Photoisomerization of retinal at 13-ene is important for phototaxis of Chlamydomonas reinhardtii: simultaneous measurements of phototactic and photophobic responses

Biochem Biophys Res Commun. 1991 Aug 15;178(3):1273-9. doi: 10.1016/0006-291x(91)91031-7.

Abstract

A real-time automated method was developed for simultaneous measurements of phototactic orientation (phototaxis) and step-up photophobic response of flagellated microorganisms. Addition of all-trans retinal restored both photoresponses in a carotenoid-deficient mutant strain of Chlamydomonas reinhardtii in a dose-dependent manner. The phototactic orientation was biphasic with respect to both the light intensity and the concentration of retinal. All-trans retinal was more effective than 11-cis retinal to regenerate both photobehavioral responses. Analogs having locked 11-cis configurations and a phenyl ring in the side chain also induced photoresponses, although at concentrations more than two orders of magnitude higher than all-trans retinal. According to the present assay method, the responses were hardly detectable in cells incubated with retinal analogs in which the 13-ene was locked in either its trans or cis configuration. The results strongly suggest that the isomerization of the 13-14 double bond is important for photobehavioral signal transduction and that a single retinal-dependent photoreceptor controls both phototactic and photophobic responses.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Cell Movement / drug effects
  • Cell Movement / radiation effects
  • Chlamydomonas / drug effects
  • Chlamydomonas / genetics
  • Chlamydomonas / physiology*
  • Chlamydomonas / radiation effects
  • Darkness
  • Isomerism
  • Light
  • Retinaldehyde / analogs & derivatives*
  • Retinaldehyde / pharmacology*
  • Retinaldehyde / radiation effects
  • Structure-Activity Relationship

Substances

  • Retinaldehyde