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Molecular Cloning and Expression of the Pyrimidine Nucleoside Phosphorylase Gene fromBacillus stearothermophilusTH 6–2
Author(s) -
Kiyoshi Okuyama,
Tomoki Hamamoto,
Toshitada Noguchi,
Yuichiro Midorikawa
Publication year - 1996
Publication title -
bioscience biotechnology and biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.509
H-Index - 116
eISSN - 1347-6947
pISSN - 0916-8451
DOI - 10.1271/bbb.60.1655
Subject(s) - phosphorolysis , escherichia coli , biology , biochemistry , purine nucleoside phosphorylase , gene , microbiology and biotechnology , thymidine phosphorylase , nucleic acid sequence , open reading frame , molecular cloning , peptide sequence , polynucleotide phosphorylase , enzyme , purine
The pyrimidine nucleoside phosphorylase (Py-NPase) of Bacillus stearothermophilus TH 6-2 is a dimer of 46-kDa subunits and catalyzes the reversible phosphorolysis of uridine and thymidine. The gene encoding this pyrimidine nucleoside phosphorylase (pyn gene) has been cloned and sequenced from B. stearothermophilus TH 6-2. The pyn gene corresponded to an open reading frame of 1299 nucleotides that translates into a putative 433 amino acid protein with a molecular weight of 46,271. The deduced amino terminal sequence of Py-NPase coincided with that previously found for the purified enzyme. The deduced amino acid sequence of Py-NPase shared significant similarity with those of human and Escherichia coli thymidine phosphorylases. The cloned pyn gene was overexpressed in E. coli cells to produce an active enzyme in large quantities that accounted for approximately 20% of the total protein.

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