Analysis of proteomic changes in colored mutants of Xanthophyllomyces dendrorhous (Phaffia rhodozyma)


Por: Barbachano-Torres A., Castelblanco-Matiz L.M., Ramos-Valdivia A.C., Cerda-García-Rojas C.M., Salgado L.M., Flores-Ortiz C.M., Ponce-Noyola T.

Publicada: 1 jun 2014
Resumen:
The yeast Xanthophyllomyces dendrorhous synthesizes astaxanthin as its most prevalent xanthophyll derivative. Comparisons between the protein profiles of mutant lines of this yeast can provide insight into the carotenogenic pathway. Differently colored mutants (red, orange, pink, yellow, and white) were obtained from this yeast species, and their protein profiles were determined using two-dimensional polyacrylamide gel electrophoresis (2DE). Individual proteins differentially expressed were identified using mass spectrometry. The red mutants hyperproduced total carotenoids (mainly astaxanthin), while in white and orange mutants, mutagenesis affected the phytoene dehydrogenase activity as indicated by the accumulation of phytoene. Inactivation of astaxanthin synthase after the mutagenic treatment was evident in beta-carotene accumulating mutants. Differences in the proteomic profiles of wild-type X. dendrorhous and its colored mutants were demonstrated using 2DE. Of the total number of spots detected in each gel (297-417), 128 proteins were present in all strains. The red mutant showed the greatest number of matches with respect to the wild type (305 spots), while the white and yellow mutants, which had reduced concentrations of total carotenoids, presented the highest correlation coefficient (0.6) between each other. A number of differentially expressed proteins were sequenced, indicating that tricarboxylic acid cycle and stress response proteins are closely related to the carotenogenic process.

Filiaciones:
Barbachano-Torres A.:
 Department of Biotechnology and Bioengineering, CINVESTAV-IPN, Av. Instituto Politécnico Nacional # 2508, Zacatenco, Gustavo A. Madero, 07360 Mexico City, Mexico

Castelblanco-Matiz L.M.:
 Department of Biotechnology and Bioengineering, CINVESTAV-IPN, Av. Instituto Politécnico Nacional # 2508, Zacatenco, Gustavo A. Madero, 07360 Mexico City, Mexico

Ramos-Valdivia A.C.:
 Department of Biotechnology and Bioengineering, CINVESTAV-IPN, Av. Instituto Politécnico Nacional # 2508, Zacatenco, Gustavo A. Madero, 07360 Mexico City, Mexico

Cerda-García-Rojas C.M.:
 Department of Chemistry, CINVESTAV-IPN, 07360 Mexico City, Mexico

Salgado L.M.:
 CICATA-Qro, Instituto Politécnico Nacional, 76090 Mexico City, Mexico

Flores-Ortiz C.M.:
 FES Iztacala UNAM, Mexico City 54090, DF, Mexico

Ponce-Noyola T.:
 Department of Biotechnology and Bioengineering, CINVESTAV-IPN, Av. Instituto Politécnico Nacional # 2508, Zacatenco, Gustavo A. Madero, 07360 Mexico City, Mexico
ISSN: 03028933
Editorial
Springer-Verlag, 233 SPRING ST, NEW YORK, NY 10013 USA, Estados Unidos America
Tipo de documento: Article
Volumen: 196 Número: 6
Páginas: 411-421
WOS Id: 000336274500004
ID de PubMed: 24676883

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