Affiliation:
1. Department of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park, Pennsylvania 16802
2. Department of Biology, University of Oslo, Blindern, N-0316, Oslo, Norway
Abstract
ABSTRACT
Bacteriochlorophylls (BChls)
c
and
d
, two of the major light-harvesting pigments in photosynthetic green sulfur bacteria, differ only by the presence of a methyl group at the C-20 methine bridge position in BChl
c
. A gene potentially encoding the C-20 methyltransferase,
bchU
, was identified by comparative analysis of the
Chlorobium tepidum
and
Chloroflexus aurantiacus
genome sequences. Homologs of this gene were amplified and sequenced from
Chlorobium phaeobacteroides
strain 1549,
Chlorobium vibrioforme
strain 8327
d
, and
C. vibrioforme
strain 8327
c
, which produce BChls
e
,
d
, and
c
, respectively. A single nucleotide insertion in the
bchU
gene of
C. vibrioforme
strain 8327
d
was found to cause a premature, in-frame stop codon and thus the formation of a truncated, nonfunctional gene product. The spontaneous mutant of this strain that produces BChl
c
(strain 8327
c
) has a second frameshift mutation that restores the correct reading frame in
bchU
. The
bchU
gene was inactivated in
C. tepidum
, a BChl
c
-producing species, and the resulting mutant produced only BChl
d
. Growth rate measurements showed that BChl
c
- and
d
-producing strains of the same organism (
C. tepidum
or
C. vibrioforme
) have similar growth rates at high and intermediate light intensities but that strains producing BChl
c
grow faster than those with BChl
d
at low light intensities. Thus, the
bchU
gene encodes the C-20 methyltransferase for BChl
c
biosynthesis in
Chlorobium
species, and methylation at the C-20 position to produce BChl
c
rather than BChl
d
confers a significant competitive advantage to green sulfur bacteria living at limiting red and near-infrared light intensities.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
71 articles.
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