نتایج جستجو برای: restriction endonucleases

تعداد نتایج: 74551  

Journal: :Indian journal of science and technology 2022

Objectives: To identify and to characterize of methicillin-resistant Staphylococcus aureus (MRSA) isolates collected from food (n=43), handler (n=8), clinical samples (n=15). Methods: Genotyping was applied for the purposes epidemiological investigation source tracking these isolates. Pulsed field gel electrophoresis (PFGE) performed using restriction endonucleases SmaI. Findings: PFGE analysis...

Journal: :Applied and environmental microbiology 1990
M Miyahara Y Kudoh K Mise

Specific restriction endonucleases were detected in three serotypes of Salmonella spp. isolated from humans in Japan from 1970 to 1987: an isoschizomer of AvaII endonuclease at a frequency of 0.91 in Salmonella infantis, an isoschizomer of KpnI at a frequency of 0.34 in Salmonella thompson, and an isoschizomer of StyI at a frequency of 0.30 in Salmonella blockley. Of interest is that restrictio...

Journal: :The Yale Journal of Biology and Medicine 1983
S. Razin M. F. Barile R. Harasawa D. Amikam G. Glaser

Recent advances on the properties of the mycoplasma genome, including size, base composition, replication, extrachromosomal DNA, and transfer of genetic material are briefly reviewed, with emphasis on their phylogenetic implications. The use of cleavage patterns of the mycoplasma genome by restriction endonucleases as "finger-prints" indicating genetic relatedness among strains is discussed. Th...

Journal: :Nucleic acids research 1991
K K Wong M McClelland

When dCTP is replaced by methyl5-dCTP in the polymerase chain reaction some templates cannot be efficiently amplified by Taq polymerase or Vent polymerase using standard cycling parameters. However, this phenomenon can be overcome by increasing the temperature of the denaturation steps to 100 degrees C, or by adding dITP to destabilize the m5dC:dG base pairs. Once the block to amplification of ...

2001
Ekrem ATALAN

To separate the unknown Streptomyces strains isolated from soil samples, the interspacer regions of 16S-23S rDNA of 14 isolates were amplified with PCR (polymerase chain reaction) and digested with three restriction endonucleases, namely, Bsp143I, HaeIII and MnlI. The restriction patterns were used for RFLP (restriction fragment length polymorphism) analysis. A dendrogram were constructed using...

Journal: :BioTechniques 1997
J H Senesac J K Romanin

Restriction endonuclease NarI cleaves DNA using a two-site mechanism, placing it in the Type IIe class of restriction endonucleases. Although these enzymes have very useful recognition sequences, the two-site mechanism limits the practical application. Site preferences often cause incomplete substrate digestion. Oligonucleotide activation of NarI eliminates incomplete digestions, making it poss...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1996
Y G Kim J Cha S Chandrasegaran

A long-term goal in the field of restriction-modification enzymes has been to generate restriction endonucleases with novel sequence specificities by mutating or engineering existing enzymes. This will avoid the increasingly arduous task of extensive screening of bacteria and other microorganisms for new enzymes. Here, we report the deliberate creation of novel site-specific endonucleases by li...

2013
Paul Hansmann

In daffodil, development of chloroplasts or chromoplasts is not accompanied by plastid DNA modification. This has been shown by comparing the fragment pattern of different restriction endonucleases, and by the lack of methylation of CCGG sequences. A physical map has been constructed for the plastome using the restriction endonucleases Sal I, Pst I, and Bgl I. The fragments containing the genes...

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