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PMID: 11425472 Published · ppublish English Journal Article

Molecular cloning and identification of UTR1 of a yeast Saccharomyces cerevisiae as a gene encoding an NAD kinase.

FEMS microbiology letters ·Vol. 200 ·No. 2 ·2001-06-25 ·Pages 181-4

Kawai S, Suzuki S, Mori S, Murata K

Abstract

UTR1 of the yeast Saccharomyces cerevisiae was cloned from the genomic DNA by polymerase chain reaction and expressed in Escherichia coli. Characterization of the purified UTR1p revealed that UTR1p is a NAD kinase consisting of six identical subunits with a molecular mass of 60 kDa. UTR1p specifically phosphorylated NAD in the presence of ATP, dATP, or CTP as phosphoryl donors, and was most active at pH 8.0, 30 degrees C. Km values of UTR1p for NAD and ATP were determined to be 0.50 mM and 0.60 mM, respectively.

MeSH Terms
Cloning, Molecular FMN Reductase NADH, NADPH Oxidoreductases/metabolism Phosphotransferases (Alcohol Group Acceptor)/genetics,metabolism Saccharomyces cerevisiae/enzymology,genetics
Chemicals
FMN Reductase NADH, NADPH Oxidoreductases ferric citrate iron reductase Phosphotransferases (Alcohol Group Acceptor) NAD kinase
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Kawai S
Research Institute for Food Science, Kyoto University, Uji, 611-0011, Kyoto, Japan.
Suzuki S
Mori S
Murata K
Article Info
Journal
FEMS microbiology letters
Abbr.
FEMS Microbiol Lett
ISSN
0378-1097
Published
2001-06-25
Pages
181-4
Language
English
Region
England
NLM ID
7705721
Subset
IM
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