Callus induction and plant regeneration from immature and mature embryos of winter durum wheat genotypes


Ozgen M., Turet M., Ozcan S., SANCAK C.

PLANT BREEDING, no.6, pp.455-458, 1996 (SCI-Expanded) identifier identifier

  • Publication Type: Article / Article
  • Publication Date: 1996
  • Doi Number: 10.1111/j.1439-0523.1996.tb00956.x
  • Journal Name: PLANT BREEDING
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.455-458
  • Keywords: Triticum aestivum, Triticum durum, embryo culture, immature embryo, mature embryo, plant regeneration, tissue culture, TRITICUM-AESTIVUM L, SOMATIC EMBRYOGENESIS, LONG-TERM, CULTURE, CULTIVARS, INFLORESCENCES, INVITRO
  • Ankara University Affiliated: Yes

Abstract

Seven genotypes of winter durum wheat (Triticum durum Desf.) were cultured to establish an efficient method of callus formation and plant regeneration from mature embryo culture, and to compare the responses of immature and mature embryo cultures. Immature embryos were aseptically dissected from seeds and placed, with the scutellum upwards, in dishes containing Murashige and Skoog's (MS) mineral salts and 2 mg 2,4-dichlorophenoxyacetic acid (2,4-D) per litre. Calli and regenerated plants were maintained on 2,4-D-free medium. Mature embryos were moved slightly on the imbibed seeds. For callus formation, the seeds with moved embryos were placed, furrow downwards, in dishes containing 8 mg 2,4-D per litre. The developed calli and regenerated plants were maintained on the MS medium. Plants regenerated from both embryo cultures were vernalized and grown to maturity in soil. Variability was observed among the wheat genotypes tested for various culture responses in both explant cultures. Callus induction rate and regeneration capacity of callus were independent of each other. Mature embryos have a low frequency of callus induction but a high regeneration capacity. Considering availability, rapidity and reliability, this form of mature embryo culture can be used as an alternative method for immature embryo culture.