Thidiazuron-induced high-frequency shoot organogenesis from leaf-derived callus of ia medicinal climber, Tylophora Indica (Burm. F.) merrill

2005 ◽  
Vol 41 (2) ◽  
pp. 124-128 ◽  
Author(s):  
T. Dennis Thomas ◽  
Boban Philip
2009 ◽  
Vol 98 (1) ◽  
pp. 59-65 ◽  
Author(s):  
Mi Jin Jeong ◽  
Hyun Jin Song ◽  
Dong Jin Park ◽  
Ji Yun Min ◽  
Jin Seong Jo ◽  
...  

HortScience ◽  
1996 ◽  
Vol 31 (5) ◽  
pp. 747b-747
Author(s):  
Xingping Zhang ◽  
Billy B. Rhodes

Tetraploids are needed to synthesize triploid watermelons, which produce “seedless” fruit with improved quality. Traditionally, the tetraploids are induced by applying colchicine to the growing apex of seedlings or soaking the seeds with colchicine solution. This method often produces low frequency of tetraploids and high frequency of chimeras. Breeding tetraploids takes much longer time than breeding diploids because of the low female fertility. We developed a tissue culture approach that allows breeders to develop desirable tetraploids with commercially acceptable volume of seed in 2 years. This tissue culture approach includes: 1) regenerate plants via shoot organogenesis from cotyledon tissue; 2) screen tetraploids based on leaf morphology (more serrated leaf margin and wider leaf shape) before transplanting, and confirm tetraploids based on pollen morphology (larger pollen with four copi) and/or seed characteristics; 3) self-pollinate tetraploids or cross the tetraploids with diploids to accurately estimate the female fertility; 4) micropropagate the best tetraploid(s) using axillary buds during the off-season; and 5) produce tetraploid seed from the cloned tetraploids in an isolation plot and evaluate the triploids derived from the tetraploid(s) in the following season. This approach has been practiced on more than 20 genotypes over the past 4 years.


2021 ◽  
Author(s):  
Silpa P ◽  
Dennis Thuruthiyil Thomas

Abstract Gymnostachyum febrifugum Benth. is a small, scapigerous, rare and endemic medicinal herb indigenous to India belonging to the family Acanthaceae. This study reports an efficient protocol for high-frequency flower bud derived callus induction and shoot organogenesis in G. febrifugum. Flower buds at 7d before anthesis (dBA) were excised from the inflorescence and cultured on MS medium supplemented with various concentrations of 2, 4-dichlorophenoxy acetic acid (2, 4-D; 0.5-2.0 mg/l) for callus induction. The optimum callus induction (78%) was obtained on MS medium supplemented with 1.5 mg/l 2, 4-D. The calli when subcultured on MS medium supplemented with different concentrations of thidiazuron (TDZ; 0.5-2.5 mg/l) or 6-benzylaminopurine BAP (0.5-2.5 mg/l) alone or in combination with 1- naphthaleneacetic acid (NAA; 0.2-0.7 mg/l) induced shoots. The highest frequency (94%) and number of shoots (44.6 shoots/unit callus) were obtained on MS medium supplemented with 2.0 mg/l TDZ and 0.5 mg/l NAA. The optimum rooting frequency (95%) and number of roots (10.2) were observed on ½ MS medium supplemented with 3.0 mg/l indole-3- butyric acid (IBA). The rooted plantlets were acclimatized and transferred to soil with 94% success.


2016 ◽  
Vol 126 (1) ◽  
pp. 141-151 ◽  
Author(s):  
Jennifer Anne Northmore ◽  
Dustin Sigurdson ◽  
Sarah Schoor ◽  
Amer Rustum ◽  
Simon D. X. Chuong

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