Yeast killer factor is a valuable phenotype used in industrial, medical, and research applications. It controls commercial fermentations, aids in identifying pathogenic biotypes, and is the active components of a topical treatment for yeast infections. It may eventually be used in the production of anti-idiotypes and of bioengineered proteins. Natural killer factor toxins vary and this variation has increased their usefulness. However, little is known about the genetic basis of killer toxin production in many killer systems. This project will increase our knowledge of natural phenotypic variation and of the genetics of killer toxin formation. To accomplish these goals, the investigator will identify and define killer phenotypes from killer Pichia collected from naturally occurring necrotic cactus tissues. The genus is composed of well defined species groups, many of which contain killer strains, Killer phenotypes will be identified by screening each killer isolate for its ability to kill a set of 70 other yeast. Physical optima will be determined for each toxin variation identified. From this database, the genetics of killer toxin production will be investigated by mating strains with different phenotypes within each group of related Pichia. Students will learn to identify yeast, to do genetic analyses, and to organize and present their data. The interdisciplinary aspects of the project will integrate concepts presented in different courses and aid in developing both quantitative and writing skills. The interdisciplinary approach will widen the students' perspectives on biology and, consequently, encourage them to widen their perspectives on choosing a career in biology.

Project Start
Project End
Budget Start
Budget End
Support Year
22
Fiscal Year
1996
Total Cost
Indirect Cost
Rana, Krupa; Whalen, Margaret (2015) Activation of protein kinase C and protein kinase D in human natural killer cells: effects of tributyltin, dibutyltin, and tetrabromobisphenol A. Toxicol Mech Methods 25:680-8
Hurd-Brown, Tasia; Udoji, Felicia; Martin, Tamara et al. (2013) Effects of DDT and triclosan on tumor-cell binding capacity and cell-surface protein expression of human natural killer cells. J Appl Toxicol 33:495-502
Sharow, Kyle A; Temkin, Boris; Asson-Batres, Mary Ann (2012) Retinoic acid stability in stem cell cultures. Int J Dev Biol 56:273-8
Hurd, Tasia; Walker, Jasmine; Whalen, Margaret M (2012) Pentachlorophenol decreases tumor-cell-binding capacity and cell-surface protein expression of human natural killer cells. J Appl Toxicol 32:627-34
Taylor, Thyneice R; Whalen, Margaret M (2011) Ziram activates mitogen-activated protein kinases and decreases cytolytic protein levels in human natural killer cells. Toxicol Mech Methods 21:577-84
Buchanan, FaMitah Q; Rochette-Egly, Cecile; Asson-Batres, Mary Ann (2011) Detection of variable levels of RAR? and RAR? proteins in pluripotent and differentiating mouse embryonal carcinoma and mouse embryonic stem cells. Cell Tissue Res 346:43-51
Hurd, Tasia; Whalen, Margaret M (2011) Tetrabromobisphenol A decreases cell-surface proteins involved in human natural killer (NK) cell-dependent target cell lysis. J Immunotoxicol 8:219-27
Udoji, Felicia; Martin, Tamara; Etherton, Rachel et al. (2010) Immunosuppressive effects of triclosan, nonylphenol, and DDT on human natural killer cells in vitro. J Immunotoxicol 7:205-12
Abraha, Abraham B; Rana, Krupa; Whalen, Margaret M (2010) Role of protein kinase C in TBT-induced inhibition of lytic function and MAPK activation in human natural killer cells. Arch Environ Contam Toxicol 59:661-9
Hinkson, Natasha C; Whalen, Margaret M (2010) Hexabromocyclododecane decreases tumor-cell-binding capacity and cell-surface protein expression of human natural killer cells. J Appl Toxicol 30:302-9

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