Open AccessRole of the Rubisco small subunit. Final report for period May 1, 1997--April 30,2000
Author(s) -
Robert J. Spreitzer
Publication year - 2000
Language(s) - English
Resource type - Reports
DOI - 10.2172/809467
Subject(s) - chlamydomonas reinhardtii , rubisco , chlamydomonas , protein subunit , specificity factor , biology , mutagenesis , site directed mutagenesis , biochemistry , gene , genetics , mutation , mutant , promoter , gene expression
CO{sub 2} and O{sub 2} are mutually competitive at the active site of ribulose-1,5-biphosphate (RuBP) carboxylase/oxygenase (Rubisco). Rubisco contains two subunits, each present in eight copies. The 15-kD small subunit is coded by a family of nuclear RbcS genes. Until now, the role of the small subunit in Rubisco structure or catalytic efficiency is not known. Because of other work in eliminating the two RbcS genes in the green algo Chlamydomonas reinhardtii, it is now possible to address questions about the structure-function relationships of the eukaryotic small subunit. There are three specific aims in this project: (1) Alanine scanning mutagenesis is being used to dissect the importance of the {beta}A/{beta}B loop, a feature unique to the eukaryotic small subunit. (2) Random mutagenesis is being used to identify additional residues or regions of the small subunit that are important for holoenzyme assembly and function. (3) Attempts are being made to express foreign small subunits in Chlamydomonas to examine the contribution of small subunits to holoenzyme assembly, catalytic efficiency, and CO{sub 2}/O{sub 2} specificity