Affiliation:
1. Department of Molecular Biology, University of Wyoming, Laramie, Wyoming
2. Department of Bacteriology, University of Wisconsin, Madison, Wisconsin
Abstract
ABSTRACT
In the facultatively phototrophic proteobacterium
Rhodobacter sphaeroides
, formation of the photosynthetic apparatus is oxygen dependent. When oxygen tension decreases, the response regulator PrrA of the global two-component PrrBA system is believed to directly activate transcription of the
puf
,
puh
, and
puc
operons, encoding structural proteins of the photosynthetic complexes, and to indirectly upregulate the photopigment biosynthesis genes
bch
and
crt
. Decreased oxygen also results in inactivation of the photosynthesis-specific repressor PpsR, bringing about derepression of the
puc
,
bch
, and
crt
operons. We uncovered a hierarchical relationship between these two regulatory systems, earlier thought to function independently. We also more accurately assessed the spectrum of gene targets of the PrrBA system. First, expression of the
appA
gene, encoding the PpsR antirepressor, is PrrA dependent, which establishes one level of hierarchical dominance of the PrrBA system over AppA-PpsR. Second, restoration of the
appA
transcript to the wild-type level is insufficient for rescuing phototrophic growth impairment of the
prrA
mutant, whereas inactivation of
ppsR
is sufficient. This suggests that in addition to controlling
appA
transcription, PrrA affects the activity of the AppA-PpsR system via an as yet unidentified mechanism(s). Third, PrrA directly activates several
bch
and
crt
genes, traditionally considered to be the PpsR targets. Therefore, in
R. sphaeroides
, the global PrrBA system regulates photosynthesis gene expression (i) by rigorous control over the photosynthesis-specific AppA-PpsR regulatory system and (ii) by extensive direct transcription activation of genes encoding structural proteins of photosynthetic complexes as well as genes encoding photopigment biosynthesis enzymes.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
20 articles.
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