Affiliation:
1. Department of Microbiology and Molecular Genetics, Harvard Medical School, Boston, Massachusetts 02115
Abstract
ABSTRACT
We describe the further utilization of a genetic screen that identifies mutations defective in the assembly of proteins into the
Escherichia coli
cytoplasmic membrane. The screen yielded mutations in each of the known genes encoding components of the
E. coli
signal recognition particle pathway:
ffh
,
ffs
, and
ftsY
, which encode Ffh, 4.5S RNA, and FtsY, respectively. In addition, the screen yielded mutations in
secM
, which is involved in regulating levels of the SecA component of the bacterium’s protein export pathway. We used a sensitive assay involving biotinylation to show that all of the mutations caused defects in the membrane insertions of three topologically distinct membrane proteins, AcrB, MalF, and FtsQ. Among the mutations that resulted in membrane protein insertion defects, only the
secM
mutations also showed defects in the translocation of proteins into the
E. coli
periplasm. Genetic evidence suggests that the S382T alteration of Ffh affects the interaction between Ffh and 4.5S RNA.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
41 articles.
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