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Molecular cloning,expression and characterization of three distinctive genes encoding methionine aminopeptidases in cyanobacterium Synechocystis sp. strain PCC6803
Authors:Anelia?Atanassova  author-information"  >  author-information__contact u-icon-before"  >  mailto:atanasso@chem.utoronto.ca"   title="  atanasso@chem.utoronto.ca"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author,Mamoru?Sugita,Masahiro?Sugiura,Tamara?Pajpanova,Ivan?Ivanov
Affiliation:(1) Institute of Molecular Biology, Bulgarian Academy of Sciences, bl. 21 Acad. G. Bonchev St., 1113 Sofia, Bulgaria;(2) Laboratory of Plant Molecular Biology and Biological Informatics, Nagoya University, Graduate School of Human Informatics, 464 – 8601 Nagoya, Japan;(3) Graduate School of Natural Sciences, Nagoya City University, 467 – 8501 Nagoya , Japan;(4) Department of Chemistry, University of Toronto, 80 St. George St., Lash Miller Chemical Laboratories, Toronto, Ontario , M5S 3H6, Canada
Abstract:Methionine aminopeptidase, known to be encoded by single genes in prokaryotes, is a cobalt-dependent enzyme that catalyzes the removal of N-terminal methionine residues from nascent polypeptides. Three ORFs encoding putative methionine aminopeptidases from the genome of cyanobacterium Synechocystis sp. strain PCC6803, designated as slr0786 (map-1), slr0918 (map-2) and sll0555 (map-3) were cloned and expressed in Escherichia coli. The purified recombinant proteins encoded by map-1 and map-3 had much higher methionine aminopeptidase activity than the recombinant protein encoded by map-2. Comparative analysis revealed that the three recombinant enzymes differed in their substrate specificity, divalent ion requirement, pH, and temperature optima. The broad activities of the iso-enzymes are discussed in light of the structural similarities with other peptidase families and their levels of specificity in the cell. Potential application of cyanobacterial MetAPs in the production of recombinant proteins used in medicine is proposed. This is the first report of a prokaryote harboring multiple methionine aminopeptidases.Abbreviations map Gene encoding methionine aminopeptidase - MetAP Methionine aminopeptidase - eMetAP-Ia Escherichia coli methionine aminopeptidase type Ia - yMetAP-Ib Yeast methionine aminopeptidase type Ib - yMetAP-IIa Yeast methionine aminopeptidase type IIa - hMetAP-IIb Human methionine aminopeptidase type IIb - pfMetAP–IIa Pyrococcus furiosis methionine aminopeptidase type Ia - bst MetAP-Ia Bacillus stearothermophilus methionine aminopeptidase type Ia - c1MetAP-Ia Cyanobacterial methionine aminopeptidase type Ia encoded by map-1 - c2MetAP-Ia Cyanobacterial methionine aminopeptidase type Ia encoded by map-2 - c3MetAP-Ib Cyanobacterial methionine aminopeptidase type Ib, ncoded by map-3
Keywords:Cobalt-dependent enzyme  Cyanobacteria  Escherichia coli  Iso-enzymes  Methionine aminopeptidase  Recombinant proteins
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