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Darkness inhibits autokinase activity of bacterial bathy phytochromes.
Huber, Christina; Strack, Merle; Schultheiß, Isabel; Pielage, Julia; Mechler, Xenia; Hornbogen, Justin; Diller, Rolf; Frankenberg-Dinkel, Nicole.
Afiliación
  • Huber C; Department of Microbiology, Rheinland-Pfälzische Technische Universität Kaiserslautern-Landau, Kaiserslautern, Germany.
  • Strack M; Department of Physics, Rheinland-Pfälzische Technische Universität Kaiserslautern-Landau, Kaiserslautern, Germany.
  • Schultheiß I; Department of Microbiology, Rheinland-Pfälzische Technische Universität Kaiserslautern-Landau, Kaiserslautern, Germany.
  • Pielage J; Department of Microbiology, Rheinland-Pfälzische Technische Universität Kaiserslautern-Landau, Kaiserslautern, Germany.
  • Mechler X; Department of Physics, Rheinland-Pfälzische Technische Universität Kaiserslautern-Landau, Kaiserslautern, Germany.
  • Hornbogen J; Department of Physics, Rheinland-Pfälzische Technische Universität Kaiserslautern-Landau, Kaiserslautern, Germany.
  • Diller R; Department of Physics, Rheinland-Pfälzische Technische Universität Kaiserslautern-Landau, Kaiserslautern, Germany.
  • Frankenberg-Dinkel N; Department of Microbiology, Rheinland-Pfälzische Technische Universität Kaiserslautern-Landau, Kaiserslautern, Germany. Electronic address: nicole.frankenberg@rptu.de.
J Biol Chem ; 300(4): 107148, 2024 Apr.
Article en En | MEDLINE | ID: mdl-38462162
ABSTRACT
Bathy phytochromes are a subclass of bacterial biliprotein photoreceptors that carry a biliverdin IXα chromophore. In contrast to prototypical phytochromes that adopt a red-light-absorbing Pr ground state, the far-red light-absorbing Pfr-form is the thermally stable ground state of bathy phytochromes. Although the photobiology of bacterial phytochromes has been extensively studied since their discovery in the late 1990s, our understanding of the signal transduction process to the connected transmitter domains, which are often histidine kinases, remains insufficient. Initiated by the analysis of the bathy phytochrome PaBphP from Pseudomonas aeruginosa, we performed a systematic analysis of five different bathy phytochromes with the aim to derive a general statement on the correlation of photostate and autokinase output. While all proteins adopt different Pr/Pfr-fractions in response to red, blue, and far-red light, only darkness leads to a pure or highly enriched Pfr-form, directly correlated with the lowest level of autokinase activity. Using this information, we developed a method to quantitatively correlate the autokinase activity of phytochrome samples with well-defined stationary Pr/Pfr-fractions. We demonstrate that the off-state of the phytochromes is the Pfr-form and that different Pr/Pfr-fractions enable the organisms to fine-tune their kinase output in response to a certain light environment. Furthermore, the output response is regulated by the rate of dark reversion, which differs significantly from 5 s to 50 min half-life. Overall, our study indicates that bathy phytochromes function as sensors of light and darkness, rather than red and far-red light, as originally postulated.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fitocromo / Proteínas Bacterianas / Oscuridad Idioma: En Revista: J Biol Chem Año: 2024 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fitocromo / Proteínas Bacterianas / Oscuridad Idioma: En Revista: J Biol Chem Año: 2024 Tipo del documento: Article País de afiliación: Alemania