PLANT BIOCHEMISTRY OF XENOBIOTICS - ISOLATION AND CHARACTERIZATION OFA SOYBEAN O-GLUCOSYLTRANSFERASE OF DDT METABOLISM

Citation
A. Wetzel et H. Sandermann, PLANT BIOCHEMISTRY OF XENOBIOTICS - ISOLATION AND CHARACTERIZATION OFA SOYBEAN O-GLUCOSYLTRANSFERASE OF DDT METABOLISM, Archives of biochemistry and biophysics, 314(2), 1994, pp. 323-328
Citations number
24
Categorie Soggetti
Biology,Biophysics
ISSN journal
00039861
Volume
314
Issue
2
Year of publication
1994
Pages
323 - 328
Database
ISI
SICI code
0003-9861(1994)314:2<323:PBOX-I>2.0.ZU;2-H
Abstract
The insecticide DDT is metabolized in soybean and wheat cell cultures to the acylglucoside of 2,2-bis-(4-chlorophenyl)-acetic acid (DDA) (M. Arjmand and H. Sandermann, 1985, Pesticide Biochem. Physiol. 23, 389- 397). An enzyme catalyzing the conjugation reaction has been highly pu rified from the soluble enzyme fraction of cultured soybean cells. Aft er the initial ammonium sulfate fractionation, quercetin and pentachlo rophenol were preferentially glucosylated. In the course of 367-fold p urification, DDA became the preferred substrate. The purified enzyme w as unstable. A molecular weight of similar to 50 kDa was estimated for the native enzyme (gel permeation chromatography) as well as the dena tured protein (sodium dodecyl sulfate-gel electrophoresis). The isoele ctric point for the enzyme was near pH 4.9. Apparent K-m values of abo ut 170 mu M were determined for UDP-glucose as well as DDA. The maxima l velocity was 257 mu kat/kg protein, corresponding to a conjugation c apacity of 855 mu g DDA/h/g fresh weight of cells. (C) 1994 Academic P ress,Inc.