scholarly journals Bioreactors in coffee micropropagation

2006 ◽  
Vol 18 (1) ◽  
pp. 45-54 ◽  
Author(s):  
Hervé Etienne ◽  
E Dechamp ◽  
D Barry-Etienne ◽  
Bernóit Bertrand

In coffee, bioreactors are the most promising way for scaling-up micropropagation processes, particularly somatic embryogenesis. The availability of an efficient somatic embryogenesis process would allow the rapid mass production of heterozygous materials such as selected Coffea canephora clones and F1 Arabica hybrid varieties. For the last fifteen years, bioreactors (mechanically or pneumatically agitated bioreactors, temporary immersion bioreactors) have mostly been used on coffee to optimize the mass regeneration of somatic embryos from embryogenic tissues. This review presents the main results, obtained with several bioreactor models, concerning the different steps of the micropropagation process : i) the multiplication of embryogenic tissues, ii) the somatic embryo mass regeneration and iii) the production of pre-germinated embryos and plantlets in bioreactors. The literature shows that scaling-up can be successful, since very efficient embryo production has been achieved for both C. arabica and C. canephora. Moreover, it was proven that the pre-germinated coffee embryos - i.e. embryonic axis elongation (10-12 mm), root tip formation, cotyledon expansion and greening - obtained in temporary immersion bioreactors were photoautotrophic and able to regenerate vigorous plantlets after sowing under nursery conditions. The feasibility to apply the bioreactor technology in an industrial micropropagation procedure is also discussed in the particular socio-economic context of coffee growing.

1970 ◽  
Vol 20 (2) ◽  
pp. 157-170 ◽  
Author(s):  
Richard M.S. Mulwa ◽  
Margaret M.A. Norton ◽  
Robert M. Skirvin

Abundant embryogenic callus was obtained from leaf and floral explants of "Chancellor" grape by continuous culture for 12 weeks on Nitsch and Nitsch basal medium supplemented with 9 μM 2, 4-D + 17 μM IASP + either 1 μM BA or 1 μM TDZ (ECIM) in darkness. They were successfully maintained by a five to six week subculture interval on NN medium containing 2 μM 2, 4-D + 0.2 μM TDZ + 4 μM IASP (LTMM). Near synchronous embryo developed from embryogenic callus on medium containing 10 μM IASP + 8 μM NOA + 1 μM TDZ + 1 μM ABA + 2.5 g/l AC (EDMM).  Individually separated somatic embryos were germinated on both NN and half strength of MS containing 0.5 μM BA + 0.025 μM NAA, respectively; normal plantlet conversion from embryos was low (35%).  Whole fruiting plants were obtained. Aberrant embryo development was characterized by failure to form functional shoot meristems following the initial cotyledon expansion during germination. These observations indicate that the embryo conversion stage of the regeneration is difficult and remains a limiting factor requiring more empirical experimentation for improvement in grape tissue culture.   Key words: Chancellor grape, Regeneration, Somatic embryogenesis   D.O.I. 10.3329/ptcb.v20i2.6895   Plant Tissue Cult. & Biotech. 20(2): 157-170, 2010 (December)


2005 ◽  
pp. 111-118 ◽  
Author(s):  
Francisco Quiroz-Figueroa ◽  
Miriam Monforte-González ◽  
Rosa M. Galaz-Ávalos ◽  
Victor M. Loyola-Vargas

PROTOPLASMA ◽  
2020 ◽  
Vol 258 (1) ◽  
pp. 45-57
Author(s):  
Paulo Marcos Amaral-Silva ◽  
Wellington Ronildo Clarindo ◽  
José Henrique Soler Guilhen ◽  
Ana Beatriz Rocha de Jesus Passos ◽  
Natália Arruda Sanglard ◽  
...  

2008 ◽  
Vol 94 (2) ◽  
pp. 171-180 ◽  
Author(s):  
A. Arroyo-Herrera ◽  
A. Ku Gonzalez ◽  
R. Canche Moo ◽  
F. R. Quiroz-Figueroa ◽  
V. M. Loyola-Vargas ◽  
...  

1999 ◽  
Vol 35 (5) ◽  
pp. 424-427 ◽  
Author(s):  
D. K. S. Goh ◽  
N. Michaux-Ferrière ◽  
O. Monteuuis ◽  
M. -C. Bon

1998 ◽  
Vol 1 (3) ◽  
pp. 216-222 ◽  
Author(s):  
Muhammad Shahidul Haque ◽  
Tomikichi Wada ◽  
Kazumi Hattori

HortScience ◽  
1992 ◽  
Vol 27 (6) ◽  
pp. 693e-693
Author(s):  
Ji-Weon Lee ◽  
Byoung-Yil Lee

The study was carried out to examine the appropriate media, explant sources, and suitable growth regulators for somatic embryogenesis to establish a rapid mass production system via somatic embryogenesis in Oenanthe stolonifera DC. Modified MS media containing higher concentrations of NO3-N were more effective for the formation and development of the somatic embryos from embryogenic callus. Liquid media were more effective for the production of somatic embryos than solidified media. Immature florets were found to be the most competent explant sources for embryogenic callus formation. 2,4-D at 1mg/l was highly effective for the formation of embryogenic callus but inhibitory for the development and differentiation of somatic embryo. Somatic embryos were developed from the translucent and friable embryogenic callus. Addition of BA promoted the callus growth synefgistically with NAA and 2,4-D, but the production of embryogenic callus was inhibited by BA.


Author(s):  
Adi Prawoto

Cocoa (Theobroma cacao L.) like most tropical trees is recalcitrant in tissue culture. Somatic embryogenesis is generally efficient micropropagation technique to multiply elite material. However, Somatic embryogenesis in cocoa is difficult and this species is considered as recalcitrant. One of the factors often considered as a component of in vitro recalsitrance is a high phenolic content and oxidation of these compounds. In cocoa tissue culture accumulate large amounts of poliphenolics compounds which probably impair further development. This study was conducted to investigate the composition of phenolic compounds in cocoa flower and leaves, and their changes troughout the somatic embryogenesis process. Calli were induced in cacao floral and leaves explants on a half-strenght Murashige and Skoog medium containing 30 g/L Glucose and combination of 2,4 dichlorophenoxyacetic acid (2,4 D) with kinetin (kin). Total polyphenol content was observed on Sulawesi 1 cocoa clone. Embryogenic and non-embryogenic callus were also compared. The percentage of callus production from flower tissue is 85%, percentage of embryogenic callus 40 %, although  the percentage of somatic embryo production from embryogenic callus callus is 70%. The conservation of callus into somatic embryos followed by decline in phenol content and an increase in peroxidase. The synthesis kinetics for these compounds in calli, under different somatic embryogenesis conditions, revealed a higher concentration under non-embryogenic conditions. So that, phenolic compound can influence the production of calli and an absence the phenolic compound can enhance production of somatic embryo.Kata kunci: Theobroma cacao L., polifenol, embrio somatik, kalus, flavonoid, katekin, in vitro recalcitance


2021 ◽  
Vol 9 (12) ◽  
pp. 2944-2950
Author(s):  
Zhi-Fang Wu ◽  
Ling-Jiao Lu ◽  
Hai-Yan Zheng ◽  
Yan Tu ◽  
Ying Shi ◽  
...  
Keyword(s):  
Root Tip ◽  

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