Hydrolysis of microcystins and nodularin by microwave radiation
ISSN: |
1612-1112
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Keywords: |
Column liquid chromatography ; Microwave hydrolysis ; Microcystin ; Nodularin ; D- and L-selective amino acid determination
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Source: |
Springer Online Journal Archives 1860-2000
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Topics: |
Chemistry and Pharmacology
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Notes: |
Summary Microwave radiation has been successfully used for hydrolysis of the hepatotoxic cyclic peptides microcystins and nodularin. Set-up of the microwave device and the operating conditions for microwave hydrolysis were optimized. Results of the microwave hydrolysis were compared with results from conventional hydrolysis for 24 h at 110°C. Microwave hydrolysis of microcystins and nodularin for as little as 10 min at 160°C results in complete cleavage of peptide bonds and high recoveries of amino acids. Enantioselective determination of amino acids was achieved by use of a previously described HPLC method after pre-column derivatization withortho-phthaldialdehyde and the chiral thiolN-iso-butyryl-cysteine.
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Type of Medium: |
Electronic Resource
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URL: |
_version_ | 1798297327971074049 |
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autor | Reichelt, M. Hummert, C. Luckas, B. |
autorsonst | Reichelt, M. Hummert, C. Luckas, B. |
book_url | http://dx.doi.org/10.1007/BF02466910 |
datenlieferant | nat_lic_papers |
hauptsatz | hsatz_simple |
identnr | NLM209137738 |
issn | 1612-1112 |
journal_name | Chromatographia |
materialart | 1 |
notes | Summary Microwave radiation has been successfully used for hydrolysis of the hepatotoxic cyclic peptides microcystins and nodularin. Set-up of the microwave device and the operating conditions for microwave hydrolysis were optimized. Results of the microwave hydrolysis were compared with results from conventional hydrolysis for 24 h at 110°C. Microwave hydrolysis of microcystins and nodularin for as little as 10 min at 160°C results in complete cleavage of peptide bonds and high recoveries of amino acids. Enantioselective determination of amino acids was achieved by use of a previously described HPLC method after pre-column derivatization withortho-phthaldialdehyde and the chiral thiolN-iso-butyryl-cysteine. |
package_name | Springer |
publikationsjahr_anzeige | 1999 |
publikationsjahr_facette | 1999 |
publikationsjahr_intervall | 8004:1995-1999 |
publikationsjahr_sort | 1999 |
publisher | Springer |
reference | 49 (1999), S. 671-677 |
schlagwort | Column liquid chromatography Microwave hydrolysis Microcystin Nodularin D- and L-selective amino acid determination |
search_space | articles |
shingle_author_1 | Reichelt, M. Hummert, C. Luckas, B. |
shingle_author_2 | Reichelt, M. Hummert, C. Luckas, B. |
shingle_author_3 | Reichelt, M. Hummert, C. Luckas, B. |
shingle_author_4 | Reichelt, M. Hummert, C. Luckas, B. |
shingle_catch_all_1 | Reichelt, M. Hummert, C. Luckas, B. Hydrolysis of microcystins and nodularin by microwave radiation Column liquid chromatography Microwave hydrolysis Microcystin Nodularin D- and L-selective amino acid determination Column liquid chromatography Microwave hydrolysis Microcystin Nodularin D- and L-selective amino acid determination Summary Microwave radiation has been successfully used for hydrolysis of the hepatotoxic cyclic peptides microcystins and nodularin. Set-up of the microwave device and the operating conditions for microwave hydrolysis were optimized. Results of the microwave hydrolysis were compared with results from conventional hydrolysis for 24 h at 110°C. Microwave hydrolysis of microcystins and nodularin for as little as 10 min at 160°C results in complete cleavage of peptide bonds and high recoveries of amino acids. Enantioselective determination of amino acids was achieved by use of a previously described HPLC method after pre-column derivatization withortho-phthaldialdehyde and the chiral thiolN-iso-butyryl-cysteine. 1612-1112 16121112 Springer |
shingle_catch_all_2 | Reichelt, M. Hummert, C. Luckas, B. Hydrolysis of microcystins and nodularin by microwave radiation Column liquid chromatography Microwave hydrolysis Microcystin Nodularin D- and L-selective amino acid determination Column liquid chromatography Microwave hydrolysis Microcystin Nodularin D- and L-selective amino acid determination Summary Microwave radiation has been successfully used for hydrolysis of the hepatotoxic cyclic peptides microcystins and nodularin. Set-up of the microwave device and the operating conditions for microwave hydrolysis were optimized. Results of the microwave hydrolysis were compared with results from conventional hydrolysis for 24 h at 110°C. Microwave hydrolysis of microcystins and nodularin for as little as 10 min at 160°C results in complete cleavage of peptide bonds and high recoveries of amino acids. Enantioselective determination of amino acids was achieved by use of a previously described HPLC method after pre-column derivatization withortho-phthaldialdehyde and the chiral thiolN-iso-butyryl-cysteine. 1612-1112 16121112 Springer |
shingle_catch_all_3 | Reichelt, M. Hummert, C. Luckas, B. Hydrolysis of microcystins and nodularin by microwave radiation Column liquid chromatography Microwave hydrolysis Microcystin Nodularin D- and L-selective amino acid determination Column liquid chromatography Microwave hydrolysis Microcystin Nodularin D- and L-selective amino acid determination Summary Microwave radiation has been successfully used for hydrolysis of the hepatotoxic cyclic peptides microcystins and nodularin. Set-up of the microwave device and the operating conditions for microwave hydrolysis were optimized. Results of the microwave hydrolysis were compared with results from conventional hydrolysis for 24 h at 110°C. Microwave hydrolysis of microcystins and nodularin for as little as 10 min at 160°C results in complete cleavage of peptide bonds and high recoveries of amino acids. Enantioselective determination of amino acids was achieved by use of a previously described HPLC method after pre-column derivatization withortho-phthaldialdehyde and the chiral thiolN-iso-butyryl-cysteine. 1612-1112 16121112 Springer |
shingle_catch_all_4 | Reichelt, M. Hummert, C. Luckas, B. Hydrolysis of microcystins and nodularin by microwave radiation Column liquid chromatography Microwave hydrolysis Microcystin Nodularin D- and L-selective amino acid determination Column liquid chromatography Microwave hydrolysis Microcystin Nodularin D- and L-selective amino acid determination Summary Microwave radiation has been successfully used for hydrolysis of the hepatotoxic cyclic peptides microcystins and nodularin. Set-up of the microwave device and the operating conditions for microwave hydrolysis were optimized. Results of the microwave hydrolysis were compared with results from conventional hydrolysis for 24 h at 110°C. Microwave hydrolysis of microcystins and nodularin for as little as 10 min at 160°C results in complete cleavage of peptide bonds and high recoveries of amino acids. Enantioselective determination of amino acids was achieved by use of a previously described HPLC method after pre-column derivatization withortho-phthaldialdehyde and the chiral thiolN-iso-butyryl-cysteine. 1612-1112 16121112 Springer |
shingle_title_1 | Hydrolysis of microcystins and nodularin by microwave radiation |
shingle_title_2 | Hydrolysis of microcystins and nodularin by microwave radiation |
shingle_title_3 | Hydrolysis of microcystins and nodularin by microwave radiation |
shingle_title_4 | Hydrolysis of microcystins and nodularin by microwave radiation |
sigel_instance_filter | dkfz geomar wilbert ipn albert fhp |
source_archive | Springer Online Journal Archives 1860-2000 |
timestamp | 2024-05-06T10:06:14.466Z |
titel | Hydrolysis of microcystins and nodularin by microwave radiation |
titel_suche | Hydrolysis of microcystins and nodularin by microwave radiation |
topic | V |
uid | nat_lic_papers_NLM209137738 |