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Plant Science
Volume 41, Issue 2, 25 October 1985, Pages 125-132
 
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doi:10.1016/0168-9452(85)90114-1    How to Cite or Link Using DOI (Opens New Window)
Copyright © 1985 Published by Elsevier Ireland Ltd.

Plant regeneration via organogenesis and embryogenesis in the maize inbred line B73

Keith Lowea, Delia Barnes Taylora, Pat Ryana and Karol E. Patersona

aStauffer Chemical Company, 1200 South 47th Street, Richmond, CA 94804, U.S.A.

Received 8 May 1985; 
revised 27 June 1985; 
accepted 8 July 1985. 
Available online 29 January 2003.

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Abstract

Immature embryos from Zea mays L. inbred line B73 were cultured on Murashige and Skoog (MS) medium containing 0.5 mg/1 2,4-dicholorophenoxyacetic acid (2,4-D) and 12% (w/v) sucrose. A compact white callus proliferated from the scutella. When this tissue was transfered to equivalent medium containing 2% (w/v) sucrose, a green organogenic tissue was selected from the compact callus. After over 2 years in culture, this tissue was still capable of regenerating plants. A sector of this tissue spontaneously became embryogenic. Embryogenic callus can be distinguished by its friability, rapid growth rate and its mucilaginous texture. Embryogenic callus and suspensions have been maintained for approx. 2 years. Plants from organogenic tissue and embryogenic callus have been grown to maturity.

Keywords: embryogenesis; organogenesis; tissue culture; Zea mays

Abbreviations: 2,4-D, 2,4-dichlorophenoxyacetic acid; MS, Murashige and Skoog


Plant Science
Volume 41, Issue 2, 25 October 1985, Pages 125-132
 
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