Pseudomonas putida

About: Pseudomonas putida is a research topic. Over the lifetime, 6854 publications have been published within this topic receiving 230572 citations.

Survival of Pseudomonas putida KT2440 in soil and in the rhizosphere of plants under greenhouse and environmental conditions.

Abstract: Pseudomonas putida KT2440 is a root colonizer of potential interest for the rhizoremediation of pollutants and the biological control of pests. The short- and long-term survival of this strain, as well as the possible eAects of its introduction on diAerent populations of indigenous soil bacteria, were tested in soil under greenhouse and field conditions. The greenhouse studies showed that inoculated P. putida KT2440 was able to establish itself after 3 d in nonvegetated soils at a density of 822 10 3 CFU g ˇ1 soil. The introduction of this strain had no significant eAect on the number of several soil bacteria including those that were resistant to tetracycline; those that utilized p-hydroxyphenylacetic acid as the sole C-source, and total fluorescent pseudomonads. In four independent field assays in nonplanted soils, the numbers of P. putida KT2440 decreased during 50 d from an initial density of 1 10 6 CFU g ˇ1 soil to approximately 221 10 2 CFU g ˇ1 soil. Thereafter, the number of cells was below detection limits (i.e. <10 2 CFU g ˇ1 soil), although they were still present because they could be recovered using selective enrichment from the soil for up to 200 d after the beginning of the experiment. This suggested that P. putida was maintained at a low cell density long after inoculation. In contrast, when P. putida KT2440 was introduced in the soil as a coating of corn (Zea mays) or broad bean (Vicia faba) seeds, the bacteria established at high cell densities in the rhizosphere (10 4 ‐10 5 CFU g ˇ1 soil in corn; 10 6 ‐10 7 CFU g ˇ1 soil in broad beans) during the growth of the crops over 12 to 16 weeks. The numbers of P. putida in the bulk soil after 2 weeks were 1 to 2 orders of magnitude below those in the rhizosphere. During the field assays, the population of p-hydroxyphenylacetic acid users was also monitored in the rhizosphere and the bulk soil. No significant seasonal variations were found. # 2000 Elsevier Science Ltd. All rights reserved.

Activity and three-dimensional distribution of toluene-degrading Pseudomonas putida in a multispecies biofilm assessed by quantitative in situ hybridization and scanning confocal laser microscopy.

Abstract: As a representative member of the toluene-degrading population in a biofilter for waste gas treatment, Pseudomonas putida was investigated with a 16S rRNA targeting probe. The three-dimensional distribution of P. putida was visualized in the biofilm matrix by scanning confocal laser microscopy, demonstrating that P. putida was present throughout the biofilm. Acridine orange staining revealed a very heterogeneous structure of the fully hydrated biofilm, with cell-free channels extending from the surface into the biofilm. This indicated that toluene may penetrate to deeper layers of the biofilm, and consequently P. putida may be actively degrading toluene in all regions of the biofilm. Furthermore, measurements of growth rate-related parameters for P. putida showed reduced rRNA content and cell size (relative to that in a batch culture), indicating that the P. putida population was not degrading toluene at a maximal rate in the biofilm environment. Assuming that the rRNA content reflected the cellular activity, a lower toluene degradation rate for P. putida present in the biofilm could be estimated. This calculation indicated that P. putida was responsible for a significant part (65%) of the toluene degraded by the entire community.

Plant growth-promoting Pseudomonas putida WCS358 produces and secretes four cyclic dipeptides: cross-talk with quorum sensing bacterial sensors.

Abstract: The most universal cell-cell signaling mechanism in Gram-negative bacteria occurs via the production and response to a class of small diffusible molecules called N-acylhomoserine lactones (AHLs). This communication is called quorum sensing and is responsible for the regulation of several physiological processes and many virulence factors in pathogenic bacteria. The detection of these molecules has been rendered possible by the utilization of genetically engineered bacterial biosensors which respond to the presence of exogenously supplied AHLs. In this study, using diverse bacterial biosensors, several biosensor activating fractions were purified by organic extraction, HPLC and TLC of cell-free culture supernatants of plant growth-promoting Pseudomonas putida WCS358. Surprisingly, it was observed that the most abundant compounds in these fractions were cyclic dipeptides (diketopiperazines, DKPs), a rather novel finding in Gram-negative bacteria. The purification, characterization, chemical synthesis of four DKPs are reported and their possible role in cell-cell signaling is discussed.