Toxic isolectins from the mushroom Boletus venenatus
Ingestion of the mushroom Boletus venenatus causes a gastrointestinal syndrome, such as diarrhea. A family of isolectins ( B. venenatus lectins, BVLs) was isolated as the toxic principles from the mushroom. BVL ingestion resulted in fetal toxicity to mice and also caused diarrhea. Ingestion of the t...
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Veröffentlicht in: | Phytochemistry (Oxford) 2010-04, Vol.71 (5), p.648-657 |
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creator | Horibe, Masashi Kobayashi, Yuka Dohra, Hideo Morita, Tatsuya Murata, Takeomi Usui, Taichi Nakamura-Tsuruta, Sachiko Kamei, Masugu Hirabayashi, Jun Matsuura, Masanori Yamada, Mina Saikawa, Yoko Hashimoto, Kimiko Nakata, Masaya Kawagishi, Hirokazu |
description | Ingestion of the mushroom
Boletus venenatus causes a gastrointestinal syndrome, such as diarrhea. A family of isolectins (
B. venenatus lectins, BVLs) was isolated as the toxic principles from the mushroom. BVL ingestion resulted in fetal toxicity to mice and also caused diarrhea.
Ingestion of the toxic mushroom
Boletus venenatus causes a severe gastrointestinal syndrome, such as nausea, repetitive vomiting, diarrhea, and stomachache. A family of isolectins (
B. venenatus lectins, BVLs) was isolated as the toxic principles from the mushroom by successive 80% ammonium sulfate-precipitation, Super Q anion-exchange chromatography, and TSK-gel G3000SW gel filtration. Although BVLs showed a single band on SDS–PAGE, they were further divided into eight isolectins (BVL-1 to -8) by BioAssist Q anion-exchange chromatography. All the isolectins showed lectin activity and had very similar molecular weights as detected by matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF-MS) analysis. Among them, BVL-1 and -3 were further characterized with their complete amino acid sequences of 99 amino acids determined and found to be identical to each other. In the hemagglutination inhibition assay, both proteins failed to bind to any mono- or oligo-saccharides tested and showed the same sugar-binding specificity to glycoproteins. Among the glycoproteins examined, asialo-fetuin was the strongest inhibitor. The sugar-binding specificity of each isolectin was also analyzed by using frontal affinity chromatography and surface plasmon resonance analysis, indicating that they recognized
N-linked sugar chains, especially Galβ1
→
4GlcNAcβ1
→
4Manβ1
→
4GlcNAcβ1
→
4GlcNAc (Type II) residues in
N-linked sugar chains. BVLs ingestion resulted in fatal toxicity in mice upon intraperitoneal administration and caused diarrhea upon oral administration in rats. |
doi_str_mv | 10.1016/j.phytochem.2009.12.003 |
format | Article |
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Boletus venenatus causes a gastrointestinal syndrome, such as diarrhea. A family of isolectins (
B. venenatus lectins, BVLs) was isolated as the toxic principles from the mushroom. BVL ingestion resulted in fetal toxicity to mice and also caused diarrhea.
Ingestion of the toxic mushroom
Boletus venenatus causes a severe gastrointestinal syndrome, such as nausea, repetitive vomiting, diarrhea, and stomachache. A family of isolectins (
B. venenatus lectins, BVLs) was isolated as the toxic principles from the mushroom by successive 80% ammonium sulfate-precipitation, Super Q anion-exchange chromatography, and TSK-gel G3000SW gel filtration. Although BVLs showed a single band on SDS–PAGE, they were further divided into eight isolectins (BVL-1 to -8) by BioAssist Q anion-exchange chromatography. All the isolectins showed lectin activity and had very similar molecular weights as detected by matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF-MS) analysis. Among them, BVL-1 and -3 were further characterized with their complete amino acid sequences of 99 amino acids determined and found to be identical to each other. In the hemagglutination inhibition assay, both proteins failed to bind to any mono- or oligo-saccharides tested and showed the same sugar-binding specificity to glycoproteins. Among the glycoproteins examined, asialo-fetuin was the strongest inhibitor. The sugar-binding specificity of each isolectin was also analyzed by using frontal affinity chromatography and surface plasmon resonance analysis, indicating that they recognized
N-linked sugar chains, especially Galβ1
→
4GlcNAcβ1
→
4Manβ1
→
4GlcNAcβ1
→
4GlcNAc (Type II) residues in
N-linked sugar chains. BVLs ingestion resulted in fatal toxicity in mice upon intraperitoneal administration and caused diarrhea upon oral administration in rats.</description><identifier>ISSN: 0031-9422</identifier><identifier>EISSN: 1873-3700</identifier><identifier>DOI: 10.1016/j.phytochem.2009.12.003</identifier><identifier>PMID: 20096904</identifier><language>eng</language><publisher>Amsterdam: Elsevier Ltd</publisher><subject>Affinity chromatography ; Agaricales - chemistry ; agglutination tests ; alpha-Fetoproteins ; Amino Acid Sequence ; amino acid sequences ; Animals ; Asialoglycoproteins ; Biological and medical sciences ; Boletaceae ; Boletus ; Boletus venenatus ; Carbohydrates - chemistry ; Chemical constitution ; Diarrhea ; Diarrhea - chemically induced ; Electrophoresis, Polyacrylamide Gel ; erythrocytes ; Fetuins ; Fundamental and applied biological sciences. Psychology ; glycoproteins ; Glycoproteins - chemistry ; glycosidic linkages ; humans ; Lectin ; lectins ; Lectins - chemistry ; Lectins - isolation & purification ; Lectins - toxicity ; Lethal toxicity ; Mice ; molecular sequence data ; monosaccharides ; Mushroom ; Mycotoxins - chemistry ; Mycotoxins - isolation & purification ; Mycotoxins - toxicity ; oligosaccharides ; Plant Lectins - chemistry ; Plant Lectins - isolation & purification ; Plant Lectins - toxicity ; Plant physiology and development ; Purification ; Rats ; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</subject><ispartof>Phytochemistry (Oxford), 2010-04, Vol.71 (5), p.648-657</ispartof><rights>2009 Elsevier Ltd</rights><rights>2015 INIST-CNRS</rights><rights>Copyright 2009 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c615t-e9938c031ec7ed460e2bcff25fe4e76e1524862fb01ed3e60d352d29600ced8f3</citedby><cites>FETCH-LOGICAL-c615t-e9938c031ec7ed460e2bcff25fe4e76e1524862fb01ed3e60d352d29600ced8f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.phytochem.2009.12.003$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27929,27930,46000</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22611479$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20096904$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Horibe, Masashi</creatorcontrib><creatorcontrib>Kobayashi, Yuka</creatorcontrib><creatorcontrib>Dohra, Hideo</creatorcontrib><creatorcontrib>Morita, Tatsuya</creatorcontrib><creatorcontrib>Murata, Takeomi</creatorcontrib><creatorcontrib>Usui, Taichi</creatorcontrib><creatorcontrib>Nakamura-Tsuruta, Sachiko</creatorcontrib><creatorcontrib>Kamei, Masugu</creatorcontrib><creatorcontrib>Hirabayashi, Jun</creatorcontrib><creatorcontrib>Matsuura, Masanori</creatorcontrib><creatorcontrib>Yamada, Mina</creatorcontrib><creatorcontrib>Saikawa, Yoko</creatorcontrib><creatorcontrib>Hashimoto, Kimiko</creatorcontrib><creatorcontrib>Nakata, Masaya</creatorcontrib><creatorcontrib>Kawagishi, Hirokazu</creatorcontrib><title>Toxic isolectins from the mushroom Boletus venenatus</title><title>Phytochemistry (Oxford)</title><addtitle>Phytochemistry</addtitle><description>Ingestion of the mushroom
Boletus venenatus causes a gastrointestinal syndrome, such as diarrhea. A family of isolectins (
B. venenatus lectins, BVLs) was isolated as the toxic principles from the mushroom. BVL ingestion resulted in fetal toxicity to mice and also caused diarrhea.
Ingestion of the toxic mushroom
Boletus venenatus causes a severe gastrointestinal syndrome, such as nausea, repetitive vomiting, diarrhea, and stomachache. A family of isolectins (
B. venenatus lectins, BVLs) was isolated as the toxic principles from the mushroom by successive 80% ammonium sulfate-precipitation, Super Q anion-exchange chromatography, and TSK-gel G3000SW gel filtration. Although BVLs showed a single band on SDS–PAGE, they were further divided into eight isolectins (BVL-1 to -8) by BioAssist Q anion-exchange chromatography. All the isolectins showed lectin activity and had very similar molecular weights as detected by matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF-MS) analysis. Among them, BVL-1 and -3 were further characterized with their complete amino acid sequences of 99 amino acids determined and found to be identical to each other. In the hemagglutination inhibition assay, both proteins failed to bind to any mono- or oligo-saccharides tested and showed the same sugar-binding specificity to glycoproteins. Among the glycoproteins examined, asialo-fetuin was the strongest inhibitor. The sugar-binding specificity of each isolectin was also analyzed by using frontal affinity chromatography and surface plasmon resonance analysis, indicating that they recognized
N-linked sugar chains, especially Galβ1
→
4GlcNAcβ1
→
4Manβ1
→
4GlcNAcβ1
→
4GlcNAc (Type II) residues in
N-linked sugar chains. BVLs ingestion resulted in fatal toxicity in mice upon intraperitoneal administration and caused diarrhea upon oral administration in rats.</description><subject>Affinity chromatography</subject><subject>Agaricales - chemistry</subject><subject>agglutination tests</subject><subject>alpha-Fetoproteins</subject><subject>Amino Acid Sequence</subject><subject>amino acid sequences</subject><subject>Animals</subject><subject>Asialoglycoproteins</subject><subject>Biological and medical sciences</subject><subject>Boletaceae</subject><subject>Boletus</subject><subject>Boletus venenatus</subject><subject>Carbohydrates - chemistry</subject><subject>Chemical constitution</subject><subject>Diarrhea</subject><subject>Diarrhea - chemically induced</subject><subject>Electrophoresis, Polyacrylamide Gel</subject><subject>erythrocytes</subject><subject>Fetuins</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>glycoproteins</subject><subject>Glycoproteins - chemistry</subject><subject>glycosidic linkages</subject><subject>humans</subject><subject>Lectin</subject><subject>lectins</subject><subject>Lectins - chemistry</subject><subject>Lectins - isolation & purification</subject><subject>Lectins - toxicity</subject><subject>Lethal toxicity</subject><subject>Mice</subject><subject>molecular sequence data</subject><subject>monosaccharides</subject><subject>Mushroom</subject><subject>Mycotoxins - chemistry</subject><subject>Mycotoxins - isolation & purification</subject><subject>Mycotoxins - toxicity</subject><subject>oligosaccharides</subject><subject>Plant Lectins - chemistry</subject><subject>Plant Lectins - isolation & purification</subject><subject>Plant Lectins - toxicity</subject><subject>Plant physiology and development</subject><subject>Purification</subject><subject>Rats</subject><subject>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</subject><issn>0031-9422</issn><issn>1873-3700</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1P4zAQhi3ECrrs_gXIBXFKdvwRJzkCggUJaQ_bni3XGVNXSVzspIJ_j6sWOHLy1_OOZx5CLigUFKj8sy42q7fRmxX2BQNoCsoKAH5EZrSueM4rgGMySzc0bwRjp-RnjGsAKEspT8jpLiIbEDMi5v7VmcxF36EZ3RAzG3yfjSvM-imugk-Hm_Q2TjHb4oCDTrtf5IfVXcTfh_WMLO7v5rcP-dO_v4-310-5kbQcc2waXpvUA5oKWyEB2dJYy0qLAiuJtGSilswugWLLUULLS9ayRgIYbGvLz8jVvu4m-JcJ46h6Fw12nR7QT1FVQkgqoSkTWe1JE3yMAa3aBNfr8KYoqJ0xtVafxtRufEWZSn5S8vzwx7Tssf3MfShKwOUB0NHozgY9GBe_OCYpFVWTuIs9Z7VX-jkkZvGfAeVAa85Lvqt0vScwOds6DCoah0Oa1YUkX7XefdvuO3s-lxw</recordid><startdate>20100401</startdate><enddate>20100401</enddate><creator>Horibe, Masashi</creator><creator>Kobayashi, Yuka</creator><creator>Dohra, Hideo</creator><creator>Morita, Tatsuya</creator><creator>Murata, Takeomi</creator><creator>Usui, Taichi</creator><creator>Nakamura-Tsuruta, Sachiko</creator><creator>Kamei, Masugu</creator><creator>Hirabayashi, Jun</creator><creator>Matsuura, Masanori</creator><creator>Yamada, Mina</creator><creator>Saikawa, Yoko</creator><creator>Hashimoto, Kimiko</creator><creator>Nakata, Masaya</creator><creator>Kawagishi, Hirokazu</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>FBQ</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7U7</scope><scope>C1K</scope><scope>M7N</scope></search><sort><creationdate>20100401</creationdate><title>Toxic isolectins from the mushroom Boletus venenatus</title><author>Horibe, Masashi ; Kobayashi, Yuka ; Dohra, Hideo ; Morita, Tatsuya ; Murata, Takeomi ; Usui, Taichi ; Nakamura-Tsuruta, Sachiko ; Kamei, Masugu ; Hirabayashi, Jun ; Matsuura, Masanori ; Yamada, Mina ; Saikawa, Yoko ; Hashimoto, Kimiko ; Nakata, Masaya ; Kawagishi, Hirokazu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c615t-e9938c031ec7ed460e2bcff25fe4e76e1524862fb01ed3e60d352d29600ced8f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Affinity chromatography</topic><topic>Agaricales - chemistry</topic><topic>agglutination tests</topic><topic>alpha-Fetoproteins</topic><topic>Amino Acid Sequence</topic><topic>amino acid sequences</topic><topic>Animals</topic><topic>Asialoglycoproteins</topic><topic>Biological and medical sciences</topic><topic>Boletaceae</topic><topic>Boletus</topic><topic>Boletus venenatus</topic><topic>Carbohydrates - chemistry</topic><topic>Chemical constitution</topic><topic>Diarrhea</topic><topic>Diarrhea - chemically induced</topic><topic>Electrophoresis, Polyacrylamide Gel</topic><topic>erythrocytes</topic><topic>Fetuins</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>glycoproteins</topic><topic>Glycoproteins - chemistry</topic><topic>glycosidic linkages</topic><topic>humans</topic><topic>Lectin</topic><topic>lectins</topic><topic>Lectins - chemistry</topic><topic>Lectins - isolation & purification</topic><topic>Lectins - toxicity</topic><topic>Lethal toxicity</topic><topic>Mice</topic><topic>molecular sequence data</topic><topic>monosaccharides</topic><topic>Mushroom</topic><topic>Mycotoxins - chemistry</topic><topic>Mycotoxins - isolation & purification</topic><topic>Mycotoxins - toxicity</topic><topic>oligosaccharides</topic><topic>Plant Lectins - chemistry</topic><topic>Plant Lectins - isolation & purification</topic><topic>Plant Lectins - toxicity</topic><topic>Plant physiology and development</topic><topic>Purification</topic><topic>Rats</topic><topic>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Horibe, Masashi</creatorcontrib><creatorcontrib>Kobayashi, Yuka</creatorcontrib><creatorcontrib>Dohra, Hideo</creatorcontrib><creatorcontrib>Morita, Tatsuya</creatorcontrib><creatorcontrib>Murata, Takeomi</creatorcontrib><creatorcontrib>Usui, Taichi</creatorcontrib><creatorcontrib>Nakamura-Tsuruta, Sachiko</creatorcontrib><creatorcontrib>Kamei, Masugu</creatorcontrib><creatorcontrib>Hirabayashi, Jun</creatorcontrib><creatorcontrib>Matsuura, Masanori</creatorcontrib><creatorcontrib>Yamada, Mina</creatorcontrib><creatorcontrib>Saikawa, Yoko</creatorcontrib><creatorcontrib>Hashimoto, Kimiko</creatorcontrib><creatorcontrib>Nakata, Masaya</creatorcontrib><creatorcontrib>Kawagishi, Hirokazu</creatorcontrib><collection>AGRIS</collection><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>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><jtitle>Phytochemistry (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Horibe, Masashi</au><au>Kobayashi, Yuka</au><au>Dohra, Hideo</au><au>Morita, Tatsuya</au><au>Murata, Takeomi</au><au>Usui, Taichi</au><au>Nakamura-Tsuruta, Sachiko</au><au>Kamei, Masugu</au><au>Hirabayashi, Jun</au><au>Matsuura, Masanori</au><au>Yamada, Mina</au><au>Saikawa, Yoko</au><au>Hashimoto, Kimiko</au><au>Nakata, Masaya</au><au>Kawagishi, Hirokazu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Toxic isolectins from the mushroom Boletus venenatus</atitle><jtitle>Phytochemistry (Oxford)</jtitle><addtitle>Phytochemistry</addtitle><date>2010-04-01</date><risdate>2010</risdate><volume>71</volume><issue>5</issue><spage>648</spage><epage>657</epage><pages>648-657</pages><issn>0031-9422</issn><eissn>1873-3700</eissn><abstract>Ingestion of the mushroom
Boletus venenatus causes a gastrointestinal syndrome, such as diarrhea. A family of isolectins (
B. venenatus lectins, BVLs) was isolated as the toxic principles from the mushroom. BVL ingestion resulted in fetal toxicity to mice and also caused diarrhea.
Ingestion of the toxic mushroom
Boletus venenatus causes a severe gastrointestinal syndrome, such as nausea, repetitive vomiting, diarrhea, and stomachache. A family of isolectins (
B. venenatus lectins, BVLs) was isolated as the toxic principles from the mushroom by successive 80% ammonium sulfate-precipitation, Super Q anion-exchange chromatography, and TSK-gel G3000SW gel filtration. Although BVLs showed a single band on SDS–PAGE, they were further divided into eight isolectins (BVL-1 to -8) by BioAssist Q anion-exchange chromatography. All the isolectins showed lectin activity and had very similar molecular weights as detected by matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF-MS) analysis. Among them, BVL-1 and -3 were further characterized with their complete amino acid sequences of 99 amino acids determined and found to be identical to each other. In the hemagglutination inhibition assay, both proteins failed to bind to any mono- or oligo-saccharides tested and showed the same sugar-binding specificity to glycoproteins. Among the glycoproteins examined, asialo-fetuin was the strongest inhibitor. The sugar-binding specificity of each isolectin was also analyzed by using frontal affinity chromatography and surface plasmon resonance analysis, indicating that they recognized
N-linked sugar chains, especially Galβ1
→
4GlcNAcβ1
→
4Manβ1
→
4GlcNAcβ1
→
4GlcNAc (Type II) residues in
N-linked sugar chains. BVLs ingestion resulted in fatal toxicity in mice upon intraperitoneal administration and caused diarrhea upon oral administration in rats.</abstract><cop>Amsterdam</cop><pub>Elsevier Ltd</pub><pmid>20096904</pmid><doi>10.1016/j.phytochem.2009.12.003</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Affinity chromatography Agaricales - chemistry agglutination tests alpha-Fetoproteins Amino Acid Sequence amino acid sequences Animals Asialoglycoproteins Biological and medical sciences Boletaceae Boletus Boletus venenatus Carbohydrates - chemistry Chemical constitution Diarrhea Diarrhea - chemically induced Electrophoresis, Polyacrylamide Gel erythrocytes Fetuins Fundamental and applied biological sciences. Psychology glycoproteins Glycoproteins - chemistry glycosidic linkages humans Lectin lectins Lectins - chemistry Lectins - isolation & purification Lectins - toxicity Lethal toxicity Mice molecular sequence data monosaccharides Mushroom Mycotoxins - chemistry Mycotoxins - isolation & purification Mycotoxins - toxicity oligosaccharides Plant Lectins - chemistry Plant Lectins - isolation & purification Plant Lectins - toxicity Plant physiology and development Purification Rats Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization |
title | Toxic isolectins from the mushroom Boletus venenatus |
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