Kvetoslava Burda

Kvetoslava Burda

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Research Focus & Metrics

Academic Career Length

35Years (1992-Present)

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

Representative Publications

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27 January 2014 in Nutrients
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JFJoanna Fiedor
Joanna Fiedor
KBKvetoslava Burda
Kvetoslava Burda
Carotenoids constitute a ubiquitous group of isoprenoid pigments. They are very efficient physical quenchers of singlet oxygen and scavengers of other reactive oxygen species. Carotenoids can also act as chemical quenchers undergoing irreversible oxygenation. The molecular mechanisms underlying these reactions are still not fully understood, especially in the context of the anti- and pro-oxidant activity of carotenoids, which, although not synthesized by humans and animals, are also present in their blood and tissues, contributing to a number of biochemical processes. The antioxidant potential of carotenoids is of particular significance to human health, due to the fact that losing antioxidant-reactive oxygen species balance results in “oxidative stress”, a critical factor of the pathogenic processes of various chronic disorders. Data coming from epidemiological studies and clinical trials strongly support the observation that adequate carotenoid supplementation may significantly reduce the risk of several disorders mediated by reactive oxygen species. Here, we would like to highlight the beneficial (protective) effects of dietary carotenoid intake in exemplary widespread modern civilization diseases, i.e., cancer, cardiovascular or photosensitivity disorders, in the context of carotenoids’ unique antioxidative properties.

1 September 2015 in Chemico-Biological Interactions
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Journal Article
Closed access
DADominika Augustynska
Dominika Augustynska
MJMalgorzata Jemiola-Rzeminska
Malgorzata Jemiola-Rzeminska
KBKvetoslava Burda
Kvetoslava Burda
KSKazimierz Strzalka
Kazimierz Strzalka

15 May 2013 in Cell Biochemistry and Biophysics
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MKMagdalena Kaczmarska
Magdalena Kaczmarska
MFMaria Fornal
Maria Fornal
FMFranz H. Messerli
Franz H. Messerli
JKJozef Korecki
Jozef Korecki
TGTomasz Grodzicki
Tomasz Grodzicki
KBKvetoslava Burda
Kvetoslava Burda

1 January 2015 in Dyes and Pigments
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Journal Article
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TKTomasz Koczorowski
Tomasz Koczorowski
WSWojciech Szczolko
Wojciech Szczolko
KBKvetoslava Burda
Kvetoslava Burda
MNMagdalena Nowak
Magdalena Nowak
MDMałgorzata Dawidowska
Małgorzata Dawidowska
TGTomasz Gośliński
Tomasz Gośliński

1 April 1995 in Zeitschrift für Naturforschung C
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KBKvetoslava Burda
Kvetoslava Burda
KSK. Strzałka
K. Strzałka
GSG. H. Schmid
G. H. Schmid
Trivalent lanthanide cations are suitable probes for Ca2+-binding sites in photosystem II (PS II). PS II membranes prepared from Nicoticinci tabacum, intact and depleted of the extrinsic polypeptides were exposed to lanthanide ions (Dy3+ and Eu3+). Small concentrations of dysprosium and europium ions enhance oxygen evolution under short saturating flashes. Higher concentrations of the rare earth cations cause the release of the three extrinsic peptides (17, 23 and 33 kDa) and reduce O2 yield. The reactivation of the PS II membranes, thus depleted of the 33 kDa subunit, by Ca2+ ions is not possible. Comparing Eu3+ with Dy3+ in this effect shows that Eu3+ is more effective than Dy3+, because a lower Eu3+-concentration in comparison to that of Dy3+ inactivates O2-evolution. The differences between europium and dysprosium can be explained by their different ionic radius. Our results suggest the existence of two Ca-binding regions: one with a low affinity for calcium would be located on the contact surface of the 23 and 33 kDa proteins and the second one with a high affinity, should be located close to the Mn-cluster and to tyrosine-161 (Z ). The more tightly-bound calcium would be responsible for the activity of the PS II system.

13 March 2021 in Antioxidants
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JFJoanna Fiedor
Joanna Fiedor
Mateusz PrzetockiMateusz Przetocki
Mateusz Przetocki
ASAleksander Siniarski
Aleksander Siniarski
GGGrzegorz Gajos
Grzegorz Gajos
NSNika Spiridis
Nika Spiridis
KBKvetoslava Burda
Kvetoslava Burda
β-Carotene (β-Crt) can be dispersed in hydrophobic regions of the membrane of red blood cells (RBC). Its location, orientation and distribution strongly depend on carotenoid concentration. In the present pilot trial (six human subjects involved), it is demonstrated that incubation of RBCs with β-Crt (1.8 × 107 β-Crt molecules per RBC, 50 μmol/L) results in expansion of the membrane of RBCs and slight elongation of the cell. The changes are of statistical significance, as verified by the Wilcoxon test at p < 0.05. They indicate (i) a highly random orientation and location of β-Crt inside the membrane and (ii) a tendency for its interaction with membrane skeleton proteins. The accompanying effect of decreased RBC resistance to lysis is possibly a result of the incorrect functioning of ion channels due to their modification/disruption. At higher β-Crt concentrations, its clustering inside membranes may occur, leading to further alterations in the shape and size of RBCs, with the most pronounced changes observed at 1.8 × 108 β-Crt molecules per RBC (500 μmol/L). Due to the reduced permeability of ions, such membranes exhibit increased resistance to haemolysis. Finally, we show that interactions of β-Crt with the membrane of RBCs lead to an alteration in haemoglobin-oxygen affinity, shifting the oxyhaemoglobin dissociation curve toward higher oxygen partial pressures. If the impact of β-Crt on a curve course is confirmed in vivo, one may consider its role in the fine tuning of O2 transportation to tissues. Hence, at low concentrations, providing unchanged elastic and functional properties of RBCs, it could serve as a beneficial agent in optimising heart performance and cardiovascular load.