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1.
J AOAC Int ; 96(6): 1189-99, 2013.
Article in English | MEDLINE | ID: mdl-24645493

ABSTRACT

A simple observation is the basis of the development of BioArena system: according to the first observations during the biological incubation after inoculation there is formaldehyde (HCHO) emission from the chromatographic spots; in this emission process, the level of HCHO molecules decreases time dependently. In fact, the antibiotic effect of an antibiotic-like compound decreases in parallel with the HCHO emission. The investigations demonstrated clearly a unique function and role of endogenous HCHO and its one main reaction product, ozone (O3), in the antiproliferative (e.g., antimicrobial) effect of different molecules with diverse chemical structures. The results in BioArena can be extended for in vivo conditions (e.g., greenhouse experiments), as well. For the pretreatment with different doses of inducers (immunostimulation-inducing molecules) there are always four bioequivalent immunostimulating response ranges (quadruple bioequivalent immune response system) in plants. The inducers (e.g., N-methylated basic amino acids, salicylic acid, cinnamic acid, and trace elements) do not participate directly in the induction of the immunostimulating effect. These new findings support a statement that HCHO and its reaction products (mainly O3), as bioreactive small molecules, are responsible for the immunostimulating activity (in vivo conditions), as well.


Subject(s)
Anti-Bacterial Agents/metabolism , Biological Assay/methods , Formaldehyde/metabolism , Ozone/metabolism , Anti-Bacterial Agents/chemistry , Bacillus subtilis/drug effects , Chromatography, Thin Layer , Formaldehyde/chemistry , Formaldehyde/isolation & purification , Ions , Ozone/chemistry , Ozone/isolation & purification , Tetrazolium Salts , Thiazoles
2.
J AOAC Int ; 96(6): 1200-8, 2013.
Article in English | MEDLINE | ID: mdl-24645494

ABSTRACT

Essential oils obtained by hydrodistillation (HD) and microwave-assisted HD (MWHD) of Origanum onites aerial parts were analyzed by GC and GCIMS. Thirty-one constituents representing 98.6% of the water-distilled oil and 52 constituents representing 99.6% of the microwave-distilled oil were identified. Carvacrol (76.8% HD and 79.2% MWHD) and thymol (4.7% HD and 4.4% MWHD) were characterized as major constituents in both essential oils. Separation of carvacrol and thymol was achieved by overpressured layer chromatography. HPTLC and TLC separations were also compared. Essential oils were evaluated for antifungal activity against the strawberry anthracnose-causing fungal plant pathogens Colletotrichum acutatum, C. fragariae, and C. gloeosporioides using a direct overlay bioautography assay. Furthermore, main oil components carvacrol and thymol were then evaluated for antifungal activity; only carvacrol demonstrated nonselective antifungal activity against the three Colletotrichum species. Thymol and carvacrol were subsequently evaluated in a 96-well microdilution broth assay against Phomopsis obscurans, Fusarium oxysporum, three Colletotrichum species, and Botrytis cinerea. No activity was observed against any of the three Colletotrichum species at or below 30 pM. However, thymol demonstrated antifungal activity and produced 31.7% growth inhibition of P. obscurans at 120 h and 0.3 pM, whereas carvacrol appeared inactive. Thymol and carvacrol at 30 pM showed 51.5 and 36.9% growth inhibition of B. cinerea at 72 h. The mechanism of antibacterial activity was studied in a bioautography-based BioArena system. Thymol and carvacrol showed similar inhibition/killing effect against Bacillus subtilis soil bacteria; the action could be enhanced by the formaldehyde generator and transporter copper (II) ions and could be decreased in the presence of L-arginine, a formaldehyde capturer. Results indicated that Origanum essential oils and its major components thymol and carvacrol appear to generate antimicrobial activity through a mechanism of action where formaldehyde and its reaction products are produced.


Subject(s)
Anti-Bacterial Agents/chemistry , Antifungal Agents/chemistry , Origanum/chemistry , Plant Extracts/chemistry , Volatile Organic Compounds/chemistry , Adsorption , Ascomycota/drug effects , Botrytis/drug effects , Chromatography, Gas , Colletotrichum/drug effects , Cymenes , Fusarium/drug effects , Gas Chromatography-Mass Spectrometry , Microbial Sensitivity Tests , Microwaves , Monoterpenes/analysis , Oils, Volatile/chemistry , Thymol/analysis
3.
Med Chem ; 8(1): 75-84, 2012 Jan.
Article in English | MEDLINE | ID: mdl-22420555

ABSTRACT

The investigations demonstrated clearly a unique function and role of endogenous formaldehyde (HCHO) and ozone (O3) in the antibiotic effect of diverse molecules having different chemical structure. Elimination of HCHO and/or O3 from the layer chromatographic spots resulted in a decrease in the antimicrobial activity. On the basis of detection and measure of endogenous HCHO and O3 BioArena enables to both direct isolation and biological evaluation of new bioactive compounds.


Subject(s)
Anti-Bacterial Agents/metabolism , Formaldehyde/metabolism , Ozone/metabolism , Anti-Bacterial Agents/chemistry , Chromatography, Thin Layer , Formaldehyde/chemistry , Formaldehyde/isolation & purification , Humans , Ozone/chemistry , Ozone/isolation & purification
4.
Med Chem ; 8(1): 85-94, 2012 Jan.
Article in English | MEDLINE | ID: mdl-22420556

ABSTRACT

Components of 50% aqueous ethanol chamomile (Matricaria recutica L.) flower extract, previously found antibacterial in a TLC-bioautographic study, were separated and isolated by the use of on-line overpressured layer chromatography (OPLC). This system consisted of an OPLC 50 BS system, an on-line coupled flow-through UV detector, and a manual fraction collector. The collected fractions were investigated by GC-MS analysis and by TLC re-chromatography with subsequent visualization, performed after use of the vanillin-sulphuric acid reagent, or under UV illumination, or applying bioautographic detection. The main compounds of the collected 11 fractions were identified by GC-MS. The results showed that the antibacterial effect of 50% aqueous ethanol extract of chamomile is ascribable to cis-, trans-spiroethers, and the coumarins like herniarin and umbelliferone.


Subject(s)
Anti-Bacterial Agents/analysis , Matricaria/chemistry , Plant Structures/chemistry , Anti-Bacterial Agents/isolation & purification , Anti-Bacterial Agents/pharmacology , Bacillus subtilis/drug effects , Biological Assay , Chromatography, Thin Layer , Gas Chromatography-Mass Spectrometry , Microbial Sensitivity Tests , Molecular Structure , Pseudomonas/drug effects
5.
J Chromatogr A ; 1232: 3-18, 2012 Apr 06.
Article in English | MEDLINE | ID: mdl-22186489

ABSTRACT

The pressurized ultramicro (UM) chamber as a closed adsorbent layer chamber enables the use of a special chromatoplate and a pump to increase and optimize the mobile phase flow velocity through an optional development distance in an adsorbent layer. This chamber is the basic instrument of overpressured-layer chromatography (OPLC), which is a separation technique that combines the advantages of conventional TLC/HPTLC with those of HPLC. The versions of OPLC instrument, the character and achievement of off-line and on-line OPLC systems in analytical and preparative use are described. The development of BioArena as a complex bioautographic system means an exploitation of the unique advantages of planar-layer system for detection, isolation and identification of new antimicrobials, antineoplastics, biopesticides and other biologically active substances as well as for studying fundamental biochemical reactions and mechanisms.


Subject(s)
Chromatography, High Pressure Liquid/instrumentation , Chromatography, High Pressure Liquid/methods , Chromatography, Thin Layer/instrumentation , Chromatography, Thin Layer/methods , Equipment Design , Pharmaceutical Preparations/analysis , Plant Extracts/analysis , Pressure
6.
Nat Prod Commun ; 6(5): 611-5, 2011 May.
Article in English | MEDLINE | ID: mdl-21615018

ABSTRACT

The effect of ascorbigen and 1'-methylascorbigen on the disease resistance of bean (Phaseolus vulgaris L.,. cv. Debreceni Tarka) to the fungal pathogen Uromyces phaseoli Pers. is reported. Contrary to ascorbigen, pretreatment of bean plants with l'-methylascorbigen, as in the case of other endogenous N-, O- and S-methyl compounds, induced the double immune response leading to the biochemical immunization of plants. The effectiveness of protection depended on the dosage of the applied l'-methylascorbigen and on the time interval between the chemical pretreatment and inoculation. Results of our greenhouse experiments revealed, in accordance with previous results, that the presence of the N-methyl group in the 1'-methylascorbigen molecule is the precondition of the effect, and formaldehyde formed from this N-methyl group and its reaction products (e.g. singlet oxygen, ozone) can have a determining role in the manifestation of the effect.


Subject(s)
Ascorbic Acid/analogs & derivatives , Basidiomycota/immunology , Indoles/pharmacology , Phaseolus/drug effects , Ascorbic Acid/pharmacology , Immunity, Innate/drug effects , Phaseolus/immunology , Phaseolus/microbiology , Plant Diseases/immunology , Plant Diseases/microbiology , Time Factors
7.
Nat Prod Commun ; 6(5): 631-8, 2011 May.
Article in English | MEDLINE | ID: mdl-21615023

ABSTRACT

On the basis of in vitro and in vivo investigations trans-resveratrol (RV) is a natural, concentration-dependent formaldehyde (HCHO) mobilizer, scavenger, capture and carrier molecule. The capturing and mobilization of HCHO from a given biological unit (e.g. tissue) with RV (first step) generates a chemopreventive effect. The reaction products between endogenous HCHO and RV (second step) may exert killing/inhibiting effects on pathogens and/or cancer cells. These two steps result in the double effect of RV. From the model reaction mixture of RV and HCHO in diluted formalin solution, different reaction products were detected, separated and identified. Similar reactions can be observed between RV and endogenous HCHO in plant and animal tissues as well. Capturing the HCHO molecules in model experiments with HCHO-capture molecules (in vitro conditions) the antibacterial activity of RV decreased substantially. The in vitro investigations were extended to in vivo conditions. The discovery of a quadruple immune response of plants to pathogens resulting from pretreatment with RV opens new horizons in the confirmation of the diverse beneficial effects of RV.


Subject(s)
Formaldehyde/chemistry , Stilbenes/chemistry , Anti-Bacterial Agents/pharmacology , Basidiomycota , Fabaceae/drug effects , Fabaceae/immunology , Models, Chemical , Pseudomonas/drug effects , Resveratrol , Stilbenes/pharmacology
8.
Nat Prod Commun ; 6(5): 657-60, 2011 May.
Article in English | MEDLINE | ID: mdl-21615027

ABSTRACT

The influence of monomethylated basic amino acids [NG-monomethyl-L-arginine (MMA) and Nepsilon-monomethyl-L-lysine (MML)] and ozone capturers (indigo carmine, d-limonene) on the antibacterial effect of the mycotoxins aflatoxins B1, B2, G1 and G2 was studied in BioArena, which is a complex bioautographic system especially suitable for investigating biochemical interactions. In the presence of the formaldehyde precursors MMA or MML, the antibacterial-toxic activity of all the aflatoxins against the phytopathogenic bacterium Pseudomonas savastanoi pv. phaseolicola was enhanced dose-dependently. Indigo carmine and d-limonene, in appropriate concentrations, decreased the inhibition zones of aflatoxins. These results support the original idea that HCHO and its derivative 03 may be involved in the antibacterial activity of aflatoxins and so, potentially, in their known toxic effect.


Subject(s)
Aflatoxins/pharmacology , Pseudomonas/drug effects , Aflatoxins/chemistry , Cyclohexenes , Formaldehyde/chemistry , Indigo Carmine , Limonene , Lysine/analogs & derivatives , Ozone/chemistry , Terpenes , omega-N-Methylarginine
9.
Nat Prod Commun ; 6(5): 719-32, 2011 May.
Article in English | MEDLINE | ID: mdl-21615038

ABSTRACT

This review briefly summarizes the overpressured layer chromatography (OPLC) technique and its progress from the beginning until today. Some theoretical aspects, important technical and methodological solutions, as well as analytical separations and isolations are demonstrated covering the last 30 years. The infusion and transfusion OPLC operations, as well as their combination, and their off-line and on-line processes, and off-line and on-line hyphenations for detection and structure elucidation are presented. The combination of OPLC separation with biological detection by direct bioautography and BioArena as an important solution touches the potential of analysis and isolation based on biological activity.


Subject(s)
Biological Products/isolation & purification , Chromatography, Thin Layer/methods , Biological Assay , Chromatography, Thin Layer/instrumentation , Chromatography, Thin Layer/trends
10.
Cell Biol Int ; 34(12): 1273-82, 2010 Dec.
Article in English | MEDLINE | ID: mdl-21067524

ABSTRACT

Formaldehyde (HCHO) may reach living organisms as an exogenous agent or produced within cells. The so-called formaldehydogenic compounds like S-adenosyl-L-methionine, N-hydroxymethyl-L-arginine, 1'-methyl ascorbigen, methanol, E-N-trimethyl lysine and methylamine are special exogenous sources of HCHO. Endogenous HCHO can be formed from hydroxymethyl groups during enzymatic methylation and demethylation processes. HCHO, as a highly reactive compound, is considered to be involved in the induction of apoptosis, consequently in the pathogenesis of atherosclerosis and neurodegenerative processes. The biological action of HCHO is dose-dependent. In vitro studies on tumour cell and endothelial cell cultures showed that HCHO in the concentration of 10.0 mM caused necrotic cell death, 1.0 mM resulted in enhanced apoptosis and reduced mitotic activity, while 0.5 and 0.1 mM enhanced cell proliferation and reduced apoptotic activity. Among formaldehydogenic compounds N-hydroxymethyl-L-arginine, 1'-methyl ascorbigen and the HCHO donor resveratrol may be considered as potential inhibitors of cell proliferation. Endogenous HCHO in plants apparently play a role in regulation of apoptosis and cell proliferation. The genotoxic and carcinogentic effects of HCHO is due to production of DNA-protein cross-links. Low doses of HCHO, reducing apoptotic activity may also accumulate cells with such cross-links. Experimental data point to the possible therapeutic use of methylated lysine residues and methylated arginine residues in the case of neoplasms.


Subject(s)
Apoptosis/drug effects , Cell Proliferation/drug effects , Formaldehyde/pharmacology , Animals , Arginine/metabolism , Arginine/pharmacology , Carcinogens/chemistry , Carcinogens/metabolism , Carcinogens/pharmacology , Carcinogens/supply & distribution , Cell Death/drug effects , Dose-Response Relationship, Drug , Formaldehyde/chemistry , Formaldehyde/metabolism , Formaldehyde/supply & distribution , Humans , Models, Biological
11.
Biomed Chromatogr ; 23(4): 412-8, 2009 Apr.
Article in English | MEDLINE | ID: mdl-19039806

ABSTRACT

The effect of ascorbigen and 1'-methylascorbigen as a model compound pair was studied on the phytopathogenic bacterium Pseudomonas savastanoi pv. phaseolicola in the BioArena experimental system after overpressured layer chromatography. Results showed a characteristic, strong antibacterial effect of 1'-methylascorbigen and weak effect of ascorbigen present on the adsorbent layer as chromatographic spot. Addition of formaldehyde capture compounds (L-arginine, glutathione, dimedone) partially or totally reduced the antibacterial effect of 1'-methylascorbigen and ascorbigen. On adding Cu(II) ions--which mobilize and coordinate formaldehyde--to the culture medium, the antibacterial effect of both compounds became stronger. It is supposed that the weak antibacterial effect of ascorbigen may have originated from the 1'-methylascorbigen formed in situ on the adsorbent layer by partial enzymatic methylation of ascorbigen.


Subject(s)
Anti-Bacterial Agents/pharmacology , Ascorbic Acid/analogs & derivatives , Formaldehyde/chemistry , Indoles/pharmacology , Pseudomonas/drug effects , Anti-Bacterial Agents/chemistry , Arginine/chemistry , Arginine/pharmacology , Ascorbic Acid/chemistry , Ascorbic Acid/pharmacology , Chromatography, Thin Layer , Copper/chemistry , Copper/pharmacology , Cyclohexanones/pharmacology , Formaldehyde/pharmacology , Glutathione/pharmacology , Indoles/chemistry
12.
Article in English | MEDLINE | ID: mdl-17587638

ABSTRACT

Compounds formed by exchanging one of the resveratrol hydroxy groups to methoxy or formyl groups are biologically important. Quantum chemical DFT calculations were applied for the simulation of some of their properties. Their optimized structures and charge distributions were computed. Based on the calculated vibrational force constants and optimized molecular structure infrared and Raman spectra were calculated. The characteristics of the vibrational modes were determined by normal coordinate analysis. Applying the calculated thermodynamic functions also for resveratrol, methanol, formaldehyde and water, thermodynamic equilibria were calculated for the equilibria between resveratrol and its methyl and formyl substituted derivatives, respectively.


Subject(s)
Spectrophotometry, Infrared/methods , Spectrum Analysis, Raman/methods , Stilbenes/chemistry , Vibration , Water/chemistry , Aldehydes/chemistry , Computer Simulation , Hydroxylation , Models, Molecular , Molecular Structure , Thermodynamics
13.
Acta Pharm Hung ; 77(1): 53-8, 2007.
Article in Hungarian | MEDLINE | ID: mdl-17518113

ABSTRACT

BioArena as a complex bioautographic system was successfully used for studying mechanism of action of some characteristic plant ingredients (e.g., 1'-methyl-ascorbigen, trans-resveratrol, salicylic acid, cinnamic acid). It has been established that the formaldehyde as a main component of formaldehyde cycle and other biochemical pathways can be studied in chromatographic spots as well. Ozone as a specially reactive reaction product of formaldehyde can be measured indirectly there. Different formaldehyde-capturing and -giving molecules and other compounds influenced (inhibited or promoted) characteristically the antibiotic effect.


Subject(s)
Formaldehyde , Plant Extracts/chemistry , Plants/chemistry , Angiogenesis Inhibitors/chemistry , Angiogenesis Inhibitors/isolation & purification , Indicators and Reagents , Plant Extracts/isolation & purification , Resveratrol , Stilbenes/chemistry , Stilbenes/isolation & purification
14.
Article in English | MEDLINE | ID: mdl-17416548

ABSTRACT

In this article the authors deal with the experimental and theoretical interpretation of the vibrational spectra of trans-resveratrol (3,5,4'-trihydroxy-trans-stilbene) of diverse beneficial biological activity. Infrared and Raman spectra of the compound were recorded; density functional calculations were carried out resulting in the optimized geometry and several properties of the molecule. Based on the calculated force constants, a normal coordinate analysis yielded the character of the vibrational modes and the assignment of the measured spectral bands.


Subject(s)
Spectrum Analysis, Raman , Stilbenes/chemistry , Vibration , Resveratrol , Spectrophotometry, Infrared
15.
Article in English | MEDLINE | ID: mdl-16387533

ABSTRACT

The structure of four natural mycotoxins, the aflatoxin B1, B2, G1 and G2 and their demethylated products were optimized with quantum chemical method. The energies and the thermodynamic functions of the molecules were calculated and applied to calculation of the reaction energies of the demethylations. Further results of the calculations are the vibrational force constants, the infrared spectra of the molecules and the assignments of the spectral bands.


Subject(s)
Aflatoxins/chemistry , Methylation , Spectrum Analysis , Thermodynamics
16.
J Chromatogr B Analyt Technol Biomed Life Sci ; 800(1-2): 231-8, 2004 Feb 05.
Article in English | MEDLINE | ID: mdl-14698259

ABSTRACT

The effect of Chamomilla recutita (L.) Rauschert is made up by several groups of active substances, among which terpenoids in the inflorescences are of greatest importance. Among cultivated species, the Hungarian BK-2 contains more chamazulene in its essential oil than the German Degumil type, which is mainly cultivated for its (-)-alpha-bisabolol. Both components have important antiinflammatory activities. Among wild chamomile populations in Hungary, a population was found in the area of Szabadkigyós containing significant amounts-on average 48%-of (-)-alpha-bisabolol in its inflorescence oil. In vitro cultures were made from this population to obtain propagation material containing a high number of active substances. The intact roots contained no (-)-alpha-bisabolol but the sesquiterpene alcohol beta-eudesmol as new compound was identified by our group. Sterile plantlets, cultured in vitro, were multiplied for phytochemical investigations. Pharmacologically important compounds of the essential oils were followed in great detail. The amount of in vitro cultured terpenoids and polyin compounds was compared with that of in vivo plants. These volatile compounds were identified by comparing their retention times with those of authentic standards, essential oils of known composition and peak enrichment. The confirmation of identity was done by comparison of their mass spectra with those reported in the literature and reference compounds. The percentage evaluation of each component was made by area normalisation. Gas chromatography (GC) and mass spectrometry (MS) showed that sterile chamomile cultures generated the most important terpenoid and polyin compounds characteristic of the parent plant. We identified germacrene-D, berkheyaradulene, 4-(2', 4', 4'-trimethyl-bicyclo[4.1.0]hept-2'-en-3'-yl)-3-buten-2-one, geranyl-isovalerate and cedrol as new components in these sterile cultures.


Subject(s)
Chamomile/chemistry , Terpenes/analysis , Biological Specimen Banks , Flowers/chemistry , Gas Chromatography-Mass Spectrometry , Hungary , Oils, Volatile/analysis , Oils, Volatile/metabolism , Plant Leaves/chemistry , Plant Roots/chemistry , Seeds
17.
Cancer Cell Int ; 1(1): 3, 2001 Dec 17.
Article in English | MEDLINE | ID: mdl-11983027

ABSTRACT

Both L-arginine supplementation and deprivation influence cell proliferation. The effect of high doses on tumours is determined by the optical configuration: L-arginine is stimulatory, D-arginine inhibitory. Arginine-rich hexapeptides inhibited tumour growth. Deprivation of L-arginine from cell cultures enhanced apoptosis. The pro-apoptotic action of NO synthase inhibitors, like NG-monomethyl-L-arginine, is manifested through inhibition of the arginase pathway. NG-hydroxymethyl-L-arginines caused apoptosis in cell cultures and inhibited the growth of various transplantable mouse tumours. These diverse biological activities become manifest through formaldehyde (HCHO) because guanidine group of L-arginine in free and bound form can react rapidly with endogenous HCHO, forming NG-hydroxymethylated derivatives. L-arginine is a HCHO capturer, carrier and donor molecule in biological systems. The role of formaldehyde generated during metabolism of NG-methylated and hydroxymethylated arginines in cell proliferation and death can be shown. The supposedly anti-apoptotic homozygous Arg 72-p53 genotype may increase susceptibility of some cancers. The diverse biological effects of L-arginine and its methylated derivatives call for further careful studies on their possible application in chemoprevention and cancer therapy.

18.
Pathol Oncol Res ; 1(1): 38-42, 1995.
Article in English | MEDLINE | ID: mdl-11173566

ABSTRACT

PC-3 human prostate carcinoma cells were treated with 100 mg/ml 1-methyl-ascorbigen (Me-Asc). This treatment resulted in a significant decrease in tumor cell number in parallel with an increase in apoptotic cells. The formaldehyde (HCHO) level in the culture medium was also increased. Dimedone (Di), a known capture molecule forming formal-demethone with HCHO, applied simultaneously with Me-Asc in 10 mg/ml doses diminished the apoptosis-inducing effect of Me-Asc. The possible role of in situ generated HCHO in the induction of apoptosis is discussed.

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