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  Functional Green-Tuned Proteorhodopsin from Modern Stromatolites

Albarracin, V. H., Kraiselburd, I., Bamann, C., Wood, P. G., Bamberg, E., Farias, M. E., et al. (2016). Functional Green-Tuned Proteorhodopsin from Modern Stromatolites. PLoS One, 11(5): e0154962. doi:10.1371/journal.pone.0154962.

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Albarracin, Virginia Helena1, 2, Author
Kraiselburd, Ivana3, Author
Bamann, Christian4, Author           
Wood, Philip G.4, Author           
Bamberg, Ernst4, Author           
Farias, María Eugenia4, Author           
Gärtner, Wolfgang5, Author
Affiliations:
1Planta Piloto de Procesos Industriales y Microbiológicos (PROIMI), CCT, CONICET. Av. Belgrano y Pasaje Caseros. 4000- S. M. de Tucumán, Argentina, ou_persistent22              
2Facultad de Ciencias Naturales e Instituto Miguel Lillo, Universidad Nacional de Tucumán, 4000, S. M. de Tucumán, Argentina, ou_persistent22              
3Instituto de Biología Molecular y Celular de Rosario (IBR - CONICET), Facultad de Ciencias Bioquímicas y Farmacéuticas (FBIOYF - UNR), Suipacha 590, 2000, Rosario, Santa Fe, Argentina, ou_persistent22              
4Department of Biophysical Chemistry, Max Planck Institute of Biophysics, Max Planck Society, ou_2068289              
5Max-Planck-Institute for Chemical Energy Conversion, Max Planck Society, Stiftstrasse 34 –36, D-45470 Mülheim, Germany, ou_persistent22              

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 Abstract: The sequenced genome of the poly-extremophile Exiguobacterium sp. S17, isolated from modern stromatolites at Laguna Socompa (3,570 m), a High-Altitude Andean Lake (HAAL) in Argentinean Puna revealed a putative proteorhodopsin-encoding gene. The HAAL area is exposed to the highest UV irradiation on Earth, making the microbial community living in the stromatolites test cases for survival strategies under extreme conditions. The heterologous expressed protein E17R from Exiguobacterium (248 amino acids, 85% sequence identity to its ortholog ESR from E. sibiricum) was assembled with retinal displaying an absorbance maximum at 524 nm, which makes it a member of the green-absorbing PR-subfamily. Titration down to low pH values (eventually causing partial protein denaturation) indicated a pK value between two and three. Global fitting of data from laser flash-induced absorption changes gave evidence for an early red-shifted intermediate (its formation being below the experimental resolution) that decayed (τ1 = 3.5 μs) into another red-shifted intermediate. This species decayed in a two-step process (τ2 = 84 μs, τ3 = 11 ms), to which the initial state of E17-PR was reformed with a kinetics of 2 ms. Proton transport capability of the HAAL protein was determined by BLM measurements. Additional blue light irradiation reduced the proton current, clearly identifying a blue light absorbing, M-like intermediate. The apparent absence of this intermediate is explained by closely matching formation and decay kinetics.

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Language(s): eng - English
 Dates: 2016-02-092016-04-212016-05-17
 Publication Status: Published online
 Pages: 18
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1371/journal.pone.0154962
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Title: PLoS One
Source Genre: Journal
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Publ. Info: San Francisco, CA : Public Library of Science
Pages: - Volume / Issue: 11 (5) Sequence Number: e0154962 Start / End Page: - Identifier: ISSN: 1932-6203
CoNE: https://pure.mpg.de/cone/journals/resource/1000000000277850