Identification and characterization of the lipoprotein N-acyltransferase in Bacteroides

  • Krista M. Armbruster
  • , Jiawen Jiang
  • , Mariana G. Sartorio
  • , Nichollas E. Scott
  • , Jenna M. Peterson
  • , Jonathan Z. Sexton
  • , Mario F. Feldman
  • , Nicole M. Koropatkin

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

Members of the Bacteroidota compose a large portion of the human gut microbiota, contributing to overall gut health via the degradation of various polysaccharides. This process is facilitated by lipoproteins, globular proteins anchored to the cell surface by a lipidated N-terminal cysteine. Despite their importance, lipoprotein synthesis by these bacteria is understudied. In Escherichia coli, the α-amino-linked lipid of lipoproteins is added by the lipoprotein N-acyltransferase Lnt. Herein, we have identified a protein distinct from Lnt responsible for the same process in Bacteroides, named lipoprotein N-acyltransferase in Bacteroides (Lnb). Deletion of Lnb yields cells that synthesize diacylated lipoproteins, with impacts on cell viability and morphology, growth on polysaccharides, and protein composition of membranes and outer membrane vesicles (OMVs). Our results not only challenge the accepted paradigms of lipoprotein biosynthesis in gram-negative bacteria but also suggest the existence of a new family of lipoprotein N-acyltransferases.

Original languageEnglish
Article numbere2410909121
JournalProceedings of the National Academy of Sciences of the United States of America
Volume121
Issue number46
DOIs
StatePublished - Nov 12 2024

Keywords

  • Bacteroides
  • acyltransferase
  • cell surface
  • lipoproteins

Fingerprint

Dive into the research topics of 'Identification and characterization of the lipoprotein N-acyltransferase in Bacteroides'. Together they form a unique fingerprint.

Cite this