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BioMed Research International
Volume 2013 (2013), Article ID 742149, 14 pages
Structure and Antimicrobial Properties of Monensin A and Its Derivatives: Summary of the Achievements
1Faculty of Chemistry, Jagiellonian University, Ingardena 3, 30-060 Krakow, Poland
2Department of Biochemistry, Faculty of Chemistry, Adam Mickiewicz University, Umultowska 89b, 61-614 Poznan, Poland
Received 29 August 2012; Revised 15 December 2012; Accepted 29 December 2012
Academic Editor: Ivayla Pantcheva-Kadreva
Copyright © 2013 Daniel Łowicki and Adam Huczyński. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
In this paper structural and microbiological studies on the ionophorous antibiotic monensin A and its derivatives have been collected. Monensin A is an ionophore which selectively complexes and transports sodium cation across lipid membranes, and therefore it shows a variety of biological properties. This antibiotic is commonly used as coccidiostat and nonhormonal growth promoter. The paper focuses on both the latest and earlier achievements concerning monensin A antimicrobial activity. The activities of monensin derivatives, including modifications of hydroxyl groups and carboxyl group, are also presented.
Ionophores are the class of compounds making complexes with cation and then transporting it as lipid-soluble complex across lipid bilayer. MonensinA is a representative of a large group of naturally occurring polyether ionophorous antibiotics. It was discovered in 1967 by Agtarap etal.  as a metabolite formed in a biosynthesis of Streptomyces cinnamonensis bacteria. The details of monensin isolation are given in a separate work . The appropriate mechanism of action of ionophores has been presented by Pressman et al.  in 1967, which marks this date as the beginning of the chemistry of ionophores. Elucidation of the crystal structure of monensin silver salt complex by Agtarap etal. , as well as that of a crystal complex of another previously known ionophore-nonactin with potassium cation by Kilbourn etal. , has significantly contributed to the understanding of this mechanism. Since that time a huge number of ionophorous antibiotics have been discovered, and their structures and antimicrobial properties have been studied. The group of carboxylic ionophores currently consists of nearly a hundred of compounds. However, only a few of them have been approved for use in veterinary practice.
2. Structure of Monensin A and Its Complexes
2.1. Studies on the Monensin A Structure
Monensin A, (Scheme 1) also called monensic acid, MONA, or MonH, occurs as a monohydrate with a water molecule complexed inside. The molecule of this ionophore contains six oxygen atoms, five of which may participate in the complexation of cations. Monensin molecule is maintained in a pseudocyclic conformation due to the presence of bifurcated intramolecular hydrogen bonds formed between carboxyl group on one side of the molecule and two hydroxyl groups on the opposite side. For the first time, the crystal structure of monensic acid monohydrate has been presented by Lutz etal. in 1971 . The host-guest system of C36H62O11-H2O formula is stabilised by inter- and intramolecular hydrogen bonds (Figure 1(a)). This complex crystallises from absolute ethanol in orthorhombic crystal system and P212121 space group.
Recently, Huczyński etal. have presented the crystal structure of monensinA monohydrate obtained by crystallisation from acetonitrile. In comparison to Lutz’s studies, the new structure contains all hydrogen atoms (Figure 1(b)) . Until now, no crystal form of monensic acid without water has been presented, which could suggest that the anhydrous monensin cannot exist. Huczyński and coauthors demonstrated that in the dichloromethane solution (DCM) monensinA also exists as monohydrate, which has been proved by FTIR and NMR spectroscopies.
A total synthesis of monensin was undertaken by Kishi et al. in 1979 [15–17]. This achievement is one of the first examples of stereoselective total synthesis through acyclic stereocontrol. Barely a year later Still and coworkers [18–20] presented another method for the synthesis of monensin.
2.2. Studies of the Monensin A Complexes
Ionophoretic properties of monensin A were widely studied in the last century [21–26]. Stability constants of monensin complexes with monovalent metal cations such as Li+, Na+, K+, Rb+, Cs+, and Ag+ were defined by various methods including fluorimetry, calorimetry, relaxation, electrochemical, and 1H NMR measurements. Determination of values was conducted in various protic, as well as polar aprotic solvents, and at different temperatures. Popov and coworkers have noted that monensin can form different types of complexes in solution, that is, monensin metal salt called monensinates of Mon−M+ formula and monensic acid with inorganic salts of MonH-M+X− formula [21, 22]. Complexation titrations with other cations have shown that the selectivity of monensin varies in the order Ag+ > Na+ > K+ > Rb+ > Cs+ > Li+ . Lutz etal.  have demonstrated that the ability to form complexes with monovalent cations by monensin is as follows: Na+ > K+ > Li+ > Rb+ > Cs+. A number of crystal salts of monensin A with different cations have been synthesized, and their structures were studied by X-ray diffraction (see Table 1 and Figure 2) [7–14]. The structure of sodium monensinate in chloroform solution was studied by Turner. The author applied nuclear Overhauser effect spectroscopy to study conformation of this complex . Full assignment of 13C and 1H NMR signals of MONA-NaCl and MONA-NaClO4 complexes in DCM solution was performed by Huczyński etal.
Three crystal complexes of monensin A with NaBr , NaCl, and NaClO4 have been synthesised  (Figure 3). Przybylski and coauthors calculated the structures of monensin A sodium, potassium and silver salts, monensin-free acid monohydrate, and some monensin derivative complexes. The semiempirical calculations were carried out by AM1, PM3, and PM5 parametric methods. Comparison of the calculated parameters (bond lengths and angles) of these structures with those in crystals has shown that the best results are achieved by PM5 method .
Recently, crystal complexes of monensin with some divalent metal cations have been synthesised by Pantcheva and coworkers [31–36]. They found that three different types of complexes can be formed, but the divalent cation is not placed in hydrophilic cavity of the ionophore in any case. The first type of complexes is formed with the cations such as Mg2+, Ca2+, Zn2+, Cd2+, Co2+, Mn2+, and Ni2+. These complexes of [M(Mon)2(H2O)2] formula, where M is divalent metal, are neutral salts with two monensinates anions bound in a bidentate coordination mode to the cation. The metal cation is additionally coordinated by two water molecules placed in axial positions of the octahedron. The crystal structure of the [Ca(Mon)2(H2O)2] complex, which is a representative of this type complexes is shown in Figure 4(a) [31–34]. In the second type of complexes with such cations as Co2+, Mn2+, and Cu2+, two molecules of monensin sodium salt are bound with a divalent metal cation, which is simultaneously bound with two chloride anions Figure 4(b) [35, 36]. The complex with Hg(II) has quite a different structure in which one cation is bound with only one molecule of monensin (Figure 4(c)). The cation is located between carboxyl anion and two hydroxyl groups. The twofold negative charge of the ligand is achieved by deprotonation of carboxylic group and secondary hydroxyl group .
3. Biosynthesis of Monensin A
As already mentioned, monensin was isolated for the first time in 1967. Several homologues of it are known (Scheme 1), but the most famous is monensin A. The isolation process involves the biosynthesis and extraction of the monensin sodium salt in the culture of Streptomyces cinnamonensis actinobacteria, which is carried out in a complex medium containing glucose, soybean oil, and grit. Cultivation process is carried out for about a week at 30 °C and under intensive aeration [37–39]. Biosynthesis of monensin proceeds through the polyketide pathway with the biochemical processes similar to those taking place in fatty acid biosynthesis. The precursors are propionyl-CoA and malonyl-CoA, which provide acethyl, propionyl, and butyrate units. During the biosynthesis the following processes occur: (i)binding of acyl groups,(ii)condensation of next malonyl-CoA molecule with emission of CO2,(iii)reduction of ketone group,(iv)emission of water molecule,(v)reduction of the double bond.In the biosynthesis performed with acetyl-CoA and malonyl-CoA, a multienzymatic protein complex is involved, which plays an important role of an acyl residue carrier. The information on the biosynthesis of monensin was obtained through research with the use of isotopes 18O- and 13C-labelled molecules . The product of biosynthesis is excreted from the bacterial cells, and its concentration in the culture averages a few grams per litre. After completion of the biosynthesis process, the solid components are filtered off, and the filtrate is acidified to pH 3 and then extracted with chloroform. The extract is purified on activated carbon, concentrated, and crystallised. If the monensin concentration in a crude biosynthesis product is higher than 10 g/L, extraction with n-hexanol is carried out directly from this mixture. Subsequently, a water is removed by azeotropic distillation, and product is crystallised .
4. Properties and Toxicity of Monensin A
Since its discovery, monensin A has become an object of scientific interest because of its biological and pharmacological properties. Brief characterisation and toxicity of monensin A are presented in Table 2. At first its cellular effects on the Golgi apparatus, both in plant and animal cells, were understood. Monensin inhibits growth of selected cells by blocking the intracellular transport of the Golgi apparatus proteins, with no apparent inhibition of the synthesis of these proteins. Also, the transfer of products formed within the Golgi structures is inhibited by monensin [20, 40].
When exposed to monensin, the culture of plant cells slows down their growth or selected cellular processes, and usually the changes in functioning and structure of the Golgi apparatus occur. However, in the animal cells monensin induces mitochondrial damage without apparent change in the operation of the Golgi structure . Monensin also slows down and reduces the process of endocytosis, that is, transport of large molecules through the cell membrane with the participation of a peptide transporter [44, 45]. The antibiotic induces pH change within the cellular structure, which can lead to a reduction in the secretion and/or transportation of the chemicals important for the proper functioning of the cell. Monensin also affects the processes of formation of external structures on the cell surface and their growth, by reducing the secretion of substances responsible for these processes (i.e., proteoglycans, collagen and procollagen, and fibronectin) . Cellular effects of monensin depend on the body subjected to its action, the route of administration, and the dose of this antibiotic.
The main cellular effects caused by monensin are listed in Table 3. The very few studies performed on the antitumor activity of monensin have demonstrated that it can inhibit the proliferation of renal cancer cells by inducing apoptosis in cancer cells and cell cycle arrest in G or G2-M phases .
5. Antimicrobial Activity of Monensin A
Monensin is one of the most widely studied ionophore antibiotics. Most of the work has been devoted to its biological activity, including the antimicrobial properties. Monensin antibacterial activity can be explained by changes in pH and the sodium-potassium balance in the cell, which leads to critical disturbances in cellular processes, resulting in cell death . Monensin and some of its derivatives have shown activity against Gram-positive bacteria of the genera Micrococcus, Bacillus, and Staphylococcus [35, 48, 49]. It has been found that only Gram-positive G(+) bacteria are sensitive to monensin, which may be due to the fact that the cell walls of Gram-negative G(−) bacteria have more complexed construction not permeable to large antibiotic molecules and the complexes formed by it. The studies devoted to the antiviral properties of monensin indicate that it is active against some viruses. Inhibition of vesicular stomatitis and Sindbis virus replication have been demonstrated [50, 51]. Monensin has been also found to inhibit Semliki Forest virus penetration into the target cells . Iacoangeli and coworkers have shown in their studies that monensin decreases DNA synthesis, effectively inhibits the replication, and induces a strong reduction of early viral antigens of murine polyoma virus . In vitro studies of monensin showed pronounced activity against Plasmodium falciparum, much stronger than that of the antimalarial drug—chloroquine. In clinical in vivo studies in mice infected with Plasmodium vinckei petteri, a 100% animals have been cured after treatment with monensin doses of 10 mg/kg. Antimalarial action of monensin can be explained by impaired function of nutrient and other vacuolar organelles of the parasite and the intracellular acidification, which eventually lead to the cell death .
6. Ion Transport
It has long been known that the biological activity of monensin arises from its ability to complex with the sodium cation and transport it across cell membranes. Initially it was thought that the mechanism of ion transport is a simple antiport of Na+/H+ cations [54–56]. The hypothesis assumes that monensin molecule binds the sodium cation as a salt, loosing proton from carboxyl group, and moves the cation as a complex on the opposite side of the lipid membrane (Figure 5(a)). Then, the sodium cation is released, and carboxylate anion undergoes protonation.
A neutral acid molecule migrates back to the other side of the membrane. This process is powered by difference of cation concentrations inside and outside the cell and tends to align the ions gradient. This mechanism of transport is electroneutral. However, microbiological studies of monensin A derivatives with blocked carboxyl groups such as amides and esters have also shown their antimicrobial properties. In 1991 Nakazato and Hatano have measured the fluxes of Na+ and H+ using monensin A containing liposomes and concluded that Na+ is transported in the form of a 1 : 1 complex between monensic acid (MonH) and Na+ cation . Recently, Huczyński etal. have synthesised two complexes of monensin acid with NaCl and NaClO4 and determined their crystal structures. The authors have proven by FT-IR study that the structure of the complexes is conserved in the hydrophobic environment like in DCM solution . These findings support the assumption that the [MonHM+X−] type complexes can exist in hydrophobic membranes and affect the Na+ transport also in electrogenic way (Figure 5(b)).
7. Applications of Monensin A
There are over 100 known ionophore antibiotics, but only three, monensin, salinomycin, and lasalocid acid, have found currently commercial application. Monensin was the first ionophoric antibiotic approved for use by the Food and Drug Administration (FDA) in the USA. Monensin A is an antibiotic which is used as coccidiostat and growth promoting agent in veterinary practice. Due to the strong antibacterial and coccidiostatic properties it has found application in industrial poultry farming. Coccidia are parasitic protozoa commonly occurring in different animal species, which multiply in the intestinal epithelial cells and propagate through the oocysts excreted in the faeces. These microorganisms cause inflammation of the mucous membrane of the small intestine, resulting in diarrheal and general weakness. The mechanism of coccidiostatic activity of monensin involves blocking the development of trophozoites of protozoa in the Eimeria genus of Coccicdium group, in the first phase of schizogony. As a result, a positive effect of antibiotic on the growth of poultry is to reduce the proliferation of parasites, thus eliminating attenuation on stockbreeding [58, 59]. For the prevention of coccidiosis in poultry Mondolar formulation, containing 10% or 20% sodium monensin, is used. Subsequent studies have shown that monensin may also improve food metabolism in ruminants, which ensures its better use and, consequently, leads to faster growth of cattle. Stimulation of growth is associated in this case with favourable changes of intestinal bovine microflora and increasing amounts of assimilable digested protein. Rumenesin containing 6.6% of monensin is used as a nonhormonal growth promoter for animals [27, 60, 61]. Monensin used as a coccidiostat in poultry or growth promoter in cattle is relatively safe if used in the recommended doses. However, the possibility of poisoning animals as well as antibiotic contamination of animal products (meat, eggs, and milk) must always be taken into account. Due to a broad spectrum of biological activity, monensin derivatives are an important object of research aimed at reducing the toxicity and to obtain new compounds with improved biological properties in terms of further use.
8. Monensin A Derivatives and Their Antimicrobial Activity
A broad spectrum of antimicrobial and biological properties of monensin has made the chemical modification of monensin a very interesting direction of research. The novel derivatives of the ionophore, depending on the location of chemical modification, differ from the parent molecule in complexation selectivity, structure of complexes formed, ion transport mechanism, and toxicity and biological properties, including antimicrobial activity. Several research groups have synthesized a wide range of monensin derivatives, some of which have been tested for antimicrobial activity.
8.1. Modifications of Hydroxyl Groups
Chemical modification of all three hydroxyl groups has already been carried out. Westley and coworkers have reported the synthesis and antimicrobial properties of a series of monensin urethanes, obtained by modification of O(XI)H group (Figure 6, compounds 1a–j) . These derivatives are very interesting in terms of chemical and microbiological properties, because they are able to transport monovalent cations about 10 times more effectively than monensin. The urethanes also show up to 10-fold higher activity compared to unmodified monensin against G(+) bacteria (MIC values varied from 0.02 to over 25 μg/mL). Moreover, some of these compounds are also active against Candida albicans fungus (MIC = 0.08 μg/mL to more than 100 μg/mL for urethane, MIC > 100 μg/mL for unmodified MONA) and Penicillium digitatum (MIC 6.3 μg/mL to more than 100 μg/mL for urethanes, MIC > 100 μg/mL for unmodified monensin).
Furthermore, four of the monensin urethanes obtained showed antimalarial properties in in vivo tests . Westley et al. have postulated that in the molecular structure of sodium monensin urethanes the oxygen of urethane carbonyl group coordinates metal cation. Recently Huczyński etal.  reinvestigated the structure of the phenyl urethane of MonNa complex and have shown that in both, solution and crystal structure, this group does not participate in the process of complexation (Figure 6). Chemical modification of monensin at the C(26) carbon atom was also carried out to prepare various derivatives of the antibiotic including: esters, ethers, amine, and sulphonate (Figure 7, compounds 2a–e). Among all of these derivatives 26-fenylaminomonensin (2c) exhibits antimicrobial activity against various bacterial strains with MIC values of 0.20–6.25 μg/mL. The activity of this compound was higher than that of monensin and even a very active derivative—26-phenylurethane of monensin (1d) . The chemical modification of monensin at position C-26 can also lead to changes in preferences of cation complexation by this ionophore. Rochdi etal.  have demonstrated that 2d and 2e monensin derivatives cause an increase in the effective transport of potassium cation through the membrane, whereas there is a decrease in the transport of sodium cations. Thus, these derivatives preferentially complex and transport potassium cations prior to sodium cations. Such inversion of complexation selectivity by the chemical modification of monensin has also led to improvement of its antibacterial activity against Bacillus cereus as well as in vivo antimalarial activity toward Plasmodium falciparum .
Among monensin derivatives with modified O(IV)H hydroxyl group the ester derivatives (Figure 8, compounds 3a–e) and ether derivatives (Figure 8, compounds 4a–k) have been synthesized [64, 65]. Acyl derivatives of monensin 3a–e showed lower antibacterial activity against both aerobic and anaerobic bacteria than the starting material. However, monensin-O(4) benzyl ethers (4d–k) showed much higher antibacterial activity than monensin. This can be related to the hydrophobic nature of the benzyl substituent, whose role is to improve the solubility of the derivatives of monensin in the bacterial cell membrane .
8.2. Modifications of Carboxyl Group
Modifications of the carboxyl group include the synthesis of amides and esters of monensin A, most of which were performed by Professor Brzezinski’s group. Recently, four new amides of monensin have been synthesised by Łowicki etal. [66–70], and their ability to complex monovalent metal cations such as Li+, Na+ and K+ has been studied (Figure 9, compounds 5a–d). The reason why polyether antibiotics exhibit several pharmacological and biological effects is their ability to form lipid-soluble pseudocyclic complexes with metal cations and transport them through cell membranes disturbing their natural Na+/ K+ ion balance. Thus, studies of the biological activity of monensin derivatives should be always connected with the studies of their ionophoretic properties.
Among all the amide complexes studied in solution, only a complex of N-phenylamide with sodium chloride showed a tendency to crystallize, therefore its structure has been determined by crystallographic methods (Figure 10(a)) . Moreover, 5b and 5c amides have been found to be able to bind alkaline earth metal cations such as Mg2+, Ca2+, Sr2+, and Ba2+ . Surprisingly, the complex of 5b with strontium perchlorate crystallized from acetonitrile solution and its structure has been determined (Figure 10(b)) . It is worth noting that the Sr2+ cation is placed inside the hydrophilic cavity of monensin amide molecule, which is the first example of that kind of complex with divalent metal cation. The ability to complex sodium cations by two complexation centres in monensin amide with 4-aminobenzo-15-crown-5 was investigated by spectroscopic and spectrometric methods. These studies have proved that the Na+ cation in 1 : 1 complex is bound in the monensin part of 5d molecule; however, the complex of 1 : 2 stoichiometry can also be formed . All the monensin amides were tested in vitro toward G(+), G(−) bacteria and yeasts, and they showed comparable, but a little bit smaller activity, against G(+) cocci than that of the parent ionophore (see Table 4).
The N-phenyl amide (5a) gave the best results in the in vitro tests on standard strains, thus it was additionally subjected to studies toward some strains of methicillin-resistant, methicillin-susceptible S. aureus (MRSA and MSSA), and methicillin-resistant S. epidermidis (MRSE). The 5a amid showed significant activity against all tested hospital strains of MRSA, MSSA, and MRSE of MIC values between 6.25 and 25 μg/mL .
In 1988 Japanese research group led by Sakakibara synthesised several amides of monensin A with chiral amino acids (Figure 9, compounds 6a–g). Subsequently, they synthesised crystal complexes of these amides with sodium bromide . Further modification of the monensylamino acids included the lactamization reaction in which the carboxyl group of the corresponding amino acid moiety is connected with monensin O(XI)H hydroxyl group (Figure 11, compounds 7a–f).
The macrocyclic lactones were tested for their activity against anaerobic bacteria and showed a lower efficiency than that of unmodified monensin A. For example, the values of the minimum inhibitory concentration of growth Peptostreptococcus anaerobius strain B-30 ranged from 25 to 50 μg/mL for compounds 7a–f, whereas the MIC value for the monensin was 1.56 μg/mL .
The largest group of monensin A derivatives are esters, most of which have been synthesised by Huczyński etal. during the last decade (Figure 12, compound 8a–m). The ability of the esters to form complexes with monovalent alkali [75–82] as well as divalent alkaline earth metal cations [83–85] has been investigated.
Two complexes of monensin esters have been obtained in crystal form, that is, aqualithium 1-naphthylmethyl ester of monensin perchlorate (Figure 13(a)) , and 1-naphthylmethyl ester of monensin with sodium perchlorate (Figure 13(b)) .
An interesting case is monensin methyl ester (8a) which is able to form a proton channel created by eight molecules of 8a each with three water molecules bounded in the hydrophilic space. Within the channel all 24 water molecules are connected by almost linear hydrogen bonds (Figure 14) . The H+ cation can be attached on one side of the channel, while the other proton is dissociated on the opposite side of the channel. These studies show that monensin methyl ester can be recognised as a channel forming ionophore, while unmodified monensin is considered to be the typical ion carrier.
Antimicrobial properties of all the esters 8a–m have been tested towards G(+), G(−) bacteria and yeasts . Among the wide range of these derivatives only three (8h, 8g, and 8k) have shown activity against some strains of Gram-positive bacteria.
Monensin A and its esters, which showed activity against the strains of Gram-positive cocci, were subjected to additional testing on hospital strains of S. aureus, including methicillin-susceptible (MSSA) and methicillin-resistant (MRSA) strains.
These studies have indicated that monensin and 2-morpholinoethyl ester (8k) show high activity against both types of S. aureus, that is, MRSA and MSSA. The other two esters (8h and 8g) show moderate activity. The MIC values of the monensin esters are compared with that of unmodified monensin in Table 5.
In the Professor Brzezinski’s group the synthesis of macromolecular derivatives of monensin (dimers and trimers) has also been developed. These derivatives are completely inactive against Gram-negative bacteria, because the compounds with high-molar masses are unable to penetrate the membrane of these bacteria. However, these compounds showed moderate activity in the assays against Gram-positive bacteria, their MIC values for G(+) bacteria ranged from 6.25 μg/mL to 200 μg/mL .
Conflict of interests
The authors declare that they have no conflict of interests.
Financial support from budget funds for science in years 2012-2013—grant “Iuventus Plus” of the Polish Ministry of Science and Higher Education—Grant no. 0179/IP3/2011/71 is gratefully acknowledged by A. Huczyński.
- A. Agtarap, J. W. Chamberlin, M. Pinkerton, and L. Steinrauf, “The structure of monensic acid, a new biologically active compound,” The Journal of the American Chemical Society, vol. 89, no. 22, pp. 5737–5739, 1967.
- M. E. Haney Jr. and M. M. Hoehn, “Monensin, a new biologically active compound. I. Discovery and isolation,” Antimicrobial Agents and Chemotherapy, vol. 7, pp. 349–352, 1967.
- B. C. Pressman, E. J. Harris, W. S. Jagger, and J. H. Johnson, “Antibiotic-mediated transport of alkali ions across lipid barriers,” Proceedings of the National Academy of Sciences of the United States of America, vol. 58, no. 5, pp. 1949–1956, 1967.
- B. T. Kilbourn, J. D. Dunitz, L. A. R. Pioda, and W. Simon, “Structure of the K+ complex with nonactin, a macrotetrolide antibiotic possessing highly specific K+ transport properties,” Journal of Molecular Biology, vol. 30, no. 3, pp. 559–563, 1967.
- W. K. Lutz, F. K. Winkler, and J. D. Dunitz, “Crystal structure of the antibiotic monensin similarities and differences betweeen free acid and metal complex,” Helvetica Chimica Acta, vol. 54, no. 4, pp. 1103–1108, 1971.
- A. Huczyński, J. Janczak, D. Łowicki, and B. Brzezinski, “Monensin A acid complexes as a model of electrogenic transport of sodium cation,” Biochimica et Biophysica Acta, no. 9, pp. 2108–2119, 1818.
- A. Huczyński, M. Ratajczak-Sitarz, A. Katrusiak, and B. Brzezinski, “Molecular structure of the 1:1 inclusion complex of monensin A lithium salt with acetonitrile,” Journal of Molecular Structure, vol. 871, no. 1–3, pp. 92–97, 2007.
- A. Huczyński, M. Ratajczak-Sitarz, A. Katrusiak, and B. Brzezinski, “Molecular structure of the 1:1 inclusion complex of monensin A sodium salt with acetonitrile,” Journal of Molecular Structure, vol. 832, no. 1–3, pp. 84–89, 2007.
- W. L. Duax, G. D. Smith, and P. D. Strong, “Complexation of metal ions by monensin. Crystal and molecular structure of hydrated and anhydrous crystal forms of sodium monensin,” The Journal of the American Chemical Society, vol. 102, no. 22, pp. 6725–6729, 1980.
- F. A. A. Paz, P. J. Gates, S. Fowler et al., “Sodium monensin dihydrate,” Acta Crystallographica Section E, vol. 59, no. 11, pp. m1050–m1052, 2003.
- W. Pangborn, W. Duax, and D. Langs, “The hydrated potassium complex of the ionophore monensin A,” The Journal of the American Chemical Society, vol. 109, no. 7, pp. 2163–2165, 1987.
- A. Huczyński, M. Ratajczak-Sitarz, A. Katrusiak, and B. Brzezinski, “Molecular structure of rubidium six-coordinated dihydrate complex with monensin A,” Journal of Molecular Structure, vol. 888, no. 1–3, pp. 224–229, 2008.
- S. Ö. Yildirim, V. McKee, F. Z. Khardli, M. Mimouni, and T. B. Hadda, “Rubidium(I) monensinate dihydrate,” Acta Crystallographica Section E, vol. 64, no. 1, pp. m154–m155, 2008.
- M. Pinkerton and L. K. Steinrauf, “Molecular structure of monovalent metal cation complexes of monensin,” Journal of Molecular Biology, vol. 49, no. 3, pp. 533–546, 1970.
- G. Schmid, T. Fukuyama, K. Akasaka, and Y. Kishi, “Total synthesis of monensin. 1. Stereocontrolled synthesis of the left half of monensin,” The Journal of the American Chemical Society, vol. 101, no. 1, pp. 259–260, 1979.
- T. Fukuyama, C.-L. Wang, and Y. Kishi, “Total synthesis of monensin. 2. Stereocontrolled synthesis of the right half of monensin,” The Journal of the American Chemical Society, vol. 101, pp. 260–262, 1979.
- T. Fukuyama, K. Akasaka, D. S. Karanewsky, C. -L. Wang, G. Schmid, and Y. Kishi, “Total synthesis of monensin. 3. Stereocontrolled total synthesis of monensin,” The Journal of the American Chemical Society, vol. 101, pp. 262–263, 1979.
- D. B. Collum, J. H. McDonald III, and W. C. Still, “Synthesis of the polyether antibiotic monensin. 1. Strategy and degradations,” Journal of the American Chemical Society, vol. 102, pp. 2117–2118, 1980.
- D. B. Collum, J. H. McDonald III, and W. C. Still, “Synthesis of the polyether antibiotic monensin. 2. Preparation of intermediates,” Journal of the American Chemical Society, vol. 102, no. 6, pp. 2118–2120, 1980.
- C. D. B. Collum, J. H. McDonald III, and W. C. Still, “Synthesis of the polyether antibiotic monensin. 3. Coupling of precursors and transformation to monensin,” Journal of the American Chemical Society, vol. 102, pp. 2120–2121, 1980.
- P. G. Gertenbach and A. I. Popov, “Solution chemistry of monensin and its alkali metal ion complexes. Potentiometric and spectroscopic studies,” The Journal of the American Chemical Society, vol. 97, no. 16, pp. 4738–4744, 1975.
- J. G. Hoogerheide and A. I. Popov, “A study of metal complexes of a naturally occurring macrocyclic ionophore-monensin,” Journal of Solution Chemistry, vol. 8, no. 1, pp. 83–95, 1979.
- G. Cornelius, W. Gärtner, and D. H. Haynes, “Cation complexation by valinomycin- and nigericin-type ionophores registered by the fluorescence signal of Tl+,” Biochemistry, vol. 13, no. 15, pp. 3052–3057, 1974.
- B. G. Cox, N. Van Truong, J. Rzeszotarska, and H. Schneider, “Rates and equilibria of alkali metal and silver ion complex formation with monensin in ethanol,” The Journal of the American Chemical Society, vol. 106, no. 20, pp. 5965–5969, 1984.
- B. G. Cox, N. Van Truong, J. Rzeszotarska, and H. Schneider, “Stability constants of complexes of monensin and lasalocid with alkali-metal and alkaline-earth-metal ions in protic and polar aprotic solvents,” Journal of the Chemical Society, Faraday Transactions 1, vol. 80, no. 12, pp. 3275–3284, 1984.
- Y. Pointud, C. Bernard, S. Touzain, L. Astier, B. Sabatier, and J. Juillard, “Thermodynamics of complexation of monovalent metal cations by the ioniophore monensin free acid in acetonitrile,” Journal of Solution Chemistry, vol. 26, no. 5, pp. 479–495, 1997.
- W. K. Lutz, H. K. Wipf, and W. Simon, “Alkali-cation specificity and carrier qualities of the antibiotics nigericin and monensin,” Helvetica Chimica Acta, vol. 53, no. 7, pp. 1741–1746, 1970.
- D. L. Turner, “The conformation of the monensin-A-sodium complex in solution determined from self-consistent NOE distance constraints,” Journal of Magnetic Resonance, Series B, vol. 108, no. 2, pp. 137–142, 1995.
- D. L. Ward, K. -T. Wei, J. G. Hoogerheide, and A. I. Popov, “The crystal and molecular structure of the sodium bromide complex of monensin, ,” Acta Crystallographica Section B, vol. B34, pp. 110–115, 2000.
- P. Przybylski, A. Huczyński, and B. Brzezinski, “The structures of monensin A derivatives and its complexes with some monovalent cations studied by the AM1d, PM3 as well as PM5 semiempirical methods,” Journal of Molecular Structure, vol. 826, no. 2-3, pp. 156–164, 2007.
- I. N. Pantcheva, R. Zhorova, M. Mitewa, S. Simova, H. Mayer-Figge, and W. S. Sheldrick, “First solid state alkaline-earth complexes of monensic acid A (MonH): crystal structure of [M(Mon)2(H2O)2] (M = Mg, Ca), spectral properties and cytotoxicity against aerobic Gram-positive bacteria,” BioMetals, vol. 23, no. 1, pp. 59–70, 2010.
- I. N. Pantcheva, J. Ivanova, R. Zhorova et al., “Nickel(II) and zinc(II) dimonensinates: single crystal X-ray structure, spectral properties and bactericidal activity,” Inorganica Chimica Acta, vol. 363, no. 8, pp. 1879–1886, 2010.
- I. N. Pantcheva, M. I. Mitewa, W. S. Sheldrick, I. M. Oppel, R. Zhorova, and P. Dorkov, “First divalent metal complexes of the polyether ionophore monensin A: X-ray structures of [Co(Mon)2(H2O)2] and [Mn(Mon)2(H2O)2] and their bactericidal properties,” Current Drug Discovery Technologies, vol. 5, no. 2, pp. 154–161, 2008.
- J. Ivanova, I. N. Pantcheva, M. Mitewa, S. Simova, H. Mayer-Figge, and W. S. Sheldrick, “Crystal structures and spectral properties of new Cd(II) and Hg(II) complexes of monensic acid with different coordination modes of the ligand,” Central European Journal of Chemistry, vol. 8, no. 4, pp. 852–860, 2010.
- P. Dorkov, I. N. Pantcheva, W. S. Sheldrick, H. Mayer-Figge, R. Petrova, and M. Mitewa, “Synthesis, structure and antimicrobial activity of manganese(II) and cobalt(II) complexes of the polyether ionophore antibiotic Sodium Monensin A,” Journal of Inorganic Biochemistry, vol. 102, no. 1, pp. 26–32, 2008.
- I. N. Pantcheva, P. Dorkov, V. N. Atanasov et al., “Crystal structure and properties of the copper(II) complex of sodium monensin A,” Journal of Inorganic Biochemistry, vol. 103, no. 10, pp. 1419–1424, 2009.
- L. E. Day, J. W. Chamberlin, E. Z. Gordee et al., “Biosynthesis of monensin,” Antimicrobial Agents and Chemotherapy, vol. 4, no. 4, pp. 410–414, 1973.
- E. Kralovcova, V. Krumphanzl, and Z. Vanek, “Improving the production of monensin by Streptomyces cinnamonensis,” Folia Microbiologica, vol. 29, no. 1, pp. 35–42, 1984.
- T. Rezanka, K. Klanova, M. Podojil, and Z. Vanek, “Fatty acids of Streptomyces cinnamonensis, producer of monensin,” Folia Microbiologica, vol. 29, no. 3, pp. 217–221, 1984.
- P. W. Ledger, N. Uchida, and M. L. Tanzer, “Immunocytochemical localization of procollagen and fibronectin in human fibroblasts: effects of the monovalent ionophore, monensin,” Journal of Cell Biology, vol. 87, no. 3, pp. 663–671, 1980.
- J. W. Westley, Chao Min Liu, and R. H. Evans, “Preparation, properties and biological activity of natural and semisynthetic urethanes of monensin,” Journal of Antibiotics, vol. 36, no. 9, pp. 1195–1200, 1983.
- A. Huczyński, M. Ratajczak-Sitarz, J. Stefańska, A. Katrusiak, B. Brzezinski, and F. Bartl, “Reinvestigation of the structure of monensin A phenylurethane sodium salt based on X-ray crystallographic and spectroscopic studies, and its activity against hospital strains of methicillin-resistant S. epidermidis and S. aureus,” Journal of Antibiotics, vol. 64, no. 3, pp. 249–256, 2011.
- H. H. Mollenhauer, D. J. Morre, and L. D. Rowe, “Alteration of intracellular traffic by monensin; mechanism, specificity and relationship to toxicity,” Biochimica et Biophysica Acta, vol. 1031, no. 2, pp. 225–246, 1990.
- M. Merion and W. S. Sly, “The role of intermediate vesicles in the adsorptive endocytosis and transport of ligand to lysosomes by human fibroblasts,” Journal of Cell Biology, vol. 96, no. 3, pp. 644–650, 1983.
- M. Marsh, J. Wellsteed, and H. Kern, “Monensin inhibits Semliki Forest virus penetration into culture cells,” Proceedings of the National Academy of Sciences of the United States of America, vol. 79, no. 17, pp. 5297–5301, 1982.
- W. H. Park, C. W. Jung, J. O. Park et al., “Monensin inhibits the growth of renal cell carcinoma cells via cell cycle arrest or apoptosis,” International Journal of Oncology, vol. 22, no. 4, pp. 855–860, 2003.
- J. B. Russell, “A proposed mechanism of monensin action in inhibiting ruminal bacterial growth: effects on ion flux and protonmotive force,” Journal of Animal Science, vol. 64, no. 5, pp. 1519–1525, 1987.
- R. Tanaka, A. Nagatsu, H. Mizukami, Y. Ogihara, and J. Sakakibara, “Studies on chemical modification of monensin VIII. Synthesis of 7-O-substituted-25-carboxymonensins and their Ca2+ ion transport activity,” Tetrahedron, vol. 57, no. 15, pp. 3005–3012, 2001.
- A. Huczyński, J. Stefańska, P. Przybylski, B. Brzezinski, and F. Bartl, “Synthesis and antimicrobial properties of Monensin A esters,” Bioorganic and Medicinal Chemistry Letters, vol. 18, no. 8, pp. 2585–2589, 2008.
- D. C. Johnson and P. G. Spear, “Monensin inhibits the processing of herpes simplex virus glycoproteins, their transport to the cell surface, and the egress of virions from infected cells,” Journal of Virology, vol. 43, no. 3, pp. 1102–1112, 1982.
- R. Schlegel, M. Willingham, and I. Pastan, “Monensin blocks endocytosis of vesicular stomatitis virus,” Biochemical and Biophysical Research Communications, vol. 102, no. 3, pp. 992–998, 1981.
- A. Iacoangeli, G. Melucci-Vigo, and G. Risuleo, “The ionophore monensin inhibits mouse polyomavirus DNA replication and destabilizes viral early mRNAs,” Biochimie, vol. 82, no. 1, pp. 35–39, 2000.
- J. Adovelande and J. Schrével, “Carboxylic ionophores in malaria chemotherapy: the effects of monensin and nigericin on Plasmodium falciparum in vitro and Plasmodium vinckei petteri in vivo,” Life Sciences, vol. 59, no. 20, pp. PL309–PL315, 1996.
- B. C. Pressman, “Ionophorous antibiotics as models for biological transport,” Federation Proceedings, vol. 27, no. 6, pp. 1283–1288, 1968.
- F. G. Riddell and M. K. Hayer, “The monensin-mediated transport of sodium ions through phospholipid bilayers studied by 23Na-NMR spectroscopy,” Biochimica et Biophysica Acta, vol. 817, no. 2, pp. 313–317, 1985.
- M. Inabayashi, S. Miyauchi, N. Kamo, and T. Jin, “Conductance change in phospholipid bilayer membrane by an electroneutral ionophore, monensin,” Biochemistry, vol. 34, no. 10, pp. 3455–3460, 1995.
- K. Nakazato and Y. Hatano, “Monensin-mediated antiport of Na+ and H+ across liposome membrane,” Biochimica et Biophysica Acta, vol. 1064, no. 1, pp. 103–110, 1991.
- R. F. Shumard and M. E. Callender, “Monensin, a new biologically active compound. VI. Anticoccidial activity,” Antimicrobial Agents and Chemotherapy, vol. 7, pp. 369–377, 1967.
- A. L. Donoho, “Biochemical studies on the fate of monensin in animals and in the environment,” Journal of Animal Science, vol. 58, no. 6, pp. 1528–1539, 1984.
- R. D. Goodrich, J. E. Garrett, D. R. Gast, M. A. Kirick, D. A. Larson, and J. C. Meiske, “Influence of monensin on the performance of cattle,” Journal of Animal Science, vol. 58, no. 6, pp. 1484–1498, 1984.
- E. L. Potter, R. L. VanDuyn, and C. O. Cooley, “Monensin toxicity in cattle,” Journal of Animal Science, vol. 58, no. 6, pp. 1499–1511, 1984.
- R. Tanaka, A. Nagatsu, H. Mizukami, Y. Ogihara, and J. Sakakibara, “Studies on chemical modification of monensin IX. Synthesis of 26-substituted monensins and their Na+ ion transport activity,” Chemical & Pharmaceutical Bulletin, vol. 49, no. 6, pp. 711–715, 2001.
- M. Rochdi, A. M. Delort, J. Guyot et al., “Ionophore properties of monensin derivatives studied on human erythrocytes by 23Na NMR and K+ and H+ potentiometry: relationship with antimicrobial and antimalarial activities,” Journal of Medicinal Chemistry, vol. 39, no. 2, pp. 588–595, 1996.
- A. Nakamura, S. Nagai, T. Takahashi et al., “Studies on the chemical modification of monensin. IV. Synthesis, sodium ion permeability, and biological activity of 7-O-acyl- and 7-O-alkylmonensins,” Chemical & Pharmaceutical Bulletin, vol. 40, no. 9, pp. 2331–2337, 1992.
- A. Nagatsu, T. Takahashi, M. Isomura et al., “Studies on chemical modification of monensin. V. Synthesis, sodium ion permeability, antibacterial activity, and crystal structure of 7-O-(4-substituted benzyl)monensins,” Chemical & Pharmaceutical Bulletin, vol. 42, no. 11, pp. 2269–2275, 1994.
- D. Łowicki, A. Huczyński, M. Ratajczak-Sitarz et al., “Structural and antimicrobial studies of a new N-phenylamide of monensin A complex with sodium chloride,” Journal of Molecular Structure, vol. 923, no. 1–3, pp. 53–59, 2009.
- D. Łowicki, A. Huczyński, J. Stefańska, and B. Brzezinski, “Structural characterization and antibacterial activity against clinical isolates of Staphylococcus of N-phenylamide of monensin A and its 1:1 complexes with monovalent cations,” European Journal of Medicinal Chemistry, vol. 45, no. 9, pp. 4050–4057, 2010.
- D. Łowicki, A. Huczyński, J. Stefańska, and B. Brzezinski, “Syntheses, structural and antimicrobial studies of a new N-allylamide of monensin A and its complexes with monovalent metal cations,” Tetrahedron, vol. 65, no. 36, pp. 7730–7740, 2009.
- D. Łowicki, A. Huczyński, B. Brzezinski, and F. Bartl, “1H, 13C NMR, FT-IR, ESI MS and PM5 studies of a new 3,6,9-trioxadecylamide of monensin A and its complexes with Li+, Na+ and K+ cations,” Journal of Molecular Structure, vol. 990, no. 1–3, pp. 121–131, 2011.
- D. Łowicki, A. Huczyński, J. Stefańska, and B. Brzezinski, “Spectroscopic, semi-empirical and antimicrobial studies of a new amide of monensin A with 4-aminobenzo-15-crown-5 and its complexes with Na+ cation at 1:1 and 1:2 ratios,” Tetrahedron, vol. 67, no. 7, pp. 1468–1478, 2011.
- D. Łowicki, Synthesis, structure and biological activity of Monensin A amides and their complexes with metal cations [Ph.D. thesis], Poznan, Poland, 2011, https://repozytorium.amu.edu.pl/jspui/handle/10593/1026.
- A. Huczyński, D. Łowicki, M. Ratajczak-Sitarz, A. Katrusiak, and B. Brzezinski, “Structural investigation of a new complex of N-allylamide of Monensin A with strontium perchlorate using X-ray, FT-IR, ESI MS and semiempirical methods,” Journal of Molecular Structure, vol. 995, no. 1–3, pp. 20–28, 2011.
- J. Sakakibara, A. Nakamura, S. I. Nagai, T. Ueda, and T. Ishida, “Studies on the chemical modification of monensin. I. Synthesis and crystal structures of NaBr complexes of monensylamino acids,” Chemical & Pharmaceutical Bulletin, vol. 36, no. 12, pp. 4776–4784, 1988.
- A. Nakamura, S. I. Nagai, T. Ueda et al., “Studies on the chemical modification of monensin. III. Synthesis and sodium ion transport activity of macrocyclic monensylamino acid-1,29-lactones,” Chemical & Pharmaceutical Bulletin, vol. 39, no. 7, pp. 1726–1730, 1991.
- A. Huczyński, P. Przybylski, B. Brzezinski, and F. Bartl, “Monensin A methyl ester complexes with Li+, Na+, and K+ cations studied by ESI-MS, 1H- and 13C-NMR, FTIR, as well as PM5 semiempirical method,” Biopolymers, vol. 81, no. 4, pp. 282–294, 2006.
- A. Huczyński, P. Przybylski, B. Brzezinski, and F. Bartl, “Spectroscopic, mass spectrometry, and semiempirical investigation of a new ester of Monensin A with ethylene glycol and its complexes with monovalent metal cations,” Biopolymers, vol. 82, no. 5, pp. 491–503, 2006.
- A. Huczyński, D. Michalak, P. Przybylski, B. Brzezinski, and F. Bartl, “Monensin A benzyl ester and its complexes with monovalent metal cations studied by spectroscopic, mass spectrometry and semiempirical methods,” Journal of Molecular Structure, vol. 797, no. 1–3, pp. 99–110, 2006.
- A. Huczyński, D. Michalak, P. Przybylski, B. Brzezinski, and F. Bartl, “Spectroscopic, mass spectrometry and semiempirical investigation of a new Monensin A allyl ester and its complexes with Li+, Na+ and K+cations,” Journal of Molecular Structure, vol. 828, no. 1–3, pp. 130–141, 2007.
- A. Huczyński, D. Łowicki, B. Brzezinski, and F. Bartl, “Spectroscopic, mass spectrometry and semiempirical investigation of a new 2-methoxyethyl ester of monensin A and its complexes with Li+, Na+ and K+ cations,” Journal of Molecular Structure, vol. 874, no. 1–3, pp. 89–100, 2008.
- A. Huczyński, P. Przybylski, and B. Brzezinski, “NMR, FTIR, ESI-MS and semiempirical study of a new 2-(2-hydroxyethoxy)ethyl ester of monensin A and its complexes with alkali metal cations,” Tetrahedron, vol. 63, no. 36, pp. 8831–8839, 2007.
- A. Huczyński, D. Łowicki, B. Brzezinski, and F. Bartl, “Spectroscopic, mass spectrometry, and semiempirical investigations of a new 2-(2-methoxyethoxy)ethyl ester of Monensin A and its complexes with monovalent cations,” Journal of Molecular Structure, vol. 879, no. 1–3, pp. 14–24, 2008.
- A. Huczyński, A. Domańska, D. Łowicki, B. Brzezinski, and F. Bartl, “Structure of 1-naphthylmethyl ester of monensin A complexes with monovalent metal cations,” Journal of Molecular Structure, vol. 920, no. 1–3, pp. 414–423, 2009.
- A. Huczyński, P. Przybylski, and B. Brzezinski, “Complexes of monensin A methyl ester with Mg2+, Ca2+, Sr2+, Ba2+ cations studied by electrospray ionization mass spectrometry and PM5 semiempirical method,” Journal of Molecular Structure, vol. 788, no. 1–3, pp. 176–183, 2006.
- A. Huczyński, P. Przybylski, G. Schroeder, and B. Brzezinski, “Investigation of complex structures of a new 2-hydroxyethyl ester of Monensin A with Mg2+, Ca2+, Sr2+, Ba2+ cations using electrospray ionization mass spectrometry and semiempirical PM5 methods,” Journal of Molecular Structure, vol. 829, no. 1–3, pp. 111–119, 2007.
- A. Huczyński, B. Brzezinski, and F. Bartl, “Structures of complexes of benzyl and allyl esters of monensin A with Mg2+, Ca2+, Sr2+, Ba2+ cations studied by ESI-MS and PM5 methods,” Journal of Molecular Structure, vol. 886, no. 1–3, pp. 9–16, 2008.
- A. Huczyński, J. Janczak, and B. Brzezinski, “Crystal structure and FT-IR study of aqualithium 1-naphthylmethyl ester of monensin A perchlorate,” Journal of Molecular Structure, vol. 985, no. 1, pp. 70–74, 2011.
- A. Huczyński, J. Janczak, and B. Brzezinski, “Structure of 1:1 complex of 1-naphthylmethyl ester of monensin A with sodium perchlorate studied by X-ray, FT-IR and ab initio methods,” Journal of Molecular Structure, vol. 1030, pp. 131–137, 2012.
- A. Huczyński, P. Przybylski, B. Brzezinski, and F. Bartl, “Spectroscopic and semiempirical studies of a proton channel formed by the methyl ester of monensin A,” Journal of Physical Chemistry B, vol. 110, no. 31, pp. 15615–15623, 2006.
- A. Huczyński, A. Domańska, I. Paluch, J. Stefańska, B. Brzezinski, and F. Bartl, “Synthesis of new semi-synthetic dipodands and tripodands from naturally occurring polyether ionophores,” Tetrahedron Letters, vol. 49, no. 39, pp. 5572–5575, 2008.