Affiliation:
1. Department of Microbiology and Molecular Genetics and The UT Center for Antimicrobial Resistance and Microbial Genomics, McGovern Medical School, The University of Texas Health Science Center at Houston, Texas, USA
Abstract
ABSTRACT
Ethanolamine (EA) is a valuable source of carbon and/or nitrogen for bacteria capable of its catabolism. Because it is derived from the membrane phospholipid phosphatidylethanolamine, it is particularly prevalent in the gastrointestinal tract, which is membrane rich due to turnover of the intestinal epithelium and the resident microbiota. Intriguingly, many gut pathogens carry the
eut
(ethanolamine utilization) genes. EA utilization has been studied for about 50 years, with most of the early work occurring in just a couple of species of
Enterobacteriaceae
. Once the metabolic pathways and enzymes were characterized by biochemical approaches, genetic screens were used to map the various activities to the
eut
genes. With the rise of genomics, the diversity of bacteria containing the
eut
genes and surprising differences in
eut
gene content were recognized. Some species contain nearly 20 genes and encode many accessory proteins, while others contain only the core catabolic enzyme. Moreover, the
eut
genes are regulated by very different mechanisms, depending on the organism and the
eut
regulator encoded. In the last several years, exciting progress has been made in elucidating the complex regulatory mechanisms that govern
eut
gene expression. Furthermore, a new appreciation for how EA contributes to infection and colonization in the host is emerging. In addition to providing an overview of EA-related biology, this minireview will give special attention to these recent advances.
Funder
HHS | NIH | National Institute of Allergy and Infectious Diseases
Publisher
American Society for Microbiology
Cited by
111 articles.
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