Cloning and expression of Escherichia coli 5′-methylthioadenosine/S-adenosylhomocysteine nucleosidase:: Identification of the pfs gene product

被引:42
作者
Cornell, KA
Riscoe, MK
机构
[1] Oregon Hlth & Sci Univ, Dept Med, Div Hematol & Med Oncol, Portland, OR 97201 USA
[2] Oregon Hlth & Sci Univ, Dept Biochem & Mol Biol, Portland, OR 97201 USA
[3] Vet Affairs Med Ctr, Med Res Serv, Portland, OR 97021 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION | 1998年 / 1396卷 / 01期
关键词
methionine; salvage; MTA/SAH nucleosidase; MTR kinase; MTA phosphorylase; pfs gene; (E-coli);
D O I
10.1016/S0167-4781(97)00169-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The enzyme 5'-methylthioadenosine/S-adenosylhomocysteine nucleosidase (EC 3.2.2.9) is responsible for cleavage of the glycosidic bond in both 5'-methylthioadenosine (MTA) and S-adenosylhomocysteine (SAH). Based on amino acid sequence analysis of this enzyme from Klebsiella. we recently speculated that an open reading frame found in E. coli (designated pfs) encoded MTA/SAH nucleosidase. To explore this possibility, we amplified, cloned, and expressed the complete pfs gene from E, coli genomic DNA. The recombinant protein exhibited a molecular weight and Michaelis constants for MTA that are in agreement with those reported for native enzyme, From this biochemical evidence we confirm our original assignment of the pfs gene as encoding MTA/SAH nucleosidase. (C) 1998 Elsevier Science B.V.
引用
收藏
页码:8 / 14
页数:7
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