Affiliation:
1. Department of Biochemistry, Leiden Institute of Chemistry, Leiden University, 2300 RA Leiden, The Netherlands
Abstract
ABSTRACT
Streptomyces ramocissimus
, the producer of elongation factor Tu (EF-Tu)-targeted antibiotic kirromycin, contains three divergent
tuf
-like genes, with
tuf1
encoding regular kirromycin-sensitive EF-Tu1; the functions of
tuf2
and
tuf3
are unknown. Analysis of the
tuf
gene organization in nine producers of kirromycin-type antibiotics revealed that they all contain homologues of
tuf1
and sometimes of
tuf3
but that
tuf2
was found in
S. ramocissimus
only. The
tuf2
-flanking regions were sequenced, and the two
tuf2
-surrounding open reading frames were shown to be oriented in opposite directions. In vivo transcription analysis of the
tuf2
gene displayed an upstream region with bidirectional promoter activity. The transcription start site of
tuf2
was located approximately 290 nucleotides upstream of the coding sequence. Very small amounts of
tuf2
transcripts were detected in both liquid- and surface-grown cultures of
S. ramocissimus
, consistent with the apparent absence of EF-Tu2 in total protein extracts. The
tuf2
transcript level was not influenced by the addition of kirromycin to exponentially growing cultures. To assess the function of
S. ramocissimus
EF-Tu2, the protein was overexpressed in
Streptomyces coelicolor
LT2. This strain is a J1501 derivative containing His
6
-tagged EF-Tu1 as the sole EF-Tu species, which facilitated the separation of EF-Tu2 from the interfering EF-Tu1.
S. ramocissimus
EF-Tu1 and EF-Tu2 were indistinguishable in their ability to stimulate protein synthesis in vitro and exhibited the same kirromycin sensitivity, which excludes the possibility that EF-Tu2 is directly involved in the kirromycin resistance mechanism of
S. ramocissimus
.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
4 articles.
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