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      Comparative genomics and functional analysis of niche-specific adaptation in Pseudomonas putida

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          Abstract

          Pseudomonas putida is a gram-negative rod-shaped gammaproteobacterium that is found throughout various environments. Members of the species P. putida show a diverse spectrum of metabolic activities, which is indicative of their adaptation to various niches, which includes the ability to live in soils and sediments contaminated with high concentrations of heavy metals and organic contaminants. Pseudomonas putida strains are also found as plant growth-promoting rhizospheric and endophytic bacteria. The genome sequences of several P. putida species have become available and provide a unique tool to study the specific niche adaptation of the various P. putida strains. In this review, we compare the genomes of four P. putida strains: the rhizospheric strain KT2440, the endophytic strain W619, the aromatic hydrocarbon-degrading strain F1 and the manganese-oxidizing strain GB-1. Comparative genomics provided a powerful tool to gain new insights into the adaptation of P. putida to specific lifestyles and environmental niches, and clearly demonstrated that horizontal gene transfer played a key role in this adaptation process, as many of the niche-specific functions were found to be encoded on clearly defined genomic islands.

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          Complete genome sequence and comparative analysis of the metabolically versatile Pseudomonas putida KT2440.

          Pseudomonas putida is a metabolically versatile saprophytic soil bacterium that has been certified as a biosafety host for the cloning of foreign genes. The bacterium also has considerable potential for biotechnological applications. Sequence analysis of the 6.18 Mb genome of strain KT2440 reveals diverse transport and metabolic systems. Although there is a high level of genome conservation with the pathogenic Pseudomonad Pseudomonas aeruginosa (85% of the predicted coding regions are shared), key virulence factors including exotoxin A and type III secretion systems are absent. Analysis of the genome gives insight into the non-pathogenic nature of P. putida and points to potential new applications in agriculture, biocatalysis, bioremediation and bioplastic production.
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            Industrial biocatalysis today and tomorrow.

            The use of biocatalysis for industrial synthetic chemistry is on the verge of significant growth. Biocatalytic processes can now be carried out in organic solvents as well as aqueous environments, so that apolar organic compounds as well as water-soluble compounds can be modified selectively and efficiently with enzymes and biocatalytically active cells. As the use of biocatalysis for industrial chemical synthesis becomes easier, several chemical companies have begun to increase significantly the number and sophistication of the biocatalytic processes used in their synthesis operations.
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              Type IV pili and twitching motility.

              Twitching motility is a flagella-independent form of bacterial translocation over moist surfaces. It occurs by the extension, tethering, and then retraction of polar type IV pili, which operate in a manner similar to a grappling hook. Twitching motility is equivalent to social gliding motility in Myxococcus xanthus and is important in host colonization by a wide range of plant and animal pathogens, as well as in the formation of biofilms and fruiting bodies. The biogenesis and function of type IV pili is controlled by a large number of genes, almost 40 of which have been identified in Pseudomonas aeruginosa. A number of genes required for pili assembly are homologous to genes involved in type II protein secretion and competence for DNA uptake, suggesting that these systems share a common architecture. Twitching motility is also controlled by a range of signal transduction systems, including two-component sensor-regulators and a complex chemosensory system.
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                Author and article information

                Journal
                FEMS Microbiol Rev
                fmr
                Fems Microbiology Reviews
                Blackwell Publishing Ltd
                0168-6445
                1574-6976
                March 2011
                26 August 2010
                : 35
                : 2
                : 299-323
                Affiliations
                [1 ]simpleBiology Department, Brookhaven National Laboratory Upton, NY, USA
                [2 ]simpleDepartment of Applied Mathematics & Statistics, State University of New York Stony Brook, NY, USA
                [3 ]simpleEEZ-CSIC Granada, Spain
                Author notes
                Daniel van der Lelie, Biology Department, Brookhaven National Laboratory, Upton, NY 11973-5000, USA. Tel.: +1 631 344 5349; fax: +1 631 344 3407; e-mail: vdlelied@ 123456bnl.gov
                Article
                10.1111/j.1574-6976.2010.00249.x
                3056050
                20796030
                816bb6e7-2cdd-4ac7-b8c1-fd056b10944a
                Journal compilation © 2010 Federation of European Microbiological Societies. Published by Blackwell Publishing Ltd. No claim to original US government works

                Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.

                History
                : 27 February 2010
                : 07 July 2010
                : 19 July 2010
                Categories
                Review Articles

                Microbiology & Virology
                pseudomonas putida,comparative genomics,w619,kt2440,f1,gb-1
                Microbiology & Virology
                pseudomonas putida, comparative genomics, w619, kt2440, f1, gb-1

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