Fungicide application is a key factor in the control of mycotoxin contamination in the harvested wheat grain. However, the practical results are often disappointing. In 2000–2004, 2006–2008 and 2007 and 2008, three experiments were made to test the efficacy of fungicide control on Fusarium Head Blight (FHB) in wheat and to find ways to improve control of the disease and toxin contamination. In a testing system we have used for 20 years, tebuconazole and tebuconazole + prothioconazole fungicides regularly reduced symptoms by about 80% with a correlating reduction in toxin contamination. Averages across the years normally show a correlation of r = 0.90 or higher. The stability differences (measured by the stability index) between the poorest and the best fungicides are about 10 or more times, differing slightly in mycotoxin accumulation, FHB index (severity) and Fusarium damaged kernels (FDK). The weak fungicides, like carbendazim, were effective only when no epidemic occurred or epidemic severity was at a very low level. Similar fungicide effects were seen on wheat cultivars which varied in FHB resistance. In this study, we found three fold differences in susceptibility to FHB between highly susceptible and moderately resistant cultivars when treated with fungicides. In the moderately resistant cultivars, about 50% of the fungicide treatments lowered the DON level below the regulatory limit. In the most susceptible cultivars, all fungicides failed to reduce mycotoxin levels low enough for grain acceptance, in spite of the fact that disease was significantly reduced. The results correlated well with the results of the large-scale field tests of fungicide application at the time of natural infection. The Turbo FloodJet nozzle reduced FHB incidence and DON contamination when compared to the TeeJet XR nozzle. Overall, the data suggest that significant decreases in FHB incidence and deoxynivalenol contamination in field situations are possible with proper fungicide applications. Additionally, small plot tests can be used to evaluate the quality of the field disease and toxin production.

The aim of this study was to apply RP-HPLC/ESI-ITMS and RP-HPLC/ESI-TOFMS to investigate and characterise six new higher molecular weight fumonisins (three pairs of isomers) extracted from a Fusarium verticillioides-infected solid rice culture. The ITMS and ITMS² spectra clearly indicated the m/z values (960, 984 and 986) of the protonated molecules and the FB₁ toxin-like structures of these compounds, respectively. Moreover, the data evaluation software of the TOFMS equipment unambiguously demonstrated the exact masses of the protonated molecules and the suggested empirical formulae (C₅₀H₈₉NO₁₆, C₅₂H₈₉NO₁₆ and C₅₂H₉₁NO₁₆) of the new fumonisins, with mass accuracy in the range between 0.1 and −1.1 ppm. Subtraction of the empirical formula of FB₁ toxin (C₃₄H₅₉NO₁₅) from these formulae and correction for the mass of water split-off from the fumonisin molecule during ester formation resulted in the empirical formulae of the fumonisin backbone esterifying agents (fatty acids): C₁₆H₃₂O₂ (palmitic acid, PA), C₁₈H₃₂O₂ (linoleic acid, LA) and C₁₈H₃₄O₂ (oleic acid, OA). We denoted the new compounds as esterified FB₁ (EFB₁) toxins, with the suggested names EFB₁ PA, iso-EFB₁ PA, EFB₁ LA, iso-EFB₁ LA, EFB₁ OA and iso-EFB₁ OA. The total amount of these new compounds comprised 0.1% of the FB₁ concentration, which may be rated as significant when it is considered that these new components are significantly more apolar than earlier-described fumonisins, and their uptake into and toxicity elicited in the various tissues of living organisms may therefore also be significantly different from those of other fumonisins.

A straightforward and reliable method for the regioselective synthesis of steroidal 1,4-disubstituted triazoles and 1,5-disubstituted tetrazoles via copper(I)-catalyzed cycloadditions is reported. Heterocycle moieties were efficiently introduced onto the starting azide compound 3β-acetoxy-16β-azidomethylandrost-5-en-17β-ol through use of the “click” chemistry approach. The antiproliferative activities of the newly-synthesized triazoles were determined in vitro on three human gynecological cell lines (HeLa, MCF7 and A2780) using the microculture tetrazolium assay.

Following the earlier detection of six new esterified fumonisin B₁ (EFB₁) isomers containing three acyl groups in a Fusarium verticillioides-inoculated rice culture, it was assumed that linoleic, palmitic or oleic acid esterifies one of the free OH groups on the fumonisin backbone. On the basis of the results of our recent investigations we now propose that these EFB₁ isomers are actually 3-O- and 5-O-acyl derivatives of FB₁ (3-O-linoleoyl-FB₁, 5-O-linoleoyl-FB₁, 3-O-palmitoyl-FB₁, 5-O-palmitoyl-FB₁, 3-O-oleoyl-FB₁ and 5-O-oleoyl-FB₁). A F. verticillioides strain was identified that produced not only O-acyl-FB₁ isomers, but also low amounts of three N-acyl derivatives (N-linoleoyl-FB₁, N-palmitoyl-FB₁ and N-oleoyl-FB₁), which eluted from the HPLC column after the six O-acyl compounds and in the same sequence as for the O-acyl compounds. The characteristic positive and negative ESI-MS/MS spectra obtained after solid-phase extraction of the culture extract facilitated identification of these N-acyl-FB₁ derivatives. The biosynthesis of N-palmitoyl-FB₁ by F. verticillioides was verified by spiking the culture extract with synthetic N-palmitoyl-FB₁. This is the first report of the separation and mass spectrometric identification of the six O-acyl- and three N-acyl-FB₁ derivatives extracted from a F. verticillioides culture.

Several new fumonisin B₅ mycotoxin isomers (iso-FB₅) present in a rice culture inoculated with Fusarium verticillioides were separated on a RP-HPLC column recommended for the separation of structural isomers, and subsequently detected by time-of-flight and ion trap mass spectrometry. The exact masses of the eluted compounds were determined by using time-of-flight mass spectrometry. The m/z values of the 20 characteristic product ions including the hydrocarbon backbone and the characteristic neutral mass losses from the molecular and product ions of the compounds obtained by ion trap mass spectrometry, unambiguously indicated of the unknown iso-FB₅ compounds. The total amount of FB₅ toxin and its isomers was 0.9% of the quantity of the main compound (FB₁ toxin), which is a noteworthy quantity considering their potential toxicity. Based on the semi-quantitative measurement data it can be assumed that, in addition to the FB₅ of unknown structure, isomers designated 1, 2, and 20 can also be isolated among the iso-FB₅ compounds.

Fumonisins are frequent food contaminants. The high exposure to fumonisins can cause harmful effects in humans and animals. Fumonisin B1 (FB1) is the most typical member of this group; however, the occurrence of several other derivatives has been reported. Acylated metabolites of FB1 have also been described as possible food contaminants, and the very limited data available suggest their significantly higher toxicity compared to FB1. Furthermore, the physicochemical and toxicokinetic properties (e.g., albumin binding) of acyl-FB1 derivatives may show large differences compared to the parent mycotoxin. Therefore, we tested the interactions of FB1, N-palmitoyl-FB1 (N-pal-FB1), 5-O-palmitoyl-FB1 (5-O-pal-FB1), and fumonisin B4 (FB4) with human serum albumin as well as the toxic effects of these mycotoxins on zebrafish embryos were examined. Based on our results, the most important observations and conclusions are the following: (1) FB1 and FB4 bind to albumin with low affinity, while palmitoyl-FB1 derivatives form highly stable complexes with the protein. (2) N-pal-FB1 and 5-O-pal-FB1 likely occupy more high-affinity binding sites on albumin. (3) Among the mycotoxins tested, N-pal-FB1 showed the most toxic effects on zebrafish, followed by 5-O-pal-FB1, FB4, and FB1. (4) Our study provides the first in vivo toxicity data regarding N-pal-FB1, 5-O-pal-FB1, and FB4.