Gene cloning, purification, and characterization of two cyanobacterial NifS homologs driving iron-sulfur cluster formation

Biosci Biotechnol Biochem. 2000 Nov;64(11):2412-9. doi: 10.1271/bbb.64.2412.

Abstract

Iron-sulfur proteins are essential in the photosynthetic system and many other biological processes. We have isolated and characterized enzymes driving the formation of iron-sulfur clusters from Synechocystis sp. PCC6803. Two genes (slr0387 and sll0704), showing similarity to nifS of Azotobacter vinelandii, were cloned, and their gene products (SsCsdl and SsCsd2) were purified. They catalyzed the desulfuration of L-cysteine. Reconstitution of a [2Fe-2S] cluster of cyanobacterial ferredoxin proceeded much faster in the presence of L-cysteine and either of these enzymes than when using sodium sulfide. These results suggest that SsCsdl and SsCsd2 facilitate the iron-sulfur cluster assembly by producing inorganic sulfur from L-cysteine. Synechocystis sp. PCC6803 has no gene coding for a protein with similarity to the N-terminal domain of NifU of A. vinelandii, which is believed to cooperate with NifS to assemble iron-sulfur clusters. Thus, the cluster formation in the cyanobacterium probably proceeds through a mechanism that is different from that in A. vinelandii.

MeSH terms

  • Bacterial Proteins / chemistry
  • Carbon-Sulfur Lyases*
  • Catalysis
  • Cloning, Molecular
  • Cyanobacteria / enzymology
  • Cyanobacteria / genetics*
  • Iron-Sulfur Proteins / genetics
  • Iron-Sulfur Proteins / isolation & purification
  • Iron-Sulfur Proteins / metabolism
  • Lyases / genetics*
  • Lyases / isolation & purification
  • Lyases / metabolism

Substances

  • Bacterial Proteins
  • Iron-Sulfur Proteins
  • nifS protein, Bacteria
  • Lyases
  • Carbon-Sulfur Lyases
  • cysteine desulfurase