Agata Ptak

Dr. Agata Ptak

University of Agriculture in Krakow, Poland
orcid

Research Focus & Metrics

Academic Career Length

27Years (2000-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 November 2016 in Scientia Horticulturae
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Journal Article
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MSMagdalena Simlat
Magdalena Simlat
PŚPatrycja Ślęzak
Patrycja Ślęzak
MMMaria Moś
Maria Moś
MWMarzena Warchoł
Marzena Warchoł
Edyta SkrzypekEdyta Skrzypek
Edyta Skrzypek
Agata PtakAgata Ptak
Agata Ptak

22 June 2018 in PeerJ
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Journal Article
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MSMagdalena Simlat
Magdalena Simlat
Agata PtakAgata Ptak
Agata Ptak
Edyta SkrzypekEdyta Skrzypek
Edyta Skrzypek
MWMarzena Warchoł
Marzena Warchoł
EMEmilia Morańska
Emilia Morańska
EPEwa Piórkowska
Ewa Piórkowska
Background: Melatonin (MEL) is a signaling molecule in plants that affects developmental processes during vegetative and reproductive growth. Investigations have proved that exogenously applied MEL also has the potential to improve seed germination and plant development.Methods: In the present study, seeds of stevia, a species with a very low germination rate, were germinated on an agar gel (AG) containing MEL at various concentrations (5, 20, 100, and 500 µM) in light. Seeds germinated on AG without MEL were used as controls. For the first 24 or 48 h of germination, the seeds were maintained in darkness as a pre-incubation step. Some seeds were not exposed to this pre-incubation step.Results: At concentrations of 20 and 5 µM, MEL significantly improved germination, but only in seeds pre-incubated in darkness for 24 h (p < 0.001). At concentrations of 100 and 500 µM, MEL had an inhibitory effect on germination, regardless of the pre-incubation time. Melatonin also affected plantlet properties. At a concentration of 20 µM, MEL increased plantlet fresh weight and leaf numbers. At a concentration of 5 µM, it promoted plantlet height. Regarding root development, the most favorable MEL concentration was 500 µM. Biochemical analysis revealed that MEL promoted higher pigment concentrations but hampered superoxide dismutase activity. On the other hand, the concentrations of sugars and phenolics, as well as the activities of catalase and peroxidase, increased at a MEL concentration of 500 µM.Discussion: The results suggest that MEL can improve germination of positively photoblastic stevia seeds and that it can play a role in plantlet development. However, the effects observed in the present study depended on the quantity of MEL that was applied.

16 February 2011 in Plant Cell, Tissue and Organ Culture (PCTOC)
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ATAnna El Tahchy
Anna El Tahchy
SBSimon Bordage
Simon Bordage
Agata PtakAgata Ptak
Agata Ptak
FDFrançois Dupire
François Dupire
EBElvina Barre
Elvina Barre
DLDominique Laurain-Mattar
Dominique Laurain-Mattar

1 March 2007 in Phytochemistry Reviews
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MDM. F. Diop
M. F. Diop
AHAlain Hehn
Alain Hehn
Agata PtakAgata Ptak
Agata Ptak
FCF. Chrétien
F. Chrétien
SDS. Doerper
S. Doerper
DLD. Laurain-Mattar
D. Laurain-Mattar

16 March 2020 in PeerJ
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Agata PtakAgata Ptak
Agata Ptak
EMEmilia Morańska
Emilia Morańska
Edyta SkrzypekEdyta Skrzypek
Edyta Skrzypek
MWMarzena Warchoł
Marzena Warchoł
RSRosella Spina
Rosella Spina
MSMagdalena Simlat
Magdalena Simlat
Background: Leucojum aestivumL. is an important medicinal plant which produces Amaryllidaceae alkaloids, especially galanthamine and lycorine. Research is currently exploring the possibility of producing these alkaloids using biotechnological methods, including in vitro cultures. The biosynthesis of alkaloids may be affected by the types and concentrations of carbohydrate sources used in the medium. In the present investigation we performed such studies on in vitro cultures ofL. aestivumwith a view to obtaining plant material of good quality, characterized, in particular, by a high content of valuable Amaryllidaceae alkaloids.Methods: We examined the effects of various types of carbohydrate sources—sucrose, glucose, fructose and maltose—at different concentrations (30, 60 and 90 g/L)—on the quality ofL. aestivumplants grown in the RITA®bioreactor. The plants’ quality was assessed by their biomass increments, as well by as analysing photosynthetic pigments, endogenous sugar, phenolics and Amaryllidaceae alkaloid content. We also investigated the effect of sugars on the activity of the antioxidant enzymes catalase (CAT), peroxidase (POD) and superoxide dismutase (SOD).Results: The highest biomass increments were observed in plants cultivated in the medium containing 90 g/L sucrose. The highest CAT activity was noted in cultures growing in the medium supplemented with 90 g/L maltose, while the highest POD activity was observed in the presence of 90 g/L fructose and 60 g/L maltose. No differences in SOD activity were observed. Moreover, the sugars did not affect the contents of chlorophyllaand carotenoids, whereas the highest amount of chlorophyllbwas recorded in plants growing in the medium with 60 g/L maltose. No statistically significant differences were observed in the contents of endogenous sugars and phenolics in any in vitro conditions. However, the addition of sugar had a decisive effect on the biosynthesis of the Amaryllidaceae alkaloids. The highest distribution of alkaloids occurred in plants cultured in the medium containing 60 g/L sucrose. Six Amaryllidaceae alkaloids were detected in the plant tissue. The addition of 30 g/L fructose in the medium resulted in the accumulation of five alkaloids, including ismine, which was not identified in other analysed tissues. The highest concentration of galanthamine was observed in plants cultured in the presence of 30 g/L fructose and 60 g/L sucrose (39.2 and 37.5 µg/g of dry weight (DW), respectively). The plants grown in the medium containing 60 g/L sucrose exhibited the highest lycorine content (1048 µg/g of DW).Conclusions: The type and concentration of sugar used in the medium have an essential influence on the biosynthesis of Amaryllidaceae alkaloids inL. aestivumplants cultured in a RITA®bioreactor. The results point to an interesting approach for commercial production of galanthamine and lycorine.

20 October 2016 in Plant Cell, Tissue and Organ Culture (PCTOC)
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Agata PtakAgata Ptak
Agata Ptak
EMEmilia Morańska
Emilia Morańska
Sahar SalibaSahar Saliba
Sahar Saliba
AZAndrzej Zieliński
Andrzej Zieliński
MSMagdalena Simlat
Magdalena Simlat
DLDominique Laurain-Mattar
Dominique Laurain-Mattar