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Academic Journal
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van Dongen KCW; Division of Toxicology, Wageningen University and Research, P.O. Box 8000, Wageningen 6700 EA, The Netherlands.
Belzer C; Laboratory of Microbiology, Wageningen University and Research, P.O. Box 8033, Wageningen 6700 EH, The Netherlands.
Bakker W; Division of Toxicology, Wageningen University and Research, P.O. Box 8000, Wageningen 6700 EA, The Netherlands.
Rietjens IMCM; Division of Toxicology, Wageningen University and Research, P.O. Box 8000, Wageningen 6700 EA, The Netherlands.
Beekmann K; Wageningen Food Safety Research (WFSR), Part of Wageningen University and Research, P.O. Box 230, Wageningen 700 AE, The Netherlands. -
Journal of agricultural and food chemistry [J Agric Food Chem] 2022 Sep 21; Vol. 70 (37), pp. 11759-11768. Date of Electronic Publication: 2022 Sep 07.
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English
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The advanced glycation endproduct carboxymethyllysine and its precursor fructoselysine are present in heated, processed food products and are considered potentially hazardous for human health. Upon dietary exposure, they can be degraded by human colonic gut microbiota, reducing internal exposure. Pronounced interindividual and intraindividual differences in these metabolic degradations were found in anaerobic incubations with human fecal slurries in vitro. The average capacity to degrade fructoselysine was 27.7-fold higher than that for carboxymethyllysine, and degradation capacities for these two compounds were not correlated ( R 2 = 0.08). Analysis of the bacterial composition revealed that interindividual differences outweighed intraindividual differences, and multiple genera were correlated with the individuals' carboxymethyllysine and fructoselysine degradation capacities (e.g., Akkermansia , Alistipes ).
Additional Information
Publisher: American Chemical Society Country of Publication: United States NLM ID: 0374755 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1520-5118 (Electronic) Linking ISSN: 00218561 NLM ISO Abbreviation: J Agric Food Chem Subsets: MEDLINE
Original Publication: Washington, American Chemical Society.
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Nucleic Acids Res. 2013 Jan;41(Database issue):D590-6. (PMID: 23193283)
PLoS Biol. 2019 Jan 23;17(1):e3000102. (PMID: 30673701)
Mol Nutr Food Res. 2017 Oct;61(10):. (PMID: 28621836)
Toxicol In Vitro. 2021 Apr;72:105078. (PMID: 33429044)
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PLoS One. 2013;8(2):e57923. (PMID: 23460914)
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Front Genet. 2020 Jan 23;10:1366. (PMID: 32117417)
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Nat Commun. 2015 Dec 01;6:10062. (PMID: 26620920)
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Food Res Int. 2021 Sep;147:110547. (PMID: 34399524)
Bioinformatics. 2004 Jan 22;20(2):289-90. (PMID: 14734327)
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Food Chem Toxicol. 2022 Jun;164:112987. (PMID: 35398182)
J Biol Chem. 1986 Apr 15;261(11):4889-94. (PMID: 3082871)
Nature. 2018 Mar 8;555(7695):210-215. (PMID: 29489753)
Keywords: 16S rRNA analysis; advanced glycation end product; human gut microbiota; interindividual differences; intraindividual differences; new approach methodologies; temporal variability
0 (Glycation End Products, Advanced)
0 (RNA, Ribosomal, 16S)
21291-40-7 (fructosyl-lysine)
70YDX3Z2O7 (N(6)-carboxymethyllysine)
K3Z4F929H6 (Lysine)
0 (RNA, Ribosomal, 16S)
21291-40-7 (fructosyl-lysine)
70YDX3Z2O7 (N(6)-carboxymethyllysine)
K3Z4F929H6 (Lysine)
Date Created: 20220907 Date Completed: 20220923 Latest Revision: 20220928
20221216
PMC9501902
10.1021/acs.jafc.2c05756
36069406