Biodiversity of Convolvulaceous species that contain ergot alkaloids,indole diterpene alkaloids,and swainsonine

Convolvulaceous species have been reported to contain several bioactive principles thought to be toxic to livestock including the calystegines, swainsonine, ergot alkaloids, and indole diterpene alkaloids. Swainsonine, ergot alkaloids, and indole diterpene alkaloids are produced by seed transmitted fungal symbionts associated with their respective plant host, while the calystegines are produced by the plant. To date, Ipomoea asarifolia and Ipomoea muelleri represent the only Ipomoea species and members of the Convolvulaceae known to contain indole diterpene alkaloids, however several other Convolvulaceous species are reported to contain ergot alkaloids. To further explore the biodiversity of species that may contain indole diterpenes, we analyzed several Convolvulaceous species (n = 30) for indole diterpene alkaloids, representing four genera, Argyreia, Ipomoea, Stictocardia, and Turbina, that had been previously reported to contain ergot alkaloids. These species were also verified to contain ergot alkaloids and subsequently analyzed for swainsonine. Ergot alkaloids were detected in 18 species representing all four genera screened, indole diterpenes were detected in two Argyreia species and eight Ipomoea species of the 18 that contained ergot alkaloids, and swainsonine was detected in two Ipomoea species. The data suggest a strong association exists between the relationship of the Periglandula species associated with each host and the occurrence of the ergot alkaloids and/or the indole diterpenes reported here. Likewise there appears to be an association between the occurrence of the respective bioactive principle and the genetic relatedness of the respective host plant species.     

The sequential appearance and metabolism of alkaloids in Heimia salicifolia

The seeds of Heimia salicifolia do not contain alkaloids. Two unidentified alkaloids were detected in 1-week-old seedlings; these alkaloids were absent from older plant samples. Lyfoline, cryogenine, and lythrine were first detected in 2-week-old plants. Sinicuichine was first observed in 3-week-old plants and nesodine in 2-month-old plants. The maximum rates of synthesis for most of these alkaloids occurred in 1- to 2-month-old plants. Following administration of ¹⁴CO₂ to H. salicifolia plants, small quantities of alkaloids were purified to constant specific activity without alkaloid dilution; 95.6% of the administered ¹⁴CO₂ was assimilated and up to 0.16% of this activity was incorporated into known alkaloids. Sinicuichine and lyfoline were shown to undergo catabolism, while cryogenine was degraded very slowly, if at all. Evidence is presented for the conversion of lyfoline to lythrine.     

Alkaloid distribution in some new world Lupinus species

Alkaloidal profiles of 21 Lupinus species indigenous to North and South America have been determined. Nineteen quinolizidine alkaloids were identified, including aphyllidine and N-methylcytisine, which have not previously been found in the genus. Two dipiperidine alkaloids were also detected. The pattern of alkaloidal distribution is related to a taxonomic classification of the genus.     

Pyrrolizidine alkaloids and other constituents from Emilia fosbergii Nicolson

Emilia fosbergii is a member of the tribe Senecioneae (Asteraceae), most species of which contain pyrrolizidine alkaloids. Notwithstanding, the phytochemistry of E. fosbergii is poorly understood, and pyrrolizidine alkaloids produced by this species have yet to be characterized. In this work, the presence of 11 pyrrolizidine alkaloids, three caffeoylquinic acid derivatives, and six flavonoids were detected by liquid chromatography coupled to high-resolution mass spectrometry analyses. Pyrrolizidine alkaloids of otonecine, retronecine, and platynecine bases are annotated in different parts of the plant. Furthermore, emiline was isolated, possibly indicating that E. fosbergii has a close phylogenetic relationship with E. coccinea. The chemophenetic implications of the presence of pyrrolizidine alkaloids in E. fosbergii and tribe Senecioneae are discussed.     

Concomitant occurrence of pyrrolizidine and quinolizidine alkaloids in the hemiparasite Osyris alba L. (Santalaceae)

The investigation of the alkaloid extracts of the hemiparasitic plant Osyris alba, collected from three different localities in southern France, revealed the concomitant presence of both pyrrolizidine (PA) and quinolizidine (QA) alkaloids in the samples from two of these localities. The sample from the third locality contained only PAs. The eight QAs identified were sparteine, N-methylcytisine, cytisine, methyl-12-cytisine acetate, hydroxy-N-methylcytisine, N-acetylcytisine, lupanine, and anagyrine. Of the eleven detected PAs, eight were identified as chysin A, chysin B, 1-carboxypyrrolizidine-7-olide, senecionine, integerrimine, retrorsine, senecivernine and a new alkaloid janfestine (7R-hydroxychysin A or 1R-carbomethoxy-7R-hydroxypyrrolizidine). PAs were mainly present as their N-oxides This is, to our knowledge, the first report demonstrating the simultaneous presence of two classes of alkaloids, quinolizidine and pyrrolizidine alkaloids, in a single parasitic plant. As these alkaloids do not occur in the same host plant, the results indicate that Osyris must have tapped more than one host plant concomitantly. Since both quinolizidine and pyrrolizidine alkaloids serve as defence compounds against herbivores, affecting different molecular targets, the simultaneous acquisition of the two types of alkaloids by a single plant could provide a novel mode of defence of hemiparasites against herbivores.     

Dereplication of Palicourea sessilis ethanol extracts by UPLC-DAD-ESI-MS/MS discloses the presence of hydroxycinnamic acid amides and the absence of monoterpene indole alkaloids

Secondary metabolites characterization of ethanol extracts of Palicourea sessilis leaves and stems by UPLC-DAD-ESI-MS/MS led to putative identification of hydrolysable tannins in leaf extract (ESI negative mode) while hydroxycinnamic acid amides (HCA) such as N-p-coumaroylputrescine and N-feruloylagmatine were detected in both leaf and stems extracts in the ESI positive mode. Secondary metabolites quantification data showed a higher content of total phenolic in the leaf extract while the total alkaloids contents are statistically equivalent in both of the extracts. Furthermore, monoterpene indole alkaloids were not detected in both extracts. The presence of HCA is here firstly reported for a Palicourea species. This finding increases the classes of secondary metabolites occurring in this genus.     

Pyrrolizidine alkaloids of Heliotropium from Mexico and adjacent U.S.A.

The levels of alkaloids were determined in leaves and stems of 24 species of Heliotropium collected in Mexico and adjacent U.S.A. All species contained unsaturated pyrrolizidines, their content in leaves ranging from 0.003 to 0.18%. Saturated pyrrolizidine alkaloids were detected in nine species. Greenhouse-grown plants of five species had a significantly higher alkaloid content in their leaves than the corresponding field samples. In all these species, except for H. indicum, the differences were due to higher levels of saturated pyrrolizidines.     

Iridoid and other constituents of Canthium subcordatum

The main constituent of the stem bark of Canthium subcordatum was found to be shanzhiside methyl ester, an iridoid recently described for two Mussaenda species; it is accompanied by the new iridoid shanzhisin methyl ester gentiobioside. No alkaloids were detected.     

Pyrrolizidine alkaloids in two endemic capeverdian Echium species

Echium hypertropicum Webb and Echium stenosiphon Webb subsp. stenosiphon are capeverdian shrubs used in folk medicine for the treatment of cough and gastrointestinal diseases. Acid-base extraction was used to obtain alkaloid-rich fractions from both species. GC–MS and ESI-MS/MS analysis indicated the presence of pyrrolizidine alkaloids (PAs) and purified substances were also analyzed by 1D and 2D NMR experiments. A total of ten alkaloids were detected, eight of which were identified by comparing their molecular masses and mass fragmentation patterns with the NIST database and data in the literature. The hepatotoxic diesters echimidine and 7-(2-methylbutyryl)-9-echimidinylretronecine were identified in both species. Echimidine was the major component in the diethyl ether fraction from leaves of E. hypertropicum, whereas the 7-(2-methylbutyryl)-9-echimidinylretronecine was the major component in the dichloromethane fraction from leaves of E. stenosiphon. To our knowledge, this is the first report on the occurrence of pyrrolizidine alkaloids in capeverdian species of Echium. This study on Echium led to the identification of constituent pyrrolizidine alkaloids, serving to assist taxonomists with the complex taxonomy of this genus.     

Distribution et activités des alcaloïdes défensifs des Coccinellidae

From a survey of 30 species and varieties of ladybugs the presence of alkaloids appears to be correlated with the existence of aposematic colour and not with being carnivorous or phytophagous. The alkaloids described until now all belong to the Coccinellini and are closely related, but other types of bases have been detected in some genera. The observed distributions are in agreement with the modern taxonomy of the family.Ladybug alkaloids constitute an effective defence against ants, Myrmica rubra, and quails, Coturnix coturnix, but all the beetles containing alkaloids do not possess the same degree of protection. Individual quail react differently towards moderately protected species.The bioassay used for the first isolation of coccinelin is described. The repulsive activities of aqueous solutions of coccinellin and convergin towards ants have been compared.     

Aporphine alkaloids and lignans formed in response to injury of sapwood in Liriodendron tulipifera

Two new phenolic aporphine alkaloids, (+)-lirioferine and (+)liriotulipiferine, were isolated from discolored sapwood of L. tulipifera. Injury to the tree stem greatly stimulated biosynthesis of glaucine and phenolic alkaloids related to glaucine including thaliporphine, predicentrine, N-methylaurotetanine and corunine as well as the above two compounds. Injury also stimulated synthesis of oxoaporphine related and other polymeric pigments. Corunine was responsible for at least part of the color of discolored sapwood. None of the above compounds except glaucine was detected in normal sapwood or heartwood of L. tulipifera. Thus, formation of alkaloids and lignans in discolored sapwood differs both quantitatively and qualitatively from that observed during the normal transition of sapwood to heartwood in this tree. The compounds formed in response to injury differed substantially from one zone of injury to another within the same tree.     

Growth and quaternary alkaloid production in differentiating and non-differentiating strains of Ruta graveolens

Cultures of Ruta graveolens have been grown and maintained on Murashige and Skoog's medium supplemented with α-naphthalene acetic acid (1 mg/l.) and kinetin (0.1 mg/l.) or 2,4-dichlorophenoxyacetic acid (1 mg/l.), and glucose (30 g/l.). The production of dihydrofuroquinoline alkaloids has been investigated in these cultures. The present study showed that: (a) cultures of Ruta produced both differentiating and non-differentiating strains; (b) quaternary alkaloids (platydesminium, ribalinium and rutalinium) were present in all the strains and maximum contents were detected at 3-4 weeks growth; (c) high platydesminium and rutalinium content was associated with differentiation and callus formation, respectively; (d) changed concentrations of quaternary alkaloids were recorded in all the five strains grown on media supplemented with tryptophan and precursors (anthranilic acid, 5-methylanthranilic acid and 2,4-dihydroxyquinoline).     

Use of repair-deficient strains of escherichia coli and liver microsomes to detect and characterise DNA damage caused by the pyrrolizidine alkaloids heliotrine and monocrotaline

E. coli WP2 and its repair-deficient derivatives were treated with the pyrrolizidine alkaloids, heliotrine and monocrotaline in the presence of a liver microsomal fraction. The doubly repair-deficient strains WP100 uvrA recA and CM611 uvrA exrA showed considerable killing. The singly repair-deficient strains WP2 uvrA, CM561 exrA and CM571 recA showed slight killing. In strains WP2 and WP2 uvrA induced reversion to Trp⁺ was not detected with either monocrotaline or mitomycin C. These results are entirely consistent with liver activation converting pyrrolizidine alkaloids into bifunctional alkylating agents.     

Peramine and other fungal alkaloids are exuded in the guttation fluid of endophyte-infected grasses

Many grasses live in association with asymptomatic fungi (Neotyphodium spp. endophytes), which grow in the intercellular spaces of the grass. These endophytes produce a range of alkaloids that protect the grass against grazing by mammals and insects. One of these alkaloids is an unusual pyrrolopyrazine, peramine. Peramine appears to be continuously produced by the endophyte, but does not progressively accumulate. No mechanism for the removal of peramine by its further metabolism or any other process has been reported. Our aim was to detect peramine or peramine metabolites in plant fluids to determine if peramine is mobilized, metabolized or excreted by the plant. We also wanted to determine if other fungal metabolites are mobilized by the plant, as has been proposed for the loline alkaloids.We developed a highly sensitive method for the analysis of peramine, using a linear ion trap mass spectrometer. We studied the fragmentation pathway of peramine using ESI MSⁿ and ESI FTICRMS. Based on these results we developed a single reaction monitoring method using the fragmentation of the guanidinium moiety. Cut leaf fluid and guttation fluid of different grass endophyte associations (Lolium perenne with Neotyphodium lolii, Festuca arundinacea with Neotyphodium coenophialum, and Elymus sp. with Epichloë sp.) were analysed. Peramine was detected in the cut leaf fluid of all grass-endophyte associations, but not in the guttation fluid of all associations. In some associations we also detected lolines and ergot peptide alkaloids. This is the first report showing the mobilization of fungal alkaloids into plant fluids by the host plant in grass-endophyte associations.     

Alkaloid chemotaxonomy of the genus Sophora

Cytisine and matrine alkaloids detected in Sophora species have been used to classify the genus chemotaxonomically.     

Ontogenetic variation of the tropane alkaloids in Datura stramonium

Alkaloid profile of Datura stramonium plant parts collected at different stages of development were investigated by GC–MS. Sixty-four tropane alkaloids were detected and 48 of them were determined. Two new tropane alkaloids, 3-phenylacetoxy-6,7-epoxynortropane and 7-hydroxyapoatropine were tentatively identified. The alkaloids scopoline, 3-(hydroxyacetoxy)tropane, 3-hydroxy-6-(2-methylbutyryloxy)tropane, 3β-tigloyloxy-6-hydroxytropane, 3,7-dihydroxy-6-tigloyloxytropane, 3-tigloyloxy-6-propionyloxytropane, 3-phenylacetoxy-6,7-epoxytropane, 3-phenylacetoxy-6-hydroxytropane, aponorscopolamine, 3β,6β-ditigloyloxytropane and 7-hydroxyhyoscyamine are reported for the first time for this species and 3-acetoxy-6-isobutyryloxytropane for the family Solanaceae. The number and the type of alkaloids in the different plant organs depend on the stages of development. The variability by types of alkaloids (monosubstituted, 3,6- and 3,7-disubstituted, 3,6,7-trisubstituted and 3-substituted-6,7-epoxytropanes) decreases from the roots of the plants in vegetative growth and immature fruits to the seeds of senile plants (mainly monosubstituted and 3-substituted-6,7-epoxytropanes).     

Effects of cold shocked Epichloë infected Festuca sinensis on ergot alkaloid accumulation

We evaluated the effects of temperature on ergot alkaloid production of three Festuca sinensis ecotypes, Xiahe (XH), Haibei (HB) and Yushu (YS) under controlled conditions. After subjecting 80 d old plants grown at 22 °C to low temperatures (5 °C or 10 °C) for 7 d, the concentrations of the ergot alkaloids ergine and ergonovine differed considerably in the three endophyte-infected ecotypes (P < 0.05), and were not detected in endophyte-free plants. The concentrations of ergine, ergonovine, and total ergot alkaloids were significantly higher at 5 °C than at 22 °C (P < 0.05). These findings showed that production of at least two secondary metabolites, the bioprotective alkaloids ergine and ergonovine, altered in response to short-term cold stress.     

Geographical variation of isoquinoline alkaloids of Annona crassiflora Mart. from cerrado,Brazil

The total content and profile of alkaloids in foliar samples of Annona crassiflora from eight different Brazilian Cerrado regions were investigated. Alkaloids were quantified and identified by GC/FID and GC/MS, respectively. Significant quantitative differences were found in these samples. Total alkaloid concentration varied from 221.1 ± 17.14 ug/g in Mogi-Guaçu (SP) to 2986.89 ± 367.1 ug/g (dry mass basis) in Brasília (DF). The alkaloids anonaine, annoretine, romucosine and xylopine were detected at different concentrations across regions. Alkaloid concentration and profile varied in A. crassiflora populations, indicating extensive phenotypic plasticity of these individuals.     

The alkaloids of Stephania sasakii: Structure of five new alkaloids

Five new alkaloids, dehydrocrebanine, 4,5-dioxodehydrocrebanine, stesakine, dehydrostesakine, bisaknadinine and four known alkaloids, lirodenine, lanuginosine, 1-tetrahydropalmatine, d-isocorydine with a few alkaloids of unknown structure were newly isolated from Stephania sasakii. The structures of the new alkaloids were determined from spectral data and chemical evidence.     

Taxonomic distribution of defensive alkaloids in Nearctic oribatid mites (Acari,Oribatida)

The opisthonotal (oil) glands of oribatid mites are the source of a wide diversity of taxon-specific defensive chemicals, and are likely the location for the more than 90 alkaloids recently identified in oribatids. Although originally recognized in temperate oribatid species, alkaloids have also been detected in related lineages of tropical oribatids. Many of these alkaloids are also present in a worldwide radiation of poison frogs, which are known to sequester these defensive chemicals from dietary arthropods, including oribatid mites. To date, most alkaloid records involve members of the superfamily Oripodoidea (Brachypylina), although few species have been examined and sampling of other taxonomic groups has been highly limited. Herein, we examined adults of more than 60 species of Nearctic oribatid mites, representing 46 genera and 33 families, for the presence of alkaloids. GC–MS analyses of whole body extracts led to the detection of 15 alkaloids, but collectively they occur only in members of the genera Scheloribates (Scheloribatidae) and Protokalumma (Parakalummidae). Most of these alkaloids have also been detected previously in the skin of poison frogs. All examined members of the oripodoid families Haplozetidae and Oribatulidae were alkaloid-free, and no mites outside the Oripodoidea contained alkaloids. Including previous studies, all sampled species of the cosmopolitan oripodoid families Scheloribatidae and Parakalummidae, and the related, mostly tropical families Mochlozetidae and Drymobatidae contain alkaloids. Our findings are consistent with a generalization that alkaloid presence is widespread, but not universal in Oripodoidea. Alkaloid presence in tropical, but not temperate members of some non-oripodoid taxa (in particular Galumnidae) deserves further study.