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<dc:creator>Laothanachareon, Thanaporm</dc:creator>
<dc:creator>Bruinsma, Lyon</dc:creator>
<dc:creator>Nijsse, Bart</dc:creator>
<dc:creator>Schonewille, Tom</dc:creator>
<dc:creator>Suarez Diez, Maria</dc:creator>
<dc:creator>Tamayo Ramos, Juan Antonio</dc:creator>
<dc:creator>Santos, Vitor AP Martins dos</dc:creator>
<dc:creator>Schaap, Peter J.</dc:creator>
<dc:date>2021-06</dc:date>
<dc:description>Aspergillus niger is the major industrial citrate producer worldwide. Export as well as&#xd;
uptake of citric acid are believed to occur by active, proton-dependent, symport systems. Both&#xd;
are major bottlenecks for industrial citrate production. Therefore, we assessed the consequences&#xd;
of deleting the citT gene encoding the A. niger citrate exporter, effectively blocking active citrate&#xd;
export. We followed the consumption of glucose and citrate as carbon sources, monitored the&#xd;
secretion of organic acids and carried out a thorough transcriptome pathway enrichment analysis.&#xd;
Under controlled cultivation conditions that normally promote citrate secretion, the knock-out strain&#xd;
secreted negligible amounts of citrate. Blocking active citrate export in this way led to a reduced&#xd;
glucose uptake and a reduced expression of high-affinity glucose transporter genes, mstG and mstH.&#xd;
The glyoxylate shunt was strongly activated and an increased expression of the OAH gene was&#xd;
observed, resulting in a more than two-fold higher concentration of oxalate in the medium. Deletion&#xd;
of citT did not affect citrate uptake suggesting that citrate export and citrate uptake are uncoupled&#xd;
from the system.</dc:description>
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<dc:identifier>http://hdl.handle.net/10259/5778</dc:identifier>
<dc:language>eng</dc:language>
<dc:publisher>MDPI</dc:publisher>
<dc:title>Global transcriptional response of aspergillus niger to blocked active citrate export through deletion of the exporter gene</dc:title>
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