The ability of enniatins to bind alkali metal, alkaline earth metal and certain transition metal ions in solution has been investigated. The complexes have been shown to form in 1:1, 2:1 and 3:2 macrocycle:cation ratios; their stability constants have been determined, and the conditions favoring their formation have been established. The enniatins were shown to be complexones of very wide spectrum, displaying low metal ion selectivity in alcoholic solutions. Two basic spatial forms, the non‐symmetric N3 form (in nonpolar solvents) and the symmetric P form (in polar solvents) have been disclosed and proposals made as to their conformational parameters. The molecular structure of the enniatin complexes has been established. Independent of the complexed ion species, of the complex stoichiometry, or of the type of solvent, the enniatin backbone of the complex is in the P form. In the 1:1 complexes, the ion is accommodated in the molecular cavity, forming iondipole bonds with all the amide and ester carbonyls. The depsipeptide chain of the enniatins is flexible, permitting “adaptation” of the complexone to the size of the ion, and thus explaining the low selectivity of these complexones. In the 2:1 and 3:2 complexes the cation is sandwiched in between two molecules of the antibiotic at the symmetry axis and interacts mainly with the N‐methylamide carbonyls. In these “sandwich” complexes the cation is much better screened from the anion and solvent than in the equimolar complexes and is highly soluble in organic solvents. The data presented here may serve as basis for interpreting the dependence between the structure, metal complexing behavior and membrane‐affecting properties in the series of the naturally occurring enniatin ionophores and their synthetic analogs.

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the Siberian wood frog Rana amurensis is a recently discovered example of extreme hypoxia tolerance that is able to survive several months without oxygen. We studied metabolomic profiles of heart and liver of R. amurensis exposed to 17 days of extreme hypoxia. Without oxygen, the studied tissues experience considerable stress with a drastic decrease of ATP, phosphocreatine, and NAD+ concentrations, and concomitant increase of AMP, creatine, and NADH. Heart and liver switch to different pathways of glycolysis with differential accumulation of lactate, alanine, succinate, as well as 2,3-butanediol (previously not reported for vertebrates as an end product of glycolysis) and depletion of aspartate. We also observed statistically significant changes in concentrations of certain osmolytes and choline-related compounds. Low succinate/fumarate ratio and high glutathione levels indicate adaptations to reoxygenation stress. Our data suggest that maintenance of the ATP/ADP pool is not required for survival of R. amurensis, in contrast to anoxia-tolerant turtles. Anoxia is a huge stress for the majority of vertebrates. Amphibians are considered to be relatively anoxia-intolerant, in contrast to a few turtle species and certain fish species 1-3 : the most resistant species are known to survive anoxia for a few days at most. However, a recent study 4 proved that the Siberian wood frog Rana amurensis can tolerate almost complete anoxia at 2-3 °C (below 0.2 mg/L oxygen, i.e., less than 1.5% of the normal concentration at this temperature) for several months. This is on par with the best vertebrate models from other classes. Moreover, while red-eared slider turtles, the most studied anoxia-tolerant tetrapods, are dormant under anoxia, the Siberian wood frog is able to react to stimuli, e.g., to flee when disturbed. R. amurensis is thus a unique model of extreme hypoxia tolerance among terrestrial vertebrates. The natural range of R. amurensis includes Northeastern China and Siberia from the Urals to the coast of the Okhotsk sea; its northern distribution is limited by about 71° N. It overwinters under ice in water bodies. Many of these lakes are shallow (< 3 m) due to thermokarst origin, i.e. resulting from local melting of permafrost. Experimental studies 4 demonstrated that during the winter oxygen is depleted in overwintering sites till almost complete anoxia. Siberian wood frogs overwinter for 6 to 7 months in different regions under hypoxia until they can leave the lakes in April-early May. The mechanisms of adaptation to the lack of oxygen are totally unknown for R. amurensis. Here we made an attempt to study this phenomenon using 1 H-NMR-based quantitative metabolomics. This method simultaneously yields concentrations of multiple metabolites 5. At the present, the detailed quantitative metabolomic composition is known for many human tissues, but for very few animals 6-8. To the best of our knowledge, this is the first report on the quantitative metabolomic analysis of amphibian tissues. We determined concentrations of ove...