<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>170(4)</volume><submitter>Regha K</submitter><pubmed_abstract>The Antarctic psychrotrophic bacterium Pseudomonas syringae Lz4W has been used as a model system to identify genes that are required for growth at low temperature. Transposon mutagenesis was carried out to isolate mutant(s) of the bacterium that are defective for growth at 4 degrees but normal at 22 degrees . In one such cold-sensitive mutant (CS1), the transposon-disrupted gene was identified to be a homolog of the recD gene of several bacteria. Trans-complementation and freshly targeted gene disruption studies reconfirmed that the inactivation of the recD gene leads to a cold-sensitive phenotype. We cloned, sequenced, and analyzed approximately 11.2 kbp of DNA from recD and its flanking region from the bacterium. recD was the last gene of a putative recCBD operon. The RecD ORF was 694 amino acids long and 40% identical (52% similar) to the Escherichia coli protein, and it could complement the E. coli recD mutation. The recD gene of E. coli, however, could not complement the cold-sensitive phenotype of the CS1 mutant. Interestingly, the CS1 strain showed greater sensitivity toward the DNA-damaging agents, mitomycin C and UV. The inactivation of recD in P. syringae also led to cell death and accumulation of DNA fragments of approximately 25-30 kbp in size at low temperature (4 degrees ). We propose that during growth at a very low temperature the Antarctic P. syringae is subjected to DNA damage, which requires direct participation of a unique RecD function. Additional results suggest that a truncated recD encoding the N-terminal segment of (1-576) amino acids is sufficient to support growth of P. syringae at low temperature.</pubmed_abstract><journal>Genetics</journal><pagination>1473-84</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC1449786</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>RecD plays an essential function during growth at low temperature in the antarctic bacterium Pseudomonas syringae Lz4W.</pubmed_title><pmcid>PMC1449786</pmcid><pubmed_authors>Satapathy AK</pubmed_authors><pubmed_authors>Regha K</pubmed_authors><pubmed_authors>Ray MK</pubmed_authors></additional><is_claimable>false</is_claimable><name>RecD plays an essential function during growth at low temperature in the antarctic bacterium Pseudomonas syringae Lz4W.</name><description>The Antarctic psychrotrophic bacterium Pseudomonas syringae Lz4W has been used as a model system to identify genes that are required for growth at low temperature. Transposon mutagenesis was carried out to isolate mutant(s) of the bacterium that are defective for growth at 4 degrees but normal at 22 degrees . In one such cold-sensitive mutant (CS1), the transposon-disrupted gene was identified to be a homolog of the recD gene of several bacteria. Trans-complementation and freshly targeted gene disruption studies reconfirmed that the inactivation of the recD gene leads to a cold-sensitive phenotype. We cloned, sequenced, and analyzed approximately 11.2 kbp of DNA from recD and its flanking region from the bacterium. recD was the last gene of a putative recCBD operon. The RecD ORF was 694 amino acids long and 40% identical (52% similar) to the Escherichia coli protein, and it could complement the E. coli recD mutation. The recD gene of E. coli, however, could not complement the cold-sensitive phenotype of the CS1 mutant. Interestingly, the CS1 strain showed greater sensitivity toward the DNA-damaging agents, mitomycin C and UV. The inactivation of recD in P. syringae also led to cell death and accumulation of DNA fragments of approximately 25-30 kbp in size at low temperature (4 degrees ). We propose that during growth at a very low temperature the Antarctic P. syringae is subjected to DNA damage, which requires direct participation of a unique RecD function. Additional results suggest that a truncated recD encoding the N-terminal segment of (1-576) amino acids is sufficient to support growth of P. syringae at low temperature.</description><dates><release>2005-01-01T00:00:00Z</release><publication>2005 Aug</publication><modification>2021-02-20T01:00:03Z</modification><creation>2019-03-27T01:26:20Z</creation></dates><accession>S-EPMC1449786</accession><cross_references><pubmed>15956672</pubmed><doi>10.1534/genetics.104.038943</doi></cross_references></HashMap>