scholarly journals Plant regeneration from cotyledon and leaf explants of Ceropegia bulbosa Roxb., an endangered medicinal plant

2017 ◽  
Author(s):  
Balakrishnan Subbaiyan ◽  
◽  
Vellaichamy Thangapandian ◽  
Author(s):  
Venkatachalam Balamurugan ◽  
Thomas Cheeran Amal ◽  
Palanisamy Karthika ◽  
Subramanian Selvakumar ◽  
Krishnan Vasanth

2007 ◽  
Vol 113 (1) ◽  
pp. 82-86 ◽  
Author(s):  
Shan-shan He ◽  
Chun-zhao Liu ◽  
Praveen K. Saxena

2011 ◽  
Vol 77 (4) ◽  
pp. 275-280 ◽  
Author(s):  
Arzu Ucar Turker ◽  
Esra Canserver Multu

<em>Solanum dulcamara</em> L. (bittersweet) is a medicinal plant that has been used to treat skin diseases, warts, tumors, felons, arthritis, rheumatism, bronchial congestion, heart ailments, ulcerative colitis, eye inflammations, jaundice and pneumonia. A reliable in vitro culture protocol for bittersweet was established. Explants (leaf and petiole segments) were cultured on Murashige and Skoog minimal organics (MSMO) medium with various plant growth regulator combinations. Leaf explants formed more shoots than petiole explants. Plant regeneration was observed through indirect organogenesis with both explants. Best shoot proliferation was obtained from leaf explants with 3 mg/l BA (benzyladenine) and 0.5 mg/l IAA (indole-3-acetic acid). Regenerated shoots were transferred to rooting media containing different levels of IAA (indole-3-acetic acid), IBA (indole-3-butyric acid), NAA (naphthalene acetic acid) or 2,4-D (2,4 dichlorophenoxyacetic acid). Most shoots developed roots on medium with 0.5 mg/l IBA. Rooted explants were transferred to vermiculate in Magenta containers for acclimatization and after 2 weeks, they were planted in plastic pots containing potting soil and maintained in the plant growth room.


2004 ◽  
Vol 4 (2) ◽  
pp. 219-223 ◽  
Author(s):  
N.A. Siddique . ◽  
M.A. Bari . ◽  
Sharmin Shahnewaz . ◽  
M.H. Rahman . ◽  
M.R. Hasan . ◽  
...  

2016 ◽  
Vol 8 (1) ◽  
Author(s):  
K. Dakshayini ◽  
C. Vaman Rao ◽  
Anitha Karun ◽  
U. Bhavyashree ◽  
P. Ujwal

<p>An efficient in vitro propagation and in vitro flowering protocols were developed for the medicinal plant Cichorium intybus (Asteraceae) using leaf disc explants. Media supplemented with the growth regulator naphthalene acetic acid (NAA) (1.5 mg/l) + 6-benzyle adenine (0.25 mg/l) was used for the initial induction of the callus and further subcultured to the same media for the proliferation of the callus. Pale yellow and green calli were noticed, which depends on incorporation of the growth hormones and their varying concentrations. Murashige and Skoog medium in addition with 2 mg/l kinetin+ 0.5 mg/l indole-3-acetic acid (IBA) + 500 mg/l casein hydrolysate resulted in maximum regeneration. Media supplemented via IBA (0.5 mg/l) and NAA (0.5 mg/l) (98%) was found to be<br />optimum for rhizogenesis for in vitro regenerated plants. For acclimatization 5-6 weeks mature in vitro regenerated plants were transferred into the greenhouse for acclimatization. The histological study revealed the presence actively dividing meristematic cells in callus. The occurrence of the peripheral meristematic zone associated with callus was noticed in after 20 days, which formed the shoot meristems after 45 days of incubation. To our knowledge, this is the first report on high-frequency plant regeneration which was carried out indirectly from the<br />leaf explants which was grown in controlled environment with varying concentration of the growth regulators and histology of callus of different stages from leaf explants of C. intybus.</p>


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