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THE STRUCTURES OF KATANOSINS A AND B
1H and 13C NMR studies on katanosin A confirmed the presence of eight usual amino acid residues which were previously deduced by amino acid analysis and suggested the presence of β-hydroxyaspartic acid, β-hydroxyleucine and β-phenylserine residues. These amino acids were isolated and confirmed, incl...
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Published in: | Journal of antibiotics 1988/06/25, Vol.41(6), pp.719-725 |
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container_end_page | 725 |
container_issue | 6 |
container_start_page | 719 |
container_title | Journal of antibiotics |
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creator | KATO, TOSHIYUKI HINOO, HIROSHI TERUI, YOSHIHIRO KIKUCHI, JUN'KO SHOJI, JUN'ICHI |
description | 1H and 13C NMR studies on katanosin A confirmed the presence of eight usual amino acid residues which were previously deduced by amino acid analysis and suggested the presence of β-hydroxyaspartic acid, β-hydroxyleucine and β-phenylserine residues. These amino acids were isolated and confirmed, including their stereochemistries, by comparison with the respective authentic specimens. Stereochemistries of the usual amino acids were determined by comparing the L-leucylated amino acids with reference compounds by HPLC. Lithium borohydride reduction and chromic acid oxidation of katanosin A and alkali-treated katanosin A elucidated a lactone linkage between the C-terminal Ser and phenylserine residues. Edman degradation on alkali-treated katanosin A clarified the total amino acid sequence. The difference in katanosins A and B was determined to be replacement of Val in A by He in B. Thus, the structures of katanosins A and B were elucidated. |
doi_str_mv | 10.7164/antibiotics.41.719 |
format | article |
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These amino acids were isolated and confirmed, including their stereochemistries, by comparison with the respective authentic specimens. Stereochemistries of the usual amino acids were determined by comparing the L-leucylated amino acids with reference compounds by HPLC. Lithium borohydride reduction and chromic acid oxidation of katanosin A and alkali-treated katanosin A elucidated a lactone linkage between the C-terminal Ser and phenylserine residues. Edman degradation on alkali-treated katanosin A clarified the total amino acid sequence. The difference in katanosins A and B was determined to be replacement of Val in A by He in B. Thus, the structures of katanosins A and B were elucidated.</description><identifier>ISSN: 0021-8820</identifier><identifier>EISSN: 1881-1469</identifier><identifier>DOI: 10.7164/antibiotics.41.719</identifier><identifier>PMID: 3403365</identifier><identifier>CODEN: JANTAJ</identifier><language>eng</language><publisher>Tokyo: JAPAN ANTIBIOTICS RESEARCH ASSOCIATION</publisher><subject>Amino Acid Sequence ; Amino Acids - analysis ; Anti-Bacterial Agents - analysis ; Biological and medical sciences ; Chemical Phenomena ; Chemistry ; Depsipeptides ; General pharmacology ; Medical sciences ; Peptides - analysis ; Pharmacology. Drug treatments ; Physicochemical properties. Structure-activity relationships</subject><ispartof>The Journal of Antibiotics, 1988/06/25, Vol.41(6), pp.719-725</ispartof><rights>Japan Antibiotics Research Association</rights><rights>1989 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5529-165c34b0170ede9d1b2766fec830aaae4069aa6f65e4f3701d46cd5c4169873c3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,1882,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=6981085$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3403365$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>KATO, TOSHIYUKI</creatorcontrib><creatorcontrib>HINOO, HIROSHI</creatorcontrib><creatorcontrib>TERUI, YOSHIHIRO</creatorcontrib><creatorcontrib>KIKUCHI, JUN'KO</creatorcontrib><creatorcontrib>SHOJI, JUN'ICHI</creatorcontrib><title>THE STRUCTURES OF KATANOSINS A AND B</title><title>Journal of antibiotics</title><addtitle>J. Antibiot.</addtitle><description>1H and 13C NMR studies on katanosin A confirmed the presence of eight usual amino acid residues which were previously deduced by amino acid analysis and suggested the presence of β-hydroxyaspartic acid, β-hydroxyleucine and β-phenylserine residues. These amino acids were isolated and confirmed, including their stereochemistries, by comparison with the respective authentic specimens. Stereochemistries of the usual amino acids were determined by comparing the L-leucylated amino acids with reference compounds by HPLC. Lithium borohydride reduction and chromic acid oxidation of katanosin A and alkali-treated katanosin A elucidated a lactone linkage between the C-terminal Ser and phenylserine residues. Edman degradation on alkali-treated katanosin A clarified the total amino acid sequence. The difference in katanosins A and B was determined to be replacement of Val in A by He in B. Thus, the structures of katanosins A and B were elucidated.</description><subject>Amino Acid Sequence</subject><subject>Amino Acids - analysis</subject><subject>Anti-Bacterial Agents - analysis</subject><subject>Biological and medical sciences</subject><subject>Chemical Phenomena</subject><subject>Chemistry</subject><subject>Depsipeptides</subject><subject>General pharmacology</subject><subject>Medical sciences</subject><subject>Peptides - analysis</subject><subject>Pharmacology. Drug treatments</subject><subject>Physicochemical properties. 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Drug treatments</topic><topic>Physicochemical properties. Structure-activity relationships</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>KATO, TOSHIYUKI</creatorcontrib><creatorcontrib>HINOO, HIROSHI</creatorcontrib><creatorcontrib>TERUI, YOSHIHIRO</creatorcontrib><creatorcontrib>KIKUCHI, JUN'KO</creatorcontrib><creatorcontrib>SHOJI, JUN'ICHI</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of antibiotics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>KATO, TOSHIYUKI</au><au>HINOO, HIROSHI</au><au>TERUI, YOSHIHIRO</au><au>KIKUCHI, JUN'KO</au><au>SHOJI, JUN'ICHI</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>THE STRUCTURES OF KATANOSINS A AND B</atitle><jtitle>Journal of antibiotics</jtitle><addtitle>J. Antibiot.</addtitle><date>1988</date><risdate>1988</risdate><volume>41</volume><issue>6</issue><spage>719</spage><epage>725</epage><pages>719-725</pages><issn>0021-8820</issn><eissn>1881-1469</eissn><coden>JANTAJ</coden><abstract>1H and 13C NMR studies on katanosin A confirmed the presence of eight usual amino acid residues which were previously deduced by amino acid analysis and suggested the presence of β-hydroxyaspartic acid, β-hydroxyleucine and β-phenylserine residues. These amino acids were isolated and confirmed, including their stereochemistries, by comparison with the respective authentic specimens. Stereochemistries of the usual amino acids were determined by comparing the L-leucylated amino acids with reference compounds by HPLC. Lithium borohydride reduction and chromic acid oxidation of katanosin A and alkali-treated katanosin A elucidated a lactone linkage between the C-terminal Ser and phenylserine residues. Edman degradation on alkali-treated katanosin A clarified the total amino acid sequence. The difference in katanosins A and B was determined to be replacement of Val in A by He in B. Thus, the structures of katanosins A and B were elucidated.</abstract><cop>Tokyo</cop><pub>JAPAN ANTIBIOTICS RESEARCH ASSOCIATION</pub><pmid>3403365</pmid><doi>10.7164/antibiotics.41.719</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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language | eng |
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source | JSTAGE |
subjects | Amino Acid Sequence Amino Acids - analysis Anti-Bacterial Agents - analysis Biological and medical sciences Chemical Phenomena Chemistry Depsipeptides General pharmacology Medical sciences Peptides - analysis Pharmacology. Drug treatments Physicochemical properties. Structure-activity relationships |
title | THE STRUCTURES OF KATANOSINS A AND B |
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