Toward a mechanism for biliprotein lyases: revisiting nucleophilic addition to phycocyanobilin

J Am Chem Soc. 2009 Apr 22;131(15):5399-401. doi: 10.1021/ja9002348.

Abstract

Biliprotein lyases attach linear-tetrapyrrolic bilins covalently to apoproteins, which is a prerequisite for the assembly of phycobiliproteins into phycobilisomes, the light-harvesting complexes of cyanobacteria. On the basis of the addition of thiol and imidazole to phycocyanobilin, we propose a generalized lyase reaction mechanism. The adducts contain isomerized phycocyanobilin that can be transferred by the lyase to apoproteins by either back-isomerization, generating phycocyanobilin-containing proteins, or direct transfer, generating phycoviolobilin-containing proteins.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoproteins / chemistry
  • Biomimetics
  • Imidazoles / chemistry
  • Light-Harvesting Protein Complexes / chemical synthesis*
  • Lyases / metabolism*
  • Phycobilins / chemistry*
  • Phycobiliproteins / metabolism*
  • Phycocyanin / chemistry*
  • Sulfhydryl Compounds / chemistry

Substances

  • Apoproteins
  • Imidazoles
  • Light-Harvesting Protein Complexes
  • Phycobilins
  • Phycobiliproteins
  • Sulfhydryl Compounds
  • Phycocyanin
  • phycocyanobilin
  • imidazole
  • Lyases