A DNA Polymerase V Homologue Encoded by TOL Plasmid pWW0 Confers Evolutionary Fitness on Pseudomonas putida under Conditions of Environmental Stress
Open Access
- 1 August 2005
- journal article
- research article
- Published by American Society for Microbiology in Journal of Bacteriology
- Vol. 187 (15) , 5203-5213
- https://doi.org/10.1128/jb.187.15.5203-5213.2005
Abstract
Plasmids in conjunction with other mobile elements such as transposons are major players in the genetic adaptation of bacteria in response to changes in environment. Here we show that a large catabolic TOL plasmid, pWW0, from Pseudomonas putida carries genes (rulAB genes) encoding an error-prone DNA polymerase Pol V homologue which increase the survival of bacteria under conditions of accumulation of DNA damage. A study of population dynamics in stationary phase revealed that the presence of pWW0-derived rulAB genes in the bacterial genome allows the expression of a strong growth advantage in stationary phase (GASP) phenotype of P. putida. When rulAB-carrying cells from an 8-day-old culture were mixed with Pol V-negative cells from a 1-day-old culture, cells derived from the aged culture out-competed cells from the nonaged culture and overtook the whole culture. At the same time, bacteria from an aged culture lacking the rulAB genes were only partially able to out-compete cells from a fresh overnight culture of the parental P. putida strain. Thus, in addition to conferring resistance to DNA damage, the plasmid-encoded Pol V genes significantly increase the evolutionary fitness of bacteria during prolonged nutritional starvation of a P. putida population. The results of our study indicate that RecA is involved in the control of expression of the pWW0-encoded Pol V.Keywords
This publication has 97 references indexed in Scilit:
- Complete Sequence and Genetic Organization of pDTG1, the 83 Kilobase Naphthalene Degradation Plasmid from Pseudomonas putida strain NCIB 9816-4Journal of Molecular Biology, 2004
- Mutagenic DNA repair potential inPseudomonasspp., and characterization of therulABPcoperon from the highly mutable strainPseudomonas cichorii302959Canadian Journal of Microbiology, 2004
- Complete nucleotide sequence and analysis of pPSR1 (72,601 bp), a pPT23A-family plasmid from Pseudomonas syringae pv. syringae A2Molecular Genetics and Genomics, 2003
- Characterization of a New LexA Binding Motif in the Marine Magnetotactic Bacterium Strain MC-1Journal of Bacteriology, 2003
- THE SOS RESPONSE: Recent Insights into umuDC-Dependent Mutagenesis and DNA Damage ToleranceAnnual Review of Genetics, 2000
- Roles of the mutagenesis proteins SamA′B and MucA′B in chemically induced frameshift mutagenesis in Salmonella typhimurium hisD3052Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 1998
- Resistance to ultraviolet light in Pseudomonas syringae: sequence and functional analysis of the plasmid-encoded rulAB genesGene, 1996
- Mutagenesis induced by bacterial UmuDC proteins and their plasmid homologuesMolecular Microbiology, 1992
- Degradative plasmid TOL provided singlet oxygen resistance for Pseudomonas strainsBiochemical and Biophysical Research Communications, 1981
- The Growth of Micro-organisms in Relation to their Energy SupplyMicrobiology, 1960