共查询到20条相似文献,搜索用时 31 毫秒
1.
Tung Hoang Thanh Thuong Tran Thi Cuong Do Manh Luan Vu Quoc Hien Vu Thi Hieu Tran Nam Nguyen Ba Phuong Hoang Thi Nhu Van The Vinh Bui Khai Hoang Dac Nhut Duong Tan 《Plant Cell, Tissue and Organ Culture》2021,145(2):393-403
Plant Cell, Tissue and Organ Culture (PCTOC) - One of the common problems in strawberry (Fragaria?×?ananassa) micropropagation is the vitrification phenomenon (succulent plantlets,... 相似文献
2.
Plant Cell, Tissue and Organ Culture (PCTOC) - In this study, we developed a repeatable in vitro micropropagation protocol for the medicinal plant Asparagus cochinchinensis, based on indirect... 相似文献
3.
Khai Hoang Dac Mai Nguyen Thi Nhu Tung Hoang Thanh Luan Vu Quoc Cuong Do Manh Ngan Ha Thi My Chau Nguyen Hoai Buu Ngo Quoc Vinh Nguyen Quang Dung Doan Manh Nhut Duong Tan 《Plant Cell, Tissue and Organ Culture》2022,150(1):113-128
Plant Cell, Tissue and Organ Culture (PCTOC) - The acclimatization stress is responsible for high mortality in tissue cultured plants, which significantly reduces micropropagation efficiency. In... 相似文献
4.
Duan Jia-Xin Duan Qing-Xue Zhang Shuang-Feng Cao Yun-Mei Yang Chao-Dong Cai Xiao-Dong 《Plant Cell, Tissue and Organ Culture》2020,142(1):177-186
Plant Cell, Tissue and Organ Culture (PCTOC) - Acclimatization of tissue cultured plants to greenhouse or field conditions is the final and most crucial step of micropropagation. Hydroponic system... 相似文献
5.
Subiramani Sivakumar Sundararajan Sathish Sivakumar Hari Priya Rajendran Venkatesh Ramalingam Sathishkumar 《Plant Cell, Tissue and Organ Culture》2019,136(1):65-74
Plant Cell, Tissue and Organ Culture (PCTOC) - In different countries, mostly in EU, rules for strawberry nursery propagation impose the use of micropropagation only to produce stock virus free... 相似文献
6.
Bychappa Muniswamy Mishra Manoj Kumar Jingade Pavankumar Huded Arun K. C. 《Plant Cell, Tissue and Organ Culture》2019,139(1):91-103
Plant Cell, Tissue and Organ Culture (PCTOC) - In coffee, the micropropagation technique can be efficiently used in mass multiplication of superior F1 hybrids which is difficult using the... 相似文献
7.
Chirumamilla Pavani Gopu Chaitanya Jogam Phanikanth Taduri Shasthree 《Plant Cell, Tissue and Organ Culture》2021,144(2):397-407
Plant Cell, Tissue and Organ Culture (PCTOC) - An efficient method of rapid micropropagation of Solanum khasianum Clarke was successfully established from the leaf, petiole, and nodal explants. The... 相似文献
8.
Plant Cell, Tissue and Organ Culture (PCTOC) - Date palm (Phoenix dactylifera L.) micropropagation still faces many problems, such as reduced growth and development of callus, low multiplication... 相似文献
9.
Nowakowska Karolina Pińkowska Anna Siedlecka Ewa Pacholczak Andrzej 《Plant Cell, Tissue and Organ Culture》2022,149(3):675-684
Plant Cell, Tissue and Organ Culture (PCTOC) - Shoot proliferation is a very important micropropagation phase, decisive for economic efficiency of this method for a given taxon. To obtain a high... 相似文献
10.
Benmahioul Benamar Dorion Noëlle Kaid-Harche Meriem Daguin Florence 《Plant Cell, Tissue and Organ Culture》2012,108(2):353-358
Plant Cell, Tissue and Organ Culture (PCTOC) - An effective pistachio (Pistacia vera L.) micropropagation system was developed involving rapid axillary bud proliferation and ex vitro rooting. The... 相似文献
11.
Manokari M. Priyadharshini S. Jogam Phanikanth Dey Abhijit Shekhawat Mahipal S. 《Plant Cell, Tissue and Organ Culture》2021,146(1):69-82
Plant Cell, Tissue and Organ Culture (PCTOC) - An advanced micropropagation protocol has been developed for the global spice crop Vanilla planifolia using meta-topolin [mT, 6-(3-hydroxybenzylamino)... 相似文献
12.
H. J. G. ten Hoopen W. M. van Gulik J. J. Heijnen 《In vitro cellular & developmental biology. Plant》1992,28(3):115-120
Summary Continuous culture is an attractive research tool in physiologic and growth and production kinetics research. However, fulfillment
of the basic assumptions of continuous culture in the experimental set-up may cause problems. The homogeneity of plant cell
cultures and effluent, particularly, may cause problems. This paper presents an experimental set-up which solves these problems
and describes the use of this equipment in a study of the growth kinetics of plant cells. Industrial application of the continuous
culture of plant cells in the production of secondary metabolites seems to be profitable when compared with batch or fed-batch
cultures. However, various problems such as uncoupled product formation and strain instability make fed-batch culture a better
choice.
Presented in the Session-in-Depth Batch Production and Fermentation at the 1991 World Congress on Cell and Tissue Culture,
Anaheim, California, June 16–20, 1991. 相似文献
13.
Davoudi Pahnekolayi Mahboubeh Tehranifar Ali Samiei Leila Shoor Mahmoud 《Plant Cell, Tissue and Organ Culture》2019,137(2):265-274
Plant Cell, Tissue and Organ Culture (PCTOC) - Tissue culture and micrografting techniques are known as effective procedures to produce healthy rose rootstocks and high quality scions. In order to... 相似文献
14.
P. C. Debergh G. de Coster W. Steurbaut 《In vitro cellular & developmental biology. Plant》1993,29(2):89-91
Summary Carbendazim is the fungitoxic ingredient of different fungicides. In our experiments it was used as a supplement to stage
II (multiplication) media for the micropropagation ofCordyline terminalis andPrunus avium. The product can be autoclaved without any loss of activity and there is no degradation of the product over a normal culture
period of 32 days. WithC. terminalis andP. avium no phytotoxic effect was revealed up to 160μg/ml. ForC. terminalis shoot height was reduced and the number of shoots smaller than 15 mm increased significantly.
Presented in the Session-in-Depth Novel Plant Growth Regulators at the 1992 World Congress on Cell and Tissue Culture, Washington,
DC, June 20–25, 1992. 相似文献
15.
Barpete Surendra Gupta Priyanka Singh Murari Kumar Shiv 《Plant Cell, Tissue and Organ Culture》2020,142(3):625-634
Plant Cell, Tissue and Organ Culture (PCTOC) - To develop low-ODAP grass pea genotypes with high protein content, in vitro tissue culture techniques were used for inducing somaclonal variation... 相似文献
16.
Kee-Yoeup Paek Eun-Joo Hahn Sung-Ho Son 《In vitro cellular & developmental biology. Plant》2001,37(2):149-157
Summary The application of bioreactor culture techniques for plant micropropagation is regarded as one of the ways to reduce production
cost by scaling-up and automation. Recent experiments are restricted to a small number of species that, however, demonstrate
the feasibility of this technology. Periodic immersion liquid culture using ebb and flood system and column-type bubble bioreactors
equipped with a raft support system to maintain plant tissues at the air and liquid interface were found to be suitable for
micropropagation of plants via the organogenic pathway. Balloon-type bubble bioreactors proved to be fit for micropropagation
via somatic embryogenesis with less shear stress on cultured cells. Several cultivars of Lilium were successfully propagated using a two-stage culture method in one bioreactor. A large number of small-scale segments were
cultured for 4 wk with periodic immersion liquid culture to induce multiple bulblets from each segment, then the bulblet induction
medium was changed into bulblet growth medium by employing a submerged liquid bioreactor system. This culture method resulted
in a nearly 10-fold increase in bulblet growth compared to conventional culture with solid medium. About 20 000 cuttings of
virus-free potato could be obtained from 120 singlenode explants in a 20-liter balloon-type bubble bioreactor after 8 wk of
culture. The percentage of ex vitro survival and root induction of the cuttings was more than 95%. Other successful results were obtained from the micropropagation
and transplant production of chrysanthemum, sweetpotato, Chinese foxglove. Propagation systems via somatic embryogenesis in
Acanthopanax koreanum and thornless Aralia elata were established using a liquid suspension of embryogenic determined cells. More than 500 000 somatic embryos in different
stages were harvested from a 10-liter balloon-type bubble bioreactor after a 6-wk culture. Further development of these embryos
in solid medium and eventually in the field was successful. The bioreactor system could reduce initial and operational cost
for micropropagation, but further development of sophisticated technology might be needed to apply this system to plant micropropagation
industries. 相似文献
17.
Michael F. Fay 《Biodiversity and Conservation》1994,3(2):176-183
Variousin vitro techniques are available for plant propagation, including seed germination, micropropagation, meristem culture and callus culture. The role of these techniques in the conservation of endangered plants is discussed, using examples drawn from the work of the Micropropagation Unit at Kew. 相似文献
18.
Roland R. Leathers Catherine Davin Jean Pierre Zrÿd 《In vitro cellular & developmental biology. Plant》1992,28(2):39-45
Summary The betalains are a class of natural pigments comprising the yellow betaxanthins and the violet betacyanins. Callus lines
developed fromBeta vulgaris, L. var. bikores monogerm exhibited cell colors ranging from white/green (nonpigmented) through yellow, orange, red, and
violet and were representative of all betalain pigments found in the whole plant. The betalains have gained particular interest
from the food industry as potential natural alternatives to synthetic food colorants in use today. Red beet extracts (E162),
which contain significant amounts of the betacyanins, are currently used in products such as yogurts and ice creams. We describe
here the characteristics of culture growth and betalain production for cell suspensions derived from the orange (predominantly
betaxanthin-producing) and violet (betacyanin producing) callus lines. The major factors affecting betalain biosynthesis in
both cultured and whole plant tissues are reviewed.
Presented in the Session-in-Depth Batch Production and Fermentation at the 1991 World Congress on Cell and Tissue Culture,
Anaheim, California, June 16–29, 1991. 相似文献
19.
The use of thidiazuron in tissue culture 总被引:15,自引:0,他引:15
Chin-Yi Lu 《In vitro cellular & developmental biology. Plant》1993,29(2):92-96
Summary Thidiazuron (N-phenyl-N’-1,2,3-thiadiazol-5-ylurea) was first reported to have cytokinin activity in 1982. Since then, thidiazuron has been used
successfully in vitro to induce adventitious shoot formation and to promote axillary shoot proliferation. Thidiazuron is especially
effective with recalcitrant woody species. Shoot numbers produced on medium containing thidiazuron are equivalent to or greater
than numbers initiated on medium with purine-type cytokinins. Low concentrations of thidiazuron (0.0022 to 0.088 mg/liter)
are effective for micropropagation. Prolonged exposure to thidiazuron should be avoided, as this may cause hyperhydricity,
abnormal shoot morphology, or problems in rooting.
Presented in the Session-in-Depth Novel Plant Growth Regulators at the 1992 World Congress on Cell and Tissue Culture, Washington,
D.C., June 20–25, 1992. 相似文献
20.
Bin Huang 《In vitro cellular & developmental biology. Plant》1992,28(2):53-58
Summary Recent advances in plant cell and molecular biology have furthered the genetic manipulation of many plant species and advanced
the options for crop improvement. Among the many targets for genetic manipulation, microspores offer several unique advantages:
they are haploid, single-celled, and highly synchronized. In many plant species microspores develop into haploid embryos,
and eventually haploid and doubled haploid plants, after in vitro anther or microspore culture. This induced in vitro developmental
pathway of microspores, termed microspore embryogenesis, can be used to recover individual homozygous plants from microspores
and microspore-derived embryos after genetic manipulation such as mutagenesis and gene transfer. The highly efficient microspore
embryogenesis system inBrassica napus has been used successfully to obtain various mutants after microspore mutagenesis, and to achieve gene transfer mediated
byAgrobacterium tumefaciens.
Presented in the Session-in-Depth In Vitro Gametophyte Biology at the 1991 World Congress on Cell and Tissue Culture held
in Anaheim, California, June 16–20, 1991. 相似文献