All Stories

  1. The soluble cytoplasmic N‐terminal domain of the FocA channel gates bidirectional formate translocation
  2. Cytochrome bd Oxidase Has an Important Role in Sustaining Growth and Development of Streptomyces coelicolor A3(2) under Oxygen-Limiting Conditions
  3. o- Phthalate derived from plastics’ plasticizers and a bacterium's solution to its anaerobic degradation
  4. A H2 -oxidizing, 1,2,3-trichlorobenzene-reducing multienzyme complex isolated from the obligately organohalide-respiring bacterium Dehalococcoides mccartyi strain CBDB1
  5. Little red floaters: gas vesicles in an enterobacterium
  6. Coordination of Synthesis and Assembly of a Modular Membrane-Associated [NiFe]-Hydrogenase Is Determined by Cleavage of the C-Terminal Peptide
  7. Of mothballs and old yellow enzymes
  8. Physiology and Bioenergetics of [NiFe]-Hydrogenase 2-Catalyzed H2-Consuming and H2-Producing Reactions in Escherichia coli
  9. Ferredoxin has a pivotal role in the biosynthesis of the hydrogen-oxidizing hydrogenases in Escherichia coli
  10. Oxygen-Dependent Control of Respiratory Nitrate Reduction in Mycelium of Streptomyces coelicolor A3(2)
  11. Pyruvate Formate-Lyase Interacts Directly with the Formate Channel FocA to Regulate Formate Translocation
  12. Identification of key residues in the formate channel FocA that control import and export of formate
  13. The importance of iron in the biosynthesis and assembly of [NiFe]-hydrogenases
  14. Novel insights into the bioenergetics of mixed-acid fermentation: Can hydrogen and proton cycles combine to help maintain a proton motive force?
  15. Hydrogen-oxidizing hydrogenases 1 and 2 of Escherichia coli regulate the onset of hydrogen evolution and ATPase activity, respectively, during glucose fermentation at alkaline pH
  16. A respiratory nitrate reductase active exclusively in resting spores of the obligate aerobeStreptomyces coelicolor A3(2)
  17. The [NiFe]-hydrogenase accessory chaperones HypC and HybG ofEscherichia coliare iron- and carbon dioxide-binding proteins
  18. A Universally Applicable and Rapid Method for Measuring the Growth of Streptomyces and Other Filamentous Microorganisms by Methylene Blue Adsorption-Desorption
  19. HypD Is the Scaffold Protein for Fe-(CN)2CO Cofactor Assembly in [NiFe]-Hydrogenase Maturation
  20. Selective selC-Independent Selenocysteine Incorporation into Formate Dehydrogenases
  21. Levels of control exerted by the Isc iron-sulfur cluster system on biosynthesis of the formate hydrogenlyase complex
  22. Regulation of reductive dehalogenase gene transcription in Dehalococcoides mccartyi
  23. Staphylococcus aureus and Pseudomonas aeruginosa Express and Secrete Human Surfactant Proteins
  24. Coordination of FocA and Pyruvate Formate-Lyase Synthesis in Escherichia coli Demonstrates Preferential Translocation of Formate over Other Mixed-Acid Fermentation Products
  25. Hydrogenase Maturation Endopeptidase
  26. Nickel in Bacteria and Archaea
  27. Periplasmic Electron-Transport Systems in Bacteria
  28. Contribution of Hydrogenase 2 to Stationary Phase H2 Production by Escherichia coli During Fermentation of Glycerol
  29. [NiFe]-hydrogenase maturation: Isolation of a HypC-HypD complex carrying diatomic CO and CN−ligands
  30. Zymographic differentiation of [NiFe]-Hydrogenases 1, 2 and 3 of Escherichia coli K-12
  31. Evidence for an oxygen-sensitive iron–sulfur cluster in an immature large subunit species of Escherichia coli [NiFe]-hydrogenase 2
  32. Terminal reduction reactions of nitrate and sulfate assimilation in Streptomyces coelicolor A3(2): identification of genes encoding nitrite and sulfite reductases
  33. Aconitase B Is Required for Optimal Growth of Xanthomonas campestris pv. vesicatoria in Pepper Plants
  34. Delivery of Iron-Sulfur Clusters to the Hydrogen-Oxidizing [NiFe]-Hydrogenases in Escherichia coli Requires the A-Type Carrier Proteins ErpA and IscA
  35. Analysis of hydrogenase 1 levels reveals an intimate link between carbon and hydrogen metabolism in Escherichia coli K-12
  36. Structure of Hydrogenase Maturation Protein HypF with Reaction Intermediates Shows Two Active Sites
  37. Characterization of Escherichia coli [NiFe]-Hydrogenase Distribution During Fermentative Growth at Different pHs
  38. Dependence on the F0F1-ATP synthase for the activities of the hydrogen-oxidizing hydrogenases 1 and 2 during glucose and glycerol fermentation at high and low pH in Escherichia coli
  39. A-Type Carrier Protein ErpA Is Essential for Formation of an Active Formate-Nitrate Respiratory Pathway in Escherichia coli K-12
  40. Metabolic Deficiences Revealed in the Biotechnologically Important Model Bacterium Escherichia coli BL21(DE3)
  41. The respiratory molybdo-selenoprotein formate dehydrogenases of Escherichia coli have hydrogen: benzyl viologen oxidoreductase activity
  42. Efficient electron transfer from hydrogen to benzyl viologen by the [NiFe]-hydrogenases of Escherichia coli is dependent on the coexpression of the iron–sulfur cluster-containing small subunit
  43. Iron restriction induces preferential down-regulation of H2-consuming over H2-evolving reactions during fermentative growth of Escherichia coli
  44. The role of the ferric-uptake regulator Fur and iron homeostasis in controlling levels of the [NiFe]-hydrogenases in Escherichia coli
  45. Development of a cell-free system reveals an oxygen-labile step in the maturation of [NiFe]-hydrogenase 2 ofEscherichia coli
  46. The obligate aerobe Streptomyces coelicolor A3(2) synthesizes three active respiratory nitrate reductases
  47. Unexpected oligomeric structure of the FocA formate channel of Escherichia coli : a paradigm for the formate–nitrite transporter family of integral membrane proteins
  48. Characterization ofcycPGene Expression inAchromobacter xylosoxidansNCIMB 11015 and High-Level Heterologous Synthesis of Cytochromec′ inEscherichia coli
  49. The ArcBA Two-Component System of Escherichia coli Is Regulated by the Redox State of both the Ubiquinone and the Menaquinone Pool
  50. Amino Acid Degradation
  51. Modulation of NO binding to cytochrome c′ by distal and proximal haem pocket residues
  52. The obligate aerobic actinomycete Streptomyces coelicolor A3(2) survives extended periods of anaerobic stress
  53. Quorum-sensing-regulated transcriptional initiation of plasmid transfer and replication genes in Rhizobium leguminosarum biovar viciae
  54. The CO and CN−ligands to the active site Fe in [NiFe]-hydrogenase ofEscherichia colihave different metabolic origins
  55. The crystal structure of Escherichia coli TdcF, a member of the highly conserved YjgF/YER057c/UK114 family
  56. The structure of the Met144Leu mutant of copper nitrite reductase from Alcaligenes xylosoxidans provides the first glimpse of a protein–protein complex with azurin II
  57. Extreme arsenic resistance by the acidophilic archaeon ‘Ferroplasma acidarmanus’ Fer1
  58. Maturation of [NiFe]-hydrogenases in Escherichia coli
  59. Insight into Catalysis of Nitrous Oxide Reductase from High-resolution Structures of Resting and Inhibitor-bound Enzyme from Achromobacter cycloclastes
  60. Differential turnover of the multiple processed transcripts of the Escherichia coli focA-pflB operon
  61. Coordinate synthesis of azurin I and copper nitrite reductase in Alcaligenes xylosoxidans during denitrification
  62. The Rhizobium leguminosarum regulator IrrA affects the transcription of a wide range of genes in response to Fe availability
  63. Aerobic activation of transcription of the anaerobically inducible Escherichia coli focA-pfl operon by fumarate nitrate regulator
  64. Regulation of the nap operon encoding the periplasmic nitrate reductase of Paracoccus pantotrophus: delineation of DNA sequences required for redox control
  65. Evidence for novel processing of the anaerobically inducible dicistronic focA-pfl mRNA transcript in Escherichia coli
  66. Atomic resolution structures of resting-state, substrate- and product-complexed Cu-nitrite reductase provide insight into catalytic mechanism
  67. Gas vesicles in actinomycetes: old buoys in novel habitats?
  68. High Resolution Structural Studies of Mutants Provide Insights into Catalysis and Electron Transfer Processes in Copper Nitrite Reductase
  69. Expression of fnr Is Constrained by an Upstream IS5 Insertion in Certain Escherichia coli K-12 Strains
  70. Proteomic analysis reveals the wide-ranging effects of the novel, iron-responsive regulator RirA in Rhizobium leguminosarum bv. viciae
  71. Transcript analysis of Escherichia coli K-12 insertion element IS 5
  72. Synthesis of the H-cluster framework of iron-only hydrogenase
  73. Formate and its role in hydrogen production in Escherichia coli
  74. Nitrate respiration in the actinomycete Streptomyces coelicolor
  75. Anaerobic Formate and Hydrogen Metabolism
  76. Fermentative Pyruvate and Acetyl-Coenzyme A Metabolism
  77. Heterologous metalloprotein biosynthesis inEscherichia coli: conditions for the overproduction of functional copper-containing nitrite reductase and azurin fromAlcaligenes xylosoxidans
  78. Insights into Redox Partner Interactions and Substrate Binding in Nitrite Reductase from Alcaligenes xylosoxidans: Crystal Structures of the Trp138His and His313Gln Mutants,
  79. Observation of an Unprecedented Cu Bis-His Site: Crystal Structure of the H129V Mutant of Nitrite Reductase
  80. The iron-sulfur cluster in thel-serine dehydratase TdcG fromEscherichia coliis required for enzyme activity
  81. mRNA Secondary Structure Modulates Translation of Tat-Dependent Formate Dehydrogenase N
  82. Anaerobic Formate and Hydrogen Metabolism
  83. Fermentative Pyruvate and Acetyl-Coenzyme A Metabolism
  84. [NiFe]-Hydrogenase Cofactor Assembly
  85. A novel mechanism controls anaerobic and catabolite regulation of the Escherichia coli tdc operon
  86. Met144Ala mutation of the copper-containing nitrite reductase fromAlcaligenes xylosoxidansreverses the intramolecular electron transfer
  87. Periplasmic Electron Transport Systems in Bacteria
  88. Characterization of Transcriptional Regulation of Shewanella frigidimarina Fe(III)-Induced Flavocytochrome c Reveals a Novel Iron-Responsive Gene Regulation System
  89. Bacterial iron (III) respiration
  90. The ECF σ factor RpoI of R. leguminosarum initiates transcription of the vbsGSO and vbsADL siderophore biosynthetic genes in vitro
  91. Crystallization and preliminary X-ray analysis of theE. colihypothetical protein TdcF
  92. Atomic Resolution Structures of Native Copper Nitrite Reductase from Alcaligenes xylosoxidans and the Active Site Mutant Asp92Glu
  93. Hierarchy of Carbon Source Selection in Paracoccus pantotrophus: Strict Correlation between Reduction State of the Carbon Substrate and Aerobic Expression of the nap Operon
  94. The vbs genes that direct synthesis of the siderophore vicibactin in Rhizobium leguminosarum: their expression in other genera requires ECF σ factor RpoI
  95. Alcaligenes xylosoxidans Dissimilatory Nitrite Reductase:  Alanine Substitution of the Surface-Exposed Histidine 139 Ligand of the Type 1 Copper Center Prevents Electron Transfer to the Catalytic Center
  96. Biochemical and crystallographic studies of the Met144Ala, Asp92Asn and His254Phe mutants of the nitrite reductase from Alcaligenes xylosoxidans provide insight into the enzyme mechanism
  97. The Rhizobium leguminosarum tonB gene is required for the uptake of siderophore and haem as sources of iron
  98. dpp Genes of Rhizobium leguminosarum Specify Uptake of δ-Aminolevulinic Acid
  99. X-ray structure of a blue copper nitrite reductase at high pH and in copper-free form at 1.9 Å resolution
  100. A novel mechanism controls anaerobic and catabolite regulation of the Escherichia coli tdc operon
  101. Constitutive Expression of Escherichia coli tat Genes Indicates an Important Role for the Twin-Arginine Translocase during Aerobic and Anaerobic Growth
  102. Catalytic and spectroscopic analysis of blue copper-containing nitrite reductase mutants altered in the environment of the type 2 copper centre: implications for substrate interaction
  103. Biosynthesis of poly-β-hydroxybutyrate (PHB) is controlled by CydR (Fnr) in the obligate aerobe Azotobacter vinelandii
  104. Escherichia coli genes whose products are involved in selenium metabolism
  105. Effects of Limited Aeration and of the ArcAB System on Intermediary Pyruvate Catabolism in Escherichia coli
  106. Site Directed Mutagenesis of Nitrite Reductase. The Crystallographic Studies of Recombinant Nitrite Reductase and Mutations
  107. Genetic Methods for Diverse Prokaryotes (Methods in Microbiology, 29).
  108. The aerobic/anaerobic interface
  109. The genetic basis of tetrathionate respiration in Salmonella typhimurium
  110. The anaerobic degradation of l -serine and l -threonine in enterobacteria: networks of pathways and regulatory signals
  111. Biochemistry, physiology and molecular biology of glycyl radical enzymes
  112. Biochemistry, physiology and molecular biology of glycyl radical enzymes
  113. A glycyl radical solution: oxygen-dependent interconversion of pyruvate formate-lyase
  114. Signal transduction and bacterial conjugation: characterization of the role of ArcA in regulating conjugative transfer of the resistance plasmid R1
  115. Novel keto acid formate-lyase and propionate kinase enzymes are components of an anaerobic pathway in Escherichia coli that degrades L-threonine to propionate
  116. The tdcE Gene in Escherichia Coli Strain W3110 is Separated from the Rest of the tdc Operon by Insertion of IS5 Elements
  117. The cydR gene product, required for regulation of cytochrome bd expression in the obligate aerobe Azotobacter vinelandii, is an Fnr-like protein
  118. Overlapping promoters modulate Fnr- and ArcA-dependent anaerobic transcriptional activation of the focApfl operon in Escherichia coli
  119. Transcriptional activation by FNR and CRP: reciprocity of binding‐site recognition
  120. Alternative regulation principles for the production of recombinant proteins in Escherichia coli
  121. Fnr activates transcription from theP6promoter of thepfloperonin vitro
  122. Purification of ArcA and analysis of is specific interaction with the pfl promoter-regulatory region
  123. Pyruvate formate-lyase is not essential for nitrate respiration by Escherichia coli
  124. Isolation and characterization of hypophosphite-resistant mutants of Escherichia coli: identification of the FocA protein, encoded by the pfl operon, as a putative formate transporter
  125. The hydrogenases and formate dehydrogenases ofEscherichia coli
  126. Specific transcriptional requirements for positive regulation of the anaerobically inducible pfl operon by ArcA and FNR
  127. Mechanism of regulation of the formate-hydrogenlyase pathway by oxygen, nitrate, and pH: definition of the formate regulon
  128. Identification and molecular characterization of a transcriptional regulator from Pseudomonas aeruginosa PAO1 exhibiting structural and functional similarity to the FNR protein of Escherichia coli
  129. Selenocysteine: the 21st amino acid
  130. Interspecies compatibility of selenoprotein biosynthesis in Enterobacteriaceae
  131. Molecular characterization of an operon (hyp) necessary for the activity of the three hydrogenase isoenzymes inEscherichia coli
  132. A radical-chemical route to acetyl-CoA: the anaerobically induced pyruvate formate-lyase system of
  133. A radical-chemical route to acetyl-CoA: the anaerobically induced pyruvate formate-lyase system of Escherichia coli
  134. Transcriptional analysis of the gene encoding pyruvate formate-lyase-activating enzyme of Escherichia coli
  135. From Nonsense to Sense: UGA Encodes Selenocysteine in Formate Dehydrogenase and Other Selenoproteins
  136. Two-dimensional gel electrophoretic analysis of Escherichia coli proteins: influence of various anaerobic growth conditions and the fnr gene product on cellular protein composition
  137. Factors affecting transcriptional regulation of the formate-hydrogen-lyase pathway of Escherichia coli
  138. Involvement of the ntrA gene product in the anaerobic metabolism of Escherichia coli
  139. Purification and properties of membrane-bound hydrogenase isoenzyme 1 from anaerobically grown Escherichia coli K12