Deletion of pyruvate decarboxylase by a new method for efficient markerless gene deletions in Gluconobacter oxydans
Autor: | Wolfgang Liebl, Katharina Brauer, David Kostner, Bernadette Mühlthaler, Björn Peters, Armin Ehrenreich, Markus Mientus, Anja Junker |
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Rok vydání: | 2012 |
Předmět: |
DNA
Bacterial Genetics Microbial Gluconobacter oxydans Molecular Sequence Data Mutant Fructose Applied Microbiology and Biotechnology chemistry.chemical_compound Pyruvic Acid Mannitol Lactic Acid Acetic acid bacteria Molecular Biology Acetic Acid chemistry.chemical_classification Uracil phosphoribosyltransferase biology Acetaldehyde Sequence Analysis DNA General Medicine biology.organism_classification Enzyme chemistry Biochemistry Pyruvate Decarboxylase Gene Deletion Pyruvate decarboxylase Bacteria Biotechnology |
Zdroj: | Applied Microbiology and Biotechnology. 97:2521-2530 |
ISSN: | 1432-0614 0175-7598 |
DOI: | 10.1007/s00253-012-4354-z |
Popis: | Gluconobacter oxydans, a biotechnologically relevant species which incompletely oxidizes a large variety of carbohydrates, alcohols, and related compounds, contains a gene for pyruvate decarboxylase (PDC). This enzyme is found only in very few species of bacteria where it is normally involved in anaerobic ethanol formation via acetaldehyde. In order to clarify the role of PDC in the strictly oxidative metabolism of acetic acid bacteria, we developed a markerless in-frame deletion system for strain G. oxydans 621H which uses 5-fluorouracil together with a plasmid-encoded uracil phosphoribosyltransferase as counter selection method and used this technique to delete the PDC gene (GOX1081) of G. oxydans 621H. The PDC deletion mutant accumulated large amounts of pyruvate but almost no acetate during growth on D-mannitol, D-fructose or in the presence of L-lactate. This suggested that in G. oxydans acetate formation occurs by decarboxylation of pyruvate and subsequent oxidation of acetaldehyde to acetate. This observation and the efficiency of the markerless deletion system were confirmed by constructing deletion mutants of two acetaldehyde dehydrogenases (GOX1122 and GOX2018) and of the acetyl-CoA-synthetase (GOX0412). Acetate formation during growth of these mutants on mannitol did not differ significantly from the wild-type strain. |
Databáze: | OpenAIRE |
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