scholarly journals In vitro clonal propagation, organogenesis and somatic embryogenesis in Bacopa monnieri (L.) Wettst

2019 ◽  
Vol 6 (4) ◽  
pp. 442-449
Author(s):  
Dipu Samanta ◽  
Bidisha Mallick ◽  
Debleena Roy
Keyword(s):  
Somatic Embryogenesis ◽  
Callus Induction ◽  
Clonal Propagation ◽  
Low Cost ◽  
Leaf Explants ◽  
Shoot Formation ◽  
Bacopa Monnieri ◽  
In Vitro Clonal Propagation

Bacopa monnieri (L.) Wettst is a well-known medicinal herb in the Ayurveda. It is also used as laxative and curative for ulcers, inflammation, anaemia, scabies, leucoderma, asthma and epilepsy, enlargement of spleen, leprosy and others. In vitro propagation and regeneration through somatic embryogenesis of B. monnieri has played an important role in the production of healthy, disease-free plants with desirable traits. In B. monnieri, there are few reports which indicate rapid regeneration and somatic embryogenesis. For in vitro clonal propagation, the highest shoot formation was obtained when BAP 2 mg/ l used. The best response for rooting was obtained in IAA 1.0 mg/ l. The recorded survival rate of the plants was 70%. Plants were without any detectable phenotypic variations. Cytological study indicated that the chromosome number remain same (2n= 64) in in vitro and in vivo roots. A rapid, simple and efficient protocol for plantlet regeneration was achieved through embryogenic callus from leaf explants of B. monnieri. Callus induction and embryogenesis were significantly affected by presence/absence and type and concentration of growth regulators. Best organogenic callus induction was obtained in MS medium supplemented with BAP 5mg/ l. For induction of somatic embryogenesis, auxin (2, 4-D 1 mg/ l) was used in the culture medium subsequently in basal media for embryo maturation. Kn 0.2 mg/ l was the best for production of plantlet from embryo. Thus, this can be an easiest protocol for stable clonal propagation and plant regeneration through somatic embryogenesis in B. monnieri. The protocol used here for propagation and regeneration is much easier, low cost and reliable.

scholarly journals IN VITRO REGENERATION AND MASS PROPAGATION OF AZIMA TETRACANTHA [LAM.] FROM THE LEAF EXPLANTS THROUGH CALLUS CULTURE

2017 ◽  
Vol 4 (2) ◽  
pp. 52-56
Author(s):  
Mallika Devi T
Keyword(s):  
Callus Induction ◽  
In Vitro Regeneration ◽  
Leaf Explants ◽  
Shoot Formation ◽  
Ms Medium ◽  
Apical Leaf ◽  
Half Strength ◽  
Regenerated Plantlets ◽  
Azima Tetracantha

In the present study the protocol for callus induction and regeneration in Azima tetracantha has been developed in culture medium. The young apical leaf explants were used for callus induction on MS medium containing BAP and NAA at 1.0 and 0.4mgl-1 respectively showed maximum callus induction (73%). The amount of callus responded for shoot formation (74%) was obtained in the MS medium containing BAP (1.5 mgl-1) and NAA (0.3mgl-1).The elongated shoots were rooted on half strength medium supplemented with IBA (1.5 mgl-1) and Kn (0.4 mgl-1) for shoots rooted. Regenerated plantlets were successfully acclimatized and hardened off inside the culture and then transferred to green house with better survival rate.

scholarly journals In vitro somatic embryogenesis of superior clones of robusta coffee from Lampung, Indonesia: Effect of genotypes and callus induction media

2020 ◽  
Vol 21 (8) ◽  
Author(s):  
Dwi Hapsoro ◽  
Rahmadyah Hamiranti ◽  
Yusnita Yusnita
Keyword(s):  
Somatic Embryogenesis ◽  
Callus Induction ◽  
Leaf Explants ◽  
Regeneration Medium ◽  
Embryogenic Calli ◽  
Robusta Coffee ◽  
Primary Callus ◽  
Ascorbic Acids ◽  
Superior Clones

Abstract. Hapsoro D, Hamiranti R, Yusnita Y. 2020. In vitro somatic embryogenesis of superior clones of robusta coffee from Lampung, Indonesia: Effect of genotypes and callus induction media. Biodiversitas 21: 3811-3817. This study aimed to investigate the effects of genotypes and primary callus induction media on somatic embryogenesis of superior robusta coffee clones of Lampung. Leaf explants of clones Tugusari, Komari, Tugino, and Wanto were cultured on two types of primary callus induction media (PCIM). PCIM1 consisted of half-strength MS salts, 30 gL-1 sucrose, added with (mgL-1) 0.1 thiamine-HCl, 0.5 nicotinic acids, 0.5 pyridoxine-HCl, 100 Myo-inositol, 200 ascorbic acids, 150 citric acids, and 1 benzyl adenine. PCIM2 consisted of NPCM salts, 30 gL-1 sucrose, added with (mgL-1) 15 thiamine-HCl, 1 nicotinic acid, 1 pyridoxine-HCl, 2 glycines, 130 Myo-inositol, 200 ascorbic acids, 150 citric acids, 1 2,4-dichlorophenoxyacetic acid, and 2 thidiazuron. The highest percentage (100%) of primary callus formation was found in Komari and Wanto clones. PCIM2 resulted in more primary calli than PCIM1. When subcultured to embryogenic callus induction medium, primary calli of clone Komari and Wanto developed into a high percentage of embryogenic calli, while those of the other two turned brown and died. PCIM2-derived primary calli developed into more embryogenic calli. When subcultured on somatic embryo (SE) regeneration medium, these calli underwent the formation of SE of various stages. When subcultured to plant regeneration medium, these SEs developed into plantlets.

scholarly journals Micropropagation of Turbinicarpus valdezianus (Möeller) Glass & Foster (Cactaceae) an Endemic Cactus in Northern Mexico

HortScience ◽  
2016 ◽  
Vol 51 (1) ◽  
pp. 94-97 ◽  
Author(s):  
Alejandro Martínez Palacios ◽  
Raúl Cárdenas Navarro ◽  
Diana Beatriz Hernández Ortega ◽  
Víctor Chávez Avila
Keyword(s):  
Clonal Propagation ◽  
Basal Medium ◽  
Shoot Proliferation ◽  
Adventitious Shoot ◽  
Shoot Formation ◽  
Inhibitory Effect ◽  
Multiplication Rate ◽  
Adventitious Shoot Formation ◽  
In Vitro Clonal Propagation

An in vitro clonal propagation protocol based on axillary bud development was generated for Turbinicarpus valdezianus. An efficient multiplication rate was obtained using either longitudinal or apical explants from in vitro germinated seedlings. The proliferation capacity of these explants was evaluated by testing the single and interaction effects of five concentrations of 6-furfurylaminopurine (KIN) (0.00, 2.32, 4.64, 9.28, and 18.56 µm) and three concentrations of α-naphthalenacetic acid (NAA) (0.00, 0.54, and 2.70 µm), using Murashige and Skoog (MS) as basal medium. Statistical analysis showed that the highest average shoot proliferation of T. valdezianus was recorded with 9.28 µm of KIN, producing 11.75 and 4.50 plantlets per initial explant, for apical and lateral explants, respectively. Addition of NAA to the medium had an inhibitory effect on shoot proliferation for both explant types. The developed shoots in 9.28 µm of KIN and plant growth regulator (PGR)-free treatments were used for a rooting subculture phase. These shoots were then transferred to PGR-free MS medium, resulting in statistically significant different rooting frequencies of 78% and 97%, respectively. When transplanted in soil, the rooted shoots showed an average survival rate of 90%, without any significant statistical differences between treatments. This propagation protocol has the capacity to produce near to 21 plantlets per seedling in 27 weeks, i.e., 11.78 and 9.00 plantlets per apical and lateral explants, respectively, without callus or adventitious shoot formation. These features made it highly attractive as an in vitro clonal propagation method for T. valdezianus plants and the later implementation of a rescue program for threatened wild populations of this cacti species.

In Vitro Clonal Propagation and Medium Term Conservation of Brahmi [Bacopa monnieri (L) Wettst]

2007 ◽  
Vol 16 (2) ◽  
pp. 139-143 ◽  
Author(s):  
Neelam Sharma ◽  
Richa Satsangi ◽  
Ruchira Pandey ◽  
S. Vimala Devi
Keyword(s):  
Clonal Propagation ◽  
Bacopa Monnieri ◽  
Medium Term ◽  
In Vitro Clonal Propagation

scholarly journals In vitro Micropropagation of Abutilon indicum L. through Leaf Explants

1970 ◽  
Vol 19 (2) ◽  
pp. 177-184 ◽  
Author(s):  
Jyoti Ranjan Rout ◽  
Manorama Mishra ◽  
Ritarani Das ◽  
Santi Lata Sahoo
Keyword(s):  
Callus Induction ◽  
Leaf Explants ◽  
Shoot Formation ◽  
Plantlet Regeneration ◽  
Root Induction ◽  
Ex Vitro ◽  
In Vitro Micropropagation ◽  
Half Strength ◽  
Abutilon Indicum

The present investigation was conducted to develop a protocol for rapid callus induction and plant regeneration from leaf explant of Abutilon indicum L. Callus induction and plantlet regeneration at various frequencies were observed on MS using different concentrations of 2,4-D alone or in combination with BAP and Kn. The highest percentage of callus induction was observed with 2.5 mg/l 2,4-D (90) and with combination of 0.5 mg/l Kn (85). Optimum shoot formation was observed on same medium but supplemented with 2.0 mg/l Kn and 1.0 mg/l NAA (11.2). Rooting experiments with half strength of MS revealed that NAA was more suitable for root induction compared to IBA and IAA. The healthy in vitro rooting plantlets were successfully transferred to the field. The survival of the plantlets under ex vitro condition was 87%. Key words: Abutilon indicum, Callus induction, Leaf explants, Micropropagation D.O.I. 10.3329/ptcb.v19i2.5435 Plant Tissue Cult. & Biotech. 19(2): 177-184, 2009 (December)

scholarly journals Somatic Embryogenesis and Plant Regeneration from in-vitro-grown Leaf Explants of Rose

HortScience ◽  
2004 ◽  
Vol 39 (6) ◽  
pp. 1378-1380 ◽  
Author(s):  
C.K. Kim ◽  
J.Y. Oh ◽  
J.D. Chung ◽  
A.M. Burrell ◽  
D.H. Byrne
Keyword(s):  
Somatic Embryogenesis ◽  
Plant Regeneration ◽  
Somatic Embryos ◽  
Leaf Explants ◽  
Basal Medium ◽  
Shoot Formation ◽  
Ms Medium ◽  
Regeneration Frequency

Somatic embryogenesis was initiated from in vitro-grown leaf explants of rose using an induction period of 4 weeks on MS basal medium supplemented with auxin followed by several subcultures on MS basal medium with cytokinin. `4th of July' showed the highest regeneration frequency (24.4%) on 5.3 μm NAA followed by culture on medium containing 18.2 μm zeatin. `Tournament of Roses' produced somatic embryos when cultured for 4 weeks on medium containing dicamba, 2.3 μm followed by three subcultures on medium containing 18.2 μm zeatin. Embryogenic callus matured on MS media containing 0.5 μm NAA, 6.8 μm zeatin, and 2.9 μm GA3. Long-term cultures were established for both cultivars. Somatic embryos germinated on MS medium containing IBA and BA. Silver nitrate (58.8 μm) enhanced shoot formation and germination of somatic embryos. Plants derived from somatic embryos were acclimatized and successfully established in the greenhouse.

Assessment of callus induction and plant regeneration potential of leaf explants derived from in vitro and in vivo shoot of strawberry

2020 ◽  
Vol 77 (1) ◽  
pp. 48
Author(s):  
Rucku Gupta ◽  
V K Wali ◽  
Parshant Bakshi ◽  
Mahital Jamwal ◽  
Pramod Kumar ◽  
...  
Keyword(s):  
Plant Regeneration ◽  
Callus Induction ◽  
Leaf Explants ◽  
Regeneration Potential

scholarly journals Proanthocyanidins against Oxidative Stress: From Molecular Mechanisms to Clinical Applications

2018 ◽  
Vol 2018 ◽  
pp. 1-11 ◽  
Author(s):  
Lingyu Yang ◽  
Dehai Xian ◽  
Xia Xiong ◽  
Rui Lai ◽  
Jing Song ◽  
...  
Keyword(s):  
Oxidative Stress ◽  
Signaling Pathways ◽  
Molecular Mechanisms ◽  
Metabolic Diseases ◽  
Low Cost ◽  
Natural Agents ◽  
Molecular Damage ◽  
And Control

Proanthocyanidins (PCs) are naturally occurring polyphenolic compounds abundant in many vegetables, plant skins (rind/bark), seeds, flowers, fruits, and nuts. Numerousin vitroandin vivostudies have demonstrated myriad effects potentially beneficial to human health, such as antioxidation, anti-inflammation, immunomodulation, DNA repair, and antitumor activity. Accumulation of prooxidants such as reactive oxygen species (ROS) exceeding cellular antioxidant capacity results in oxidative stress (OS), which can damage macromolecules (DNA, lipids, and proteins), organelles (membranes and mitochondria), and whole tissues. OS is implicated in the pathogenesis and exacerbation of many cardiovascular, neurodegenerative, dermatological, and metabolic diseases, both through direct molecular damage and secondary activation of stress-associated signaling pathways. PCs are promising natural agents to safely prevent acute damage and control chronic diseases at relatively low cost. In this review, we summarize the molecules and signaling pathways involved in OS and the corresponding therapeutic mechanisms of PCs.

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