Callus induction, clonal propagation and in vitrogermplasm conservation of ‘hualtaco’ Loxopterygium huasangoSpruce ex Engl. (Anacardiaceae)

2021 ◽  
Vol 12 (4) ◽  
pp. 545-556
Author(s):  
Guillermo Delgado Paredes ◽  
Ana Millones-Yamunaque ◽  
Cecilia Vásquez-Díaz ◽  
Consuelo Rojas-Idrogo
2020 ◽  
Vol 8 (5) ◽  
pp. 277-289
Author(s):  
Duque-Aurazo Yohonatan A. ◽  
Rojas-Idrogo Consuelo ◽  
Delgado-Paredes Guillermo E.

Muntingia calabura L. (Muntingiaceae) is a fast-growing tree native to tropical America, abundant in the seasonally dry forest of the north coast of Peru. Tissue culture is an effective procedure to produce healthy plants, rapid clonal propagation and several morphogenic process. The objective of this study was to formulate an efficient method for micropropagation, morphogenesis callus induction and germplasm conservation of this species. In this study, seeds, shoot-tips and nodal segments of seedlings were used as explants, inducing various morphogenic processes in different combinations of growth regulators and osmoregulatory substances. In vitro seeds germination was 100% up to four months after the ripe fruits were collected and after 12 months the germination rate was 0.0%. The highest elongation of shoot was observed with 0.5 mg L-1 2iP (3.11 cm) although the highest number of shoots formed (18.0 and 16.5) was observed with 0.5 mg/L KIN or TDZ, respectively, after 30 days of culture. The best callus induction was obtained in  0.5 and 1.0 mg L-1 TDZ, 1.0 and 2.0 mg L-1 2,4-D, 2.0 mg L-1 NAA or 2.0 mg L-1 NAA with 0.1 and 0.5 mg L-1 BAP, after 45 days of culture period. Shoot regeneration (> 10 shoots/explant) was observed with 0.1 to 2.0 mg L-1 NAA. Root induction was observed in all shoots cultured in various concentrations of IBA and NAA-GA3, after 30 days of culture. After two months, well rooted plantlets were transplanted in greenhouse conditions, however, the survival rate was less than 10%. Only in treatment with mannitol 2.0% in explants without roots, the highest in vitro conservation rate (50%) was reached, after 6 months of culture, while in the control treatment in culture medium without ABA and mannitol, but supplemented with 0.02-0.02 mg L-1 (IAA-GA3), the conservation rate reached 100%. The results demonstrated the applicability of tissue culture in the micropropagation and in vitro germplasm conservation of M. calabura.  


2021 ◽  
Author(s):  
Sani Muhammad Tajo ◽  
Zhao Pan ◽  
Salisu Bello Sadau ◽  
Shahid Iqbal ◽  
KM Yusuf ◽  
...  

Abstract Gossypium hirsutm undergoes a rapid clonal propagation to regenerate a mature plant through tissue culture. In this research, cotton leaf regeneration level for 21 accessions in the field (new leaves) was observed after the first harvest, and a comparison between field regeneration level and callus induction with its regeneration capacity (new shoots and roots) for the same 21 accessions was carried out. During the flowering stage of Gossypium hirsutum, biochemical (Proline), physiological (chlorophyll and carotenoid content) analysis was carried out. Phenotypic observations (plant height, leaf area, fresh leaf weight, dry leaf weight, flower and boll number) were also carried out on 21 accessions for each accession. Callus induction and regeneration capacity of roots and shoots for hypocotyl, cotyledons and shoot tip tissues was used to validate field regeneration capacity through analysis of variance. ZS061, LuMian378, JiMian863, and ZS065 have highest drought tolerance while ZhongMianSuo24, LiaoYangDuoMaoMian, and BeiZheGongSheMian have the lowest tolerance to drought stress. Accessions with both field and callus regeneration capacity were identified.


2019 ◽  
Vol 6 (4) ◽  
pp. 442-449
Author(s):  
Dipu Samanta ◽  
Bidisha Mallick ◽  
Debleena Roy

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.


1994 ◽  
Vol 90 (4) ◽  
pp. 739-747 ◽  
Author(s):  
Diana Lee ◽  
Barbara A. Moffatt

2009 ◽  
Vol 24 ◽  
pp. 82-88 ◽  
Author(s):  
Saraswoti Aryal ◽  
Sanu Devi Joshi

Rauvolfia serpentina (L.) ex. Kurz is an important medicinal plant. Callus induction and regeneration was studied from stem explant of in-vitro grown plant of Rauvolfia serpentina(L.) Benth. ex Kurz (Apocynaceae) on Murashige Skoog (1962) medium supplemented with 1mg/l 2,4-Dichlorophenocy acetic acid (2,4-D) and 1mg/l Kinetin (Kn). Vigorous growth of callus occurs after 4 weeks of culture. Callus was sub-cultured on Murashige and Skoog (MS) medium supplemented with different concentration of 2, 4-D (0.5-3.0 mg/l) and 10% coconut milk. Regeneration of plantlets occurred on MS medium containing 3 mg/1 of 2, 4-D and 10% coconut milk. These plantlets were rooted on MS medium supplemented with 1 mg/l IAA .The regenerated plantlets were able to grow on soil after short period ofacclimatization. Key words: Explant; In-vitro culture; MS medium;  2, 4 Dichlorophenoxy acetic acid; Kinetin; Callus; Tissue culture; Coconut milk. Journal of Natural History Museum Vol. 24, 2009 Page: 82-88


2014 ◽  
Vol 49 (5) ◽  
pp. 595 ◽  
Author(s):  
Feng Huan ◽  
Yi Shuli ◽  
Xie Jiaheng ◽  
Lei Mengqi ◽  
Huang Xuan

Crop Science ◽  
1982 ◽  
Vol 22 (6) ◽  
pp. 1193-1197 ◽  
Author(s):  
J. V. Krans ◽  
V. T. Henning ◽  
K. C. Torres

Crop Science ◽  
1978 ◽  
Vol 18 (1) ◽  
pp. 157-159 ◽  
Author(s):  
B. V. Conger ◽  
J. V. Carabia

2021 ◽  
Vol 286 ◽  
pp. 110193
Author(s):  
Su-Fang Li ◽  
Tian-Wen Ye ◽  
Xin Xu ◽  
De-Yi Yuan ◽  
Shi-Xin Xiao

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