The origin and ecological significance of multiple branches for histidine utilization in Pseudomonas aeruginosa PAO1.

Pseudomonas proliferate in a wide spectrum of harsh and variable environments. In many of these environments, amino acids, such as histidine, are a valuable source of carbon, nitrogen and energy. Here, we demonstrate that the histidine uptake and utilization (hut) pathway of Pseudomonas aeruginosa PAO1 contains two branches from the intermediate formiminoglutamate to the product glutamate. Genetic analysis revealed that the four-step route is dispensable as long as the five-step route is present (and vice versa). Mutants with deletions of either the four-step (HutE) or five-step (HutFG) branches were competed against each other and the wild-type strain to test the hypothesis of ecological redundancy; that is, that the presence of two pathways confers no benefit beyond that delivered by the individual pathways. Fitness assays performed under several environmental conditions led us to reject this hypothesis; the four-step pathway can provide an advantage when histidine is the sole carbon source. An IclR-type regulator (HutR) was identified that regulates the four-step pathway. Comparison of sequenced genomes revealed that P.aeruginosa strains and P.fluorescens Pf-5 have branched hut pathways. Phylogenetic analyses suggests that the gene encoding formiminoglutamase (hutE) was acquired by horizontal gene transfer from a Ralstonia-like ancestor. Potential barriers to inter-species transfer of the hutRE module were explored by transferring it from P.aeruginosa PAO1 to P.fluorescens SBW25. Transfer of the operon conferred the ability to utilize histidine via the four-step pathway in a single step, but the fitness cost of acquiring this new operon was found to be environment dependent.

[1]  Bas Teusink,et al.  A critical view of metabolic network adaptations , 2009, HFSP journal.

[2]  P. Rainey,et al.  Construction and validation of a neutrally-marked strain of Pseudomonas fluorescens SBW25. , 2007, Journal of microbiological methods.

[3]  M. Welch,et al.  Comparative microarray analysis reveals that the core biofilm-associated transcriptome of Pseudomonas aeruginosa comprises relatively few genes. , 2010, Environmental microbiology reports.

[4]  R Mahadevan,et al.  The degree of redundancy in metabolic genes is linked to mode of metabolism. , 2008, Biophysical journal.

[5]  Ying Xu,et al.  Operon prediction using both genome-specific and general genomic information , 2006, Nucleic acids research.

[6]  P. H. Clarke,et al.  An inducible amidase produced by a strain of Pseudomonas aeruginosa. , 1962, Journal of general microbiology.

[7]  J. Mekalanos,et al.  Effect of Metabolic Imbalance on Expression of Type III Secretion Genes in Pseudomonas aeruginosa , 2004, Infection and Immunity.

[8]  R. Hancock,et al.  Swarming of Pseudomonas aeruginosa Is Controlled by a Broad Spectrum of Transcriptional Regulators, Including MetR , 2009, Journal of bacteriology.

[9]  Chung-Dar Lu,et al.  Polyamines Induce Resistance to Cationic Peptide, Aminoglycoside, and Quinolone Antibiotics in Pseudomonas aeruginosa PAO1 , 2006, Antimicrobial Agents and Chemotherapy.

[10]  B. Magasanik,et al.  Urocanase and N-formimino-L-glutamate formiminohydrolase of Bacillus subtilis, two enzymes of the histidine degradation pathway. , 1970, The Journal of biological chemistry.

[11]  Ian T. Paulsen,et al.  High-Throughput Phenotypic Characterization of Pseudomonas aeruginosa Membrane Transport Genes , 2008, PLoS genetics.

[12]  G. Edelman,et al.  Degeneracy and complexity in biological systems , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[13]  M. Bailey,et al.  Survival, Colonization and Dispersal of Genetically Modified Pseudomonas fluorescens SBW25 in the Phytosphere of Field Grown Sugar Beet , 1995, Bio/Technology.

[14]  C. Kurland,et al.  Compensatory gene amplification restores fitness after inter‐species gene replacements , 2010, Molecular microbiology.

[15]  J. Ramos,et al.  Members of the IclR family of bacterial transcriptional regulators function as activators and/or repressors. , 2006, FEMS microbiology reviews.

[16]  H. Schweizer,et al.  mini-Tn7 insertion in bacteria with single attTn7 sites: example Pseudomonas aeruginosa , 2006, Nature Protocols.

[17]  G. Ditta,et al.  Broad host range DNA cloning system for gram-negative bacteria: construction of a gene bank of Rhizobium meliloti. , 1980, Proceedings of the National Academy of Sciences of the United States of America.

[18]  F. Neidhardt,et al.  REVERSAL OF THE GLUCOSE INHIBITION OF HISTIDASE BIOSYNTHESIS IN AEROBACTER AEROGENES , 1957, Journal of bacteriology.

[19]  R. Helling,et al.  Why does Escherichia coli have two primary pathways for synthesis of glutamate? , 1994, Journal of bacteriology.

[20]  F. Montero,et al.  Optimization of Metabolism: The Evolution of Metabolic Pathways Toward Simplicity Through the Game of the Pentose Phosphate Cycle , 1994 .

[21]  F. Neidhardt,et al.  Induction and repression of the histidine-degrading enzymes in Aerobacter aerogenes. , 1965, The Journal of biological chemistry.

[22]  Martin G. Reese,et al.  Application of a Time-delay Neural Network to Promoter Annotation in the Drosophila Melanogaster Genome , 2001, Comput. Chem..

[23]  James R. Cole,et al.  The Ribosomal Database Project: improved alignments and new tools for rRNA analysis , 2008, Nucleic Acids Res..

[24]  Ludmila Chistoserdova,et al.  Multiple Formaldehyde Oxidation/Detoxification Pathways in Burkholderia fungorum LB400 , 2004, Journal of bacteriology.

[25]  Raymond Lo,et al.  Pseudomonas Genome Database: facilitating user-friendly, comprehensive comparisons of microbial genomes , 2008, Nucleic Acids Res..

[26]  Ronald W. Davis,et al.  Role of duplicate genes in genetic robustness against null mutations , 2003, Nature.

[27]  J. Arthur,et al.  Gene expression of Pseudomonas aeruginosa in a mucin-containing synthetic growth medium mimicking cystic fibrosis lung sputum. , 2010, Journal of medical microbiology.

[28]  Kelly P Williams,et al.  Phylogeny of Gammaproteobacteria , 2010, Journal of bacteriology.

[29]  Y. Itoh,et al.  Histidine Catabolism and Catabolite Regulation , 2007 .

[30]  Dmitri A. Petrov,et al.  Pervasive and Persistent Redundancy among Duplicated Genes in Yeast , 2008, PLoS genetics.

[31]  P. Rainey Adaptation of Pseudomonas fluorescens to the plant rhizosphere. , 1999, Environmental microbiology.

[32]  A. T. Phillips,et al.  Organization and multiple regulation of histidine utilization genes in Pseudomonas putida , 1988, Journal of bacteriology.

[33]  H. Tabor,et al.  Isolation of N-formyl-L-glutamic acid as an intermediate in the enzymatic degradation of L-histidine. , 1954, The Journal of biological chemistry.

[34]  I. Kukavica-Ibrulj,et al.  Characterization of Alanine Catabolism in Pseudomonas aeruginosa and Its Importance for Proliferation In Vivo , 2009, Journal of bacteriology.

[35]  J. Young,et al.  Probable synonymy of the nitrogen-fixing genus Azotobacter and the genus Pseudomonas. , 2007, International journal of systematic and evolutionary microbiology.

[36]  P. Barrow,et al.  l-Serine Catabolism via an Oxygen-Labile l-Serine Dehydratase Is Essential for Colonization of the Avian Gut by Campylobacter jejuni , 2004, Infection and Immunity.

[37]  C. Pál,et al.  Adaptive evolution of bacterial metabolic networks by horizontal gene transfer , 2005, Nature Genetics.

[38]  R. Rodriguez,et al.  Histidine operon control region of Klebsiella pneumoniae: analysis with an Escherichia coli promoter-probe plasmid vector , 1984, Journal of bacteriology.

[39]  Axel Bender,et al.  Degeneracy: a design principle for achieving robustness and evolvability. , 2009, Journal of theoretical biology.

[40]  S. Oliver,et al.  Plasticity of genetic interactions in metabolic networks of yeast , 2007, Proceedings of the National Academy of Sciences.

[41]  Wei Qian,et al.  Selection of conserved blocks from multiple alignments for their use in phylogenetic analysis. , 2000, Molecular biology and evolution.

[42]  Thomas Pfeiffer,et al.  Evolution under Fluctuating Environments Explains Observed Robustness in Metabolic Networks , 2010, PLoS Comput. Biol..

[43]  M. Whiteley,et al.  Nutritional Cues Control Pseudomonas aeruginosa Multicellular Behavior in Cystic Fibrosis Sputum , 2007, Journal of bacteriology.

[44]  H. L. Wang,et al.  Release of proteinase from mycelium of Mucor hiemalis. , 1967, Journal of bacteriology.

[45]  L. Pease,et al.  Gene splicing and mutagenesis by PCR-driven overlap extension , 2007, Nature Protocols.

[46]  C. Harwood,et al.  Responses of Pseudomonas aeruginosa to low oxygen indicate that growth in the cystic fibrosis lung is by aerobic respiration , 2007, Molecular microbiology.

[47]  S. Lory,et al.  Complete genome sequence of Pseudomonas aeruginosa PAO1, an opportunistic pathogen , 2000, Nature.

[48]  B. Magasanik,et al.  Genetic and metabolic control of enzymes responsible for histidine degradation in Salmonella typhimurium. 4-imidazolone-5-propionate amidohydrolase and N-formimino-L-glutamate formiminohydrolase. , 1971, The Journal of biological chemistry.

[49]  M. Whiteley,et al.  Staphylococcus aureus Serves as an Iron Source for Pseudomonas aeruginosa during In Vivo Coculture , 2005, Journal of bacteriology.

[50]  M. Savageau,et al.  Inhibition of growth by imadazol(on)e propionic acid: Evidence in vivo for coordination of histidine catabolism with the catabolism of other amino acids , 1979, Molecular and General Genetics MGG.

[51]  J. Vanderleyden,et al.  Azotobacter vinelandii: a Pseudomonas in disguise? , 2004, Microbiology.

[52]  W. Verstraete,et al.  Genetic and Genomic Insights into the Role of Benzoate-Catabolic Pathway Redundancy in Burkholderia xenovorans LB400 , 2006, Applied and Environmental Microbiology.

[53]  Jannell V. Bazurto,et al.  Plasticity in the Purine–Thiamine Metabolic Network of Salmonella , 2011, Genetics.

[54]  Alexandros Stamatakis,et al.  RAxML-VI-HPC: maximum likelihood-based phylogenetic analyses with thousands of taxa and mixed models , 2006, Bioinform..

[55]  C. Kurland,et al.  Evolution of microbial genomes: sequence acquisition and loss. , 2002, Molecular biology and evolution.

[56]  Francisco J. Planes,et al.  Recovering metabolic pathways via optimization , 2007, Bioinform..

[57]  Rodrigo Lopez,et al.  Clustal W and Clustal X version 2.0 , 2007, Bioinform..

[58]  Rainer Fischer,et al.  Genetic determinants of Pseudomonas aeruginosa biofilm establishment. , 2010, Microbiology.

[59]  F. Neidhardt,et al.  Formation and Operation of the Histidine-degrading Pathway in Pseudomonas aeruginosa , 1967, Journal of bacteriology.

[60]  Peer Bork,et al.  Interactive Tree Of Life v2: online annotation and display of phylogenetic trees made easy , 2011, Nucleic Acids Res..

[61]  H. Ochman,et al.  Lateral gene transfer and the nature of bacterial innovation , 2000, Nature.

[62]  P. Rainey,et al.  Genetic Analysis of the Histidine Utilization (hut) Genes in Pseudomonas fluorescens SBW25 , 2007, Genetics.

[63]  L. Mulfinger,et al.  Purification and properties of formylglutamate amidohydrolase from Pseudomonas putida , 1987, Journal of bacteriology.

[64]  J. Ramos,et al.  The IclR family of transcriptional activators and repressors can be defined by a single profile , 2006, Protein science : a publication of the Protein Society.

[65]  R. Lenski,et al.  Long-term experimental evolution in Escherichia coli , 1991 .

[66]  B. Magasanik,et al.  Genetic basis of histidine degradation in Bacillus subtilis. , 1970, The Journal of biological chemistry.

[67]  B. Ames,et al.  The Histidine Operon , 1963 .

[68]  José B. Pereira-Leal,et al.  Loss of Genetic Redundancy in Reductive Genome Evolution , 2011, PLoS Comput. Biol..

[69]  Ricardo Martí-Arbona,et al.  Annotating enzymes of unknown function: N-formimino-L-glutamate deiminase is a member of the amidohydrolase superfamily. , 2006, Biochemistry.

[70]  P. H. Clarke The Aliphatic Amidases of Pseudomonas aeruginosa , 1969 .