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Encapsulation of Photosystem I in Organic Microparticles Increases Its Photochemical Activity and Stability for Ex Vivo Photocatalysis
Author(s) -
Arianna Cherubin,
L. Destefanis,
Michele Bovi,
Federico Perozeni,
Ilaria Bargigia,
Gabriel de la Cruz Valbuena,
Cosimo D’Andrea,
Alessandro Romeo,
Matteo Ballottari,
Massimiliano Perduca
Publication year - 2019
Publication title -
acs sustainable chemistry and engineering
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.878
H-Index - 109
ISSN - 2168-0485
DOI - 10.1021/acssuschemeng.9b00738
Subject(s) - photochemistry , chemistry , photosystem i , redox , electron transfer , photosynthesis , plastocyanin , photocatalysis , plga , electron acceptor , photosystem ii , biophysics , organic chemistry , catalysis , biochemistry , in vitro , biology
Photosystem I (PSI) is a pigment binding multisubunit protein complex involved in the light phase of photosynthesis, catalyzing a light-dependent electron transfer reaction from plastocyanin to ferredoxin. PSI is characterized by a photochemical efficiency close to one, suggesting its possible application in light-dependent redox reaction in an extracellular context. The stability of PSI complexes isolated from plant cells is however limited if not embedded in a protective environment. Here we show an innovative solution for exploiting the photochemical properties of PSI, by encapsulation of isolated PSI complexes in PLGA (poly lactic- co -glycolic acid) organic microparticles. These encapsulated PSI complexes were able to catalyze light-dependent redox reactions with electron acceptors and donors outside the PLGA microparticles. Moreover, PSI complexes encapsulated in PLGA microparticles were characterized by a higher photochemical activity and stability compared with PSI complexes in detergent solution, suggesting their possible application for ex vivo photocatalysis.

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