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Aerobic-Type Ribonucleotide Reductase in the Anaerobe Bacteroides fragilis

dc.contributor.authorSmalley, Darrenen_US
dc.contributor.authorRocha, Edson R.en_US
dc.contributor.authorSmith, C. Jeffreyen_US
dc.date.accessioned2011-04-28T18:44:52Zen_US
dc.date.accessioned2011-05-17T01:40:11Z
dc.date.available2011-04-28T18:44:52Zen_US
dc.date.available2011-05-17T01:40:11Z
dc.date.issued2002-02en_US
dc.description.abstractBacteroides fragilis, a component of the normal intestinal flora, is an obligate anaerobe capable of long-term survival in the presence of air. Survival is attributed to an elaborate oxidative stress response that controls the induction of more than 28 peptides, but there is limited knowledge concerning the identities of these peptides. In this report, RNA fingerprinting by arbitrarily primed PCR identified five new genes whose expression increased following exposure to O2. Nucleotide sequence analysis of the cloned genes indicated that they encoded an outer membrane protein, an aspartate decarboxylase, an efflux pump, heat shock protein HtpG, and an NrdA ortholog constituting the large subunit of a class Ia ribonucleotide reductase (RRase). Attention was focused on the nrdA gene since class I RRases are obligate aerobic enzymes catalyzing the reduction of ribonucleoside 5'-diphosphates by a mechanism that requires molecular oxygen for activity. Sequence analysis of the nrd locus showed that two genes, nrdA and nrdB, are located in the same orientation in a 4.5-kb region. Northern hybridization and primer extension experiments confirmed induction of the genes by O2 and suggested they are an operon. The B. fragilis nrdA and nrdB genes were overexpressed in Escherichia coli, and CDP reductase assays confirmed that they encoded an active enzyme. The enzyme activity was inhibited by hydroxyurea, and ATP was shown to be a positive effector of CDP reductase activity, while dATP was an inhibitor, indicating that the enzyme was a class Ia RRase. A nrdA mutant was viable under anaerobic conditions but had decreased survival following exposure to O2, and it could not rapidly resume growth after O2 treatment. The results presented indicate that during aerobic conditions B. fragilis NrdAB may have a role in maintaining deoxyribonucleotide pools for DNA repair and growth recovery. Originally published Journal of Bacteriology, Vol. 184, No. 4, Feb 2002en_US
dc.identifier.citationJournal of Bacteriology; 184:4 p. 895-903en_US
dc.identifier.doi10.1128/jb.184.4.895-903.2002
dc.identifier.pmidPMC134816en_US
dc.identifier.urihttp://hdl.handle.net/10342/3425en_US
dc.language.isoen_USen_US
dc.publisherEast Carolina Universityen_US
dc.relation.urihttp://jb.asm.org/archive/2002.dtlen_US
dc.rightsAuthor notified of opt-out rights by Cammie Jennings prior to upload of this article.en_US
dc.subjectBacteroides fragilisen_US
dc.subjectRibonucleotide Reductasesen_US
dc.subjectAerobic environmenten_US
dc.titleAerobic-Type Ribonucleotide Reductase in the Anaerobe Bacteroides fragilisen_US
dc.typeArticleen_US
ecu.journal.issue4
ecu.journal.nameJournal of Bacteriology
ecu.journal.pages895-903
ecu.journal.volume184

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