Literature DB >> 16448509

Munumbicins E-4 and E-5: novel broad-spectrum antibiotics from Streptomyces NRRL 3052.

Uvidelio F Castillo1, Gary A Strobel, Kirby Mullenberg, Margaret M Condron, David B Teplow, Vincenzo Folgiano, Monica Gallo, Rosalia Ferracane, Luisa Mannina, Stepanie Viel, Marissa Codde, Richard Robison, Heide Porter, James Jensen.   

Abstract

Streptomyces NRRL 30562 was originally isolated as an endophyte from Kennedia nigriscans, snakevine, in the Northern Territory of Australia. This plant has been used for centuries by Aboriginal peoples to treat open bleeding wounds to prevent sepsis. A solvent extract of the crude fluid from cultures of this endophyte possesses wide-spectrum antibiotic activity. Some of the bioactivity is associated with the appearance of actinomycins X2, D, and Xobeta, the first two of which had been previously designated munumbicins A and B, respectively. Other novel compounds bearing wide-spectrum antibiotic activity are also produced by Streptomyces NRRL 30562, and these are designated munumbicins E-4 and E-5. Mass spectrometric analyses of these peptide antibiotics show that they have identical masses (1445.00) but different retention times on HPLC. Both compounds showed activity against gram-positive and gram-negative bacteria. The plant pathogenic fungus, Pythium ultimum is sensitive to both munumbicins at 5.0 microg mL(-1) The malarial parasite, Plasmodium falciparum has IC50 values of 0.50+/-0.08 and 0.87+/-0.0.26 microg mL(-1) for E-4 and E-5, respectively. It appears that other bioactive compounds, related to E-4 and E-5, are also produced making it the most biologically active endophytic Streptomyces spp. on record.

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Year:  2006        PMID: 16448509     DOI: 10.1111/j.1574-6968.2005.00080.x

Source DB:  PubMed          Journal:  FEMS Microbiol Lett        ISSN: 0378-1097            Impact factor:   2.742


  20 in total

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Review 9.  Endophytic actinobacteria of medicinal plants: diversity and bioactivity.

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10.  Endophytic bacteria as a source of novel antibiotics: An overview.

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Journal:  Pharmacogn Rev       Date:  2013-01
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