Structure and mechanism of the tRNA-dependent lantibiotic dehydratase NisB

Nature. 2015 Jan 22;517(7535):509-12. doi: 10.1038/nature13888. Epub 2014 Oct 26.

Abstract

Lantibiotics are a class of peptide antibiotics that contain one or more thioether bonds. The lantibiotic nisin is an antimicrobial peptide that is widely used as a food preservative to combat food-borne pathogens. Nisin contains dehydroalanine and dehydrobutyrine residues that are formed by the dehydration of Ser/Thr by the lantibiotic dehydratase NisB (ref. 2). Recent biochemical studies revealed that NisB glutamylates Ser/Thr side chains as part of the dehydration process. However, the molecular mechanism by which NisB uses glutamate to catalyse dehydration remains unresolved. Here we show that this process involves glutamyl-tRNA(Glu) to activate Ser/Thr residues. In addition, the 2.9-Å crystal structure of NisB in complex with its substrate peptide NisA reveals the presence of two separate domains that catalyse the Ser/Thr glutamylation and glutamate elimination steps. The co-crystal structure also provides insights into substrate recognition by lantibiotic dehydratases. Our findings demonstrate an unexpected role for aminoacyl-tRNA in the formation of dehydroamino acids in lantibiotics, and serve as a basis for the functional characterization of the many lantibiotic-like dehydratases involved in the biosynthesis of other classes of natural products.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins / chemistry*
  • Bacterial Proteins / classification
  • Bacterial Proteins / metabolism*
  • Bacteriocins / biosynthesis
  • Bacteriocins / metabolism*
  • Crystallography, X-Ray
  • Escherichia coli / genetics
  • Glutamic Acid / metabolism
  • Hydro-Lyases / chemistry*
  • Hydro-Lyases / classification
  • Hydro-Lyases / metabolism*
  • Lactococcus lactis / enzymology*
  • Lactococcus lactis / genetics
  • Membrane Proteins / chemistry*
  • Membrane Proteins / classification
  • Membrane Proteins / metabolism*
  • Models, Molecular
  • Nisin / biosynthesis
  • Nisin / metabolism
  • Phylogeny
  • Protein Structure, Tertiary
  • RNA, Transfer, Glu / genetics
  • RNA, Transfer, Glu / metabolism*
  • Serine / metabolism
  • Threonine / metabolism

Substances

  • Bacterial Proteins
  • Bacteriocins
  • Membrane Proteins
  • NisB protein, Lactococcus lactis
  • RNA, Transfer, Glu
  • Nisin
  • Threonine
  • Glutamic Acid
  • Serine
  • Hydro-Lyases