Please use this identifier to cite or link to this item: https://doi.org/10.1534/genetics.104.038943
Title: RecD plays an essential function during growth at low temperature in the antarctic bacterium Pseudomonas syringae Lz4W
Authors: Regha, K 
Satapathy, AK
Ray, MK
Keywords: Alkylating Agents
Amino Acid Sequence
Antarctic Regions
Apoptosis
Cell Death
Cloning, Molecular
Cold Temperature
DNA
DNA Damage
DNA Transposable Elements
Drug Tolerance
Escherichia coli
Escherichia coli Proteins
Gene Expression Regulation, Bacterial
Genes, Bacterial
Genetic Complementation Test
Mitomycin
Molecular Sequence Data
Mutagenesis, Site-Directed
Mutation
Open Reading Frames
Operon
Pseudomonas syringae
Radiation Tolerance
Sequence Analysis, DNA
Sequence Homology, Amino Acid
Ultraviolet Rays
Issue Date: 1-Aug-2005
Publisher: Oxford University Press (OUP)
Citation: Regha, K, Satapathy, AK, Ray, MK (2005-08-01). RecD plays an essential function during growth at low temperature in the antarctic bacterium Pseudomonas syringae Lz4W. Genetics 170 (4) : 1473-1484. ScholarBank@NUS Repository. https://doi.org/10.1534/genetics.104.038943
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° but normal at 22°. 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 ∼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 ∼25-30 kbp in size at low temperature (4°). 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. Copyright © 2005 by the Genetics Society of America.
Source Title: Genetics
URI: https://scholarbank.nus.edu.sg/handle/10635/213516
ISSN: 00166731
19432631
DOI: 10.1534/genetics.104.038943
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