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Inhibiting NAD+-dependent DNA ligase activity with 2-(cyclopentyloxy)-5'-deoxyadenosine (CPOdA) offers a new tool for DNA replication and repair studies in the model archaeon Haloferax volcanii.
Giroux, Xavier; MacNeill, Stuart A.
Affiliation
  • Giroux X; School of Biology, University of St Andrews, North Haugh, St Andrews, Fife KY16 9ST, UK.
  • MacNeill SA; School of Biology, University of St Andrews, North Haugh, St Andrews, Fife KY16 9ST, UK sam31@st-and.ac.uk.
FEMS Microbiol Lett ; 362(21)2015 Nov.
Article in En | MEDLINE | ID: mdl-26420852
ABSTRACT
DNA ligases play an essential role in many aspects of DNA metabolism in all three domains of life. The haloarchaeal organism Haloferax volcanii encodes both ATP- and NAD(+)-dependent DNA ligase enzymes designated LigA and LigN, respectively. Neither LigA nor LigN alone is required for cell viability but they share an essential function, most likely the ligation of Okazaki fragments during chromosome replication. Here we show that 2-(cyclopentyloxy)-5'-deoxyadenosine (referred to as CPOdA), originally developed as a inhibitor of bacterial NAD(+)-dependent DNA ligases, is a potent inhibitor of the growth of Hfx. volcanii cells expressing LigN alone, causing chromosome fragmentation and cell death, while cells expressing LigA are unaffected. Growth inhibition occurs at significantly lower CPOdA concentrations (MIC ≤ 50 ng ml(-1)) than those required for inhibition of bacterial growth (≥2 µg ml(-1)). CPOdA has the potential to become a vital tool in DNA replication and repair studies in this important model organism.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA Ligases / Haloferax volcanii / DNA Replication / Enzyme Inhibitors Language: En Journal: FEMS Microbiol Lett Year: 2015 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA Ligases / Haloferax volcanii / DNA Replication / Enzyme Inhibitors Language: En Journal: FEMS Microbiol Lett Year: 2015 Document type: Article Affiliation country: