Use of the metabolic grid to explain the metabolism of quinolizidine alkaloids in Leguminosae

Evidence from feeding experiments with lysine-[2-¹⁴C] and from metabolism experiments published previously suggest the operation of a gridlike conversion of quinolizidine alkaloids in Leguminosae. Using these results and the taxonomical distribution of alkaloids a metabolic grid was devised to explain the conversion of lysine into lupin alkaloids and their interconversions.     

Metabolism of l-sparteine,dl-lupanine and l-thermopsine in species of Leguminosae

l-Sparteine-[¹⁴C], dl-lupanine-[¹⁴C] and l-thermopsine-[¹⁴C] fed to plants served as precursors to the more highly oxidized alkaloids. Radioactivity was also found in amino acids.     

Determination of quinolizidine alkaloids in Sophora tonkinensis by HPCE

A simple, rapid and reliable high-performance capillary electrophoresis method has been developed to determine quantitatively the alkaloid content of Sophora tonkinensis, a Chinese herb commonly known as shan-dou-gen. A total of seven quinolizidine alkaloids (cytisine, sophocarpine, matrine, lehmannine, sophoranol, oxymatrine and oxysophocarpine) could be readily separated within 15 min. The running buffer was 50 mM phosphate buffer (pH 2.5) containing 1% hydroxypropyl-beta-cyclodextrin and 3.3% isopropanol in water. The applied voltage was 25 kV, the capillary temperature was 25 degrees C, the detection wavelength was 200 nm and scopolamine butylbromide was used as internal standard. The method was used to analyse the chemical constituents of two commercial alternatives to shan-dou-gen. The alkaloid constituents of authentic shan-dou-gen gave a specific HPCE electropherogram that could be used to distinguish the drug from potential substitutes. Furthermore, the content of oxymatrine and the total content of the seven quinolizidine alkaloids could be used as quantitative markers in order to assess the quality of S. tonkinensis.     

Leontidine-type quinolizidine alkaloids in Orphanodendron (Leguminosae)

Herbarium leaf fragments of the two known species of Orphanodendron (Leguminosae), O. bernalii and O. grandiflorum, were found to contain the quinolizidine alkaloids camoensine (1), camoensidine (2) and guianodendrine (3), supporting the recent phylogenetic placement of the genus in the genistoid clade of subfamily Papilionoideae rather than its traditional placement in subfamily Caesalpinioideae.     

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.     

A phytochemical study of the quinolizidine alkaloids from Genista tenera by gas chromatography-mass spectrometry

Gas chromatography coupled with mass spectrometry has been used to analyse the alkaloids present in the aerial parts of Genista tenera. Anagyrine, cytisine, N-formylcytisine, N-methylcytisine and lupanine were the major compounds, the last two alkaloids being known for their hypoglycaemic activity. Dehydrocytisine, 5,6-dehydrolupanine, rhombifoline, aphylline and thermopsine were the minor alkaloids. The characterisation of the constituents was based on comparison of their Kovats retention indexes and electron impact-mass spectrometric data recorded on-line with those of reference compounds and literature data.     

Distribution of quinolizidine alkaloid types in nine Ormosia species (Leguminosae-Papilionoideae)

Quinolizidine alkaloids were surveyed in 22 plant samples, representing nineOrmosia species and up to five different plant parts per species, using combined gas chromatography and mass spectroscopy. The detected alkaloids were classified into 40 structural types. There was a remarkable degree of dissimilarity of alkaloid-type profiles between any two plant samples, including those obtained from the same species and even from a single tree. The similarity of alkaloid-type profiles among the studied samples varied between 0% and 79% (Jaccard similarity coefficient). Of chemotaxonomic interest was the finding of acosmine inO. isthmensis, which previously had been reported only from the related genusAcosmium. Furthermore, the alkaloid-type profile ofO. panamensis seeds was distinct from that of all other samples, supporting the hypothesis that this species is only distantly related to the other Latin AmericanOrmosia species.     

Biosynthesis of radiolabelled alkaloids from 14C-tyrosine in Erythrina crista-galli

Alkaloid biosynthesis has been demonstrated in the young expanding tissues of Erythrina crista-galli shoots, the stem part of which elaborated, from [2-^14C]-tyrosine, alkaloid of specific radioactivity 2μuCi mmol^?1, 10-fold greater than previously reported.     

A survey of alkaloids in the genera Harpalyce and Brongniartia (Fabaceae—Brongniartieae)

The presence of alkaloids in six species of Brongniartia and three species of Harpalyce is reported. This survey revealed remarkable qualitative differences in the alkaloid profiles of these two genera. B. discolor, B. lupinoides, B. sousae and B. intermedia showed a typical -pyridone pattern, with cytisine, anagyrine and baptifoline as major alkaloids. In leaves of the first three species ormosanine-type alkaloids occurred additionally. B. flava and B. vazquezii are devoid of -pyridones, but accumulate lupanine, hydroxylated lupanines and ester alkaloids. All three species of Harpalyce were similar in accumulating -pyridones, but H. formosa differed from H. brasiliana and H. pringlei in the presence of epilupinine. In general the alkaloid profiles of Brongniartia and Harpalyce show similarities to those of the Australian genera Hovea, Lamprolobium, Plagiocarpus and Templetonia and support therefore the actual concept of the enlarged tribe Brongniartieae.     

Quinolizidine alkaloids in petteria ramentacea and the infesting aphids, Aphis cytisorum

Alkaloid extracts of Petteria ramentacea (leaves, fruits, stem) contained cytisine, N-methylcytisine, anagyrine as major alkaloids, and lupanine, 5,6-dehydrolupanine and rhombifoline as minor constituents. Aphids (Aphis cytisorum) feeding on this plant accumulated cytisine in a concentration of 21 mmol/kg fresh weight (0.4 %).     

Directed biosynthesis of unnatural alkaloids in Dolichothele sphaerica

Using appropriate precursors, the two unnatural alkaloids 4(5)-[N-isocaproylaminomethyl]imidazole and 3-[2-N-isovalerylaminoethyl]pyrazole were produced by Dolichothele sphaerica. The former compound represents an unnatural alkaloid formed by the simultaneous introduction of two unnatural precursors, namely isocaproic acid and 4(5)-aminomethylimidazole. The latter compound represents an aberrant alkaloid formed by the introduction of a precursor of different heterocyclic entity, 3-aminoethylpyrazole.     

Identification of the quinolizidine alkaloids in Sophora leachiana

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Molecular Phylogeny of the Papilionoideae (Family Leguminosae): RbcL Gene Sequences versus Chemical Taxonomy

Total DNA was extracted from 67 species (30 genera) of the subfamily Papilionoideae (family Leguminosae). The rbcL gene was amplified by polymerase chain reaction (PCR) and sequenced directly. RbcL sequences were evaluated with character-state (maximum parsimony; PAUP) and distance methods (neighbour-joining; MEGA). Morphology-based classifications of tribes and subtribes are mostly congruent with rbcL phylogeny. Differences occur for members of the genus Sophora and for intratribal relationships within the Genista/Cytisus complex: Sophora appears in two clades; one clade with S. japonica at the base of the Papilionoideae and a second more advanced group (with S. davidii, S. jaubertii, and S.flavescens) which represents a sister clade of the Thermopsideae. The Cytisus complex includes the genera Cytisus, Chamaecytisus, Calicotome and Spartocytisus but not Cytisophyllum which appears as a distinct member of the Genista complex. Chamaespartium sagittale is very close to Genista supporting the view that it does not represent an independent genus but should be treated as Genista sagittalis. Close to Genista are Teline and Spartium, whereas Argyrolobium, Retama, Cytisophyllum, Ulex, Petteria, Adenocarpus, Chamaespartium tridentatum and Laburnum can be considered as “outliers” of the Genista-group sensu stricto. RbcL phylogeny is compared with profiles of alkaloids and other natural products. First results indicate that secondary metabolite profiles, if compared with morphology or rbcL sequences, are of limited value as a taxonomic marker.     

Pyrrolizidine alkaloids from seeds of Crotalaria scassellatii

Three pyrrolizidine alkaloids were isolated from the seeds of Crotalaria scassellatii. Axillaridine and axillarine were the two major alkaloids whereas the third minor alkaloid was a new compound. Its structure was determined as desoxyaxillarine.     

Optical rotation of quinolizidine alkaloids: An important variable in chemosystematic studies ofFabaceae

The anomalous distribution of (+)-lupanine and (–)-lupanine inPodalyria species provides circumstantial evidence that hydroxylation and subsequent esterification of lupanine is only possible when (–)-sparteine and (+)-lupanine are the precursors. The optical rotation of lupanine and/or sparteine isolated from different genera, in combination with literature data, provide evidence of a separate biosynthetic pathway which leads to lupanine-type esters rather than -pyridones. The occurrence of this pathway can be predicted from the optical rotation of sparteine and/or lupanine, even in the absence of end products. Enantiomers-specificity is thus an important variable for establishing homology in comparative studies.