Biology and function of the reversible sulfation pathway catalysed by human sulfotransferases and sulfatases
- PMID: 9566730
- DOI: 10.1016/s0009-2797(97)00117-8
Biology and function of the reversible sulfation pathway catalysed by human sulfotransferases and sulfatases
Abstract
Sulfation and sulfate conjugate hydrolysis play an important role in metabolism, and are catalysed by members of the sulfotransferase and sulfatase enzyme super-families. In general, sulfation is a deactivating, detoxication pathway, but for some chemicals the sulfate conjugates are much more reactive than the parent compound. The range of compounds which are sulfated is enormous, yet we still understand relatively little of the function of this pathway. This review summarises current knowledge of the sulfation system and the enzymes involved, and illustrates how heterologous expression of sulfotransferases (SULTs) and sulfatases is aiding our appreciation of the properties of these important proteins. The role of sulfation in the bioactivation of procarcinogens and promutagens is discussed, and new data on the inhibition of the sulfotransferase(s) involved by common dietary components such as tea and coffee are presented. The genetic and environmental factors which are known to influence the activity and expression of human SULTs and sulfatases are also reviewed.
Similar articles
-
Sulfotransferases and sulfatases in mycobacteria.Chem Biol. 2002 Jul;9(7):767-76. doi: 10.1016/s1074-5521(02)00175-8. Chem Biol. 2002. PMID: 12144918 Review.
-
24-hydroxycholesterol sulfation by human cytosolic sulfotransferases: formation of monosulfates and disulfates, molecular modeling, sulfatase sensitivity, and inhibition of liver x receptor activation.Drug Metab Dispos. 2009 Oct;37(10):2069-78. doi: 10.1124/dmd.108.025759. Epub 2009 Jul 9. Drug Metab Dispos. 2009. PMID: 19589875 Free PMC article.
-
Current status of the cytosolic sulfotransferases in the metabolic activation of promutagens and procarcinogens.Curr Drug Metab. 2000 Jul;1(1):1-30. doi: 10.2174/1389200003339234. Curr Drug Metab. 2000. PMID: 11467078 Review.
-
Sulfotransferases, sulfatases and formylglycine-generating enzymes: a sulfation fascination.Curr Opin Chem Biol. 2008 Oct;12(5):573-81. doi: 10.1016/j.cbpa.2008.06.018. Curr Opin Chem Biol. 2008. PMID: 18625336 Review.
-
Phytoestrogens are potent inhibitors of estrogen sulfation: implications for breast cancer risk and treatment.J Clin Endocrinol Metab. 2004 Apr;89(4):1779-87. doi: 10.1210/jc.2003-031631. J Clin Endocrinol Metab. 2004. PMID: 15070945
Cited by
-
Understanding catecholamine metabolism as a guide to the biochemical diagnosis of pheochromocytoma.Rev Endocr Metab Disord. 2001 Aug;2(3):297-311. doi: 10.1023/a:1011572617314. Rev Endocr Metab Disord. 2001. PMID: 11708294 Review. No abstract available.
-
Algal blooms in the ocean: hot spots for chemically mediated microbial interactions.Nat Rev Microbiol. 2024 Mar;22(3):138-154. doi: 10.1038/s41579-023-00975-2. Epub 2023 Oct 13. Nat Rev Microbiol. 2024. PMID: 37833328 Review.
-
Pre-ADMET studies of 5-(3',4'-dihydroxyphenyl)-γ-valerolactone, the bioactive intestinal metabolite of proanthocyanidins.Arch Pharm (Weinheim). 2025 Jan;358(1):e2400575. doi: 10.1002/ardp.202400575. Epub 2024 Nov 11. Arch Pharm (Weinheim). 2025. PMID: 39526505 Free PMC article.
-
Urine Metabolome during Parturition.Metabolites. 2020 Jul 16;10(7):290. doi: 10.3390/metabo10070290. Metabolites. 2020. PMID: 32708819 Free PMC article.
-
Detoxication versus Bioactivation Pathways of Lapatinib In Vitro: UGT1A1 Catalyzes the Hepatic Glucuronidation of Debenzylated Lapatinib.Drug Metab Dispos. 2021 Mar;49(3):233-244. doi: 10.1124/dmd.120.000236. Epub 2020 Dec 29. Drug Metab Dispos. 2021. PMID: 33376146 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources