Microbiome Metabolic Engineering Theme, Carl R. Woese Institute for Genomic Biology, Urbana, Illinois, USA.
Department of Animal Sciences, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA.
Appl Environ Microbiol. 2018 May 1;84(10). doi: 10.1128/AEM.00235-18. Print 2018 May 15.
Bile acids are important cholesterol-derived nutrient signaling hormones, synthesized in the liver, that act as detergents to solubilize dietary lipids. Bile acid 7α-dehydroxylating gut bacteria generate the toxic bile acids deoxycholic acid and lithocholic acid from host bile acids. The ability of these bacteria to remove the 7-hydroxyl group is partially dependent on 7α-hydroxysteroid dehydrogenase (HSDH) activity, which reduces 7-oxo-bile acids generated by other gut bacteria. 3α-HSDH has an important enzymatic activity in the bile acid 7α-dehydroxylation pathway. 12α-HSDH activity has been reported for the low-activity bile acid 7α-dehydroxylating bacterium ; however, this activity has not been reported for high-activity bile acid 7α-dehydroxylating bacteria, such as , , and Here, we demonstrate that these strains express bile acid 12α-HSDH. The recombinant enzymes were characterized from each species and shown to preferentially reduce 12-oxolithocholic acid to deoxycholic acid, with low activity against 12-oxochenodeoxycholic acid and reduced activity when bile acids were conjugated to taurine or glycine. Phylogenetic analysis suggests that 12α-HSDH is widespread among , in the family, and human gut 12α-HSDH activity has been established in the medically important bile acid 7α-dehydroxylating bacteria , , and Experiments with recombinant 12α-HSDHs from these strains are consistent with culture-based experiments that show a robust preference for 12-oxolithocholic acid over 12-oxochenodeoxycholic acid. Phylogenetic analysis identified novel members of the gut microbiome encoding 12α-HSDH. Future reengineering of 12α-HSDH enzymes to preferentially oxidize cholic acid may provide a means to industrially produce the therapeutic bile acid ursodeoxycholic acid. In addition, a cholic acid-specific 12α-HSDH expressed in the gut may be useful for the reduction in deoxycholic acid concentration, a bile acid implicated in cancers of the gastrointestinal (GI) tract.
胆汁酸是一种重要的胆固醇衍生营养信号激素,在肝脏中合成,作为清洁剂溶解膳食脂质。胆汁酸 7α-脱羟肠道细菌将宿主胆汁酸转化为有毒胆汁酸脱氧胆酸和石胆酸。这些细菌去除 7-羟基的能力部分依赖于 7α-羟甾酮脱氢酶(HSDH)的活性,该酶降低其他肠道细菌产生的 7-氧代胆汁酸。3α-HSDH 在胆汁酸 7α-脱羟化途径中具有重要的酶活性。已经报道了低活性胆汁酸 7α-脱羟化细菌的 12α-HSDH 活性;然而,尚未报道高活性胆汁酸 7α-脱羟化细菌,如 、 、 和 。在这里,我们证明这些菌株表达胆汁酸 12α-HSDH。从每个物种中分离出重组酶并对其进行了表征,结果表明它们优先将 12-氧代石胆酸还原为脱氧胆酸,对 12-氧代鹅脱氧胆酸的活性较低,当胆汁酸与牛磺酸或甘氨酸结合时活性降低。系统发育分析表明,12α-HSDH 在 、 科的 中广泛存在,人类肠道中的 也存在 12α-HSDH 活性。在医学上重要的胆汁酸 7α-脱羟化细菌 、 、 和 中已经建立了 12α-HSDH 活性。这些菌株的重组 12α-HSDH 的实验与基于培养的实验一致,表明它们对 12-氧代石胆酸具有很强的偏好,而对 12-氧代鹅脱氧胆酸的偏好较弱。系统发育分析鉴定了肠道微生物组中编码 12α-HSDH 的新成员。未来对 12α-HSDH 酶的重新设计以优先氧化胆酸可能为工业生产治疗性胆汁酸熊去氧胆酸提供一种方法。此外,在肠道中表达的特异性胆汁酸 12α-HSDH 可能有助于降低与胃肠道(GI)癌有关的脱氧胆酸浓度。