Most cited article - PubMed ID 8123690
Fast atom bombardment mass spectrometry of elymoclavine glycosides
Oligosaccharides produced by submerged cultures of C. africana and C. sorghi were isolated by semipreparative HPLC. Structure of 6-O-beta-D-fructofuranosyl-D-glucopyranose (blastose), 1,6-bis-O-(beta-D-fructofuranosyl)-alpha-D-glucopyranoside (neokestose) and two sugar alcohols, 1-O-beta-D-fructofuranosyl-D-mannitol (fructosylmannitol) and 1,6-bis-O-(beta-D-fructofuranosyl)-D-mannitol (bisfructosylmannitol) was determined by NMR spectrometry. MALDI TOF MS analysis revealed molecular ions [M+Na]+ that indicate the presence of other tetra- and pentasaccharides (m/z = 689.4 and 851.5, respectively) and corresponding sugar alcohol (m/z = 691.4). Rapid conversion of sucrose into series of oligosaccharides and corresponding sugar alcohols was observed in all tested strains.
- MeSH
- Claviceps growth & development isolation & purification metabolism pathogenicity MeSH
- Sugar Alcohols chemistry metabolism MeSH
- Fermentation MeSH
- Molecular Structure MeSH
- Plant Diseases microbiology MeSH
- Nuclear Magnetic Resonance, Biomolecular MeSH
- Oligosaccharides biosynthesis chemistry isolation & purification MeSH
- Sorghum microbiology MeSH
- Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization MeSH
- Chromatography, High Pressure Liquid MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Sugar Alcohols MeSH
- Oligosaccharides MeSH
A total of 307 new compounds, natural, semisynthetic or synthetic, were isolated at the Institute of microbiology during the last twelve years. Due to the development of separation (chromatographic) methods and of analytical methods used to determine the chemical structure of these compounds, i.e. NMR, MS and X-ray diffraction, many new metabolites could be described.
- MeSH
- Biological Factors chemistry isolation & purification MeSH
- Peptides, Cyclic chemistry isolation & purification MeSH
- Enzymes chemistry isolation & purification MeSH
- Molecular Sequence Data MeSH
- Ergot Alkaloids chemistry isolation & purification MeSH
- Carbohydrate Sequence MeSH
- Carbohydrates chemistry isolation & purification MeSH
- Amino Acid Sequence MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Review MeSH
- Names of Substances
- Biological Factors MeSH
- Peptides, Cyclic MeSH
- Enzymes MeSH
- Ergot Alkaloids MeSH
- Carbohydrates MeSH
Natural sources, i.e. fungal strains and species producing ergot alkaloids (EA), are surveyed together with the chemical structures of EA and a list of new natural EA discovered in the last three decades. Other topics include new efficient chromatographic methods (HPLC) for the separation and isolation of new natural EA and also immunological methods of EA detection.
- MeSH
- Fungi chemistry MeSH
- Immunoassay methods MeSH
- Humans MeSH
- Molecular Structure MeSH
- Ergot Alkaloids chemistry isolation & purification pharmacology MeSH
- Chromatography, High Pressure Liquid methods MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Review MeSH
- Names of Substances
- Ergot Alkaloids MeSH