Thais Regiani Cataldi

Dr. Thais Regiani Cataldi

orcid

Research Focus & Metrics

Academic Career Length

19Years (2008-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 2011 in Journal of Nanomaterials
Verified
Journal Article
Open access
PDF file
Hernane Silva BarudHernane Silva Barud
Hernane Silva Barud
TCThais Regiani Cataldi
Thais Regiani Cataldi
RMRodrigo F. C. Marques
Rodrigo F. C. Marques
WLWilton Rogério Rogério Lustri
Wilton Rogério Rogério Lustri
YMYounes Messaddeq
Younes Messaddeq
SRSidney Ribeiro
Sidney Ribeiro
Antimicrobial bacterial cellulose-silver nanoparticles composite membranes have been obtained by“in situ”preparation of Ag nanoparticles from hydrolytic decomposition of silver nitrate solution using triethanolamine as reducing and complexing agent. The formation of silver nanoparticles was evidenced by the X-ray diffraction, scanning electron microscopy (SEM), transmission electron microscopy (TEM), and absorption in the UV-Visible (350 nm to 600 nm). Thermal and mechanical properties together with swelling behavior for water were considered. TEA concentration was observed to be important in order to obtain only Ag particles and not a mixture of silver oxides. It was also observed to control particle size and amount of silver contents in bacterial cellulose. The composite membranes exhibited strong antimicrobial activity against Gram-negative and Gram-positive bacteria.

1 May 2008 in Materials Science and Engineering: C
Verified
Journal Article
Closed access
HBHernane S. Barud
Hernane S. Barud
CBCelina Barrios
Celina Barrios
TCThais Regiani Cataldi
Thais Regiani Cataldi
RMRodrigo F.C. Marques
Rodrigo F.C. Marques
MVMarc Verelst
Marc Verelst
SRSidney Ribeiro
Sidney Ribeiro

14 January 2011 in Analytical Chemistry
Verified
Journal Article
Closed access
VSVanessa G. Santos
Vanessa G. Santos
TCThais Regiani Cataldi
Thais Regiani Cataldi
Fernanda F G DiasFernanda F G Dias
Fernanda F G Dias
WRWanderson Romão
Wanderson Romão
JJJose Luis Paz Jara
Jose Luis Paz Jara
MEMarcos N. Eberlin
Marcos N. Eberlin

26 October 2015 in Journal of Assisted Reproduction and Genetics
Verified
Journal Article
Closed access
PDF file
Fernanda Bertuccez CordeiroFernanda Bertuccez Cordeiro
Fernanda Bertuccez Cordeiro
TCThais Regiani Cataldi
Thais Regiani Cataldi
KPKayla Jane Perkel
Kayla Jane Perkel
LCLívia Do Vale Teixeira da Costa
Lívia Do Vale Teixeira da Costa
RRRaquel Cellin Rochetti
Raquel Cellin Rochetti
ETEdson Guimarães Lo Turco
Edson Guimarães Lo Turco

1 September 2014 in Chemistry – A European Journal
Verified
Journal Article
Closed access
PDF file
VSVanessa G. Santos
Vanessa G. Santos
MGMarla N. Godoi
Marla N. Godoi
TCThais Regiani Cataldi
Thais Regiani Cataldi
FGFernando H. S. Gama
Fernando H. S. Gama
MCMirela B. Coelho
Mirela B. Coelho
SGSimon J. Garden
Simon J. Garden

31 May 2017 in Frontiers in Plant Science
Verified
Journal Article
Open access
PSPatricia D. C. Schaker
Patricia D. C. Schaker
LPLeila P. Peters
Leila P. Peters
TCThais Regiani Cataldi
Thais Regiani Cataldi
CLCarlos A. Labate
Carlos A. Labate
CCCamila Caldana
Camila Caldana
CMClaudia Barros Monteiro-Vitorello
Claudia Barros Monteiro-Vitorello
Sugarcane smut disease, caused by the biotrophic fungus Sporisorium scitamineum, is characterized by the development of a whip-like structure from the plant meristem. The disease causes negative effects on sucrose accumulation, fiber content and juice quality. The aim of this study was to examine whether the transcriptomic changes already described during the infection of sugarcane by S. scitamineum result in changes at the metabalomic level. To address this question, an analysis was conducted during the initial stage of the interaction and through disease progression in a susceptible sugarcane genotype. GC-TOF-MS allowed the identification of seventy-three primary metabolites. A set of these compounds were quantitatively altered at each analyzed point as compared with healthy plants. The results revealed that energetic pathways and amino acid pools were affected throughout the interaction. Raffinose levels increased shortly after infection but decreased remarkably after whip emission. Changes related to cell wall biosynthesis were characteristic of disease progression and suggested a loosening of its structure to allow whip growth. Lignin biosynthesis related to whip formation may rely on Tyr metabolism through the overexpression of a bifunctional PTAL. The altered levels of Met residues along with overexpression of SAM synthetase and ACC synthase genes suggested a role for ethylene in whip emission. Moreover, unique secondary metabolites antifungal-related were identified using LC-ESI-MS approach, which may have potential biomarker applications. Lastly, a putative toxin was the most important fungal metabolite identified whose role during infection remains to be established.