Maristentorin, a novel pigment from the positively phototactic marine ciliate Maristentor dinoferus, is structurally related to hypericin and stentorin

J Phys Chem B. 2006 Mar 30;110(12):6359-64. doi: 10.1021/jp055871f.

Abstract

The photoreceptor pigment of the heterotrich ciliate, Maristentor dinoferus, has been characterized. It is structurally similar to those of Stentor coeruleus and Blepharisma japonicum but differs significantly in that it bears no aromatic hydrogens. The structure of the pigment, maristentorin, is based upon the hypericin skeleton, and its spectra are nearly identical to those of hypericin but shifted toward the red. Within experimental error, its fluorescence lifetime is identical to that of hypericin, approximately 5.5 ns in dimethylsulfoxide. It is remarkable that while the pigments are structurally similar in S. coeruleus and M. dinoferus, in the former there is an abrupt photophobic response, whereas in the latter there is a slow response toward light. The roles of the hypericin-like pigments in the heterotrich ciliates are discussed as potentially analogous in Maristentor.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Anthracenes
  • Chromatography, Gel
  • Ciliophora / chemistry*
  • Marine Biology
  • Mass Spectrometry
  • Nuclear Magnetic Resonance, Biomolecular
  • Perylene / analogs & derivatives*
  • Perylene / chemistry
  • Polycyclic Compounds / chemistry*

Substances

  • Anthracenes
  • Polycyclic Compounds
  • maristentorin
  • Perylene
  • hypericin