"In vitro" somatic embryogenesis of Texas ebony [Ebenopsis ebano [Berland.] Barneby & J.W. Grimes
Texas ebony (Ebenopsis ebano [Berland.] Barneby & J.W. Grimes) is a member of the Fabaceae that is native to Mexico. Its wood has multiple uses, and its natural propagation is limited and only by seed. The present investigation describes the first report of Texas ebony somatic embryogenesis with...
Gespeichert in:
Veröffentlicht in: | In vitro cellular & developmental biology. Plant 2021-11, Vol.57 (6), p.942-953 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 953 |
---|---|
container_issue | 6 |
container_start_page | 942 |
container_title | In vitro cellular & developmental biology. Plant |
container_volume | 57 |
creator | Ibarra-López, Alejandro del Carmen Ojeda-Zacarías, Ma Lozoya-Saldaña, Héctor Vázquez-Alvarado, Rigoberto E. Olivares-Sáenz, Emilio Treviño-Ramírez, José E. |
description | Texas ebony (Ebenopsis ebano [Berland.] Barneby & J.W. Grimes) is a member of the Fabaceae that is native to Mexico. Its wood has multiple uses, and its natural propagation is limited and only by seed. The present investigation describes the first report of Texas ebony somatic embryogenesis with the objective of identifying medium, growth regulator components, and culture conditions. Immature cotyledons were cultured on semisolid and in liquid media containing Murashige and Skoog (MS) basal salts plus 0.0 to 9.06 µM 2,4-dichlorophenoxyacetic acid (2,4-D). The most frequent generation of embryogénie callus occurred with cotyledons cultured in the dark in liquid medium containing 9.06 2,4-D. For the maturation phase, the embryogénie calluses were subcultured on semisolid MS medium with 3.78 to 30.24 µM abscisic acid (ABA), 3% and 6% polyethylene glycol (PEG) 4000, or 3 to 5% sucrose. Sucrose at 4% and 5% induced the greatest total number of somatic embryos; however, the maturation frequency and embryo quality were both higher with 6% PEG. Histological analysis revealed the ontogeny, morphology, and development of somatic embryos. Finally, the mature somatic embryos were subcultured for germination in halfstrength MS medium plus 6-benzylaminopurine (BAP; 2.22 µM and 4.44 µM), gibberellic acid (GA3; 1.45 µM and 2.89 µM), or BAP (2.22 µM) and GA 3 (1.45 µM). Embryo germination was superior with 2.22 µM BAP; however, radicle generation was poor in all of the treatments. This study demonstrated that for each phase of somatic embryogenesis, specific combinations of culture medium components and incubation environment are required. |
format | Article |
fullrecord | <record><control><sourceid>jstor</sourceid><recordid>TN_cdi_jstor_primary_45407350</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><jstor_id>45407350</jstor_id><sourcerecordid>45407350</sourcerecordid><originalsourceid>FETCH-jstor_primary_454073503</originalsourceid><addsrcrecordid>eNqFissKwjAQAIMo-PwEYfHgrSW1idWrUl_ngociJdGtVGxSskXs31vBu6cZmOmwQSAi6S2Wq3W3dS6FJ0W07LMh0YNzHvAgGjA1Oxp4FbWzMyBbqrq4ApbaNfaOBqkgsDkk-FYEqK1pII01Glt9C2plLKQbdE9lbv4FNsoZ1A3M4eSffdi7okQas16unoSTH0dsuouT7cF7UG1dVrWTck0mpOBRKHn4r38AMORARA</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>"In vitro" somatic embryogenesis of Texas ebony [Ebenopsis ebano [Berland.] Barneby & J.W. Grimes</title><source>SpringerLink Journals - AutoHoldings</source><creator>Ibarra-López, Alejandro ; del Carmen Ojeda-Zacarías, Ma ; Lozoya-Saldaña, Héctor ; Vázquez-Alvarado, Rigoberto E. ; Olivares-Sáenz, Emilio ; Treviño-Ramírez, José E.</creator><creatorcontrib>Ibarra-López, Alejandro ; del Carmen Ojeda-Zacarías, Ma ; Lozoya-Saldaña, Héctor ; Vázquez-Alvarado, Rigoberto E. ; Olivares-Sáenz, Emilio ; Treviño-Ramírez, José E.</creatorcontrib><description>Texas ebony (Ebenopsis ebano [Berland.] Barneby & J.W. Grimes) is a member of the Fabaceae that is native to Mexico. Its wood has multiple uses, and its natural propagation is limited and only by seed. The present investigation describes the first report of Texas ebony somatic embryogenesis with the objective of identifying medium, growth regulator components, and culture conditions. Immature cotyledons were cultured on semisolid and in liquid media containing Murashige and Skoog (MS) basal salts plus 0.0 to 9.06 µM 2,4-dichlorophenoxyacetic acid (2,4-D). The most frequent generation of embryogénie callus occurred with cotyledons cultured in the dark in liquid medium containing 9.06 2,4-D. For the maturation phase, the embryogénie calluses were subcultured on semisolid MS medium with 3.78 to 30.24 µM abscisic acid (ABA), 3% and 6% polyethylene glycol (PEG) 4000, or 3 to 5% sucrose. Sucrose at 4% and 5% induced the greatest total number of somatic embryos; however, the maturation frequency and embryo quality were both higher with 6% PEG. Histological analysis revealed the ontogeny, morphology, and development of somatic embryos. Finally, the mature somatic embryos were subcultured for germination in halfstrength MS medium plus 6-benzylaminopurine (BAP; 2.22 µM and 4.44 µM), gibberellic acid (GA3; 1.45 µM and 2.89 µM), or BAP (2.22 µM) and GA 3 (1.45 µM). Embryo germination was superior with 2.22 µM BAP; however, radicle generation was poor in all of the treatments. This study demonstrated that for each phase of somatic embryogenesis, specific combinations of culture medium components and incubation environment are required.</description><identifier>ISSN: 1054-5476</identifier><identifier>EISSN: 1475-2689</identifier><language>eng</language><publisher>Springer Science + Business Media, LLC</publisher><subject>PLANT TISSUE CULTURE</subject><ispartof>In vitro cellular & developmental biology. Plant, 2021-11, Vol.57 (6), p.942-953</ispartof><rights>2021 The Society for in Vitro Biology</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780</link.rule.ids></links><search><creatorcontrib>Ibarra-López, Alejandro</creatorcontrib><creatorcontrib>del Carmen Ojeda-Zacarías, Ma</creatorcontrib><creatorcontrib>Lozoya-Saldaña, Héctor</creatorcontrib><creatorcontrib>Vázquez-Alvarado, Rigoberto E.</creatorcontrib><creatorcontrib>Olivares-Sáenz, Emilio</creatorcontrib><creatorcontrib>Treviño-Ramírez, José E.</creatorcontrib><title>"In vitro" somatic embryogenesis of Texas ebony [Ebenopsis ebano [Berland.] Barneby & J.W. Grimes</title><title>In vitro cellular & developmental biology. Plant</title><description>Texas ebony (Ebenopsis ebano [Berland.] Barneby & J.W. Grimes) is a member of the Fabaceae that is native to Mexico. Its wood has multiple uses, and its natural propagation is limited and only by seed. The present investigation describes the first report of Texas ebony somatic embryogenesis with the objective of identifying medium, growth regulator components, and culture conditions. Immature cotyledons were cultured on semisolid and in liquid media containing Murashige and Skoog (MS) basal salts plus 0.0 to 9.06 µM 2,4-dichlorophenoxyacetic acid (2,4-D). The most frequent generation of embryogénie callus occurred with cotyledons cultured in the dark in liquid medium containing 9.06 2,4-D. For the maturation phase, the embryogénie calluses were subcultured on semisolid MS medium with 3.78 to 30.24 µM abscisic acid (ABA), 3% and 6% polyethylene glycol (PEG) 4000, or 3 to 5% sucrose. Sucrose at 4% and 5% induced the greatest total number of somatic embryos; however, the maturation frequency and embryo quality were both higher with 6% PEG. Histological analysis revealed the ontogeny, morphology, and development of somatic embryos. Finally, the mature somatic embryos were subcultured for germination in halfstrength MS medium plus 6-benzylaminopurine (BAP; 2.22 µM and 4.44 µM), gibberellic acid (GA3; 1.45 µM and 2.89 µM), or BAP (2.22 µM) and GA 3 (1.45 µM). Embryo germination was superior with 2.22 µM BAP; however, radicle generation was poor in all of the treatments. This study demonstrated that for each phase of somatic embryogenesis, specific combinations of culture medium components and incubation environment are required.</description><subject>PLANT TISSUE CULTURE</subject><issn>1054-5476</issn><issn>1475-2689</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqFissKwjAQAIMo-PwEYfHgrSW1idWrUl_ngociJdGtVGxSskXs31vBu6cZmOmwQSAi6S2Wq3W3dS6FJ0W07LMh0YNzHvAgGjA1Oxp4FbWzMyBbqrq4ApbaNfaOBqkgsDkk-FYEqK1pII01Glt9C2plLKQbdE9lbv4FNsoZ1A3M4eSffdi7okQas16unoSTH0dsuouT7cF7UG1dVrWTck0mpOBRKHn4r38AMORARA</recordid><startdate>20211101</startdate><startdate>20211201</startdate><enddate>20211101</enddate><enddate>20211201</enddate><creator>Ibarra-López, Alejandro</creator><creator>del Carmen Ojeda-Zacarías, Ma</creator><creator>Lozoya-Saldaña, Héctor</creator><creator>Vázquez-Alvarado, Rigoberto E.</creator><creator>Olivares-Sáenz, Emilio</creator><creator>Treviño-Ramírez, José E.</creator><general>Springer Science + Business Media, LLC</general><scope/></search><sort><creationdate>20211101</creationdate><title>"In vitro" somatic embryogenesis of Texas ebony [Ebenopsis ebano [Berland.] Barneby & J.W. Grimes</title><author>Ibarra-López, Alejandro ; del Carmen Ojeda-Zacarías, Ma ; Lozoya-Saldaña, Héctor ; Vázquez-Alvarado, Rigoberto E. ; Olivares-Sáenz, Emilio ; Treviño-Ramírez, José E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-jstor_primary_454073503</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>PLANT TISSUE CULTURE</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ibarra-López, Alejandro</creatorcontrib><creatorcontrib>del Carmen Ojeda-Zacarías, Ma</creatorcontrib><creatorcontrib>Lozoya-Saldaña, Héctor</creatorcontrib><creatorcontrib>Vázquez-Alvarado, Rigoberto E.</creatorcontrib><creatorcontrib>Olivares-Sáenz, Emilio</creatorcontrib><creatorcontrib>Treviño-Ramírez, José E.</creatorcontrib><jtitle>In vitro cellular & developmental biology. Plant</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ibarra-López, Alejandro</au><au>del Carmen Ojeda-Zacarías, Ma</au><au>Lozoya-Saldaña, Héctor</au><au>Vázquez-Alvarado, Rigoberto E.</au><au>Olivares-Sáenz, Emilio</au><au>Treviño-Ramírez, José E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>"In vitro" somatic embryogenesis of Texas ebony [Ebenopsis ebano [Berland.] Barneby & J.W. Grimes</atitle><jtitle>In vitro cellular & developmental biology. Plant</jtitle><date>2021-11-01</date><date>2021-12-01</date><risdate>2021</risdate><risdate>2021</risdate><volume>57</volume><issue>6</issue><spage>942</spage><epage>953</epage><pages>942-953</pages><issn>1054-5476</issn><eissn>1475-2689</eissn><abstract>Texas ebony (Ebenopsis ebano [Berland.] Barneby & J.W. Grimes) is a member of the Fabaceae that is native to Mexico. Its wood has multiple uses, and its natural propagation is limited and only by seed. The present investigation describes the first report of Texas ebony somatic embryogenesis with the objective of identifying medium, growth regulator components, and culture conditions. Immature cotyledons were cultured on semisolid and in liquid media containing Murashige and Skoog (MS) basal salts plus 0.0 to 9.06 µM 2,4-dichlorophenoxyacetic acid (2,4-D). The most frequent generation of embryogénie callus occurred with cotyledons cultured in the dark in liquid medium containing 9.06 2,4-D. For the maturation phase, the embryogénie calluses were subcultured on semisolid MS medium with 3.78 to 30.24 µM abscisic acid (ABA), 3% and 6% polyethylene glycol (PEG) 4000, or 3 to 5% sucrose. Sucrose at 4% and 5% induced the greatest total number of somatic embryos; however, the maturation frequency and embryo quality were both higher with 6% PEG. Histological analysis revealed the ontogeny, morphology, and development of somatic embryos. Finally, the mature somatic embryos were subcultured for germination in halfstrength MS medium plus 6-benzylaminopurine (BAP; 2.22 µM and 4.44 µM), gibberellic acid (GA3; 1.45 µM and 2.89 µM), or BAP (2.22 µM) and GA 3 (1.45 µM). Embryo germination was superior with 2.22 µM BAP; however, radicle generation was poor in all of the treatments. This study demonstrated that for each phase of somatic embryogenesis, specific combinations of culture medium components and incubation environment are required.</abstract><pub>Springer Science + Business Media, LLC</pub></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1054-5476 |
ispartof | In vitro cellular & developmental biology. Plant, 2021-11, Vol.57 (6), p.942-953 |
issn | 1054-5476 1475-2689 |
language | eng |
recordid | cdi_jstor_primary_45407350 |
source | SpringerLink Journals - AutoHoldings |
subjects | PLANT TISSUE CULTURE |
title | "In vitro" somatic embryogenesis of Texas ebony [Ebenopsis ebano [Berland.] Barneby & J.W. Grimes |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-28T11%3A48%3A28IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-jstor&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=%22In%20vitro%22%20somatic%20embryogenesis%20of%20Texas%20ebony%20%5BEbenopsis%20ebano%20%5BBerland.%5D%20Barneby%20&%20J.W.%20Grimes&rft.jtitle=In%20vitro%20cellular%20&%20developmental%20biology.%20Plant&rft.au=Ibarra-L%C3%B3pez,%20Alejandro&rft.date=2021-11-01&rft.volume=57&rft.issue=6&rft.spage=942&rft.epage=953&rft.pages=942-953&rft.issn=1054-5476&rft.eissn=1475-2689&rft_id=info:doi/&rft_dat=%3Cjstor%3E45407350%3C/jstor%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rft_jstor_id=45407350&rfr_iscdi=true |