Hydrolysis of microcystins and nodularin by microwave radiation

Reichelt, M. ; Hummert, C. ; Luckas, B.
Springer
Published 1999
ISSN:
1612-1112
Keywords:
Column liquid chromatography ; Microwave hydrolysis ; Microcystin ; Nodularin ; D- and L-selective amino acid determination
Source:
Springer Online Journal Archives 1860-2000
Topics:
Chemistry and Pharmacology
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.
Type of Medium:
Electronic Resource
URL:
_version_ 1798297327971074049
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
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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