4.6 Article

Regulation of antimycin biosynthesis by the orphan ECF RNA polymerase sigma factor σAntA

Journal

PEERJ
Volume 2, Issue -, Pages -

Publisher

PEERJ INC
DOI: 10.7717/peerj.253

Keywords

Streptomyces; Antibiotics; Secondary metabolites; Actinomycetes; Gene regulation; ECF sigma factor; Antimycin

Funding

  1. Medical Research Council [G0801721]
  2. Natural Environment Research Council [NE/J01074X/1]
  3. John and Pamela Salter Charitable Trust
  4. Biotechnology and Biological Sciences Research Council [BBS/E/T/000PR6193] Funding Source: researchfish
  5. Medical Research Council [G0801721] Funding Source: researchfish
  6. Natural Environment Research Council [NE/J01074X/1] Funding Source: researchfish
  7. BBSRC [BBS/E/T/000PR6193] Funding Source: UKRI
  8. MRC [G0801721] Funding Source: UKRI
  9. NERC [NE/J01074X/1] Funding Source: UKRI

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Antimycins are an extended family of depsipeptides that arc made by filamentous actinomycete bacteria and were first isolated more than 60 years ago. Recently, antimycins have attracted renewed interest because of their activities against the antiapoptotic machineries inside human cells which could make them promising anticancer compounds. The biosynthetic pathway for antimycins was recently characterised but very little is known about the organisation and regulation of the antimycin (ant) gene cluster. here we report that the ant gene cluster in Streptomyces albus is organized into four transcriptional units; the antBA, antCDE, antGF and antHIJKLMNO operons. Unusually for secondary metabolite clusters, the antG and antH promoters are regulated by an extracytoplasmic function (ECF) RNA polymerase sigma factor named sigma(AntA) which represents a new sub-family of ECU sigma factors that is only found in antimycin producing strains. We show that sigma(AnIA) controls production of the unusual precursor 3-aminosalicylate which is absolutely required for the production of antimycins. sigma(AntA) is highly conserved in antimycin producing strains and the 10 and 35 elements at the sigma(AntA) regulated antG and antH promoters are also highly conserved suggesting a common mechanism of regulation. We also demonstrate that altering the C-terminal Ala-Ala residues found in all sigma(AntA) proteins to Asp-Asp increases expression of the antFG and antGHIJKLMNO operons and we speculate that this Ala-Ala motif may be a signal for the protease ClpXP.

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