Clonal propagation of mulberry (Morus indica L. cultivar M-5) through in vitro culture of nodal explants

1999 ◽  
Vol 80 (3-4) ◽  
pp. 289-298 ◽  
Author(s):  
D.S Vijaya Chitra ◽  
G Padmaja
1979 ◽  
Vol 11 (3) ◽  
pp. 241-246 ◽  
Author(s):  
Joseph Roggemans ◽  
Marie-Christine Claes

2021 ◽  
Vol 27 (1) ◽  
pp. 68-77
Author(s):  
Mina Taghizadeh ◽  
Mahboubeh Ganji Dastjerdi

Abstract During different phases of in vitro culture, plant tissues may be exposed to some stresses that never encounter in their natural habitats. The most significant stresses which interfere with in vitro culture are pathogenic contamination and browning disorder. Since browning sign is occurred during all phases of in vitro culture of Spartium junceum L., the present study was done preventing explants from browning during disinfection and callogenesis phases using exposure time of sterilants (ethanol 0, 30, 60 s and home bleach 0, 10, 15 min), antioxidant compounds (PVP 0.5%, Activated charcoal 0.1%, Curcumin 0.1%), Running water (30 and 60 min) plant growth regulators (2,4-D 0, 0.5, 1 and 2 mg L-1 and BA 0, 0.1 and 0.2 mg L-1), and by changing light/dark conditions was designed. The results showed that ethanol 70% (30 s) in combination with home bleach 20% (10 min) had the best effect in control contaminations and browning sign in nodal explants of S. junceum. The application of PVP 0.5% in medium was the best treatment to control of browning nodal explants in callus induction phase. The highest callus formation and the lowest explant browning were obtained on the medium supplemented with 0.5 mg L-1 2,4-D under the darkness condition. According to the results of this study, how disinfection methods, culture medium compositions and light conditions were effective on the browning and callogenesis of Spartium junceum L.


1999 ◽  
Vol 4 (1) ◽  
pp. 47-51 ◽  
Author(s):  
Sukartiningsih ◽  
Kentaro Nakamura ◽  
Yuji Ide

2012 ◽  
Vol 2 (1) ◽  
pp. 1-5 ◽  
Author(s):  
Wesely Edward Gnanaraj ◽  
Johnson Marimuthu@Antonisamy ◽  
RB Mohanamathi ◽  
Kavitha Marappampalyam Subramanian

2017 ◽  
Vol 13 (15) ◽  
pp. 274
Author(s):  
Aurélien Mokea-Niaty ◽  
Samson Daudet Medza Mve ◽  
Alexis Nicaise Lepengue ◽  
Antoine Mitte Mbeang Beyeme ◽  
Christian Moupela ◽  
...  

Trichloroisocyanuric acid is a swimming pool disinfectant and is readily accessible. As a result, there is the need to use it as a substitute for conventional disinfectants in in vitro culture. Nodal explants of Alchornea cordifolia, harvested in a natural environment, have been rinsed abundantly with Dettol under running water. Then it was soaked in Talo Plus (550 g/l carbendazim and 100 g/l Chlorothalonil) at 5 ml/liter, which is a broad spectrum fungicide. After then, it was immersed in 70% alcohol for 10 minutes before being soaked in different solutions of trichloroisocyanuric acid to: 6, 4, 3, 2, 1, 0.3, 0.1, and 0.08%. The explants were disinfected completely of all contaminating bacterial and fungal exogenous. This was after a treatment in solutions of acidic trichloroisocyanurique of 6 to 0.08%. The results showed that the losses of active chlorine remained low during storage at temperatures of 4 to 18 ± 2°C. They reach only 5.29% after 72 hours. At room temperature of 27 ± 2 ° C, these losses are more than 30% after three days. Concentrations of 0.1 to 0.3% are effective for the disinfection of explants. This protocol of explants disinfection in vitro culture could therefore be advantageously substituted using the hypochlorite of calcium or the chloride of mercury.


HortScience ◽  
1990 ◽  
Vol 25 (9) ◽  
pp. 1137c-1137
Author(s):  
Azza Tawfik ◽  
P. E. Read ◽  
S. S. Salac

A method is described for obtaining explants free of bacterial contamination and for clonal propagation by in vitro culture of liatris axillary buds. Axillary bud growth was stimulated by removal of the shoot tips of greenhouse grown stock plants. Prior to using this approach, extreme bacterial contamination occured when explants were taken from stock plants that had not been decapitated. However, these axillary buds (0.3-0.5 cm long) were successfully established free of bacterial contamination when excised, surface disinfested and cultured on Murashige & Skoog (MS) medium supplemented with various levels of benzyladenine (BA) or kinetin and gibberellic acid (GA3). The highest number of leaves and greatest shoot length were produced by buds cultured on a medium supplemented with 1.0 mg/l BA plus 1.5 mg/l GA3. Shoot number was increased on medium containing 1.0 or 2.0 mg/l BA plus 0.5 mg/l GA3. Kinetin significantly increased the leaf number of the buds but there was no effect of kinetin on the shoot length or number. Shoots formed roots in a medium supplemented with 3 mg/l indole-3-butyric acid (IBA) plus 9 mg/l GA3. The plantlets were transferred to vermiculite and acclimatized successfully under intermittent mist in a greenhouse.


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