The low affinity glucose transporter HxtB is also involved in glucose signalling and metabolism in Aspergillus nidulans

Reis TF dos, Benjamin M. Nitsche, Lima PBA de, Assis LJ de, Laura Mellado, Steven D. Harris, Vera Meyer, Santos RAC dos, Diego M. Riaño-Pachón, Laure Nicolas Annick Ries*, Gustavo H. Goldman

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

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>
Original languageEnglish
Number of pages0
JournalScientific Reports
Volume7
Issue number1
DOIs
Publication statusE-pub ahead of print - 31 Mar 2017

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