Page 54 - PC2019 Program & Proceedings
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PLANT CANADA 2019



                                             PS1. Monday, July 8, morning session at 8:30 am




                                             Dr. Maureen Hanson and Myat T. Lin
                                             Cornell University, NY


                                             Improving photosynthesis in C3 plants



               Abstract: Rubisco, which catalyzes the first step in carbon fixation, is a target for efforts to improve
               photosynthetic efficiency. Modifying the cellular environment surrounding Rubisco to enhance the CO2
               concentration, in order to prevent photorespiration, is one strategy underway in our lab.  Another strategy is to
               alter the properties of Rubisco itself to increase its enzymatic efficiency and/or to increase its affinity for CO2.
               Manajit Hayer-Hartl’s group recently demonstrated assembly of active Rubisco in E. coli, where the effects of
               mutagenesis can be quickly examined. Assembly of Rubisco requires multiple chaperones: Cpn60α, Cpn60β and
               Cpn20, as well as RbcX, Raf1, Raf2 and BSD2, for assembly of large and small subunits into L8S8 holoenzymes.
               We modified Hayer-Hartl’s Arabidopsis vectors to express tobacco Rubisco by replacing the Arabidopsis
               assembly factor genes with tobacco ones. We used this system to survey the activity of enzymes comprised of
               individual members of the tobacco Rubisco small subunit family, by co-expressing each one with the single
               large subunit gene in E. coli. These novel E. coli-expressed Rubisco enzymes have carboxylation kinetics very
               similar to that of the native tobacco Rubisco. We also produced tobacco Rubisco with a recently discovered
               trichome small subunit in E. coli and found that it has a higher catalytic rate and a lower CO2 affinity compared
               to the enzymes with other small subunits.



               Bio:

               Dr. Maureen Hanson is Liberty Hyde Bailey Professor in the Department of Molecular Biology and Genetics at
               Cornell University in Ithaca, NY.  She  previously was on the Biology faculty at the  University of Virginia,
               Charlottesville.  She  holds a Ph.D. in Cell and Developmental  Biology from Harvard University, where she
               subsequently held an NIH NRSA postdoctoral fellowship. She is a Fellow and recipient of the Lawrence Bogorad
               Award of the American Society of Plant Biologists and a Fellow of the American Association for the Advancement
               of Science.  She received the SUNY Chancellor’s Award for Faculty Service and the Cornell Award for Outstanding
               Accomplishments in Basic Research.  Her lab is known for identifying the first single dominant fertility restorer
               (Rf) gene that suppresses the expression of a toxic mitochondrial gene encoding cytoplasmic male sterility, the
               rediscovery of stromules and the demonstration that molecules pass through them between chloroplasts, and
               identification of several gene families previously unknown to comprise plant organelle RNA editing machinery.
               Her group  has ongoing  projects concerning improving photosynthetic  efficiency  through synthesizing the
               cyanobacterial carbon-concentrating  mechanism in chloroplasts or through engineering  of the carbon-fixing
               enzyme Rubisco. https://hansonlab.org/




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