Chlamydomonas reinhardtii genetic variants as probes for fluorescence sensing system in detection of pollutants

ABSTRACT: The unicellular green alga Chlamydomonas reinhardtii is employed here for the setup of a biosensor demonstrator based on multibiomediators for the detection of herbicides. The detection is based on the activity of photosystem II, the multienzymatic chlorophyll–protein complex located in th...

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Autores:
Pezzotti, Gianni
Scognamiglio, Viviana
Dimova Lambreva, Maya
Tibuzzi, Arianna
Johanningmeier, U.
Raffi, D.
Rea, Giuseppina
Giardi, María Teresa
Tipo de recurso:
Article of investigation
Fecha de publicación:
2009
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/34441
Acceso en línea:
https://hdl.handle.net/10495/34441
Palabra clave:
Chlamydomonas reinhardtii
Técnicas Biosensibles
Biosensing Techniques
Mutagénesis Sitio-Dirigida
Mutagenesis, Site-Directed
Contaminantes Ambientales
Environmental Pollutants
Fluorescencia
Fluorescence
Variación Genética
Genetic Variation
Herbicidas - análisis
Herbicides - analysis
Complejo de Proteína del Fotosistema II
Photosystem II Protein Complex
Factores de Tiempo
Time Factors
Sensibilidad y Especificidad
Sensitivity and Specificity
Rights
openAccess
License
http://creativecommons.org/licenses/by-nc-nd/2.5/co/
Description
Summary:ABSTRACT: The unicellular green alga Chlamydomonas reinhardtii is employed here for the setup of a biosensor demonstrator based on multibiomediators for the detection of herbicides. The detection is based on the activity of photosystem II, the multienzymatic chlorophyll–protein complex located in the thylakoid membrane that catalyzes the light-dependent photosynthetic primary charge separation and the electron transfer chain in cyanobacteria, algae, and higher plants. Several C. reinhardtii mutants modified on the D1 photosystem II protein are generated by site-directed mutagenesis and experimentally tested for the development of a biosensor revealing the modification of the fluorescence parameter (1−VJ) in the presence of herbicides. The A250R, A250L, A251C, and I163N mutants are highly sensitive to the urea and triazine herbicide classes; the newly generated F255N mutant is shown to be especially resistant to the class of urea. It follows that the response of the multibiomediators is associated to a particular herbicide subclass and can be useful to monitor several species of pollutants