Factors controlling the reactivity of divalent metal ions towards pheophytin a

• Published in: Journal of biological inorganic chemistry Vol. 22; no. 6; pp. 941 - 952
• Main Authors: Orzeł, Ł., Waś, J., Kania, A., Susz, A., Rutkowska-Zbik, D., Staroń, J., Witko, M., Stochel, G., Fiedor, L.
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer Berlin Heidelberg 01-08-2017; Springer Nature B.V
• Subjects: Absorption spectroscopy; Biochemistry; Biomedical and Life Sciences; Catalysis; Cations; Cations, Divalent - chemistry; Computer applications; Deactivation; Enthalpy; Inorganic chemistry; Ions; Kinetics; Life Sciences; Magnesium; Metals; Microbiology; Original Paper; Pheophytins - chemistry; Quantum Theory; Solvents; Spectroscopy; Thermodynamics; Zinc; Metallochlorophylls; Metal ion insertion; Metal ion activation; Heavy metals
• ISSN: 0949-8257; 1432-1327
• DOI: 10.1007/s00775-017-1472-1

In this study, we evaluate the factors which determine the reactivity of divalent metal ions in the spontaneous formation of metallochlorophylls, using experimental and computational approaches. Kinetic studies were carried out using pheophytin
a
in reactions with various divalent metal ions combined with non- or weakly-coordinative counter ions in a series of organic solvents. To obtain detailed insights into the solvent effect, the metalations with the whole set of cations were investigated in three solvents and with Zn
2+
in seven solvents. The reactions were monitored using electronic absorption spectroscopy and the stopped-flow technique. DFT calculations were employed to shed light on the role of solvent in activating the metal ions towards porphyrinoids. This experimental and computational analysis gives detailed information regarding how the solvent and the counter ion assist/hinder the metalation reaction as activators/inhibitors. The metalation course is dictated to a large extent by the reaction medium, via either the activation or deactivation of the incoming metal ion. The solvent may affect the metalation in several ways, mainly via H-bonding with pyrrolenine nitrogens and the activation/deactivation of the incoming cation. It also seems to affect the activation enthalpy by causing slight conformational changes in the macrocyclic ligand. These new mechanistic insights contribute to a better understanding of the “metal–counterion–solvent” interplay in the metalation of porphyrinoids. In addition, they are highly relevant to the mechanisms of metalation reactions catalyzed by chelatases and explain the differences between the insertion of Mg
2+
and other divalent cations.