We extended the measurable time scale of DNA dynamics to microsecond using [Ru(phen)(2)(dppz)](2+)(phen = 1,10-phenanthroline, dppz=dipyrido[3,2-a:2',3'-c]phenazine)(RuPD) , which displays a mean lifetime near 500 ns. To evaluate the usefulness of this luminophore (RuPD) for probing nucleic acid dynamics, its intensity and anisotropy decays when intercalated into supercoiled and linear pBluescript (pBS) II SK(+) phagemids were examined using frequency-domain fluorometry with a blue light-emitting diode (LED) as the modulated light source. The mean lifetime for the supercoiled phagemids (
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http://dx.doi.org/10.5483/bmbrep.2005.38.1.104 | DOI Listing |
Indian J Microbiol
September 2019
Dpto. de Biotecnología, Facultad de Ciencias Químicas, Universidad Nacional de Asunción, Campus Universitario, San Lorenzo, Paraguay.
Filamentous bacteriophages are widely used in phage display technology. The most common quantification method is lysis plaque formation test (PFT). This technique has several disadvantages, and only quantifies infective phages and is not effective when phagemids are used.
View Article and Find Full Text PDFPLoS One
October 2017
Key Laboratory of Special Pathogens and Biosafety, Center for Emerging Infectious Diseases, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, China.
Proc Natl Acad Sci U S A
July 2016
Department of Biochemistry and Biophysics, University of North Carolina, Chapel Hill, NC 27599
The hydrolytic deamination of cytosine and 5-methylcytosine residues in DNA appears to contribute significantly to the appearance of spontaneous mutations in microorganisms and in human disease. In the present work, we examined the mechanism of cytosine deamination and the response of the uncatalyzed reaction to changing temperature. The positively charged 1,3-dimethylcytosinium ion was hydrolyzed at a rate similar to the rate of acid-catalyzed hydrolysis of 1-methylcytosine, for which it furnishes a satisfactory kinetic model and a probable mechanism.
View Article and Find Full Text PDFPLoS One
July 2014
Department of Microbiology, University of Delhi South Campus, Benito Juarez Road, New Delhi, India.
Phagemid-based expression of cloned genes fused to the gIIIP coding sequence and rescue using helper phages, such as VCSM13, has been used extensively for constructing large antibody phage display libraries. However, for randomly primed cDNA and gene fragment libraries, this system encounters reading frame problems wherein only one of 18 phages display the translated foreign peptide/protein fused to phagemid-encoded gIIIP. The elimination of phages carrying out-of-frame inserts is vital in order to improve the quality of phage display libraries.
View Article and Find Full Text PDFWei Sheng Yan Jiu
September 2012
School of Life Science, Jiangxi Science and Technology Normal University, Nanchang 330013, China.
Objective: Traditional ochratoxin A(OTA) competitive antigen are high toxicity, high price and difficult preparation. Non-toxic and easy prepared OTA competitive antigen substitutes were expressed by recombinant filamentous phage which have OTA mimotope displayed on its p VI surface.
Methods: Recombinant phagemid pC89-COTA which contain OTA mimotope nucleotide sequence was constructed.
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