Purification and characterization of NfrA1, a Bacillus subtilis nitro/flavin reductase capable of interacting with the bacterial luciferase

Biosci Biotechnol Biochem. 1998 Oct;62(10):1978-87. doi: 10.1271/bbb.62.1978.

Abstract

ipa-43d is a hypothetical gene identified by the Bacillus subtilis genome project (Mol. Microbiol. 10, 371-384 1993; Nature 390, 249-256 1997). The ipa-43d protein overexpressed in E. coli was purified to homogeneity and its properties were analyzed biochemically. The ipa-43d protein was found to be tightly associated with FMN and to be capable of reducing both nitrofurazone and FMN effectively. Although the ipa-43d protein catalysis obeys the ping-pong Bi-Bi mechanism, catalysis mode was changed to the sequential mechanism upon coupling with the bioluminescent reaction. Database search showed that B. subtilis possessed four genes (ipa-44d, ytmO, yddN, and yvbT), encoding proteins similar in amino acid sequence to LuxA and LuxB of Photobacterium fischeri, and, in particular, ipa-44d is immediately adjacent to the ipa-43d gene on the chromosome.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Bacillus subtilis / enzymology*
  • Bacterial Proteins*
  • Flavin Mononucleotide / metabolism
  • Gene Expression Regulation, Bacterial
  • Luciferases / metabolism*
  • Molecular Sequence Data
  • Nitrofurazone / metabolism
  • Nitroreductases / isolation & purification*
  • Nitroreductases / metabolism
  • Sequence Homology, Amino Acid

Substances

  • Bacterial Proteins
  • Flavin Mononucleotide
  • Luciferases
  • Nitroreductases
  • NfrA1 protein, Bacillus subtilis
  • Nitrofurazone