37 results on '"Jacek, Switala"'
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2. Characterization of Extremely Drug-Resistant and Hypervirulent Acinetobacter baumannii AB030
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Manu Singh, P. Malaka De Silva, Yasser Al-Saadi, Jacek Switala, Peter C. Loewen, Georg Hausner, Wangxue Chen, Ismael Hernandez, Santiago Castillo-Ramirez, and Ayush Kumar
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multidrug resistance ,virulence ,gram-negative ,comparative genomics ,insertion elements ,Therapeutics. Pharmacology ,RM1-950 - Abstract
Acinetobacter baumannii is an important nosocomial bacterial pathogen. Multidrug-resistant isolates of A. baumannii are reported worldwide. Some A. baumannii isolates display resistance to nearly all antibiotics, making treatment of infections very challenging. As the need for new and effective antibiotics against A. baumannii becomes increasingly urgent, there is a need to understand the mechanisms of antibiotic resistance and virulence in this organism. In this work, comparative genomics was used to understand the mechanisms of antibiotic resistance and virulence in AB030, an extremely drug-resistant and hypervirulent strain of A. baumannii that is a representative of a recently emerged lineage of A. baumannii International Clone V. In order to characterize AB030, we carried out a genomic and phenotypic comparison with LAC-4, a previously described hyper-resistant and hypervirulent isolate. AB030 contains a number of antibiotic resistance- and virulence-associated genes that are not present in LAC-4. A number of these genes are present on mobile elements. This work shows the importance of characterizing the members of new lineages of A. baumannii in order to determine the development of antibiotic resistance and virulence in this organism.
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- 2020
- Full Text
- View/download PDF
3. Identification of Interactions between Abscisic Acid and Ribulose-1,5-Bisphosphate Carboxylase/Oxygenase.
- Author
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Marek M Galka, Nandhakishore Rajagopalan, Leann M Buhrow, Ken M Nelson, Jacek Switala, Adrian J Cutler, David R J Palmer, Peter C Loewen, Suzanne R Abrams, and Michele C Loewen
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Medicine ,Science - Abstract
Abscisic acid ((+)-ABA) is a phytohormone involved in the modulation of developmental processes and stress responses in plants. A chemical proteomics approach using an ABA mimetic probe was combined with in vitro assays, isothermal titration calorimetry (ITC), x-ray crystallography and in silico modelling to identify putative (+)-ABA binding-proteins in crude extracts of Arabidopsis thaliana. Ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) was identified as a putative ABA-binding protein. Radiolabelled-binding assays yielded a Kd of 47 nM for (+)-ABA binding to spinach Rubisco, which was validated by ITC, and found to be similar to reported and experimentally derived values for the native ribulose-1,5-bisphosphate (RuBP) substrate. Functionally, (+)-ABA caused only weak inhibition of Rubisco catalytic activity (Ki of 2.1 mM), but more potent inhibition of Rubisco activation (Ki of ~ 130 μM). Comparative structural analysis of Rubisco in the presence of (+)-ABA with RuBP in the active site revealed only a putative low occupancy (+)-ABA binding site on the surface of the large subunit at a location distal from the active site. However, subtle distortions in electron density in the binding pocket and in silico docking support the possibility of a higher affinity (+)-ABA binding site in the RuBP binding pocket. Overall we conclude that (+)-ABA interacts with Rubisco. While the low occupancy (+)-ABA binding site and weak non-competitive inhibition of catalysis may not be relevant, the high affinity site may allow ABA to act as a negative effector of Rubisco activation.
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- 2015
- Full Text
- View/download PDF
4. Insights on the Mechanism of Action of INH-C10 as an Antitubercular Prodrug
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Peter C. Loewen, Miguel Machuqueiro, Bruno L. Victor, Filomena Martins, Diogo Vila-Viçosa, Diana Machado, Miguel Viveiros, Jacek Switala, Ruben Elvas Leitão, and Jorge Ramos
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0301 basic medicine ,Tuberculosis ,Activation ,Pharmaceutical Science ,Pharmacology ,medicine.disease_cause ,Ativação ,Mycobacterium tuberculosis ,03 medical and health sciences ,In vivo ,Drug Discovery ,medicine ,Tuberculose ,heterocyclic compounds ,Mutação ,Mutation ,biology ,business.industry ,Isoniazid ,KatG ,Membrane ,Wild type ,respiratory system ,biochemical phenomena, metabolism, and nutrition ,Prodrug ,bacterial infections and mycoses ,biology.organism_classification ,medicine.disease ,respiratory tract diseases ,3. Good health ,030104 developmental biology ,Mechanism of action ,Molecular Medicine ,medicine.symptom ,business ,medicine.drug - Abstract
Tuberculosis remains one of the top causes of death worldwide, and combating its spread has been severely complicated by the emergence of drug-resistance mutations, highlighting the need for more effective drugs. Despite the resistance to isoniazid (INH) arising from mutations in the katG gene encoding the catalase-peroxidase KatG, most notably the S315T mutation, this compound is still one of the most powerful first-line antitubercular drugs, suggesting further pursuit of the development of tailored INH derivatives. The N′-acylated INH derivative with a long alkyl chain (INH-C10) has been shown to be more effective than INH against the S315T variant of Mycobacterium tuberculosis, but the molecular details of this activity enhancement are still unknown. In this work, we show that INH N′-acylation significantly reduces the rate of production of both isonicotinoyl radical and isonicotinyl–NAD by wild type KatG, but not by the S315T variant of KatG mirroring the in vivo effectiveness of the compound. Restrai...
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- 2017
5. Characterization of Extremely Drug-Resistant and Hypervirulent Acinetobacter baumannii AB030
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Jacek Switala, P. Malaka De Silva, Peter C. Loewen, Wangxue Chen, Manu Singh, Yasser Alsaadi, Santiago Castillo-Ramírez, Ismael Hernandez, Georg Hausner, and Ayush Kumar
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0301 basic medicine ,Microbiology (medical) ,medicine.drug_class ,030106 microbiology ,Antibiotics ,Virulence ,comparative genomics ,Drug resistance ,Biochemistry ,Microbiology ,03 medical and health sciences ,Antibiotic resistance ,multidrug resistance ,medicine ,Pharmacology (medical) ,General Pharmacology, Toxicology and Pharmaceutics ,Pathogen ,Comparative genomics ,biology ,lcsh:RM1-950 ,biochemical phenomena, metabolism, and nutrition ,bacterial infections and mycoses ,biology.organism_classification ,gram-negative ,Acinetobacter baumannii ,virulence ,Multiple drug resistance ,lcsh:Therapeutics. Pharmacology ,030104 developmental biology ,Infectious Diseases ,bacteria ,insertion elements - Abstract
Acinetobacter baumannii is an important nosocomial bacterial pathogen. Multidrug-resistant isolates of A. baumannii are reported worldwide. Some A. baumannii isolates display resistance to nearly all antibiotics, making treatment of infections very challenging. As the need for new and effective antibiotics against A. baumannii becomes increasingly urgent, there is a need to understand the mechanisms of antibiotic resistance and virulence in this organism. In this work, comparative genomics was used to understand the mechanisms of antibiotic resistance and virulence in AB030, an extremely drug-resistant and hypervirulent strain of A. baumannii that is a representative of a recently emerged lineage of A. baumannii International Clone V. In order to characterize AB030, we carried out a genomic and phenotypic comparison with LAC-4, a previously described hyper-resistant and hypervirulent isolate. AB030 contains a number of antibiotic resistance- and virulence-associated genes that are not present in LAC-4. A number of these genes are present on mobile elements. This work shows the importance of characterizing the members of new lineages of A. baumannii in order to determine the development of antibiotic resistance and virulence in this organism.
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- 2020
6. Structure and function of a lignostilbene-α,β-dioxygenase orthologue from Pseudomonas brassicacearum
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Michele C. Loewen, Fang Huang, James P. Wells, Jacek Switala, Anthony T. Zara, Peter C. Loewen, John S. Allingham, and University of Manitoba
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0301 basic medicine ,Oxygenase ,Lignostilbene cleaving oxygenase ,Protein Conformation ,In silico ,lcsh:Animal biochemistry ,Crystallography, X-Ray ,Biochemistry ,Dioxygenases ,Substrate Specificity ,lcsh:Biochemistry ,03 medical and health sciences ,In vivo ,Oxidoreductase ,Dioxygenase ,Pseudomonas ,lcsh:QD415-436 ,lcsh:QP501-801 ,Molecular Biology ,Phylogeny ,Soil Microbiology ,Carotenoid ,chemistry.chemical_classification ,In silico modeling ,030102 biochemistry & molecular biology ,biology ,Crystal structure ,Reproducibility of Results ,biology.organism_classification ,Recombinant Proteins ,Molecular Docking Simulation ,030104 developmental biology ,Enzyme ,chemistry ,Resveratrol ,Docking (molecular) ,Pseudomonas brassicacearum ,Research Article - Abstract
Background Stilbene cleaving oxygenases (SCOs), also known as lignostilbene-α,β-dioxygenases (LSDs) mediate the oxidative cleavage of the olefinic double bonds of lignin-derived intermediate phenolic stilbenes, yielding small modified benzaldehyde compounds. SCOs represent one branch of the larger carotenoid cleavage oxygenases family. Here, we describe the structural and functional characterization of an SCO-like enzyme from the soil-born, bio-control agent Pseudomonas brassicacearum. Methods In vitro and in vivo assays relying on visual inspection, spectrophotometric quantification, as well as liquid-chormatographic and mass spectrometric characterization were applied for functional evaluation of the enzyme. X-ray crystallographic analyses and in silico modeling were applied for structural investigations. Results In vitro assays demonstrated preferential cleavage of resveratrol, while in vivo analyses detected putative cleavage of the straight chain carotenoid, lycopene. A high-resolution structure containing the seven-bladed β-propeller fold and conserved 4-His-Fe unit at the catalytic site, was obtained. Comparative structural alignments, as well as in silico modelling and docking, highlight potential molecular factors contributing to both the primary in vitro activity against resveratrol, as well as the putative subsidiary activities against carotenoids in vivo, for future validation. Conclusions The findings reported here provide validation of the SCO structure, and highlight enigmatic points with respect to the potential effect of the enzyme’s molecular environment on substrate specificities for future investigation.
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- 2018
7. KatG-mediated oxidation leading to reduced susceptibility of bacteria to kanamycin
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Jacylyn Villanueva, Lynda J. Donald, Ignacio Fita, Jacek Switala, P. Malaka De Silva, Peter C. Loewen, Ayush Kumar, Natural Sciences and Engineering Research Council of Canada, Canada Research Chairs, National Research Council of Canada, Canadian Institutes of Health Research, University of Saskatchewan, Government of Canada, University of Manitoba, Loewen, Peter C. [0000-0003-4507-4356], Kumar, Ayush [0000-0001-6395-7932], Loewen, Peter C., and Kumar, Ayush
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0301 basic medicine ,medicine.drug_class ,General Chemical Engineering ,030106 microbiology ,Antibiotics ,education ,ComputingMilieux_LEGALASPECTSOFCOMPUTING ,Article ,Microbiology ,lcsh:Chemistry ,Mycobacterium tuberculosis ,03 medical and health sciences ,Oxidoreductase ,Data_FILES ,medicine ,chemistry.chemical_classification ,biology ,Bacteria ,Aminoglycoside ,Isoniazid ,Proteins ,Kanamycin ,General Chemistry ,biochemical phenomena, metabolism, and nutrition ,bacterial infections and mycoses ,biology.organism_classification ,3. Good health ,030104 developmental biology ,Enzyme ,lcsh:QD1-999 ,chemistry ,Crystal structures ,Protein structure ,bacteria ,Molecular structure ,medicine.drug - Abstract
This is an open access article published under an ACS AuthorChoice License, which permits copying and redistribution of the article or any adaptations for non-commercial purposes., Resistance to antibiotics has become a serious problem for society, and there are increasing efforts to understand the reasons for and sources of resistance. Bacterial-encoded enzymes and transport systems, both innate and acquired, are the most frequent culprits for the development of resistance, although in Mycobacterium tuberculosis, the catalase-peroxidase, KatG, has been linked to the activation of the antitubercular drug isoniazid. While investigating a possible link between aminoglycoside antibiotics and the induction of oxidative bursts, we observed that KatG reduces susceptibility to aminoglycosides. Investigation revealed that kanamycin served as an electron donor for the peroxidase reaction, reducing the oxidized ferryl intermediates of KatG to the resting state. Loss of electrons from kanamycin was accompanied by the addition of a single oxygen atom to the aminoglycoside. The oxidized form of kanamycin proved to be less effective as an antibiotic. Kanamycin inhibited the crystallization of KatG, but the smaller, structurally related glycoside maltose did cocrystallize with KatG, providing a suggestion as to the possible binding site of kanamycin, This work was supported by Discovery Grants 2012-9600 (to P.C.L.) and 2015-05550 (to A.K.) from the Natural Sciences and Engineering Research Council (NSERC) of Canada, and by the Canada Research Chair Program (to P.C.L.). The Canadian Light Source is supported by the Natural Sciences and Engineering Research Council of Canada, the National Research Council Canada, the Canadian Institutes of Health Research, the Province of Saskatchewan, Western Economic Diversification Canada, and the University of Saskatchewan. P.M.D.S. is supported by the University of Manitoba Graduate Fellowship.
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- 2018
8. Insights on the Mechanism of Action of INH-C
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Diogo, Vila-Viçosa, Bruno L, Victor, Jorge, Ramos, Diana, Machado, Miguel, Viveiros, Jacek, Switala, Peter C, Loewen, Ruben, Leitão, Filomena, Martins, and Miguel, Machuqueiro
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Acylation ,Antitubercular Agents ,Microbial Sensitivity Tests ,Mycobacterium tuberculosis ,Molecular Dynamics Simulation ,Catalase ,NAD ,Bacterial Proteins ,Drug Resistance, Bacterial ,Mutation ,Isoniazid ,Tuberculosis ,Prodrugs ,Peroxidase - Abstract
Tuberculosis remains one of the top causes of death worldwide, and combating its spread has been severely complicated by the emergence of drug-resistance mutations, highlighting the need for more effective drugs. Despite the resistance to isoniazid (INH) arising from mutations in the katG gene encoding the catalase-peroxidase KatG, most notably the S315T mutation, this compound is still one of the most powerful first-line antitubercular drugs, suggesting further pursuit of the development of tailored INH derivatives. The N'-acylated INH derivative with a long alkyl chain (INH-C
- Published
- 2017
9. Unprecedented access of phenolic substrates to the heme active site of a catalase: Substrate binding and peroxidase-like reactivity ofBacillus pumiluscatalase monitored by X-ray crystallography and EPR spectroscopy
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Anabella Ivancich, Lynda J. Donald, Jacylyn Villanueva, Jacek Switala, and Peter C. Loewen
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chemistry.chemical_classification ,0303 health sciences ,biology ,Bacillus pumilus ,Stereochemistry ,030302 biochemistry & molecular biology ,Substrate (chemistry) ,Active site ,biology.organism_classification ,Biochemistry ,03 medical and health sciences ,chemistry.chemical_compound ,Heme B ,Enzyme ,chemistry ,Structural Biology ,Catalase ,biology.protein ,Molecular Biology ,Heme ,030304 developmental biology ,Peroxidase - Abstract
Heme-containing catalases and catalase-peroxidases catalyze the dismutation of hydrogen peroxide as their predominant catalytic activity, but in addition, individual enzymes support low levels of peroxidase and oxidase activities, produce superoxide, and activate isoniazid as an antitubercular drug. The recent report of a heme enzyme with catalase, peroxidase and penicillin oxidase activities in Bacillus pumilus and its categorization as an unusual catalase-peroxidase led us to investigate the enzyme for comparison with other catalase-peroxidases, catalases, and peroxidases. Characterization revealed a typical homotetrameric catalase with one pentacoordinated heme b per subunit (Tyr340 being the axial ligand), albeit in two orientations, and a very fast catalatic turnover rate (kcat = 339,000 s−1). In addition, the enzyme supported a much slower (kcat = 20 s−1) peroxidatic activity utilizing substrates as diverse as ABTS and polyphenols, but no oxidase activity. Two binding sites, one in the main access channel and the other on the protein surface, accommodating pyrogallol, catechol, resorcinol, guaiacol, hydroquinone, and 2-chlorophenol were identified in crystal structures at 1.65–1.95 A. A third site, in the heme distal side, accommodating only pyrogallol and catechol, interacting with the heme iron and the catalytic His and Arg residues, was also identified. This site was confirmed in solution by EPR spectroscopy characterization, which also showed that the phenolic oxygen was not directly coordinated to the heme iron (no low-spin conversion of the FeIII high-spin EPR signal upon substrate binding). This is the first demonstration of phenolic substrates directly accessing the heme distal side of a catalase. Proteins 2015; 83:853–866. © 2015 Wiley Periodicals, Inc.
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- 2015
10. The Catalase Activity of Catalase-Peroxidases Is Modulated by Changes in the pK
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Miguel, Machuqueiro, Bruno, Victor, Jacek, Switala, Jacylyn, Villanueva, Carme, Rovira, Ignacio, Fita, and Peter C, Loewen
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Hemeproteins ,Models, Molecular ,Burkholderia pseudomallei ,Protein Conformation ,Recombinant Fusion Proteins ,Static Electricity ,Titrimetry ,Computational Biology ,Hydrogen-Ion Concentration ,Catalase ,Crystallography, X-Ray ,Peptide Fragments ,Recombinant Proteins ,Amino Acid Substitution ,Bacterial Proteins ,Peroxidases ,Catalytic Domain ,Mutation ,Biocatalysis ,Histidine - Abstract
The unusual Met-Tyr-Trp adduct composed of cross-linked side chains along with an associated mobile Arg is essential for catalase activity in catalase-peroxidases. In addition, acidic residues in the entrance channel, in particular an Asp and a Glu ∼7 and ∼15 Å, respectively, from the heme, significantly enhance catalase activity. The mechanism by which these channel carboxylates influence catalase activity is the focus of this work. Seventeen new variants with fewer and additional acidic residues have been constructed and characterized structurally and for enzymatic activity, revealing that their effect on activity is roughly inversely proportional to their distance from the heme and adduct, suggesting that the electrostatic potential of the heme cavity may be affected. A discrete group of protonable residues are contained within a 15 Å sphere surrounding the heme iron, and a computational analysis reveals that the pK
- Published
- 2017
11. The catalase activity of catalase-reroxidases Is modulated by changes in the pKa of the distal histidine
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Jacek Switala, Carme Rovira, Peter C. Loewen, Ignacio Fita, Jacylyn Villanueva, Bruno L. Victor, Miguel Machuqueiro, Natural Sciences and Engineering Research Council of Canada, National Research Council of Canada, Canadian Institutes of Health Research, University of Saskatchewan, Fundação para a Ciência e a Tecnologia (Portugal), Machuqueiro, Miguel, Rovira, Carme, Loewen, Peter C., Machuqueiro, Miguel [0000-0001-6923-8744], Rovira, Carme [0000-0003-1477-5010], and Loewen, Peter C. [0000-0003-4507-4356]
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0301 basic medicine ,chemistry.chemical_classification ,biology ,Stereochemistry ,010402 general chemistry ,01 natural sciences ,Biochemistry ,0104 chemical sciences ,3. Good health ,Adduct ,03 medical and health sciences ,chemistry.chemical_compound ,030104 developmental biology ,Protein structure ,Enzyme ,chemistry ,Oxidoreductase ,Catalase ,biology.protein ,Heme ,Histidine ,Peroxidase - Abstract
The unusual Met-Tyr-Trp adduct composed of cross-linked side chains along with an associated mobile Arg is essential for catalase activity in catalase-peroxidases. In addition, acidic residues in the entrance channel, in particular an Asp and a Glu ∼7 and ∼15 Å, respectively, from the heme, significantly enhance catalase activity. The mechanism by which these channel carboxylates influence catalase activity is the focus of this work. Seventeen new variants with fewer and additional acidic residues have been constructed and characterized structurally and for enzymatic activity, revealing that their effect on activity is roughly inversely proportional to their distance from the heme and adduct, suggesting that the electrostatic potential of the heme cavity may be affected. A discrete group of protonable residues are contained within a 15 Å sphere surrounding the heme iron, and a computational analysis reveals that the pKa of the distal His112, alone, is modulated within the pH range of catalase activity by the remote acidic residues in a pattern consistent with its protonated form having a key role in the catalase reaction cycle. The electrostatic potential also impacts the catalatic reaction through its influence on the charged status of the Met-Tyr-Trp adduct., This work was supported by a Discovery Grant 9600 from the Natural Sciences and Engineering Research Council (NSERC) of Canada (to P.C.L.) and the Canada Research Chair Program (to P.C.L.). The Canadian Light Source is supported by the Natural Sciences and Engineering Research Council of Canada, the National Research Council Canada, the Canadian Institutes of Health Research, the Province of Saskatchewan, Western Economic Diversification Canada, and the University of Saskatchewan. We also acknowledge financial support from the Portuguese Fundaca̧ o para a Ciencia e a Tecnologia through ̂ Project UID/MULTI/00612/2013.
- Published
- 2017
12. Comparative study of catalase-peroxidases (KatGs)
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Jacek Switala, Vikash Jha, Taweewat Deemagarn, Peter C. Loewen, Rahul Singh, and Ben Wiseman
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Azides ,Burkholderia pseudomallei ,Antitubercular Agents ,Biophysics ,Biochemistry ,Multienzyme Complexes ,Isoniazid ,Histidine ,NADH, NADPH Oxidoreductases ,Enzyme kinetics ,Enzyme Inhibitors ,Molecular Biology ,chemistry.chemical_classification ,Binding Sites ,Cyanides ,Rhodobacter ,Bacteria ,biology ,Synechocystis ,Hydrogen Peroxide ,Mycobacterium tuberculosis ,Hydrogen-Ion Concentration ,Catalase ,biology.organism_classification ,Lyase ,Anti-Bacterial Agents ,Kinetics ,Enzyme ,Peroxidases ,chemistry ,biology.protein ,Peroxidase - Abstract
Catalase-peroxidases or KatGs from seven different organisms, including Archaeoglobus fulgidus, Bacillus stearothermophilus , Burkholderia pseudomallei , Escherichia coli , Mycobacterium tuberculosis , Rhodobacter capsulatus and Synechocystis PCC 6803, have been characterized to provide a comparative picture of their respective properties. Collectively, the enzymes exhibit similar turnover rates with the catalase and peroxidase reactions varying between 4900 and 15,900 s −1 and 8–25 s −1 , respectively. The seven enzymes also exhibited similar pH optima for the peroxidase (4.25–5.0) and catalase reactions (5.75), and high sensitivity to azide and cyanide with IC 50 values of 0.2–20 μM and 50–170 μM, respectively. The K M s of the enzymes for H 2 O 2 in the catalase reaction were relatively invariant between 3 and 5 mM at pH 7.0, but increased to values ranging from 20 to 225 mM at pH 5, consistent with protonation of the distal histidine (pKa approximately 6.2) interfering with H 2 O 2 binding to Cpd I. The catalatic k cat was 2- to 3-fold higher at pH 5 compared to pH 7, consistent with the uptake of a proton being involved in the reduction of Cpd I. The turnover rates for the INH lyase and isonicotinoyl-NAD synthase reactions, responsible for the activation of isoniazid as an anti-tubercular drug, were also similar across the seven enzymes, but considerably slower, at 0.5 and 0.002 s −1 , respectively. Only the NADH oxidase reaction varied more widely between 10 −4 and 10 −2 s −1 with the fastest rate being exhibited by the enzyme from B. pseudomallei .
- Published
- 2008
13. Identification of interactions between abscisic acid and ribulose-1,5-bisphosphate carboxylase/oxygenase
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Peter C. Loewen, Nandhakishore Rajagopalan, Michele C. Loewen, Suzanne R. Abrams, Marek M. Galka, Adrian J. Cutler, Leann M. Buhrow, Jacek Switala, Ken M. Nelson, and David R. J. Palmer
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electron ,Oxygenase ,spinach ,Arabidopsis ,lcsh:Medicine ,ribulosebisphosphate carboxylase ,abscisic acid ,chemistry.chemical_compound ,binding affinity ,vegetable protein ,lcsh:Science ,Abscisic acid ,enzyme inhibition ,comparative study ,hormone binding protein ,Multidisciplinary ,biology ,food and beverages ,structure analysis ,unclassified drug ,enzyme activity ,enzyme structure ,isothermal titration calorimetry ,Biochemistry ,validation study ,protein protein interaction ,enzyme active site ,Protein Binding ,Research Article ,Ribulose-Bisphosphate Carboxylase ,Molecular Sequence Data ,Amino Acid Sequence ,Binding site ,enzyme substrate ,Ribulose 1,5-bisphosphate ,Binding Sites ,catalysis ,organic chemicals ,RuBisCO ,lcsh:R ,fungi ,Active site ,Isothermal titration calorimetry ,enzyme activation ,molecular docking ,Lyase ,oxygenase ,chemistry ,biology.protein ,lcsh:Q ,ribulose 1,5 bisphosphate oxygenase ,computer model - Abstract
Abscisic acid ((+)-ABA) is a phytohormone involved in the modulation of developmental processes and stress responses in plants. A chemical proteomics approach using an ABA mimetic probe was combined with in vitro assays, isothermal titration calorimetry (ITC), x-ray crystallography and in silico modelling to identify putative (+)-ABA binding-proteins in crude extracts of Arabidopsis thaliana. Ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) was identified as a putative ABA-binding protein. Radiolabelled-binding assays yielded a Kd of 47 nM for (+)-ABA binding to spinach Rubisco, which was validated by ITC, and found to be similar to reported and experimentally derived values for the native ribulose-1,5-bisphosphate (RuBP) substrate. Functionally, (+)-ABA caused only weak inhibition of Rubisco catalytic activity (Ki of 2.1 mM), but more potent inhibition of Rubisco activation (Ki of ~ 130 μM). Comparative structural analysis of Rubisco in the presence of (+)-ABA with RuBP in the active site revealed only a putative low occupancy (+)-ABA binding site on the surface of the large subunit at a location distal from the active site. However, subtle distortions in electron density in the binding pocket and in silico docking support the possibility of a higher affinity (+)-ABA binding site in the RuBP binding pocket. Overall we conclude that (+)-ABA interacts with Rubisco. While the low occupancy (+)-ABA binding site and weak non-competitive inhibition of catalysis may not be relevant, the high affinity site may allow ABA to act as a negative effector of Rubisco activation.
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- 2015
14. A molecular switch and electronic circuit modulate catalase activity in catalase‐peroxidases
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Rahul Singh, Anabella Ivancich, Taweewat Deemagarn, Peter C. Loewen, Ben Wiseman, Jacek Switala, Xavier Carpena, and Ignacio Fita
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Models, Molecular ,Burkholderia pseudomallei ,Arginine ,Protein Conformation ,Stereochemistry ,Scientific Report ,Heme ,Heme oxidation ,Crystallography, X-Ray ,Biochemistry ,Adduct ,chemistry.chemical_compound ,Bacterial Proteins ,Oxidoreductase ,Genetics ,Molecular Biology ,Catalase-peroxidase ,chemistry.chemical_classification ,Binding Sites ,biology ,Chemistry ,Water ,Hydrogen Peroxide ,Hydrogen-Ion Concentration ,Catalase ,Kinetics ,Models, Chemical ,Peroxidases ,biology.protein ,Electronics ,Oxidation-Reduction ,Peroxidase - Abstract
The catalase reaction of catalase-peroxidases involves catalase-specific features built into a peroxidase core. An arginine, 20 Å from the active-site heme, acts as a molecular switch moving between two conformations, one that activates heme oxidation and one that activates oxoferryl heme reduction by H2O2, facilitating the catalatic pathway in a peroxidase. The influence of the arginine is imparted to the heme through its association with or dissociation from a tyrosinate that modulates reactivity through a Met-Tyr-Trp crosslinked adduct and a π electron interaction of the heme with the adduct Trp. © 2005 European Molecular Biology Organization., This work was supported by grant BIO2002-04419 from Ministerio de Ciencia y Technologia, Spain (to I.F.), by grant OGP9600 from the Natural Sciences and Engineering Research Council of Canada (to P.C.L.), by the Canada Research Chair Program (to P.C.L.) and by fellowship EX-2003-0866 from the Ministerio de Educación Cultura y Deporte, Spain (to X.C.)
- Published
- 2005
15. Characterization of a Large Subunit Catalase Truncated by Proteolytic Cleavage
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Xavier Carpena, Ignacio Fita, Prashen Chelikani, Peter C. Loewen, R. Perez-Luque, Jacek Switala, Lynda J. Donald, and Harry W. Duckworth
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Models, Molecular ,Spectrometry, Mass, Electrospray Ionization ,Stereochemistry ,Protein subunit ,Heme ,Crystallography, X-Ray ,Cleavage (embryo) ,Biochemistry ,chemistry.chemical_compound ,Catalytic Domain ,Escherichia coli ,Binding site ,Protein Structure, Quaternary ,Binding Sites ,biology ,Chemistry ,Escherichia coli Proteins ,Genetic Variation ,Active site ,Substrate (chemistry) ,Hydrogen Peroxide ,Catalase ,Peptide Fragments ,Protein Structure, Tertiary ,Kinetics ,Protein Subunits ,biology.protein ,NADPH binding ,Protein quaternary structure ,Peptide Hydrolases - Abstract
The large subunit catalase HPII from Escherichia coli can be truncated by proteolysis to a structure similar to small subunit catalases. Mass spectrometry analysis indicates that there is some heterogeneity in the precise cleavage sites, but approximately 74 N-terminal residues, 189 C-terminal residues, and a 9-11-residue internal fragment, including residues 298-308, are removed. Crystal structure refinement at 2.8 A reveals that the tertiary and quaternary structure of the native enzyme is retained with only very subtle changes despite the loss of 36% of the sequence. The truncated variant exhibits a 1.8 times faster turnover rate and enhanced sensitivity to high concentrations of H(2)O(2), consistent with easier access of the substrate to the active site. In addition, the truncated variant is more sensitive to inhibition, particularly by reagents such as aminotriazole and azide which are larger than substrate H(2)O(2). The main channel leading to the heme cavity is largely unaffected by the truncation, but the lateral channel is shortened and its entrance widened by removal of the C-terminal domain, providing an explanation for easier access to the active site. Opening of the entrance to the lateral channel also opens the putative NADPH binding site, but NADPH binding could not be demonstrated. Despite the lack of bound NADPH, the compound I species of both native and truncated HPII are reduced back to the resting state with compound II being evident in the absorbance spectrum only of the heme b-containing H392A variant.
- Published
- 2005
16. Unprecedented access of phenolic substrates to the heme active site of a catalase: substrate binding and peroxidase-like reactivity of Bacillus pumilus catalase monitored by X-ray crystallography and EPR spectroscopy
- Author
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Peter C, Loewen, Jacylyn, Villanueva, Jacek, Switala, Lynda J, Donald, and Anabella, Ivancich
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Models, Molecular ,Catalytic Domain ,Electron Spin Resonance Spectroscopy ,Polyphenols ,Bacillus ,Heme ,Catalase ,Crystallography, X-Ray ,Peroxidase ,Protein Binding ,Substrate Specificity - Abstract
Heme-containing catalases and catalase-peroxidases catalyze the dismutation of hydrogen peroxide as their predominant catalytic activity, but in addition, individual enzymes support low levels of peroxidase and oxidase activities, produce superoxide, and activate isoniazid as an antitubercular drug. The recent report of a heme enzyme with catalase, peroxidase and penicillin oxidase activities in Bacillus pumilus and its categorization as an unusual catalase-peroxidase led us to investigate the enzyme for comparison with other catalase-peroxidases, catalases, and peroxidases. Characterization revealed a typical homotetrameric catalase with one pentacoordinated heme b per subunit (Tyr340 being the axial ligand), albeit in two orientations, and a very fast catalatic turnover rate (kcat = 339,000 s(-1) ). In addition, the enzyme supported a much slower (kcat = 20 s(-1) ) peroxidatic activity utilizing substrates as diverse as ABTS and polyphenols, but no oxidase activity. Two binding sites, one in the main access channel and the other on the protein surface, accommodating pyrogallol, catechol, resorcinol, guaiacol, hydroquinone, and 2-chlorophenol were identified in crystal structures at 1.65-1.95 Å. A third site, in the heme distal side, accommodating only pyrogallol and catechol, interacting with the heme iron and the catalytic His and Arg residues, was also identified. This site was confirmed in solution by EPR spectroscopy characterization, which also showed that the phenolic oxygen was not directly coordinated to the heme iron (no low-spin conversion of the Fe(III) high-spin EPR signal upon substrate binding). This is the first demonstration of phenolic substrates directly accessing the heme distal side of a catalase.
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- 2014
17. Catalase HPII from Escherichia coli Exhibits Enhanced Resistance to Denaturation
- Author
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Joe D. O’NeilJ.D. O’Neil, Peter C. Loewen, and Jacek Switala
- Subjects
Models, Molecular ,Protein Denaturation ,Hot Temperature ,Stereochemistry ,Dimer ,medicine.disease_cause ,Biochemistry ,Dissociation (chemistry) ,chemistry.chemical_compound ,Enzyme Stability ,Escherichia coli ,medicine ,Urea ,Protein secondary structure ,Guanidine ,chemistry.chemical_classification ,biology ,Circular Dichroism ,Sodium Dodecyl Sulfate ,Catalase ,Enzyme Activation ,Enzyme ,chemistry ,Covalent bond ,Mutagenesis, Site-Directed ,biology.protein ,Homotetramer - Abstract
Catalase HPII from Escherichia coli is a homotetramer of 753 residue subunits. The multimer displays a number of unusual structural features, including interwoven subunits and a covalent bond between Tyr415 and His392, that would contribute to its rigidity and stability. As the temperature of a solution of HPII in 50 mM potassium phosphate buffer (pH 7) is raised from 50 to 92 degrees C, the enzyme begins to lose activity at 78 degrees C and 50% inactivation has occurred at 83 degrees C. The inactivation is accompanied by absorbance changes at 280 and 407 nm and by changes in the CD spectrum consistent with small changes in secondary structure. The subunits in the dimer structure remain associated at 95 degrees C and show a significant level of dissociation only at 100 degrees C. The exceptional stability of the dimer association is consistent with the interwoven nature of the subunits and provides an explanation for the resistance to inactivation of the enzyme. For comparison, catalase-peroxidase HPI of E. coli and bovine liver catalase are 50% inactivated at 53 and 56 degrees C, respectively. In 5.6 M urea, HPII exhibits a coincidence of inactivation, CD spectral change, and dissociation of the dimer structure with a midpoint of 65 degrees C. The inactive mutant variants of HPII which fold poorly during synthesis and which lack the Tyr-His covalent bond undergo spectral changes in the 78 to 84 degrees C range, revealing that the extra covalent linkage is not important in the enhanced resistance to denaturation and that problems in the folding pathway do not affect the ultimate stability of the folded structure.
- Published
- 1999
18. Identification of a novel bond between a histidine and the essential tyrosine in catalase HPII ofEscherichia coli
- Author
-
Jacek Switala, Peter C. Loewen, Werner Ens, Ignacio Fita, Jerónimo Bravo, Alex Hillar, and Juan C. Ferrer
- Subjects
Models, Molecular ,Protein Conformation ,Stereochemistry ,Molecular Sequence Data ,Heme ,Crystallography, X-Ray ,Ring (chemistry) ,Biochemistry ,Histidine-tyrosine linkage ,chemistry.chemical_compound ,Escherichia coli ,Imidazole ,Molecule ,Histidine ,Trypsin ,Amino Acid Sequence ,Molecular Biology ,Binding Sites ,biology ,Active site ,Catalase ,Peptide Fragments ,Protein modification ,Heme B ,chemistry ,Covalent bond ,Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization ,Crystal structures ,biology.protein ,Thermodynamics ,Tyrosine ,Research Article - Abstract
8 pages, 7 figures, 1 table.-- PMID: 9144772 [PubMed].-- PMCID: PMC2143697., A bond between the N delta of the imidazole ring of His 392 and the C beta of the essential Tyr 415 has been found in the refined crystal structure at 1.9 A resolution of catalase HPII of Escherichia coli. This novel type of covalent linkage is clearly defined in the electron density map of HPII and is confirmed by matrix-assisted laser desorption/ionization mass spectrometry analysis of tryptic digest mixtures. The geometry of the bond is compatible with both the sp3 hybridization of the C beta atom and the planarity of the imidazole ring. Two mutated variants of HPII active site residues, H128N and N201H, do not contain the His 392-Tyr 415 bond, and their crystal structures show that the imidazole ring of His 392 was rotated, in both cases, by 80 degrees relative to its position in HPII. These mutant forms of HPII are catalytically inactive and do not convert heme b to heme d, suggesting a relationship between the self-catalyzed heme conversion reaction and the formation of the His-Tyr linkage. A model coupling the two processes and involving the reaction of one molecule of H2O2 on the proximal side of the heme with compound 1 is proposed., n. Thwiso rk was supported by an operating grant from the Natural Sciences and Engineering Research Council (NSERC (OGP9600) to P.C.L. and a postgraduate scholarship from NSERC to A.H. Work in Barcelona was supported by grants PB92-0707 and PB95-0218 to I.F. J.B. was the recipient of a doctoral fellowship from the Generalitat de Catalunya. Data collection in Hamburg was supporbteyd the Human Capital Mobility Project on contract CHGE-CT93-0040
- Published
- 1997
19. Structure of Pisum sativum Rubisco with bound ribulose 1,5-bisphosphate
- Author
-
Jacek Switala, Ignacio Fita, Allison L. Didychuk, Rosa Pérez-Luque, Michele C. Loewen, and Peter C. Loewen
- Subjects
Models, Molecular ,Rubisco ,Protein Conformation ,Ribulose-Bisphosphate Carboxylase ,Ribulose 1,5-bisphosphate ,Biophysics ,Biology ,Crystallography, X-Ray ,Biochemistry ,Pisum ,chemistry.chemical_compound ,Ribulosephosphates ,Structural Biology ,Catalytic Domain ,Genetics ,Structural Communications ,Pisum sativum ,Plant Proteins ,ribulose 1,5-bisphosphate ,Ribulose ,Lysine ,RuBisCO ,fungi ,Peas ,Active site ,Substrate (chemistry) ,food and beverages ,Condensed Matter Physics ,biology.organism_classification ,Molecular replacement ,molecular replacement ,Crystallography ,chemistry ,biology.protein ,Protein quaternary structure ,Protein Multimerization - Abstract
The first structure of a ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) from a pulse crop is reported. Rubisco was purified from Pisum sativum (garden pea) and diffraction-quality crystals were obtained by hanging-drop vapour diffusion in the presence of the substrate ribulose 1,5-bisphosphate. X-ray diffraction data were recorded to 2.20 Ã… resolution from a single crystal at the Canadian Light Source. The overall quaternary structure of non-activated P. sativum Rubisco highlights the conservation of the form I Rubisco hexadecameric complex. The electron density places the substrate in the active site at the interface of the large-subunit dimers. Lys201 in the active site is not carbamylated as expected for this non-activated structure. Some heterogeneity in the small-subunit sequence is noted, as well as possible variations in the conformation and contacts of ribulose 1,5-bisphosphate in the large-subunit active sites. Overall, the active-site conformation most closely correlates with the 'closed' conformation observed in other substrate/inhibitor- bound Rubisco structures. © 2013 International Union of Crystallography. All rights reserved., This work was supported by the National Research Council of Canada (to MCL), the Canada Research Chair Program (to PCL) and the Natural Sciences and Engineering Research Council Discovery Grants Program (to both MCL and PCL). This manuscript represents NRC Communication No. 54669.
- Published
- 2013
20. NADPH binding and control of catalase compound II formation: comparison of bovine, yeast, and Escherichia coli enzymes
- Author
-
Jacek Switala, Peter C. Loewen, A Hillar, and Peter Nicholls
- Subjects
Saccharomyces cerevisiae ,Biochemistry ,Peroxide ,Chromatography, Affinity ,chemistry.chemical_compound ,Escherichia coli ,Animals ,Molecular Biology ,chemistry.chemical_classification ,Binding Sites ,biology ,Cytochrome c peroxidase ,Cell Biology ,Catalase ,Yeast ,Peroxides ,Spectrometry, Fluorescence ,Enzyme ,Liver ,chemistry ,biology.protein ,NADPH binding ,Cattle ,Electrophoresis, Polyacrylamide Gel ,Ferrocyanide ,Oxidation-Reduction ,NADP ,Research Article ,Peroxidase - Abstract
1. NADPH binds to bovine catalase and to yeast catalases A and T, but not to Escherichia coli catalase HPII. The association was demonstrated using chromatography and fluorimetry. Bound NADPH fluoresces in a similar way to NADPH in solution. 2. Bound NADPH protects bovine and yeast catalases against forming inactive peroxide compound II either via endogenous reductant action or by ferrocyanide reduction during catalytic activity in the presence of slowly generated peroxide. 3. Bound NADPH reduces neither compound I nor compound II of catalase. It apparently reacts with an intermediate formed during the decay of compound I to compound II; this postulated intermediate is an immediate precursor of stable compound II either when the latter is formed by endogenous reductants or when ferrocyanide is used. It represents therefore a new type of hydrogen donor that is not included in the original classification of Keilin and Nicholls [Keilin, D. and Nicholls, P. (1958) Biochim. Biophys. Acta 29, 302-307] 4. A model for NADPH action is presented in which concerted reduction of the ferryl iron and of a neighbouring protein free radical is responsible for the observed NADPH effects. The roles of migrant radical species in mammalian and yeast catalases are compared with similar events in metmyoglobin and cytochrome c peroxidase reactions with peroxides.
- Published
- 1994
21. The delta (argF-lacZ)205(U169) deletion greatly enhances resistance to hydrogen peroxide in stationary-phase Escherichia coli
- Author
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Jacek Switala, Peter C. Loewen, Michael R. Volkert, David J. Crowley, and Matthew Conley
- Subjects
Genotype ,Molecular Sequence Data ,Mutant ,lac operon ,Molecular cloning ,medicine.disease_cause ,Microbiology ,Open Reading Frames ,Escherichia coli ,medicine ,Insertion ,Beta-galactosidase ,Promoter Regions, Genetic ,Molecular Biology ,Gene ,Alleles ,Base Sequence ,biology ,Drug Resistance, Microbial ,Hydrogen Peroxide ,beta-Galactosidase ,biology.organism_classification ,Enterobacteriaceae ,Molecular biology ,Kinetics ,Mutagenesis, Insertional ,Phenotype ,Genes, Bacterial ,biology.protein ,Gene Deletion ,Research Article - Abstract
In this study, we demonstrate that a strain bearing the delta (argF-lacZ)205(U169) deletion exhibits a high level of resistance to hydrogen peroxide compared with its undeleted parent. Our initial investigation of the mechanism behind the observed differences in peroxide resistance when parent and mutant strains are compared indicates that the parent strain carries a region near argF that is responsible for the H2O2-sensitive phenotype, which we have named katC. The H2O2 resistance phenotype of the delta katC [delta (argF-lacZ)205(U169)] mutant strain can be duplicated by Tn9 insertion in a specific locus (katC5::Tn9) which maps near argF. The increased H2O2 resistance of the delta katC and katC5::Tn9 mutant strains can be seen only when cells are grown to stationary phase; exponential-phase cells are unaffected by the presence or absence of katC. This H2O2 resistance mechanism requires functional katE and katF genes, which suggests that the mechanism of H2O2 resistance may involve the activity of the stationary-phase-specific catalase HPII. Cloning, DNA sequencing, and analysis of the katC5::Tn9 insertion allele in comparison with its parent allele implicate two insertion elements, IS1B and IS30B, and suggest that their presence sensitizes parent cells to H2O2.
- Published
- 1994
22. Distinct role of specific tryptophans in facilitating electron transfer or as [Fe(IV)=O Trp(*)] intermediates in the peroxidase reaction of Bulkholderia pseudomallei catalase-peroxidase: a multifrequency EPR spectroscopy investigation
- Author
-
Peter C. Loewen, Julie Colin, Anabella Ivancich, Jacek Switala, and Ben Wiseman
- Subjects
Models, Molecular ,Burkholderia pseudomallei ,Chemistry ,Peroxidase reaction ,Reactive intermediate ,Electron Spin Resonance Spectroscopy ,Tryptophan ,Electrons ,General Chemistry ,biochemical phenomena, metabolism, and nutrition ,bacterial infections and mycoses ,Photochemistry ,Biochemistry ,Catalysis ,law.invention ,Electron transfer ,Colloid and Surface Chemistry ,Bacterial Proteins ,Peroxidases ,law ,Mutagenesis ,bacteria ,Electron paramagnetic resonance ,Catalase-peroxidase ,Iron Compounds - Abstract
We have characterized the reactive intermediates of the peroxidase-like reaction of Bulkholderia pseudomallei KatG using multifrequency EPR spectroscopy. The aim was to investigate the putative role of tryptophanyl radicals as alternative intermediates to the [Fe(IV)=O Por(*+)] species or as short-lived species involved in superexchange-coupled pathways between redox cofactors. Three distinct sites for the formation of radical intermediates, Trp330, Trp139 and Trp153, were identified using single, double and triple variants of Bulkholderia pseudomallei KatG. The proximal Trp330 is the site for a radical in magnetic interaction with the ferryl heme iron [Fe(IV)=O Trp(*+)], formed at the expense of a short-lived [Fe(IV)=O Por(*+)] species as in the cases of Mycobacterium tuberculosis KatG and cytochrome c peroxidase. Formation of the Trp153 radical at a site close to the enzyme surface crucially depends on the integrity of the H-bonding network of the heme distal side, that includes Trp95, the radical site in the Synechocystis KatG. Accordingly, the extended H-bonding network and Trp94 provide an electron transfer pathway between Trp153 and the heme. The distal tryptophan (Trp111) being part of the KatG-specific adduct required for the catalase-like activity, is involved in facilitating electron transfer for the formation of the Trp139 radical. We propose a comprehensive description of the role of specific Trp residues that takes into account not only the apparent differences in sites for the Trp(*) intermediates in other catalase-peroxidases but also the similar cases observed in monofunctional peroxidases.
- Published
- 2009
23. Catalase-peroxidase KatG of Burkholderia pseudomallei at 1.7A resolution
- Author
-
Suvit Loprasert, Skorn Mongkolsuk, Xavi Carpena, Peter C. Loewen, Ignacio Fita, and Jacek Switala
- Subjects
Models, Molecular ,Protein Folding ,Burkholderia pseudomallei ,Stereochemistry ,Protein Conformation ,Dimer ,Antitubercular Agents ,Photochemistry ,Crystallography, X-Ray ,Adduct ,Electron transfer ,chemistry.chemical_compound ,Bacterial Proteins ,Structural Biology ,Oxidoreductase ,Isoniazid ,Molecular Biology ,Heme ,chemistry.chemical_classification ,Binding Sites ,Ligand ,Hydrogen bond ,Hydrogen Bonding ,chemistry ,Peroxidases ,Covalent bond ,Crystallization - Abstract
The catalase-peroxidase encoded by katG of Burkholderia pseudomallei (BpKatG) is 65% identical with KatG of Mycobacterium tuberculosis , the enzyme responsible for the activation of isoniazid as an antibiotic. The structure of a complex of BpKatG with an unidentified ligand, has been solved and refined at 1.7 A resolution using X-ray synchrotron data collected from crystals flash-cooled with liquid nitrogen. The crystallographic agreement factors R and R free are 15.3% and 18.6%, respectively. The crystallized enzyme is a dimer with one modified heme group and one metal ion, likely sodium, per subunit. The modification on the heme group involves the covalent addition of two or three atoms, likely a perhydroxy group, to the secondary carbon atom of the vinyl group on ring I. The added group can form hydrogen bonds with two water molecules that are also in contact with the active-site residues Trp111 and His112, suggesting that the modification may have a catalytic role. The heme modification is in close proximity to an unusual covalent adduct among the side-chains of Trp111, Tyr238 and Met264. In addition, Trp111 appears to be oxidized on C δ1 of the indole ring. The main channel, providing access of substrate hydrogen peroxide to the heme, contains a region of unassigned electron density consistent with the binding of a pyridine nucleotide-like molecule. An interior cavity, containing the sodium ion and an additional region of unassigned density, is evident adjacent to the adduct and is accessible to the outside through a second funnel-shaped channel. A large cleft in the side of the subunit is evident and may be a potential substrate-binding site with a clear pathway for electron transfer to the active-site heme group through the adduct.
- Published
- 2003
24. Diversity of properties among catalases
- Author
-
Peter C. Loewen and Jacek Switala
- Subjects
Models, Molecular ,Hot Temperature ,Cyanide ,Kinetics ,Biophysics ,In Vitro Techniques ,Biochemistry ,chemistry.chemical_compound ,Hydroxylamine ,Species Specificity ,Catalytic Domain ,Animals ,Humans ,Enzyme Inhibitors ,Molecular Biology ,chemistry.chemical_classification ,biology ,Bacteria ,Substrate (chemistry) ,Hydrogen Peroxide ,Catalase ,Recombinant Proteins ,Heat inactivation ,Protein Subunits ,Enzyme ,chemistry ,biology.protein ,Azide - Abstract
Catalases from 16 different organisms including representatives from all three phylogenetic clades were purified and characterized to provide a comparative picture of their respective properties. Collectively the enzymes presented a diverse range of activities and properties. Specific activities ranged from 20,700 to 273,800 units per milligram of protein and maximal turnover rates ranged from 54,000 to 833,000 per second. The effective concentrations of common catalase inhibitors, cyanide, azide, hydroxylamine, aminotriazole, and mercaptoethanol, varied over a 100- to 1000-fold concentration range, and a broad range of sensitivities to heat inactivation was observed. Michaelis–Menten kinetics were approximately followed only at the low substrate concentrations. At high H2O2 concentrations, inactivation of small-subunit enzymes resulted in lower velocities than what were predicted, whereas large-subunit enzymes had velocities higher than predicted. Kinetic constants such as Km and Vmax for catalases must be labeled as “apparent.”
- Published
- 2002
25. Template secondary structure can increase the error frequency of the DNA polymerase from Thermus aquaticus
- Author
-
Peter C. Loewen and Jacek Switala
- Subjects
DNA polymerase ,Operon ,Molecular Sequence Data ,DNA-Directed DNA Polymerase ,Polymerase Chain Reaction ,law.invention ,law ,Genetics ,Escherichia coli ,Taq Polymerase ,Thermus ,Protein secondary structure ,Gene ,Polymerase chain reaction ,Thermus aquaticus ,biology ,Base Sequence ,Inverse polymerase chain reaction ,General Medicine ,biology.organism_classification ,Stem-loop ,Catalase ,Molecular biology ,biology.protein ,Nucleic Acid Conformation ,Artifacts - Abstract
Amplification of portions of the intergenic spacer between the katE gene and cryptic cel operon of Escherichia coli was accomplished by the polymerase chain reaction using the DNA polymerase from Thermus aquaticus. Nine different segments were amplified and cloned without error, but one 83-bp fragment was amplified with a high error rate such that 32 of 34 selected clones had three or more nucleotide changes from the expected sequence. The changes were all located in two 9-bp segments immediately adjacent to the 3'-ends of the two primers. Moving the end points of the primers to increase the spacing between them resulted in the isolation of significantly fewer error-containing products. It is proposed that stem-loop structures in the template immediately downstream from the primers interfere with an early stage of elongation and cause misincorporation. This is supported by the observation that destabilisation of one of the stem-loop structures reduced the frequency of errors.
- Published
- 1995
26. Catalase HPII of Escherichia coli catalyzes the conversion of protoheme to cis-heme d
- Author
-
Ingemar von Ossowski, Peter C. Loewen, Peter Nicholls, Alex Hillar, Andrew Christie, Jacek Switala, and Brenda Tattrie
- Subjects
Azides ,Stereochemistry ,Mutant ,Molecular Sequence Data ,Ascorbic Acid ,Heme ,medicine.disease_cause ,Biochemistry ,Polymerase Chain Reaction ,chemistry.chemical_compound ,Residue (chemistry) ,Isomerism ,medicine ,Escherichia coli ,Amino Acid Sequence ,Hydrogen peroxide ,Mercaptoethanol ,chemistry.chemical_classification ,biology ,Base Sequence ,Hydrogen Peroxide ,Catalase ,Recombinant Proteins ,Kinetics ,Enzyme ,chemistry ,Oligodeoxyribonucleotides ,biology.protein ,Mutagenesis, Site-Directed ,Peroxidase ,Plasmids - Abstract
Catalase HPII from aerobically grown Escherichia coli normally contains heme d but cultures grown with poor or no aeration produce HPII containing a mixture of heme d and protoheme IX. The protoheme component of HPII from anaerobically grown cells is converted into heme d during treatment of the purified enzyme with hydrogen peroxide. It is concluded that heme d found in catalase HPII is formed by the cis-hydroxylation of protoheme in a reaction catalyzed by catalase HPII using hydrogen peroxide as a substrate. The distal His128 residue of HPII is absolutely required for the protoheme to heme d conversion. Two mutant enzymes, Ala128 and Asn128, are catalytically inactive and contain only protoheme, which is unaffected by hydrogen peroxide treatment. The Asn201 residue is not an absolute requirement for heme conversion. The mutant enzyme Ala201 contains predominantly heme d and is partially active. However, insertion of a histidyl residue to give the His201 enzyme interferes with the heme conversion reaction. This mutant form is isolated as a protoheme enzyme with limited activity, and a reversible conversion to a heme d-like species occurs in vitro in the presence of continuously generated hydrogen peroxide.
- Published
- 1993
27. The alternative sigma factor katF (rpoS) regulates Salmonella virulence
- Author
-
Stephen J. Libby, Donald G. Guiney, Julia Harwood, Peter C. Loewen, Ferric C. Fang, Nancy A. Buchmeier, and Jacek Switala
- Subjects
Salmonella typhimurium ,Salmonella ,DNA Repair ,Mutant ,Molecular Sequence Data ,Virulence ,Sigma Factor ,Biology ,medicine.disease_cause ,Polymerase Chain Reaction ,Microbiology ,Mice ,Plasmid ,Sigma factor ,Gene expression ,medicine ,Animals ,Regulation of gene expression ,Genetics ,Salmonella Infections, Animal ,Multidisciplinary ,Base Sequence ,Gene Expression Regulation, Bacterial ,Hydrogen-Ion Concentration ,Catalase ,Methyl Methanesulfonate ,Oligodeoxyribonucleotides ,Genes, Bacterial ,rpoS ,Research Article ,DNA Damage - Abstract
Nutrient limitation is a critical signal in Salmonella virulence gene regulation. The katF (rpoS) gene mediates the expression of the Salmonella spv plasmid virulence genes during bacterial starvation. A katF Salmonella mutant has increased susceptibility to nutrient deprivation, oxidative stress, acid stress, and DNA damage, conditions which are relevant to the intraphagosomal environment of host macrophages. Moreover, the katF mutant has significantly reduced virulence in mice. katF encodes an alternative sigma factor of RNA polymerase which coordinately regulates Salmonella virulence.
- Published
- 1992
28. Homology among bacterial catalase genes
- Author
-
Jacek Switala, Peter C. Loewen, and Barbara Triggs-Raine
- Subjects
DNA, Bacterial ,Immunology ,Applied Microbiology and Biotechnology ,Microbiology ,Homology (biology) ,Enterobacteriaceae ,Escherichia ,Sequence Homology, Nucleic Acid ,Genetics ,Escherichia coli ,Molecular Biology ,Gene ,Southern blot ,chemistry.chemical_classification ,Gel electrophoresis ,biology ,Nucleic Acid Hybridization ,General Medicine ,biology.organism_classification ,Catalase ,Blotting, Southern ,Enzyme ,chemistry ,Biochemistry ,biology.protein ,bacteria ,DNA Probes ,Bacteria - Abstract
Catalase activities in crude extracts of exponential and stationary phase cultures of various bacteria were visualized following gel electrophoresis for comparison with the enzymes from Escherichia coli. Citrobacter freundii, Edwardsiella tarda, Enterobacter aerogenes, Klebsiella pneumoniae, and Salmonella typhimurium exhibited patterns of catalase activity similar to E. coli, including bifunctional HPI-like bands and a monofunctional HPII-like band. Proteus mirabilis, Erwinia carotovora, and Serratia marcescens contained a single band of monofunctional catalase with a mobility intermediate between the HPI-like and HPII-like bands. The cloned genes for catalases HPI (katG) and HPII (katE) from E. coli were used as probes in Southern hybridization analyses for homologous sequences in genomic DNA of the same bacteria. katG was found to hybridize with fragments from C. freundii, Ent. aerogenes, Sal. typhimurium, and K. pneumoniae but not at all with Ed. tarda, P. mirabilis, S. marcesens, or Er. carotovora. katE hydridized with C. freundii and K. pneumoniae DNAs and not with the other bacterial DNAs. Key words: catalase genes, bacteria, homology.
- Published
- 1990
29. Molecular characterization of three mutations in katG affecting the activity of hydroperoxidase I of Escherichia coli
- Author
-
Mark Smolenski, Barbara Triggs-Raine, Jacek Switala, and Peter C. Loewen
- Subjects
Mutant ,Molecular Sequence Data ,medicine.disease_cause ,Biochemistry ,Structure-Activity Relationship ,medicine ,Escherichia coli ,Phosphofructokinase 2 ,Cloning, Molecular ,Molecular Biology ,Gene ,Peptide sequence ,Nitrosoguanidines ,chemistry.chemical_classification ,biology ,Base Sequence ,Escherichia coli Proteins ,Spectrum Analysis ,Chromosome Mapping ,Cell Biology ,Hydrogen Peroxide ,Hydrogen-Ion Concentration ,Catalase ,Molecular biology ,Enzyme Activation ,Kinetics ,Enzyme ,chemistry ,Mutation ,biology.protein ,Leucine ,Peroxidase - Abstract
Hydroperoxidase I (HPI) of Escherichia coli is a bifunctional enzyme exhibiting both catalase and peroxidase activities. Mutants lacking appreciable HPI have been generated using nitrosoguanidine and the gene encoding HPI, katG, has been cloned from three of these mutants using either classical probing methods or polymerase chain reaction amplification. The mutant genes were sequenced and the changes from wild-type sequence identified. Two mutants contained G to A changes in the coding strand, resulting in glycine to aspartate changes at residues 119 (katG15) and 314 (katG16) in the deduced amino acid sequence of the protein. A third mutant contained a C to T change resulting in a leucine to phenylalanine change at residue 139 (katG14). The Phe139-, Asp119-, and Asp314-containing mutants exhibited 13
- Published
- 1990
30. Crystallization and preliminary X-ray diffraction analysis of catalase HPII from Escherichia coli
- Author
-
José Tormo, Jacek Switala, Peter C. Loewen, and Ignacio Fita
- Subjects
Diffraction ,biology ,Chemistry ,Resolution (electron density) ,Catalase ,biology.organism_classification ,medicine.disease_cause ,Enterobacteriaceae ,law.invention ,Crystallography ,X-Ray Diffraction ,Structural Biology ,law ,X-ray crystallography ,Escherichia coli ,biology.protein ,medicine ,Crystallization ,Molecular Biology ,Monoclinic crystal system - Abstract
Green crystals of the hexameric catalase HPII from Escherichia coli have been obtained by the hanging-drop method. The crystals belong to the monoclinic space group P 2 with a = 123 A, b = 132 A, c = 93 A, β = 112·5°. There are three subunits in the asymmetric unit. The crystals diffract at least to 3·2 A resolution and are suitable for further X-ray diffraction studies.
- Published
- 1990
31. Purification and characterization of catalase-1 from Bacillus subtilis
- Author
-
Jacek Switala and Peter C. Loewen
- Subjects
Macromolecular Substances ,Cyanide ,Heme ,Bacillus subtilis ,Biochemistry ,chemistry.chemical_compound ,Amino Acids ,Hydrogen peroxide ,Molecular Biology ,chemistry.chemical_classification ,biology ,Spectrum Analysis ,Tryptophan ,Cell Biology ,Hydrogen-Ion Concentration ,Catalase ,biology.organism_classification ,Molecular Weight ,Kinetics ,Enzyme ,chemistry ,biology.protein ,Cysteine - Abstract
The catalase activity produced in vegetative Bacillus subtilis, catalase-1, has been purified to homogeneity. The apparent native molecular weight was determined to be 395 000. Only one subunit type with a molecular weight of 65 000 was present, suggesting a hexamer structure for the enzyme. In other respects, catalase-1 was a typical catalase. Protoheme IX was identified as the heme component on the basis of the spectra of the enzyme and of the isolated hemochromogen. The ratio of protoheme/subunit was 1. The enzyme remained active over a broad pH range of 5–11 and was only slowly inactivated at 65 °C. It was inhibited by cyanide, azide, and various sulfhydryl compounds. The apparent Km for hydrogen peroxide was 40.1 mM. The amino acid composition was typical of other catalases in having relatively low amounts of tryptophan and cysteine.
- Published
- 1987
32. Proposed structure for the prosthetic group of the catalase HPII from Escherichia coli
- Author
-
Russell Timkovich, Jen Ting Chiu, Jacek Switala, Robert B. Gennis, and Peter C. Loewen
- Subjects
Hemeprotein ,biology ,Stereochemistry ,Cytochrome b6f complex ,General Chemistry ,Chromophore ,medicine.disease_cause ,Photochemistry ,Biochemistry ,Porphyrin ,Catalysis ,Cofactor ,chemistry.chemical_compound ,Colloid and Surface Chemistry ,chemistry ,medicine ,biology.protein ,Carbon monoxide binding ,Heme ,Escherichia coli - Abstract
Escherichia coli contains two catalases designated HPI and HPII. The heme prosthetic group of HPII is an unusual green chromophore that was believed to be a member of the family of d-type hemes. The heme was extracted and compared to the heme of the terminal oxidase cytochrome complex in E. coli. The two hemes were very similar by visible spectroscopy but were resolved by chromatography. The heme was converted to a free-base, esterified derivative that was characterized by 'H NMR spectroscopy, infrared spectroscopy, and mass spectrometry. The proposed structure for the free base is 12-hydroxy- 1 3-cis-spirolactone-2,7,12,18-tetramethyl-3,8-divinyl- 17-propionylporphyrin. The respiratory electron-transport chain of certain aeorobic bacteria contains an unusual prosthetic group for the terminal oxidase. This group, originally called heme a2 but later renamed to heme d, is the oxygen, carbon monoxide binding site. It is spectroscopically characterized by a red shift of the a band in the visible spectrum. In 1956 Barrett' extensively investigated the properties of heme a2 and the porphyrin derived by iron removal and tentatively proposed that it was a dihydroporphyrin. In 1985 it was shown by isolation and purification of the chlorin derived from the heme of the terminal oxidase in E. coli that the basic
- Published
- 1989
33. Purification and characterization of catalase HPII from Escherichia coli K12
- Author
-
Jacek Switala and Peter C. Loewen
- Subjects
Catalase HPII ,biology ,Macromolecular Substances ,Chemistry ,Cell Biology ,Catalase ,medicine.disease_cause ,Biochemistry ,Molecular biology ,Isoenzymes ,Molecular Weight ,Kinetics ,Peroxidases ,Escherichia coli ,medicine ,biology.protein ,Hydroperoxidase II ,Molecular Biology ,Catalase HPI ,Peroxidase - Abstract
Catalase (hydroperoxidase II or HPII) of Escherichia coli K12 has been purified using a protocol that also allows the purification of the second catalase HPI in large amounts. The purified HPII was found to have equal amounts of two subunits with molecular weights of 90 000 and 92 000. Only a single 92 000 subunit was present in the immunoprecipitate created when HPII antiserum was added directly to a crude extract, suggesting that proteolysis was responsible for the smaller subunit. The apparent native molecular weight was determined to be 532 000, suggesting a hexamer structure for the enzyme, an unusual structure for a catalase. HPII was very stable, remaining maximally active over the pH range 4–11 and retaining activity even in a solution of 0.1% sodium dodecyl sulfate and 7 M urea. The heme cofactor associated with HPII was also unusual for a catalase, in resembling heme d (a2) both spectrally and in terms of solubility. On the basis of heme-associated iron, six heme groups were associated with each molecule of enzyme or one per subunit.
- Published
- 1986
34. Catalases HPI and HPII in Escherichia coli are induced independently
- Author
-
Peter C. Loewen, Barbara Triggs-Raine, and Jacek Switala
- Subjects
Transposable element ,Biophysics ,Succinic Acid ,Lactose ,Ascorbic Acid ,Citrate (si)-Synthase ,medicine.disease_cause ,Biochemistry ,Electron Transport ,Malate Dehydrogenase ,Carbon source ,medicine ,Tn10 ,Escherichia coli ,Enzyme inducer ,Molecular Biology ,Polyacrylamide gel electrophoresis ,biology ,Succinates ,biochemical phenomena, metabolism, and nutrition ,Catalase ,Culture Media ,Citric acid cycle ,Glucose ,Peroxidases ,Enzyme Induction ,Mutation ,biology.protein ,bacteria ,Electrophoresis, Polyacrylamide Gel - Abstract
Three strains of Escherichia coli differing only in the catalase locus mutated by transposon Tn10 were constructed. These strains produced only catalase HPI (katE::Tn10 and katF::Tn10 strains) or catalase HPII (katG::Tn10). HPI levels increased gradually about twofold during logarithmic growth but did not increase during growth into stationary phase in rich medium. HPII levels, which were initially threefold lower than HPI levels, did not change during logarithmic growth but did increase tenfold during growth into stationary phase. HPI levels increased in response to ascorbate or H2O2 being added to the medium but HPII levels did not. In minimal medium, any carbon source derived from the tricarboxylic acid cycle caused five- to tenfold higher HPII levels during logarithmic growth but had very little effect on HPI levels. Active electron transport did not affect either HPI or HPII levels.
- Published
- 1985
35. Effect of ascorbate on oxygen uptake and growth of Escherichia coli B
- Author
-
Peter C. Loewen, Jacek Switala, and Holly E. Richter
- Subjects
Immunology ,Stimulation ,Ascorbic Acid ,medicine.disease_cause ,Applied Microbiology and Biotechnology ,Microbiology ,chemistry.chemical_compound ,Oxygen Consumption ,Nitrate ,Genetics ,medicine ,Escherichia coli ,Anaerobiosis ,Molecular Biology ,Edetic Acid ,chemistry.chemical_classification ,biology ,General Medicine ,Electron acceptor ,biology.organism_classification ,Ascorbic acid ,Enterobacteriaceae ,Culture Media ,chemistry ,Biochemistry ,Bacteria - Abstract
The addition of ascorbate to aerobically growing cultures of Escherichia coli B caused only a short pause in growth and no subsequent change in the rate or extent of growth. The effect of ascorbate on oxygen uptake varied from inhibition in minimal medium to stimulation in rich medium. Cyanide-resistant growth and oxygen uptake were stimulated by ascorbate. Both the rate and extent of anaerobic growth were stimulated in proportion to the amount of ascorbate added when fumarate was the terminal electron acceptor. Ascorbate had no effect on any aspect of anaerobic growth in the absence of a terminal electron acceptor or in the presence of nitrate.
- Published
- 1988
36. Purification and characterization of spore-specific catalase-2 from Bacillus subtilis
- Author
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Peter C. Loewen and Jacek Switala
- Subjects
chemistry.chemical_classification ,Spores, Bacterial ,biology ,Chemistry ,Cyanide ,Ether ,Cell Biology ,Bacillus subtilis ,biology.organism_classification ,Catalase ,Biochemistry ,Molecular Weight ,chemistry.chemical_compound ,Enzyme ,Bacterial Proteins ,Spectrophotometry ,biology.protein ,Urea ,Azide ,Amino Acids ,Molecular Biology ,Heme - Abstract
Catalase-2, the catalase found in spores of Bacillus subtilis, has been purified to homogeneity from a nonsporulating strain. The apparent native molecular weight is 504 000. The enzyme appears to be composed of six identical protomers with a molecular weight of 81 000 each. The amino acid composition is similar to the composition of other catalases. Like most catalases, catalase-2 exhibits a broad pH optimum from pH 4 to pH 12 and is sensitive to cyanide, azide, thiol reagents, and amino triazole. The apparent Km for H2O2 is 78 mM. The enzyme exhibits extreme stability, losing activity only slowly at 93 °C and remaining active in 1% SDS – 7 M urea. The green-colored enzyme exhibits a spectrum like heme d with a Soret absorption at 403 nm and a molar absorptivity consistent with one heme per subunit. The heme cannot be extracted with acetone–HCl or ether, suggesting that it is covalently bound to the protein.
- Published
- 1988
37. DNA repair is more important than catalase for Salmonella virulence in mice
- Author
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Peter C. Loewen, Yisheng Xu, Ferric C. Fang, Nancy A. Buchmeier, Donald G. Guiney, Jacek Switala, and Stephen J. Libby
- Subjects
Salmonella typhimurium ,DNA Repair ,DNA repair ,Acatalasia ,Mutant ,Molecular Sequence Data ,Virulence ,medicine.disease_cause ,Microbiology ,Mice ,medicine ,Animals ,chemistry.chemical_classification ,Reactive oxygen species ,Mice, Inbred BALB C ,biology ,Base Sequence ,Escherichia coli Proteins ,Macrophages ,General Medicine ,Hydrogen Peroxide ,medicine.disease ,Catalase ,Survival Analysis ,Respiratory burst ,Oxidative Stress ,chemistry ,biology.protein ,Female ,Oxidative stress ,Research Article - Abstract
Pathogenic microorganisms possess antioxidant defense mechanisms for protection from reactive oxygen metabolites such as hydrogen peroxide (H2O2), which are generated during the respiratory burst of phagocytic cells. These defense mechanisms include enzymes such as catalase, which detoxify reactive oxygen species, and DNA repair systems which repair damage resulting from oxidative stress. To determine the relative importance of these two potentially protective defense mechanisms against oxidative stress encountered by Salmonella during infection of the host, a Salmonella typhimurium double mutant unable to produce either the HPI or HPII catalase was constructed, and compared with an isogenic recA mutant deficient in DNA repair. The recA mutant was hypersusceptible to H2O2 at low cell densities in vitro, while the catalase mutant was more susceptible to high H2O2 concentrations at high cell densities. The catalase mutant was found to be resistant to macrophages and retained full murine virulence, in contrast to the recA mutant which previously was shown to be macrophage-sensitive and attenuated in mice. These observations suggest that Salmonella is subjected to low concentrations of H2O2 while at relatively low cell density during infection, conditions requiring an intact DNA repair system but not functional catalase activity.
Catalog
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