نتایج جستجو برای: dna supercoiling

تعداد نتایج: 507474  

2014
Alejandra Gutiérrez-Estrada Jesús Ramírez-Santos María del Carmen Gómez-Eichelmann

Escherichia coli stationary-phase (SP) cells contain relaxed DNA molecules and recover DNA supercoiling once nutrients become available. In these cells, the reactivation of DNA gyrase, which is a DNA topoisomerase type IIA enzyme, is responsible for the recovery of DNA supercoiling. The results presented in this study show that DNA gyrase reactivation does not require cellular chaperones or pol...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1977
M Gellert K Mizuuchi M H O'Dea T Itoh J I Tomizawa

ATP-dependent DNA supercoiling catalyzed by Escherichia coli DNA gyrase was inhibited by oxolinic acid, a compound similar to but more potent than nalidixic acid and a known inhibitor of DNA replication in E. coli. The supercoiling activity of DNA gyrase purified from nalidixic acid-resistant mutant (nalA(R)) bacteria was resistant to oxolinic acid. Thus, the nalA locus is responsible for a sec...

Journal: :Nano letters 2016
Mahipal Ganji Sung Hyun Kim Jaco van der Torre Elio Abbondanzieri Cees Dekker

DNA supercoiling crucially affects cellular processes such as DNA replication, gene expression, and chromatin organization. However, mechanistic understanding of DNA supercoiling and the related DNA-processing enzymes has remained limited, mainly due to the lack of convenient experimental tools to probe these phenomena. Here, we report a novel high-throughput single-molecule assay for real-time...

Journal: :Cell cycle 2011
Guillaume Witz Giovanni Dietler Andrzej Stasiak

Type II DNA topoisomerases permit passages of double stranded DNA segments through each other and this is achieved via a complex mechanism involving a transient cleavage of one duplex, a passage of the second duplex through the topoisomerase-spanned cleavage site and finally resealing of the cut duplex. Type II DNA topoisomerases facilitate many DNA transactions requiring manipulation of long D...

2015
DongHee Park Bong-Kwang Jung Hyunjin Park Hyungbeen Lee Gyudo Lee Jingam Park Unchul Shin Jong Ho Won Yong Jun Jo Jin Woo Chang Sangwoo Lee Daesung Yoon Jongbum Seo Chul-Woo Kim

Supercoiling DNA (folding DNA into a more compact molecule) from open circular forms requires significant bending energy. The double helix is coiled into a higher order helix form; thus it occupies a smaller footprint. Compact packing of DNA is essential to improve the efficiency of gene delivery, which has broad implications in biology and pharmaceutical research. Here we show that low-intensi...

Journal: :Journal of Bacteriology 1984

Journal: :Physical review letters 2004
Sébastien Neukirch

We use an elastic rod model with contact to study the extension versus rotation diagrams of single supercoiled DNA molecules. We reproduce quantitatively the supercoiling response of overtwisted DNA and, using experimental data, we obtain an estimate of the effective supercoiling radius and of the twist rigidity of B-DNA. We find that the twist rigidity of DNA seems to vary widely with the natu...

2016
Sally Hassan Eli Keshavarz‐Moore John Ward

With the recent revival of the promise of plasmid DNA vectors in gene therapy, a novel synthetic biology approach was used to enhance the quantity, (yield), and quality of the plasmid DNA. Quality was measured by percentage supercoiling and supercoiling density, as well as improving segregational stability in fermentation. We examined the hypothesis that adding a Strong Gyrase binding Site (SGS...

2016
Airat Gubaev Daniela Weidlich Dagmar Klostermeier

The topological state of DNA is important for replication, recombination and transcription, and is regulated in vivo by DNA topoisomerases. Gyrase introduces negative supercoils into DNA at the expense of ATP hydrolysis. It is the accepted view that gyrase achieves supercoiling by a strand passage mechanism, in which double-stranded DNA is cleaved, and a second double-stranded segment is passed...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1978
L F Liu J C Wang

Two active components alpha and beta of micrococcus luteus DNA gyrase, of peptide weights of 115,000 and 97,000, respectively, have been purified. Each individual component exhibits little DNA gyrase activity; the ATP-dependent negative supercoiling of a covalently closed circular DNA duplex is catalyzed by a combination of the two. Covalent closure by Escherichia coli ligase of a circular DNA ...

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