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Wyświetlanie 1-3 z 3
Tytuł:
Mg2+ ions do not induce expansion of the melted DNA region in the open complex formed by Escherichia coli RNA polymerase at a cognate synthetic Pa promoter. A quantitative KMnO4 footprinting study
Autorzy:
Łoziński, Tomasz
Wierzchowski, Kazimierz
Powiązania:
https://bibliotekanauki.pl/articles/1044146.pdf
Data publikacji:
2001
Wydawca:
Polskie Towarzystwo Biochemiczne
Tematy:
permanganate footprinting
open promoter complex
thymine oxidation
effect of magnesium ions
RNA polymerase
Opis:
Footprinting studies of prokaryotic open transcription complexes (RPO), based on oxidation of pyrimidine residues by KMnO4 and/or OsO4 at a single oxidant dose, have suggested that the extent of DNA melting in the transcription bubble region increases in the presence of Mg2+. In this work, quantitative KMnO4 footprinting in function of the oxidant dose of RPO, using Escherichia coli RNA polymerase (Eσ70 ) at a fully functional synthetic promoter Pa having -35 and -10 consensus hexamers, has been used to determine individual rate constants of oxidation of T residues in this region at 37°C in the absence of Mg2+ and in the presence of 10 mM MgCl2, and to evaluate therefrom the effect of Mg2+ on the extent of DNA melting. Population distributions of end-labeled DNA fragments corresponding to oxidized Ts were quantified and analyzed according to the single-hit kinetic model. Pseudo-first order reactivity rate constants, ki, thus obtained demonstrated that Mg2+ ions bound to RPO merely enhanced the reactivity of all 11 oxidizable thymines between the +3 and -11 promoter sites by a position-dependent factor: 3-4 for those located close to the transcription start point +1 in either DNA strand, and about 1.6 for those located more distantly therefrom. On the basis of these observations, we conclude that Mg2+ ions bound to RPO at Pa do not influence the length of the melted DNA region and propose that the higher reactivity of thymines results mainly from lower local repulsive electrostatic barriers to MnO4- diffusion around carboxylate binding sites in the catalytic center of RPO and promoter DNA phosphates.
Źródło:
Acta Biochimica Polonica; 2001, 48, 2; 495-510
0001-527X
Pojawia się w:
Acta Biochimica Polonica
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Footprinting, czyli mierzenie śladu pozostawionego w środowisku
Footprinting as environmental impact measure
Autorzy:
Śleszyński, Jerzy
Powiązania:
https://bibliotekanauki.pl/articles/956173.pdf
Data publikacji:
2016
Wydawca:
Uniwersytet w Białymstoku. Wydawnictwo Uniwersytetu w Białymstoku
Tematy:
footprinting
ecological footprint
carbon footprint
wskaźniki śladu
ślad ekologiczny
ślad węglowy
Opis:
Celem artykułu jest przedstawienie silnych i słabych stron wskaźników z rodziny wskaźników ,,śladowych”, a więc wskaźników, które, podobnie jak ślad ekologiczny (Ecological Footprint), opisują presję wywieraną na środowisko przez istniejące modele produkcji i wzorce konsumpcji. Środowisko udziela nam zasobów i przyjmuje zanieczyszczenia, ale może to czynić tylko w granicach wyznaczonych: pojemnością, odpornością i stabilnością ekosystemów. W zakończeniu kwestia przydatności mierników ,,śladu” prowadzi do wskazania kierunków ich bardziej powszechnego i pożytecznego zastosowania.
The paper enumerates the strengths and weaknesses of indicators belonging to the family of footprint indicators. They follow the Ecological Footprint method and describe the anthropogenic pressure on the natural environment stemming from the functioning of production models and consumption patterns. The environment provides us with resources and also absorbs pollution. However, all these benefits are available to an extent limited by the capacity, resilience and stability of ecosystems. In the conclusion of the paper, recommendations for a more frequent and productive application of footprint indicators are offered.
Źródło:
Optimum. Economic Studies; 2016, 1(79); 56-73
1506-7637
Pojawia się w:
Optimum. Economic Studies
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Effect of Mg2+ on kinetics of oxidation of pyrimidines in duplex DNA by potassium permanganate.
Autorzy:
Łoziński, Tomasz
Wierzchowski, Kazimierz
Powiązania:
https://bibliotekanauki.pl/articles/1044147.pdf
Data publikacji:
2001
Wydawca:
Polskie Towarzystwo Biochemiczne
Tematy:
oxidation of pyrimidines
thymine glycol
magnesium ions
rate constant of oxidation
pDS3 plasmid DNA
quantitative permanganate footprinting
Opis:
Potassium permanganate oxidation of pyrimidine bases is often used to probe single-stranded regions in functional DNA-protein complexes. However, so far reactivity of these bases in double-stranded DNA has not been studied quantitatively. We have investigated the kinetics of oxidation of pyrimidines in supercoiled pDS3 plasmid dsDNA by quantitative KMnO4 footprinting, in connection with parallel studies on the effect of Mg2+ on kinetics of oxidation of individual thymines in the single-stranded region of the open transcription complex of Escherichia coli RNA polymerase at a cognate Pa promoter contained in this plasmid. Rate constants of oxidation for pyrimidines, kj, in selected regions of pDS3 DNA, including Pa promoter, were determined under single-hit reaction conditions in the absence and presence of 10 mM MgCl2. Their values appeared to be sequence-dependent and were: (i) the largest for Ts in 5'TA3' and 5'TC3' steps, while 2-4 times smaller for 5'-adjacent ones in TT(A,G,C) and TTT(A) runs, (ii) for Cs in 5'TC3' steps 2-4 fold smaller than for adjacent Ts, and (iii) in the presence of Mg2+ generally larger by a sequence-dependent factor: in 5'TC3' steps of about 2 and 4 for Ts and Cs, respectively, in 5'TA3' steps of TTA and TTTA sequences for 3'-terminal Ts of about 3, while for their 5'-neighbors of a distinctly smaller value of about 2. Comparison of kj data for corresponding Ts located between +1 and -10 regions of Pa promoter in dsDNA and in ssDNA form in the open transcription complex, reported elsewhere, demonstrates that reactivity of pyrimidines in dsDNA is by 2-3 orders of magnitude smaller. The effect of Mg2+ in dsDNA is interpreted in terms of electrostatic barrier to diffusion of MnO4- on DNA surface, which is lowered by diffusive binding of these ions to backbone phosphates, involving also sequence-specific contacts with bases in the minor and major grooves of B-DNA.
Źródło:
Acta Biochimica Polonica; 2001, 48, 2; 511-523
0001-527X
Pojawia się w:
Acta Biochimica Polonica
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-3 z 3

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