Two Pathways for Glutamate Biosynthesis in the Syntrophic Bacterium Syntrophus aciditrophicus
Autor: | Michael J. McInerney, Wolfgang Buckel, Yinjie J. Tang, Marie Kim, Housna Mouttaki, Xueyang Feng, Huynh M. Le, Xiulan Xie |
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Jazyk: | angličtina |
Rok vydání: | 2015 |
Předmět: |
Syntrophus aciditrophicus
Deltaproteobacteria Magnetic Resonance Spectroscopy Decarboxylation Physiology Succinic Acid Glutamic Acid Hydroxybutyrates Citrate (si)-Synthase Acetates medicine.disease_cause Applied Microbiology and Biotechnology Methanospirillum Acetyl Coenzyme A medicine Citrate synthase Hydro-Lyases Alanine chemistry.chemical_classification Ecology biology Clostridium kluyveri Glutamic acid biology.organism_classification Amino acid chemistry Biochemistry biology.protein Microbial Interactions Acyl Coenzyme A Oxidation-Reduction Metabolic Networks and Pathways Food Science Biotechnology |
Popis: | The anaerobic metabolism of crotonate, benzoate, and cyclohexane carboxylate by Syntrophus aciditrophicus grown syntrophically with Methanospirillum hungatei provides a model to study syntrophic cooperation. Recent studies revealed that S. aciditrophicus contains Re -citrate synthase but lacks the common Si -citrate synthase. To establish whether the Re -citrate synthase is involved in glutamate synthesis via the oxidative branch of the Krebs cycle, we have used [1- 13 C]acetate and [1- 14 C]acetate as well as [ 13 C]bicarbonate as additional carbon sources during axenic growth of S. aciditrophicus on crotonate. Our analyses showed that labeled carbons were detected in at least 14 amino acids, indicating the global utilization of acetate and bicarbonate. The labeling patterns of alanine and aspartate verified that pyruvate and oxaloacetate were synthesized by consecutive carboxylations of acetyl coenzyme A (acetyl-CoA). The isotopomer profile and 13 C nuclear magnetic resonance (NMR) spectroscopy of the obtained [ 13 C]glutamate, as well as decarboxylation of [ 14 C]glutamate, revealed that this amino acid was synthesized by two pathways. Unexpectedly, only the minor route used Re -citrate synthase (30 to 40%), whereas the majority of glutamate was synthesized via the reductive carboxylation of succinate. This symmetrical intermediate could have been formed from two acetates via hydration of crotonyl-CoA to 4-hydroxybutyryl-CoA. 4-Hydroxybutyrate was detected in the medium of S. aciditrophicus when grown on crotonate, but an active hydratase could not be measured in cell extracts, and the annotated 4-hydroxybutyryl-CoA dehydratase (SYN_02445) lacks key amino acids needed to catalyze the hydration of crotonyl-CoA. Besides Clostridium kluyveri , this study reveals the second example of a microbial species to employ two pathways for glutamate synthesis. |
Databáze: | OpenAIRE |
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