Growth and Secondary Product Formation of in vitro Cultures from the Liverwort Reboulia hemisphaerica

1991 ◽  
Vol 46 (1-2) ◽  
pp. 28-32 ◽  
Author(s):  
Rui M. S. C. Morais ◽  
Hans Becker

Abstract Reboulia hemisphaerica has been cultivated on Gamborg B5 medium with various sugars. Differentiated cultures grew best on agar medium with the addition of 0.5% sucrose and a light regime of 18 h light/6h dark . Callus was induced either by a combination of phytohor­mones (2 mg/l α-naphthylacetic acid + 1 mg/l kinetin) or by 4% glucose. The differentiated cultures on agar produced sesquiterpenes in a tenfold increased amount compared to undiffer­ entiated suspension cultures. Cultures kept in da rk produced no sesquiterpenes, but 5-hydroxy-7,8,4′-trimethoxyflavone was present whereas apigenin-7,4′-dimethylether was the only flavonoid in cultures cultivated in the light.

2011 ◽  
Vol 74 (1) ◽  
pp. 17-21 ◽  
Author(s):  
Izabela Grzegorczyk ◽  
Ireneusz Bilichowski ◽  
Elżbieta Mikiciuk-Olasik ◽  
Halina Wysokińska

The concentrations of carnosic acid, carnosol and rosmarinic acid in different materials from differentiated (multiple shoot cultures and regenerated plants) and undifferentiated (callus and cell suspension) in vitro cultures of <em>Salvia officinalis</em> were determined by HPLC. The results suggested that diterpenoid (carnosic acid and carnosol) production is closely related to shoot differentiation. The highest diterpenoid yield (11.4 mg g<sup>-1</sup> for carnosic acid and 1.1 mg g<sup>-1</sup> for carnosol) was achieved in shoots of 10-week-old micropropagated plants. The levels were comparable to those found in shoots of naturally growing plants. Undifferentiated callus and cell suspension cultures produced only very low amounts of carnosol (ca. 0.05 mg g<sup>-1</sup> of dry weight). In contrast, content of rosmarinic acid in callus and suspension cultures as well as shoots growing in vitro and in vivo was similar and ranged between 11.2 and 18.6 mg g<sup>-1</sup> of dry weight.


IAWA Journal ◽  
1993 ◽  
Vol 14 (1) ◽  
pp. ins1-11
Author(s):  
I. C. Nielsen

Stern 'chips' from large-diameter stern regions of Larix laricina were produced free of contaminating organisms. These chips, consisting of dormant vascular cambium sandwiched intact between mature xylem and phloem, were grown as in vitro cultures on the surface of an agar medium that supports apparently normal cambial cell division and xylogenesis. It was determined that auxin (l-naphthaIene acetic acid) together with nutrients at low concentrations in the medium was essential for cambial growth, whether chips were grown in continuous light or darkness. Fusiform cambial cells underwent successive periclinal divisions to produce radial files of enlarged, bordered-pitted, secondary-walled, lignified and autolysed earlywood tracheids. As many as 20 new tracheids per radial file were produced, and > 95% of these were autolysed after 35 days of culture.


1997 ◽  
Vol 87 (8) ◽  
pp. 868-876 ◽  
Author(s):  
Geza Hrazdina ◽  
Wlodzimierz Borejsza-Wysocki ◽  
Cathy Lester

Cell suspension cultures of the scab-resistant apple (Malus × domestica) cultivar Liberty were challenged with yeast extract to mimic the effect of biological stress such as fungal invasion. The cells responded to the challenge by production of novel compounds. Suspension cultures of the scab-susceptible cultivar McIntosh, when similarly challenged, showed no detectable response. The major compound produced by scab-resistant cells in response to the challenge has been identified as the 2,4-methoxy-3-hydroxy-9-O-β-D-glucosyloxydibenzofuran by UV, mass spectrometry, 1H-nuclear magnetic resonance (NMR), and 13C-NMR spectroscopy. We suggest the trivial name malusfuran for the compound. Malusfuran production was initiated approximately 24 h after being challenged. Malusfuran inhibited spore germination and growth of Venturia inaequalis at millimolar concentrations, indicating its role as a possible phytoalexin. The aglycone of malusfuran, 2,4-methoxy-3,9-hydroxy-dibenzofuran, showed higher toxicity to V. inaequalis than to the parent malusfuran. In vitro cultures of V. inaequalis produced a β-glucosidase that hydrolyzed ortho- and para-substituted nitrophenyl-β-glucosides, suggesting that the aglycone may act as the actual phytoalexin.


Planta Medica ◽  
2012 ◽  
Vol 78 (11) ◽  
Author(s):  
K Sykłowska-Baranek ◽  
A Pietrosiuk ◽  
M Grech-Baran ◽  
M Bonfill ◽  
P Mistrzak

Planta Medica ◽  
2013 ◽  
Vol 79 (13) ◽  
Author(s):  
K Sykłowska-Baranek ◽  
A Pietrosiuk ◽  
K Graikou ◽  
H Damianakos ◽  
M Jeziorek ◽  
...  

2008 ◽  
Vol 21 (2) ◽  
pp. 103-106 ◽  
Author(s):  
Barbara Sparzak ◽  
Mirosława Krauze-Baranowska ◽  
Loretta Pobłocka-Olech
Keyword(s):  

2020 ◽  
Vol 26 (24) ◽  
pp. 2817-2842
Author(s):  
Ewa Skała ◽  
Joanna Makowczyńska ◽  
Joanna Wieczfinska ◽  
Tomasz Kowalczyk ◽  
Przemysław Sitarek

Background: For a long time, the researchers have been looking for new efficient methods to enhance production and obtain valuable plant secondary metabolites, which would contribute to the protection of the natural environment through the preservation of various plant species, often rare and endangered. These possibilities offer plant in vitro cultures which can be performed under strictly-controlled conditions, regardless of the season or climate and environmental factors. Biotechnological methods are promising strategies for obtaining the valuable plant secondary metabolites with various classes of chemical compounds including caffeoylquinic acids (CQAs) and their derivatives. CQAs have been found in many plant species which are components in the daily diet and exhibit a wide spectrum of biological activities, including antioxidant, immunomodulatory, antihypertensive, analgesic, anti-inflammatory, hepato- and neuroprotective, anti-hyperglycemic, anticancer, antiviral and antimicrobial activities. They have also been found to offer protection against Alzheimer’s disease, and play a role in weight reduction and lipid metabolism control, as well as modulating the activity of glucose-6-phosphatase involved in glucose metabolism. Methods: This work presents the review of the recent advances in use in vitro cultures of various plant species for the alternative system to the production of CQAs and their derivatives. Production of the secondary metabolites in in vitro culture is usually performed with cell suspension or organ cultures, such as shoots and adventitious or transformed roots. To achieve high production of valuable secondary metabolites in in vitro cultures, the optimization of the culture condition is necessary with respect to both biomass accumulation and metabolite content. The optimization of the culture conditions can be achieved by choosing the type of medium, growth regulators or growth conditions, selection of high-productivity lines or culture period, supplementation of the culture medium with precursors or elicitor treatments. Cultivation for large-scale in bioreactors and genetic engineering: Agrobacterium rhizogenes transformation and expression improvement of transcriptional factor or genes involved in the secondary metabolite production pathway are also efficient strategies for enhancement of the valuable secondary metabolites. Results: Many studies have been reported to obtain highly productive plant in vitro cultures with respect to CQAs. Among these valuable secondary metabolites, the most abundant compound accumulated in in vitro cultures was 5-CQA (chlorogenic acid). Highly productive cultures with respect to this phenolic acid were Leonurus sibiricus AtPAP1 transgenic roots, Lonicera macranthoides and Eucomia ulmoides cell suspension cultures which accumulated above 20 mg g-1 DW 5-CQA. It is known that di- and triCQAs are less common in plants than monoCQAs, but it was also possible to obtain them by biotechnological methods. Conclusion: The results indicate that the various in vitro cultures of different plant species can be a profitable approach for the production of CQAs. In particular, an efficient production of these valuable compounds is possible by Lonicera macranthoides and Eucomia ulmoides cell suspension cultures, Leonurus sibiricus transformed roots and AtPAP1 transgenic roots, Echinacea angustifolia adventitious shoots, Rhaponticum carthamoides transformed plants, Lavandula viridis shoots, Sausera involucrata cell suspension and Cichorium intybus transformed roots.


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