Affiliation:
1. School of Microbiology and Immunology, University of New South Wales, Sydney, New South Wales 2052, Australia
Abstract
ABSTRACT
We report the cloning, sequencing, and characterization of the
rpoE
homolog in
Vibrio angustum
S14. The
rpoE
gene encodes a protein with a predicted molecular mass of 19.4 kDa and has been demonstrated to be present as a single-copy gene by Southern blot analysis. The deduced amino acid sequence of RpoE is most similar to that of the RpoE homolog of
Sphingomonas aromaticivorans
, ς
24
, displaying sequence similarity and identity of 63 and 43%, respectively. Northern blot analysis demonstrated the induction of
rpoE
6, 12, and 40 min after a temperature shift to 40°C. An
rpoE
mutant was constructed by gene disruption. There was no difference in viability during logarithmic growth, stationary phase, or carbon starvation between the wild type and the
rpoE
mutant strain. In contrast, survival of the mutant was impaired following heat shock during exponential growth, as well as after oxidative stress at 24 h of carbon starvation. The mutant exhibited microcolony formation during optimal growth temperatures (22 to 30°C), and cell area measurements revealed an increase in cell volume of the mutant during growth at 30°C, compared to the wild-type strain. Moreover, outer membrane and periplasmic space protein analysis demonstrated many alterations in the protein profiles for the mutant during growth and carbon starvation, as well as following oxidative stress, in comparison with the wild-type strain. It is thereby concluded that RpoE has an extracytoplasmic function and mediates a range of specific responses in stressed as well as unstressed cells of
V. angustum
S14.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
18 articles.
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