Generation and multiplication of plantlets from callus derived from Haplopappus gracilus (Nutt.) Gray and their karyotype analysis

Unopened flower heads of Haplopappus gracilis (2n = 4) provided primary explants for callus production and subsequent induction of organized growth. Callus was initiated from small (3-5 mm in length) floral buds with benzylaminopurine (BAP) (44.4 micromoles; 10 mg/l) and naphthalene acetic acid (NA...

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Détails bibliographiques
Publié dans:Plant science : an international journal of experimental plant biology. - 1985. - 75(1991) vom: 20., Seite 245-55
Auteur principal: Kann, R P (Auteur)
Autres auteurs: O'Connor, S A (Autre), Levine, H G, Krikorian, A D
Format: Article
Langue:English
Publié: 1991
Accès à la collection:Plant science : an international journal of experimental plant biology
Sujets:Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S. NASA Discipline Number 40-50 NASA Discipline Plant Biology NASA Program Space Biology Non-NASA Center Benzyl Compounds Culture Media Plant Growth Regulators plus... Purines Adenine JAC85A2161 benzylaminopurine KXG6A989PS Kinetin P39Y9652YJ
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520 |a Unopened flower heads of Haplopappus gracilis (2n = 4) provided primary explants for callus production and subsequent induction of organized growth. Callus was initiated from small (3-5 mm in length) floral buds with benzylaminopurine (BAP) (44.4 micromoles; 10 mg/l) and naphthalene acetic acid (NAA) (0.54 micromole; 0.1 mg/l). Lowering the BAP level to 4.44 micromoles (1 mg/l) but maintaining the NAA level, gave rise to organized but highly compressed shoot growing points from an otherwise undifferentiated callus mass. Shoots selected from such cultures were maintainable and could be proliferated by growing 1-1.5-cm stem tip cuttings on Murashige and Skoog basal medium (solidified with agar) containing 0.444 micromole (0.1 mg/l) BAP and 0.054 micromole (0.01 mg/l) NAA. The stem tip multiplication rates obtainable by these means permit reliable strategies for shoot multiplication or production of rooted plantlets. Prolonged subculture and maintenance of shoots on growth regulator-free medium leads to in vitro flowering and greatly reduces rooting capacity. Karyotype analysis of chromosomes from root tip cells at metaphase and chromosome measurements show that karyologically uniform plantlets (based on chromosome number and morphology) can be obtained 
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700 1 |a Krikorian, A D  |e investigator  |4 oth 
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