PEDRO AGUILAR-ZÁRATE

Dr. PEDRO AGUILAR-ZÁRATE

Instituto Tecnológico de Ciudad Valles, Tecnológico Nacional de México/ I. T. de Ciudad Valles, Ciudad Valles, San Luis Potosí, Mexico
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Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

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

Representative Publications

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14 February 2024 in Foods
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Journal Article
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AAAngélica Almanza-Oliveros
Angélica Almanza-Oliveros
IHIsrael Bautista Hernández
Israel Bautista Hernández
CCCecilia Castro-López
Cecilia Castro-López
PEDRO AGUILAR-ZÁRATEPEDRO AGUILAR-ZÁRATE
PEDRO AGUILAR-ZÁRATE
ZMZahidd Meza-Carranco
Zahidd Meza-Carranco
Guillermo Cristian Guadalupe Martínez-ÁvilaGuillermo Cristian Guadalupe Martínez-Ávila
Guillermo Cristian Guadalupe Martínez-Ávila
From a circular economy perspective, the appropriate management and valorization of winery wastes and by-products are crucial for sustainable development. Nowadays, grape pomace (GP) has attracted increasing interest within the food field due to its valuable content, comprising nutritional and bioactive compounds (e.g., polyphenols, organic and fatty acids, vitamins, etc.). Particularly, GP polyphenols have been recognized as exhibiting technological and health-promoting effects in different food and biological systems. Hence, GP valorization is a step toward offering new functional foods and contributing to solving waste management problems in the wine industry. On this basis, the use of GP as a food additive/ingredient in the development of novel products with technological and functional advantages has recently been proposed. In this review, we summarize the current knowledge on the bioactivity and health-promoting effects of polyphenolic-rich extracts from GP samples. Advances in GP incorporation into food formulations (enhancement of physicochemical, sensory, and nutritional quality) and information supporting the intellectual property related to GP potential applications in the food industry are also discussed.

23 May 2017 in Phytochemical Analysis
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PEDRO AGUILAR-ZÁRATEPEDRO AGUILAR-ZÁRATE
PEDRO AGUILAR-ZÁRATE
JWJorge E. Wong-Paz
Jorge E. Wong-Paz
MMMariela Ramona Michel
Mariela Ramona Michel
JBJuan Buenrostro‐Figueroa
Juan Buenrostro‐Figueroa
HDHugo R. Díaz
Hugo R. Díaz
Cristobal N. AguilarCristobal N. Aguilar
Cristobal N. Aguilar

30 December 2015 in Microbial Cell Factories
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PEDRO AGUILAR-ZÁRATEPEDRO AGUILAR-ZÁRATE
PEDRO AGUILAR-ZÁRATE
MCMario A. Cruz
Mario A. Cruz
JMJulio Cesar Montanez
Julio Cesar Montanez
RRRaul Rodriguez
Raul Rodriguez
JWJorge E. Wong-Paz
Jorge E. Wong-Paz
Cristobal N. AguilarCristobal N. Aguilar
Cristobal N. Aguilar
Tannase is an enzyme that catalyses the breakdown of ester bonds in gallotannins such as tannic acid. In recent years, the interest on bacterial tannases has increased because of its wide applications. The lactic acid bacteria (LAB) plays an important role in food tannin biotransformation, it has the ability of hydrolyse tannins in ruminants intestine. The finding of tannin hydrolysis by LAB has sparked their use as tannase producer. The bacterial strains used in the present work were identified as Bacillus subtilis AM1 and Lactobacillus plantarum CIR1. The maximal tannase production levels were 1400 and 1239 U/L after 32 and 36 h of fermentation respectively, for B. subtilis AM1 and L. plantarum CIR1. Maximum gallic acid release was 24.16 g/L for B. subtilis AM1 and 23.73 g/L for L. plantarum CIR1. HPLC analysis showed the formation of another peaks in the retention time range of 9–14 min, which could be attributed to the formation of di or tri-galloyl glucose. According to database, the strains were identified as Bacillus subtilis AM1 and Lactobacillus plantarum CIR1. In conclusion, both strains had the capability to produce good titres of extracellular tannase and release gallic acid.

1 March 2021 in Food Chemistry
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Journal Article
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JWJorge E. Wong-Paz
Jorge E. Wong-Paz
SGSylvain Guyot
Sylvain Guyot
PEDRO AGUILAR-ZÁRATEPEDRO AGUILAR-ZÁRATE
PEDRO AGUILAR-ZÁRATE
DMDiana B. Muñiz-Márquez
Diana B. Muñiz-Márquez
JCJuan C. Contreras-Esquivel
Juan C. Contreras-Esquivel
Cristobal N. AguilarCristobal N. Aguilar
Cristobal N. Aguilar

8 August 2018 in Mini-Reviews in Medicinal Chemistry
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PEDRO AGUILAR-ZÁRATEPEDRO AGUILAR-ZÁRATE
PEDRO AGUILAR-ZÁRATE
JWJorge E. Wong-Paz
Jorge E. Wong-Paz
JBJuan J. Buenrostro-Figueroa
Juan J. Buenrostro-Figueroa
JAJuan A. Ascacio
Juan A. Ascacio
JCJuan C. Contreras-Esquivel
Juan C. Contreras-Esquivel
Cristobal N. AguilarCristobal N. Aguilar
Cristobal N. Aguilar
The ellagitannins are a group of phenolic compounds with biological activities. The ellagic acid is the product obtained from hydrolysis of ellagitannins. Information related to the biosynthesis of ellagitannins still been scarce and confused. The ellagitannins are obtained from plants and their purification process implies mainly the use of chromatographic techniques. The ellagitannin acyl hydrolase (EAH) also known as ellagitannase is an enzyme capable to hydrolyze the ester bonds of ellagitannins and the consequent releasing of ellagic acid. Information about the EAH is not clear because the enzyme had showed different activities due to the low purity or complexity of substrates and there are no available information about the biochemical, physicochemical and molecular characteristics of EAH. The present review describes information related to the sources, biosynthesis and the purification of ellagitannins and a current assessment on the production of ellagitannase.

1 April 2014 in Phytochemical Analysis
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Journal Article
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JWJorge E. Wong‐Paz
Jorge E. Wong‐Paz
DMDiana B. Muñiz‐Márquez
Diana B. Muñiz‐Márquez
PEDRO AGUILAR-ZÁRATEPEDRO AGUILAR-ZÁRATE
PEDRO AGUILAR-ZÁRATE
RRRaúl Rodríguez‐Herrera
Raúl Rodríguez‐Herrera
Cristobal N. AguilarCristobal N. Aguilar
Cristobal N. Aguilar