Cristiane Moriwaki
UEM Group
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Featured researches published by Cristiane Moriwaki.
Food Chemistry | 2014
Camila Sampaio Mangolim; Cristiane Moriwaki; Ana Claudia Nogueira; Francielle Sato; M. L. Baesso; Antonio Medina Neto; Graciette Matioli
Curcumin was complexed with β-CD using co-precipitation, freeze-drying and solvent evaporation methods. Co-precipitation enabled complex formation, as indicated by the FT-IR and FT-Raman techniques via the shifts in the peaks that were assigned to the aromatic rings of curcumin. In addition, photoacoustic spectroscopy and X-ray diffraction, with the disappearance of the band related to aromatic rings, by Gaussian fitting, and modifications in the spectral lines, respectively, also suggested complex formation. The possible complexation had an efficiency of 74% and increased the solubility of the pure colourant 31-fold. Curcumin-β-CD complex exhibited a sunlight stability 18% higher than the pure colourant. This material was stable to pH variations and storage at -15 and 4°C. With an isothermal heating at 100 and 150°C for 2h, the material exhibited a colour retention of approximately 99%. The application of curcumin-β-CD complex in vanilla ice creams intensified the colour of the products and produced a great sensorial acceptance.
Molecules | 2012
Rúbia Pazzetto; Sabrina Barbosa de Souza Ferreira; Elder James Silva Santos; Cristiane Moriwaki; Teresinha Aparecida Guedes; Graciette Matioli
The preservation of Bacillus firmus strain 37 cells by lyophilization was evaluated and response surface methodology (RSM) was used to optimize the β-cyclodextrin (β-CD) production by cells immobilized on loofa sponge. Interactions were studied with the variables temperature, pH and dextrin concentration using a central composite design (CCD). Immobilization time influence on β-CD production was also investigated. B. firmus strain 37 cells remained viable after one year of storage, showing that the lyophilization is a suitable method for preservation of the microorganism. From the three-dimensional diagrams and contour plots, the best conditions for β-CD production were determined: temperature 60 °C, pH 8, and 18% dextrin. Considering that the amount of dextrin was high, a new assay was carried out, in which dextrin concentrations of 10, 15, and 18% were tested and the temperature of 60 °C and pH 8 were maintained. The results achieved showed very small differences and therefore, for economic reasons, the use of 10% dextrin is suggested. Increasing the immobilization time of cells immobilized on synthetic sponge the β-CD production decreased and did not change for cells immobilized on loofa sponge. The results of this research are important for microorganism preservation and essential in the optimization of the biosynthesis of CD.
International Journal of Molecular Sciences | 2012
Tieles Carina de Oliveira Delani; Rúbia Pazzetto; Camila Sampaio Mangolim; Vanderson Carvalho Fenelon; Cristiane Moriwaki; Graciette Matioli
This study aimed to improve the production of β-cyclodextrin (β-CD) by microbial cells immobilized on synthetic or loofa sponges both with and without the use of alginate or chitosan. The most suitable matrix for the immobilization of Bacillus firmus strain 7B was synthetic sponge and for Bacillus sphaericus strain 41 was loofa sponge. After 330 days of storage, the β-CD production by Bacillus firmus and Bacillus sphaericus remained at around 41% and 49%, respectively, of initial levels. After 24 days of immobilization on loofa sponge, Bacillus sphaericus strain 41 achieved an improved operational stability, reaching 86.6 mM β-CD after 20 days of production, compared to only 32.8 mM of β-CD produced by free Bacillus sphaericus strain 41 cells. The expected increase in β-CD production by immobilized cells of Bacillus firmus strain 7B on synthetic sponge for 4 days was not statistically different to that for cells immobilized for 24 days. The application of this process on an industrial scale using loofa sponge, an inexpensive and renewable matrix, will allow the stable production of β-CD.
Biochemical Engineering Journal | 2009
Cristiane Moriwaki; Lívia Rosas Ferreira; Júlia Regina Tedesco Rodella; Graciette Matioli
Process Biochemistry | 2007
Cristiane Moriwaki; Glauciane de Lara Costa; Rúbia Pazzetto; Gisella Maria Zanin; Flávio Faria de Moraes; Márcia Portilho; Graciette Matioli
Biochemical Engineering Journal | 2008
Cassiana Mazzer; Lívia Rosas Ferreira; Júlia Regina Tedesco Rodella; Cristiane Moriwaki; Graciette Matioli
Journal of Molecular Catalysis B-enzymatic | 2007
Cristiane Moriwaki; Franciele Maria Pelissari; Regina Aparecida Correia Gonçalves; José Eduardo Gonçalves; Graciette Matioli
Biochemical Engineering Journal | 2014
Cristiane Moriwaki; Camila Sampaio Mangolim; Graziele Brescansin Ruiz; Gutierrez Rodrigues de Morais; M. L. Baesso; Graciette Matioli
Acta Scientiarum. Biological Sciences | 2008
Graciette Matioli; Cristiane Moriwaki; Regiane Barbieri Mazzoni; G. M. Zanin; Flávio Faria de Moraes
Acta Scientiarum. Health Science | 2009
Cassiana Mazzer; Rúbia Pazzetto; Cristiane Moriwaki; Graciette Matioli