Affiliation:
1. Institut für Mikrobiologie und Weinforschung, Johannes Gutenberg-Universität, Becherweg 15, 55099 Mainz, Germany
Abstract
C
4
-dicarboxylates, like succinate, fumarate,
L
- and
D
-malate, tartrate, and the C
4
-dicarboxylic amino acid aspartate, support aerobic and anaerobic growth of
Escherichia coli
and related bacteria and can serve as carbon and energy sources. In aerobic growth, the C
4
-dicarboxylates are oxidized in the citric acid cycle. Due to the interruption of the citric acid cycle under anaerobic conditions, anaerobic metabolism of the C
4
-dicarboxylates depends on fumarate reduction to succinate. In some related bacteria (e.g.,
Klebsiella
), degradation of C
4
-dicarboxylates, like tartrate, uses a different mechanism and pathway. It requires the functioning of an Na
+
-dependent and membrane-associated oxaloacetate decarboxylase. Due to the incomplete function of the citric acid cycle in anaerobic growth, succinate supports only aerobic growth of
E. coli
. This chapter describes the pathways of and differences in aerobic and anaerobic C
4
-dicarboxylate metabolism and the physiological consequences. The citric acid cycle, fumarate respiration, and fumarate reductase are discussed here only in the context of aerobic and anaerobic C
4
-dicarboxylate metabolism. Some recent aspects of C
4
-dicarboxylate metabolism, such as transport and sensing of C
4
-dicarboxylates, and their relationships are treated in more detail.
Publisher
American Society for Microbiology
Cited by
14 articles.
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