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  • 1985-1989  (2)
  • Symphytum  (1)
  • bioconversions  (1)
Materialart
Erscheinungszeitraum
Jahr
  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Plant systematics and evolution 167 (1989), S. 113-127 
    ISSN: 1615-6110
    Schlagwort(e): Angiosperms ; Boraginaceae ; Symphytum ; S. officinale agg. ; Chemotaxonomy ; pyrrolizidine alkaloids ; isobauerenol
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie
    Notizen: Abstract In a chemotaxonomic study of the genusSymphytum pyrrolizidine alkaloids and triterpenes were used as chemotaxonomical markers. A micro-extraction methods was developed for screening compounds of very small pieces of herbarium material. The occurrence of the pyrrolizidine alkaloids symphytine and (acetyl-)lycopsamine is very general forSymphytum taxa. Echimidine is present in someS. officinale L. plants and inS. tanaicense Steven. The triterpene isobauerenol is present inS. officinale, S. bohemicum Schmidt,S. tanaicense and inS. officinale var.lanceolatum Weinm. The chemotaxonomic hypothesis, proposed byGadella and collaborators, based on the presence of the triterpene isobauerenol inS. officinale and its absence inS. asperum Lepech. and the presence of the pyrrolizidine alkaloid echimidine inS. asperum and its absence inS. officinale, can no longer be applied absolutely to theS. officinale species complex. The pyrrolizidine alkaloid and triterpene pattern ofS. officinale (2n = 24) andS. bohemicum (2n = 24) is identical.S. bohemicum is morphologically, cytologically and phytochemically very similar toS. officinale. Furthermore, it readily crosses with the white flowered W. European diploids ofS. officinale. Therefore it seems likely that these two taxa are conspecific.S. tanaicense shows a pyrrolizidine alkaloid and triterpene pattern similar toS. officinale (2n = 40). Also on morphological and cytological grounds they are very similar. It seems highly probable thatS. tanaicense is conspecific withS. officinale (2n = 40) and represents an intraspecific variant only.S. officinale var.lanceolatum contained no pyrrolizidine alkaloids but did contain isobauerenol. This feature points to an origin fromS. officinale.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    ISSN: 1573-5044
    Schlagwort(e): Mucuna pruriens ; entrapped plant cells ; bioconversions ; catechols ; isolation ; mass spectrometry
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie
    Notizen: Abstract Alginate-entrapped cells ofM. pruriens were able to convert a number of parasubstituted monophenolic compounds into the corresponding catechols. All catechols produced were released into the medium, which offered the opportunity to isolate these products via a relatively simple procedure. Prepurification was performed on a Sephadex G10 gel and catechols were concentrated on Affigel 601. The identity of all products was confirmed with combined liquid chromatography/mass spectrometry (LC/MS) or MS using the desorption chemical ionization technique, depending on the catechol. For the entrapped cells and for a cell homogenate prepared of the same cell line ofM. pruriens the substrate specificities were qualitatively identical when judged on initial rates of synthesis calculated on protein basis.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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