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http://purl.uniprot.org/citations/12044150http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/12044150http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/12044150http://www.w3.org/2000/01/rdf-schema#comment"The gene encoding for the methionyl aminopeptidase from the hyperthermophilic archaeon Pyrococcus furiosus (PfMetAP-II; EC 3.4.11.18) has been inserted into a pET 27b(+) vector and overexpressed in Escherichia coli. The new expression system resulted in a 5-fold increase in purified enzyme obtained from a 5 L fermentor growth. The as-purified PfMetAP-II enzyme, to which no exogenous metal ions or EDTA was added, was found to have 1.2 equiv of zinc and 0.1 equiv of iron present by ICP-AES analysis. This enzyme had a specific activity of 5 units/mg, a 60-fold decrease from the fully loaded Fe(II) enzymes. When an additional 2 equiv of Zn(II) was added to the as-purified PfMetAP-II, no activity could be detected. The combination of these data with previously reported whole cell studies on EcMetAP-I further supports the suggestion that the in vivo metal ion for all MetAP's is Fe(II). Both Co(II)- and Fe(II)-loaded PfMetAP-II showed similar substrate specificities to EcMetAP-I. Substrate binding was largely affected by the amino acid in the P1 position and the length of the polypeptide. The substrates MSSHRWDW and MP-p-NA showed the smallest K(m) values while the substrates MGMM and MP-p-NA provided the highest turnover. The catalytic efficiency (k(cat)/K(m)) of PfMetAP-II for MP-p-NA at 30 degrees C was 799 500 and 340 930 M(-1) s(-1) for Co(II)- and Fe(II)-loaded PfMetAP-II, respectively. Maximum catalytic activity was obtained with 1 equiv of Co(II) or Fe(II), and the dissociation constants (K(d)) for the first metal binding site were found to be 50 +/- 15 and 20 +/-15 nM for Co(II)- and Fe(II)-substituted PfMetAP-II, respectively. Electronic absorption spectral titration of a 1 mM sample of apo-PfMetAP-II with Co(II) provided a dissociation constant of 0.35 +/-0.02 mM for the second metal binding site, a 17500-fold increase compared to the first metal binding site. The electronic absorption data also indicated that both Co(II) ions reside in a pentacoordinate geometry. PfMetAP-II shows unique thermostability and the optimal temperature for substrate turnover was found to be approximately 85 degrees C at pH 7.5 in 25 mM Hepes and 150 mM KCl buffer. The hydrolysis of MGMM was measured in triplicate between 25 and 85 degrees C at eight substrate concentrations ranging from 2 to 20 mM. Both specific activity and K(m) values increased with increasing temperature. An Arrhenius plot was constructed from the k(cat) values and was found to be linear over the temperature range 25-85 degrees C, indicating that the rate-limiting step in PfMetAP-II peptide hydrolysis does not change as a function of temperature. Co(II)- and Fe(II)-loaded PfMetAP-II have similar activation energies (13.3 and 19.4 kJ/mol, respectively). The thermodynamic parameters calculated at 25 degrees C are as follows: DeltaG++ = 46.23 kJ/mol, DeltaH++ = 10.79 kJ/mol, and DeltaS++ = -119.72 J.mol(-1).K(-1) for Co(II)-loaded PfMetAP; DeltaG++ = 46.44 kJ/mol, DeltaH++ = 16.94 kJ/mol, and DeltaS++ = -99.67 J.mol(-1).K(-1) for Fe(II)-loaded PfMetAP. Interestingly, at higher temperatures (> 50 degrees C), Fe(II)-loaded PfMetAP-II is more active (1.4-fold at 85 degrees C) than Co(II)-loaded PfMetAP-II."xsd:string
http://purl.uniprot.org/citations/12044150http://purl.org/dc/terms/identifier"doi:10.1021/bi020138p"xsd:string
http://purl.uniprot.org/citations/12044150http://purl.org/dc/terms/identifier"doi:10.1021/bi020138p"xsd:string
http://purl.uniprot.org/citations/12044150http://purl.uniprot.org/core/author"Tsunasawa S."xsd:string
http://purl.uniprot.org/citations/12044150http://purl.uniprot.org/core/author"Tsunasawa S."xsd:string
http://purl.uniprot.org/citations/12044150http://purl.uniprot.org/core/author"Holz R.C."xsd:string
http://purl.uniprot.org/citations/12044150http://purl.uniprot.org/core/author"Holz R.C."xsd:string
http://purl.uniprot.org/citations/12044150http://purl.uniprot.org/core/author"Copik A.J."xsd:string
http://purl.uniprot.org/citations/12044150http://purl.uniprot.org/core/author"Copik A.J."xsd:string
http://purl.uniprot.org/citations/12044150http://purl.uniprot.org/core/author"D'souza V.M."xsd:string
http://purl.uniprot.org/citations/12044150http://purl.uniprot.org/core/author"D'souza V.M."xsd:string
http://purl.uniprot.org/citations/12044150http://purl.uniprot.org/core/author"Meng L."xsd:string
http://purl.uniprot.org/citations/12044150http://purl.uniprot.org/core/author"Meng L."xsd:string
http://purl.uniprot.org/citations/12044150http://purl.uniprot.org/core/author"Ruebush S."xsd:string
http://purl.uniprot.org/citations/12044150http://purl.uniprot.org/core/author"Ruebush S."xsd:string
http://purl.uniprot.org/citations/12044150http://purl.uniprot.org/core/date"2002"xsd:gYear
http://purl.uniprot.org/citations/12044150http://purl.uniprot.org/core/date"2002"xsd:gYear
http://purl.uniprot.org/citations/12044150http://purl.uniprot.org/core/name"Biochemistry"xsd:string
http://purl.uniprot.org/citations/12044150http://purl.uniprot.org/core/name"Biochemistry"xsd:string
http://purl.uniprot.org/citations/12044150http://purl.uniprot.org/core/pages"7199-7208"xsd:string
http://purl.uniprot.org/citations/12044150http://purl.uniprot.org/core/pages"7199-7208"xsd:string
http://purl.uniprot.org/citations/12044150http://purl.uniprot.org/core/title"Overexpression and divalent metal binding properties of the methionyl aminopeptidase from Pyrococcus furiosus."xsd:string
http://purl.uniprot.org/citations/12044150http://purl.uniprot.org/core/title"Overexpression and divalent metal binding properties of the methionyl aminopeptidase from Pyrococcus furiosus."xsd:string
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