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Job contenders: roles of the β‐barrel assembly machinery and the translocation and assembly module in autotransporter secretion
Author(s) -
Albenne Cécile,
Ieva Raffaele
Publication year - 2017
Publication title -
molecular microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.857
H-Index - 247
eISSN - 1365-2958
pISSN - 0950-382X
DOI - 10.1111/mmi.13832
Subject(s) - biology , secretion , barrel (horology) , chromosomal translocation , microbiology and biotechnology , order (exchange) , genetics , engineering , mechanical engineering , gene , biochemistry , finance , economics
Summary In Gram‐negative bacteria, autotransporters secrete effector protein domains that are linked to virulence. Although they were once thought to be simple and autonomous secretion machines, mounting evidence reveals that multiple factors of the bacterial envelope are necessary for autotransporter assembly. Secretion across the outer membrane of their soluble effector “passenger domain” is promoted by the assembly of an outer membrane‐spanning “β‐barrel domain”. Both reactions require BamA, an essential component of the β‐barrel assembly machinery (BAM complex) that catalyzes the final reaction step by which outer membrane proteins are integrated into the lipid bilayer. A large amount of data generated in the last decade has shed key insights onto the mechanistic coordination of autotransporter β‐barrel domain assembly and passenger domain secretion. These results, together with the recently solved structures of the BAM complex, offer an unprecedented opportunity to discuss a detailed model of autotransporter assembly. Importantly, some autotransporters benefit from the presence of an additional machinery, the translocation and assembly module (TAM), a two‐membrane spanning complex, which contains a BamA‐homologous subunit. Although it remains unclear how the BAM complex and the TAM cooperate, it is evident that multiple preparatory steps are necessary for efficient autotransporter biogenesis.