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The Escherichia coli protein YjjG is a house-cleaning nucleotidase in vivo.
Titz, Björn; Häuser, Roman; Engelbrecher, Anne; Uetz, Peter.
Afiliação
  • Titz B; Institute of Genetics, Forschungszentrum Karlsruhe, Karlsruhe, Germany. bjoern@itg.fzk.de
FEMS Microbiol Lett ; 270(1): 49-57, 2007 May.
Article em En | MEDLINE | ID: mdl-17286574
ABSTRACT
House-cleaning enzymes protect cells from the adverse effects of noncanonical metabolic chemical compounds. The Escherichia coli nucleotide phosphatase YjjG (B4374, JW4336) functions as a house-cleaning phosphatase in vivo. YjjG protects the cell against noncanonical pyrimidine derivatives such as 5-fluoro-2'-deoxyuridine (5-FdUridine), 5-fluorouridine, 5-fluoroorotic acid (5-FOA), 5-fluorouracil, and 5-aza-2'-deoxycytidine. YjjG prevents the incorporation of potentially mutagenic nucleotides into DNA as shown for 5-bromo-2'-deoxyuridine (BrdU). Its enzymatic activity in vitro towards noncanonical 5-fluoro-2'-deoxyuridine monophosphate (5-FdUMP) is higher than towards canonical thymidine monophosphate (dTMP). The closest homolog in humans, HDHD4, does not show a protective effect against noncanonical nucleotides, excluding an involvement of HDHD4 in resistance against noncanonical nucleotides used for cancer chemotherapy. The substrate spectrum of YjjG suggests that its in vivo substrates are noncanonical pyrimidine derivatives, which might also include oxidized nucleobases such as 5-formyluracil and 5-hydroxyuracil.
Assuntos
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Coleções: 01-internacional Temas: Geral Base de dados: MEDLINE Assunto principal: Proteínas de Escherichia coli / Escherichia coli / N-Glicosil Hidrolases / Nucleotidases Idioma: En Revista: FEMS Microbiol Lett Ano de publicação: 2007 Tipo de documento: Article País de afiliação: Alemanha
Buscar no Google
Coleções: 01-internacional Temas: Geral Base de dados: MEDLINE Assunto principal: Proteínas de Escherichia coli / Escherichia coli / N-Glicosil Hidrolases / Nucleotidases Idioma: En Revista: FEMS Microbiol Lett Ano de publicação: 2007 Tipo de documento: Article País de afiliação: Alemanha