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dc.contributor.authordos Reis, TF
dc.contributor.authorNitsche, BM
dc.contributor.authorde Lima, PBA
dc.contributor.authorde Assis, LJ
dc.contributor.authorMellado, L
dc.contributor.authorHarris, SD
dc.contributor.authorMeyer, V
dc.contributor.authordos Santos, RAC
dc.contributor.authorRiaño-Pachón, DM
dc.contributor.authorRies, LNA
dc.contributor.authorGoldman, GH
dc.date.accessioned2024-02-27T13:50:23Z
dc.date.available2024-02-27T13:50:23Z
dc.date.issued2017
dc.identifier.issn2045-2322
dc.identifier.issn2045-2322
dc.identifier.other45073
dc.identifier.urihttps://pearl.plymouth.ac.uk/handle/10026.1/22104
dc.description.abstract

<jats:title>Abstract</jats:title><jats:p>One of the drawbacks during second-generation biofuel production from plant lignocellulosic biomass is the accumulation of glucose, the preferred carbon source of microorganisms, which causes the repression of hydrolytic enzyme secretion by industrially relevant filamentous fungi. Glucose sensing, subsequent transport and cellular signalling pathways have been barely elucidated in these organisms. This study therefore characterized the transcriptional response of the filamentous fungus <jats:italic>Aspergillus nidulans</jats:italic> to the presence of high and low glucose concentrations under continuous chemostat cultivation with the aim to identify novel factors involved in glucose sensing and signalling. Several transcription factor- and transporter-encoding genes were identified as being differentially regulated, including the previously characterized glucose and xylose transporter HxtB. HxtB was confirmed to be a low affinity glucose transporter, localizing to the plasma membrane under low- and high-glucose conditions. Furthermore, HxtB was shown to be involved in conidiation-related processes and may play a role in downstream glucose signalling. A gene predicted to encode the protein kinase PskA was also identified as being important for glucose metabolism. This study identified several proteins with predicted roles in glucose metabolic processes and provides a foundation for further investigation into the response of biotechnologically important filamentous fungi to glucose.</jats:p>

dc.format.extent45073-
dc.format.mediumElectronic
dc.languageen
dc.publisherSpringer Science and Business Media LLC
dc.subjectAspergillus nidulans
dc.subjectCarbohydrate Metabolism
dc.subjectComputational Biology
dc.subjectCyclic AMP
dc.subjectCyclic AMP-Dependent Protein Kinases
dc.subjectGene Deletion
dc.subjectGene Expression Profiling
dc.subjectGene Expression Regulation, Fungal
dc.subjectGene Ontology
dc.subjectGlucose
dc.subjectGlucose Transport Proteins, Facilitative
dc.subjectPhenotype
dc.subjectProtein Binding
dc.subjectProtein Transport
dc.subjectSignal Transduction
dc.subjectTranscription, Genetic
dc.subjectras Proteins
dc.titleThe low affinity glucose transporter HxtB is also involved in glucose signalling and metabolism in Aspergillus nidulans
dc.typejournal-article
dc.typeArticle
plymouth.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/28361917
plymouth.issue1
plymouth.volume7
plymouth.publisher-urlhttp://dx.doi.org/10.1038/srep45073
plymouth.publication-statusPublished online
plymouth.journalScientific Reports
dc.identifier.doi10.1038/srep45073
plymouth.organisational-group|Plymouth
plymouth.organisational-group|Plymouth|Faculty of Health
plymouth.organisational-group|Plymouth|REF 2021 Researchers by UoA
plymouth.organisational-group|Plymouth|Users by role
plymouth.organisational-group|Plymouth|Users by role|Academics
plymouth.organisational-group|Plymouth|REF 2021 Researchers by UoA|UoA01 Clinical Medicine
plymouth.organisational-group|Plymouth|Faculty of Health|Peninsula Medical School
plymouth.organisational-group|Plymouth|Faculty of Health|School of Biomedical Sciences
plymouth.organisational-group|Plymouth|REF 2028 Researchers by UoA
plymouth.organisational-group|Plymouth|REF 2028 Researchers by UoA|UoA01 Clinical Medicine
dc.publisher.placeEngland
dcterms.dateAccepted2017-02-17
dc.date.updated2024-02-27T13:50:22Z
dc.identifier.eissn2045-2322
dc.rights.embargoperiodforever
rioxxterms.versionofrecord10.1038/srep45073


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