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Photoactivated ethidium monoazide directly cleaves bacterial DNA and is applied to PCR for discrimination of live and dead bacteria.

Photoactivated ethidium monoazide directly cleaves bacterial DNA and is applied to PCR for discrimination of live and dead bacteria. Research Abstract Details 

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  • Photoactivated ethidium monoazide directly cleaves bacterial DNA and is applied to PCR for discrimination of live and dead bacteria. Abstract Text:

    takashi soejimaTakashi Soejima,ken-ichiro iidaKen-ichiro Iida,tian qinTian Qin,hiroaki taniaiHiroaki Taniai,masanori sekiMasanori Seki,akemi takadeAkemi Takade,shin-ichi yoshidaShin-ichi Yoshida,takashi soejimaTakashi Soejima,ken-ichiro iidaKen-ichiro Iida,tian qinTian Qin,hiroaki taniaiHiroaki Taniai,masanori sekiMasanori Seki,akemi takadeAkemi Takade,shin-ichi yoshidaShin-ichi Yoshida,

    Ethidium monoazide (EMA) is a DNA intercalating agent and a eukaryotic topoisomerase II poison. We found that EMA treatment and subsequent visible light irradiation (photoactivation or photolysis) shows a bactericidal effect, hence the mechanism was analyzed. When bacterial cells were treated with more than 10 microg/ml of EMA for 1 hr plus photoactivation for 20 min, cleavage of bacterial DNA was confirmed by agarose gel electrophoresis and electron microscopic studies. The cleavage of chromosomal DNA was seen when it was treated in vitro with EMA and photolysis, which showed that the cleavage directly took place without the assistance of DNA gyrase/topoisomerase IV and the DNA repair enzymes of bacteria. It was also verified, by using negatively supercoiled pBR322 DNA, that medium/high concentrations of EMA (1 to 100 microg/ml) led to breaks of double-stranded DNA and that low concentrations of EMA (10 to 100 ng/ml) generated a single-stranded break. EMA is known to easily penetrate dead but not live bacteria. After treatment of 10 microg/ml of EMA for 30 min and photoactivation for 5 min, EMA cleaved the DNA of dead but not live Klebsiella oxytoca. When the cleaved DNA was used for templates in PCR targeting 16S rDNA, PCR product from the dead bacteria was completely suppressed. We demonstrated that EMA and photolysis directly cleaved bacterial DNA and are effective tools for discriminating live from dead bacteria by PCR.

    Photoactivated ethidium monoazide directly cleaves bacterial DNA and is applied to PCR for discrimination of live and dead bacteria. Publishing Authors By Initials

    t soejimaT Soejima,k iidaK Iida,t qinT Qin,h taniaiH Taniai,m sekiM Seki,a takadeA Takade,s yoshidaS Yoshida,t soejimaT Soejima,k iidaK Iida,t qinT Qin,h taniaiH Taniai,m sekiM Seki,a takadeA Takade,s yoshidaS Yoshida,

    For similar abstracts research abstracts see: abstracts research

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    Photoactivated ethidium monoazide directly cleaves bacterial DNA and is applied to PCR for discrimination of live and dead bacteria. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Microbiology and immunology

    VOLUME: 51

    Page Numbers: 763-75

    Journal Abbreviation: Microbiol. Immunol.

    ISSN: 0385-5600

    DAY: 20

    MONTH: 08

    YEAR: 2007

    Photoactivated ethidium monoazide directly cleaves bacterial DNA and is applied to PCR for discrimination of live and dead bacteria. Information

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    LANGUAGE: eng

    NlmUniqueID: 7703966

    Photoactivated ethidium monoazide directly cleaves bacterial DNA and is applied to PCR for discrimination of live and dead bacteria. Keywords Mesh Terms:

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    Grant and Affiliation Information for Photoactivated ethidium monoazide directly cleaves bacterial DNA and is applied to PCR for discrimination of live and dead bacteria.

    AFFILIATION: Department of Bacteriology, Faculty of Medical Sciences, Kyushu University, Fukuoka 812-8582, Japan. t_soezim@morinagamilk.co.jp

    Country: Japan

    Japan Research PublicationJapan Research Publication

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    MEDLINETA: Microbiol Immunol

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