The psychrophilic lifestyle as revealed by the genome sequence of Colwellia psychrerythraea 34H through genomic and proteomic analyses.

The completion of the 5,373,180-bp genome sequence of the marine psychrophilic bacterium Colwellia psychrerythraea 34H, a model for the study of life in permanently cold environments, reveals capabilities important to carbon and nutrient cycling, bioremediation, production of secondary metabolites, and cold-adapted enzymes. From a genomic perspective, cold adaptation is suggested in several broad categories involving changes to the cell membrane fluidity, uptake and synthesis of compounds conferring cryotolerance, and strategies to overcome temperature-dependent barriers to carbon uptake. Modeling of three-dimensional protein homology from bacteria representing a range of optimal growth temperatures suggests changes to proteome composition that may enhance enzyme effectiveness at low temperatures. Comparative genome analyses suggest that the psychrophilic lifestyle is most likely conferred not by a unique set of genes but by a collection of synergistic changes in overall genome content and amino acid composition.

[1]  Theofanis Sapatinas,et al.  Discriminant Analysis and Statistical Pattern Recognition , 2005 .

[2]  K. Nealson,et al.  Low-Temperature Growth of Shewanella oneidensis MR-1 , 2005, Applied and Environmental Microbiology.

[3]  R. Amann,et al.  The genome of Desulfotalea psychrophila, a sulfate-reducing bacterium from permanently cold Arctic sediments. , 2004, Environmental microbiology.

[4]  D. Y. Lee,et al.  Substitution of aspartic acid with glutamic acid increases the unfolding transition temperature of a protein. , 2004, Biochemical and biophysical research communications.

[5]  G. Feller,et al.  A perspective on cold enzymes: current knowledge and frequently asked questions. , 2004, Cellular and molecular biology.

[6]  B. Methé,et al.  Purification, Characterization, and Sequencing of an Extracellular Cold-Active Aminopeptidase Produced by Marine Psychrophile Colwellia psychrerythraea Strain 34H , 2004, Applied and Environmental Microbiology.

[7]  Rekha Seshadri,et al.  The genome sequence of the anaerobic, sulfate-reducing bacterium Desulfovibrio vulgaris Hildenborough , 2004, Nature Biotechnology.

[8]  R. Sleator,et al.  Molecular and Physiological Analysis of the Role of Osmolyte Transporters BetL, Gbu, and OpuC in Growth of Listeria monocytogenes at Low Temperatures , 2004, Applied and Environmental Microbiology.

[9]  J. Cronan,et al.  Isolation and Characterization of β-Ketoacyl-Acyl Carrier Protein Reductase (fabG) Mutants of Escherichia coli and Salmonella enterica Serovar Typhimurium , 2004 .

[10]  G. Feller,et al.  Some like it cold: biocatalysis at low temperatures. , 2004, FEMS microbiology reviews.

[11]  M. Bonato,et al.  Preferred amino acids and thermostability. , 2003, Genetics and molecular research : GMR.

[12]  J A Eisen,et al.  Genome of Geobacter sulfurreducens: Metal Reduction in Subsurface Environments , 2003, Science.

[13]  G. Feller,et al.  Psychrophilic enzymes: hot topics in cold adaptation , 2003, Nature Reviews Microbiology.

[14]  G. Bourenkov,et al.  Coenzyme F420-dependent methylenetetrahydromethanopterin dehydrogenase (Mtd) from Methanopyrus kandleri: a methanogenic enzyme with an unusual quarternary structure. , 2003, Journal of molecular biology.

[15]  S. Lee,et al.  Identification and Characterization of a New Enoyl Coenzyme A Hydratase Involved in Biosynthesis of Medium-Chain-Length Polyhydroxyalkanoates in Recombinant Escherichia coli , 2003, Journal of bacteriology.

[16]  J. Deming,et al.  Motility of Colwellia psychrerythraea Strain 34H at Subzero Temperatures , 2003, Applied and Environmental Microbiology.

[17]  Paramvir S. Dehal,et al.  Mechanisms of thermal adaptation revealed from the genomes of the Antarctic Archaea Methanogenium frigidum and Methanococcoides burtonii. , 2003, Genome research.

[18]  N. Trachtmann,et al.  Homologous npdGI Genes in 2,4-Dinitrophenol- and 4-Nitrophenol-Degrading Rhodococcus spp , 2003, Applied and Environmental Microbiology.

[19]  J. Deming,et al.  High concentrations of exopolymeric substances in Arctic winter sea ice: implications for the polar ocean carbon cycle and cryoprotection of diatoms , 2002 .

[20]  M. Roberts,et al.  Solute accumulation in the deep-sea bacterium Photobacterium profundum , 2002, Extremophiles.

[21]  L. Xun,et al.  Organization and Regulation of Pentachlorophenol-Degrading Genes in Sphingobium chlorophenolicum ATCC 39723 , 2002, Journal of bacteriology.

[22]  A. Steinbüchel,et al.  Technical-Scale Production of Cyanophycin with Recombinant Strains of Escherichia coli , 2002, Applied and Environmental Microbiology.

[23]  Young Lee,et al.  Production of Chiral and other Valuable Compounds from Microbial Polyesters , 2002 .

[24]  J. Browse,et al.  Production of Polyunsaturated Fatty Acids by Polyketide Synthases in Both Prokaryotes and Eukaryotes , 2001, Science.

[25]  J. Berdagué,et al.  Roles of superoxide dismutase and catalase of Staphylococcus xylosus in the inhibition of linoleic acid oxidation. , 2001, FEMS microbiology letters.

[26]  W. Wiebe,et al.  Temperature and substrates as interactive limiting factors for marine heterotrophic bacteria , 2001 .

[27]  in chief George M. Garrity Bergey’s Manual® of Systematic Bacteriology , 1989, Springer New York.

[28]  J. Kirschvink,et al.  Paleoproterozoic snowball earth: extreme climatic and geochemical global change and its biological consequences. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[29]  Charles O. Rock,et al.  β-Ketoacyl-Acyl Carrier Protein Synthase III (FabH) Is a Determining Factor in Branched-Chain Fatty Acid Biosynthesis , 2000, Journal of bacteriology.

[30]  S. Salzberg,et al.  Improved microbial gene identification with GLIMMER. , 1999, Nucleic acids research.

[31]  G. Olsen,et al.  Thermal adaptation analyzed by comparison of protein sequences from mesophilic and extremely thermophilic Methanococcus species. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[32]  Gjalt W. Huisman,et al.  Metabolic Engineering of Poly(3-Hydroxyalkanoates): From DNA to Plastic , 1999, Microbiology and Molecular Biology Reviews.

[33]  B. Momen,et al.  WATERSHED CLASSIFICATION BY DISCRIMINANT ANALYSES OF LAKEWATER‐CHEMISTRY AND TERRESTRIAL CHARACTERISTICS , 1998 .

[34]  J. Knight,et al.  LIFE ON ICE , 1998 .

[35]  N. Russell Psychrophilic bacteria--molecular adaptations of membrane lipids. , 1997, Comparative biochemistry and physiology. Part A, Physiology.

[36]  Søren Brunak,et al.  A Neural Network Method for Identification of Prokaryotic and Eukaryotic Signal Peptides and Prediction of their Cleavage Sites , 1997, Int. J. Neural Syst..

[37]  Roland L. Dunbrack,et al.  Prediction of protein side-chain rotamers from a backbone-dependent rotamer library: a new homology modeling tool. , 1997, Journal of molecular biology.

[38]  R. Y. Morita,et al.  Posttranscriptional modification of tRNA in psychrophilic bacteria , 1997, Journal of bacteriology.

[39]  J. Lobry Asymmetric substitution patterns in the two DNA strands of bacteria. , 1996, Molecular biology and evolution.

[40]  P. Argos,et al.  Knowledge‐based protein secondary structure assignment , 1995, Proteins.

[41]  Lening Zhang,et al.  Sequence Analysis of Sarcosine Oxidase and Nearby Genes Reveals Homologies with Key Enzymes of Folate One-carbon Metabolism (*) , 1995, The Journal of Biological Chemistry.

[42]  G. McLachlan Discriminant Analysis and Statistical Pattern Recognition , 1992 .

[43]  李幼升,et al.  Ph , 1989 .