Chapter VII: The Dissociation of Molecular Oxygen, The Recombination of Oxygen Atoms and Isotopic Exchange with Molecular Oxygen

2019 ◽  
Vol 150 (20) ◽  
pp. 201103 ◽  
Author(s):  
Ryan C. Fortenberry ◽  
Tarek Trabelsi ◽  
Brent R. Westbrook ◽  
Weston A. Del Rio ◽  
Joseph S. Francisco

2015 ◽  
Vol 19 (09) ◽  
pp. 1007-1013 ◽  
Author(s):  
Patrick C. Loughlin ◽  
Robert D. Willows ◽  
Min Chen

Following extraction from photosynthetic organisms, chlorophylls are prone to reactions including demetalation, dephytylation and specific oxidations of the exocyclic ring E, termed allomerizations. Allomerization of chlorophylls has been well-characterized in methanol and to a lesser extent in aqueous solution. Here we detail novel allomerization-like reactions of chlorophyll a and chlorophyll b. In the presence of heme, detergent-solubilized chlorophyll a is hydroxylated at its C 132 position in ring E and, surprisingly, the C 18 position in ring D. Two major oxidation products are synthesized — a C 132- OH and a C 132- OH , C 18- OH derivative of chlorophyll a. We track the origin of the oxygen atoms added in these hydroxylated chlorophylls using 18 O 2 labeling and demonstrate that the additional oxygen atoms are derived from molecular oxygen. A similar heme-catalyzed reaction is also observed using chlorophyll b as a substrate. These results highlight the need for care when dealing with extracted chlorophylls and demonstrate an unusual hydroxylation of the C 18 position of chlorophylls in the presence of heme.


Author(s):  
Kh. M. Minachev ◽  
E. N. Savost'yanov ◽  
D. A. Kondrat'ev ◽  
Sui Nu Ch'ang ◽  
G. V. Antoshin

Sign in / Sign up

Export Citation Format

Share Document