“Woah! It's like Spotify but for academic articles.”

Instant Access to Thousands of Journals for just $40/month

Mutual orientation of absorbing chromophores and long wavelength pigments in photosystem I particles

Mutual orientation of absorbing chromophores and long wavelength pigments in photosystem I particles The fluorescence anisotropy of photosystem I particles, isolated from spinach chloroplasts and containing approximately 200 chlorophyll molecules per reaction center, has been investigated at low temperatures. Fluorescence anisotropy has been measured upon excitation with laser lines at 476.5 and 632.8 nm. Using our data for the fluorescence anisotropy at these conditions and the new `practical' formula for the degree of polarization of a triple-chromophore complex under steady-state excitation, derived recently by Demidov, we estimate the mutual orientation of absorbing chromophores and long wavelength pigments—chlorophyll a molecules, that absorb at wavelengths longer than the corresponding reaction center, in Photosystem I particles. The angle between the transition dipole moments of chlorophyll a , belonging to the light-harvesting complex of PS I and absorbing the excitation at 632.8 nm, and the emitting long wavelength pigment at 735 nm is estimated to be 40°, whereas the angle between the transition dipole moments of chlorophyll b , belonging to the light-harvesting complex of PS I and absorbing the excitation at 476.5 nm, and the emitting long wavelength pigment at 735 nm—60°. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy Elsevier
Loading next page...
 
/lp/elsevier/mutual-orientation-of-absorbing-chromophores-and-long-wavelength-MtVEhBAhNo

You're reading a free preview. Subscribe to read the entire article.

And millions more from thousands of peer-reviewed journals, for just $40/month

To be the best researcher, you need access to the best research

  • With DeepDyve, you can stop worrying about how much articles cost, or if it's too much hassle to order — it's all at your fingertips. Your research is important and deserves the top content.
  • Read from thousands of the leading scholarly journals from Springer, Elsevier, Nature, IEEE, Wiley-Blackwell and more.
  • All the latest content is available, no embargo periods.

Stop missing out on the latest updates in your field

  • We’ll send you automatic email updates on the keywords and journals you tell us are most important to you.
  • There is a lot of content out there, so we help you sift through it and stay organized.