<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Henry LG</submitter><funding>NIDCR NIH HHS</funding><pagination>7985-93</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2593216</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>190(24)</volume><pubmed_abstract>The persistence of Porphyromonas gingivalis in the inflammatory environment of the periodontal pocket requires an ability to overcome oxidative stress. DNA damage is a major consequence of oxidative stress. Unlike the case for other organisms, our previous report suggests a role for a non-base excision repair mechanism for the removal of 8-oxo-7,8-dihydroguanine (8-oxo-G) in P. gingivalis. Because the uvrB gene is known to be important in nucleotide excision repair, the role of this gene in the repair of oxidative stress-induced DNA damage was investigated. A 3.1-kb fragment containing the uvrB gene was PCR amplified from the chromosomal DNA of P. gingivalis W83. This gene was insertionally inactivated using the ermF-ermAM antibiotic cassette and used to create a uvrB-deficient mutant by a</pubmed_abstract><journal>Journal of bacteriology</journal><pubmed_title>DNA repair of 8-oxo-7,8-dihydroguanine lesions in Porphyromonas gingivalis.</pubmed_title><pmcid>PMC2593216</pmcid><funding_grant_id>R01 DE019730</funding_grant_id><funding_grant_id>R01 DE013664</funding_grant_id><funding_grant_id>R01 DE013664-06</funding_grant_id><funding_grant_id>R01 DE022508</funding_grant_id><pubmed_authors>Zhang K</pubmed_authors><pubmed_authors>Sandberg L</pubmed_authors><pubmed_authors>Henry LG</pubmed_authors><pubmed_authors>Fletcher HM</pubmed_authors></additional><is_claimable>false</is_claimable><name>DNA repair of 8-oxo-7,8-dihydroguanine lesions in Porphyromonas gingivalis.</name><description>The persistence of Porphyromonas gingivalis in the inflammatory environment of the periodontal pocket requires an ability to overcome oxidative stress. DNA damage is a major consequence of oxidative stress. Unlike the case for other organisms, our previous report suggests a role for a non-base excision repair mechanism for the removal of 8-oxo-7,8-dihydroguanine (8-oxo-G) in P. gingivalis. Because the uvrB gene is known to be important in nucleotide excision repair, the role of this gene in the repair of oxidative stress-induced DNA damage was investigated. A 3.1-kb fragment containing the uvrB gene was PCR amplified from the chromosomal DNA of P. gingivalis W83. This gene was insertionally inactivated using the ermF-ermAM antibiotic cassette and used to create a uvrB-deficient mutant by a</description><dates><release>2008-01-01T00:00:00Z</release><publication>2008 Dec</publication><modification>2025-04-04T13:38:59.807Z</modification><creation>2019-03-27T00:19:37Z</creation></dates><accession>S-EPMC2593216</accession><cross_references><pubmed>18849425</pubmed><doi>10.1128/jb.00919-08</doi><doi>10.1128/JB.00919-08</doi></cross_references></HashMap>