Development of a new culture medium and efficient protocol for "in vitro" micropropagation of "Ceratonia siliqua L."
A new basal culture medium was developed and tested using a rapid and efficient protocol of in vitro axillary shoot bud proliferation of Ceratonia siliqua L., an important Mediterranean Fabaceae plant species. In a first experiment, the new formulated 'LA' mineral composition significantly...
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Veröffentlicht in: | In vitro cellular & developmental biology. Plant 2019-10, Vol.55 (5), p.615-624 |
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description | A new basal culture medium was developed and tested using a rapid and efficient protocol of in vitro axillary shoot bud proliferation of Ceratonia siliqua L., an important Mediterranean Fabaceae plant species. In a first experiment, the new formulated 'LA' mineral composition significantly improved shoot growth and proliferation as compared with Murashige and Skoog medium (MS, 1962) in both solid and liquid culture media. However, the liquid culture system proved to be the most suitable for shoot induction, shoot length (about fourfold higher), and multiplication rate (about two-fold higher), the difference being significant. The measured growth and proliferation parameters were further improved when LA mineral composition was optimized, in a second experiment. The highest multiplication rate (6.3) was achieved during the second subculture using the optimized 'LAC' medium. Noticeably, hyperhydricity and shoot-tip necrosis symptoms were absent in both formulated LA and LAC compositions when using the liquid culture system. In vitro rooting in solid medium showed 41.7 to 46.3% response on a solid medium which was more suitable than the liquid culture system, the difference being significant. In contrast, pretreated microcuttings with 3 μM IBA (indole-3-butyric acid) were successfully rooted ex vitro, showing significantly higher response (91.7%), average root number (8.3), and root length (31.5 mm). The plantlets were successfully acclimatized showing more than 90% survivability and normal morphology. The present study is a first cost-effective protocol for carob micropropagation combining the use of the newly formulated LAC basal medium, a liquid culture system, and ex vitro rooting. |
doi_str_mv | 10.1007/s11627-019-09990-6 |
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In a first experiment, the new formulated 'LA' mineral composition significantly improved shoot growth and proliferation as compared with Murashige and Skoog medium (MS, 1962) in both solid and liquid culture media. However, the liquid culture system proved to be the most suitable for shoot induction, shoot length (about fourfold higher), and multiplication rate (about two-fold higher), the difference being significant. The measured growth and proliferation parameters were further improved when LA mineral composition was optimized, in a second experiment. The highest multiplication rate (6.3) was achieved during the second subculture using the optimized 'LAC' medium. Noticeably, hyperhydricity and shoot-tip necrosis symptoms were absent in both formulated LA and LAC compositions when using the liquid culture system. In vitro rooting in solid medium showed 41.7 to 46.3% response on a solid medium which was more suitable than the liquid culture system, the difference being significant. In contrast, pretreated microcuttings with 3 μM IBA (indole-3-butyric acid) were successfully rooted ex vitro, showing significantly higher response (91.7%), average root number (8.3), and root length (31.5 mm). The plantlets were successfully acclimatized showing more than 90% survivability and normal morphology. The present study is a first cost-effective protocol for carob micropropagation combining the use of the newly formulated LAC basal medium, a liquid culture system, and ex vitro rooting.</description><identifier>ISSN: 1054-5476</identifier><identifier>EISSN: 1475-2689</identifier><identifier>DOI: 10.1007/s11627-019-09990-6</identifier><language>eng</language><publisher>New York: Springer Science + Business Media, LLC</publisher><subject>Acclimatization ; Biomedical and Life Sciences ; Butyric acid ; Carob ; Cell Biology ; Ceratonia siliqua ; Composition ; Culture media ; Developmental Biology ; Indole-3-butyric acid ; Life Sciences ; Liquid culture ; Micropropagation ; Mineral composition ; Morphology ; Multiplication ; Necrosis ; Plant Breeding/Biotechnology ; Plant Genetics and Genomics ; Plant Sciences ; Plant species ; PLANT TISSUE CULTURE ; Plantlets ; Rooting ; Subculture ; Survivability</subject><ispartof>In vitro cellular & developmental biology. 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All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c349t-1f76be37ed3f4c8ab15392a336098daa270c6507f9785710a522929121fa123a3</citedby><cites>FETCH-LOGICAL-c349t-1f76be37ed3f4c8ab15392a336098daa270c6507f9785710a522929121fa123a3</cites><orcidid>0000-0002-2040-637X ; 0000-0003-3980-9811</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/45222667$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/45222667$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,780,784,803,27924,27925,41488,42557,51319,58017,58250</link.rule.ids></links><search><creatorcontrib>Lozzi, Assia</creatorcontrib><creatorcontrib>Abdelwahd, Rabha</creatorcontrib><creatorcontrib>Mentag, Rachid</creatorcontrib><creatorcontrib>Abousalim, Abdelhadi</creatorcontrib><title>Development of a new culture medium and efficient protocol for "in vitro" micropropagation of "Ceratonia siliqua L."</title><title>In vitro cellular & developmental biology. Plant</title><addtitle>In Vitro Cell.Dev.Biol.-Plant</addtitle><description>A new basal culture medium was developed and tested using a rapid and efficient protocol of in vitro axillary shoot bud proliferation of Ceratonia siliqua L., an important Mediterranean Fabaceae plant species. In a first experiment, the new formulated 'LA' mineral composition significantly improved shoot growth and proliferation as compared with Murashige and Skoog medium (MS, 1962) in both solid and liquid culture media. However, the liquid culture system proved to be the most suitable for shoot induction, shoot length (about fourfold higher), and multiplication rate (about two-fold higher), the difference being significant. The measured growth and proliferation parameters were further improved when LA mineral composition was optimized, in a second experiment. The highest multiplication rate (6.3) was achieved during the second subculture using the optimized 'LAC' medium. Noticeably, hyperhydricity and shoot-tip necrosis symptoms were absent in both formulated LA and LAC compositions when using the liquid culture system. In vitro rooting in solid medium showed 41.7 to 46.3% response on a solid medium which was more suitable than the liquid culture system, the difference being significant. In contrast, pretreated microcuttings with 3 μM IBA (indole-3-butyric acid) were successfully rooted ex vitro, showing significantly higher response (91.7%), average root number (8.3), and root length (31.5 mm). The plantlets were successfully acclimatized showing more than 90% survivability and normal morphology. The present study is a first cost-effective protocol for carob micropropagation combining the use of the newly formulated LAC basal medium, a liquid culture system, and ex vitro rooting.</description><subject>Acclimatization</subject><subject>Biomedical and Life Sciences</subject><subject>Butyric acid</subject><subject>Carob</subject><subject>Cell Biology</subject><subject>Ceratonia siliqua</subject><subject>Composition</subject><subject>Culture media</subject><subject>Developmental Biology</subject><subject>Indole-3-butyric acid</subject><subject>Life Sciences</subject><subject>Liquid culture</subject><subject>Micropropagation</subject><subject>Mineral composition</subject><subject>Morphology</subject><subject>Multiplication</subject><subject>Necrosis</subject><subject>Plant Breeding/Biotechnology</subject><subject>Plant Genetics and Genomics</subject><subject>Plant Sciences</subject><subject>Plant species</subject><subject>PLANT TISSUE CULTURE</subject><subject>Plantlets</subject><subject>Rooting</subject><subject>Subculture</subject><subject>Survivability</subject><issn>1054-5476</issn><issn>1475-2689</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9UEtLxDAQLqLguvoHPIWKx-okaZPmKOsTFrzoOWS7yZKlbbpJuuK_N2sFPXmagfle82XZJYYbDMBvA8aM8AKwKEAIAQU7yma45FVBWC2O0w5VWVQlZ6fZWQhbAMCA-SyL93qvWzd0uo_IGaRQrz9QM7Zx9Bp1em3HDql-jbQxtrEH1OBddI1rkXEe5bZHexu9y1FnG-_ScVAbFa3rD3L5QnsVXW8VCra1u1Gh5U1-np0Y1QZ98TPn2fvjw9viuVi-Pr0s7pZFQ0sRC2w4W2nK9ZqasqnVCldUEEUpA1GvlSIcGlYBN4LXFcegKkIEEZhgozChis6zq0k3pdqNOkS5daPvk6UkFLigtIY6ociESvFD8NrIwdtO-U-JQR7alVO7MrUrv9uVLJHoRAoJ3G-0_5X-l3U9sbYhOv_X55BHlukBwhinX_yyiBQ</recordid><startdate>20191001</startdate><enddate>20191001</enddate><creator>Lozzi, Assia</creator><creator>Abdelwahd, Rabha</creator><creator>Mentag, Rachid</creator><creator>Abousalim, Abdelhadi</creator><general>Springer Science + Business Media, LLC</general><general>Springer US</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>4T-</scope><scope>4U-</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>S0X</scope><orcidid>https://orcid.org/0000-0002-2040-637X</orcidid><orcidid>https://orcid.org/0000-0003-3980-9811</orcidid></search><sort><creationdate>20191001</creationdate><title>Development of a new culture medium and efficient protocol for "in vitro" micropropagation of "Ceratonia siliqua L."</title><author>Lozzi, Assia ; Abdelwahd, Rabha ; Mentag, Rachid ; Abousalim, Abdelhadi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c349t-1f76be37ed3f4c8ab15392a336098daa270c6507f9785710a522929121fa123a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Acclimatization</topic><topic>Biomedical and Life Sciences</topic><topic>Butyric acid</topic><topic>Carob</topic><topic>Cell Biology</topic><topic>Ceratonia siliqua</topic><topic>Composition</topic><topic>Culture media</topic><topic>Developmental Biology</topic><topic>Indole-3-butyric acid</topic><topic>Life Sciences</topic><topic>Liquid culture</topic><topic>Micropropagation</topic><topic>Mineral composition</topic><topic>Morphology</topic><topic>Multiplication</topic><topic>Necrosis</topic><topic>Plant Breeding/Biotechnology</topic><topic>Plant Genetics and Genomics</topic><topic>Plant Sciences</topic><topic>Plant species</topic><topic>PLANT TISSUE CULTURE</topic><topic>Plantlets</topic><topic>Rooting</topic><topic>Subculture</topic><topic>Survivability</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lozzi, Assia</creatorcontrib><creatorcontrib>Abdelwahd, Rabha</creatorcontrib><creatorcontrib>Mentag, Rachid</creatorcontrib><creatorcontrib>Abousalim, Abdelhadi</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Docstoc</collection><collection>University Readers</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</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>Agricultural & Environmental Science Collection</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>Agricultural Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Science Database</collection><collection>Biological Science 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>SIRS Editorial</collection><jtitle>In vitro cellular & developmental biology. Plant</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lozzi, Assia</au><au>Abdelwahd, Rabha</au><au>Mentag, Rachid</au><au>Abousalim, Abdelhadi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of a new culture medium and efficient protocol for "in vitro" micropropagation of "Ceratonia siliqua L."</atitle><jtitle>In vitro cellular & developmental biology. Plant</jtitle><stitle>In Vitro Cell.Dev.Biol.-Plant</stitle><date>2019-10-01</date><risdate>2019</risdate><volume>55</volume><issue>5</issue><spage>615</spage><epage>624</epage><pages>615-624</pages><issn>1054-5476</issn><eissn>1475-2689</eissn><abstract>A new basal culture medium was developed and tested using a rapid and efficient protocol of in vitro axillary shoot bud proliferation of Ceratonia siliqua L., an important Mediterranean Fabaceae plant species. In a first experiment, the new formulated 'LA' mineral composition significantly improved shoot growth and proliferation as compared with Murashige and Skoog medium (MS, 1962) in both solid and liquid culture media. However, the liquid culture system proved to be the most suitable for shoot induction, shoot length (about fourfold higher), and multiplication rate (about two-fold higher), the difference being significant. The measured growth and proliferation parameters were further improved when LA mineral composition was optimized, in a second experiment. The highest multiplication rate (6.3) was achieved during the second subculture using the optimized 'LAC' medium. Noticeably, hyperhydricity and shoot-tip necrosis symptoms were absent in both formulated LA and LAC compositions when using the liquid culture system. In vitro rooting in solid medium showed 41.7 to 46.3% response on a solid medium which was more suitable than the liquid culture system, the difference being significant. In contrast, pretreated microcuttings with 3 μM IBA (indole-3-butyric acid) were successfully rooted ex vitro, showing significantly higher response (91.7%), average root number (8.3), and root length (31.5 mm). The plantlets were successfully acclimatized showing more than 90% survivability and normal morphology. The present study is a first cost-effective protocol for carob micropropagation combining the use of the newly formulated LAC basal medium, a liquid culture system, and ex vitro rooting.</abstract><cop>New York</cop><pub>Springer Science + Business Media, LLC</pub><doi>10.1007/s11627-019-09990-6</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-2040-637X</orcidid><orcidid>https://orcid.org/0000-0003-3980-9811</orcidid></addata></record> |
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subjects | Acclimatization Biomedical and Life Sciences Butyric acid Carob Cell Biology Ceratonia siliqua Composition Culture media Developmental Biology Indole-3-butyric acid Life Sciences Liquid culture Micropropagation Mineral composition Morphology Multiplication Necrosis Plant Breeding/Biotechnology Plant Genetics and Genomics Plant Sciences Plant species PLANT TISSUE CULTURE Plantlets Rooting Subculture Survivability |
title | Development of a new culture medium and efficient protocol for "in vitro" micropropagation of "Ceratonia siliqua L." |
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