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2.

Figure. From: Chemical transformation of xenobiotics by the human gut microbiota.

Human gut microbes metabolize xenobiotics. Themicroorganisms that inhabit the human gut alter the chemical structures of ingested compounds, including dietarycomponents, industrial chemicals, and drugs.These changes affect xenobiotic toxicity, biological activity, and bioavailability.The gutmicrobialenzymesresponsibleformanyofthesetransformationsarepoorlyunderstood.Me,methyl.

Nitzan Koppel, et al. Science. 2018;356(6344):eaag2770.
3.
Fig. 1

Fig. 1. From: Chemical transformation of xenobiotics by the human gut microbiota.

Identifying gut microbial genes that predict cardiac drug metabolism. (A) E. lenta reductive metabolism leads to cardiac drug inactivation. (B) A combination of culture-based studies, sequencing, and bioinformatics helped to identify microbial genes associated with digoxin metabolism in humans.

Nitzan Koppel, et al. Science. 2018;356(6344):eaag2770.
4.
Fig. 2

Fig. 2. From: Chemical transformation of xenobiotics by the human gut microbiota.

Uncovering gut microbial enzymes that convert dietary choline to disease-associated metabolites. (A) Choline is metabolized by a gut microbial-human co-metabolic pathway into the disease-associated metabolites trimethylamine (TMA) and trimethylamine N-oxide (TMAO). (B) A chemically guided, rational genome-mining effort enabled the identification and characterization of enzymes involved in gut microbial anaerobic choline metabolism.

Nitzan Koppel, et al. Science. 2018;356(6344):eaag2770.
5.
Fig. 3

Fig. 3. From: Chemical transformation of xenobiotics by the human gut microbiota.

Preventing drug reactivation and toxicity by inhibiting gut microbial enzymes. (A) Microbial cleavage of the glucuronidated drug conjugate of the cancer chemotherapeutic SN-38 leads to drug reactivation and toxicity within the gut. UDP, uridine diphosphate. (B) High-throughput screening identified specific inhibitors of bacterial β-glucuronidases. These compounds alleviated the GI toxicity associated with irinotecan metabolism. Et, ethyl.

Nitzan Koppel, et al. Science. 2018;356(6344):eaag2770.
6.
Fig. 4

Fig. 4. From: Chemical transformation of xenobiotics by the human gut microbiota.

Potential implications of understanding gut microbial xenobiotic metabolism. (A) Interfacing clinical studies and hypothesis-driven research in model systems is essential for elucidating the biological consequences of gut microbial xenobiotic metabolism. Incorporating a mechanistic understanding of microbial transformations, along with knowledge of host genetics and metabolism, could (B) inform personalized nutrition, (C) improve toxicological risk assessment, and (D) enable personalized medicine.

Nitzan Koppel, et al. Science. 2018;356(6344):eaag2770.

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