ArticleJournal of bacteriology2002
The unique tuf2 gene from the kirromycin producer Streptomyces ramocissimus encodes a minor and kirromycin-sensitive elongation factor Tu.
Article in Journal of bacteriology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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Who cites it
3 citing papers in PubMed, 5 citations in OpenAlex.
- Avoidance of suicide in antibiotic-producing microbes.Journal of industrial microbiology & biotechnology · 2010Review
- Elongation factor Tu3 (EF-Tu3) from the kirromycin producer Streptomyces ramocissimus Is resistant to three classes of EF-Tu-specific inhibitors.Journal of bacteriology · 2007Article
- Archaeal elongation factor 1alpha from Sulfolobus solfataricus interacts with the eubacterial antibiotic GE2270A.Extremophiles : life under extreme conditions · 2004Article
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Authors and funding
3 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
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.
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