Plant regeneration of wildGlycine species from suspension culture-derived protoplasts View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1989-02

AUTHORS

James R. Myers, Paul A. Lazzeri, Glenn B. Collins

ABSTRACT

Protoplasts isolated from four-week old cell suspension cultures ofGlycine canescens F. J. Herm andG. clandestina Wendl. were cultured in 8P or modified 8P to a multicellular stage. Colonies of 0.5 to 1.0 mm diameter were transferred to solid media for callus growth and regeneration. Callus consisted of friable masses with compact green nodular areas. Organogenesis of both species occurred primarily from the green nodular areas. Shoot buds ofG. clandestina did not mature, but shoots ofG. canescens proliferated on MS medium, with B5 vitamins, 0.33 mgL(-1) each BA, KN, ZN, and 0.15 mgL(-1) NAA. Shoots failed to root after multiple subcultures on four different rooting media.In vitro grafting ofG. canescens scions ontoG. max root stocks allowed plants to be transferred to soil. An overall protoplast division efficiency of 48% was achieved with moderately efficient shoot regeneration inG. canescens. Division efficiencies forG. clandestina were lower (11%). Refinements of this protocol should result in high efficiencies of regeneration which would allowin vitro manipulations of these wild soybean relatives at the single cell level and would make the derivation of somatic hybrid plants possible within the genusGlycine. More... »

PAGES

112-115

Journal

TITLE

Plant Cell Reports

ISSUE

2

VOLUME

8

Author Affiliations

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf00716852

DOI

http://dx.doi.org/10.1007/bf00716852

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1016023072

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/24232998


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