نتایج جستجو برای: 46 amino uracil

تعداد نتایج: 294386  

Journal: :Journal of bacteriology 1995
J Martinussen P Glaser P S Andersen H H Saxild

Uracil phosphoribosyltransferase (UPRTase) catalyzes the key reaction in the salvage of uracil in many microorganisms. Surprisingly, two genes encoding UPRTase activity were cloned from Bacillus subtilis by complementation of an Escherichia coli mutant. The genes were sequenced, and the putative amino acid sequences were deduced. One gene showed a high level of homology to UPRTases from other o...

Journal: :The Journal of chemical physics 2004
Iwona Dabkowska Janusz Rak Maciej Gutowski J Michael Nilles Sarah T Stokes Kit H Bowen

The photoelectron spectrum of the uracil-alanine anionic complex (UA)(-) has been recorded with 2.540 eV photons. This spectrum reveals a broad feature with a maximum between 1.6 and 2.1 eV. The vertical electron detachment energy is too large to be attributed to an (UA)(-) anionic complex in which an intact uracil anion is solvated by alanine, or vice versa. The neutral and anionic complexes o...

2008
Denis A. Semenov

A simple explanation for the symmetry of the genetic code has been suggested. An alternative to the wobble hypothesis has been proposed. The facts revealed in this study offer a new insight into physical mechanisms of the functioning of the genetic code. The wobble hypothesis, which was first proposed more than 40 years ago [1], can explain two events: 1) formation of the uracil­guanine pair as...

Journal: :European journal of biochemistry 1998
K Purnapatre U Varshney

Deamination of cytosine residues contributes to the appearance of uracil in DNA. Uracil DNA glycosylase (UDG) initiates uracil excision repair to safeguard the genomic integrity. To study the mechanism of uracil excision in mycobacteria (organisms with G+C rich genomes), we have purified UDG from Mycobacterium smegmatis by more than 3000-fold. The molecular mass of M. smegmatis UDG, as determin...

Journal: :ACS omega 2023

Herein, we report an efficient method for synthesis of novel selenocyanates amino pyrazole, uracil, and isoxazole derivatives using in situ triselenium dicyanide from the combination malononitrile selenium dioxide DMSO medium. Using same but changing stoichiometry reagents sequence addition temperature, symmetrical selenoethers pyrazoles uracils were prepared good yields. Furthermore, utilized ...

Journal: :DNA repair 2006
Sibghat-Ullah Lari Cheng-Yao Chen Béata G Vertéssy Jeff Morré Samuel E Bennett

The steady-state levels of uracil residues in DNA extracted from strains of Escherichia coli were measured and the influence of defects in the genes for uracil-DNA glycosylase (ung), double-strand uracil-DNA glycosylase (dug), and dUTP pyrophosphatase (dut) on uracil accumulation was determined. A sensitive method, called the Ung-ARP assay, was developed that utilized E. coli Ung, T4pdg, and th...

2013
Tomas T. Richardson Xiaohua Wu Brian J. Keith Pauline Heslop Anita C. Jones Bernard A. Connolly

Archaeal family-B DNA polymerases bind tightly to deaminated bases and stall replication on encountering uracil in template strands, four bases ahead of the primer-template junction. Should the polymerase progress further towards the uracil, for example, to position uracil only two bases in front of the junction, 3'-5' proof-reading exonuclease activity becomes stimulated, trimming the primer a...

Journal: :Journal of the American Chemical Society 1919

Journal: :Analytica chimica acta 2010
Takayuki Shibata Shin-ya Kawasaki Jun-ya Fujita Tsutomu Kabashima Masaaki Kai

Facile and specific methods to quantify a nucleobase in biological samples are of great importance for diagnosing disorders in nucleic acid metabolism. In the present study, a novel fluorogenic reaction specific for uracil has been developed. The reaction was carried out in an alkaline medium containing benzamidoxime and K(3)[Fe(CN)(6)] which were heated for 2.0 min. Under the optimum reaction ...

Journal: :Protein expression and purification 2004
Xipeng Liu Jianhua Liu

A uracil-DNA glycosylase gene was cloned from Chlamydia pneumoniae AR39 and expressed in E. coli strains BL21 (DE3) and BL21 (DE3) pLysS. After purification by Ni-NTA His x Bind Resin and DEAE Sepharose Fast Flow column chromatography, recombinant CpUDG with a specific activity of 1,000,000 U/mg was obtained. The enzymatic activity of the purified CpUDG protein was further characterized using o...

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