mullenite
Well-Known Member
Lots to read as a result of my EBSCO search, primarily dealing with fungi that infect barley such as Fusarium complex and Ochratoxin A.
When it comes to Ochratoxin A (symbols that don't show are ^-1):
For Fusarium mychotoxins (important note: this is during the brewing process, not the beer itself DON levels were tested in 14 US beers and none were found to contain the toxin. In the paper itself they cover this and say that while toxins were found to be transferred more research is needed.):
One paper that was pretty interesting looked for a correlation between home-brewed beer consumption and esophageal cancer in Africa due to a higher iron content in home-brewed beers vs. commercial. They found that while home-brewed beer did have a significantly higher iron content (258-fold actually) there was no correlation. The patients who drank home-brewed beer did not suffer from iron-overload.
If anyone is interested in these papers let me know and I will email them to you. I have the PDFs saved.
When it comes to Ochratoxin A (symbols that don't show are ^-1):
Estimations of ochratoxin A (OTA) and 4-deoxynivalenol (DON) exposure of the Belgian population through beer
consumption were made using the results of the recent Belgian food survey and the compiled data set of OTA and DON
levels in conventionally and organically produced beers in 2003–05. For the consumers of organic beers, the daily intake
of OTA was 0.86 (in 2003), 1.76 (in 2004) and 0.72 (in 2005) ng kg1 body weight (bw), considering the mean beer
consumption (0.638 litres) and the average level of OTA in 2003, 2004 and 2005, respectively. Using the 97.5th percentile
of beer consumption (1.972 litres), the corresponding OTA daily intakes were 2.65, 5.44 and 2.24 ng kg1 bw, which are
close or above the tolerable daily intake (TDI) of 5 ng kg1 bw. For the consumers of conventional beers, the OTA intakes
were low: 0.23, 0.23 and 0.11 ng kg1 bw day1 for the average beer consumption, in 2003, 2004 and 2005 against 0.72,
0.73 and 0.34 ng kg1 bw day1 when the 97.5th percentile level was considered. As for the DON intake, the estimates were
quite low for both conventional and organic beer consumers when the provisional maximum TDI (PMTDI) of 1 mg kg1 bw
was considered. Average consumption of organic beer led to daily intakes of 0.05 and 0.04 mgDONkg1 bw in 2003 and
2004, respectively, whilst for conventional beer, daily intakes were 0.07 and 0.05 mgDONkg1 bw. At the 97.5th percentile
level of beer consumption, daily intakes of 0.15 and 0.13 mg kg1 bw were obtained for organic beers against 0.23 and
0.17 mg kg1 bw for conventional ones. The results showed that beer could be an important contributor to OTA exposure in
Belgium, even though a declining trend seems to be apparent during the last year of monitoring. Therefore, efforts should
be devoted to maintain the OTA levels as low as reasonably achievable, especially for organic beer.
For Fusarium mychotoxins (important note: this is during the brewing process, not the beer itself DON levels were tested in 14 US beers and none were found to contain the toxin. In the paper itself they cover this and say that while toxins were found to be transferred more research is needed.):
The fate of five Fusarium toxins — deoxynivalenol (DON), sum of 15- and 3-acetyl-deoxynivalenol (ADONs),
HT-2 toxin (HT-2) representing the main trichothecenes and zearalenone (ZON) during the malting and brewing
processes — was investigated. In addition to these ‘free’ mycotoxins, the occurrence of deoxynivalenol-
3-glucoside (DON-3-Glc) was monitored for the first time in a beer production chain (currently, only DON and
ZON are regulated). Two batches of barley, naturally infected and artificially inoculated with Fusarium spp.
during the time of flowering, were used as a raw material for processing experiments. A highly sensitive procedure
employing high-performance liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS) was
validated for the analysis of ‘free’ Fusarium mycotoxins and DON-conjugate in all types of matrices. The method
was also able to detect nivalenol (NIV), fusarenon-X (FUS-X) and T-2 toxin (T-2); nevertheless, none of these
toxins was found in any of the samples. While steeping of barley grains (the first step in the malting process)
apparently reduced Fusarium mycotoxin levels to below their quantification limits (5–10 mgkg1), their successive
accumulation occurred during germination. In malt, the content of monitored mycotoxins was higher compared
with the original barley. The most significant increase was found for DON-3-Glc. During the brewing process,
significant further increases in levels occurred. Concentrations of this ‘masked’ DON in final beers exceeded ‘free’
DON, while in malt grists this trichothecene was the most abundant, with the DON/DON-3-Glc ratio being
approximately 5:1 in both sample series. When calculating mass balance, no significant changes were observed
during brewing for ADONs. The content of DON and ZON slightly decreased by a maximum of 30%. Only
traces of HT-2 were detected in some processing intermediates (wort after trub removal and green beer).
One paper that was pretty interesting looked for a correlation between home-brewed beer consumption and esophageal cancer in Africa due to a higher iron content in home-brewed beers vs. commercial. They found that while home-brewed beer did have a significantly higher iron content (258-fold actually) there was no correlation. The patients who drank home-brewed beer did not suffer from iron-overload.
If anyone is interested in these papers let me know and I will email them to you. I have the PDFs saved.