Confirmation of Frm2 as a novel nitroreductase in Saccharomyces cerevisiae

  • Seo Young Bang
  • , Jeong Hoon Kim
  • , Phil Young Lee
  • , Kwang Hee Bae
  • , Jong Suk Lee
  • , Pan Soo Kim
  • , Do Hee Lee
  • , Pyung Keun Myung
  • , Byoung Chul Park
  • , Sung Goo Park

Research output: Contribution to journalArticlepeer-review

16 Scopus citations

Abstract

Nitroreductases comprise a group of FMN- or FAD-dependent enzymes that reduce nitrosubstituted compounds by using NAD(P)H, and are found in bacterial species and yeast. Although there is little information on the biological functions of nitroreductases, some studies suggest their possible involvement in oxidative stress responses. In the yeast Saccharomyces cerevisiae, a putative nitroreductase protein, Frm2, has been identified based on its sequence similarity with known bacterial nitroreductases. Frm2 has been reported to function in the lipid signaling pathway. To study the functions of Frm2, we measured the nitroreductase activity of purified Frm2 on 4-nitroquinoline-N-oxide (4-NQO) using NADH. LC-MS analysis of the reaction products revealed that Frm2 reduced NQO into 4-aminoquinoline-N-oxide (4-AQO) via 4-hydroxyaminoquinoline (4-HAQO). An Frm2 deletion mutant exhibited growth inhibition in the presence of 4-NQO. Thus, in this study, we demonstrate a novel nitroreductase activity of Frm2 and its involvement in the oxidative stress defense system.

Original languageEnglish
Pages (from-to)638-641
Number of pages4
JournalBiochemical and Biophysical Research Communications
Volume423
Issue number4
DOIs
StatePublished - 13 Jul 2012
Externally publishedYes

Keywords

  • 4-AQO
  • 4-NQO
  • Frm2
  • Nitroreductase
  • Oxidative stress

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