Beronda Montgomery-Kaguri
Assistant Professor
- Ph.D, 2001, University of California, Davis
montg133@msu.edu
MSU-DOE Plant Research Lab
322 Plant Biology Building
Michigan State University
East Lansing, MI 48824
Office: 517-353-7802
Lab: 517-353-3992
Fax: (517) 353-9168
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Beronda Montgomery-Kaguri Research Interests continued
We have initiated molecular studies to broaden our understanding of organ-specific phytochrome responses in plants. It has been demonstrated previously that constitutive expression of the mammalian enzyme biliverdin IX-alpha reductase (BVR) in transgenic Arabidopsis and Tobacco plants alters light-dependent growth and development by metabolically inactivating the precursors of the phytochrome chromophore (Figure 1; Montgomery et al, 1999; 2001). We are adapting transgenic BVR expression as a molecular tool for probing localized phytochrome responses. Preliminary studies have shown that localized BVR expression affects distinct aspects of light-mediated plant growth and development. The phytochrome dependent phenotypes that are disrupted differ for lines using constitutive or tissue-specific promoters for BVR expression (Figure 2).
A second area of study focuses on complementary chromatic adaptation (CCA). Cells of the cyanobacterium Fremyella diplosiphon appear brick red in color when grown under green light (GL) due to the accumulation of GL-absorbing proteins. When grown under red light (RL), cells appear blue-green due to the accumulation of pigments that maximally absorb RL. CCA, a specific form of photomorphogenesis in some cyanobacteria, is controlled by a biliprotein photoreceptor with significant similarity to plant phytochromes. Biochemical characterization of the light-regulated signal transduction cascade controlling CCA will expand our current knowledge of the complex signaling cascades controlled by phytochrome-like proteins in prokaryotic systems. In summary, our current studies focus on the synthesis of photosensory biliproteins and investigations into their physiological roles during selected aspects of photomorphogenesis in the model plant Arabidopsis and cyanobacteria.
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