Somatic embryogenesis and organogenesis induced on the immature zygotic embryo of sunflower (Helianthus annum L.) cultivated in vitro: role of the sugar

1995 ◽  
Vol 15 (3-4) ◽  
pp. 200-204 ◽  
Author(s):  
Geneviève Jeannin ◽  
Roberte Bronner ◽  
Günther Hahne
Keyword(s):  
Somatic Embryogenesis ◽  
Zygotic Embryo ◽  
Immature Zygotic Embryo

scholarly journals Reproductive Characteristics of the Selected Cocoa (Theobroma cacao L.) Clones after Regenerated from the Somatic Embryogenesis Culture

2021 ◽  
Vol 18 (24) ◽  
pp. 1406
Author(s):  
Gibson Entuni ◽  
Hollena Nori ◽  
Rebicca Edward ◽  
Ahmad Kamil bin Mohammad Jaafar
Keyword(s):  
Somatic Embryogenesis ◽  
Reproductive Cycle ◽  
Embryo Culture ◽  
Zygotic Embryo ◽  
Reproductive Organ ◽  
Immature Zygotic Embryo ◽  
Reproductive Characteristics ◽  
Zygotic Embryo Culture ◽  
Typical Period ◽  
Immature Zygotic Embryo Culture

This study was conducted to evaluate the reproductive characteristics of 4 elite cocoa clones (MCBC1, PBC230, KKM22 and KKM4) propagated via somatic embryogenesis culture. From the findings, all clones have similar reproductive characteristics with clones from conventional grafted. However, only KKM4 clone from immature zygotic embryo culture produced the shortest staminode to style distance of 1.83 mm. This consequently influenced flower stability by reducing the efficiency of pollination by insects. It was found that this clone also has the highest number of flowers drop after anthesis (5 flowers) and lowest production of cherelle (5 cherelles). Further observation revealed that floral development from first bud visible (BBCH51) to flower anthesis (BBCH68) of all clones took around 31 days. These cocoa flowers which remained receptive soon after anthesis at 10 am (day-31) until the next day (day-32) suggesting 2 days’ period of receptivity. HIGHLIGHTS It is crucial to assess the presence of off-type characteristics in the reproductive organ structure such as the distance between staminode to style, period of reproductive cycle and stigmatic receptivity of cocoa clones regenerated from somatic embryogenesis The converging and parallel type of staminode to style distances are the ideal flower spatial arrangements for the optimal pollination in cocoa plant compared to splay type Only KKM4 clone propagated from immature zygotic embryo culture showed variation in the distance between staminode to style distance and this caused pollination failure by insect which then consequently caused minimum cherelle production All regenerated cocoa clones observed with typical period of the reproductive cycle and stigmatic receptivity GRAPHICAL ABSTRACT

scholarly journals Developmental changes of catalase and superoxide dismutase isoenzymes in zygotic and somatic embryos of horse chestnut

1998 ◽  
Vol 25 (8) ◽  
pp. 909 ◽  
Author(s):  
F. Bagnoli ◽  
M. Capuana ◽  
M. L. Racchi
Keyword(s):  
Superoxide Dismutase ◽  
Somatic Embryogenesis ◽  
Somatic Embryo ◽  
Zygotic Embryo ◽  
Electrophoretic Analysis ◽  
Horse Chestnut ◽  
Zygotic Embryogenesis ◽  
Native Page ◽  
Cat Isoforms

Catalase (CAT) and superoxide dismutase (SOD), two of the major antioxidant enzyme systems, were examined by native PAGE at different stages of zygotic and somatic embryogenesis of horse chestnut (Aesculus hippocastanum L.). During both zygotic and somatic embryogenesis, CAT and SOD specific activities increased, but electrophoretic analysis revealed remarkable differences in the isoenzyme patterns. Two CAT isoforms were differentially present during zygotic embryogenesis. The transition from the fast to the slow migrating form occurred in July, approximately 2 months after pollination. In contrast to zygotic, the two isoforms were continuously detectable during somatic embryo-genesis. In fact, with the exception of the callus stage, in which only one form was present, both of the CAT isoforms are equally active during the somatic embryo development. Unlike CAT, all SOD isoenzymes, one Mn-SOD and five Cu/Zn-SODs, were present during all the stages of zygotic embryo formation, but only Mn-SOD and an Fe-SOD were detected during somatic embryogenesis. These results suggest the occurrence of oxidative stress conditions during in vitro culture which, in horse chestnut, could account for the difficulties observed in the development of the somatic embryo into a plantlet.

scholarly journals 5-Azacytidine: A Promoter of Epigenetic Changes in the Quest to Improve Plant Somatic Embryogenesis

2018 ◽  
Vol 19 (10) ◽  
pp. 3182 ◽  
Author(s):  
Pedro Osorio-Montalvo ◽  
Luis Sáenz-Carbonell ◽  
Clelia De-la-Peña
Keyword(s):  
Gene Expression ◽  
Dna Methylation ◽  
Somatic Embryogenesis ◽  
Regulation Of Gene Expression ◽  
Culture Conditions ◽  
Short Time ◽  
Time Frames ◽  
Different Sources

Somatic embryogenesis (SE) is a widely studied process due to its biotechnological potential to generate large quantities of plants in short time frames and from different sources of explants. The success of SE depends on many factors, such as the nature of the explant, the microenvironment generated by in vitro culture conditions, and the regulation of gene expression, among others. Epigenetics has recently been identified as an important factor influencing SE outcome. DNA methylation is one of the most studied epigenetic mechanisms due to its essential role in gene expression, and its participation in SE is crucial. DNA methylation levels can be modified through the use of drugs such as 5-Azacytidine (5-AzaC), an inhibitor of DNA methylation, which has been used during SE protocols. The balance between hypomethylation and hypermethylation seems to be the key to SE success. Here, we discuss the most prominent recent research on the role of 5-AzaC in the regulation of DNA methylation, highlighting its importance during the SE process. Also, the molecular implications that this inhibitor might have for the increase or decrease in the embryogenic potential of various explants are reviewed.

High-frequency plant regeneration from immature zygotic embryo cultures of Houttuynia cordata Thunb via somatic embryogenesis

2013 ◽  
Vol 7 (4) ◽  
pp. 527-534 ◽  
Author(s):  
Myung Jin Oh ◽  
Myung Suk Ahn ◽  
Eun Yee Jie ◽  
Jang Ryol Liu ◽  
Byung Whan Min ◽  
...  
Keyword(s):  
Somatic Embryogenesis ◽  
Plant Regeneration ◽  
High Frequency ◽  
Zygotic Embryo ◽  
Immature Zygotic Embryo ◽  
Houttuynia Cordata ◽  
Embryo Cultures ◽  
Houttuynia Cordata Thunb

Somatic embryogenesis and plant regeneration in immature zygotic embryo, ovule, and anther filament cultures of Chinese cabbage

1998 ◽  
Vol 72 (2) ◽  
pp. 151-155 ◽  
Author(s):  
Pil S Choi ◽  
Sung R Min ◽  
Min Y Ahn ◽  
Woong Y Soh ◽  
Jang R Liu
Keyword(s):  
Somatic Embryogenesis ◽  
Plant Regeneration ◽  
Chinese Cabbage ◽  
Zygotic Embryo ◽  
Immature Zygotic Embryo

scholarly journals SOMATIC EMBRYOGENESIS OF CASSAVA (MANIHOT ESCULENTA CRANTZ) VAR. KM297

2011 ◽  
Vol 14 (3) ◽  
pp. 14-22
Author(s):  
Kien Van Vu ◽  
Sanh Du Nguyen
Keyword(s):  
Somatic Embryogenesis ◽  
Manihot Esculenta ◽  
Somatic Embryos ◽  
Light Condition ◽  
Ms Medium ◽  
Dark Condition ◽  
Manihot Esculenta Crantz ◽  
Immature Leaf

Somatic embryos of cassava var. KM297 received from pieces of in vitro immature leaf lobes or cotyledon of somatic embryos, were induced on the MS medium supplemented with 8mg/l picloram after 13 days inoculation in the dark condition. Different states of embryo were obtained after 10 days cultured on MS medium supplemented with 0.1 mg/l BA and 0.01mg/l NAA, in the light condition. Role of endogenous AIA and Zeatin of the globular state of embryos was studied.

GhAIL6, a Member of the AP2 Family Gene, Promotes Somatic Embryogenesis in Cotton.

2021 ◽  
Author(s):  
Congcong Ma ◽  
Yilin Li ◽  
Xiaorui Zhang ◽  
Dan Ma ◽  
Ruibin Sun ◽  
...  
Keyword(s):  
Somatic Embryogenesis ◽  
Large Family ◽  
Intact Plants ◽  
Transgenic Breeding ◽  
Callus Production ◽  
Transcription Factor Genes ◽  
Family Gene ◽  
Ap2 Family

Abstract Background Somatic embryogenesis (SE) is the process by which plant somatic cells are cultured in vitro without fertilization to regenerate embryos and develop into intact plants, the difficulty of cotton regeneration has severely limited functional gene research and transgenic breeding. The AP2 family is a relatively large family of transcription factor genes that regulate the process of growth and development, but the role of Aintegumenta-Like6 ( AIL6) in cotton SE has not been reported. Methods The 35S::AIL6:GR vector was constructed and transformed into cotton JH713 by Agrobacterium-mediated method, after 3 years of self-breeding, stable genetic T3 generation positive plants were obtained, identified by Southern, and three lines were selected for the following regeneration experiments.Results The results showed that overexpression of GhAIL6 significantly inhibited the proliferation of callus during the first 30 days, and promoted the embryogenic callus production at about 45 days.Couclusion Our results indicated that GhAIL6 was a key regulator of cotton SE, overexpression of GhAIL6 helped to improve the regeneration efficiency of cotton SE

scholarly journals Regulation of in vitro somatic embryogenesis with emphasis on to the role of endogenous hormones

2001 ◽  
Vol 13 (2) ◽  
pp. 196-223 ◽  
Author(s):  
VÍCTOR M. JIMÉNEZ
Keyword(s):  
Somatic Embryogenesis ◽  
Plant Growth ◽  
Growth Regulators ◽  
Culture Medium ◽  
Endogenous Hormones ◽  
Tissue Cultures ◽  
Factors Associated ◽  
General Aspects

Different aspects of the in vitro somatic embryogenesis regulation are reviewed in this paper.work. A description of g General aspects, such as terminology, uses, stages of development and factors associated with the somatic embryogenesis, are described. is carried out. Although a brief description ofn the effects of the addition of different plant growth regulators to the culture medium wasis given, the article is centereds itself on the effect that the endogenous hormone concentrations in the initial explants and in the tissue cultures derived from them could play oin the induction and expression of somatic embryogenesis. It is significant that few to emphasize the low amount of systematic studies have been conducted, in this subject, in which different species and hormone groups were compared in cultures with and without embryogenic capacity. Moreover, the lack of correlation between the results presented in different studies the distinct works indicates that the hormone content of the cultures is not the only factor involved.

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