Retroconversion of estrogens into androgens by bacteria via a cobalamin-mediated methylation.

Wang, Po-Hsiang; Chen, Yi-Lung; Wei, Sean Ting-Shyang; Wu, Kan; Lee, Tzong-Huei; Wu, Tien-Yu; Chiang, Yin-Ru · Proc Natl Acad Sci U S A · 2020

basic_science · Level V

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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.

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