Redox-dependent interaction between thaumatin-like protein and β-glucan influences malting quality of barley.
Identifieur interne : 000078 ( Main/Exploration ); précédent : 000077; suivant : 000079Redox-dependent interaction between thaumatin-like protein and β-glucan influences malting quality of barley.
Auteurs : Surinder Singh [Canada] ; Rajiv K. Tripathi [Canada] ; Peggy G. Lemaux [États-Unis] ; Bob B. Buchanan [États-Unis] ; Jaswinder Singh [États-Unis]Source :
- Proceedings of the National Academy of Sciences of the United States of America [ 1091-6490 ] ; 2017.
Descripteurs français
- KwdFr :
- Chromosomes de plante (MeSH), Hordeum (génétique), Hordeum (physiologie), Locus de caractère quantitatif (MeSH), Oryza (génétique), Oxydoréduction (MeSH), Phylogenèse (MeSH), Protéines végétales (composition chimique), Protéines végétales (génétique), Protéines végétales (métabolisme), Régulation de l'expression des gènes végétaux (MeSH), Sites de fixation (MeSH), bêta-Glucanes (métabolisme).
- MESH :
- composition chimique : Protéines végétales.
- génétique : Hordeum, Oryza, Protéines végétales.
- métabolisme : Protéines végétales, bêta-Glucanes.
- physiologie : Hordeum.
- Chromosomes de plante, Locus de caractère quantitatif, Oxydoréduction, Phylogenèse, Régulation de l'expression des gènes végétaux, Sites de fixation.
English descriptors
- KwdEn :
- Binding Sites (MeSH), Chromosomes, Plant (MeSH), Gene Expression Regulation, Plant (MeSH), Hordeum (genetics), Hordeum (physiology), Oryza (genetics), Oxidation-Reduction (MeSH), Phylogeny (MeSH), Plant Proteins (chemistry), Plant Proteins (genetics), Plant Proteins (metabolism), Quantitative Trait Loci (MeSH), beta-Glucans (metabolism).
- MESH :
- chemical , chemistry : Plant Proteins.
- genetics : Hordeum, Oryza, Plant Proteins.
- chemical , metabolism : Plant Proteins, beta-Glucans.
- physiology : Hordeum.
- Binding Sites, Chromosomes, Plant, Gene Expression Regulation, Plant, Oxidation-Reduction, Phylogeny, Quantitative Trait Loci.
Abstract
Barley is the cornerstone of the malting and brewing industry. It is known that 250 quantitative trait loci (QTLs) of the grain are associated with 19 malting-quality phenotypes. However, only a few of the contributing genetic components have been identified. One of these, on chromosome 4H, contains a major malting QTL, QTL2, located near the telomeric region that accounts, respectively, for 28.9% and 37.6% of the variation in the β-glucan and extract fractions of malt. In the current study, we dissected the QTL2 region using an expression- and microsynteny-based approach. From a set of 22 expressed sequence tags expressed in seeds at the malting stage, we identified a candidate gene, TLP8 (thaumatin-like protein 8), which was differentially expressed and influenced malting quality. Transcript abundance and protein profiles of TLP8 were studied in different malt and feed varieties using quantitative PCR, immunoblotting, and enzyme-linked immunosorbent assay (ELISA). The experiments demonstrated that TLP8 binds to insoluble (1, 3, 1, 4)-β-D glucan in grain extracts, thereby facilitating the removal of this undesirable polysaccharide during malting. Further, the binding of TLP8 to β-glucan was dependent on redox. These findings represent a stride forward in our understanding of the malting process and provide a foundation for future improvements in the final beer-making process.
DOI: 10.1073/pnas.1701824114
PubMed: 28634304
PubMed Central: PMC5530668
Affiliations:
Links toward previous steps (curation, corpus...)
Le document en format XML
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It is known that 250 quantitative trait loci (QTLs) of the grain are associated with 19 malting-quality phenotypes. However, only a few of the contributing genetic components have been identified. One of these, on chromosome 4H, contains a major malting QTL, QTL2, located near the telomeric region that accounts, respectively, for 28.9% and 37.6% of the variation in the β-glucan and extract fractions of malt. In the current study, we dissected the QTL2 region using an expression- and microsynteny-based approach. From a set of 22 expressed sequence tags expressed in seeds at the malting stage, we identified a candidate gene, <i>TLP8</i> (<i>thaumatin-like protein 8</i>), which was differentially expressed and influenced malting quality. Transcript abundance and protein profiles of <i>TLP8</i> were studied in different malt and feed varieties using quantitative PCR, immunoblotting, and enzyme-linked immunosorbent assay (ELISA). The experiments demonstrated that TLP8 binds to insoluble (1, 3, 1, 4)-β-D glucan in grain extracts, thereby facilitating the removal of this undesirable polysaccharide during malting. Further, the binding of TLP8 to β-glucan was dependent on redox. These findings represent a stride forward in our understanding of the malting process and provide a foundation for future improvements in the final beer-making process.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">28634304</PMID><DateCompleted><Year>2018</Year><Month>05</Month><Day>24</Day></DateCompleted><DateRevised><Year>2018</Year><Month>11</Month><Day>13</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1091-6490</ISSN><JournalIssue CitedMedium="Internet"><Volume>114</Volume><Issue>29</Issue><PubDate><Year>2017</Year><Month>07</Month><Day>18</Day></PubDate></JournalIssue><Title>Proceedings of the National Academy of Sciences of the United States of America</Title><ISOAbbreviation>Proc Natl Acad Sci U S A</ISOAbbreviation></Journal><ArticleTitle>Redox-dependent interaction between thaumatin-like protein and β-glucan influences malting quality of barley.</ArticleTitle><Pagination><MedlinePgn>7725-7730</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1073/pnas.1701824114</ELocationID><Abstract><AbstractText>Barley is the cornerstone of the malting and brewing industry. It is known that 250 quantitative trait loci (QTLs) of the grain are associated with 19 malting-quality phenotypes. However, only a few of the contributing genetic components have been identified. One of these, on chromosome 4H, contains a major malting QTL, QTL2, located near the telomeric region that accounts, respectively, for 28.9% and 37.6% of the variation in the β-glucan and extract fractions of malt. In the current study, we dissected the QTL2 region using an expression- and microsynteny-based approach. From a set of 22 expressed sequence tags expressed in seeds at the malting stage, we identified a candidate gene, <i>TLP8</i> (<i>thaumatin-like protein 8</i>), which was differentially expressed and influenced malting quality. Transcript abundance and protein profiles of <i>TLP8</i> were studied in different malt and feed varieties using quantitative PCR, immunoblotting, and enzyme-linked immunosorbent assay (ELISA). The experiments demonstrated that TLP8 binds to insoluble (1, 3, 1, 4)-β-D glucan in grain extracts, thereby facilitating the removal of this undesirable polysaccharide during malting. Further, the binding of TLP8 to β-glucan was dependent on redox. These findings represent a stride forward in our understanding of the malting process and provide a foundation for future improvements in the final beer-making process.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Singh</LastName><ForeName>Surinder</ForeName><Initials>S</Initials><AffiliationInfo><Affiliation>Plant Science Department, McGill University, Montreal, QC H9X 3V9, Canada.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Tripathi</LastName><ForeName>Rajiv K</ForeName><Initials>RK</Initials><AffiliationInfo><Affiliation>Plant Science Department, McGill University, Montreal, QC H9X 3V9, Canada.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Lemaux</LastName><ForeName>Peggy G</ForeName><Initials>PG</Initials><AffiliationInfo><Affiliation>Department of Plant and Microbial Biology, University of California, Berkeley, CA 94720.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Buchanan</LastName><ForeName>Bob B</ForeName><Initials>BB</Initials><AffiliationInfo><Affiliation>Department of Plant and Microbial Biology, University of California, Berkeley, CA 94720 view@berkeley.edu jaswinder.singh@mcgill.ca.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Singh</LastName><ForeName>Jaswinder</ForeName><Initials>J</Initials><AffiliationInfo><Affiliation>Plant Science Department, McGill University, Montreal, QC H9X 3V9, Canada; view@berkeley.edu jaswinder.singh@mcgill.ca.</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="D013486">Research Support, U.S. Gov't, Non-P.H.S.</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2017</Year><Month>06</Month><Day>20</Day></ArticleDate></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>Proc Natl Acad Sci U S A</MedlineTA><NlmUniqueID>7505876</NlmUniqueID><ISSNLinking>0027-8424</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D010940">Plant Proteins</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D047071">beta-Glucans</NameOfSubstance></Chemical><Chemical><RegistryNumber>53850-34-3</RegistryNumber><NameOfSubstance UI="C003427">thaumatin protein, plant</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D001665" MajorTopicYN="N">Binding Sites</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D032461" MajorTopicYN="N">Chromosomes, Plant</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D018506" MajorTopicYN="N">Gene Expression Regulation, Plant</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D001467" MajorTopicYN="N">Hordeum</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D012275" MajorTopicYN="N">Oryza</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010084" MajorTopicYN="N">Oxidation-Reduction</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D010802" MajorTopicYN="N">Phylogeny</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D010940" MajorTopicYN="N">Plant Proteins</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName><QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D040641" MajorTopicYN="N">Quantitative Trait Loci</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D047071" MajorTopicYN="N">beta-Glucans</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading></MeshHeadingList><KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="Y">Hordeum vulgare</Keyword><Keyword MajorTopicYN="Y">malting</Keyword><Keyword MajorTopicYN="Y">quantitative trait loci</Keyword><Keyword MajorTopicYN="Y">thaumatin-like protein</Keyword><Keyword MajorTopicYN="Y">β-glucan</Keyword></KeywordList><CoiStatement>The authors declare no conflict of interest.</CoiStatement></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>2017</Year><Month>6</Month><Day>22</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate 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Tripathi</name></country><country name="États-Unis"><region name="Californie"><name sortKey="Lemaux, Peggy G" sort="Lemaux, Peggy G" uniqKey="Lemaux P" first="Peggy G" last="Lemaux">Peggy G. Lemaux</name></region><name sortKey="Buchanan, Bob B" sort="Buchanan, Bob B" uniqKey="Buchanan B" first="Bob B" last="Buchanan">Bob B. Buchanan</name><name sortKey="Singh, Jaswinder" sort="Singh, Jaswinder" uniqKey="Singh J" first="Jaswinder" last="Singh">Jaswinder Singh</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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