Influence of surfactants on growth and regeneration from mature internodal stem segments of sweet orange (Citrus sinensis) cv. Hamlin

被引:13
作者
Curtis, Ian S. [1 ]
Mirkov, T. Erik [1 ]
机构
[1] Texas A&M Univ Syst, Weslaco, TX 78596 USA
关键词
Citrus; Mature tissue; Pluronic F-68; Shoot regeneration; Surfactant; Triton X-100; Tween; 20; AGROBACTERIUM-MEDIATED TRANSFORMATION; SHOOT REGENERATION; GENETIC-TRANSFORMATION; PROTOPLAST FUSION; JUTE COTYLEDONS; PLANTS; SYSTEM; EXPRESSION; ROOTSTOCK; EXPLANTS;
D O I
10.1007/s11240-011-0037-1
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The development of a reliable shoot regeneration system for mature tissue of citrus is of major importance to accelerate the evaluation of commercial traits. Three non-ionic surfactants were evaluated independently in terms of their affects on the growth and regeneration of mature internodal stem segments of sweet orange cv. Hamlin in culture. Growth and shoot development of explants were influenced by type of surfactant added to the regeneration medium DBA3, its concentration and order of flush growth used for explant preparation. Supplementation of Pluronic F-68 at 0.001% (w/v) to the medium was the superior treatment resulting in significantly higher fresh weight gain of explant, improved mean number of shoots per explant and the percentage of explants giving shoots (33.5% from first flush) and shoot yield was twofold higher compared to treatments without surfactant (17%). Triton X-100 was the least responsive in terms of its affect on the growth and regeneration of stem segments but such shoots had a normal phenotype. Explants cultured on DBA3 medium containing Tween 20 exhibited growth and shoot yield similar to treatments without surfactant, but at concentrations 0.01-0.5% (v/v), the shoots became vitrified and failed to graft successfully in vivo. Growth and shoot yield of explants showed a general decline between flushes especially from second and third harvests. Shoots derived from stem segments which were cultured on media containing Pluronic F-68 and no surfactant had a higher survival rate (70-80%, respectively) compared to treatments using Triton X-100 at 0.001-0.1% (v/v) (33% survival). All acclimatized grafts exhibited typical mature wood characteristics and flowered 14-16 months after transfer to the greenhouse.
引用
收藏
页码:345 / 352
页数:8
相关论文
共 32 条
[1]   Genetic transformation and plant recovery from mature tissues of Citrus sinensis L.!Osbeck [J].
Almeida, WAB ;
Mourao, FAA ;
Pino, LE ;
Boscariol, RL ;
Rodriguez, APM ;
Mendes, BMJ .
PLANT SCIENCE, 2003, 164 (02) :203-211
[2]   Selectable marker-free transgenic orange plants recovered under non-selective conditions and through PCR analysis of all regenerants [J].
Ballester, A. ;
Cervera, M. ;
Pena, L. .
PLANT CELL TISSUE AND ORGAN CULTURE, 2010, 102 (03) :329-336
[3]   Agrobacterium-mediated transformation of the commercially important citrus cultivar Washington navel orange [J].
Bond, JE ;
Roose, ML .
PLANT CELL REPORTS, 1998, 18 (3-4) :229-234
[4]   Genetic transformation and regeneration of mature tissues of woody fruit plants bypassing the juvenile stage [J].
Cervera M. ;
Juárez J. ;
Navarro A. ;
Pina J.A. ;
Durán-Vila N. ;
Navarro L. ;
Peña L. .
Transgenic Research, 1998, 7 (1) :51-59
[5]   Production of transgenic adult plants from clementine mandarin by enhancing cell competence for transformation and regeneration [J].
Cervera, Magdalena ;
Navarro, Antonio ;
Navarro, Luis ;
Pena, Leandro .
TREE PHYSIOLOGY, 2008, 28 (01) :55-66
[6]  
Deng XX, 2006, TREE TRANSGENESIS: RECENT DEVELOPMENTS, P47, DOI 10.1007/3-540-32199-3_3
[7]  
DENG XX, 1992, SCI HORTIC-AMSTERDAM, V49, P55, DOI 10.1016/0304-4238(92)90142-Y
[8]   Regeneration and characterization of transgenic kumquat plants containing the Arabidopsis APETALA1 gene [J].
Duan, Yan-Xin ;
Fan, Jing ;
Guo, Wen-Wu .
PLANT CELL TISSUE AND ORGAN CULTURE, 2010, 100 (03) :273-281
[9]   Effects of antioxidants on Agrobacterium-mediated transformation and accelerated production of transgenic plants of Mexican lime (Citrus aurantifolia Swingle) [J].
Dutt, M. ;
Vasconcellos, M. ;
Grosser, J. W. .
PLANT CELL TISSUE AND ORGAN CULTURE, 2011, 107 (01) :79-89
[10]   An embryogenic suspension cell culture system for Agrobacterium-mediated transformation of citrus [J].
Dutt, M. ;
Grosser, J. W. .
PLANT CELL REPORTS, 2010, 29 (11) :1251-1260