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Tissue Culture and Plant Regeneration of Blue Grama Grass, Bouteloua gracilis (H.B.K.) Lag. ex Steud
As a first step towards applying biotechnology to blue grama, Bouteloua gracilis (H.B.K.) Lag. ex Steud., we have developed a regenerable tissue culture system for this grass. Shoot apices were isolated from 3-d-old seedlings and cultured in 15 different growth regulator formulations combining 2,4-d...
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Published in: | In vitro cellular & developmental biology. Plant 2001-03, Vol.37 (2), p.182-189 |
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description | As a first step towards applying biotechnology to blue grama, Bouteloua gracilis (H.B.K.) Lag. ex Steud., we have developed a regenerable tissue culture system for this grass. Shoot apices were isolated from 3-d-old seedlings and cultured in 15 different growth regulator formulations combining 2,4-dichlorophenoxyacetic acid (2,4-D), Picloram (4-amino-3,5,6-trichloropicolinic acid),$N^6-benzyladenine (BA)$or adenine (6-aminopurine). The highest induction of organogenic callus was obtained with formulations containing$1 mg l^{-1} (4.52 \mu M) 2,4-D plus 0.5 mg l^{-1} (2.22 \mu M) BA$, and$2 mg l^{-1} (8.88 \mu M) BA plus 1 mg l^{-1} (4.14 \mu M) Picloram$with or without$40 mg l^{-1} (296.08 \mu M) adenine$. Lower frequencies of induction were obtained for embryogenic as compared to organogenic callus. The most efficient treatments for induction of embryogenic callus contained$2 mg l^{-1} (9.05 \mu M) 2,4-D combined$with$0.25 (1.11 \mu M)$or$0.50 mg l^{-1} (2.22 \mu M) BA$, or$1 mg l^{-1} (4.52 \mu M) 2,4-D$with$0.50 mg l^{-1} (2.22 \mu M) BA$. Regeneration was achieved in hormone-free Murashige anmd Skoog (MS) medium, half-strength MS medium or MS medium plus$1 mg l^{-1} (1.44 \mu M) gibberellic acid$. The number of plantlets regenerated per 500 mg callus fresh weight on MS medium ranged from$9 for 2 mg l^{-1} (9.05 \mu M) 2,4-D to 62.2$for induction medium containing$2 mg l^{-1} (8.28 \mu M) Picloram$,$1 mg l^{-1} (4.44 \mu M) BA$and$40 mg l^{-1} (296.08 \mu M) adenine$. Regenerated plants grown in soil under greenhouse conditions reached maturity and produced seeds. |
doi_str_mv | 10.1007/s11627-001-0032-z |
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Lag. ex Steud</title><source>Springer Link</source><source>JSTOR Archival Journals</source><creator>Gerardo Armando Aguado-Santacruz ; Cabrera-Ponce, José Luis ; Victor Olalde-Portugal ; Ma. Rosario Sánchez-González ; Márquez-Guzmán, Judith ; Herrera-Estrella, Luis</creator><creatorcontrib>Gerardo Armando Aguado-Santacruz ; Cabrera-Ponce, José Luis ; Victor Olalde-Portugal ; Ma. Rosario Sánchez-González ; Márquez-Guzmán, Judith ; Herrera-Estrella, Luis</creatorcontrib><description>As a first step towards applying biotechnology to blue grama, Bouteloua gracilis (H.B.K.) Lag. ex Steud., we have developed a regenerable tissue culture system for this grass. Shoot apices were isolated from 3-d-old seedlings and cultured in 15 different growth regulator formulations combining 2,4-dichlorophenoxyacetic acid (2,4-D), Picloram (4-amino-3,5,6-trichloropicolinic acid),$N^6-benzyladenine (BA)$or adenine (6-aminopurine). The highest induction of organogenic callus was obtained with formulations containing$1 mg l^{-1} (4.52 \mu M) 2,4-D plus 0.5 mg l^{-1} (2.22 \mu M) BA$, and$2 mg l^{-1} (8.88 \mu M) BA plus 1 mg l^{-1} (4.14 \mu M) Picloram$with or without$40 mg l^{-1} (296.08 \mu M) adenine$. Lower frequencies of induction were obtained for embryogenic as compared to organogenic callus. The most efficient treatments for induction of embryogenic callus contained$2 mg l^{-1} (9.05 \mu M) 2,4-D combined$with$0.25 (1.11 \mu M)$or$0.50 mg l^{-1} (2.22 \mu M) BA$, or$1 mg l^{-1} (4.52 \mu M) 2,4-D$with$0.50 mg l^{-1} (2.22 \mu M) BA$. Regeneration was achieved in hormone-free Murashige anmd Skoog (MS) medium, half-strength MS medium or MS medium plus$1 mg l^{-1} (1.44 \mu M) gibberellic acid$. The number of plantlets regenerated per 500 mg callus fresh weight on MS medium ranged from$9 for 2 mg l^{-1} (9.05 \mu M) 2,4-D to 62.2$for induction medium containing$2 mg l^{-1} (8.28 \mu M) Picloram$,$1 mg l^{-1} (4.44 \mu M) BA$and$40 mg l^{-1} (296.08 \mu M) adenine$. Regenerated plants grown in soil under greenhouse conditions reached maturity and produced seeds.</description><identifier>ISSN: 1054-5476</identifier><identifier>EISSN: 1475-2689</identifier><identifier>DOI: 10.1007/s11627-001-0032-z</identifier><language>eng</language><publisher>Wallingford: CABI Publishing</publisher><subject>Biological and medical sciences ; Biotechnology ; Callus ; Embryos ; Eukaryotic cell cultures ; Fundamental and applied biological sciences. Psychology ; Grasses ; In vitro propagation: entire plant regeneration from tissues and cell cultures ; Methods. Procedures. Technologies ; Plant cells and fungal cells ; Plantlets ; Plants ; Protocols and Research Reports ; Regeneration ; Seedlings ; Somatic embryogenesis ; Tissue culture techniques</subject><ispartof>In vitro cellular & developmental biology. Plant, 2001-03, Vol.37 (2), p.182-189</ispartof><rights>Copyright 2001 The Society for In Vitro Biology</rights><rights>2001 INIST-CNRS</rights><rights>Copyright Society for In Vitro Biology Mar/Apr 2001</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c251t-6146397ba5397d9264be6c97b3c656eb288c362a37e1d3d1bff095d9667dd65d3</citedby><cites>FETCH-LOGICAL-c251t-6146397ba5397d9264be6c97b3c656eb288c362a37e1d3d1bff095d9667dd65d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/4293441$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/4293441$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>309,310,314,780,784,789,790,23930,23931,25140,27924,27925,58238,58471</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=992845$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Gerardo Armando Aguado-Santacruz</creatorcontrib><creatorcontrib>Cabrera-Ponce, José Luis</creatorcontrib><creatorcontrib>Victor Olalde-Portugal</creatorcontrib><creatorcontrib>Ma. Rosario Sánchez-González</creatorcontrib><creatorcontrib>Márquez-Guzmán, Judith</creatorcontrib><creatorcontrib>Herrera-Estrella, Luis</creatorcontrib><title>Tissue Culture and Plant Regeneration of Blue Grama Grass, Bouteloua gracilis (H.B.K.) Lag. ex Steud</title><title>In vitro cellular & developmental biology. Plant</title><description>As a first step towards applying biotechnology to blue grama, Bouteloua gracilis (H.B.K.) Lag. ex Steud., we have developed a regenerable tissue culture system for this grass. Shoot apices were isolated from 3-d-old seedlings and cultured in 15 different growth regulator formulations combining 2,4-dichlorophenoxyacetic acid (2,4-D), Picloram (4-amino-3,5,6-trichloropicolinic acid),$N^6-benzyladenine (BA)$or adenine (6-aminopurine). The highest induction of organogenic callus was obtained with formulations containing$1 mg l^{-1} (4.52 \mu M) 2,4-D plus 0.5 mg l^{-1} (2.22 \mu M) BA$, and$2 mg l^{-1} (8.88 \mu M) BA plus 1 mg l^{-1} (4.14 \mu M) Picloram$with or without$40 mg l^{-1} (296.08 \mu M) adenine$. Lower frequencies of induction were obtained for embryogenic as compared to organogenic callus. The most efficient treatments for induction of embryogenic callus contained$2 mg l^{-1} (9.05 \mu M) 2,4-D combined$with$0.25 (1.11 \mu M)$or$0.50 mg l^{-1} (2.22 \mu M) BA$, or$1 mg l^{-1} (4.52 \mu M) 2,4-D$with$0.50 mg l^{-1} (2.22 \mu M) BA$. Regeneration was achieved in hormone-free Murashige anmd Skoog (MS) medium, half-strength MS medium or MS medium plus$1 mg l^{-1} (1.44 \mu M) gibberellic acid$. The number of plantlets regenerated per 500 mg callus fresh weight on MS medium ranged from$9 for 2 mg l^{-1} (9.05 \mu M) 2,4-D to 62.2$for induction medium containing$2 mg l^{-1} (8.28 \mu M) Picloram$,$1 mg l^{-1} (4.44 \mu M) BA$and$40 mg l^{-1} (296.08 \mu M) adenine$. Regenerated plants grown in soil under greenhouse conditions reached maturity and produced seeds.</description><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Callus</subject><subject>Embryos</subject><subject>Eukaryotic cell cultures</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Grasses</subject><subject>In vitro propagation: entire plant regeneration from tissues and cell cultures</subject><subject>Methods. Procedures. Technologies</subject><subject>Plant cells and fungal cells</subject><subject>Plantlets</subject><subject>Plants</subject><subject>Protocols and Research Reports</subject><subject>Regeneration</subject><subject>Seedlings</subject><subject>Somatic embryogenesis</subject><subject>Tissue culture techniques</subject><issn>1054-5476</issn><issn>1475-2689</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><recordid>eNo9kF1LwzAUhosoOKc_QPAi6I2CrflOc-mGbuJA0Xkd0iYdHV07kxR0v96Myi7OB-c85z3wJsklghmCUDx4hDgWKYQoBsHp7igZISpYinkuj2MPGU0ZFfw0OfN-DSMIkRglZll731sw7ZvQOwt0a8B7o9sAPuzKttbpUHct6CowaSI2c3qj99n7ezDp-mCbrtdg5XRZN7UHt_Nskr1md2ChVxmwP-Az2N6cJyeVbry9-K_j5Ov5aTmdp4u32cv0cZGWmKGQckQ5kaLQLGYjMaeF5WUckJIzbguc5yXhWBNhkSEGFVUFJTOSc2EMZ4aMk-tBd-u67976oNZd79r4UiEpoiimIkJogErXee9spbau3mj3qxBUey_V4KWKFqm9l2oXb27-hbUvdVM53Za1PxxKiXPKInU1UGsfOnfYUiwJpYj8AeEXet4</recordid><startdate>20010301</startdate><enddate>20010301</enddate><creator>Gerardo Armando Aguado-Santacruz</creator><creator>Cabrera-Ponce, José Luis</creator><creator>Victor Olalde-Portugal</creator><creator>Ma. 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Lag. ex Steud</title><author>Gerardo Armando Aguado-Santacruz ; Cabrera-Ponce, José Luis ; Victor Olalde-Portugal ; Ma. Rosario Sánchez-González ; Márquez-Guzmán, Judith ; Herrera-Estrella, Luis</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c251t-6146397ba5397d9264be6c97b3c656eb288c362a37e1d3d1bff095d9667dd65d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>Callus</topic><topic>Embryos</topic><topic>Eukaryotic cell cultures</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Grasses</topic><topic>In vitro propagation: entire plant regeneration from tissues and cell cultures</topic><topic>Methods. Procedures. Technologies</topic><topic>Plant cells and fungal cells</topic><topic>Plantlets</topic><topic>Plants</topic><topic>Protocols and Research Reports</topic><topic>Regeneration</topic><topic>Seedlings</topic><topic>Somatic embryogenesis</topic><topic>Tissue culture techniques</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gerardo Armando Aguado-Santacruz</creatorcontrib><creatorcontrib>Cabrera-Ponce, José Luis</creatorcontrib><creatorcontrib>Victor Olalde-Portugal</creatorcontrib><creatorcontrib>Ma. 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Plant</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gerardo Armando Aguado-Santacruz</au><au>Cabrera-Ponce, José Luis</au><au>Victor Olalde-Portugal</au><au>Ma. Rosario Sánchez-González</au><au>Márquez-Guzmán, Judith</au><au>Herrera-Estrella, Luis</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tissue Culture and Plant Regeneration of Blue Grama Grass, Bouteloua gracilis (H.B.K.) Lag. ex Steud</atitle><jtitle>In vitro cellular & developmental biology. Plant</jtitle><date>2001-03-01</date><risdate>2001</risdate><volume>37</volume><issue>2</issue><spage>182</spage><epage>189</epage><pages>182-189</pages><issn>1054-5476</issn><eissn>1475-2689</eissn><abstract>As a first step towards applying biotechnology to blue grama, Bouteloua gracilis (H.B.K.) Lag. ex Steud., we have developed a regenerable tissue culture system for this grass. Shoot apices were isolated from 3-d-old seedlings and cultured in 15 different growth regulator formulations combining 2,4-dichlorophenoxyacetic acid (2,4-D), Picloram (4-amino-3,5,6-trichloropicolinic acid),$N^6-benzyladenine (BA)$or adenine (6-aminopurine). The highest induction of organogenic callus was obtained with formulations containing$1 mg l^{-1} (4.52 \mu M) 2,4-D plus 0.5 mg l^{-1} (2.22 \mu M) BA$, and$2 mg l^{-1} (8.88 \mu M) BA plus 1 mg l^{-1} (4.14 \mu M) Picloram$with or without$40 mg l^{-1} (296.08 \mu M) adenine$. Lower frequencies of induction were obtained for embryogenic as compared to organogenic callus. The most efficient treatments for induction of embryogenic callus contained$2 mg l^{-1} (9.05 \mu M) 2,4-D combined$with$0.25 (1.11 \mu M)$or$0.50 mg l^{-1} (2.22 \mu M) BA$, or$1 mg l^{-1} (4.52 \mu M) 2,4-D$with$0.50 mg l^{-1} (2.22 \mu M) BA$. Regeneration was achieved in hormone-free Murashige anmd Skoog (MS) medium, half-strength MS medium or MS medium plus$1 mg l^{-1} (1.44 \mu M) gibberellic acid$. The number of plantlets regenerated per 500 mg callus fresh weight on MS medium ranged from$9 for 2 mg l^{-1} (9.05 \mu M) 2,4-D to 62.2$for induction medium containing$2 mg l^{-1} (8.28 \mu M) Picloram$,$1 mg l^{-1} (4.44 \mu M) BA$and$40 mg l^{-1} (296.08 \mu M) adenine$. Regenerated plants grown in soil under greenhouse conditions reached maturity and produced seeds.</abstract><cop>Wallingford</cop><pub>CABI Publishing</pub><doi>10.1007/s11627-001-0032-z</doi><tpages>8</tpages></addata></record> |
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subjects | Biological and medical sciences Biotechnology Callus Embryos Eukaryotic cell cultures Fundamental and applied biological sciences. Psychology Grasses In vitro propagation: entire plant regeneration from tissues and cell cultures Methods. Procedures. Technologies Plant cells and fungal cells Plantlets Plants Protocols and Research Reports Regeneration Seedlings Somatic embryogenesis Tissue culture techniques |
title | Tissue Culture and Plant Regeneration of Blue Grama Grass, Bouteloua gracilis (H.B.K.) Lag. ex Steud |
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