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A metal-free blue chromophore derived from plant pigments.
Freitas-Dörr, B C; Machado, C O; Pinheiro, A C; Fernandes, A B; Dörr, F A; Pinto, E; Lopes-Ferreira, M; Abdellah, M; Sá, J; Russo, L C; Forti, F L; Gonçalves, L C P; Bastos, E L.
Afiliación
  • Freitas-Dörr BC; Departamento de Química Fundamental, Instituto de Química, Universidade de São Paulo, 05508-000 São Paulo, SP, Brazil.
  • Machado CO; Departamento de Química Fundamental, Instituto de Química, Universidade de São Paulo, 05508-000 São Paulo, SP, Brazil.
  • Pinheiro AC; Departamento de Química Fundamental, Instituto de Química, Universidade de São Paulo, 05508-000 São Paulo, SP, Brazil.
  • Fernandes AB; Departamento de Química Fundamental, Instituto de Química, Universidade de São Paulo, 05508-000 São Paulo, SP, Brazil.
  • Dörr FA; Departamento de Análises Clínicas e Toxicológicas, Faculdade de Ciências Farmacêuticas, Universidade de São Paulo, 05508-000 São Paulo, SP, Brazil.
  • Pinto E; Departamento de Análises Clínicas e Toxicológicas, Faculdade de Ciências Farmacêuticas, Universidade de São Paulo, 05508-000 São Paulo, SP, Brazil.
  • Lopes-Ferreira M; Immunoregulation Unit of the Special Laboratory of Applied Toxinology (Center for Toxins, Immune-Response and Cell Signaling/CEPID/FAPESP), Butantan Institute, 05503-900 São Paulo, SP, Brazil.
  • Abdellah M; Physical Chemistry Division, Department of Chemistry, Ångström Laboratory, Uppsala University, 75120 Uppsala, Sweden.
  • Sá J; Department of Chemistry, Qena Faculty of Science, South Valley University, 83523 Qena, Egypt.
  • Russo LC; Physical Chemistry Division, Department of Chemistry, Ångström Laboratory, Uppsala University, 75120 Uppsala, Sweden.
  • Forti FL; Institute of Physical Chemistry, Polish Academy of Sciences, 01-224 Warsaw, Poland.
  • Gonçalves LCP; Departamento de Bioquímica, Instituto de Química, Universidade de São Paulo, 05508-000 São Paulo, SP, Brazil.
  • Bastos EL; Departamento de Bioquímica, Instituto de Química, Universidade de São Paulo, 05508-000 São Paulo, SP, Brazil.
Sci Adv ; 6(14): eaaz0421, 2020 04.
Article en En | MEDLINE | ID: mdl-32284978
ABSTRACT
Blue natural pigments are rare, especially among plants. However, flowering species that evolved to attract Hymenoptera pollinators are colored by blue anthocyanin-metal complexes. Plants lacking anthocyanins are pigmented by betalains but are unable to produce blue hues. By extending the π-system of betalains, we designed a photostable and metal-free blue dye named BeetBlue that did not show toxicity to human hepatic and retinal pigment epithelial cells and does not affect zebrafish embryonal development. This chiral dye can be conveniently synthesized from betalamic acid obtained from hydrolyzed red beetroot juice or by enzymatic oxidation of l-dopa. BeetBlue is blue in the solid form and in solution of acidified polar molecular solvents, including water. Its capacity to dye natural matrices makes BeetBlue the prototype of a new class of low-cost bioinspired chromophores suitable for a myriad of applications requiring a blue hue.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Pigmentos Biológicos / Plantas / Colorantes Idioma: En Revista: Sci Adv Año: 2020 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Pigmentos Biológicos / Plantas / Colorantes Idioma: En Revista: Sci Adv Año: 2020 Tipo del documento: Article