Abstract

Ochratoxin A (OTA) is a toxic secondary metabolite produced by several fungal species of the genus Penicillium and Aspergillus. 2′R-Ochratoxin A (2′R-OTA) is a thermal isomerization product of OTA formed during food processing at high temperatures. Both compounds are detectable in human blood in concentrations between 0.02 and 0.41 µg/L with 2′R-OTA being only detectable in the blood of coffee drinkers. Humans have approximately a fifty-fold higher exposure through food consumption to OTA than to 2′R-OTA. In human blood, however, the differences between the concentrations of the two compounds is, on average, only a factor of two. To understand these unexpectedly high 2′R-OTA concentrations found in human blood, the affinity of this compound to the most abundant protein in human blood the human serum albumin (HSA) was studied and compared to that of OTA, which has a well-known high binding affinity. Using fluorescence spectroscopy, equilibrium dialysis, circular dichroism (CD), high performance affinity chromatography (HPAC), and molecular modelling experiments, the affinities of OTA and 2′R-OTA to HSA were determined and compared with each other. For the affinity of HSA towards OTA, a logK of 7.0–7.6 was calculated, while for its thermally produced isomer 2′R-OTA, a lower, but still high, logK of 6.2–6.4 was determined. The data of all experiments showed consistently that OTA has a higher affinity to HSA than 2′R-OTA. Thus, differences in the affinity to HSA cannot explain the relatively high levels of 2′R-OTA found in human blood samples.

Highlights

  • Ochratoxin A (OTA) is a toxic secondary metabolite produced by fungal species of the genusPenicillium and Aspergillus which can contaminate several agricultural commodities

  • To determine the binding of OTA and 20 R-OTA to human serum albumin (HSA), one In compartment of the cell was loaded a mixtureofoftwo and the respective this experiment, an equilibrium dialysiswith cell consisting compartments separatedochratoxin by a in buffer, while the second compartment was solely loaded with buffer

  • Equilibrium is reached, analysis of the ochratoxin concentration in both dialysis chambers makes it. This experiment was performed individually in triplicate for 25 nM OTA or 20 R-OTA using a possible to determine the ratio between unbound and HSA-bound ochratoxins

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Summary

Introduction

Ochratoxin A (OTA) is a toxic secondary metabolite produced by fungal species of the genus. Penicillium and Aspergillus which can contaminate several agricultural commodities. Within the Ochratoxin (OTA)and is a toxic secondary metabolite produced by fungal species themain genussources, European Union (EU) A cereals cereal products such as pasta, bread and beer areofthe. Within the0 R-OTA, while roasted coffee contributes ca.contaminate. 20 R-Ochratoxin A (2 European Union (EU). Cereals and cereal products such as pasta, bread and beer are the main sources, previously reported as 14R-ochratoxin A, Figure 1) is a diastereomer of OTA that is not produced by while roasted coffee only contributes ca. 10% to OTA exposure [1]. Cereals and cereal products such as pasta, bread and beer are the main sources, previously reported as 14R-ochratoxin A, Figure 1) is a diastereomer of OTA that is not produced by while roasted coffee only contributes ca. 10% to OTA exposure [1]. 2’R-Ochratoxin A

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