Literature DB >> 26453144

The UDP-glycosyltransferase (UGT) superfamily expressed in humans, insects and plants: Animal-plant arms-race and co-evolution.

Karl Walter Bock1.   

Abstract

UDP-glycosyltransferases (UGTs) are major phase II enzymes of a detoxification system evolved in all kingdoms of life. Lipophilic endobiotics such as hormones and xenobiotics including phytoalexins and drugs are conjugated by vertebrates mainly with glucuronic acid, by invertebrates and plants mainly with glucose. Plant-herbivore arms-race has been the major driving force for evolution of large UGT and other enzyme superfamilies. The UGT superfamily is defined by a common protein structure and signature sequence of 44 amino acids responsible for binding the UDP moiety of the sugar donor. Plants developed toxic phytoalexins stored as glucosides. Upon herbivore attack these conjugates are converted to highly reactive compounds. In turn, animals developed large families of UGTs in their intestine and liver to detoxify these phytoalexins. Interestingly, phytoalexins, exemplified by quercetin glucuronides and glucosinolate-derived isocyanates, are known insect attractant pigments in plants, and antioxidants, anti-inflammatory and chemopreventive compounds of humans. It is to be anticipated that phytochemicals may provide a rich source in beneficial drugs.
Copyright © 2015. Published by Elsevier Inc.

Entities:  

Keywords:  Glucosinolates; Humans; Phytoalexins; Quercetin; Quercetin (PubChem CID: 5280343); Quercetin 3-O-glucuronide (PubChem CID: 5274585); Steviol (PubChem CID: 452967); Sulforaphane (PubChem CID: 5350); Sulforaphane glucosinolate (PubChem CID: 9548634); UDP-glycosyltransferases

Mesh:

Substances:

Year:  2015        PMID: 26453144     DOI: 10.1016/j.bcp.2015.10.001

Source DB:  PubMed          Journal:  Biochem Pharmacol        ISSN: 0006-2952            Impact factor:   5.858


  41 in total

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