Actinorhodin

Actinorhodin
Names
IUPAC name
[3'-carboxymethyl-5,5',10,10'-tetrahydroxy-1,1'-dimethyl-6,6',9,9'-tetraoxo-3,3',4,4'6,6'9,9'-octahydro-1H,1'H-8,8'-bi(benzo[g]isochromen)-3-yl]acetic acid[1]
Identifiers
1397-77-9 N
3D model (Jmol) Interactive image
ChEBI CHEBI:2448 N
ChemSpider 16735642 YesY
Properties
C32H26O14
Molar mass 634.54 g mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

Actinorhodin is a benzoisochromanequinone polyketide antibiotic produced by Streptomyces coelicolor.[2][3] The gene cluster responsible for actinorhodin production contains the biosynthetic enzymes and genes responsible for export of the antibiotic.[4] The antibiotic also has the effect of being a pH indicator due to its pH-dependent color change.[5]

References

  1. "Actinorhodin (CHEBI:2448)". EBI Small Molecule Database. 18 February 2008. Retrieved 9 February 2010.
  2. Magnolo SK, Leenutaphong DL, DeModena JA, et al. (May 1991). "Actinorhodin production by Streptomyces coelicolor and growth of Streptomyces lividans are improved by the expression of a bacterial hemoglobin". Biotechnology (N.Y.). 9 (5): 473–6. doi:10.1038/nbt0591-473. PMID 1367312.
  3. Brian P, Riggle PJ, Santos RA, Champness WC (June 1996). "Global negative regulation of Streptomyces coelicolor antibiotic synthesis mediated by an absA-encoded putative signal transduction system". J. Bacteriol. 178 (11): 3221–31. PMC 178074Freely accessible. PMID 8655502.
  4. Tahlan, K; Ahn SK; Sing A; Bodnaruk TD; Willems AR; Davidson AR; Nodwell JR. (February 2007). "Initiation of actinorhodin export in Streptomyces coelicolor". Molecular Microbiology. 63: 951–961. doi:10.1111/j.1365-2958.2006.05559.x. PMID 17338074.
  5. Bystrykh, LV; Fernández-Moreno MA; Herrema JK; Malpartida F; Hopwood DA; Dijkhuizen L (April 1996). "Production of actinorhodin-related "blue pigments" by Streptomyces coelicolor A3(2)". Journal of Bacteriology. 178: 2238–44. PMID 8636024.


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