TY - JOUR
T1 - Identification and characterization of the lipoprotein N-acyltransferase in Bacteroides
AU - Armbruster, Krista M.
AU - Jiang, Jiawen
AU - Sartorio, Mariana G.
AU - Scott, Nichollas E.
AU - Peterson, Jenna M.
AU - Sexton, Jonathan Z.
AU - Feldman, Mario F.
AU - Koropatkin, Nicole M.
N1 - Publisher Copyright:
© 2024 the Author(s).
PY - 2024/11/12
Y1 - 2024/11/12
N2 - 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.
AB - 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.
KW - Bacteroides
KW - acyltransferase
KW - cell surface
KW - lipoproteins
UR - https://www.scopus.com/pages/publications/85208517169
U2 - 10.1073/pnas.2410909121
DO - 10.1073/pnas.2410909121
M3 - Article
C2 - 39495918
AN - SCOPUS:85208517169
SN - 0027-8424
VL - 121
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 46
M1 - e2410909121
ER -