Experimental Cell Research 1984-10-01

An isozyme-specific selective system for the recovery of mammalian cells deficient in hepatic alcohol dehydrogenase activity.

A M Killary, R E Fournier

Index: Exp. Cell Res. 154(2) , 442-53, (1984)

Full Text: HTML

Abstract

A selective system toxic towards mammalian cells expressing the liver-specific isozyme of alcohol dehydrogenase (L-ADH) has been developed. A number of alpha-unsaturated primary and secondary alcohols were assayed for their ability to serve as substrates for rat liver ADH and were screened for cytotoxicity towards L-ADH+ and L-ADH- cells. 1-Propen-3-ol and 1-penten-3-ol were identified as agents showing selective cytotoxicity. Reconstruction experiments demonstrated that 1-propen-3-ol at a concentration of 15 microM could be used to recover L-ADH- clones from mixed populations of L-ADH+ and L-ADH cells. Cells expressing the non-allelic S-ADH isozyme were not killed under these conditions. The selective system defined in this report is thus isozyme-specific.


Related Compounds

  • 1-Penten-3-ol

Related Articles:

Off-flavour masking of secondary lipid oxidation products by pea dextrin.

2015-02-15

[Food Chem. 169 , 492-8, (2014)]

Characterization of Volatile Flavor Compounds in Chinese Rice Wine Fermented from Enzymatic Extruded Rice.

2015-07-01

[J. Food Sci. 80 , C1476-89, (2015)]

Higher sterol content regulated by CYP51 with concomitant lower phospholipid content in membranes is a common strategy for aluminium tolerance in several plant species.

2015-02-01

[J. Exp. Bot. 66(3) , 907-18, (2015)]

Tolerance to 1-pentene-3-ol and to 1-pentene-3-one in relation to alcohol dehydrogenase (ADH) and aldo keto reductase (AKR) activities in Drosophila melanogaster.

1990-10-01

[Biochem. Genet. 28(9-10) , 513-22, (1990)]

Photooxidation of leaf-wound oxygenated compounds, 1-penten-3-ol, (Z)-3-hexen-1-ol, and 1-penten-3-one, initiated by OH radicals and sunlight.

2009-03-15

[Environ. Sci. Technol. 43(6) , 1831-7, (2009)]

More Articles...