A Na+-coupled C4-dicarboxylate transporter (Asuc_0304) and aerobic growth of Actinobacillus succinogenes on C4-dicarboxylates
| Autor: | Ok Bin Kim, Sandra Zedler, Gottfried Unden, Hyo Eun Yoon, Mi Na Rhie, Hye Yun Oh |
|---|---|
| Rok vydání: | 2014 |
| Předmět: |
Molecular Sequence Data
medicine.disease_cause Models Biological Microbiology Divalent Bacterial Proteins Fumarates medicine Dicarboxylic Acids Amino Acid Sequence Anaerobiosis Carbon Radioisotopes Escherichia coli Phylogeny Dicarboxylic Acid Transporters chemistry.chemical_classification biology Sodium Biological Transport Succinates Actinobacillus Gene Expression Regulation Bacterial Fumarate reductase biology.organism_classification Aerobiosis Transport protein Actinobacillus succinogenes Glucose Biochemistry chemistry Symporter Fermentation Cotransporter Sequence Alignment |
| Zdroj: | Microbiology. 160:1533-1544 |
| ISSN: | 1465-2080 1350-0872 |
| DOI: | 10.1099/mic.0.076786-0 |
| Popis: | Actinobacillus succinogenes, which is known to produce large amounts of succinate during fermentation of hexoses, was able to grow on C4-dicarboxylates such as fumarate under aerobic and anaerobic conditions. Anaerobic growth on fumarate was stimulated by glycerol and the major product was succinate, indicating the involvement of fumarate respiration similar to succinate production from glucose. The aerobic growth on C4-dicarboxylates and the transport proteins involved were studied. Fumarate was oxidized to acetate. The genome of A. succinogenes encodes six proteins with similarity to secondary C4-dicarboxylate transporters, including transporters of the Dcu (C4-dicarboxylate uptake), DcuC (C4-dicarboxylate uptake C), DASS (divalent anion : sodium symporter) and TDT (tellurite resistance dicarboxylate transporter) family. From the cloned genes, Asuc_0304 of the DASS family protein was able to restore aerobic growth on C4-dicarboxylates in a C4-dicarboxylate-transport-negative Escherichia coli strain. The strain regained succinate or fumarate uptake, which was dependent on the electrochemical proton potential and the presence of Na+. The transport had an optimum pH ~7, indicating transport of the dianionic C4-dicarboxylates. Transport competition experiments suggested substrate specificity for fumarate and succinate. The transport characteristics for C4-dicarboxylate uptake by cells of aerobically grown A. succinogenes were similar to those of Asuc_0304 expressed in E. coli, suggesting that Asuc_0304 has an important role in aerobic fumarate uptake in A. succinogenes. Asuc_0304 has sequence similarity to bacterial Na+-dicarboxylate cotransporters and contains the carboxylate-binding signature. Asuc_0304 was named SdcA (sodium-coupled C4-dicarboxylate transporter from A . succinogenes). |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|