A membrane-bound prenyltransferase catalyzes the O-prenylation of 1,6-dihydroxyphenazine in the marine bacterium Streptomyces sp. CNQ-509

Chembiochem. 2014 Nov 3;15(16):2385-92. doi: 10.1002/cbic.201402394. Epub 2014 Sep 15.

Abstract

Streptomyces sp. CNQ-509 produces the rare O-prenylated phenazines marinophenazines A and B. To identify the enzyme catalyzing the O-prenyl transfer in marinophenazine biosynthesis, we sequenced the genome of S. sp. CNQ-509. This led to the identification of two genomic loci harboring putative phenazine biosynthesis genes. The first locus contains orthologues for all seven genes involved in phenazine-1-carboxylic acid biosynthesis in pseudomonads. The second locus contains two known phenazine biosynthesis genes and a putative prenyltransferase gene termed cnqPT1. cnqPT1 codes for a membrane protein with sequence similarity to the prenyltransferase UbiA of ubiquinone biosynthesis. The enzyme CnqPT1 was identified as a 1,6-dihydroxyphenazine geranyltransferase, which catalyzes the C-O bond formation between C-1 of the geranyl moiety and O-6 of the phenazine scaffold. CnqPT1 is the first example of a prenyltransferase catalyzing O-prenyl transfer to a phenazine.

Keywords: Streptomyces; biosynthesis; enzyme catalysis; phenazine; prenyltransferase.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins / metabolism*
  • Biocatalysis
  • Dimethylallyltranstransferase / metabolism*
  • Kinetics
  • Multigene Family
  • Phenazines / chemistry
  • Phenazines / metabolism*
  • Prenylation
  • Streptomyces / enzymology*
  • Streptomyces / genetics
  • Substrate Specificity

Substances

  • Bacterial Proteins
  • Phenazines
  • 1-phenazinecarboxylic acid
  • Dimethylallyltranstransferase