6533b856fe1ef96bd12b1c94
RESEARCH PRODUCT
DcuA of aerobically grownEscherichia coliserves as a nitrogen shuttle (L‐aspartate/fumarate) for nitrogen uptake
Christopher SchubertPhilipp Aloysius SteinmetzAlexander StreckerSandra ZedlerGottfried Undensubject
Glycerol0301 basic medicineendocrine system diseasesAntiporter030106 microbiologyMalateschemistry.chemical_elementBiologymedicine.disease_causeMicrobiology03 medical and health scienceschemistry.chemical_compoundBacterial ProteinsFumaratesAspartic acidEscherichia colimedicineGlycerolMolecular BiologyEscherichia coliDicarboxylic Acid TransportersAspartic AcidEscherichia coli Proteinsnutritional and metabolic diseasesBiological TransportTransporterbiology.organism_classificationNitrogen030104 developmental biologychemistryBiochemistryAnaerobic exercisehormones hormone substitutes and hormone antagonistsBacteriadescription
DcuA of Escherichia coli is known as an alternative C4 -dicarboxylate transporter for the main anaerobic C4 -dicarboxylate transporter DcuB. Since dcuA is expressed constitutively under aerobic and anaerobic conditions, DcuA was suggested to serve aerobically as a backup for the aerobic (DctA) transporter, or for the anabolic uptake of C4 -dicarboxylates. In this work, it is shown that DcuA is required for aerobic growth with L-aspartate as a nitrogen source, whereas for growth with L-aspartate as a carbon source, DctA was needed. Strains with DcuA catalyzed L-aspartate and C4 -dicarboxylate uptake (like DctA), or an L-aspartate/C4 -dicarboxylate antiport (unlike DctA). DcuA preferred L-aspartate to succinate in transport (KM = 43 and 844 µM, respectively), whereas DctA has higher affinity for C4 -dicarboxylates like succinate compared to L-aspartate. When L-aspartate was supplied as the sole nitrogen source together with glycerol as the carbon source, L-aspartate was taken up by the bacteria and fumarate (or L-malate) was excreted in equimolar amounts. Both reactions depended on DcuA. L-Aspartate was taken up in amounts required for nitrogen metabolism but not for carbon metabolism. Therefore, DcuA catalyzes an L-aspartate/C4 -dicarboxylate antiport serving as a nitrogen shuttle for nitrogen supply without net carbon supply.
year | journal | country | edition | language |
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2018-02-28 | Molecular Microbiology |