Cell suspension culture: A potential in vitro culture method for clonal propagation of coconut plantlets via somatic embryogenesis

2020 ◽  
Vol 147 ◽  
pp. 112125 ◽  
Author(s):  
Eveline Y.Y. Kong ◽  
Julianne Biddle ◽  
Mike Foale ◽  
Steve W. Adkins
Proceedings ◽  
2020 ◽  
Vol 36 (1) ◽  
pp. 55
Author(s):  
Mu

Coconut (Cocos nucifera L.) is one of the most important tropical palm crops worldwide, but the gap between decreasing productivity and expanding demand is growing and is now becoming a major problem. The global coconut industry is threatened not only by palm senility but by pests/pathogen attack which is becoming exacerbated by climate change. However, conventional breeding methods cannot provide sufficient new planting materials to meet the replacement of senile and damaged palms. Hence, coconut clonal propagation via somatic embryogenesis (SE) is being developed to help meet the demand of the growing market. However, with refined medium composition, improved technical skills, optimized environmental conditions, proper acclimatization steps employed and the application of a cell suspension culture step, a much higher multiplication rate can be predicted. Several factors that affect the rate of clonal propagation are being studied: 1) determination of the effect of a non-activated charcoal (AC) medium and 2) the development of culture induction medium composition with a reduced auxin concentration. Results of the study so far show that a non-activated charcoal medium with more frequent subculture (monthly) and a lower auxin concentration is an efficient alternative approach to the traditional mainstream AC-containing medium for the initiation of embryogenic callus. With a better understanding of the callus induction medium composition, and with a liquid cell suspension culture step medium to be applied in the future, should elevate the multiplication rate of clonal plantlet production.


2008 ◽  
Vol 43 (10) ◽  
pp. 1325-1330 ◽  
Author(s):  
Lucymeire Souza Morais-Lino ◽  
Janay Almeida dos Santos-Serejo ◽  
Sebastião de Oliveira e Silva ◽  
José Raniere Ferreira de Santana ◽  
Adilson Kenji Kobayashi

The objective of this study was to establish cell suspension culture and plant regeneration via somatic embryogenesis of a Brazilian plantain, cultivar Terra Maranhão, AAB. Immature male flowers were used as explant source for generating highly embryogenic cultures 45 days after inoculation, which were used for establishment of cell suspension culture and multiplication of secondary somatic embryos. Five semisolid culture media were tested for differentiation, maturation, somatic embryos germination and for plant regeneration. An average of 558 plants per one milliliter of 5% SCV (settled cell volume) were regenerated in the MS medium, with 11.4 µM indolacetic acid and 2.2 µM 6-benzylaminopurine. Regenerated plants showed a normal development, and no visible somaclonal variation was observed in vitro. It is possible to regenerate plants from cell suspensions of plantain banana cultivar Terra using MS medium supplemented with 11.4 µM of IAA and 2.2 µM of BAP.


2017 ◽  
Vol 16 (1) ◽  
pp. 1-11
Author(s):  
Aryani Leksonowati ◽  
Witjaksono Witjaksono ◽  
Diah Ratnadewi

Aquilaria malaccensis Lam. is a plant species producing fragrant woody material that contains some resin. The compounds can be used as medicine and perfume. Sesquiterpenoid, one group of compounds has been found being synthesized and subsequently extracted from callus and cell suspension culture of Aquilaria species. The aim of this research was to find a method of producing friable calli and cell suspension cultures from leaves or internodes of A. malaccensis in vitro by using suitable plant growth regulators; cell suspension that will suitably serve as material to produce sesquiterpenoid afterwards. Calli were established in almost all treatments of auxin-cytokinin on both leaves and internod explants. The treatment of 10 mg/L IBA induced the highest percentage of callus coverage from leaves with a rather compact structure. The combined treatment of 1–2 mg/L 2.4-D and 0.2–0.3 mg/L BA induced friable callus formation in more than 80% of cultures with 27–32% callus coverage percentage.  The use of 2,4-D induced a better formation of cell suspension than Picloram, with maximum volume up to 7 mL. Cell suspension culture with fine and homogenous aggregate could be established in the medium supplemented with 0.5 –1 mg/L 2,4-D.


2016 ◽  
Vol 8 (1) ◽  
Author(s):  
U. Bhavyashree ◽  
K. Lakshmi Jayaraj ◽  
K. S. Muralikrishna ◽  
K. K. Sajini ◽  
M. K. Rajesh ◽  
...  

<p>An attempt was made to establish highly competent embryogenic cell suspension culture in coconut, a species recalcitrant to in vitro culture. Embryogenic calli were initiated from shoot meristem explants of coconut. Y3 medium supplemented with 2.4-D (4.5 μM) and glutamine (34.2 μM) was found to be the best medium to initiate cell suspension. Growth evaluation was done by packed cell volume (PCV) and it was found that maximum growth volume of 9.9% was reached at 200 days of culture initiation. About 52% of viable cells were detected through fluorescent microscopy. Cell aggregation was noticed in Y3 medium supplemented with glutamine (34.2 μM), malt extract (100mg/l), biotin (40.9 μM) and kinetin (9.3 μM), but further progress could not be achieved. It was also observed that embryogenic calli were not of a friable type, but were associated with densely aggregated cells. Because of its hard nature, we were unsuccessful to obtain high quality cell suspension.</p>


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