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Essential factors for in vitro regeneration of rose and a protocol for plant regeneration from leaves
In vitro propagation of Rosa hybrida, L. cv. ‘Eiffel Tower’ was improved by the addition of thidiazuron (TDZ) and silver nitrate (AgNo3) to the culture medium. The combination of auxin and cytokinins was indispensable for inducing response from leaf discs. Maintaining cultures under dark was better...
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Published in: | Horticultural science (Praha) 2018-01, Vol.45 (2), p.83-91 |
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description | In vitro propagation of Rosa hybrida, L. cv. ‘Eiffel Tower’ was improved by the addition of thidiazuron (TDZ) and silver nitrate (AgNo3) to the culture medium. The combination of auxin and cytokinins was indispensable for inducing response from leaf discs. Maintaining cultures under dark was better than light for callus formation and quality. The source of explants was vital in the regeneration process wherein situ explants produced callus while, in vitro explants regenerated somatic embryos and shoots. Gibberellic acid (GA3) had a favorable effect where in vitro explants showed somatic embryogenesis with no shoots on media containing TDZ however, 37% of explants regenerated shoots directly on medium containing GA3. The presence of benzyl adenine (BA) was essential for shoot elongation, and indole butyric acid (IBA) was better than indole acetic acid (IAA) for rooting. The optimum conditions produced rooted plants from leaf discs within ten weeks. The reported results clarify factors controlling in vitro regeneration of R. hybrida, and provide a rapid protocol allowing further improvements of rose. |
doi_str_mv | 10.17221/12/2017-HORTSCI |
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The combination of auxin and cytokinins was indispensable for inducing response from leaf discs. Maintaining cultures under dark was better than light for callus formation and quality. The source of explants was vital in the regeneration process wherein situ explants produced callus while, in vitro explants regenerated somatic embryos and shoots. Gibberellic acid (GA3) had a favorable effect where in vitro explants showed somatic embryogenesis with no shoots on media containing TDZ however, 37% of explants regenerated shoots directly on medium containing GA3. The presence of benzyl adenine (BA) was essential for shoot elongation, and indole butyric acid (IBA) was better than indole acetic acid (IAA) for rooting. The optimum conditions produced rooted plants from leaf discs within ten weeks. The reported results clarify factors controlling in vitro regeneration of R. hybrida, and provide a rapid protocol allowing further improvements of rose.</description><subject>Acetic acid</subject><subject>Adenine</subject><subject>Butyric acid</subject><subject>Callus</subject><subject>Cytokinins</subject><subject>direct regeneration</subject><subject>Elongation</subject><subject>embryogenesis</subject><subject>Embryonic growth stage</subject><subject>Embryos</subject><subject>Explants</subject><subject>Gibberellic acid</subject><subject>Indole-3-butyric acid</subject><subject>leaf discs</subject><subject>Leaves</subject><subject>organogenesis</subject><subject>Plants</subject><subject>Propagation</subject><subject>Regeneration</subject><subject>Rooting</subject><subject>rosa hybrida</subject><subject>Shoots</subject><subject>Silver</subject><subject>Silver nitrate</subject><subject>Somatic embryogenesis</subject><subject>Thidiazuron</subject><issn>0862-867X</issn><issn>1805-9333</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpVkc1rHDEMxU1poUuae4-GnKex_D3HsKTNQiCQptCbkb_CLJPx1nYC_e872Q2FnATip_ckPUK-AvsGhnO4BH7JGZjh5u7-4ed294FswDI1jEKIj2TDrOaD1eb3Z3Le2p4xBmqUFtiGpOvW0tInnGnG0EttNJdKp4W-TL0WWtNjWlLFPpWFlkxraYniEinSQy29hDIfBw4zLv09nWt5onPCl9S-kE8Z55bO3-oZ-fX9-mF7M9ze_dhtr26HIMzYB6OzTpIFQPDWq5CD8pCTj6O2GI0FERNEYT3DPOYYhGTSW5QGlfYAXJyR3Uk3Fty7Q52esP51BSd3bJT66LD2KczJRcGVyBosaimVYR5VXE20N0LJBHbVujhprXf-eU6tu315rsu6vuOKrZSwSq4UO1Fh_UyrKf93BeaO2Tjg7jUb95aN-AeXsIMj</recordid><startdate>20180101</startdate><enddate>20180101</enddate><creator>Mahmoud, Inas Mohamed Ali</creator><creator>Hassanein, Anber Mahmoud Ahmed</creator><general>Czech Academy of Agricultural Sciences (CAAS)</general><general>Czech Academy of Agricultural Sciences</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X2</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>M0K</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>DOA</scope></search><sort><creationdate>20180101</creationdate><title>Essential factors for in vitro regeneration of rose and a protocol for plant regeneration from leaves</title><author>Mahmoud, Inas Mohamed Ali ; Hassanein, Anber Mahmoud Ahmed</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c379t-76f6e40c1a1b8b5cfc5b1febd968ad7813de1d38b0af9fdc3404b8a47a56b1123</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Acetic acid</topic><topic>Adenine</topic><topic>Butyric acid</topic><topic>Callus</topic><topic>Cytokinins</topic><topic>direct regeneration</topic><topic>Elongation</topic><topic>embryogenesis</topic><topic>Embryonic growth stage</topic><topic>Embryos</topic><topic>Explants</topic><topic>Gibberellic acid</topic><topic>Indole-3-butyric acid</topic><topic>leaf discs</topic><topic>Leaves</topic><topic>organogenesis</topic><topic>Plants</topic><topic>Propagation</topic><topic>Regeneration</topic><topic>Rooting</topic><topic>rosa hybrida</topic><topic>Shoots</topic><topic>Silver</topic><topic>Silver nitrate</topic><topic>Somatic embryogenesis</topic><topic>Thidiazuron</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mahmoud, Inas Mohamed Ali</creatorcontrib><creatorcontrib>Hassanein, Anber Mahmoud Ahmed</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Agricultural Science Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>SciTech Premium Collection</collection><collection>Agriculture Science Database</collection><collection>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</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 China</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Horticultural science (Praha)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mahmoud, Inas Mohamed Ali</au><au>Hassanein, Anber Mahmoud Ahmed</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Essential factors for in vitro regeneration of rose and a protocol for plant regeneration from leaves</atitle><jtitle>Horticultural science (Praha)</jtitle><date>2018-01-01</date><risdate>2018</risdate><volume>45</volume><issue>2</issue><spage>83</spage><epage>91</epage><pages>83-91</pages><issn>0862-867X</issn><eissn>1805-9333</eissn><abstract>In vitro propagation of Rosa hybrida, L. cv. ‘Eiffel Tower’ was improved by the addition of thidiazuron (TDZ) and silver nitrate (AgNo3) to the culture medium. The combination of auxin and cytokinins was indispensable for inducing response from leaf discs. Maintaining cultures under dark was better than light for callus formation and quality. The source of explants was vital in the regeneration process wherein situ explants produced callus while, in vitro explants regenerated somatic embryos and shoots. Gibberellic acid (GA3) had a favorable effect where in vitro explants showed somatic embryogenesis with no shoots on media containing TDZ however, 37% of explants regenerated shoots directly on medium containing GA3. The presence of benzyl adenine (BA) was essential for shoot elongation, and indole butyric acid (IBA) was better than indole acetic acid (IAA) for rooting. The optimum conditions produced rooted plants from leaf discs within ten weeks. The reported results clarify factors controlling in vitro regeneration of R. hybrida, and provide a rapid protocol allowing further improvements of rose.</abstract><cop>Prague</cop><pub>Czech Academy of Agricultural Sciences (CAAS)</pub><doi>10.17221/12/2017-HORTSCI</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acetic acid Adenine Butyric acid Callus Cytokinins direct regeneration Elongation embryogenesis Embryonic growth stage Embryos Explants Gibberellic acid Indole-3-butyric acid leaf discs Leaves organogenesis Plants Propagation Regeneration Rooting rosa hybrida Shoots Silver Silver nitrate Somatic embryogenesis Thidiazuron |
title | Essential factors for in vitro regeneration of rose and a protocol for plant regeneration from leaves |
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