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The role of the local environment on the structural heterogeneity of carotenoid β-ionone rings.

Roman Y PishchalnikovIgor A YaroshevichDmitry V ZlenkoGeorgy V TsoraevEvgenii M OsipovVladimir A LazarenkoEvgenia Yu ParshinaDenis D ChesalinNikolai N SluchankoEugene G Maksimov
Published in: Photosynthesis research (2022)
Our analysis of the X-ray crystal structure of canthaxanthin (CAN) showed that its ketolated β-ionone rings can adopt two energetically equal, but structurally distinct puckers. Quantum chemistry calculations revealed that the potential energy surface of the β-ionone ring rotation over the plane of the conjugated π-system in carotenoids depends on the pucker state of the β-ring. Considering different pucker states and β-ionone ring rotation, we found six separate local minima on the potential energy surface defining the geometry of the keto-β-ionone ring-two cis and one trans orientation for each of two pucker states. We observed a small difference in energy and no difference in relative orientation for the cis-minima, but a pronounced difference for the position of trans-minimum in alternative pucker configurations. An energetic advantage of β-ionone ring rotation from a specific pucker type can reach up to 8 kJ/mol ([Formula: see text]). In addition, we performed the simulation of linear absorption of CAN in hexane and in a unit cell of the CAN crystal. The electronic energies of [Formula: see text] transition were estimated both for the CAN monomer and in the CAN crystal. The difference between them reached [Formula: see text], which roughly corresponds to the energy gap between A and B pucker states predicted by theoretical estimations. Finally, we have discussed the importance of such effects for biological systems whose local environment determines conformational mobility, and optical/functional characteristics of carotenoid.
Keyphrases
  • single cell
  • molecular dynamics
  • smoking cessation
  • human milk
  • high resolution
  • molecular dynamics simulations
  • photodynamic therapy
  • risk assessment
  • mass spectrometry
  • bone marrow
  • mesenchymal stem cells
  • drug discovery