FEBS Letters · 2004 · 45 citations · 22 references
Life SciencesBiochemistryMicrobiologyEnzymologyMicrobial GeneticsMicrobial MetabolismCitric Acid CycleLactic Acid BacteriaLactic Acid FermentationMalic Acid MetabolismMetabolic Pathways In FermentationCatalytic ResiduesCitrate MetabolismDecarboxylase EnzymesEnzyme Activity During FermentationEscherichia ColiMalate DecarboxylationMalate DehydrogenaseMicrobial Enzyme Function
The citM gene from Lactococcus lactis CRL264 was demonstrated to encode for an oxaloacetate decarboxylase. The enzyme exhibits high levels of similarity to malic enzymes (MEs) from other organisms. CitM was expressed in Escherichia coli, purified and its oxaloacetate decarboxylase activity was demonstrated by biochemical and genetic studies. The highest oxaloacetate decarboxylation activity was found at low pH in the presence of manganese, and the Km value for oxaloacetate was 0.52+/-0.03 mM. However, no malic activity was found for this enzyme. Our studies clearly show a new group of oxaloacetate decarboxylases associated with the citrate fermentation pathway in gram-positive bacteria. Furthermore, the essential catalytic residues were found to be conserved in all members of the ME family, suggesting a common mechanism for oxaloacetate decarboxylation.
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Julie Thompson, Desmond G. Higgins, Toby J. Gibson · Nucleic Acids Research · 1994 · 64.9K citations · Full text
The use of gene clusters to infer functional coupling
Ross Overbeek, Michael Fonstein, Mark D’Souza et al. · Proceedings of the National Academy of Sciences · 1999 · 1.3K citations
Two plasmid-determined restriction and modification systems in Streptococcus lactis
Alain Chopin, Marie‐Christine Chopin, A Moillo-Batt et al. · Plasmid · 1984 · 406 citations