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In this research paper, the total phenols (TP), flavonoids (TF), and tannins (TT) content in the acetone and ethyl acetate extracts of Najas marina L. and the identification and quantification of phenolic acids and flavonoids from the ethyl acetate extract were performed. Antioxidant, antimicrobial, and antibiofilm properties of the mentioned extracts were investigated in vitro. The genotoxic potential was analyzed in cultured human peripheral blood lymphocytes (PBL). The TP and TF content was higher in the ethyl acetate extract, dominated by quercetin (172.4 µg mg−1) and ferulic acid (22.74 µg mg−1), while the TT content was slightly higher in the acetone extract. Both extracts tested showed limited antioxidant effects compared to ascorbic acid. The strongest antibacterial activity was observed with Gram-positive bacteria, particularly Staphylococcus aureus (MIC and MMC at 0.31 mg ml−1) and S. aureus ATCC 25923 (MIC at

This is the first study on antioxidant and antibacterial activity of essential oils of A. sylvestris and A. pancicii against the human pathogens. In the oil of A. sylvestris, the main compounds wer...

In this paper, we investigated the hydrophobicity, ability to adhere to solvents and the pig epithelium and co-aggregation of members of family Enterobacteriaceae and Enterococcus faecalis KGPMF 49. The bacteria used in this study were isolated from traditionally made autochthonous cheese from Southeastern Serbia (Sokobanja). The percentage of adhered bacteria was different in three solvents (chloroform, ethyl acetate and xylene). The highest percentage was detected in the presence of chloroform, and the lowest percentage was detected in the presence of xylene (chloroform < ethyl acetate < xylene). A different degree of co-aggregation of enterobacteria with E. faecalis KGPMF 49 was observed. Klebsiella ornithinolytica KGPMF 8 demonstrated the highest percentage of co-aggregation with E. faecalis KGPMF49 (32.29%). Klebsiella pneumoniae KGPMF 13, K. ornithinolytica KGPMF 9 and Serratia marcescens biogp 1 KGPMF 19 were found to have the ability to adhere to the pig epithelium, whereas Escherichia coli KGPMF 22 showed no such ability. The ability to co-aggregate with other species and the ability to adhere to the pig epithelium are very important characteristics of the isolated bacteria.

Seven new zinc(II) complexes, K[Zn(dClQ)3]·2DMF (1), K[Zn(dClQ)3]·2DMF·H2O (2), [Zn(dBrQ)2(H2O)]2·DMF·H2O (3), [Zn(BrQ)2(H2O)]2·H2O (4), (HdClQ)2[ZnCl4]·2H2O (5), [Zn(dClQ)2(H2O)2]·H2O (6) and [Zn(CQ)2(H2O)2] (7) (5,7-dichloroquinolin-8-ol (dClQ), protonated 5,7-dichloroquinolin-8-ol (HdClQ), 5,7-dibromoquinolin-8-ol (dBrQ), 7-bromoquinolin-8-ol (BrQ), 5-chloro-7-iodoquinolin-8-ol (CQ)) have been prepared. All complexes were characterized by IR spectroscopy, elemental analysis and, except 7, by X-ray structure analysis. Stability of complexes in dimethyl sulfoxide was verified by NMR spectra. Antimicrobial activity was tested against nine strains of pathogenic bacteria, five mould species and two yeast species. Cytotoxic activity was tested against colon cancer cell line HCT 116 and non-cancerous cell line CCD-18Co. While all complexes showed higher cytotoxicity than cisplatin, poor selectivity to normal cells was observed.

This study monitors the influence of basic automotive paints on plankton and biofilms of selected microorganisms isolated from the wastewater of an automotive factory. Minimum Biofilm Eradication Concentration-High Throughput Plates system was used for the simultaneous tolerance testing. Minimal inhibitory concentration and minimal lethal concentration of the tested substances were determined for both planktonic cells and their biofilms. The resistance level of biofilms was also tested in standard 96 microtiter plates, whereby the results for bacteria and yeasts were confirmed by the fluorescence microscopy. The results were mutually compared for both plankton and biofilms, as well as for plankton and biofilm of the same microorganisms. In no case, the resistance of the planktonic form was higher than the biofilm for the same microorganism. Saccharomyces cerevisiae PMFKG-F7 in the presence of basic color, as well as Rhodotorula mucilaginosa PMFKG-F8 in the presence of the thinner for rinsing paint, shows high sensitivity in planktonic form, whereby the same species are the most resistant in the form of biofilm for the same substances. The highest resistance to all test substances was shown by the biofilm of R. mucilaginosa PMFKG-F8, as well as Candida utilis PMFKG-F9 which was significantly resistant in both tested forms. The obtained results suggest that autochthonous microorganisms that form biofilms can significantly improve the process of removing car paints from the wastewater and being thus new grounds for the development of new biotechnologies.

The five coumarin derivatives 3-(1-(2-hydroxypropylamino)ethylidene)-chroman-2,4-dione (L1), 3-(1-(phenylamino)ethylidene)-chroman-2,4-dione (L2), 3-(1-(o-toluidino)ethylidene)-chroman-2,4-dione (L3), 3-(1-(m-toluidino)ethylidene)-chroman-2,4-dione (L4), 3-(1-(2-mercaptoethylamino)ethylidene)-chroman-2,4-dione (L5) and its corresponding complexes 3-(1-(2-hydroxypropylamino)-ethylidene)-chroman-2,4-dione-palladium(II) (C1), 3-(1-(phenylamino)-ethylidene)-chroman-2,4-dione-palladium(II) (C2), 3-(1-(o-toluidino)-ethylidene)-chroman-2,4-dione-palladium(II) (C3), 3-(1-(m-toluidino)ethylidene)-chroman-2,4-dione-palladium(II) (C4), 3-(1-(2-mercaptoethylamino)ethylidene)-chroman-2,4-dione-palladium(II) (C5), were synthesized and characterized with microanalysis, infrared, 1H and 13C NMR spectroscopy. The proposed structures of ligands L3 and L4 were confirmed on the basis of the X-ray structural study. The ligands and their complexes were tested for their in vitro antimicrobial activity against 17 species of bacteria and fungi. Testing is performed by the microdilution method, with the minimum inhibitory concentration (MIC) and the minimum microbicidal concentration (MMC) being determined.

In this study, the effects of different temperature, pH, salt and glucose concentrations on the planktonic growth, biofilm formation, and formed biofilm of Serratia odorifera and Serratia marcescens, isolated from traditionally made cheese, were investigated using spectrophotometric method. The investigated strains demonstrated best planktonic growth and biofilm formation in Tryptic soy broth. The limiting factors for the planktonic growth and biofilm formation were temperature below 4 °C and salt concentration above 4%. Temperature of 37 °C and 44 °C, as well as various concentrations of glucose, stimulated the planktonic growth of bacteria. Moderate influence on biofilm formation was demonstrated at 37 °C as well as at various concentrations of glucose. These results were in accordance with the origin of bacteria, since the isolates were obtained from cheese.

In this study, the effects of different temperature, pH, different concentrations of salt, glucose and lactose, on the planktonic growth, biofilm formation and formed biofilm of Enterococcus hirae KGPMF9, Streptococcus uberis KGPMF2, Lactococcus lactis subsp. lactis KGPMF23 and Lactobacillus fermentum KGPMF29 was investigated. These lactic acid bacteria were previously isolated from traditionally made cheese from Southeastern Serbia. Evaluation of the effect of different environmental conditions on the planktonic growth, biofilm formation and formed biofilm were determined by spectrophotometric method. The limiting factor for the planktonic growth of tested bacteria was the salt concentration above 6.5%, while temperature of 4 °C was limiting factor for planktonic growth and biofilm formation. Temperature of 37 °C as well as various concentrations of glucose and lactose, stimulated planktonic growth and biofilm formation of all tested bacteria, except E. hirae KGPMF9. S. uberis KGPMF2 showed no ability of biofilm formation. Tested bacteria showed better planktonic growth and ability of biofilm formation in acidic media. Basic media was limiting factor for biofim formation. These results provide a basis for further research of influence of more environmental conditions on the development of lactic acid bacteria and their use like probiotics or starter cultures.

The biological activities of two binuclear copper(II) complexes containing S-alkenyl derivatives of thiosalicylic acid are reported [alkenyl = propenyl (L1), isobutenyl (L2)]. The structure of the complex with the S-isobutenyl derivative (C2) was confirmed by single-crystal X-ray structure analysis, which revealed that the structure consists of centrosymmetric, dinuclear complex molecules [Cu-2(S-i-butenyl-thiosal)(4)(DMSO)(2)] containing two Cu(II) centers bridged by four S-isobutyl-thiosalicylate ligands in a paddle-wheel type structure. The Cu(II) atom is situated in a distorted square-pyramidal environment formed by carboxylate oxygen atoms in the basal plane and a DMSO ligand in the axial position. The reactivities of the complexes toward guanosine-5-monophosphate (5-GMP) were investigated. Complex C2 ([Cu-2(S-i-butenyl-thiosal)(4)(H2O)(2)]) reacted more rapidly with 5-GMP than complex C1. The interactions of complexes C1 and C2 with calf thymus DNA (CT-DNA) were examined by absorption (UV-Vis) and emission spectral studies (ethidium bromide displacement studies), revealing good DNA interaction abilities. The antimicrobial activities of the free ligands and their complexes were tested by microdilution method, and both minimal inhibitory and microbicidal concentrations were determined. All the tested substances demonstrated selective and moderate antibacterial activity on gram-positive bacteria, but low antibacterial activity on gram-negative bacteria. Also, the tested substances demonstrated low antifungal activity.

In this study, the effects of environmental factors (different media, temperature, pH, salt and sugar concentrations) on the planktonic growth, biofilm formation and formed biofilm of Escherichia coli KGPMF 16 and Escherichia coli KGPMF 17 were investigated. Tested bacteria were isolated from traditionally made cheese produced in Southeastern Serbia (Sokobanja region). The influence on planktonic growth, biofilm formation and formed biofilm was determined using spectrophotometric method. The limiting factors for the planktonic growth and biofilm formation were temperature of 4 °C and all tested concentrations of salt. The growth of tested bacteria was higher in media enriched with lactose than in media containing glucose. TSB was more congenial media to the planktonic growth of bacteria than MHB broth. None of the tested bacteria demonstrated the ability to form biofilm at 4 °C and 44 °C. Only E. coli KGPMF 17 showed ability to form biofilm in TSB at 37 °C. Different concentrations of salt, glucose and lactose exhibited inhibitory effect on biofilm formation, but all tested concentrations of lactose showed stimulating effect on formed biofilm of E. coli KGPMF 17. These results contribute to better understanding of the effects of environmental factors on the development of E. coli in cheese.

The aim of the study was to examine heavy metal tolerance (Cd2+, Zn2+, Ni2+ and Cu2+) of single- and mixed-species biofilms (Rhodotorula mucilaginosa and Escherichia coli) and to determine metal removal efficiency (Cd2+, Zn2+, Ni2+, Cu2+, Pb2+ and Hg2+). Metal tolerance was quantified by crystal violet assay and results were confirmed by fluorescence microscopy. Metal removal efficiency was determined by batch biosorption assay. The tolerance of the mixed-species biofilm was higher than the single-species biofilms. Single- and mixed-species biofilms showed the highest sensitivity in the presence of Cu2+ (E. coli-MIC 4 mg/ml, R. mucilaginosa-MIC 8 mg/ml, R. mucilaginosa/E. coli-MIC 64 mg/ml), while the highest tolerance was observed in the presence of Zn2+ (E. coli-MIC 80 mg/ml, R. mucilaginosa-MIC 161 mg/ml, R. mucilaginosa-E. coli-MIC 322 mg/ml). The mixed-species biofilm exhibited better efficiency in removal of all tested metals than single-species biofilms. The highest efficiency in Cd2+ removal was shown by the E. coli biofilm (94.85%) and R. mucilaginosa biofilm (97.85%), individually. The highest efficiency in Cu2+ (99.88%), Zn2+ (99.26%) and Pb2+ (99.52%) removal was shown by the mixed-species biofilm. Metal removal efficiency was in the range of 81.56%–97.85% for the single- and 94.99%–99.88% for the mixed-species biofilm.

The objectives of this research project were isolation, identification, and evaluation of the safety aspect and probiotics properties of 21 Enterococcus faecium strains isolated from sausages originated from southeastern Serbia. Analyzed E. faecium isolates showed tolerance to simulated gastrointestinal conditions. All the examined isolates grew well on media with 0.1% and 0.2% of phenol. None of the tested isolates were histamine-producers, while the synthesis of tyramine was observed for E. faecium sk8-1 and sk8-17. Full resistance to antibiotics was not observed for any examined isolate of E. faecium (penicillin, amoxicillin, and ofloxacin showed the effect on all tested isolates). An inhibition zone against examined pathogens was exhibited by all strains, with the largest inhibition zone against Pseudomonas spp., Proteus spp. and E. coli (12–30 mm/MIC values ranged from 0.5 to 12 mg mL−1). The results indicated that E. faecium isolates from spontaneously fermented sausage showed a potential for further investigation and possible application as probiotics.

The objective of this study was to evaluate the probiotic potential as well as the ability of adhesion and aggregation of natural and autochthonous lactic acid bacteria, isolated from traditionally made cheese. Lactic acid bacteria from natural food sources can be promising probiotic candidates and they can be used in natural food preservation or like starter cultures. Tested autochthonous isolates showed tolerance to the simulated gastrointestinal condition as well as the sensitivity to clinically relevant antibiotics, especially to ampicillin (MIC at 0.195 μg mL−1 for lactobacilli and from 0.195 to 3.125 μg mL−1 for lactococci). Among isolates, the highest percentage of adhesion was detected with chloroform, while the adhesion ability of selected isolates to pig intestinal epithelium was in the correlation with the results of adhesion ability with solvents. The auto-aggregation ability of isolates was demonstrated, while co-aggregation with Escherichia coli was strain specific. The results indicated the potential probiotic properties of the isolates and give evidence for further investigation and potential application in the dairy industry.

Starting from well-defined NH2(CH3)2[PdCl2(XQ)] complexes, coordination compounds of general formula Cat[PdCl2(XQ)] have been prepared by cationic exchange of NH2(CH3)2+ and Cat cations, where XQ are biologically active halogen derivatives of quinolin-8-ol (5-chloro-7-iodo-quinolin-8-ol (CQ), 5,7-dibromo-quinolin-8-ol (dBrQ) and 5,7-dichloro-quinolin-8-ol (dClQ)) and Cat is K+ or Cs+. The cation exchange of all prepared complexes, K[PdCl2(CQ)] (1), K[PdCl2(dClQ)] (2), K[PdCl2(dBrQ)] (3), Cs[PdCl2(CQ)] (4), Cs[PdCl2(dClQ)] (5) and Cs[PdCl2(dBrQ)] (6) was approved using IR spectroscopy, their structures in DMSO solution were elucidated by one- and two-dimensional NMR experiments, whereas their stability in solution was verified by UV-VIS spectroscopy. Interaction of complexes to ctDNA was investigated using UV-VIS and fluorescence emission spectroscopy. The minimum inhibitory concentration and the minimum microbicidal concentration values were detected against 15 bacterial strains and 4 yeast strains to examine the antimicrobial activity for the complexes. The in vitro antitumor properties of the complexes were studied by testing the complexes on leukemic cell line L1210, ovarian cancer cell line A2780 and non-cancerous cell line HEK293. The majority of the prepared compounds exhibited moderate antimicrobial and very high cytotoxic activity.

The influence of 5 new Platinum(IV) (Pt(IV)) complexes with S-alkyl derivatives of thiosalicylic acid (C1-benzyl, C2-methyl, C3-ethyl, C4-propyl and C5- butyl) was studied on 16 strains of bacteria. Antibacterial activity was tested using microdilution method with resazurin while antibiofilm activity was observed by tissue culture plate method, using doxycycline as a positive control. The results were expressed as minimum inhibitory concentration (MIC), minimum bactericidal concentration (MBC) and biofilm inhibitory concentration (BIC). The best result on Gram positive bacteria exhibited C1 and MIC was

The spectroscopically predicted structure of the obtained copper(II)-complex with S-propyl derivative of thiosalicylic acid was confirmed by X-ray structural study. The binuclear copper(II)-complex with S-propyl derivative of thiosalicylic acid crystallized in two polymorphic forms with main structural difference in the orientation of phenyl rings relative to corresponding carboxylate groups. The antibacterial activity was tested determining the minimum inhibitory concentration (MIC) and the minimum bactericidal concentration (MBC) by using microdilution method. The influence on bacterial biofilm formation was determined by tissue culture plate method. In general, the copper(II)-complexes manifested a selective and moderate activity. The most sensitive bacteria to the effects of Cu(II)-complexes was a clinical isolate of Pseudomonas aeruginosa. For this bacteria MIC and biofilm inhibitory concentration (BIC) values for all tested complexes were in the range or better than the positive control, doxycycline. Also, for the established biofilm of clinical isolate Staphylococcus aureus, BIC values for the copper(II)-complex with S-ethyl derivative of thiosalicylic acid, [Cu-2(S-et-thiosal)(4)(H2O)(2)] (C3) and copper(II)-complex with S-butyl derivative of thiosalicylic acid, [Cu-2(S-bu-thiosal)(4)(H2O)(2)] (C5) were in range or better than the positive control. All the complexes acted better against Gram-positive bacteria (Staphylococcus aureus and Staphylococcus aureus ATCC 25923) than Gram-negative bacteria (Proteus mirabilis ATCC 12453, Pseudomonas aeruginosa, and P. aeruginosa. ATCC 27855). The complexes showed weak antioxidative properties tested by two methods (1,1-diphenyl-2-picrylhydrazyl (DPPH) and reducing power assay). (C) 2016 Elsevier B.V. All rights reserved.

Negative effects of available antibiotics and the constant development of bacterial resistance motivate a search for new antimicrobial agents. Aromatics plants have traditionally been used as antibacterial agents and are well accepted today as a source of antioxidants. The present study evaluated the antibacterial activities and antioxidant capacity of eight aromatic plants, indigenous to the flora of the Balkan Peninsula, which are used as medicinal plants in traditional medicine. The plants studied were Hyssopus officinalis , Angelica pancicii, Angelica sylvestris, Laserpitium latifolium , Achillea grandifolia, Achillea crithmifolia, Artemisia absinthium and Tanacetum parthenium . The antimicrobial activities of methanolic extracts of the plant tissues against 16 bacterial isolates of Escherichia coli , Pseudomonas aeruginosa , Klebsiella sp. , Proteus mirabilis , Acinetobacter sp. , Staphylococcus aureus , Streptococcus pyogenes , Streptococcus pneumoniae and Enterococcus faecalis were investigated using a microwell dilution assay. Minimal inhibitory concentration (MIC) of the extracts ranged from 6.3 to 100 mg mL -1 , and minimal bactericidal concentration (MBC) ranged from 12.5 to 100 mg mL -1 . Antioxidant potential of the extracts was analyzed as contents of total phenols and flavonoids; radical scavenging activity by the ABTS + and DPPH methods, and reducing power by the iron (III) to iron (II) reduction assay, and the ferric reducing antioxidant power assay (FRAP). Results of antioxidative activities from the 4 methods demonstrated similar sequence of activity: A. crithmifolia > A. grandifolia > H. officinalis > A. absinthium > T. parthenium > L. latifolium > A. pancicii > A. sylvestris. The total content of polyphenols and flavonoids in the methanol extracts of the studied species positively correlated with their antioxidant properties, confirming their major role in antioxidant activity of these species.

Four new platinum(IV) complexes C1–C4 of general formula [PtBr4(R2-S,S-eddv)], (R = ethyl, propyl, butyl and pentyl; S,S-eddv = (S,S)--ethylenediamine-N,N′-di-2-(3-methyl)butanoate) have been synthesized and characterized by microanalysis, infrared, 1H and 13C NMR spectroscopy. In vitro antimicrobial activity for these and [PtBr4(R2-S,S-eddp)] complexes (S,S-eddp = (S,S)-ethylenediamine-N,N′-di-2-propanoate) has been investigated. The antibacterial activity was tested against 16 strains of bacteria determining the minimum inhibitory concentration (MIC) and the minimum bactericidal concentration (MBC) using microdilution method. In general, platinum(IV) complexes manifested moderate activity against the Gram positive bacteria and low activity against the Gram negative bacteria. The complexes showed weak antioxidative properties tested by two methods (DPPH and reducing power assay).

A series of four new ligands of general formula R2-S,S-eddtrp·2HCl (L1–L4) and their palladium(II) complexes of general formula [PdCl2(R2-S,S-eddtrp)] (C1–C4) where R = ethyl, 1-propyl, 1-butyl and 1-pentyl; S,S-eddtrp·2HCl = ethylenediamine-N,N′-di-(3,3′-1H-indol-3yl)propionic acid dihydrochloride have been synthesized and characterized by elemental microanalysis, infrared, 1H and 13C NMR spectroscopy. The proposed structures of all compounds were examined by density functional theory (DFT). The ligands (L1–L4) and Pd(II) complexes (C1–C4) were screened for their antimicrobial activity against 19 microorganisms and minimum inhibitory concentrations (MIC) and minimum microbicidal concentration (MMC) were determinated. All tested ligands and complexes exhibited the highest antimicrobial activity on Escherichia coli ATCC 25922, being in range or higher than positive control, tetracycline.

In this study, inhibitory effects of crude silk produced by 5th larval instar of moth Plodia interpunctella , as well as ethanol, acetone, ethyl acetate, hexane and dichloromethane silk extracts were evaluated against 18 bacterial strains (ATCC strains/isolates) and 6 fun-gal ATCC strains in vitro . Among the tested extracts, the acetone silk extract had the highest activity against Gram-negative bacteria,while all the extracts showed moderate to high activity against Gram-positive bacteria and fungi. The dilution of 1/2, 1/4 of stock samples showed higher microbial activity. The crude silk was not bioactive. This is the first report on antimicrobial activity of different extracts of silk of P. interpunctella larvae. These results open new ave-nues for future research in using this major storage insect pest in biomedical applications.

In the present manuscript, palladium(II) complexes (C1, C2) with newly synthesized coumarine ligands 3-(1-((3-chlorophenyl)amino)ethylidene)-chroman-2,4-dione (L1) and 3-(1-((4-chlorophenyl)amino)ethylidene)-chroman-2,4-dione (L2) were prepared and structurally characterized by spectroscopic techniques (FT-IR, 1H NMR, 13C NMR) in combination with elemental analysis and theoretical methods (DFT). The structures of all compounds were fully optimized using the B3LYP-D3BJ theoretical method. Cytotoxic activity of investigated compounds was tested against two cells lines (human colorectal carcinoma, HCT-116, and human fibroblast lung MRC-5), while their antimicrobial activity was screened against nine strains of pathogenic bacteria, five mould species and two yeast species. Unfortunately, their cytotoxic and antibacterial activities were weak. Docking studies for all compounds with epidermal growth factor receptor (EGFR) were performed. It was found that hydrophobic interactions that include chlorine atom have somewhat lower values of the pairwise interaction energies compared to the purely hydrophobic interactions. In addition, it was found the chlorine atom in the para position contributes to the slightly higher binding free energy and lower values of constant of inhibition.

A series of new 3d metal complexes with 5-chloro-quinolin-8-ol (ClQ), [Mn(ClQ)2] (1), [Fe(ClQ)3] (2), [Co(ClQ)2(H2O)2] (3), [Ni(ClQ)2(H2O)2] (4), [Cu(ClQ)2] (5), [Zn(ClQ)2(H2O)2] (6), [Mn(ClQ)3]·DMF (7) and [Co(ClQ)3]·DMF·(EtOH)0.35 (8) (DMF=N,N-dimethylformamide), has been synthesized and characterized by elemental analysis, IR spectroscopy and TG-DTA thermal analysis. X-ray structure analysis of 7 and 8 revealed that these molecular complexes contain three chelate ClQ molecules coordinated to the central atoms in a deformed octahedral geometry and free space between the complex units is filled by solvated DMF and ethanol molecules. Antimicrobial activity of 1-6 was tested by determining the minimum inhibitory concentration and minimum microbicidal concentration against 12 strains of bacteria and 5 strains of fungi. The intensity of antimicrobial action varies depending on the group of microorganism and can be sorted: 1>ClQ>6>3/4>2>5. Complexes 1-6 exhibit high cytotoxic activity against MDA-MB, HCT-116 and A549 cancer cell lines. Among them, complex 2 is significantly more cytotoxic against MDA-MB cells than cisplatin at all tested concentrations and is not cytotoxic against control mesenchymal stem cells indicating that this complex seems to be a good candidate for future pharmacological evaluation. Interaction of 1-6 with DNA was investigated using UV-VIS spectroscopy, fluorescence spectroscopy and agarose gel electrophoresis. The binding studies indicate that 1-6 can interact with CT-DNA through intercalation; complex 2 has the highest binding affinity. Moreover, complexes 1-6 inhibit the catalytic activity of topoisomerase I.

The aim of this study was to examine heavy metal tolerance (lead (Pb2+) and mercury (Hg2+)) of single- and mixed-species biofilms, formed by yeast Rhodotorula mucilaginosa and bacteria Escherichia coli LM1. Single- and mixed-species biofilms were quantified by crystal violet test and the absorbance was measured using microplate reader (OD570). The minimal inhibitory concentration (MIC) and the minimal lethal concentration (MLC) were determined and the results were confirmed by fluorescence microscopy. The significant difference in lead tolerance was observed between the mixed- and the single-species biofilms. The MIC of lead (Pb2+) for the examined biofilms (E. coli LM1, R. mucilaginosa and R. mucilaginosa / E. coli) was recorded at concentrations of 4000 μg/ml, 4000 μg/ml and 16000 μg/ml, respectively. The MIC of mercury (Hg2+) for the biofilms was noticed at concentrations of 31.25 μg/ml, 250 μg/ml and 250 μg/ml, respectively. Standard antibiotics (amphotericin B and tetracycline) were used as positive control. Results obtained for single-species biofilms were compared in between and with the results obtained for mixed-species biofilm. The tolerance of the mixed- species biofilm was higher in comparison to the singlespecies biofilms and the results were confirmed by a fluoresecence microscope. The obtained results suggest that the R. mucilaginosa / E. coli biofilm may have a potential to be used in bioremediation of wastewaters contaminated with lead and mercury.

The aim of study was to investigate the antimicrobial and antibiofilm activities as well as chemical analysis of aquatic, acetone and ethyl acetate extracts Vinca minor L. collected in Balkan mountains (Dinaric Alps, Serbia). Antimicrobial testing was performed by microdilution method. Minimum inhibitory concentration and minimal microbicidal concentration were determined for 26 species of microorganisms. Strong antimicrobial activity was detected against Gram-positive bacteria, especially from genus Bacillus. Gramnegative bacteria were not sensitive within the tested extracts concentrations. Ethyl acetate extract from V. minor caused some antifungal effect on Rhodotorula and Candida. Trichoderma viride was sensitive to aquatic extract of the plant. Antibiofilm activity was tested by crystal violet assay. Only ethyl acetate extract was effective against formation of biofilm by Proteus mirabilis and biofilm inhibitory concentration (BIC50) was at 22.8 mg/mL. Phytochemical analysis involved determining the amount of total phenols, flavonoids and tannins as well as antioxidant activity monitoring capability to neutralize 2.2-diphenyl-1-picrylhydrazyl (DPPH) free radicals and reduction potential. Total phenolic content, DPPH and reduction potential of the aquatic extract of V. minor was significantly stronger compared to the acetone and ethyl acetate extracts.

Ethnopharmacological relevance: Trapa natans L. (water chestnut or water caltrop) is a widespread aquatic plant, which has been cultivated for food and traditional medicine since ancient times. Pharmacological studies showed that water chestnut exhibits the wide range of biological activities, such as antimicrobial, antioxidative, analgesic, anti-inflammatory, as well as antiulcer. Aim of the study: Evaluation of anti-virulence potential and toxicity of T. natans methanol (TnM), acetone (TnA) and ethyl acetate (TnEA) leaf extracts. Materials and methods: The anti-quorum sensing activity of Tn extracts was addressed by measuring their effects on biofilm formation, swarming motility and pyocyanin and elastase production in Pseudomonas aeruginosa. Specific P. aeruginosa biosensors were used to identify which of the signaling pathways were affected. The lethal and developmental toxicity of extracts were addressed in vivo using the zebrafish (Danio rerio) model system. The phenolic composition of T. natans leafs extracts was analyzed by a linear ion trap-OrbiTrap hybrid mass spectrometer (LTQ OrbiTrapMS) and UHPLC system configured with a diode array detector (DAD) hyphenated with the triple quadrupole mass spectrometer. Results: Subinhibitory concentrations of Tn leaf extracts (0.2 MIC) inhibited pyocyanin and elastase production up to 50% and 60%, respectively, and reduced swarming zones, comparing to non-treated P. aeruginosa. TnA inhibited biofilm formation by 15%, TnM showed a stimulatory effect on biofilm formation up to 20%, while TnEA showed no effect. The bioactive concentrations of TnM and TnA were not toxic in the zebrafish model system. Twenty-two phenolic compounds were tentatively identified in TnM, where thirteen of them were identified in T. natans for the first time. Tn extracts, as well as their major components, ellagic and ferulic acids, demonstrated the ability to interfere with P. aeruginosa Las and PQS signaling pathways. Conclusions: This study demonstrates anti-virulence potential of Tn leaf extracts against medically important pathogen P. aeruginosa and confirms the ethnopharmacological application of this plant against microbial infections. This is the peer-reviewed version of the following article: Aleksic, I.; Ristivojevic, P.; Pavic, A.; Radojević, I.; Čomić, L. R.; Vasiljevic, B.; Opsenica, D.; Milojković-Opsenica, D.; Senerovic, L. Anti-Quorum Sensing Activity, Toxicity in Zebrafish (Danio Rerio) Embryos and Phytochemical Characterization of Trapa Natans Leaf Extracts. Journal of Ethnopharmacology 2018, 222, 148–158. [https://doi.org/10.1016/j.jep.2018.05.005] Supplementary material: [http://cherry.chem.bg.ac.rs/handle/123456789/2933]

Management of water resources such as lakes and reservoirs involves many stakeholders and a huge amount of data that comes from various information systems and in different formats. These systems are typically very difficult to integrate, analyze and customize. This requires a new breed of information systems capable to answer the challenges of modern water information management. In this paper, we introduce the new application model for designing such systems and accompanying i-SeLaR software system - composite, service-oriented and multilayered web information system for management of Serbian lakes and reservoirs. We describe architecture and services of the application model, together with structure and functionalities of the software solution. i-SeLaR integrates data, tools and applications for collaboration, data and knowledge management, process automation, and analytics. Architecture and features of i-SeLaR provide scalability and flexibility, so the system can be scaled, customized and implemented in organizations of different types and sizes. i-SeLaR web portal is the central component which serves as a unique gateway to different data sources and services, and provides a seamless and unified web interface for monitoring and management of water resources. Practical results showed several benefits in terms of better integration and flexibility, enhanced collaboration, higher data quality, knowledge-based analysis and more informed decision making.

The octahedral cobalt(III) complexes with (S,S)-ethylenediamine-N,N-di-2-propionic (S,S-eddp) and (S,S)-ethylenediamine-N,N-di-2-(3-methyl)-butanoic (S,S-eddv) acids and oxalato and malonato ligands, as additional bidentate ligands, were prepared and characterized. The complexes were purified by ionexchange chromatography. The geometry of the complexes has been supposed on the basis of the infrared, electronic absorption and NMR spectra. The A absolute configurations of the isolated complexes have been predicted on the basis of their circular dichroism (CD) spectra and it was confirmed by single-crystal X-ray analysis of potassium-Delta-(-)(589)-s-cis-oxalato-(S,S)-ethylenediamine-N,N-di-(2-propanoato)-cobaltate(III)-semihydrate, K-Delta-(-)(589)-s-cis-[Co(S,S-eddp)(ox)]center dot 0.5H(2)O. Antimicrobial activity of ligands and obtained cobalt(III) complexes was evaluated by determining the minimum inhibitory concentration (MIC) and minimum microbicidal concentration (MMC) in relation to 13 species of microorganisms (five strains of pathogenic bacteria, five species pathogenic fungi and three species of probiotic). Tested ligands and complexes demonstrated moderate and low antibacterial and antifungal activity. There was no difference in activities between the ligands and complexes. (C) 2014 Elsevier Ltd. All rights reserved.

In this paper, the presence of enterobacteria in autochthonous cheese from Southeast Serbia (Sokobanja), made in the traditional way, was investigated. The samples from different households, was taken during the summer and the autumn. Chemical and physical characteristics of samples (water content, fat content, acidity, pH, and sodium chloride content) were examined. In the analyzed samples of cheese, four different genera of family Enterobacteriaceae (Klebsiella [65%], Escherichia [20%], Serratia [10%], and Enterobacter [5%]) were identified. The members of genus Klebsiella were Klebsiella oxytoca, Klebsiella pneumoniae, and Klebsiella ornithinolytica, while in the genus Escherichia only one species, Escherichia coli was identified. Besides, two species of the genus Serratia, Serratia odorifera and Serratia marcescens biogp 1, and one species of the genus Enterobacter, Enterobacter gergoviae, were identified. Biochemical characteristics, proteolytic and lipolytic activity, sensitivity to streptomycin, chloramphenicol, and tetracycline were, also, determined. According to the rapid latex agglutination test, of the four E. coli isolates, two isolates belong to serotype E. coli O157. Practical applications The results of this study contribute to better understanding of unexplored microflora of cheese from Sokobanja. The isolated genera were Klebsiella sp., Escherichia sp., Enterobacter sp., and Serratia sp. with twenty identified species. It is well known that bacteria from family Enterobacteriaceae could affect organoleptic properties of cheese. Bacteria isolated from cheese from Sokobanja mostly did not manifest proteolytic and lipolytic activity. The most number of isolates were susceptible to tested antibiotics. Further researches may contribute to better understanding of interaction between enterobacteria and lactic acid bacteria in autochthonous cheeses.

The five new copper(II) complexes with some S-alkyl derivatives of thiosalicylic acid (alkyl = benzyl (L1), methyl (L2), ethyl (L3), propyl (L4), butyl (L5)) have been synthesized and characterized by microanalysis and infrared spectra. The spectroscopically predicted structure of the obtained binuclear copper(II) complex with S-methyl derivative of thiosalicylic acid was confirmed by X-ray analysis. Single crystals suitable for X-ray measurements were obtained by slow crystallization from a water solution. The compound crystallizes with two binuclear Cu(II) complex molecules in the asymmetric unit. Both molecules have typical paddle-wheel structure with apical positions occupied by water molecules. The independent molecules showed slight difference in configuration mainly reflected in the different orientation of the phenyl rings relating to their carboxylate groups. Antimicrobial activity of these complexes was tested by microdilution method and both minimal inhibitory and microbicidal concentration were determined. The intensity of the antimicrobial activity varied depending on the species of microorganism and the compound type. In general, the activity of the complexes was higher than or similar to the corresponding ligands. All the tested complexes demonstrated moderate or selective antibacterial activity and low antifungal activity. (C) 2014 Elsevier Ltd. All rights reserved.

Five 3d metal [M(H2O)2(SQ)]n complexes, where M is Mn (1), Co (2), Ni (3), Zn (4) and Cu (5), and SQ is the dianion of 8-hydroxyquinoline-5-sulfonic acid have been prepared and characterized by IR spectroscopy and elemental analysis. X-ray structure analysis of 1 and 5 in combination with IR spectroscopy of all five complexes showed that complexes 1–4 are isostructural 2D polymers, while 5 is 1D polymer due to the different bonding character of SQ. Stability of all complexes in DMSO was proved by UV–Vis spectroscopy and for 4 also verified by 1H and 13C NMR spectroscopy. Cytotoxic activity tests against cervical carcinoma HeLa, colon carcinoma HCT116 and normal human fibroblast MRC-5 cell lines showed moderate but selective cytotoxicity of all complexes. Complex 1 exhibited highest activity with IC50 = 39.1 and 33.4 µM, respectively, but is lower than activity of cisplatin (CP) which IC50 = 24.3 and 14.3 µM, respectively. However, their cytotoxic activity against healthy MRC-5 cells (IC50 > 92 µM) is much lower than CP (IC50 = 19.7 µM). Antimicrobial activity of all complexes against 9 strains of pathogenic bacteria, five mould species and two yeast species is negligible.

This research presents complete data about phytochemical analysis and biological activities of a new dietary supplement for commercial use “Oligo Grapes” (OG), and its individual constituents: lyophilized pomace (LP), clay supplemented with red wine extract, lyophilized pomace ethanolic extract (PE), and red wine extract. OG, as a commercially available food supplement, has not been previously tested for its biological activity. Now we want to present new data about its phytochemical screening, antioxidant and antibacterial activities, and anticancer properties with respect to its cytotoxicity and effects on redox status in colon cancer cell lines. The tested extracts expressed strong antibacterial activity against Proteus mirabilis and Proteus mirabilis ATCC 12453, where the synergy of contents inside the supplement demonstrated a higher influence on the bacteria than its separately tested constituents. Among the investigated extracts, PE, as the extract with the highest phenolics concentration, had remarkable cytotoxic activity on HCT-116 and SW-480 colon cancer cells. Also, the treatments modulated redox status in the investigated cancer cells, by inducing oxidative and nitrosative stress, which could be one of the preferred mechanisms of the anticancer action. Based on the achieved antimicrobial and anticancer properties, there is a need for producing different food supplements and nutritional products originating from grapes. In this respect, the food supplement OG and its health benefits deserve scientific attention and further research.

Antibacterial, antibiofilm and antioxidant activity of acetone, ethanol, ethyl acetate and diethyl ether extracts of P. nodosus Poir. were tested. In vitro antibacterial activity was investigated by microdilution method. Minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) have been determined. The values were in the range from 5 to > 5 mg/ml. Antibiofilm activity was tested by crystal violet assay. The biofilm inhibitory concentration (BIC) values were from 2.03 to > 10 mg/ml. The best results against biofilm formation had ethanol and ethyl acetate extracts. The total phenolic content was established by using Folin-Ciocalteu method. The highest total phenol content was found in the ethyl acetate extract (28.45 mg GA/g) while the lowest content in the ethanol extract (22.74 mg GA/g). The concentrations of flavonoids were determined using aluminium chloride method. The concentration of total flavonoid content was 102.09 mg RU/g for the ethyl acetate extract, while the lowest content was noticed in diethyl ether extract (32.93 mg RU/g). The antioxidant activity was determined by the DPPH free radicals assay. Antioxidative efficiency was in the range from 641.77 to 8811.63 μg/ml. The tested extracts showed weak antioxidant activity (AAI < 0.5).

The antibacterial and anti-biofilm activity of ethanolic extract from the rhizome of Zingiber officinale were evaluated. In vitro antibacterial activity was investigated by microdilution method. Minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) have been determined. The values were in the range from 0.0024 to > 20 mg/ml. The most sensitive bacteria were Gram-positive bacteria: Staphylococcus aureus and Staphylococcus aureus ATCC 25923. Anti-biofilm activity was tested by crystal violet assay. Pseudomonas aeruginosa ATCC 27853, Proteus mirabilis and Escherichia coli ATCC 25922 were used as the test organisms. Ethanolic extract showed the best result on Proteus mirabilis biofilm where biofilm inhibitory concentration (BIC50) was 19 mg/ml.

This study investigated the antimicrobial activity as well as some phytochemical analysis of ethanol and diethyl ether extracts from plant species Vinca minor L. In vitro antimicrobial activity of extracts was studied on 20 strains of microorganisms (16 bacteria and four yeasts). Testing was performed by microdilution method and minimum inhibitory concentration (MIC) and minimum microbicidal concentration (MMC) were determined. The strongest antimicrobial activity wa s detected on G+ bacteria of the genus Bacillus . Tested G - bacteria and yeasts were not sensitive to the acti on of the extracts or the sensitivity was insignificant. Phytochemical analysis involved determining the amount of total phenolics, flavonoids and tannins, as well as the determination of antioxidan t activity monitoring capability to neutralize free radicals (DPPH) and the reductive p otential. Phytochemical examination indicates that the total phenolic compounds were mo re in the ethanolic extract and the content of flavonoids and tannins marginally higher in the diethyl ether extract. The antioxidant activity (DPPH) of the ethanolic extrac t of V. minor was significantly stronger as compared to the diethyl ether extract, and the redu ction potential was approximately the same.

The s-cis -[Cr( S , S- eddv)L]-complexes ( 1 , 2 ) ( S , S -eddv = ( S , S )-ethylenediamine- N , N ′-di-2-(3 - methyl ) butanoato ion; L = oxalate or malonate ion) were prepared. The complexes were purified by ion-exchange chromatography. The geometry of the complexes has been supposed on the basis of the infrared and electronic absorption spectra, and the absolute configurations of the isolated s-cis -[Cr( S , S -eddv)L]-complexes have been predicted on the basis of their circular dichroism (CD) spectra. Also, the results of thermal decomposition have been discussed. Antimicrobial activity of the prepared complexes ( 1 – 4 ) was investigated against 28 species of microorganisms. Testing was performed by microdilution method and minimum inhibitory concentrations (MIC) and minimum microbicidal concentration (MMC) have been determined. Complexes demonstrated in generally low antibacterial and antifungal activity.

The present work was undertaken to determine the total phenol, flavonoid and tannin content in five extracts of Origanum vulgare growing wild in southwest Serbia as well as to evaluate antioxidant and antimicrobial activity towards 29 strains of human pathogenic and food spoilage bacteria and fungi. In order to define a chemotype of this O. vulgare, chemical composition of essential oil was determined. The major compounds were: sabinene, terpinen-4-ol, 1.8 cineole, γ-terpinene and caryophyllene oxide. The concentrations of total phenols were examined using Folin–Ciocalteu reagent and the obtained values ranged from 84.5 to 235 mg GA/g. By using aluminium chloride method, the concentrations of flavonoids were obtained and the values ranged from 57.1 to 132 mg RU/g. In determining the amount of tannins, the method with butanol–HCl reagent was used and the obtained values were between 1.25 and 4.02 mg CCh/g. Antioxidant activity was evaluated by measuring the scavenging capacity of extracts on DPPH. Tested extracts expressed strong scavenger activity with IC50 values between 34.5 and 86 μg/ml. The ethanol extract was the most active. The strongest antibacterial activity, determined by microdilution method, was detected on G+ bacteria such as Bacillus species and Staphylococcus aureus, obtaining minimal inhibitory concentration (MIC) 0.16 mg/ml while antifungal activity was moderate with MICs between 2.5 and 20 mg/mL.

This study compares the effect of heavy metals (Hg2+, Cu2+, and Pb2+) on the Rhodotorula mucilaginosa and Saccharomyces boulardii biofilm and planktonic cells. A MBECTM-HTP assay was used to test the levels of tolerance to heavy metals. The minimum inhibitory concentration (MICp) and minimum lethal concentration (MLCp) of the R. mucilaginosa and S. boulardii planktonic cells were determined, as well as minimum biofilm eradication concentration (MBEC). Metal removal efficiency was determined by batch biosorption assay. Previous studies had focused on heavy metal tolerance and removal efficiency of planktonic cells from Rhodotorula species only. Hence, our study presents and compares results for metal tolerance and removal efficiency of the R. mucilaginosa planktonic cells and biofilm. Biofilm tolerance was higher than the planktonic cells. The R. mucilaginosa planktonic cells showed the tolerance in the presence of Hg2+ (MICp 0.08 mM), Cu2+ (MICp 6.40 mM), and Pb2+ (MICp 3.51 mM), while the S. boulardii planktonic cells only tolerated Pb2+ (MICp 0.43 mM). The R. mucilaginosa biofilm showed the highest tolerance in the presence of Hg2+ (MBEC >0.31 mM), Cu2+(MBEC >12.81 mM), Pb2+ (MBEC >7.12 mM), and obtained results were confirmed by fluorescence microscopy. S. boulardii did not show potential in biofilm formation. The R. mucilaginosa biofilm exhibited better efficiency in removal of all tested metals than the planktonic cells. Metal removal efficiency was in the range from 4.79–10.25% for planktonic cells and 91.71–95.39% for biofilm.

The interest in determining the influence of new metal complexes on microorganisms is increasing due to the growing pathogenic resistance. This investigation showed influence of 5 new Pt(IV) complexes on 16 strains of bacteria. Antibacterial activity was tested using microdilution method with resazurin while antibiofilm activity was observed by tissue culture plate method and antibiotic doxycycline was used as positive control. The results were expressed as minimum inhibitory concentration (MIC), minimum bactericidal concentration (MBC) and biofilm inhibitory concentration (BIC). The complexes were labeled as: C1 for Pt(S-bz-thiosal)3, C2 for Pt(S-met-thiosal)3, C3 for Pt(S-et-thiosal)3, C4 for Pt(S-pr-thiosal)3 and C5 for Pt(S-bu-thiosal)3. The best result on Gram positive bacteria was obtained with C1 and MIC on Staphylococcus aureus ATCC 25923 was ˂7.81 μg/ml. Bifidobacterium animalis subsp. lactis (probiotic) was sensitive to C2 (MIC at 15.625 μg/ml). The best sensitivity on Gram negative bacteria was observed on Escherichia coli ATCC 25922 with C1, C2, C3 and C4, on Proteus mirabilis ATCC 12453 with C1, and on Pseudomonas aeruginosa with C2, C3 and C5 (all MICs at 250 μg/ml). The tested complexes were more efficient as antibiofilm agents and the best results were obtained with C2 acting against S. aureus and S. aureus ATCC 25923 biofilm. In conclusion, we noticed that the tested compounds exhibited promising properties as antibacterial agents and antibiofilm agents

A series of 22 synthetic drug-like hydantoin derivatives, including aryl or alkenyl 5,5-disubstituted hydantoins, spirohydantoins and annulated bicyclic and tricyclic hydantoins, was assayed for in vitro antibacterial and antifungal activity. The antimicrobial activity was tested by determination of the minimum inhibitory concentration (MIC) and the minimum bactericidal concentration (MBC) using microdilution method. The tested hydantoin derivatives showed moderate antibacterial and weak antifungal activity. The intensity of acting varied depending on the structure and concentration of the test substances and the type of test organisms. The bicyclic benzeneselenenyl derivatives of hydantoin have shown the highest inhibitory activity. The tested compounds appeared as promising for a fragment-based drug design approach and further bioactivity studies.

The reaction of K(2)PtCl(4) with anticancer-alkylating agent mechlorethamine hydrochloride (CH(3)NH(C(2)H(4)Cl)(2) x HCl = HN2×HCl), in the molar ratio 1 : 2, affords the complex [H2N2](2)[PtCl(4)]. In vitro antimicrobial and lipoxygenase inhibitory activities of the complex and its precursor were evaluated. Antimicrobial activity of the HN2×HCl and [H2N2](2)[PtCl(4)] complex was investigated against 29 species of microorganisms. Testing is performed by microdilution method. Minimum inhibitory concentration (MIC) and minimum microbicidal concentration (MMC) have been determined. The difference between antimicrobial activity of precursor and corresponding platinum(II) complex is noticed and the activity of the precursor was higher. Tested compounds demonstrated the high and significant antifungal activity and low to moderate antibacterial activity. It was shown that the gram-positive bacteria were more sensitive than the gram-negative. UV absorbance-based enzyme assays were performed with HN2×HCl and [H2N2](2)[PtCl(4)] complex, in order to evaluate their in vitro inhibitory activity of soybean lipoxygenase (LOX), also. Assay with LOX showed significantly greater inhibitory activity of the complex, than the precursor.

In vitro antimicrobial activity of 21 crude extracts obtained from seven taxa of the genus Teucrium (T. chamaedrys, T. montanum, T. arduini, T. polium, T. scordium subsp. scordium, T. scordium subsp. scordioides and T. botrys) was tested against bacterial and fungal species. Minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) were determined using a microdilution analysis method. Total phenolic content and flavonoid concentrations were measured spectrophotometrically. Total phenols were determined using Folin-Ciocalteu reagent and their amounts ranged from 28.49 up to 159.84 mg CA/g of extract (chlorogenic acid equivalent). The amounts of flavonoids ranged from 38.17 up to 190.45 mg RU/g of extract (rutin equivalent).The plant extracts showed greater potential of antibacterial than antifungal activity. A relationship was found between total phenolics and biological activity. The highest level of total phenols was measured in the methanol extracts, which demonstrated higher antimicrobial activity than acetone and ethyl acetate extracts. Staphylococcus aureus ATCC 25923 appeared to be the most sensitive organism. Our results indicate that Teucrium spp extracts are rich sources of phenolic compounds and are promising candidates for further development as natural antimicrobial agents.

Information technologies provide a significant support in the management of lakes and reservoirs. Existing information systems mostly did not comprise all the necessary data and enabled collecting only a limited set of reports. More complex data analyses such as statistical analyses and data research were conducted in separate environments and recquired additional preparation of the data. Information system of lakes and reservoirs in Serbia (SeLaR) was produced in order to provide all the neccessary information for lake and reservoir management. The information system integrates a large data set and provide users with necessary information in the form of reports and charts. The users of the system are scientists and experts who study these issues, as well as students with the objective of continuous education. Furthermore, an interface was produced to enable linking with data research software. In this way a unique working environment was created to provide users with an efficient model of acquiring all the information necessary for the management and to find out new facts in data interaction, and also to make a forecast. This study presents an overview of the information system, its production model, the information available and the possibilities of data research.

The antimicrobial activity of the ionic liquids triethanolamine acetate [TEA][HOAc] and diethanolamine chloride [HDEA][Cl], as well as of their Pd(II) complexes trans-dichlorobis(triethanolamine-N)palladium(II) (trans-[PdCl2(TEA)2]) and diethanolammonium–tetrachloridopalladate(II) ([HDEA]2[PdCl4]), is presented. The investigated compounds showed low antibacterial activity. Better results were for antifungal activity. [TEA][HOAc] exhibited better activity than corresponding complex. Aspergillus species were especially sensitive to [HDEA]2[PdCl4]. The activity of this complex against A. restrictus, A. fumigatus was up to ten times higher than the activity of positive control, fluconazole.

Carlinae radix is an herbal drug, commonly used by the locals in southeastern Serbia for the treatment of respiratory and urogenital diseases and, externally, for various skin conditions. There still seems to be no detailed studies correlating the chemical composition of this drug and its ethnopharmacological uses.Chemical composition, antimicrobial activity and mode of action of C. radix essential oil, isolated from commercial samples (confirmation of whose true biological identity was also the aim of this work) were analyzed. Antimicrobial potential of decoctions (extracts prepared by boiling plant material in a given solvent), used in ethnomedicine preferentially to the pure essential oil, was also investigated.The essential oil obtained by hydrodistillation was screened for antimicrobial activity by disc diffusion and broth microdilution methods. Effects of the oil on the growth of Staphylococcus aureus cells were investigated using turbidimetric measurements and visualized using scanning electron microscopy. Analyses of the chemical composition of the oils were done using gas chromatography and gas chromatography/mass spectrometry.Both the essential oil and the decocts exhibited a very high antimicrobial activity against all tested strains, with S. aureus as the most sensitive one [e.g., for the oil sample the values for minimal inhibitory concentration (MIC) and minimal bactericidal concentration (MBC) were 0.02, 0.04 µL/mL, respectively]. Growth curves of S. aureus demonstrated a significant decrease in turbidity (for the MIC concentration this amounted to ca. 70%) showing a concentration-dependent lysis of the cells, confirmed by scanning electron microscopy. Chemical composition, anatomical and morphological features of the sample pointed to Carlina acanthifolia L. (Asteraceae) instead of Carlina acaulis L. (Asteraceae).The results showed significant antimicrobial effect of the essential oil and the decoctions and support the use of this plant in ethnomedicine for the treatment of various human infections, especially those caused by S. aureus. Adulteration of the drug would not cause significant differences in its biological activity, since chemical composition of the sample showed high similarity with those containing C. acaulis roots.

S-Alkyl (R = benzyl, methyl, ethyl, propyl and butyl) derivatives of thiosalicylic acid and the corresponding palladium(II) complexes were prepared and their structures were proposed on the basis of infrared, 1H and 13C NMR spectroscopy. The cis geometrical configurations of the isolated complexes were proposed on the basis of an X-ray structural study of the bis(S-benzyl-thiosalicylate)–palladium(II), [Pd(S-bz-thiosal)2] complex. Antimicrobial activity of the tested compounds was evaluated by determining the minimum inhibitory concentration (MIC) and minimum microbicidal concentration (MMC) in relation to 26 species of microorganisms. The tested ligands, with a few exceptions, show low antimicrobial activity. The palladium(II) complexes, [Pd(S-R-thiosal)2], have statistically significant higher activity than the corresponding ligands. The complexes [Pd(S-et-thiosal)2] and [Pd(S-pro-thiosal)2] displayed the strongest activity amongst the all tested compounds. The palladium(II) complexes show selective and moderate antibacterial activity and significant antifungal activity. The most sensitive were Aspergillus fumigatus and Aspergillus flavus.

The synthesis of ethyl esters of (S,S)-ethylenediamine-N,N′-di-2-propanoic and (S,S)-ethylenediamine-N,N′-di-2-(3-methyl)-butanoic acids and corresponding platinum(IV) complexes are reported. The complexes have been prepared by direct reaction of K2[PtCl6] and ethyl esters of the acids mentioned above. The esters and complexes were characterized by elemental microanalysis, infrared, 1H and 13C NMR spectroscopy. The spectroscopically predicted structures of the synthesized complexes were confirmed by X-ray analysis of the [PtCl4(det-(S,S)-eddp)]. Antimicrobial activity of ligands and corresponding platinum(IV) complexes was investigated against 29 species of microorganisms. Testing was performed by microdilution method and minimum inhibitory concentrations (MIC) and minimum microbicidal concentration (MMC) have been determined. Tested ligands and corresponding platinum(IV) complexes demonstrated the significant activity against some G+ bacteria. On the other hand, these complexes demonstrated moderate and low antibacterial and antifungal activity.