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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
Main Authors: Gerardo Armando Aguado-Santacruz, Cabrera-Ponce, José Luis, Victor Olalde-Portugal, Ma. Rosario Sánchez-González, Márquez-Guzmán, Judith, Herrera-Estrella, Luis
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container_title In vitro cellular & developmental biology. Plant
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creator Gerardo Armando Aguado-Santacruz
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Herrera-Estrella, Luis
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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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 &amp; 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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source Springer Link; JSTOR Archival Journals
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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