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Spectral and photochemical diversity of tandem cysteine cyanobacterial phytochromes.
Song, Ji-Young; Lee, Ha Yong; Yang, Hee Wook; Song, Ji-Joon; Lagarias, J Clark; Park, Youn-Il.
Afiliación
  • Song JY; Department of Biological Sciences, Chungnam National University, Daejeon 34134, Korea.
  • Lee HY; Department of Biological Sciences, Chungnam National University, Daejeon 34134, Korea.
  • Yang HW; Department of Biological Sciences, Chungnam National University, Daejeon 34134, Korea.
  • Song JJ; Department of Biological Science and KI for the BioCentury, Korea Advanced Institute of Science and Technology, Daejeon 34141, Korea.
  • Lagarias JC; Department of Molecular and Cellular Biology, University of California Davis, Davis, California 95616 jclagarias@ucdavis.edu.
  • Park YI; Department of Biological Sciences, Chungnam National University, Daejeon 34134, Korea yipark@cnu.ac.kr.
J Biol Chem ; 295(19): 6754-6766, 2020 05 08.
Article en En | MEDLINE | ID: mdl-32184354
ABSTRACT
The atypical trichromatic cyanobacterial phytochrome NpTP1 from Nostoc punctiforme ATCC 29133 is a linear tetrapyrrole (bilin)-binding photoreceptor protein that possesses tandem-cysteine residues responsible for shifting its light-sensing maximum to the violet spectral region. Using bioinformatics and phylogenetic analyses, here we established that tandem-cysteine cyanobacterial phytochromes (TCCPs) compose a well-supported monophyletic phytochrome lineage distinct from prototypical red/far-red cyanobacterial phytochromes. To investigate the light-sensing diversity of this family, we compared the spectroscopic properties of NpTP1 (here renamed NpTCCP) with those of three phylogenetically diverged TCCPs identified in the draft genomes of Tolypothrix sp. PCC7910, Scytonema sp. PCC10023, and Gloeocapsa sp. PCC7513. Recombinant photosensory core modules of ToTCCP, ScTCCP, and GlTCCP exhibited violet-blue-absorbing dark-states consistent with dual thioether-linked phycocyanobilin (PCB) chromophores. Photoexcitation generated singly-linked photoproduct mixtures with variable ratios of yellow-orange and red-absorbing species. The photoproduct ratio was strongly influenced by pH and by mutagenesis of TCCP- and phytochrome-specific signature residues. Our experiments support the conclusion that both photoproduct species possess protonated 15E bilin chromophores, but differ in the ionization state of the noncanonical "second" cysteine sulfhydryl group. We found that the ionization state of this and other residues influences subsequent conformational change and downstream signal transmission. We also show that tandem-cysteine phytochromes present in eukaryotes possess similar amino acid substitutions within their chromophore-binding pocket, which tune their spectral properties in an analogous fashion. Taken together, our findings provide a roadmap for tailoring the wavelength specificity of plant phytochromes to optimize plant performance in diverse natural and artificial light environments.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fitocromo / Proteínas Bacterianas / Cianobacterias / Fotorreceptores Microbianos Tipo de estudio: Prognostic_studies Idioma: En Revista: J Biol Chem Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fitocromo / Proteínas Bacterianas / Cianobacterias / Fotorreceptores Microbianos Tipo de estudio: Prognostic_studies Idioma: En Revista: J Biol Chem Año: 2020 Tipo del documento: Article