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1.
J Biol Chem ; 299(9): 105110, 2023 Sep.
Article in English | MEDLINE | ID: mdl-37517696

ABSTRACT

Marine animals display diverse vibrant colors, but the mechanisms underlying their specific coloration remain to be clarified. Blue coloration is known to be achieved through a bathochromic shift of the orange carotenoid astaxanthin (AXT) by the crustacean protein crustacyanin, but other examples have not yet been well investigated. Here, we identified an ependymin (EPD)-related water-soluble blue carotenoprotein responsible for the specific coloration of the marine blue sponge Haliclona sp. EPD was originally identified in the fish brain as a protein involved in memory consolidation and neuronal regeneration. The purified blue protein, designated as EPD-related blue carotenoprotein-1, was identified as a secreted glycoprotein. We show that it consists of a heterodimer that binds orange AXT and mytiloxanthin and exhibits a bathochromic shift. Our crystal structure analysis of the natively purified EPD-related blue carotenoprotein-1 revealed that these two carotenoids are specifically bound to the heterodimer interface, where the polyene chains are aligned in parallel to each other like in ß-crustacyanin, although the two proteins are evolutionary and structurally unrelated. Furthermore, using reconstitution assays, we found that incomplete bathochromic shifts occurred when the protein bound to only AXT or mytiloxanthin. Taken together, we identified an EPD in a basal metazoan as a blue protein that decorates the sponge body by binding specific structurally unrelated carotenoids.

2.
Article in English | MEDLINE | ID: mdl-30533902

ABSTRACT

Hydrogenophilus spp., which are moderately thermophilic aerobic betaproteobacteria, are widely distributed in geothermal environments. They fix carbon dioxide via the Calvin-Benson-Bassham cycle and exhibit rapid autotrophic growth using hydrogen as an energy source. Here, we report the complete genome sequence of Hydrogenophilus thermoluteolus strain TH-1.

3.
Chem Commun (Camb) ; 54(87): 12385-12388, 2018 Oct 30.
Article in English | MEDLINE | ID: mdl-30328414

ABSTRACT

Citrobacter sp. S-77 [NiFe]-hydrogenase harbors a standard [4Fe-4S] cluster proximal to the Ni-Fe active site. The presence of relocatable water molecules and a flexible aspartate enables the [4Fe-4S] to display redox-dependent conformational changes. These structural features are proposed to be the key aspects that protect the active site from O2 attack.


Subject(s)
Hydrogenase/chemistry , Iron-Sulfur Proteins/chemistry , Oxygen/chemistry , Catalytic Domain , Electron Spin Resonance Spectroscopy , Hydrogen Bonding , Models, Molecular , Oxidation-Reduction , Protein Conformation , Spectroscopy, Fourier Transform Infrared
4.
Chembiochem ; 18(17): 1712-1715, 2017 09 05.
Article in English | MEDLINE | ID: mdl-28660650

ABSTRACT

The design of protein oligomers with multiple active sites has been gaining interest, owing to their potential use for biomaterials, which has encouraged researchers to develop a new design method. Three-dimensional domain swapping is the unique phenomenon in which protein molecules exchange the same structural region between each other. Herein, to construct oligomeric heme proteins with different active sites by utilizing domain swapping, two c-type cytochrome-based chimeric proteins have been constructed and the domains swapped. According to X-ray crystallographic analysis, the two chimeric proteins formed a domain-swapped dimer with two His/Met coordinated hemes. By mutating the heme coordination structure of one of the two chimeric proteins, a domainswapped heterodimer with His/Met and His/H2 O coordinated hemes was formed. Binding of an oxygen molecule to the His/H2 O site of the heterodimer was confirmed by resonance Raman spectroscopy, in which the Fe-O2 stretching band was observed at 580 cm-1 for the reduced/oxygenated heterodimer (at 554 cm-1 under an 18 O2 atmosphere). These results show that domain swapping is a useful method to design multiheme proteins.


Subject(s)
Cytochrome c Group/metabolism , Aquifoliaceae/enzymology , Circular Dichroism , Crystallography, X-Ray , Cytochrome c Group/chemistry , Cytochrome c Group/genetics , Dimerization , Heme/chemistry , Heme/metabolism , Oxygen/chemistry , Protein Engineering , Protein Structure, Tertiary , Pseudomonas aeruginosa/enzymology , Recombinant Fusion Proteins/biosynthesis , Recombinant Fusion Proteins/chemistry , Recombinant Fusion Proteins/isolation & purification , Spectrum Analysis, Raman
5.
Mol Biosyst ; 11(12): 3218-21, 2015 Dec.
Article in English | MEDLINE | ID: mdl-26451671

ABSTRACT

High-order oligomers of Hydrogenobacter thermophilus cytochrome c552 increased with the insertion of more Gly residues between Ala18 and Lys19 at the major hinge loop of the wild-type protein. N-Terminal domain swapping and C-terminal domain swapping were elucidated by using X-ray crystallography for the mutant with the insertion of three Gly residues at the hinge loop.


Subject(s)
Cytochrome c Group/chemistry , Models, Molecular , Protein Interaction Domains and Motifs , Protein Multimerization , Thermodynamics , Binding Sites , Catalytic Domain , Cytochrome c Group/genetics , Cytochrome c Group/metabolism , Protein Array Analysis , Protein Conformation
6.
Acta Crystallogr F Struct Biol Commun ; 71(Pt 1): 96-9, 2015 Jan 01.
Article in English | MEDLINE | ID: mdl-25615977

ABSTRACT

NAD+-reducing [NiFe] hydrogenases catalyze the oxidoreduction of dihydrogen concomitant with the interconversion of NAD+ and NADH. Here, the isolation, purification and crystallization of the NAD+-reducing [NiFe] hydrogenase from Hydrogenophilus thermoluteolus TH-1 are reported. Crystals of the NAD+-reducing [NiFe] hydrogenase were obtained within one week from a solution containing polyethylene glycol using the sitting-drop vapour-diffusion method and micro-seeding. The crystal diffracted to 2.58 Šresolution and belonged to space group C2, with unit-cell parameters a=131.43, b=189.71, c=124.59 Å, ß=109.42°. Assuming the presence of two NAD+-reducing [NiFe] hydrogenase molecules in the asymmetric unit, VM was calculated to be 2.2 Å3 Da(-1), which corresponds to a solvent content of 43%. Initial phases were determined by the single-wavelength anomalous dispersion method using the anomalous signal from the Fe atoms.


Subject(s)
Bacterial Proteins/chemistry , Hydrogenase/chemistry , Hydrogenophilaceae/enzymology , Crystallization , Crystallography, X-Ray
7.
Chem Sci ; 6(12): 7336-7342, 2015 Dec 01.
Article in English | MEDLINE | ID: mdl-28791095

ABSTRACT

Protein nanostructures have been gaining in interest, along with developments in new methods for construction of novel nanostructures. We have previously shown that c-type cytochromes and myoglobin form oligomers by domain swapping. Herein, we show that a four-helix bundle protein cyt cb562, with the cyt b562 heme attached to the protein moiety by two Cys residues insertion, forms a domain-swapped dimer. Dimeric cyt cb562 did not dissociate to monomers at 4 °C, whereas dimeric cyt b562 dissociated under the same conditions, showing that heme attachment to the protein moiety stabilizes the domain-swapped structure. According to X-ray crystallographic analysis of dimeric cyt cb562, the two helices in the N-terminal region of one protomer interacted with the other two helices in the C-terminal region of the other protomer, where Lys51-Asp54 served as a hinge loop. The heme coordination structure of the dimer was similar to that of the monomer. In the crystal, three domain-swapped cyt cb562 dimers formed a unique cage structure with a Zn-SO4 cluster inside the cavity. The Zn-SO4 cluster consisted of fifteen Zn2+ and seven SO42- ions, whereas six additional Zn2+ ions were detected inside the cavity. The cage structure was stabilized by coordination of the amino acid side chains of the dimers to the Zn2+ ions and connection of two four-helix bundle units through the conformation-adjustable hinge loop. These results show that domain swapping can be applied in the construction of unique protein nanostructures.

8.
ACS Synth Biol ; 4(4): 383-92, 2015 Apr 17.
Article in English | MEDLINE | ID: mdl-25171735

ABSTRACT

Enzymatic regio- and stereoselective hydroxylation are valuable for the production of hydroxylated chiral ingredients. Proline hydroxylases are representative members of the nonheme Fe(2+)/α-ketoglutarate-dependent dioxygenase family. These enzymes catalyze the conversion of L-proline into hydroxy-L-prolines (Hyps). L-Proline cis-4-hydroxylases (cis-P4Hs) from Sinorhizobium meliloti and Mesorhizobium loti catalyze the hydroxylation of L-proline, generating cis-4-hydroxy-L-proline, as well as the hydroxylation of L-pipecolic acid (L-Pip), generating two regioisomers, cis-5-Hypip and cis-3-Hypip. To selectively produce cis-5-Hypip without simultaneous production of two isomers, protein engineering of cis-P4Hs is required. We therefore carried out protein engineering of cis-P4H to facilitate the conversion of the majority of L-Pip into the cis-5-Hypip isomer. We first solved the X-ray crystal structure of cis-P4H in complex with each of L-Pro and L-Pip. Then, we conducted three rounds of directed evolution and successfully created a cis-P4H triple mutant, V97F/V95W/E114G, demonstrating the desired regioselectivity toward cis-5-Hypip.


Subject(s)
Bacterial Proteins , Mesorhizobium/enzymology , Pipecolic Acids , Prolyl Hydroxylases , Sinorhizobium meliloti/enzymology , Bacterial Proteins/chemistry , Bacterial Proteins/metabolism , Crystallography, X-Ray , Hydroxylation , Pipecolic Acids/chemistry , Pipecolic Acids/metabolism , Prolyl Hydroxylases/chemistry , Prolyl Hydroxylases/metabolism , Protein Structure, Tertiary
9.
Angew Chem Int Ed Engl ; 54(2): 511-5, 2015 Jan 07.
Article in English | MEDLINE | ID: mdl-25370865

ABSTRACT

Protein design is a useful method to create novel artificial proteins. A rational approach to design a heterodimeric protein using domain swapping for horse myoglobin (Mb) was developed. As confirmed by X-ray crystallographic analysis, a heterodimeric Mb with two different active sites was produced efficiently from two surface mutants of Mb, in which the charges of two amino acids involved in the dimer salt bridges were reversed in each mutant individually, with the active site of one mutant modified. This study shows that the method of constructing heterodimeric Mb with domain swapping is useful for designing artificial multiheme proteins.


Subject(s)
Myoglobin/chemistry , Dimerization
10.
Biochem Biophys Res Commun ; 430(1): 284-8, 2013 Jan 04.
Article in English | MEDLINE | ID: mdl-23159801

ABSTRACT

[NiFe] hydrogenase catalyzes reversible oxidation of molecular hydrogen. Its active site is constructed of a hetero dinuclear Ni-Fe complex, and the oxidation state of the Ni ion changes according to the redox state of the enzyme. We found that the Ni-A state (an inactive unready, oxidized state) of [NiFe] hydrogenase from Desulfovibrio vulgaris Miyazaki F (DvMF) is light sensitive and forms a new state (Ni-AL) with irradiation of visible light. The Fourier transform infrared (FT-IR) bands at 1956, 2084 and 2094 cm(-1) of the Ni-A state shifted to 1971, 2086 and 2098 cm(-1) in the Ni-AL state. The g-values of g(x)=2.30, g(y)=2.23 and g(z)=2.01 for the signals in the electron paramagnetic resonance (EPR) spectrum of the Ni-A state at room temperature varied for -0.009, +0.012 and +0.010, respectively, upon light irradiation. The light-induced Ni-AL state converted back immediately to the Ni-A state under dark condition at room temperature. These results show that the coordination structure of the Fe site of the Ni-A state of [NiFe] hydrogenase is perturbed significantly by light irradiation with relatively small coordination change at the Ni site.


Subject(s)
Desulfovibrio vulgaris/enzymology , Hydrogenase/radiation effects , Light , Photochemical Processes , Hydrogenase/chemistry , Iron/chemistry , Nickel/chemistry , Spectroscopy, Fourier Transform Infrared
11.
FEBS Lett ; 586(20): 3705-9, 2012 Oct 19.
Article in English | MEDLINE | ID: mdl-22975312

ABSTRACT

The bacterial translational GTPases release factor RF3 promotes translation termination by recycling RF1 or RF2. Here, we present the crystal structures of RF3 complexed with GDP and guanosine 3',5'-(bis)diphosphate (ppGpp) at resolutions of 1.8 and 3.0Å, respectively. ppGpp is involved in the so-called "stringent response" of bacteria. ppGpp binds at the same site as GDP, suggesting that GDP and ppGpp are two alternative physiologically relevant ligands of RF3. We also found that ppGpp decelerates the recycling of RF1 by RF3. These lines of evidence suggest that RF3 functions both as a cellular metabolic sensor and as a regulator.


Subject(s)
Escherichia coli Proteins/chemistry , Escherichia coli Proteins/metabolism , Peptide Termination Factors/chemistry , Peptide Termination Factors/metabolism , Crystallography, X-Ray , Desulfovibrio vulgaris , Guanosine Diphosphate/metabolism , Guanosine Triphosphate/metabolism , Models, Molecular , Protein Conformation
12.
Dalton Trans ; 41(37): 11378-85, 2012 Oct 07.
Article in English | MEDLINE | ID: mdl-22885714

ABSTRACT

Myoglobin (Mb) stores dioxygen in muscles, and is a fundamental model protein widely used in molecular design. The presence of dimeric Mb has been known for more than forty years, but its structural and oxygen binding properties remain unknown. From an X-ray crystallographic analysis at 1.05 Å resolution, we found that dimeric metMb exhibits a domain-swapped structure with two extended α-helices. Each new long α-helix is formed by the E and F helices and the EF-loop of the original monomer, and as a result the proximal and distal histidines of the heme originate from different protomers. The heme orientation in the dimer was in the normal mode as in the monomer, but regulated faster from the reverse to normal orientation. The dimer possessed the oxygen binding property, although it exhibited a slightly higher oxygen binding affinity (∼1.4 fold) compared to the monomer and showed no cooperativity for oxygen binding. The oxygen binding rate constant (k(on)) of the dimer ((14.0 ± 0.7) × 10(6) M(-1) s(-1)) was similar to that of the monomer, whereas the oxygen dissociation rate constant (k(off)) of the dimer (8 ± 1 s(-1)) was smaller than that of the monomer (12 ± 1 s(-1)). We attribute the similar k(on) values to their active site structures being similar, whereas the faster regulation of the heme orientation and the smaller k(off) in the dimer are presumably due to the slight change in the active site structure and/or more rigid structure compared to the monomer. These results show that domain swapping may be a new tool for protein engineering.


Subject(s)
Myoglobin/chemistry , Oxygen/chemistry , Animals , Circular Dichroism , Crystallography, X-Ray , Dimerization , Horses , Magnetic Resonance Spectroscopy , Models, Molecular , Myoglobin/metabolism , Oxygen/metabolism
13.
J Biol Chem ; 287(34): 28409-19, 2012 Aug 17.
Article in English | MEDLINE | ID: mdl-22740694

ABSTRACT

As a remarkable structural feature of hydrogenase active sites, [NiFe]-hydrogenases harbor one carbonyl and two cyano ligands, where HypE and HypF are involved in the biosynthesis of the nitrile group as a precursor of the cyano groups. HypF catalyzes S-carbamoylation of the C-terminal cysteine of HypE via three steps using carbamoylphosphate and ATP, producing two unstable intermediates: carbamate and carbamoyladenylate. Although the crystal structures of intact HypE homodimers and partial HypF have been reported, it remains unclear how the consecutive reactions occur without the loss of unstable intermediates during the proposed reaction scheme. Here we report the crystal structures of full-length HypF both alone and in complex with HypE at resolutions of 2.0 and 2.6 Å, respectively. Three catalytic sites of the structures of the HypF nucleotide- and phosphate-bound forms have been identified, with each site connected via channels inside the protein. This finding suggests that the first two consecutive reactions occur without the release of carbamate or carbamoyladenylate from the enzyme. The structure of HypF in complex with HypE revealed that HypF can associate with HypE without disturbing its homodimeric interaction and that the binding manner allows the C-terminal Cys-351 of HypE to access the S-carbamoylation active site in HypF, suggesting that the third step can also proceed without the release of carbamoyladenylate. A comparison of the structure of HypF with the recently reported structures of O-carbamoyltransferase revealed different reaction mechanisms for carbamoyladenylate synthesis and a similar reaction mechanism for carbamoyltransfer to produce the carbamoyl-HypE molecule.


Subject(s)
Bacterial Proteins/chemistry , Hydrogenase/chemistry , Multiprotein Complexes/chemistry , Protein Multimerization , Protein Processing, Post-Translational/physiology , Thermoanaerobacter/chemistry , Bacterial Proteins/genetics , Bacterial Proteins/metabolism , Crystallography, X-Ray , Hydrogenase/genetics , Hydrogenase/metabolism , Multiprotein Complexes/genetics , Multiprotein Complexes/metabolism , Protein Structure, Quaternary , Thermoanaerobacter/genetics , Thermoanaerobacter/metabolism
14.
Protein Sci ; 21(5): 707-16, 2012 May.
Article in English | MEDLINE | ID: mdl-22407814

ABSTRACT

BacD is an ATP-dependent dipeptide ligase responsible for the biosynthesis of L-alanyl-L-anticapsin, a precursor of an antibiotic produced by Bacillus spp. In contrast to the well-studied and phylogenetically related D-alanine: D-alanine ligase (Ddl), BacD synthesizes dipeptides using L-amino acids as substrates and has a low substrate specificity in vitro. The enzyme is of great interest because of its potential application in industrial protein engineering for the environmentally friendly biological production of useful peptide compounds, such as physiologically active peptides, artificial sweeteners and antibiotics, but the determinants of its substrate specificity and its catalytic mechanism have not yet been established due to a lack of structural information. In this study, we report the crystal structure of BacD in complex with ADP and an intermediate analog, phosphorylated phosphinate L-alanyl-L-phenylalanine, refined to 2.5-Å resolution. The complex structure reveals that ADP and two magnesium ions bind in a manner similar to that of Ddl. However, the dipeptide orientation is reversed, and, concomitantly, the entrance to the amino acid binding cavity differs in position. Enzymatic characterization of two mutants, Y265F and S185A, demonstrates that these conserved residues are not catalytic residues at least in the reaction where L-phenylalanine is used as a substrate. On the basis of the biochemical and the structural data, we propose a reaction scheme and a catalytic mechanism for BacD.


Subject(s)
Bacillus subtilis/enzymology , Bacterial Proteins/chemistry , Dipeptides/chemistry , Ligases/chemistry , Adenosine Diphosphate/chemistry , Adenosine Diphosphate/metabolism , Bacterial Proteins/antagonists & inhibitors , Bacterial Proteins/metabolism , Catalytic Domain , Dipeptides/metabolism , Ligases/antagonists & inhibitors , Ligases/metabolism , Models, Molecular , Protein Conformation
15.
Nature ; 479(7372): 253-6, 2011 Oct 16.
Article in English | MEDLINE | ID: mdl-22002607

ABSTRACT

Membrane-bound respiratory [NiFe]-hydrogenase (MBH), a H(2)-uptake enzyme found in the periplasmic space of bacteria, catalyses the oxidation of dihydrogen: H(2) → 2H(+) + 2e(-) (ref. 1). In contrast to the well-studied O(2)-sensitive [NiFe]-hydrogenases (referred to as the standard enzymes), MBH has an O(2)-tolerant H(2) oxidation activity; however, the mechanism of O(2) tolerance is unclear. Here we report the crystal structures of Hydrogenovibrio marinus MBH in three different redox conditions at resolutions between 1.18 and 1.32 Å. We find that the proximal iron-sulphur (Fe-S) cluster of MBH has a [4Fe-3S] structure coordinated by six cysteine residues--in contrast to the [4Fe-4S] cubane structure coordinated by four cysteine residues found in the proximal Fe-S cluster of the standard enzymes--and that an amide nitrogen of the polypeptide backbone is deprotonated and additionally coordinates the cluster when chemically oxidized, thus stabilizing the superoxidized state of the cluster. The structure of MBH is very similar to that of the O(2)-sensitive standard enzymes except for the proximal Fe-S cluster. Our results give a reasonable explanation why the O(2) tolerance of MBH is attributable to the unique proximal Fe-S cluster; we propose that the cluster is not only a component of the electron transfer for the catalytic cycle, but that it also donates two electrons and one proton crucial for the appropriate reduction of O(2) in preventing the formation of an unready, inactive state of the enzyme.


Subject(s)
Hydrogenase/chemistry , Hydrogenase/metabolism , Iron-Sulfur Proteins/chemistry , Iron/chemistry , Oxygen/metabolism , Piscirickettsiaceae/enzymology , Sulfur/chemistry , Biocatalysis , Crystallography, X-Ray , Cysteine/chemistry , Desulfovibrio gigas/enzymology , Iron-Sulfur Proteins/metabolism , Models, Chemical , Models, Molecular , Oxidation-Reduction , Protein Multimerization , Protein Structure, Quaternary , Protein Subunits/chemistry , Protein Subunits/metabolism , Protons , Structure-Activity Relationship
16.
Article in English | MEDLINE | ID: mdl-21795788

ABSTRACT

Coiled-coil DIX1 (Ccd1) is a positive regulator that activates the canonical Wnt signalling pathway by inhibiting the degradation of the key signal transducer ß-catenin. The C-terminal DIX domain of Ccd1 plays an important role in the regulation of signal transduction through homo-oligomerization and protein complex formation with other DIX domain-containing proteins, i.e. axin and dishevelled proteins. Here, the expression, purification, crystallization and X-ray data collection of the Ccd1 DIX domain are reported. The crystals of the Ccd1 DIX domain belonged to space group P2(1)2(1)2(1), with unit-cell parameters a=72.9, b=75.7, c=125.6 Å. An X-ray diffraction data set was collected at 3.0 Šresolution.


Subject(s)
Intracellular Signaling Peptides and Proteins/chemistry , Signal Transduction , Animals , Crystallography, X-Ray , Intracellular Signaling Peptides and Proteins/metabolism , Mice , Wnt Proteins/metabolism
17.
Article in English | MEDLINE | ID: mdl-21795805

ABSTRACT

Membrane-bound respiratory [NiFe] hydrogenase is an H2-uptake enzyme found in the periplasmic space of bacteria that plays a crucial role in energy-conservation processes. The heterodimeric unit of the enzyme from Hydrogenovibrio marinus was purified to homogeneity using chromatographic procedures. Crystals were grown using the sitting-drop vapour-diffusion method at room temperature. Preliminary crystallographic analysis revealed that the crystals belonged to space group P2(1), with unit-cell parameters a=75.72, b=116.59, c=113.40 Å, ß=91.3°, indicating that two heterodimers were present in the asymmetric unit.


Subject(s)
Hydrogenase/chemistry , Membrane Proteins/chemistry , Piscirickettsiaceae/enzymology , Crystallization , Crystallography, X-Ray
18.
Acta Crystallogr Sect F Struct Biol Cryst Commun ; 66(Pt 11): 1470-2, 2010 Nov 01.
Article in English | MEDLINE | ID: mdl-21045297

ABSTRACT

Dissimilatory sulfite reductase (Dsr) plays an important role in sulfate respiration in many sulfate-reducing bacteria. Dsr from Desulfovibrio vulgaris Miyazaki F has been purified and crystallized at 277 K using the sitting-drop vapour-diffusion method with PEG 3350 and potassium thiocyanate as precipitants. A data set was collected to 3.7 Šresolution from a single crystal at 100 K using synchrotron radiation. The Dsr crystal belonged to space group P4(1)2(1)2, with unit-cell parameters a = b = 163.26, c = 435.32 Å. The crystal structure of Dsr was determined by the molecular-replacement method based on the three-dimensional structure of Dsr from D. vulgaris Hildenborough. The crystal contained three α(2)ß(2)γ(2) units per asymmetric unit, with a Matthews coefficient (V(M)) of 2.35 Å(3) Da(-1); the solvent content was estimated to be 47.7%.


Subject(s)
Desulfovibrio vulgaris/enzymology , Hydrogensulfite Reductase/chemistry , Crystallization , Crystallography, X-Ray , Hydrogensulfite Reductase/isolation & purification , Models, Molecular , Protein Structure, Tertiary
19.
J Biol Chem ; 285(34): 26484-93, 2010 Aug 20.
Article in English | MEDLINE | ID: mdl-20519496

ABSTRACT

N-terminal truncation of the Escherichia coli ethanolamine ammonia-lyase beta-subunit does not affect the catalytic properties of the enzyme (Akita, K., Hieda, N., Baba, N., Kawaguchi, S., Sakamoto, H., Nakanishi, Y., Yamanishi, M., Mori, K., and Toraya, T. (2010) J. Biochem. 147, 83-93). The binary complex of the truncated enzyme with cyanocobalamin and the ternary complex with cyanocobalamin or adeninylpentylcobalamin and substrates were crystallized, and their x-ray structures were analyzed. The enzyme exists as a trimer of the (alphabeta)(2) dimer. The active site is in the (beta/alpha)(8) barrel of the alpha-subunit; the beta-subunit covers the lower part of the cobalamin that is bound in the interface of the alpha- and beta-subunits. The structure complexed with adeninylpentylcobalamin revealed the presence of an adenine ring-binding pocket in the enzyme that accommodates the adenine moiety through a hydrogen bond network. The substrate is bound by six hydrogen bonds with active-site residues. Argalpha(160) contributes to substrate binding most likely by hydrogen bonding with the O1 atom. The modeling study implies that marked angular strains and tensile forces induced by tight enzyme-coenzyme interactions are responsible for breaking the coenzyme Co-C bond. The coenzyme adenosyl radical in the productive conformation was modeled by superimposing its adenine ring on the adenine ring-binding site followed by ribosyl rotation around the N-glycosidic bond. A major structural change upon substrate binding was not observed with this particular enzyme. Glualpha(287), one of the substrate-binding residues, has a direct contact with the ribose group of the modeled adenosylcobalamin, which may contribute to the substrate-induced additional labilization of the Co-C bond.


Subject(s)
Cobamides/chemistry , Escherichia coli Proteins/chemistry , Ethanolamine Ammonia-Lyase/chemistry , Catalytic Domain , Cobamides/metabolism , Escherichia coli/chemistry , Escherichia coli Proteins/metabolism , Ethanolamine Ammonia-Lyase/metabolism , Hydrogen Bonding , Organometallic Compounds/chemistry , Organometallic Compounds/metabolism , Protein Binding , Protein Subunits , Substrate Specificity , Vitamin B 12/chemistry , Vitamin B 12/metabolism
20.
Article in English | MEDLINE | ID: mdl-20516606

ABSTRACT

Ethanolamine ammonia-lyase (EAL) catalyzes the adenosylcobalamin-dependent conversion of ethanolamine to acetaldehyde and ammonia. The wild-type enzyme shows a very low solubility. N-terminal truncation of the Escherichia coli EAL beta-subunit dramatically increases the solubility of the enzyme without altering its catalytic properties. Two deletion mutants of the enzyme [EAL(betaDelta4-30) and EAL(betaDelta4-43)] have been overexpressed, purified and crystallized using the sitting-drop vapour-diffusion method. Crystals of EAL(betaDelta4-30) and EAL(betaDelta4-43) diffracted to approximately 8.0 and 2.1 A resolution, respectively.


Subject(s)
Escherichia coli/enzymology , Ethanolamine Ammonia-Lyase/chemistry , Crystallization , Crystallography, X-Ray , Ethanolamine Ammonia-Lyase/genetics , Gene Expression , Mutation
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