Abstract
Selection for allyl alcohol resistance in respiratory incompetent yeast is a highly specific method for isolating functional mutations at ADH1, the gene coding for the cytoplasmic alcohol dehydrogenase, ADHI. Because of the nature of this selection scheme, the ADHI activity of such mutants is retained, but the kinetic characteristics of the enzymes are altered. The high specificity for targeting functional mutations at this locus suggested that selection for enzyme variants with more subtle phenotypic effects might be possible. Here, we describe functional ADHI mutants that are temperature-conditional in their allyl alcohol resistance. Haploid cells of one of these mutants grow well on plates at 10 mm allyl alcohol at 19°, but not at 37°, the restrictive temperature. A second mutant grows well at 10 mm at 37°, but its growth is restricted at 19°. What distinguishes these mutants from other temperature-sensitive mutants is that the temperature-conditional growth phenotypes described here must be due to interactions between allyl alcohol levels and ADHI functional properties and cannot be due to lability of the enzyme at the restrictive temperature. This system shows promise for the investigation of functional enzyme variants that differ by only one or two amino acid residues but have significant temperature- and substrate-conditional effects on growth phenotypes in both the haploids and the diploids.
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Selected References
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- Batzinger R. P., Ou S. Y., Bueding E. Saccharin and other sweeteners: mutagenic properties. Science. 1977 Dec 2;198(4320):944–946. doi: 10.1126/science.337489. [DOI] [PubMed] [Google Scholar]
- Fersht A. R., Shi J. P., Knill-Jones J., Lowe D. M., Wilkinson A. J., Blow D. M., Brick P., Carter P., Waye M. M., Winter G. Hydrogen bonding and biological specificity analysed by protein engineering. Nature. 1985 Mar 21;314(6008):235–238. doi: 10.1038/314235a0. [DOI] [PubMed] [Google Scholar]
- Izard C., Libermann C. Acrolein. Mutat Res. 1978;47(2):115–138. doi: 10.1016/0165-1110(78)90016-7. [DOI] [PubMed] [Google Scholar]
- Pielak G. J., Mauk A. G., Smith M. Site-directed mutagenesis of cytochrome c shows that an invariant Phe is not essential for function. Nature. 1985 Jan 10;313(5998):152–154. doi: 10.1038/313152a0. [DOI] [PubMed] [Google Scholar]
- Taguchi A. K., Ciriacy M., Young E. T. Carbon source dependence of transposable element-associated gene activation in Saccharomyces cerevisiae. Mol Cell Biol. 1984 Jan;4(1):61–68. doi: 10.1128/mcb.4.1.61. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wilkinson A. J., Fersht A. R., Blow D. M., Carter P., Winter G. A large increase in enzyme-substrate affinity by protein engineering. Nature. 1984 Jan 12;307(5947):187–188. doi: 10.1038/307187a0. [DOI] [PubMed] [Google Scholar]
- Wills C. Production of yeast alcohol dehydrogenase isoenzymes by selection. Nature. 1976 May 6;261(5555):26–29. doi: 10.1038/261026a0. [DOI] [PubMed] [Google Scholar]
- Wills C. Three kinds of genetic variability in yeast populations. Proc Natl Acad Sci U S A. 1968 Nov;61(3):937–944. doi: 10.1073/pnas.61.3.937. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yancey P. H., Clark M. E., Hand S. C., Bowlus R. D., Somero G. N. Living with water stress: evolution of osmolyte systems. Science. 1982 Sep 24;217(4566):1214–1222. doi: 10.1126/science.7112124. [DOI] [PubMed] [Google Scholar]
