrib><creatorcontrib>Cusidó, Rosa</creatorcontrib><creatorcontrib>Goleniowski, Marta Ester</creatorcontrib><creatorcontrib>aMinisterio de Ciencia y Tecnologia Unidad CEPROCOR</creatorcontrib><creatorcontrib>bCatedra de Fisiologia Vegetal Facultad de Farmacia Universidad de Barcelona</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biological & Pharmaceutical Bulletin</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Palacio, Lorena</au><au>Baeza, María Cecilia</au><au>Cantero, Juan José</au><au>Cusidó, Rosa</au><au>Goleniowski, Marta Ester</au><aucorp>aMinisterio de Ciencia y Tecnologia Unidad CEPROCOR</aucorp><aucorp>bCatedra de Fisiologia Vegetal Facultad de Farmacia Universidad de Barcelona</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In Vitro Propagation of “Jarilla” (Larrea divaricata CAV.) and Secondary Metabolite Production</atitle><jtitle>Biological & Pharmaceutical Bulletin</jtitle><addtitle>Biol Pharm Bull</addtitle><date>2008-12-01</date><risdate>2008</risdate><volume>31</volume><issue>12</issue><spage>2321</spage><epage>2325</epage><pages>2321-2325</pages><issn>0918-6158</issn><eissn>1347-5215</eissn><abstract>An efficient protocol for the in vitro germination and propagation of Larrea divaricata CAV. (Jarilla) was established. To determine the effect of different growth regulators on the growth rates and phenol production, apical-node microshoots from in vitro germinated plantlets were incubated on the following media: 1) full-strength MS (Murashige and Skoog) salt medium with different ratios of α-naphthaleneacetic acid (NAA) and N6-benzyladenine (BA); 2) after pre-treatment with indolebutyric acid (IBA), transfer to MS medium of different inorganic salt strengths; and 3) full-strength MS salt medium with different ratios of sucrose and IBA. Successful microshoot rooting percentages were achieved by the second and third strategies, the highest being 87.5—100%. The maximum principal shoot length and node number obtained by the second strategy corresponded to the plantlets previously induced with 50 μM IBA, and grown on half- or full-strength MS salt media (7.03±0.93 and 9.86±1.07 cm, respectively) while in the third strategy the most efficient micropropagation medium was full-strength MS salt medium supplemented with 7.5 μM IBA: 3% (w/v) sucrose (7.05±1.08 and 7.0±1.51 cm, respectively). The phenol concentration was determined by analytical HPLC. The highest content of nordihydroguiaretic acid (NDGA) accumulated in microplants of L. divaricata cultivated on half-strength MS salt medium (35.90±3.82 mg/g DW). Reducing the MS medium salt concentration by half, in the absence of IBA, it resulted in a higher NDGA production. NDGA production was not sensitive to the variation of IBA concentration. The medium supplemented with 5% (w/v) sucrose and 2.5 μM IBA induced not only a higher NDGA production but also a higher quercetin production.</abstract><cop>Japan</cop><pub>The Pharmaceutical Society of Japan</pub><pmid>19043220</pmid><doi>10.1248/bpb.31.2321</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acclimatization apical-double node microshoot Culture Media Germination Larrea - growth & development Larrea - metabolism micropropagation nordihydroguaiaretic acid plant growth regulator Plant Roots - growth & development Plant Roots - metabolism Quercetin - biosynthesis Quercetin - chemistry rooting Seeds - chemistry shoot elongation Solvents Tissue Culture Techniques - methods |
title | In Vitro Propagation of “Jarilla” (Larrea divaricata CAV.) and Secondary Metabolite Production |
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