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Sequence Diversity of the oprI Gene, Coding for Major Outer Membrane Lipoprotein I, among rRNA Group I Pseudomonads
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ABSTRACT
The sequence of
oprI
, the gene coding for the major outer membrane lipoprotein I, was determined by PCR sequencing for representatives of 17 species of rRNA group I pseudomonads, with a special emphasis on
Pseudomonas aeruginosa
and
Pseudomonas fluorescens
. Within the
P. aeruginosa
species,
oprI
sequences for 25 independent isolates were found to be identical, except for one silent substitution at position 96. The
oprI
sequences diverged more for the other rRNA group I pseudomonads (85 to 91% similarity with
P. aeruginosa oprI
). An accumulation of silent and also (but to a much lesser extent) nonsilent substitutions in the different sequences was found. A clustering according to the respective presence and/or positions of the
Hae
III,
Pvu
II, and
Sph
I sites could also be obtained. A sequence cluster analysis showed a rather widespread distribution of
P. fluorescens
isolates. All other rRNA group I pseudomonads clustered in a manner that was in agreement with other studies, showing that the
oprI
gene can be useful as a complementary phylogenetic marker for classification of rRNA group I pseudomonads.
American Society for Microbiology
Title: Sequence Diversity of the
oprI
Gene, Coding for Major Outer Membrane Lipoprotein I, among rRNA Group I Pseudomonads
Description:
ABSTRACT
The sequence of
oprI
, the gene coding for the major outer membrane lipoprotein I, was determined by PCR sequencing for representatives of 17 species of rRNA group I pseudomonads, with a special emphasis on
Pseudomonas aeruginosa
and
Pseudomonas fluorescens
.
Within the
P.
aeruginosa
species,
oprI
sequences for 25 independent isolates were found to be identical, except for one silent substitution at position 96.
The
oprI
sequences diverged more for the other rRNA group I pseudomonads (85 to 91% similarity with
P.
aeruginosa oprI
).
An accumulation of silent and also (but to a much lesser extent) nonsilent substitutions in the different sequences was found.
A clustering according to the respective presence and/or positions of the
Hae
III,
Pvu
II, and
Sph
I sites could also be obtained.
A sequence cluster analysis showed a rather widespread distribution of
P.
fluorescens
isolates.
All other rRNA group I pseudomonads clustered in a manner that was in agreement with other studies, showing that the
oprI
gene can be useful as a complementary phylogenetic marker for classification of rRNA group I pseudomonads.
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