Literature DB >> 8236282

Saccharomyces cerevisiae: an alternative source for human microsomal liver enzymes and its use in drug interaction studies.

H P Eugster1, C Sengstag.   

Abstract

Heterologous expression of human cDNAs in the yeast Saccharomyces cerevisiae represents an attractive alternative source of human enzymes and allows metabolic studies to be performed without the need of human tissue. Here we report on the functional expression of human microsomal epoxide hydrolase (hmEH) and cytochrome P450 1A1 and 1A2 in yeast. Microsomal fractions of corresponding yeast strains exhibited enzyme specific activities which allowed the characterization of the heterologous enzymes. The use of these microsomes enabled us to study drug interactions on the respective enzymes with pharmacologically relevant drugs such as carbamazepine epoxide, valpromide and ketoconazole.

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Year:  1993        PMID: 8236282     DOI: 10.1016/0300-483x(93)90060-6

Source DB:  PubMed          Journal:  Toxicology        ISSN: 0300-483X            Impact factor:   4.221


  5 in total

1.  Sulforaphane- and phenethyl isothiocyanate-induced inhibition of aflatoxin B1-mediated genotoxicity in human hepatocytes: role of GSTM1 genotype and CYP3A4 gene expression.

Authors:  Kerstin Gross-Steinmeyer; Patricia L Stapleton; Julia H Tracy; Theo K Bammler; Stephen C Strom; David L Eaton
Journal:  Toxicol Sci       Date:  2010-05-04       Impact factor: 4.849

2.  Effects of furanocoumarins from apiaceous vegetables on the catalytic activity of recombinant human cytochrome P-450 1A2.

Authors:  Ah-Young Kang; Lindsay R Young; Carlus Dingfelder; Sabrina Peterson
Journal:  Protein J       Date:  2011-10       Impact factor: 2.371

3.  Expression of a human cytochrome p450 in yeast permits analysis of pathways for response to and repair of aflatoxin-induced DNA damage.

Authors:  Yingying Guo; Linda L Breeden; Helmut Zarbl; Bradley D Preston; David L Eaton
Journal:  Mol Cell Biol       Date:  2005-07       Impact factor: 4.272

4.  Modulation of aflatoxin B1-mediated genotoxicity in primary cultures of human hepatocytes by diindolylmethane, curcumin, and xanthohumols.

Authors:  Kerstin Gross-Steinmeyer; Patricia L Stapleton; Julia H Tracy; Theo K Bammler; Stephen C Strom; Donald R Buhler; David L Eaton
Journal:  Toxicol Sci       Date:  2009-09-21       Impact factor: 4.849

5.  A further interaction study of quinine with clinically important drugs by human liver microsomes: determinations of inhibition constant (Ki) and type of inhibition.

Authors:  X J Zhao; T Ishizaki
Journal:  Eur J Drug Metab Pharmacokinet       Date:  1999 Jul-Sep       Impact factor: 2.569

  5 in total

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