Literature DB >> 24213691

A rapid and efficient regeneration system for pea (Pisum sativum), suitable for transformation.

B Nauerby1, M Madsen, J Christiansen, R Wyndaele.   

Abstract

A method for plant regeneration via organogenesis in pea (Pisum sativum) using nodal thin cell layer segments has been developed.From 10 to 12 days old sterile pea seedlings, nodal expiants were excised from which leaves and axillary buds were removed. Shoot regeneration was consistently obtained from liquid cultures where the expiants were floated on the medium. Shoots could be harvested after two weeks and thereafter up to ten weeks and no important effect of the cultivar (Bodil, Puget, Rondo and Trille) used could be observed as far as shooting capacity was concerned.Rooting frequency of the regenerated shoots was cultivar dependent. Plantlets were obtained within 7 weeks after expiant excision. Agrobacterium tumefaciens carrying a disarmed Tiplasmid and a binary vector containing the ß-glucuronidase reporter gene, were used in cocultivation experiments on pea nodal expiants in order to obtain transgenic shoots.

Entities:  

Year:  1991        PMID: 24213691     DOI: 10.1007/BF00235355

Source DB:  PubMed          Journal:  Plant Cell Rep        ISSN: 0721-7714            Impact factor:   4.570


  13 in total

1.  Plant regeneration from pea protoplasts via somatic embyogenesis.

Authors:  R Lehminger-Mertens; H J Jacobsen
Journal:  Plant Cell Rep       Date:  1989-10       Impact factor: 4.570

2.  Haploid plants from pollen grains.

Authors:  J P Nitsch; C Nitsch
Journal:  Science       Date:  1969-01-03       Impact factor: 47.728

Review 3.  Basic processes underlying Agrobacterium-mediated DNA transfer to plant cells.

Authors:  P Zambryski
Journal:  Annu Rev Genet       Date:  1988       Impact factor: 16.830

4.  Direct flower neoformation from superficial tissue of small explants of Nicotiana tabacum L.

Authors:  M T Van
Journal:  Planta       Date:  1973-03       Impact factor: 4.116

5.  Nutrient requirements of suspension cultures of soybean root cells.

Authors:  O L Gamborg; R A Miller; K Ojima
Journal:  Exp Cell Res       Date:  1968-04       Impact factor: 3.905

6.  Light microscopic staining and histochemical applications for plant meristems embedded in Spurr's medium.

Authors:  J Lin; T L Rost; C Elmore
Journal:  Mikroskopie       Date:  1974-10

7.  Specificity of strain and genotype in the susceptibility of pea to Agrobacterium tumefaciens.

Authors:  S L Hobbs; J A Jackson; J D Mahon
Journal:  Plant Cell Rep       Date:  1989-05       Impact factor: 4.570

8.  Agrobacterium tumefaciens-mediated transformation of Pisum sativum L. using binary and cointegrate vectors.

Authors:  A De Kathen; H J Jacobsen
Journal:  Plant Cell Rep       Date:  1990-09       Impact factor: 4.570

9.  Plant Regeneration from Pea Leaflets Cultured in vitro and Genetic Stability of Regenerants.

Authors:  A Rubluo; K K Kartha; L A Mroginski; J Dyck
Journal:  J Plant Physiol       Date:  2012-01-20       Impact factor: 3.549

10.  Ti plasmid vector for the introduction of DNA into plant cells without alteration of their normal regeneration capacity.

Authors:  P Zambryski; H Joos; C Genetello; J Leemans; M V Montagu; J Schell
Journal:  EMBO J       Date:  1983       Impact factor: 11.598

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  2 in total

1.  High frequency adventitious shoot regeneration from immature cotyledons of pea (Pisum sativum L.).

Authors:  S Ozcan; M Barghchi; S Firek; J Draper
Journal:  Plant Cell Rep       Date:  1992-02       Impact factor: 4.570

2.  Thidiazuron-induced high frequency of shoot induction and plant regeneration in protoplast derived pea callus.

Authors:  P Böhmer; B Meyer; H J Jacobsen
Journal:  Plant Cell Rep       Date:  1995-01       Impact factor: 4.570

  2 in total

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