Transition metal complexes of phyllobilins - a new realm of bioinorganic chemistry

Natural cyclic tetrapyrroles feature outstanding capacity for binding transition metal ions, furnishing Nature with the important metallo-porphyrinoid 'Pigments of Life', such as heme, chlorophyll (Chl) and vitamin B 12 . In contrast, linear tetrapyrroles are not generally ascribed a biolo...

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Veröffentlicht in:Dalton transactions : an international journal of inorganic chemistry 2015-06, Vol.44 (22), p.1116-1127
Hauptverfasser: Li, Chengjie, Kräutler, Bernhard
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Sprache:eng
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Zusammenfassung:Natural cyclic tetrapyrroles feature outstanding capacity for binding transition metal ions, furnishing Nature with the important metallo-porphyrinoid 'Pigments of Life', such as heme, chlorophyll (Chl) and vitamin B 12 . In contrast, linear tetrapyrroles are not generally ascribed a biologically relevant ability for metal-binding. Indeed, when heme or Chl are degraded to natural linear tetrapyrroles, their central Fe- or Mg-ions are set free. Some linear tetrapyrroles are, however, effective multi-dentate ligands and their transition metal complexes have remarkable chemical properties. The focus of this short review is centred on such complexes of the linear tetrapyrroles derived from natural Chl-breakdown, called phyllobilins. These natural bilin-type compounds are massively produced in Nature and in highly visible processes. Colourless non-fluorescing Chl-catabolites (NCCs) and the related dioxobilin-type NCCs, which typically accumulate in leaves as 'final' products of Chl-breakdown, show low affinity for transition metal-ions. However, NCCs are oxidized in leaves to give less saturated coloured phyllobilins, such as yellow or pink Chl-catabolites (YCCs or PiCCs). YCCs and PiCCs are ligands for various biologically relevant transition metal-ions, such as Zn( ii )-, Ni( ii )- and Cu( ii )-ions. Complexation of Zn( ii )- and Cd( ii )-ions by the effectively tridentate PiCC produces blue metal-complexes that exhibit an intense red fluorescence, thus providing a tool for the sensitive detection of these metal ions. Outlined here are fundamental aspects of structure and metal coordination of phyllobilins, including a comparison with the corresponding properties of bilins. This knowledge may be valuable in the quest of finding possible biological roles of the phyllobilins. Thanks to their capacity for metal-ion coordination, phyllobilins could, e.g. , be involved in heavy-metal transport and detoxification, and some of their metal-complexes could act as sensitizers for singlet oxygen or as plant toxins against pathogens. Phyllobilins may function as natural ligand molecules for biologically important transition metal ions, giving complexes with remarkable chemical and photophysical properties.
ISSN:1477-9226
1477-9234
DOI:10.1039/c5dt00474h