Synthesis of microbial signaling molecules and their stereochemistry-activity relationships.
Identifieur interne : 001651 ( Main/Exploration ); précédent : 001650; suivant : 001652Synthesis of microbial signaling molecules and their stereochemistry-activity relationships.
Auteurs : Arata Yajima [Japon]Source :
- Bioscience, biotechnology, and biochemistry [ 1347-6947 ] ; 2011.
Descripteurs français
- KwdFr :
- Bactériocines (pharmacologie), Bactériocines (synthèse chimique), Cétones (pharmacologie), Cétones (synthèse chimique), Diterpènes (pharmacologie), Diterpènes (synthèse chimique), Détection du quorum (MeSH), Phytophthora (effets des médicaments et des substances chimiques), Phytophthora (métabolisme), Relation structure-activité (MeSH), Rhizobium leguminosarum (effets des médicaments et des substances chimiques), Rhizobium leguminosarum (métabolisme), Stéréoisomérie (MeSH), Vibrio cholerae (effets des médicaments et des substances chimiques), Vibrio cholerae (métabolisme), Xanthomonadaceae (effets des médicaments et des substances chimiques), Xanthomonadaceae (métabolisme).
- MESH :
- effets des médicaments et des substances chimiques : Phytophthora, Rhizobium leguminosarum, Vibrio cholerae, Xanthomonadaceae.
- métabolisme : Phytophthora, Rhizobium leguminosarum, Vibrio cholerae, Xanthomonadaceae.
- pharmacologie : Bactériocines, Cétones, Diterpènes.
- synthèse chimique : Bactériocines, Cétones, Diterpènes.
- Détection du quorum, Relation structure-activité, Stéréoisomérie.
English descriptors
- KwdEn :
- Bacteriocins (chemical synthesis), Bacteriocins (pharmacology), Diterpenes (chemical synthesis), Diterpenes (pharmacology), Ketones (chemical synthesis), Ketones (pharmacology), Phytophthora (drug effects), Phytophthora (metabolism), Quorum Sensing (MeSH), Rhizobium leguminosarum (drug effects), Rhizobium leguminosarum (metabolism), Stereoisomerism (MeSH), Structure-Activity Relationship (MeSH), Vibrio cholerae (drug effects), Vibrio cholerae (metabolism), Xanthomonadaceae (drug effects), Xanthomonadaceae (metabolism).
- MESH :
- chemical , chemical synthesis : Bacteriocins, Diterpenes, Ketones.
- chemical , pharmacology : Bacteriocins, Diterpenes, Ketones.
- drug effects : Phytophthora, Rhizobium leguminosarum, Vibrio cholerae, Xanthomonadaceae.
- metabolism : Phytophthora, Rhizobium leguminosarum, Vibrio cholerae, Xanthomonadaceae.
- Quorum Sensing, Stereoisomerism, Structure-Activity Relationship.
Abstract
Microbial signaling molecules such as autoinducers and microbial hormones play important roles in intercellular communication in microorganisms. Information transfer between the individual cells of a microorganism is one of the most important biological events among them. Researchers often suffer from extremely low levels of microbial signaling molecule contents, which prevent them from understanding chemistry and biology of intercellular communication in microorganisms. Chemical synthesis is a powerful tool to obtain sufficient amounts of sample and to clarify the structure of a molecule. This review focuses on the synthesis and stereochemistry-bioactivity relationships of five microbial signaling molecules, Vibrio cholerae autoinducer-1 (CAI-1), AI-2 precursor (DPD), an acylhomoserine lactone from Rhizobium leguminosarum (small bacteriocin), a diffusible extracellular factor of Xanthomondas campestris pv. campestris, and Phytophthora mating hormone α1.
DOI: 10.1271/bbb.110283
PubMed: 21821958
Affiliations:
Links toward previous steps (curation, corpus...)
Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Synthesis of microbial signaling molecules and their stereochemistry-activity relationships.</title><author><name sortKey="Yajima, Arata" sort="Yajima, Arata" uniqKey="Yajima A" first="Arata" last="Yajima">Arata Yajima</name><affiliation wicri:level="3"><nlm:affiliation>Department of Fermentation Science, Faculty of Applied Biological Science, Tokyo University of Agriculture (NODAI), Setagaya-ku, Tokyo, Japan. ayaji@nodai.ac.jp</nlm:affiliation><country xml:lang="fr">Japon</country><wicri:regionArea>Department of Fermentation Science, Faculty of Applied Biological Science, Tokyo University of Agriculture (NODAI), Setagaya-ku, Tokyo</wicri:regionArea><placeName><settlement type="city">Tokyo</settlement><region type="région">Région de Kantō</region></placeName></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2011">2011</date><idno type="RBID">pubmed:21821958</idno><idno type="pmid">21821958</idno><idno type="doi">10.1271/bbb.110283</idno><idno type="wicri:Area/Main/Corpus">001652</idno><idno type="wicri:explorRef" wicri:stream="Main" wicri:step="Corpus" wicri:corpus="PubMed">001652</idno><idno type="wicri:Area/Main/Curation">001652</idno><idno type="wicri:explorRef" wicri:stream="Main" wicri:step="Curation">001652</idno><idno type="wicri:Area/Main/Exploration">001652</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Synthesis of microbial signaling molecules and their stereochemistry-activity relationships.</title><author><name sortKey="Yajima, Arata" sort="Yajima, Arata" uniqKey="Yajima A" first="Arata" last="Yajima">Arata Yajima</name><affiliation wicri:level="3"><nlm:affiliation>Department of Fermentation Science, Faculty of Applied Biological Science, Tokyo University of Agriculture (NODAI), Setagaya-ku, Tokyo, Japan. ayaji@nodai.ac.jp</nlm:affiliation><country xml:lang="fr">Japon</country><wicri:regionArea>Department of Fermentation Science, Faculty of Applied Biological Science, Tokyo University of Agriculture (NODAI), Setagaya-ku, Tokyo</wicri:regionArea><placeName><settlement type="city">Tokyo</settlement><region type="région">Région de Kantō</region></placeName></affiliation></author></analytic><series><title level="j">Bioscience, biotechnology, and biochemistry</title><idno type="eISSN">1347-6947</idno><imprint><date when="2011" type="published">2011</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Bacteriocins (chemical synthesis)</term><term>Bacteriocins (pharmacology)</term><term>Diterpenes (chemical synthesis)</term><term>Diterpenes (pharmacology)</term><term>Ketones (chemical synthesis)</term><term>Ketones (pharmacology)</term><term>Phytophthora (drug effects)</term><term>Phytophthora (metabolism)</term><term>Quorum Sensing (MeSH)</term><term>Rhizobium leguminosarum (drug effects)</term><term>Rhizobium leguminosarum (metabolism)</term><term>Stereoisomerism (MeSH)</term><term>Structure-Activity Relationship (MeSH)</term><term>Vibrio cholerae (drug effects)</term><term>Vibrio cholerae (metabolism)</term><term>Xanthomonadaceae (drug effects)</term><term>Xanthomonadaceae (metabolism)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Bactériocines (pharmacologie)</term><term>Bactériocines (synthèse chimique)</term><term>Cétones (pharmacologie)</term><term>Cétones (synthèse chimique)</term><term>Diterpènes (pharmacologie)</term><term>Diterpènes (synthèse chimique)</term><term>Détection du quorum (MeSH)</term><term>Phytophthora (effets des médicaments et des substances chimiques)</term><term>Phytophthora (métabolisme)</term><term>Relation structure-activité (MeSH)</term><term>Rhizobium leguminosarum (effets des médicaments et des substances chimiques)</term><term>Rhizobium leguminosarum (métabolisme)</term><term>Stéréoisomérie (MeSH)</term><term>Vibrio cholerae (effets des médicaments et des substances chimiques)</term><term>Vibrio cholerae (métabolisme)</term><term>Xanthomonadaceae (effets des médicaments et des substances chimiques)</term><term>Xanthomonadaceae (métabolisme)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="chemical synthesis" xml:lang="en"><term>Bacteriocins</term><term>Diterpenes</term><term>Ketones</term></keywords><keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en"><term>Bacteriocins</term><term>Diterpenes</term><term>Ketones</term></keywords><keywords scheme="MESH" qualifier="drug effects" xml:lang="en"><term>Phytophthora</term><term>Rhizobium leguminosarum</term><term>Vibrio cholerae</term><term>Xanthomonadaceae</term></keywords><keywords scheme="MESH" qualifier="effets des médicaments et des substances chimiques" xml:lang="fr"><term>Phytophthora</term><term>Rhizobium leguminosarum</term><term>Vibrio cholerae</term><term>Xanthomonadaceae</term></keywords><keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Phytophthora</term><term>Rhizobium leguminosarum</term><term>Vibrio cholerae</term><term>Xanthomonadaceae</term></keywords><keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Phytophthora</term><term>Rhizobium leguminosarum</term><term>Vibrio cholerae</term><term>Xanthomonadaceae</term></keywords><keywords scheme="MESH" qualifier="pharmacologie" xml:lang="fr"><term>Bactériocines</term><term>Cétones</term><term>Diterpènes</term></keywords><keywords scheme="MESH" qualifier="synthèse chimique" xml:lang="fr"><term>Bactériocines</term><term>Cétones</term><term>Diterpènes</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Quorum Sensing</term><term>Stereoisomerism</term><term>Structure-Activity Relationship</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Détection du quorum</term><term>Relation structure-activité</term><term>Stéréoisomérie</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Microbial signaling molecules such as autoinducers and microbial hormones play important roles in intercellular communication in microorganisms. Information transfer between the individual cells of a microorganism is one of the most important biological events among them. Researchers often suffer from extremely low levels of microbial signaling molecule contents, which prevent them from understanding chemistry and biology of intercellular communication in microorganisms. Chemical synthesis is a powerful tool to obtain sufficient amounts of sample and to clarify the structure of a molecule. This review focuses on the synthesis and stereochemistry-bioactivity relationships of five microbial signaling molecules, Vibrio cholerae autoinducer-1 (CAI-1), AI-2 precursor (DPD), an acylhomoserine lactone from Rhizobium leguminosarum (small bacteriocin), a diffusible extracellular factor of Xanthomondas campestris pv. campestris, and Phytophthora mating hormone α1.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">21821958</PMID><DateCompleted><Year>2012</Year><Month>01</Month><Day>17</Day></DateCompleted><DateRevised><Year>2011</Year><Month>08</Month><Day>26</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1347-6947</ISSN><JournalIssue CitedMedium="Internet"><Volume>75</Volume><Issue>8</Issue><PubDate><Year>2011</Year></PubDate></JournalIssue><Title>Bioscience, biotechnology, and biochemistry</Title><ISOAbbreviation>Biosci Biotechnol Biochem</ISOAbbreviation></Journal><ArticleTitle>Synthesis of microbial signaling molecules and their stereochemistry-activity relationships.</ArticleTitle><Pagination><MedlinePgn>1418-29</MedlinePgn></Pagination><Abstract><AbstractText>Microbial signaling molecules such as autoinducers and microbial hormones play important roles in intercellular communication in microorganisms. Information transfer between the individual cells of a microorganism is one of the most important biological events among them. Researchers often suffer from extremely low levels of microbial signaling molecule contents, which prevent them from understanding chemistry and biology of intercellular communication in microorganisms. Chemical synthesis is a powerful tool to obtain sufficient amounts of sample and to clarify the structure of a molecule. This review focuses on the synthesis and stereochemistry-bioactivity relationships of five microbial signaling molecules, Vibrio cholerae autoinducer-1 (CAI-1), AI-2 precursor (DPD), an acylhomoserine lactone from Rhizobium leguminosarum (small bacteriocin), a diffusible extracellular factor of Xanthomondas campestris pv. campestris, and Phytophthora mating hormone α1.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Yajima</LastName><ForeName>Arata</ForeName><Initials>A</Initials><AffiliationInfo><Affiliation>Department of Fermentation Science, Faculty of Applied Biological Science, Tokyo University of Agriculture (NODAI), Setagaya-ku, Tokyo, Japan. ayaji@nodai.ac.jp</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType><PublicationType UI="D016454">Review</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2011</Year><Month>08</Month><Day>07</Day></ArticleDate></Article><MedlineJournalInfo><Country>England</Country><MedlineTA>Biosci Biotechnol Biochem</MedlineTA><NlmUniqueID>9205717</NlmUniqueID><ISSNLinking>0916-8451</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="C525620">3-hydroxytridecan-4-one</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D001430">Bacteriocins</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D004224">Diterpenes</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D007659">Ketones</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="C504077">mating hormone alpha1, Phytophthora</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D001430" MajorTopicYN="N">Bacteriocins</DescriptorName><QualifierName UI="Q000138" MajorTopicYN="Y">chemical synthesis</QualifierName><QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D004224" MajorTopicYN="N">Diterpenes</DescriptorName><QualifierName UI="Q000138" MajorTopicYN="Y">chemical synthesis</QualifierName><QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D007659" MajorTopicYN="N">Ketones</DescriptorName><QualifierName UI="Q000138" MajorTopicYN="Y">chemical synthesis</QualifierName><QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010838" MajorTopicYN="N">Phytophthora</DescriptorName><QualifierName UI="Q000187" MajorTopicYN="N">drug effects</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D053038" MajorTopicYN="Y">Quorum Sensing</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D016961" MajorTopicYN="N">Rhizobium leguminosarum</DescriptorName><QualifierName UI="Q000187" MajorTopicYN="N">drug effects</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D013237" MajorTopicYN="N">Stereoisomerism</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D013329" MajorTopicYN="N">Structure-Activity Relationship</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D014734" MajorTopicYN="N">Vibrio cholerae</DescriptorName><QualifierName UI="Q000187" MajorTopicYN="N">drug effects</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D044166" MajorTopicYN="N">Xanthomonadaceae</DescriptorName><QualifierName UI="Q000187" MajorTopicYN="N">drug effects</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="entrez"><Year>2011</Year><Month>8</Month><Day>9</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2011</Year><Month>8</Month><Day>9</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2012</Year><Month>1</Month><Day>18</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">21821958</ArticleId><ArticleId IdType="pii">JST.JSTAGE/bbb/110283</ArticleId><ArticleId IdType="doi">10.1271/bbb.110283</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>Japon</li></country><region><li>Région de Kantō</li></region><settlement><li>Tokyo</li></settlement></list><tree><country name="Japon"><region name="Région de Kantō"><name sortKey="Yajima, Arata" sort="Yajima, Arata" uniqKey="Yajima A" first="Arata" last="Yajima">Arata Yajima</name></region></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Bois/explor/PhytophthoraV1/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 001651 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 001651 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien
|wiki= Bois
|area= PhytophthoraV1
|flux= Main
|étape= Exploration
|type= RBID
|clé= pubmed:21821958
|texte= Synthesis of microbial signaling molecules and their stereochemistry-activity relationships.
}}
Pour générer des pages wiki
HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Exploration/RBID.i -Sk "pubmed:21821958" \
| HfdSelect -Kh $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd \
| NlmPubMed2Wicri -a PhytophthoraV1
| This area was generated with Dilib version V0.6.38. |  |