Establishment of Tissue Culture Protocol in Brassica (B. napus L.)

2004 ◽  
Vol 7 (2) ◽  
pp. 277-278 ◽  
Author(s):  
Ihsan Ullah ◽  
Hamid Rashid . ◽  
M. Ramzan Khan .
2015 ◽  
Vol 804 ◽  
pp. 227-230 ◽  
Author(s):  
Duongruitai Nicomrat ◽  
Jackrit Anantasaran

Murashige and Skoog (MS) medium, a common tissue culture media for orchids which is mostly supplemented with various natural organic substances with high nutritional values can accelerate the growth of plant tissues. Nevertheless, the knowledge of actual compositions of these natural added substances is limited, causing various culture results. In this study, we have investigated the effects of added natural organic nutrient ratios on 2 orchid tissue cultures, Dendrobium, Dendrobium farmeri Paxt. and Dendrobium griffithianum Lindl. Additionally, simple, affordable medium recipes, MS media supplemented with banana were thus economically sterilized by either a simple type steaming vapor boiler or an autoclave for reliability improvement. The results showed that the orchids grew better in medium supplemented with Namwa banana especially at 150 g/L for Dendrobiumfarmeri Paxt. and 75 g/L for Dendrobium griffithianum Lindl. The suitable steaming procedure at 100°C for 60 minutes was adequate for eliminating most pathogens from the media and helped both orchid seedlings cultivated very well. Moreover, the optimized homemade tissue culture protocol provides fast effectiveness, simplicity, consistently high nutritional values, and practically being suitable technique for ready transferring to the community.


2012 ◽  
Vol 11 (8) ◽  
pp. 1862-1867 ◽  
Author(s):  
Skorić Marijana ◽  
Živković Suzana ◽  
Savić Jelena ◽  
Scaron iler Branislav ◽  
Sabovljević Aneta ◽  
...  

2002 ◽  
Vol 68 (4) ◽  
pp. 424-429 ◽  
Author(s):  
J.C. Chukwujekwu ◽  
C.W. Fennell ◽  
J. van Staden

Scientifica ◽  
2016 ◽  
Vol 2016 ◽  
pp. 1-7 ◽  
Author(s):  
Mahipal S. Shekhawat ◽  
M. Manokari ◽  
C. P. Ravindran

A tissue culture protocol was developed for an important medicinal plantRungia pectinataL. in the present study. Nodal shoots were used as explants and surface-sterilized with 0.1% HgCl2solution. Murashige and Skoog (MS) medium was used to establish the cultures ofR. pectinata. The bud break was reported on MS medium supplemented with 1.0 mg L−16-benzylaminopurine (BAP). About 98% response was observed with this media combination and maximum 3.2 shoots per explant with 4.3 cm length were recorded. The shoots were further multiplied using MS medium augmented with 0.5 mg L−1each of BAP and kinetin (Kin) + 0.1 mg L−1indole-3 acetic acid (IAA). Maximum 13.2 shoots per explant with 5.2 cm length were observed. All the shoots were rooted (4.9 roots per shoot with 3.5 cm length) on half strength MS medium fortified with 2.0 mg L−1indole-3 butyric acid (IBA).In vitroflowering was induced from the shoots on half strength MS medium supplemented with same concentrations and combinations of growth regulators used for shoot multiplication under 12/12 hr light/dark photoperiod. The plantlets were hardened in the greenhouse for two months and finally transferred to the field. The foliar micromorphological studies revealed the developmental changes in stomata, vein density, and trichomes during the culture of shoots underin vitroconditions.


2015 ◽  
Vol 27 (1) ◽  
pp. 3-14 ◽  
Author(s):  
Jaime A. Teixeira da Silva ◽  
Budi Winarto ◽  
Judit Dobránszki ◽  
Songjun Zeng

Abstract Disinfection of plant material is the most important step of the tissue culture protocol. In this process, an attempt is made to eliminate microbial contaminants from the surface and interior of plant material, thus giving the explant a fighting chance at survival in vitro. Initial cultures of Anthurium species and cultivars, which are usually established from ex vitro material grown in a greenhouse, pots or in the field, easily contaminate the in vitro milieu. This review highlights the differences in disinfection protocols that exist for different species or cultivars of Anthurium. The protocol needs to be adjusted based on the material used: spadices, spathes, seeds, leaves, or roots. Regrettably, most of the currently published protocols, derived from a literature that spans over 100 published papers, have numerous weaknesses and flaws in the information provided pertaining to disinfection and infection levels. Advice for future Anthurium researchers should thus be followed cautiously.


2020 ◽  
Vol 8 (1) ◽  
pp. 2721-2726
Author(s):  
Sinchana NS ◽  
Kattimani KN ◽  
Prabhuling G ◽  
Sudesh K ◽  
Jagadeesha N

2022 ◽  
Author(s):  
Najamuddin Solangi ◽  
Mushtaque Ahmed Jatoi ◽  
Ghulam Sarwar Markhand ◽  
Adel Ahmed Abul-Soad ◽  
Muhammad Aslam Solangi ◽  
...  

2019 ◽  
Vol 7 (4) ◽  
pp. 547-555
Author(s):  
Asfandyar Chaudhary ◽  
◽  
Kashif Ali ◽  
Neha Farid ◽  
Nosheen Maqsood ◽  
...  

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