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Deletion of pyruvate decarboxylase by a new method for efficient markerless gene deletions in Gluconobacter oxydans

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 an...

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Published in:Applied microbiology and biotechnology 2013-03, Vol.97 (6), p.2521-2530
Main Authors: Peters, Björn, Junker, Anja, Brauer, Katharina, Mühlthaler, Bernadette, Kostner, David, Mientus, Markus, Liebl, Wolfgang, Ehrenreich, Armin
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container_title Applied microbiology and biotechnology
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creator Peters, Björn
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description 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.
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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). 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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.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><pmid>22940799</pmid><doi>10.1007/s00253-012-4354-z</doi><tpages>10</tpages></addata></record>
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subjects Acetic acid
Acetic Acid - metabolism
Antibiotics
Applied Genetics and Molecular Biotechnology
Bacteria
Bacterial genetics
Biomedical and Life Sciences
Biotechnology
Carbohydrates
Chemicals
Dehydrogenases
DNA, Bacterial - chemistry
DNA, Bacterial - genetics
E coli
Enzymes
Ethanol
Fructose - metabolism
Gene Deletion
Gene expression
Genes
Genetic aspects
Genetics
Genetics, Microbial - methods
Gluconobacter oxydans
Gluconobacter oxydans - enzymology
Gluconobacter oxydans - genetics
Gram-negative bacteria
Lactic Acid - metabolism
Life Sciences
Mannitol - metabolism
Metabolism
Metabolites
Microbial Genetics and Genomics
Microbiology
Molecular Biology - methods
Molecular Sequence Data
Mutagenesis
Physiological aspects
Plasmids
Pyruvate Decarboxylase - genetics
Pyruvates
Pyruvic Acid - metabolism
Sequence Analysis, DNA
Studies
title Deletion of pyruvate decarboxylase by a new method for efficient markerless gene deletions in Gluconobacter oxydans
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