Plant regeneration of sweet orange (Citrus sinensis) from thin sections of mature stem segments
Identifieur interne : 000727 ( PascalFrancis/Corpus ); précédent : 000726; suivant : 000728Plant regeneration of sweet orange (Citrus sinensis) from thin sections of mature stem segments
Auteurs : A. K. Kobayashi ; J. C. Bespalhok ; L. F. P. Pereira ; L. G. E. VieiraSource :
- Plant cell, tissue and organ culture [ 0167-6857 ] ; 2003.
Abstract
An efficient system for in vitro plant regeneration from thin transversal stem sections explants (1-2 mm) using mature tissues of sweet orange cv. Pera was developed. Explants were cultured in different media to evaluate the frequency of regeneration and size of buds. A high percentage of explants (54% with 3.1 buds/explant) producing large buds (1-4 mm) was observed when the explants were cultivated for 2 weeks on Murashige and Skoog medium and then transferred to Woody Plant medium (WPM). Both media were supplemented with 1.8 μM 6-benzylaminopurine and 0.7 μM gibberellic acid. Adventitious buds were regenerated into whole plants by in vitro shoot-tip grafting. Regenerated plants started to flower after 12 months in the greenhouse, confirming their mature nature.
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NO : | PASCAL 03-0479314 INIST |
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ET : | Plant regeneration of sweet orange (Citrus sinensis) from thin sections of mature stem segments |
AU : | KOBAYASHI (A. K.); BESPALHOK (J. C.); PEREIRA (L. F. P.); VIEIRA (L. G. E.) |
AF : | Laboratório de Biotecnologia Vegetal, Instituto Agronômico do Paraná (IAPAR), C.P. 481/CEP 86001-970, Londrina, Paraná/Brésil (1 aut., 2 aut., 3 aut., 4 aut.) |
DT : | Publication en série; Niveau analytique |
SO : | Plant cell, tissue and organ culture; ISSN 0167-6857; Coden PTCEDJ; Pays-Bas; Da. 2003; Vol. 74; No. 1; Pp. 99-102; Bibl. 10 ref. |
LA : | Anglais |
EA : | An efficient system for in vitro plant regeneration from thin transversal stem sections explants (1-2 mm) using mature tissues of sweet orange cv. Pera was developed. Explants were cultured in different media to evaluate the frequency of regeneration and size of buds. A high percentage of explants (54% with 3.1 buds/explant) producing large buds (1-4 mm) was observed when the explants were cultivated for 2 weeks on Murashige and Skoog medium and then transferred to Woody Plant medium (WPM). Both media were supplemented with 1.8 μM 6-benzylaminopurine and 0.7 μM gibberellic acid. Adventitious buds were regenerated into whole plants by in vitro shoot-tip grafting. Regenerated plants started to flower after 12 months in the greenhouse, confirming their mature nature. |
CC : | 002A |
LO : | INIST-19374.354000111089750110 |
ID : | 03-0479314 |
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Pascal:03-0479314Le document en format XML
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<ET>Plant regeneration of sweet orange (Citrus sinensis) from thin sections of mature stem segments</ET>
<AU>KOBAYASHI (A. K.); BESPALHOK (J. C.); PEREIRA (L. F. P.); VIEIRA (L. G. E.)</AU>
<AF>Laboratório de Biotecnologia Vegetal, Instituto Agronômico do Paraná (IAPAR), C.P. 481/CEP 86001-970, Londrina, Paraná/Brésil (1 aut., 2 aut., 3 aut., 4 aut.)</AF>
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<EA>An efficient system for in vitro plant regeneration from thin transversal stem sections explants (1-2 mm) using mature tissues of sweet orange cv. Pera was developed. Explants were cultured in different media to evaluate the frequency of regeneration and size of buds. A high percentage of explants (54% with 3.1 buds/explant) producing large buds (1-4 mm) was observed when the explants were cultivated for 2 weeks on Murashige and Skoog medium and then transferred to Woody Plant medium (WPM). Both media were supplemented with 1.8 μM 6-benzylaminopurine and 0.7 μM gibberellic acid. Adventitious buds were regenerated into whole plants by in vitro shoot-tip grafting. Regenerated plants started to flower after 12 months in the greenhouse, confirming their mature nature.</EA>
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