Iriani Rodrigues Maldonade

Prof. Iriani Rodrigues Maldonade

Brazilian Agricultural Research Corporation, Brasília, Distrito Federal, Brazil
orcid

Research Focus & Metrics

Academic Career Length

27Years (2000-Present)

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

Representative Publications

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9 December 2020 in Molecules
Verified
Journal Article
Open access
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GMGabriela Marcelino
Gabriela Marcelino
David Johane MachateDavid Johane Machate
David Johane Machate
KFKarine Freitas
Karine Freitas
PHPRISCILA HIANE
PRISCILA HIANE
IMIriani Rodrigues Maldonade
Iriani Rodrigues Maldonade
RGRita De Cássia Avellaneda Guimarães
Rita De Cássia Avellaneda Guimarães
Carotenoids are vital antioxidants for plants and animals. They protect cells from oxidative events and act against the inflammatory process and carcinogenesis. Among the most abundant carotenoids in human and foods is β-carotene. This carotenoid has the highest level of provitamin A activity, as it splits into two molecules of retinol through the actions of the cytosolic enzymes: β-carotene-15,15′-monooxygenase (β-carotene-15,15′-oxygenase 1) and β-carotene-9′,10′-dioxygenase (β-carotene-9′,10′-oxygenase 2). The literature supports the idea that β-carotene acts against type 2 diabetes mellitus, cardiovascular diseases, obesity, and metabolic syndrome. Due to the many processes involved in β-carotene biosynthesis and metabolic function, little is known about such components, since many mechanisms have not yet been fully elucidated. Therefore, our study concisely described the relationships between the consumption of carotenoids, with emphasis on β-carotene, and obesity and type 2 diabetes mellitus and its associated parameters in order to understand the preventive role of carotenoids better and encourage their consumption.

1 November 2021 in Food Research International
Verified
Journal Article
Closed access
LMLilian Regina Barros Mariutti
Lilian Regina Barros Mariutti
KRKemilla Sarmento Rebelo
Kemilla Sarmento Rebelo
ABAntonio Bisconsin-Junior
Antonio Bisconsin-Junior
JMJanne Santos de Morais
Janne Santos de Morais
MMMarciane Magnani
Marciane Magnani
CCCinthia Baú Betim Cazarin
Cinthia Baú Betim Cazarin

1 March 2008 in Food Chemistry
Verified
Journal Article
Closed access
IMIriani Rodrigues Maldonade
Iriani Rodrigues Maldonade
DRDelia B. Rodriguez-Amaya
Delia B. Rodriguez-Amaya
ASAdilma R.P. Scamparini
Adilma R.P. Scamparini

1 May 2021 in Food Chemistry
Verified
Journal Article
Closed access
MLMaria Isabel Ordoñez Lozada
Maria Isabel Ordoñez Lozada
IMIriani Rodrigues Maldonade
Iriani Rodrigues Maldonade
Daniele Bobrowski RodriguesDaniele Bobrowski Rodrigues
Daniele Bobrowski Rodrigues
DSDébora Silva Santos
Débora Silva Santos
BSBeatriz Alejandra Ortega Sanchez
Beatriz Alejandra Ortega Sanchez
Livia de Lacerda de Lacerda de OliveiraLivia de Lacerda de Lacerda de Oliveira
Livia de Lacerda de Lacerda de Oliveira

19 June 2022 in Nutrients
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Journal Article
Open access
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GMGabriela Marcelino
Gabriela Marcelino
PHPRISCILA HIANE
PRISCILA HIANE
APArnildo Pott
Arnildo Pott
WFWander Fernando de Oliveira Filiú
Wander Fernando de Oliveira Filiú
Anderson R. L. CairesAnderson R. L. Caires
Anderson R. L. Caires
RGRita De Cássia Avellaneda Guimarães
Rita De Cássia Avellaneda Guimarães
Mauritia flexuosa (Buriti) pulp oil contains bioactive substances and lipids that are protective against cardiovascular and inflammatory diseases. We performed physical and chemical analyses to verify its quality and stability. Buriti oil was stable according to the Rancimat test, presenting an induction period of 6.6 h. We evaluated the effect of supplementation with crude buriti oil and olive oil on metabolic parameters in 108 Swiss mice for 90 days. We investigated six groups: extra virgin olive oil (EVOO) 1 and 2 (1000 and 2000 mg/kg), buriti oil (BO) 1 and 2 (1000 and 2000 mg/kg), synergic (S) (BO1 + EVOO1), and control (water dose 1000 mg/kg). The animals were euthanized to examine their blood, livers, and fats. The supplementation did not interfere with food consumption, weight gain, and histological alterations in the liver. Group S showed the strongest relationship with the fractions HDL-c and non-HDL-c, indicating a possible cardioprotective effect. Moreover, we observed significantly higher IL-6 levels in the control, EVOO2, and BO1 groups than in the EVOO1 group. Resistin was also significantly higher for the synergic treatment than for the control. We conclude that BO combined with EVOO could be an excellent food supplement for human consumption.

1 March 2007 in Brazilian Journal of Microbiology
Verified
Journal Article
Open access
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IMIriani Rodrigues Maldonade
Iriani Rodrigues Maldonade
ASAdilma R. P. Scamparini
Adilma R. P. Scamparini
DRDélia B. Rodriguez-Amaya
Délia B. Rodriguez-Amaya
The objective of the present study was to select and identify yeasts from Brazil capable of producing carotenoids. Pigmented yeasts were isolated from soil, leaves, fruits, flowers and a processed product. The samples were incubated at 30ºC in Erlenmeyer flasks, containing YM broth. After 48 hours, they were inoculated in Petri dishes with YM agar, and incubated at 30ºC during 120 hours. The yeast colonies, which presented yellow to red coloration, were transferred to culture tubes containing YM agar, and incubated at 30ºC for 72 hours. Out of 242 samples, only five had yellow to red color at high intensity. These highly pigmented yeasts were re-isolated in Petri dishes with YM agar and then transferred to tubes with GPYM agar. Identification through morphological and reproduction characteristics, along with physiological and biochemical tests, classified four strains as R. mucilaginosa and one strain as R. graminis. The main carotenoids extracted from them were identified through HPLC analysis as beta-carotene and torulene. The strains showed potential as promising microorganisms for the commercial production of carotenoids.Este trabalho teve como objetivo selecionar e identificar leveduras encontradas no Brasil capazes de produzir carotenóides. As leveduras pigmentadas foram isoladas de amostras de solos, folhas, frutos, flores e um alimento processado. As amostras foram colocadas em frascos de erlenmeyer, contendo meio de Extrato de Malte e Levedura (YM), e incubadas a 30ºC. Após 48 horas, as amostras foram inoculadas em placas de petri contendo meio YM ágar e incubadas a 30ºC por 120 horas. As colônias, que apresentaram coloração entre amarelo e vermelho, foram transferidas para os tubos de culturas, contendo meio YM ágar e incubadas a 30ºC por 72 horas. Das 242 amostras, somente cinco delas apresentaram coloração intensa entre amarelo e vermelho. Estas colônias de leveduras foram reisoladas, em placas de petri contendo YM ágar e, posteriormente, transferidas para tubos de ensaios contendo GPYM ágar. A identificação das leveduras, baseada nas características morfológicas, de reprodução, além dos testes fisiológicos e bioquímicos, classificou quatro linhagens como Rhodotorula mucilaginosa e uma como Rhodotorula graminis. Os principais pigmentos extraídos destas linhagens foram identificados através da análise de cromatografia de alta eficiência como beta-caroteno e toruleno. As linhagens de leveduras mostraram potencial como microrganismos promissores para a produção comercial de carotenóides por fermentação