Busca avançada
Ano de início
Entree
(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Evaluation of secretion reporters to microalgae biotechnology: Blue to red fluorescent proteins

Texto completo
Autor(es):
Dutra Molino, Joao Vitor [1] ; Monteiro de Carvalho, Joao Carlos [1] ; Mayfield, Stephen [2]
Número total de Autores: 3
Afiliação do(s) autor(es):
[1] Univ Sao Paulo, Fac Pharmaceut Sci, Dept Biochem & Pharmaceut Technol, Av Prof Lineu Prestes 580, Bl 16, BR-05508900 Sao Paulo - Brazil
[2] Univ Calif San Diego, Calif Ctr Algae Biotechnol, Div Biol Sci, 9500 Gilman Dr, La Jolla, CA 92093 - USA
Número total de Afiliações: 2
Tipo de documento: Artigo Científico
Fonte: ALGAL RESEARCH-BIOMASS BIOFUELS AND BIOPRODUCTS; v. 31, p. 252-261, APR 2018.
Citações Web of Science: 2
Resumo

Efficient protein secretion could potentially be exploited for improving the performance of heterologous protein expression system. However, efficient protein secretion depends on numerous factors that are not always known, and rapid development of protein secretion depends on efficient reporters. This study aimed to compare the secretion efficiency of seven fluorescent proteins (FPs)-mTagBFP, mCerulean, Emerald, CrGFP, cOFP, tdTomato, and mCherry-which are photoactive across the visible light spectrum in the microalgal expression system, Chlamydomonas reinhardtii. To fully compare the efficiency of FPs, three expression vectors-a non-secreting vector used as a control and two secreting vectors employing arylsulfatase 1 (ARS1) signal peptide-were used. Up to 94 transformants for each construct were evaluated to better determine the secretion detection efficiency and variability of each FP construct. Fluorescence measurements of all FPs in the whole culture and supernatant were conducted using a microplate reader. Furthermore, we observed fluorescence of six FPs, among the seven tested, in the secretory pathway by confocal fluorescence microscopy. The results indicated that orange and red FPs are the most suitable for this photosynthetic pigment-rich organism, but the FP reporter for secretion should be selected carefully, since some may be deleteriously modified, as observed in the case of tdTomato, in our study. Overall, cOFP and mCherry performed admirably with a high fluorescence signal to noise ratio (S/N > 6) for all constructs as compared to that of the wild type auto-fluorescence, and showed a high positive rate of transformants (> 75%). This FP may play an important role in protein secretion studies, supporting the development of this potential expression system based on microalgae. (AU)

Processo FAPESP: 13/18224-2 - Produção de proteína heteróloga em microalga
Beneficiário:João Vitor Dutra Molino
Modalidade de apoio: Bolsas no Brasil - Doutorado