CC-4664 prk1-R64C/G326S mt+ (R203-16A revertant of 12-2B)
$30.00
From Robert J. Spreitzer, University of Nebraska, March 2014
Following MMS mutagenesis of prk1-R64C mt+ (CGC-TGC), Bryan Smith in Spreitzer’s group selected photosynthesis-competent revertants at a frequency of 1 X 10E-8 cells (Smith 2000). Revertant R203-16A has reduced photosynthetic growth relative to wild type. It was found to result from intragenic suppression that converts phosphoribulokinase Gly-326 (GGC) to Ser (AGC). The mutant protein has not been analyzed. This strain has been maintained with acetate medium in darkness since its isolation.
Smith BD (2000) Isolation and analysis of Chlamydomonas reinhardtii phosphoribulokinase mutants and revertants. Undergraduate Honors Thesis, Department of Biochemistry, University of Nebraska (available from the Chlamydomonas Resource Center)