Retroconversion of estrogens into androgens by bacteria via a cobalamin-mediated methylation.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 31848239.
- Also identified by DOI 10.1073/pnas.1914380117 and PMC identifier 6983444.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
Steroid estrogens modulate physiology and development of vertebrates. Conversion of C<sub>19</sub> androgens into C<sub>18</sub> estrogens is thought to be an irreversible reaction. Here, we report a denitrifying <i>Denitratisoma</i> sp. strain DHT3 capable of catabolizing estrogens or androgens anaerobically. Strain DHT3 genome contains a polycistronic gene cluster, <i>emtABCD</i>, differentially transcribed under estrogen-fed conditions and predicted to encode a cobalamin-dependent methyltransferase system conserved among estrogen-utilizing anaerobes; an <i>emtA</i>-disrupted DHT3 derivative could catabolize androgens but not estrogens. These data, along with the observed androgen production in estrogen-fed strain DHT3 cultures, suggested the occurrence of a cobalamin-dependent estrogen methylation to form androgens. Consistently, the estrogen conversion into androgens in strain DHT3 cell extracts requires methylcobalamin and is inhibited by propyl iodide, a specific inhibitor of cobalamin-dependent enzymes. The identification of the cobalamin-dependent estrogen methylation thus represents an unprecedented metabolic link between cobalamin and steroid metabolism and suggests that retroconversion of estrogens into androgens occurs in the biosphere.
Medical subject headings
- Androgens
- Bacterial Proteins
- Betaproteobacteria
- Estrogens
- Methyltransferases
- Vitamin B 12