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1.
World J Microbiol Biotechnol ; 31(7): 1137-45, 2015 Jul.
Article in English | MEDLINE | ID: mdl-25940328

ABSTRACT

Quercetins, vitisin A and hydroxytyrosol are phenolic compounds possessing several positive properties to human health. This paper refers on the possible effects of two wine yeast species, Saccharomyces cerevisiae and Starmerella bacillaris (synonym Candida zemplinina) on the accumulation of these compounds in experimental Sangiovese wines. A single lot of Sangiovese grapes was fermented by S. cerevisiae alone or by sequential inoculum of C. zemplinina and S. cerevisiae under two aeration conditions. The accumulation of quercetin and its glycosides resulted only influenced by must aeration. However, yeast species occurring in the fermentative process affected the relative abundances among the different forms of quercetin. Vitisin A contents were higher in wines produced in the presence of C. zemplinina. Finally, higher concentrations of hydroxytyrosol and tyrosol were found in wines produced by S. cerevisiae alone under non-aerated condition. The fermentation of different Sangiovese grape musts carried out by the assayed S. cerevisiae strain pointed out that slow fermentation kinetics lead to higher levels of hydroxytyrosol and tyrosol. The study underlines the role of yeast species in determining the accumulation of bioactive compounds in Sangiovese wine.


Subject(s)
Candida/physiology , Saccharomyces cerevisiae/physiology , Vitis/microbiology , Wine/analysis , Benzofurans/metabolism , Fermentation , Kinetics , Phenols/metabolism , Phenylethyl Alcohol/analogs & derivatives , Phenylethyl Alcohol/metabolism , Quercetin/metabolism , Vitis/chemistry , Wine/microbiology
2.
Curr Med Chem ; 17(9): 826-46, 2010.
Article in English | MEDLINE | ID: mdl-20156173

ABSTRACT

Many enzymes and proteins are regulated by their quaternary structure and/or by their association in homo- and/or hetero-oligomer complexes. Thus, these protein-protein interactions can be good targets for blocking or modulating protein function therapeutically. The large number of oligomeric structures in the Protein Data Bank (http://www.rcsb.org/) reflects growing interest in proteins that function as multimeric complexes. In this review, we consider the particular case of homodimeric enzymes as drug targets. There is intense interest in drugs that inhibit dimerization of a functionally obligate homodimeric enzyme. Because amino acid conservation within enzyme interfaces is often low compared to conservation in active sites, it may be easier to achieve drugs that target protein interfaces selectively and specifically. Two main types of dimerization inhibitors have been developed: peptides or peptidomimetics based on sequences involved in protein-protein interactions, and small molecules that act at hot spots in protein-protein interfaces. Examples include inhibitors of HIV protease and HIV integrase. Studying the mechanisms of action and locating the binding sites of such inhibitors requires different techniques for different proteins. For some enzymes, ligand binding is only detectable in vivo or after unfolding of the complexes. Here, we review the structural features of dimeric enzymes and give examples of inhibition through interference in dimer stability. Several techniques for studying these complex phenomena will be presented.


Subject(s)
Enzyme Inhibitors/chemistry , Enzymes/chemistry , Anti-HIV Agents/chemistry , Anti-HIV Agents/pharmacology , Binding Sites , Biomimetic Materials/chemistry , Biomimetic Materials/pharmacology , Dimerization , Enzyme Inhibitors/pharmacology , Enzymes/metabolism , HIV Integrase/chemistry , HIV Integrase/metabolism , HIV Protease/chemistry , HIV Protease/metabolism , Protein Binding
3.
J Mol Biol ; 336(3): 707-16, 2004 Feb 20.
Article in English | MEDLINE | ID: mdl-15095982

ABSTRACT

The catalytic domain of matrix metalloproteinase-10 (MMP-10) has been expressed in Escherichia coli and its crystal structure solved at 2.1 A resolution. The availability of this structure allowed us to critically examine the small differences existing between the catalytic domains of MMP-3 and MMP-10, which show the highest sequence identity among all MMPs. Furthermore, the binding mode of N-isobutyl-N-[4-methoxyphenylsulfonyl]glycyl hydroxamic acid (NNGH), which is one of the most known commercial inhibitors of MMPs, is described for the first time.


Subject(s)
Metalloendopeptidases/chemistry , Protein Structure, Tertiary , Amino Acid Sequence , Catalytic Domain , Crystallography, X-Ray , Humans , Matrix Metalloproteinase 10 , Metalloendopeptidases/genetics , Metalloendopeptidases/metabolism , Models, Molecular , Molecular Sequence Data , Molecular Structure , Sequence Alignment
4.
Acta Paediatr Suppl ; 91(441): 12-7, 2003 Sep.
Article in English | MEDLINE | ID: mdl-14599037

ABSTRACT

Inappropriate infant feeding including a lack of breastfeeding and the early introduction of cow's milk are the most common forms of infant feeding malpractice. To evaluate the hypothesis that infant feeding malpractices are associated with mothers' low level of education, questionnaires were administered to 400 mothers of infants below 12 mo of age divided into 3 groups according to their various educational levels. Items included the type of milk given at birth and at 1, 3 and 6 mo of age. To investigate the efficacy of paediatricians in orienting infant feeding, the same questionnaire was given to 30 paediatricians in primary paediatric healthcare, in hospitals or in private practices. Initiation of breastfeeding was similar in the three groups. An analysis of the data showed that an increasing number of infants born to mothers of low and intermediate educational level did not receive exclusive breastfeeding compared with those with a higher level of education, a difference that was significant as early as 1 mo of age. In infants aged 3 mo, the prevalence of exclusive breastfeeding was 37%, 40% and 65% in the three groups, respectively, in relation to progressively increasing levels of education. In infants of 6 mo, the respective prevalence rates were 13%, 15% and 48%. Early introduction of cow's milk showed a similar correlation with educational level. A greater number of infants born to mothers with a low level of education received cow's milk at 3 mo of age compared with those born to mothers with an intermediate education (12% vs 5%). A similar difference was observed between the latter group and infants born to mothers with a high educational level (0%). This pattern was supported by data for infants at 6 mo of age with prevalence rates for cow's milk feeding of 39%, 20% and 0% in the three groups in association with progressively increasing level of educational (p < 0.05). The analysis of the paediatricians' response to the questionnaire showed that while physicians know and correctly prescribe age-related infant nutrition regimens, they are unaware that a substantial number of mothers do not comply with what they prescribe. Overall, these data support the relationship between a low educational level and infant feeding malpractice and suggest that a more effective role should be played by paediatricians in supporting an adequate duration of breastfeeding and the use of formula rather than cow's milk protein.


Subject(s)
Breast Feeding , Educational Status , Adult , Animals , Female , Humans , Infant , Infant, Newborn , Milk , Pediatrics , Physician's Role , Surveys and Questionnaires , Time Factors
5.
J Synchrotron Radiat ; 9(Pt 2): 103-4, 2002 Mar 01.
Article in English | MEDLINE | ID: mdl-11872932

ABSTRACT

The proceedings of BIOXAS 2001 (Siena, Italy, 2001) and both current and planned activities in the field of biological X-ray absorption spectroscopy are discussed against the perspective of changes in the perception of the technique since ICBIC 1 (Florence, Italy, 1983).


Subject(s)
Spectrum Analysis/methods , X-Rays , Humans
6.
J Biol Inorg Chem ; 6(8): 778-90, 2001 Oct.
Article in English | MEDLINE | ID: mdl-11713685

ABSTRACT

The structure of Bacillus pasteurii urease (BPU) inhibited with phosphate was solved and refined using synchrotron X-ray diffraction data from a vitrified crystal (1.85 A resolution, 99.3% completeness, data redundancy 4.6, R-factor 17.3%, PDB code 6UBP). A distance of 3.5 A separates the two Ni ions in the active site. The binding mode of the inhibitor involves the formation of four coordination bonds with the two Ni ions: one phosphate oxygen atom symmetrically bridges the two metal ions (1.9-2.0 A), while two of the remaining phosphate oxygen atoms bind to the Ni atoms at 2.4 A. The fourth phosphate oxygen is directed into the active site channel. Analysis of the H-bonding network around the bound inhibitor indicates that phosphate is bound as the H2PO4- anion, and that an additional proton is present on the Odelta2 atom of Asp(alpha363), an active site residue involved in Ni coordination through Odelta1. The flexible flap flanking the active site cavity is in the open conformation. Analysis of the complex reveals why phosphate is a relatively weak inhibitor and why sulfate does not bind to the nickels in the active site. The implications of the results for the understanding of the urease catalytic mechanism are reviewed. A novel alternative for the proton donor is presented.


Subject(s)
Phosphates/pharmacology , Urease/antagonists & inhibitors , Bacillus/chemistry , Bacillus/enzymology , Binding Sites , Crystallization , Models, Molecular , Nickel/chemistry , Phosphates/chemistry , Protein Conformation , Structure-Activity Relationship , Urease/chemistry , X-Ray Diffraction
7.
Chem Res Toxicol ; 14(10): 1353-62, 2001 Oct.
Article in English | MEDLINE | ID: mdl-11599926

ABSTRACT

The interactions between Cu(II)-amikacin complexes [Cu(II)-Ami] and hydrogen peroxide were studied by spectroscopy (EPR, UV-vis, CD, XAS) and cyclic voltammetry. A monomer-dimer equilibrium was detected at complex concentrations above 5 mM (log K(dim) = 1.84 +/- 0.03). The dimeric complex undergoes easy, although irreversible oxidation (ca. 0.5-0.6 V) to a Cu(III) species on platinum electrode. However, the monomeric complexes are able to catalyze hydrogen peroxide disproportionation reaction at pH 7.4 in a multistep process, mediated by hydroxyl radicals and involving both Cu(I)/Cu(II) and Cu(II)/Cu(III) redox pairs.


Subject(s)
Amikacin/chemistry , Anti-Bacterial Agents/chemistry , Copper/chemistry , Hydrogen Peroxide/chemistry , Oxidants/chemistry , Catalysis , Electrodes , Hydrogen-Ion Concentration , Oxidation-Reduction , Platinum , Spectrum Analysis
8.
Biochemistry ; 39(40): 12391-7, 2000 Oct 10.
Article in English | MEDLINE | ID: mdl-11015219

ABSTRACT

The three-dimensional structure of a possible intermediate in the hydration reaction of cyanamide to urea catalyzed by human carbonic anhydrase II (hCAII) has been determined by cryocrystallographic techniques. The crystal structure shows that two different adducts are formed under the experimental conditions and that they have different occupancy in the crystal. The high occupancy form consists of a binary hCAII-cyanamide complex where the substrate has replaced the zinc-bound hydroxide anion present in the native enzyme, maintaining the tetrahedral geometry around the metal ion. The second, low-occupancy form consists of a hCAII-cyanamide-water ternary complex where the catalytic zinc ion, still being bound to cyanamide, is approached by a water molecule in a five-coordinate adduct. While the first form can be considered a nonproductive complex, the second form may represent an intermediate state of the catalyzed reaction where the water molecule is about to perform a nucleophilic attack on the zinc-activated cyanamide substrate. The structural evidence is consistent with the kinetic data previously reported about this recently described hydrolytic reaction catalyzed by hCAII, and indicates that a different mechanism with respect to that generally accepted for the physiologic carbon dioxide hydration reaction may be adopted by the enzyme, depending on the substrate chemical properties.


Subject(s)
Carbonic Anhydrases/chemistry , Cyanamide/chemistry , Binding Sites , Carbonic Anhydrase Inhibitors/chemistry , Carbonic Anhydrases/metabolism , Catalysis/drug effects , Crystallization , Crystallography, X-Ray/methods , Fourier Analysis , Freezing , Humans , Hydrogen Bonding , Kinetics , Models, Molecular , Nitrates/chemistry , Urea/chemistry , Urea/metabolism , Water , Zinc/chemistry
9.
J Biol Inorg Chem ; 5(1): 110-8, 2000 Feb.
Article in English | MEDLINE | ID: mdl-10766443

ABSTRACT

The structure of Bacillus pasteurii urease inhibited with acetohydroxamic acid was solved and refined anisotropically using synchrotron X-ray cryogenic diffraction data (1.55 A resolution, 99.5% completeness, data redundancy = 26, R-factor = 15.1%, PDB code 4UBP). The two Ni ions in the active site are separated by a distance of 3.53 A. The structure clearly shows the binding mode of the inhibitor anion, symmetrically bridging the two Ni ions in the active site through the hydroxamate oxygen and chelating one Ni ion through the carbonyl oxygen. The flexible flap flanking the active site cavity is in the open conformation. The possible implications of the results on structure-based molecular design of new urease inhibitors are discussed.


Subject(s)
Bacillus/enzymology , Hydroxamic Acids/chemistry , Urease/chemistry , Anions , Binding Sites , Enzyme Inhibitors/chemistry , Models, Molecular , Protein Conformation , Urease/antagonists & inhibitors , X-Ray Diffraction
10.
J Biol Inorg Chem ; 4(5): 528-36, 1999 Oct.
Article in English | MEDLINE | ID: mdl-10550681

ABSTRACT

The interaction of human carbonic anhydrase (hCA) isozymes I and II with cyanamide, a linear molecule isoelectronic with the main physiological substrate of the enzyme, CO(2), was investigated through spectroscopic, kinetic, and X-ray crystallographic studies. We show here that cyanamide is hydrated to urea in the presence of CAs, and that it also acts as a weak non-competitive inhibitor (K(I)=61+/-3 mM and 238+/-9 mM for hCA II and hCA I, respectively) towards the esterasic activity of these enzymes, as tested with 4-nitrophenyl acetate. Changes in the spectrum of the Co(II)-hCA II derivative observed in the presence of cyanamide suggest that it likely binds the metal ion within the CA active site, adding to the coordination sphere, not substituting the metal-bound solvent molecule. It thereafter undergoes a nucleophilic attack from the metal-bound hydroxide ion, forming urea which remains bound to the metal, as observed in the X-ray crystal structure of hCA II soaked in cyanamide solutions for several hours. The urea molecule is directly coordinated to the active site Zn(II) ion through a protonated nitrogen atom. Several hydrogen bonds involving active site residues Thr199 and Thr200 as well as three water molecules (Wat99, Wat122, and Wat123) further stabilize the urea-hCA II adduct. Kinetic studies in solution further proved that urea acts as a tight binding inhibitor of the two isozymes hCA I and hCA II, with very slow binding kinetics (k(on) = 2.5 x 10(-5)s(-1)M(-1)). A mechanism to explain the hydration process of cyanamide by CAs, as well as the tight binding of urea in the active site, is also proposed based on the hypothesis that urea is deprotonated when bound to the enzyme. Cyanamide is thus the first true suicide substrate of this enzyme for which binding has been documented by means of X-ray crystallographic and spectroscopic studies.


Subject(s)
Carbonic Anhydrases/metabolism , Cyanamide/metabolism , Carbonic Anhydrases/chemistry , Catalysis , Crystallography, X-Ray , Humans , In Vitro Techniques , Kinetics , Models, Molecular , Protein Conformation , Recombinant Proteins/metabolism , Urea/metabolism , Water/metabolism
11.
Structure ; 7(2): 205-16, 1999 Feb 15.
Article in English | MEDLINE | ID: mdl-10368287

ABSTRACT

BACKGROUND: Urease catalyzes the hydrolysis of urea, the final step of organic nitrogen mineralization, using a bimetallic nickel centre. The role of the active site metal ions and amino acid residues has not been elucidated to date. Many pathologies are associated with the activity of ureolytic bacteria, and the efficiency of soil nitrogen fertilization with urea is severely decreased by urease activity. Therefore, the development of urease inhibitors would lead to a reduction of environmental pollution, to enhanced efficiency of nitrogen uptake by plants, and to improved therapeutic strategies for treatment of infections due to ureolytic bacteria. Structure-based design of urease inhibitors would require knowledge of the enzyme mechanism at the molecular level. RESULTS: The structures of native and inhibited urease from Bacillus pasteurii have been determined at a resolution of 2.0 A by synchrotron X-ray cryogenic crystallography. In the native enzyme, the coordination sphere of each of the two nickel ions is completed by a water molecule and a bridging hydroxide. A fourth water molecule completes a tetrahedral cluster of solvent molecules. The enzyme crystallized in the presence of phenylphosphorodiamidate contains the tetrahedral transition-state analogue diamidophosphoric acid, bound to the two nickel ions in an unprecedented mode. Comparison of the native and inhibited structures reveals two distinct conformations of the flap lining the active-site cavity. CONCLUSIONS: The mode of binding of the inhibitor, and a comparison between the native and inhibited urease structures, indicate a novel mechanism for enzymatic urea hydrolysis which reconciles the available structural and biochemical data.


Subject(s)
Bacillus/enzymology , Urease/chemistry , Binding Sites , Crystallization , Crystallography, X-Ray , Drug Design , Enzyme Inhibitors/metabolism , Helix-Turn-Helix Motifs , Models, Molecular , Molecular Sequence Data , Nickel/chemistry , Organophosphates/chemistry , Protein Binding , Protein Conformation , Urea/metabolism , Urease/metabolism
12.
J Mol Biol ; 288(3): 413-26, 1999 May 07.
Article in English | MEDLINE | ID: mdl-10329151

ABSTRACT

The crystal structure of the engineered monomeric human Cu,ZnSOD triple mutant F50E/G51E/E133Q (Q133M2SOD) is reported at atomic resolution (1.02 A). This derivative has about 20 % of the wild-type activity. Crystals of Q133M2SOD have been obtained in the presence of CdCl2. The metal binding site is disordered, with both cadmium and copper ions simultaneously binding to the copper site. The cadmium (II) ions occupy about 45 % of the copper sites by binding the four histidine residues which ligate copper in the native enzyme, and two further water molecules to complete octahedral coordination. The copper ion is tri-coordinate, and the fourth histidine (His63) is detached from copper and bridges cadmium and zinc. X-ray absorption spectroscopy performed on the crystals suggests that the copper ion has undergone partial photoreduction upon exposure to the synchrotron light. The structure is also disordered in the disulfide bridge region of loop IV that is located at the subunit/subunit interface in the native SOD dimer. As a consequence, the catalytically relevant Arg143 residue is disordered. The present structure has been compared to other X-ray structures on various isoenzymes and to the solution structure of the same monomeric form. The structural results suggest that the low activity of monomeric SOD is due to the disorder in the conformation of the side-chain of Arg143 as well as of loop IV. It is proposed that the subunit-subunit interactions in the multimeric forms of the enzyme are needed to stabilize the correct geometry of the cavity and the optimal orientation of the charged residues in the active channel. Furthermore, the different coordination of cadmium and copper ions, contemporaneously present in the same site, are taken as models for the oxidized and reduced copper species, respectively. These properties of the structure have allowed us to revisit the enzymatic mechanism.


Subject(s)
Superoxide Dismutase/chemistry , Binding Sites , Cadmium/metabolism , Catalysis , Copper/metabolism , Crystallography, X-Ray , Humans , Models, Molecular , Mutagenesis , Protein Conformation , Spectrometry, X-Ray Emission , Superoxide Dismutase/genetics , Superoxide Dismutase/metabolism
13.
Acta Crystallogr D Biol Crystallogr ; 55(Pt 4): 901-3, 1999 Apr.
Article in English | MEDLINE | ID: mdl-10089329

ABSTRACT

Hydroxyquinol 1,2-dioxygenase (HQ1,2O) from Nocardioides simplex 3E, an enzyme involved in the aerobic biodegradation of a large class of chloroaromatic compounds such as 2,4-dichlorophenoxyacetate (2,4-D) and 2,4,5-trichlorophenoxyacetate (2,4,5-T), has been crystallized. HQ1,2O, which specifically catalyzes the intradiol cleavage of hydroxyquinol (1,2,4-trihydroxybenzene), an intermediate in the degradation of a variety of aromatic pollutants, to maleylacetate, has been recently purified to homogeneity. The enzyme is an homodimer composed of two identical subunits in a alpha 2-type quaternary structure, has a molecular weight of about 65 kDa and contains a catalytically essential Fe(III) ion. Crystals of HQ1,2O obtained using 2% PEG 400 and 2 M ammonium sulfate at pH 7.5 as precipitants belong to the orthorhombic space group P212121, with unit-cell parameters a = 81.15 (6), b = 86.79 (7), c = 114.93 (8). Assuming one dimer per asymmetric unit, the Vm value is 2.51 A3 Da-1. A complete native data set to 1.8 A resolution has been collected on a laboratory source. This is the first intradiol dioxygenase which specifically catalyzes the cleavage of hydroxyquinol to give diffraction-quality crystals.


Subject(s)
Actinomycetales/enzymology , Dioxygenases , Hydrocarbons, Chlorinated/metabolism , Oxygenases/chemistry , Oxygenases/metabolism , Biodegradation, Environmental , Crystallization , X-Ray Diffraction
14.
J Biol Inorg Chem ; 4(6): 795-803, 1999 Dec.
Article in English | MEDLINE | ID: mdl-10631612

ABSTRACT

The solution structure of a mutated (Phe50Glu, Gly51Glu, Val148Lys, Ile151Lys), reduced, monomeric form of human copper,zinc superoxide dismutase (SOD; 153 amino acids) has been determined through 2237 meaningful nuclear Overhauser enhancements, out of 2492, and 43 dihedral angle constraints. A characteristic of this mutant is that of having the same overall charge as the dimeric protein, but an activity of only 20% with respect to wild-type SOD. This protein, at variance with a previously characterized monomeric form (Phe50Glu, Gly51Glu, Glu133Gln), does not contain mutations in the active site. Therefore, its characterization allows us to understand the structural changes independently induced by the monomerization and by the active site mutation. The family of 36 conformers, which have a target function with respect to the experimental constraints lower than 1.5 A2, has RMSD values with respect to the average structure of 0.94 +/- 0.14 A2 and 1.50 +/- 0.14 A2 for the backbone and the heavy atoms, respectively. The overall folding, which includes the classical eight-stranded Greek-key beta-barrel and a short alpha-helix, is very close to that of the previously characterized monomeric mutant E133QM2SOD and to that of wild-type SOD. The region involved in the subunit-subunit interactions in the dimeric protein is confirmed to be disordered in the monomeric species. It is also observed that a sizable rearrangement of the charged groups of the electrostatic loop and of Arg143 takes place in the monomeric species. The width of the active site channel, both at its entrance and at the bottleneck of the active site, is discussed in the light of the influence on the enzymatic activity and the latter with respect to the overall charge. It is also confirmed that the NH proton of His63 shields the Cu(I) from the bulk solvent, thus supporting the suggestion that superoxide may interact with the reduced metal ion in an outer-sphere fashion.


Subject(s)
Superoxide Dismutase/chemistry , Binding Sites , Catalysis , Copper/metabolism , Humans , Magnetic Resonance Spectroscopy , Protein Conformation , Static Electricity , Superoxide Dismutase/metabolism , Zinc/metabolism
15.
Acta Crystallogr D Biol Crystallogr ; 54(Pt 3): 409-12, 1998 May 01.
Article in English | MEDLINE | ID: mdl-9761912

ABSTRACT

Hexagonal crystals of urease from Bacillus pasteurii have been obtained by vapour diffusion at 293 K in 20 mM Tris-HCl, neutral pH, containing 50 mM Na2SO3. Isomorphous crystals of urease inhibited with beta-mercaptoethanol were also obtained by including 4 mM of the inhibitor in the enzyme solution. Crystals of the native and inhibited enzyme diffract respectively to 2.00 A (96.7% completeness) and to 1.65 A (98.7% completeness) using synchrotron X-ray cryogenic (100 K) conditions. The space group is P6322 for both forms, and the unit-cell parameters are a = b = 131.36, c = 189. 76 A for native urease and a = b = 131.34, c = 190.01 A for inhibited urease. Under the same conditions, single crystals of B. pasteurii urease inhibited with acetohydroxamic acid, cisteamine, and phenylphosphorodiamidate were also obtained.


Subject(s)
Bacillus/enzymology , Enzyme Inhibitors/pharmacology , Mercaptoethanol/pharmacology , Urease/antagonists & inhibitors , Crystallization , Cysteamine/pharmacology , Hydroxamic Acids/pharmacology , Synchrotrons , X-Ray Diffraction
16.
FEBS Lett ; 433(1-2): 58-62, 1998 Aug 14.
Article in English | MEDLINE | ID: mdl-9738933

ABSTRACT

The intradiol cleaving dioxygenases hydroxyquinol 1,2-dioxygenase (HQI,20) from Nocardiodes simplex 3E, chlorocatechol 1,2-dioxygenase (CIC1,20) from Rhodococcus erythropolis ICP, and their anaerobic substrate adducts (hydroxyquinol-HQ1,20 and 4-chlorocatechol-CIC1,20) have been characterized through X-ray absorption spectroscopy. In both enzymes the iron(III) is pentacoordinated and the distance distribution inside the Fe(III) first coordination shell is close to that already found in the extensively characterized protocatechuate 3,4-dioxygenase. The coordination number and the bond lengths are not significantly affected by the substrate binding. Therefore it is confirmed that the displacement of a protein donor upon substrate binding has to be considered a general step valid for all intradiol dioxygenases.


Subject(s)
Dioxygenases , Oxygenases/chemistry , Spectrum Analysis , Actinomycetales/enzymology , Binding Sites , Catechols/metabolism , Ferric Compounds/chemistry , Hydroquinones/metabolism , Oxygenases/metabolism , Rhodococcus/enzymology , Substrate Specificity , X-Rays
17.
Biometals ; 10(4): 239-46, 1997 Oct.
Article in English | MEDLINE | ID: mdl-9353870

ABSTRACT

Three strains of Saccharomyces cerevisiae, SC-1, DBVPG 6173 and DBVPG 6037, were studied for vanadate resistance in complex Sabouraud medium since they did not thrive in different minimal media (yeast nitrogen base with and without amino acids). The strain SC-1 was resistant up to 16 mM of vanadate, whereas the strains DBVPG 6173 and DBVPG 6037 were inhibited by 8 mM and 4 mM vanadate, respectively. The vanadate resistance in strain SC-1 was constitutive and due to the reduction of this oxyanion to vanadyl, which was detected by EPR spectroscopy and visible spectroscopy. The transformation of vanadate to vanadyl took place during the exponential growth phase; 10 mM of vanadate was reduced to vanadyl outside the cells since the oxyanion was not detected in the cell biomass and only a negligible concentration of vanadyl (25 nmoles mg-1 cells dry weight) was found in the biomass. The other two vanadate-sensitive yeast strains only accumulated vanadate and did not reduce the oxyanion to vanadyl.


Subject(s)
Saccharomyces cerevisiae/metabolism , Vanadates/metabolism , Biomass , Culture Media , Drug Resistance , Electron Spin Resonance Spectroscopy , Magnetic Resonance Spectroscopy , Oxidation-Reduction , Saccharomyces cerevisiae/genetics , Saccharomyces cerevisiae/growth & development , Spectrophotometry , Vanadates/chemistry
18.
Biochemistry ; 36(34): 10384-92, 1997 Aug 26.
Article in English | MEDLINE | ID: mdl-9265618

ABSTRACT

The interaction of native and Co(II)-substituted isozymes I and II of carbonic anhydrase (CA) with histamine, a well-known activator, was investigated kinetically, spectroscopically, and X-ray crystallographically. This activator is of the noncompetitive type with 4-nitrophenyl acetate and CO2 as substrates for both HCA I and HCA II. The electronic spectrum of the adduct of Co(II)-HCA II with histamine is similar to the spectrum of the Co(II)-HCA II-phenol adduct, being only slightly different from that of the uncomplexed enzyme. This is the first spectroscopic evidence that the activator molecule binds within the active site, but not directly to the metal ion. X-ray crystallographic data for the adduct of HCA II with histamine showed that the activator molecule is bound at the entrance of the active site cavity in a position where it may actively participate in shuttling protons between the active site and the bulk solvent. The role of the activators and the reported X-ray crystal structure of the HCA II-histamine adduct has prompted us to reexamine the X-ray structures of the different CA isozymes in order to find a structural basis accounting for their large differences in catalytic rate. A tentative explanation is proposed on the basis of possible pathways of proton transfer, which constitute the rate-limiting step in the catalytic reaction.


Subject(s)
Carbonic Anhydrases/chemistry , Histamine/metabolism , Carbonic Anhydrases/metabolism , Cobalt/metabolism , Crystallography, X-Ray , Enzyme Activation , Histamine/chemistry , Humans , Hydrogen Bonding , Models, Molecular , Nitrophenols/metabolism , Protein Conformation , Protein Structure, Tertiary , Spectrophotometry , Zinc
19.
Eur J Biochem ; 239(1): 61-6, 1996 Jul 01.
Article in English | MEDLINE | ID: mdl-8706719

ABSTRACT

X-ray absorption spectroscopy (XAS) has been applied to urease from Bacillus pasteurii, a highly ureolytic soil bacterium, with the aim of elucidating the structural details of the nickel-containing active site. The results indicate the presence of octahedrally coordinated Ni2+, in a sphere of six N/O donors at an average distance of 0.203 nm. An average of two histidine residues are bound to nickel. The experimental evidence suggests direct binding of the urease inhibitor phenylphosphorodiamidate to Ni2+. These spectroscopic results are in agreement with previous findings on both plant and microbial ureases, but differ in some respect from the results obtained by X-ray crystallography analysis of Klebsiella aerogenes urease.


Subject(s)
Bacillus/enzymology , Enzyme Inhibitors/pharmacology , Organophosphorus Compounds/pharmacology , Urease/antagonists & inhibitors , Spectrum Analysis
20.
J Mol Biol ; 251(2): 282-96, 1995 Aug 11.
Article in English | MEDLINE | ID: mdl-7643403

ABSTRACT

Cu,Zn superoxide dismutase was investigated crystallographically in the reduced form. Co-ordinate errors were estimated by comparing two independently refined models, based on two different data sets. This gave a detailed error estimation as opposed to the standard sigma A and Luzzati plots, which estimate only the overall error. The high quality of the final model, obtained after scaling together the two data sets, combined with the error estimates allowed a detailed analysis of the protein and solvent structures. An automatic procedure for building and refining solvent structure was tested and found to give reproducible results. Contrary to results obtained from spectroscopic studies, the co-ordination of the metal ions in the catalytic site is preserved in the crystal structure of the reduced enzyme, as compared with the crystal structure of the oxidised form. Analysis of the solvent reveals a well-defined chain of closely packed, hydrogen-bonded water molecules filling the active site groove. This structural feature could serve as a hydrogen bond relay for efficient delivery of protons to the active centre. Analysis of electron density suggests that Glu119 is covalently modified. The modification, if originated in vivo, could have a role in the catalytic mechanism and could affect the overall electrostatic field in the active site. There are significant differences between the active sites of the two crystallographically independent monomers. They are explained in terms of local differences in the crystal environment.


Subject(s)
Erythrocytes/enzymology , Superoxide Dismutase/chemistry , Amino Acid Sequence , Animals , Binding Sites , Cattle , Crystallography, X-Ray , Electron Spin Resonance Spectroscopy , Hydrogen Bonding , Models, Molecular , Molecular Sequence Data , Protein Conformation , Solvents/chemistry , Superoxide Dismutase/blood , Temperature
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