Changes in enzyme activities and amino acids and their relations with phenolic compounds contents in okra treated by LED lights of different colors

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Author listWilawan N., Ngamwonglumlert L., Devahastin S., Chiewchan N.

PublisherElsevier

Publication year2019

JournalLWT - Food Science and Technology (0023-6438)

Volume number12

Issue number11

Start page1945

End page1954

Number of pages10

ISSN0023-6438

URLhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85075939508&doi=10.1016%2fj.lwt.2019.108841&partnerID=40&md5=873086430c0916605a579f55337bf154

LanguagesEnglish-Great Britain (EN-GB)


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Abstract

A novel and rapid method to identify contamination of Vibrio parahaemolyticus during an enrichment was developed. The principle was based on the bacteria's capability of carbohydrate fermentation and amino acid decarboxylation. Six different broths were developed with four sugar substrates, namely, dextrose (DEX), arabinose (ARA), mannose (MAO), mannitol (MAI), and two amino acids, namely, lysine (LYS) and ornithine (ODB). Bromocresol purple (BP) and phenol red (PR) were added to detect pH changes of the broths. The absorbance of the color change was determined for all sugar broths at 600 nm and both amino acids at 550 nm. Salinity and pH were adjusted to suppress competitive bacteria. The optimal conditions for the sugar substrates and the amino acids were 8% NaCl/pH = 9.0 and 6% NaCl/pH = 6.0, respectively. In real samples, this method was capable of detecting V. parahaemolyticus with a limit of detection of 0.1–1.0 log CFU/mL (measured as an initial cell concentration in the samples). At 24 h, this method also yielded a 100% sensitivity and improved a specificity to 95%–100%, compared to the 88% specificity as obtained in the conventional method. Integrating the detection of V. parahaemolyticus provided a quick and effective screening for the presence of V. parahaemolyticus. © 2019 Elsevier Ltd


Keywords

Amino acid decarboxylationBacterial contaminationCarbohydrate fermentation


Last updated on 2023-03-10 at 07:36