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1.
J Appl Microbiol ; 120(4): 900-11, 2016 Apr.
Article in English | MEDLINE | ID: mdl-26811095

ABSTRACT

AIMS: The aim was to isolate, identify and characterize endophytes from Solanum nigrum L. as a new source of the cytotoxic steroidal alkaloid solamargine. METHODS AND RESULTS: Three endophytic fungi; SNFSt, SNFL and SNFF were isolated from S. nigrum and identified by molecular methods. Preliminary TLC screening showed a common metabolite between the plant and one of these fungi, SNFSt which was identified as Aspergillus flavus based on the phylogenetic analysis of its ITS sequence. Subsequent LC-HRESIMS analysis unambiguously established the identity of the compound based on its molecular formula and its characteristic MS(2) fragmentation pattern as solamargine. To ascertain its identity, fungal solamargine was isolated using preparative TLC and its structure was fully characterized using NMR spectroscopic techniques and high-resolution mass spectrometric analysis. Solamargine production could be followed and quantified for a total of 11 generations of this fungus with a titer of ~250-300 µg l(-1) . This study represents one of the first examples where host plant-derived compounds have been demonstrated to be steadily produced by an endophytic fungi in sizeable quantities. CONCLUSIONS: The production of solamargine (found in the host plant) by a cultivable fungal endophyte at a significant yield is a new observation. Further experiments such as media optimization, OSMAC (One Strain Many Compounds) or epigenetic modifiers could be applied to enhance the fungal solamargine production. SIGNIFICANCE AND IMPACT OF THE STUDY: The endophytic fungus SNFSt isolated from S. nigrum may be utilized for quantitative production of the potent cytotoxic metabolite solamargine.


Subject(s)
Endophytes/metabolism , Fungi/metabolism , Solanaceous Alkaloids/biosynthesis , Solanum nigrum/microbiology , Endophytes/classification , Endophytes/genetics , Endophytes/isolation & purification , Fungi/classification , Fungi/genetics , Fungi/isolation & purification , Mass Spectrometry , Molecular Sequence Data , Phylogeny
2.
Neuroscience ; 305: 26-35, 2015 Oct 01.
Article in English | MEDLINE | ID: mdl-26247694

ABSTRACT

Anhydroexfoliamycin (1) and undecylprodigiosin (2) have been previously described as neuroprotective molecules against oxidative stress in neurons. Since oxidative stress is strongly correlated with neurodegenerative diseases, we have evaluated their effects over the principal hallmarks of Alzheimer's disease (AD). Both compounds were tested in vitro in two different neuroblastoma cellular models, one for amyloid precursor protein metabolism studies (BE(2)-M17) and another one specific for taupathology in AD (SH-SY5Y-TMHT441). Amyloid-beta (Aß) levels, ß-secretase (BACE1) activity, tau phosphorylation, extracellular signal-regulated kinase (ERK) and glycogen synthase kinase-3beta (GSK3ß) expression were analyzed and while undecylprodigiosin (2) produced poor results, anhydroexfoliamycin (1) strongly inhibited GSK3ß, reducing tau phosphorylation in vitro (0.1 µM). A competitive assay of anhydroexfoliamycin (1) and the specific c-Jun N-terminal kinase (JNK) inhibitor, SP600125, showed that the reduction of the phosphorylated tau levels is mediated by the JNK pathway in SH-SY5Y-TMHT441 cells. Thus, this compound was tested in vivo by intraperitoneal administration in 3xTg-AD mice, confirming the positive results registered in the in vitro assays. This work presents anhydroexfoliamycin (1) as a promising candidate for further studies in drug development against neurodegenerative diseases.


Subject(s)
Alzheimer Disease/drug therapy , Anthracenes/therapeutic use , Antipsychotic Agents/therapeutic use , Brain/metabolism , Prodigiosin/analogs & derivatives , Alzheimer Disease/genetics , Amyloid Precursor Protein Secretases/antagonists & inhibitors , Amyloid Precursor Protein Secretases/metabolism , Amyloid beta-Peptides/metabolism , Amyloid beta-Protein Precursor/genetics , Animals , Antipsychotic Agents/chemistry , Aspartic Acid Endopeptidases/antagonists & inhibitors , Aspartic Acid Endopeptidases/metabolism , Brain/drug effects , Cell Line, Tumor , Disease Models, Animal , Glycogen Synthase Kinase 3/metabolism , Glycogen Synthase Kinase 3 beta , Humans , MAP Kinase Kinase Kinases/metabolism , Mice , Mice, Transgenic , Mutation/genetics , Neuroblastoma/pathology , Peptide Fragments/metabolism , Presenilin-1/genetics , Prodigiosin/chemistry , Prodigiosin/therapeutic use , tau Proteins/genetics
3.
ACS Chem Neurosci ; 6(2): 331-8, 2015 Feb 18.
Article in English | MEDLINE | ID: mdl-25387680

ABSTRACT

Bromoalkaloids are secondary metabolites with a demonstrated high activity in several therapeutic areas. In this research, we probe the neuroprotective and antioxidant activities of hymenialdisine and hymenin. Both structures were tested in an oxidative stress cellular model, consisting of cortical neurons that are incubated with the oxidative stress inducer hydrogen peroxide and the tested compound. Several oxidation biomarkers were analyzed, and the results of the oxidative stress induced neurons in the presence and absence of bromoalkaloids were compared. Both compounds demonstrated significant neuroprotective ability under stress conditions at low nanomolar concentrations, with hymenialdisine highlighted for demonstrating a more complete protection. Also, the activity of hymenialdisine and hymenin was studied in the nuclear factor erythroid 2-related factor 2 (Nrf2)-antioxidant response element (ARE) pathway, and, for the first time, these halogenated metabolites are described as Nrf2 inducers, reinforcing the antioxidant capacity observed and therefore opening a new path of investigation. These results, added to the previously described effect of this compound family in negatively modulating several kinases and proinflammatory cytokines, position hymenialdisine and hymenin as good candidates for the development of new drugs for neurodegenerative diseases.


Subject(s)
Azepines/pharmacology , Cerebral Cortex/drug effects , Neurons/drug effects , Neuroprotective Agents/pharmacology , Oxidative Stress/drug effects , Pyrroles/pharmacology , Sesquiterpenes/pharmacology , Alkaloids/chemistry , Alkaloids/pharmacology , Animals , Antioxidant Response Elements/physiology , Azepines/chemistry , Blotting, Western , Cell Membrane/drug effects , Cell Membrane/metabolism , Cell Survival/drug effects , Cell Survival/physiology , Cells, Cultured , Cerebral Cortex/pathology , Cerebral Cortex/physiology , Lipid Peroxidation/drug effects , Lipid Peroxidation/physiology , Mice , Microscopy, Confocal , Mitochondria/drug effects , Mitochondria/metabolism , NF-E2-Related Factor 2/metabolism , Neurons/pathology , Neurons/physiology , Oxidative Stress/physiology , Pyrroles/chemistry , Sesquiterpenes/chemistry , Signal Transduction/drug effects
4.
Anal Chim Acta ; 642(1-2): 257-65, 2009 May 29.
Article in English | MEDLINE | ID: mdl-19427484

ABSTRACT

A reverse phase high performance liquid chromatography (HPLC) separation was established for profiling water soluble compounds in extracts from tea. Whole chromatograms were pre-processed by techniques including baseline correction, binning and normalisation. In addition, peak alignment by correction of retention time shifts was performed using correlation optimization warping (COW) producing a correlation score of 0.96. To extract the chemically relevant information from the data, a variety of chemometric approaches were employed. Principle component analysis (PCA) was used to group the tea samples according to their chromatographic differences. Three principal components (PCs) described 78% of the total variance after peak alignment (64% before) and analysis of the score and loading plots provided insight into the main chemical differences between the samples. Finally, PCA, support vector machines (SVMs) and random forest (RF) machine learning methods were evaluated comparatively on their ability to predict unknown tea samples using models constructed from a predetermined training set. The best predictions of identity were obtained by using RF.


Subject(s)
Chromatography, High Pressure Liquid/methods , Tea/chemistry , Algorithms , Artificial Intelligence , Mass Spectrometry , Pattern Recognition, Automated , Principal Component Analysis , Time Factors
5.
J Thromb Haemost ; 6(1): 166-73, 2008 Jan.
Article in English | MEDLINE | ID: mdl-17944992

ABSTRACT

BACKGROUND: Anti-inflammatory analgesics, including ibuprofen and naproxen, are known to interfere with the antiplatelet effect of aspirin, presumably as a result of a drug-drug interaction at the level of platelet cyclooxygenase-1 (COX-1). OBJECTIVE: We studied whether dipyrone, which has recently been reported to inhibit COX isoforms by a mechanism different from conventional non-steroidal anti-inflammatory drugs (NSAIDs), also interferes with the antiplatelet effect of aspirin. METHODS: Arachidonic acid- and collagen-induced aggregation, as well as thromboxane formation, were measured in human platelet-rich plasma. Platelet P-selectin expression was determined by flow cytometry and cell-free COX enzyme activity was quantified by luminol-enhanced luminescence of human platelet microsomes. In addition, computerized docking was performed based on the crystal structure of COX-1. RESULTS: 4-Methylaminoantipyrine (MAA), the active metabolite of dipyrone, largely attenuated or even completely abolished the inhibition of arachidonic acid-induced platelet aggregation, thromboxane formation and P-selectin expression by aspirin. Similar results were obtained for other pyrazolinones, as well as for the conventional NSAIDs ibuprofen and naproxen. Moreover, MAA attenuated the effect of aspirin on COX activity of platelet microsomes, suggesting a competition with aspirin at the COX-1 enzyme. This was confirmed by docking studies, which revealed that MAA forms a strong hydrogen bond with serine 530 within the COX-1, thereby preventing enzyme acetylation by aspirin. CONCLUSION: This study demonstrates for the first time that dipyrone and other pyrazolinones have a high potential to attenuate or prevent the antiplatelet effect of aspirin. This should be considered if pyrazolinone analgesics are administered to patients with cardiovascular disease requiring antiplatelet aspirin therapy.


Subject(s)
Analgesics/pharmacology , Aspirin/antagonists & inhibitors , Blood Platelets/metabolism , Dipyrone/pharmacology , Thromboxanes/biosynthesis , Anti-Inflammatory Agents, Non-Steroidal , Binding Sites , Blood Platelets/drug effects , Cells, Cultured , Cyclooxygenase 1/drug effects , Cyclooxygenase 1/metabolism , Dipyrone/analogs & derivatives , Dipyrone/metabolism , Drug Antagonism , Humans , Platelet Aggregation/drug effects , Pyrazolones/metabolism , Pyrazolones/pharmacology
6.
Prog Mol Subcell Biol ; 43: 261-75, 2006.
Article in English | MEDLINE | ID: mdl-17153347

ABSTRACT

Opisthobranchs of the genus Tylodina are found at exceedingly distant geographical regions in the marine environment but are always associated with sponges of the order Verongida (e.g., Aplysina species) which serve as prey for these gastropods. We investigated the chemical ecology of the Mediterranean species T. perversa that commonly feeds on A. aerophoba. The gastropod sequesters a set of sponge-derived brominated isoxazoline alkaloids which are accumulated in the mantle and egg masses and are furthermore exuded as part of the mucus when the animal is molested. Based on the documented feeding deterrent properties of the sponge alkaloids against fish, it is speculated that the sequestered sponge alkaloids serve also as a defense for T. perversa. Interestingly, specimens of T. perversa that were either collected while feeding on A. aerophoba or had been kept on these sponges under controlled conditions for several weeks almost always contained the brominated alkaloid aerothionin, which is not detected in A. aerophoba but occurs in the sibling species A. cavernicola instead. The latter sponge is also accepted as a food source by the gastropod, at least under experimental conditions. The possible origin of aerothionin in T. perversa is discussed.


Subject(s)
Alkaloids/chemistry , Alkaloids/pharmacokinetics , Diet , Marine Biology , Mollusca/chemistry , Animals , Feeding Behavior/physiology , Mollusca/physiology , Porifera/chemistry , Species Specificity
7.
J Anim Physiol Anim Nutr (Berl) ; 90(3-4): 165-72, 2006 Apr.
Article in English | MEDLINE | ID: mdl-16519762

ABSTRACT

An experiment was conducted to evaluate the metabolic products of chlorocholine chloride (CCC) in eggs and meat of laying hens fed a diet containing (15)N-CCC. Ten brown laying hens were randomly divided into two groups of five each. One group was offered (15)N-CCC free diet while the other group received a diet with 100 ppm (15)N-CCC for 11 days. Samples of eggs and meat from the laying hens were collected. Egg yolks and albumen were separated. Meat was collected from the breast and femur. The metabolic products of CCC were measured using ion trap electrospray ionisation mass spectrometry (ion trap-ESI-MS/MS). Determination of CCC or its metabolites in eggs and meat showed that CCC was metabolised to choline. Corresponding MS/MS spectra were obtained for m/z 104 (choline) or 105 ((15)N-choline), whereas nothing was detected at m/z 122 (CCC) or 123 ((15)N-CCC). The results from this study indicate that CCC will be metabolised in tissues of laying hens.


Subject(s)
Chickens/metabolism , Chlormequat/pharmacology , Eggs/analysis , Meat/analysis , Plant Growth Regulators/pharmacology , Animals , Choline/analysis , Consumer Product Safety , Drug Residues/analysis , Female , Gas Chromatography-Mass Spectrometry/veterinary , Nitrogen Isotopes , Random Allocation
8.
Arch Virol ; 151(3): 599-606, 2006 Mar.
Article in English | MEDLINE | ID: mdl-16328136

ABSTRACT

The nucleotide sequences of RNAs 1 and 2 of a German isolate of Raspberry ringspot virus (RpRSV) infecting grapevine (RpRSV-Grapevine), as well as partial sequences of another grapevine isolate from Switzerland (RAC815) were determined. The sequences of the protease-polymerase region encoded by RNA1, and the movement protein and coat protein genes encoded by RNA 2, of these isolates were compared with those of other isolates available in databases. The coat proteins of the grapevine isolates formed a sister group to all those from other RpRSV isolates, but whether this resulted from divergence or recombination was uncertain.


Subject(s)
Nepovirus/genetics , Vitis/virology , Base Sequence , Molecular Sequence Data , Nepovirus/isolation & purification , Nepovirus/pathogenicity , Phylogeny , RNA, Viral/genetics , Recombination, Genetic , Sequence Homology, Amino Acid , Viral Proteins/genetics
9.
J Nat Prod ; 67(9): 1532-43, 2004 Sep.
Article in English | MEDLINE | ID: mdl-15387655

ABSTRACT

Fractionation of the EtOAc extract of a static culture of Aspergillus niger isolated from the Mediterranean sponge Axinella damicornis yielded eight secondary metabolites, out of which seven compounds (2-8) proved to be new natural products, whereas one was identified as the known fungal pigment cycloleucomelone (1). The new compounds included the 3,3'-bicoumarin bicoumanigrin (2), the structurally unusual 4-benzyl-1H-pyridin-6-one derivatives aspernigrins A and B (3 and 4), and pyranonigrins A-D (5-8), the latter featuring a novel pyrano[3,2-b]pyrrole skeleton hitherto unprecedented in nature. All structures were elucidated on the basis of extensive one- and two-dimensional NMR spectroscopic studies ((1)H, (13)C, COSY, HMQC, HMBC, NOE difference spectra) and mass spectral analysis. For the two chiral molecules 4 and 5, the absolute configurations were established by quantum chemical calculations of their circular dichroism (CD) spectra. In each case, two independent methods, i.e., a molecular dynamics approach taking into consideration the molecular flexibility, and a conformational analysis followed by Boltzmann weighting of the single CD spectra calculated for the conformers thus obtained, led to identical results without the need of any empirical comparison of chiroptical data reported for reference compounds. Bicoumanigrin (2) showed moderate cytotoxicity against human cancer cell lines in vitro. In addition, aspernigrin B (4) was found to display a strong neuroprotective effect against glutamic acid.


Subject(s)
Aspergillus niger/chemistry , Heterocyclic Compounds/isolation & purification , Animals , Calcium/analysis , Circular Dichroism , Drug Screening Assays, Antitumor , Glutamic Acid/pharmacology , Heterocyclic Compounds/chemistry , Heterocyclic Compounds/pharmacology , Humans , Mediterranean Sea , Molecular Structure , Nuclear Magnetic Resonance, Biomolecular , Porifera , Stereoisomerism , Tumor Cells, Cultured
10.
Virus Res ; 97(2): 141-4, 2003 Nov.
Article in English | MEDLINE | ID: mdl-14602206

ABSTRACT

The complete nucleotide sequence of the RNAs 1 and 2 of the nepovirus Raspberry ringspot virus cherry isolate (RpRSV-ch) from grapevine was determined. The RNA 1 is 7935 nucleotides (nt) long excluding the poly(A) tail, and contains one long open reading frame (ORF) encoding a polypeptide of 2367 amino acids. This ORF is preceeded by a 136nt 5' non-coding region, and followed by a 695nt 3' non-coding region. Conserved amino acid motifs, characteristic of the viral protease cofactor, the NTP-binding protein, proteinase and polymerase, were found in the sequence of the RNA 1-encoded polyprotein. The RNA 2 is 3915nt long excluding the poly(A) tail, and contains one long ORF encoding a polypeptide of 1106 amino acids. This ORF is preceeded by a 203nt 5' non-coding region, and followed by a 390nt 3' non-coding region. When compared to the corresponding sequences of other nepoviruses, a maximum level of 34% identity was found between the RNA 1-encoded polypetides of RpRSV-ch and other nepoviruses. For the RNA 2-encoded polypeptide, 88% identity was found between RpRSV-ch and RpRSV-S, a Scottish isolate of RpRSV from raspberry, and a maximum 29% identity between RpRSV-ch and other nepoviruses.


Subject(s)
Nepovirus/genetics , Nepovirus/isolation & purification , Vitis/virology , 3' Untranslated Regions/genetics , 5' Untranslated Regions/genetics , Amino Acid Motifs/genetics , Base Sequence , Cloning, Molecular , Molecular Sequence Data , Open Reading Frames/genetics , Polyproteins/genetics , RNA, Viral/genetics , RNA, Viral/isolation & purification , Sequence Analysis, DNA , Transcription, Genetic , Viral Proteins/genetics
11.
Prog Mol Subcell Biol ; 37: 117-42, 2003.
Article in English | MEDLINE | ID: mdl-15825642

ABSTRACT

Marine natural products with their unique structural features and pronounced biological activities continue to provide lead structures in the search for new drugs from nature. Invertebrates such as sponges, tunicates, mollusks and others that are either sessile or slow moving and mostly lack morphological defense structures have so far provided the largest number of marine-derived secondary constituents including some of the most interesting drug candidates. This review highlights recent research findings of our group related to natural products from marine invertebrates. Areas that are covered include ecological functions of secondary constituents from sponges against predatory fish, the search for new pharmacologically active constituents from sponges and tunicates, and sponge-associated fungi as an evolving source for new bioactive natural products.


Subject(s)
Fungal Proteins/metabolism , Fungi/metabolism , Porifera/microbiology , Alkaloids/metabolism , Animals , Biodiversity , Biological Products , Biotechnology , Marine Biology/methods , Marine Toxins , Models, Chemical , Oxazoles/chemistry , Staurosporine/pharmacology , Urochordata/chemistry
12.
Appl Microbiol Biotechnol ; 59(2-3): 125-34, 2002 Jul.
Article in English | MEDLINE | ID: mdl-12111137

ABSTRACT

The oceans are the source of a large group of structurally unique natural products that are mainly accumulated in invertebrates such as sponges, tunicates, bryozoans, and molluscs. Several of these compounds (especially the tunicate metabolite ET-743) show pronounced pharmacological activities and are interesting candidates for new drugs primarily in the area of cancer treatment. Other compounds are currently being developed as an analgesic (ziconotide from the mollusc Conus magus) or to treat inflammation. Numerous natural products from marine invertebrates show striking structural similarities to known metabolites of microbial origin, suggesting that microorganisms (bacteria, microalgae) are at least involved in their biosynthesis or are in fact the true sources of these respective metabolites. This assumption is corroborated by several studies on natural products from sponges that proved these compounds to be localized in symbiotic bacteria or cyanobacteria. Recently, molecular methods have successfully been applied to study the microbial diversity in marine sponges and to gain evidence for an involvement of bacteria in the biosynthesis of the bryostatins in the bryozoan Bugula neritina.


Subject(s)
Marine Biology , Water Microbiology , Animals , Bryozoa/metabolism , Bryozoa/microbiology , Mollusca/metabolism , Mollusca/microbiology , Porifera/metabolism , Porifera/microbiology , Urochordata/metabolism , Urochordata/microbiology
13.
J Org Chem ; 66(21): 6847-51, 2001 Oct 19.
Article in English | MEDLINE | ID: mdl-11597201

ABSTRACT

A human 15-lipoxygenase (15-HLO) assay has been employed to discover new marine-sponge-derived bioactive compounds. Extracts from two different sponges, Jaspis splendens (order Choristida, family Jaspidae) and Suberea sp. (order Verongida, family Aplysinellidae), exhibited potent IC(50) values of 0.4 and 0.1 microg/mL, respectively. Both are sources of terpenoids, and the former is a known source of (+)-jasplakinolide (7), which is inactive as a 15-HLO inhibitor. The terpenoids included (+)-(5S,6S)-subersin (1, IC(50) > 100 microM), (-)-(5R,10R)-subersic acid (2, IC(50) = 15 microM), jaspaquinol (3, IC(50) = 0.3 microM), and (-)-jaspic acid (4, IC(50) = 1.4 microM). Structure elucidations and lipoxygenase activity studies of these compounds are reported.


Subject(s)
Lipoxygenase Inhibitors , Porifera/chemistry , Terpenes/pharmacology , Animals , Humans , Inhibitory Concentration 50 , Molecular Structure , Stereoisomerism , Structure-Activity Relationship
14.
J Nat Prod ; 64(9): 1216-20, 2001 Sep.
Article in English | MEDLINE | ID: mdl-11575959

ABSTRACT

A phytochemical analysis of the leaves of Aglaia dasyclada collected in Yunnan Province (People's Republic of China) yielded five cyclopentabenzofurans (1-5) of the rocaglamide family that are common secondary metabolites of Aglaia species as well as four biogenetically related compounds of the aglain (7), aglaforbesin (8) and forbaglin (9, 10) types. In addition, the cinnamic acid amide dasyclamide (6), which is a putative biogenetic precursor of these compounds (7-10), was isolated. The structures of the new compounds (6-10) were assigned unambiguously from the combined use of 1D and 2D NMR spectroscopy and mass spectrometry.


Subject(s)
Benzofurans/isolation & purification , Glycosides/isolation & purification , Insecticides/isolation & purification , Meliaceae/chemistry , Animals , Benzofurans/chemistry , Benzofurans/pharmacology , China , Chromatography, High Pressure Liquid , Chromatography, Thin Layer , Circular Dichroism , Dose-Response Relationship, Drug , Feeding Behavior/drug effects , Glycosides/chemistry , Glycosides/pharmacology , Insecticides/chemistry , Insecticides/pharmacology , Larva/drug effects , Larva/metabolism , Magnetic Resonance Spectroscopy , Mass Spectrometry , Molecular Structure , Plant Leaves/chemistry , Plants, Medicinal/chemistry , Putrescine/analogs & derivatives , Putrescine/chemistry , Putrescine/isolation & purification , Putrescine/pharmacology , Spodoptera/drug effects , Spodoptera/metabolism , Stereoisomerism
15.
J Nat Prod ; 64(5): 651-2, 2001 May.
Article in English | MEDLINE | ID: mdl-11374967

ABSTRACT

The fungus Hortaea werneckii isolated from the Mediterranean sponge Aplysina aerophoba, collected at Banyuls-sur-Mer in southern France, yielded a new compound named hortein (1), which possesses a unique ring system hitherto unknown for natural products. The structure of 1 was established on the basis of 1D and 2D NMR spectroscopic and mass spectrometric (ESI, CI, FAB, EI) data.


Subject(s)
Polycyclic Aromatic Hydrocarbons/chemistry , Porifera/microbiology , Animals , Bacteria/drug effects , Fungi/drug effects , Insecticides/pharmacology , Magnetic Resonance Spectroscopy , Mediterranean Sea , Microbial Sensitivity Tests , Polycyclic Aromatic Hydrocarbons/isolation & purification , Polycyclic Aromatic Hydrocarbons/pharmacology , Spectrometry, Mass, Electrospray Ionization , Spectrometry, Mass, Fast Atom Bombardment
16.
J Nat Prod ; 64(4): 415-20, 2001 Apr.
Article in English | MEDLINE | ID: mdl-11325219

ABSTRACT

Organic-soluble extracts of the twigs of Aglaia oligophylla collected in Vietnam yielded four insecticidal cyclopentatetrahydrobenzofurans of the rocaglamide type including one new natural product (compound 4). Moreover, two cyclopentatetrahydrobenzopyran derivatives, belonging to the aglain and aglaforbesin types, respectively, were also isolated. The aglaforbesin derivative 6 proved likewise to be a new natural product. All isolated rocaglamide, aglain, and aglaforbesin derivatives have a characteristic methylenedioxy substituent linked to C-6 and C-7 or to C-7 and C-8, respectively. Structure elucidation of the new natural products and the determination of the absolute configuration of compound 1 by calculation of its CD spectrum with molecular dynamics simulation are described. All isolated rocaglamide derivatives exhibited strong insecticidal activity toward neonate larvae of the polyphageous pest insect Spodoptera littoralis when incorporated into an artificial diet, with LC(50) values varying between 2.15 and 6.52 ppm.


Subject(s)
Benzofurans/isolation & purification , Insecticides/isolation & purification , Rosales/chemistry , Animals , Benzofurans/chemistry , Circular Dichroism , Insecticides/chemistry , Magnetic Resonance Spectroscopy , Mass Spectrometry/methods , Models, Molecular , Molecular Structure , Spodoptera , Stereoisomerism
17.
J Nat Prod ; 64(12): 1521-6, 2001 Dec.
Article in English | MEDLINE | ID: mdl-11754603

ABSTRACT

Four new metabolites, aglacins A-D (1-4), were identified from the methanol extract of the stem bark of Aglaia cordata. These compounds represent a new class of aryltetralin cyclic ether lignan. The structure of aglacin A (1) including the absolute configuration was elucidated by interpretation of spectral data, X-ray crystal structure determination, and employing the modified Mosher's method. In addition, three other derivatives, aglacins B-D (2-4), were isolated and identified by spectral means.


Subject(s)
Ethers, Cyclic/isolation & purification , Lignans/isolation & purification , Meliaceae/chemistry , Plants, Medicinal/chemistry , Chromatography, High Pressure Liquid , Crystallography, X-Ray , Drug Screening Assays, Antitumor , Ethers, Cyclic/chemistry , HL-60 Cells/drug effects , Humans , Indonesia , Lignans/chemistry , Molecular Conformation , Molecular Structure , Nuclear Magnetic Resonance, Biomolecular , Plant Bark/chemistry , Plant Stems/chemistry , Stereoisomerism , Tumor Cells, Cultured/drug effects
18.
J Nat Prod ; 63(6): 739-45, 2000 Jun.
Article in English | MEDLINE | ID: mdl-10869191

ABSTRACT

An undescribed fungus of the genus Microsphaeropsis, isolated from the Mediterranean sponge Aplysina aerophoba, produces two new betaenone derivatives (1, 2) and three new 1,3,6, 8-tetrahydroxyanthraquinone congeners (5-7). The structures of the compounds were established on the basis of NMR spectroscopic and mass spectrometric data and by CD spectroscopy. This is the first report wherein the (1)H and (13)C NMR data of the betaenone congeners are fully and unambiguously assigned on the basis of two-dimensional NMR spectroscopy. Furthermore, we describe the first elucidation of the absolute configuration of 1-(2'-anthraquinonyl)ethanols such as 5 and 6, by quantum chemical calculation of their circular dichroism (CD) and comparison with experimentally measured spectra. Moreover, it was shown that compounds 1, 5, 6, and 7 are inhibitors of PKC-epsilon, CDK4, and EGF receptor tyrosine kinases.


Subject(s)
Anthraquinones/chemistry , Enzyme Inhibitors/chemical synthesis , Ketones/chemistry , Mitosporic Fungi/chemistry , Naphthols/chemistry , Porifera/microbiology , Protein Kinase Inhibitors , Animals , Circular Dichroism , Magnetic Resonance Spectroscopy , Mass Spectrometry , Protein Conformation
19.
J Nat Prod ; 59(6): 591-4, 1996 Jun.
Article in English | MEDLINE | ID: mdl-8786366

ABSTRACT

Aeroplysinin-1 (1) and the structurally related dienone 2 were cytotoxic to Ehrlich ascites tumor (EAT) cells and HeLa tumor cells in the microculture tetrazolium (MTT) and clonogenic assays. Both compounds are bromotyrosine derivatives, isolated from the marine spong Aplysina aerophoba. As the effective concentrations in the MTT assay were lower than in the clonogenic assay, 1 and 2 are able to cause growth inhibition as well as actual cell death in these cell lines. With an IC50 value of 8.2 microM (MTT assay, 2-h incubation, EAT cells), 1 was the more toxic compound. When the cells were depleted of glutathione by pretreatment with buthionine sulfoximine, they were significantly more sensitive toward 1 and 2 in the MTT assay. A dose-enhancement factor as high as 11.8 was found in EAT cells after 2-h incubation with 2. Using electron paramagnetic resonance we were able to measure free radical formation of 1 and 2, yielding the semiquinone structures 3 and 4, respectively, in a culture medium with tumor cells. It is concluded that free radicals are, at least in part, responsible for the cytotoxicity of 1 and 2. This conclusion is in line with expectations derived from the chemical structures of both compounds.


Subject(s)
Acetamides/isolation & purification , Acetonitriles/isolation & purification , Antineoplastic Agents/isolation & purification , Benzoquinones/isolation & purification , Porifera/chemistry , Acetamides/chemistry , Acetamides/pharmacology , Acetonitriles/chemistry , Acetonitriles/pharmacology , Animals , Antineoplastic Agents/chemistry , Antineoplastic Agents/pharmacology , Benzoquinones/chemistry , Benzoquinones/pharmacology , Carcinoma, Ehrlich Tumor/drug therapy , Cyclohexenes , Drug Screening Assays, Antitumor , Electron Spin Resonance Spectroscopy , Glutathione/metabolism , HeLa Cells , Humans , Mice , Tetrazolium Salts , Thiazoles , Tumor Cells, Cultured , Tumor Stem Cell Assay
20.
Biochim Biophys Acta ; 1292(1): 133-9, 1996 Jan 04.
Article in English | MEDLINE | ID: mdl-8547335

ABSTRACT

Structural analysis of a monomeric hemoglobin from the cyanobacterium Nostoc commune strain UTEX 584, cyanoglobin (Potts et al. (1992) Science 256, 1690-1692), is presented. Cyanoglobin binds molecular oxygen reversibly, with high oxygen affinity and non-cooperativity. There was no evidence for decreased stability of the pigment at 37 degrees C. Cyanoglobin-specific antibodies showed no cross-reactivity with two reference hemoglobins, leghemoglobin a and sperm whale myoglobin. The absorption spectral properties of cyanoglobin differ significantly from those of the two reference hemoglobins. The spectrum of oxy-cyanoglobin most closely resembles that of an oxy-hemoglobin from the protozoan Tetrahymena pyriformis, a hemoprotein that shares substantial amino-acid sequence identity with cyanoglobin. Met-cyanoglobin possesses spectral characteristics at pH 7.0-9.0 that resemble those of the alkaline met-hemoglobin (a putative hemichrome) of another protozoan, Paramecium caudatum. The spin-state character of met-cyanoglobin is pH-dependent. Met-cyanoglobin does not coordinate the strong-field ligands, cyanide and azide, at pH 7.0. The capacity of cyanoglobin to coordinate cyanide increased with decreasing pH. Far-UV CD spectra of cyanoglobin are indicative of a protein with a significant amount of alpha-helical structure. Data from Soret-region CD spectra suggest that the orientations of the heme moieties in cyanoglobin and leghemoglobin a are similar to one another.


Subject(s)
Cyanobacteria/chemistry , Hemoglobins/chemistry , Blotting, Western , Circular Dichroism , Escherichia coli/genetics , Heme/metabolism , Hemoglobins/genetics , Hemoglobins/isolation & purification , Hemoglobins/metabolism , Hydrogen-Ion Concentration , Leghemoglobin/chemistry , Leghemoglobin/immunology , Methemoglobin/chemistry , Myoglobin/immunology , Nitrogen Fixation , Oxygen/metabolism , Recombinant Proteins/chemistry , Recombinant Proteins/isolation & purification , Recombinant Proteins/metabolism , Spectrophotometry
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