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Identification and Characterization of the Dicarboxylate Uptake System DccT inCorynebacterium glutamicum
Author(s) -
Jung-Won Youn,
Elena Jolkver,
Reinhard Krämer,
Kay Marin,
Volker F. Wendisch
Publication year - 2008
Publication title -
journal of bacteriology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.652
H-Index - 246
eISSN - 1067-8832
pISSN - 0021-9193
DOI - 10.1128/jb.00780-08
Subject(s) - corynebacterium glutamicum , biology , mutant , fumarase , biochemistry , tricarboxylic acid , citric acid cycle , corynebacterium , succinic acid , symporter , bacteria , fumarate reductase , malate dehydrogenase , citrate synthase , succinate dehydrogenase , gene , metabolism , enzyme , transporter , genetics
Many bacteria can utilize C4 -carboxylates as carbon and energy sources. However,Corynebacterium glutamicum ATCC 13032 is not able to use tricarboxylic acid cycle intermediates such as succinate, fumarate, andl -malate as sole carbon sources. Upon prolonged incubation, spontaneous mutants which had gained the ability to grow on succinate, fumarate, andl -malate could be isolated. DNA microarray analysis showed higher mRNA levels of cg0277, which subsequently was nameddccT , in the mutants than in the wild type, and transcriptional fusion analysis revealed that a point mutation in the promoter region ofdccT was responsible for increased expression. The overexpression ofdccT was sufficient to enable theC. glutamicum wild type to grow on succinate, fumarate, andl -malate as the sole carbon sources. Biochemical analyses revealed that DccT, which is a member of the divalent anion/Na+ symporter family, catalyzes the effective uptake of dicarboxylates like succinate, fumarate,l -malate, and likely also oxaloacetate in a sodium-dependent manner.

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