Structural and mechanistic aspects of carotenoid cleavage dioxygenases (CCDs)

Biochim Biophys Acta Mol Cell Biol Lipids. 2020 Nov;1865(11):158590. doi: 10.1016/j.bbalip.2019.158590. Epub 2019 Dec 23.

Abstract

Carotenoid cleavage dioxygenases (CCDs) comprise a superfamily of mononuclear non-heme iron proteins that catalyze the oxygenolytic fission of alkene bonds in carotenoids to generate apocarotenoid products. Some of these enzymes exhibit additional activities such as carbon skeleton rearrangement and trans-cis isomerization. The group also includes a subfamily of enzymes that split the interphenyl alkene bond in molecules such as resveratrol and lignostilbene. CCDs are involved in numerous biological processes ranging from production of light-sensing chromophores to degradation of lignin derivatives in pulping waste sludge. These enzymes exhibit unique features that distinguish them from other families of non-heme iron enzymes. The distinctive properties and biological importance of CCDs have stimulated interest in their modes of catalysis. Recent structural, spectroscopic, and computational studies have helped clarify mechanistic aspects of CCD catalysis. Here, we review these findings emphasizing common and unique properties of CCDs that enable their variable substrate specificity and regioselectivity. This article is part of a Special Issue entitled Carotenoids recent advances in cell and molecular biology edited by Johannes von Lintig and Loredana Quadro.

Keywords: Beta-propeller; Dioxetane; Monotopic membrane protein; Nitric oxide; Non-heme iron; Resveratrol.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Review

MeSH terms

  • Carbon / metabolism
  • Carotenoids / chemistry*
  • Carotenoids / metabolism
  • Dioxygenases / chemistry
  • Dioxygenases / genetics*
  • Dioxygenases / metabolism
  • Humans
  • Light
  • Nonheme Iron Proteins / chemistry
  • Nonheme Iron Proteins / genetics*
  • Nonheme Iron Proteins / metabolism
  • Oxygen / metabolism*
  • Resveratrol / pharmacology
  • Substrate Specificity

Substances

  • Nonheme Iron Proteins
  • Carotenoids
  • Carbon
  • Dioxygenases
  • Resveratrol
  • Oxygen