Risk assessment of the mycotoxin zearalenone
Trans-zearalenone, a resorcylic acid lactone, additionally referred to as F-2 poisonous substance, may be a nonsteroidal steroid hormone phytotoxin created by various species of Fusarium. As a result zearalenone is found in an exceedingly range of cereal crops and their derived food merchandise. A closely connected substance “zeranol” (zearalanol) is at this time being employed within the u. s. Associate in Nursingd North American country as an anabolic agent in Bos taurus. Zearalenone has been concerned in various incidences of mycotoxicosis in domestic animals, particularly pigs. 
Risk assessment of the mycotoxin ochratoxin A.
Ochratoxin A (OA) may be a plant toxin that has been found to occur in foods of plant origin, in edible animal tissues, in addition as in human blood sera and tissues. the flexibility of OA to maneuver up the organic phenomenon is assisted by its long half-life in bound edible animal species. during this report, associate analysis of the health risks to Canadians because of the presence of OA in food product is conferred. the primary a part of the report deals with the chemical science aspects, mycology, laboratory production, analytical ways, and natural incidence in plant product, animal product, and human tissues. the soundness of OA in foods and feeds, the consequences of food process, and also the removal from foods and feeds by physiochemical means that are mentioned. From these information, the worst case estimate for the daily exposure of Canadians to OA, from the consumption of pork-based food product and cereal foods, is or so five weight unit OA/kg body wt (mean of eaters) for young youngsters, the very best consumption cluster on a weight basis. 
Biosensors and multiple mycotoxin analysis
An chemistry biosensor assay for the detection of multiple mycotoxins in an exceedingly sample is delineated .
The inhibition assay is intended to live four completely different mycotoxins in an exceedingly single activity, following extraction, sample clean-up Associate in Nursingd incubation with an acceptable cocktail of anti-mycotoxin antibodies.
The different mycotoxins may be detected at the same time in relevant concentrations inside a time-frame of twenty five minutes, as well as the time required for detector regeneration. 
Variable protein homeostasis in housekeeping and non-housekeeping pathways under mycotoxins stress
Transcript levels are the first issue determinative supermolecule levels, except for the bulk of genes, fold changes in transcript levels are larger than the corresponding changes in supermolecule levels, a development that’s termed “protein homeostasis”. However, this development isn’t well characterised within the context of environmental changes. during this study, we tend to sequenced the complete transcriptome and protein of chicken primary hepatocytes administered 3 phytotoxin treatments biological weapon B1 (AFB1), Ochoratoxin A (OTA) and Zearalenone (ZEN). every phytotoxin iatrogenic distinctive set of differential expressed transcripts and proteins, suggesting variable toxicity and organic chemistry action in cell. we tend to found a weak direct correlation between transcript and supermolecule changes, and also the transcript changes were above the supermolecule changes. 
The Presence of Mycotoxins in Kenya’s Kalenjin Traditional Fermented Milk “Mursik”
The study aimed toward finishing up quantification of mycotoxins contaminating Mursik. Mursik is historically hard milk ready from freshly milked cow milk. Fermentation doesn’t happen in controlled systems or sterilized conditions; as a result contamination with yeasts, moulds and a few infective bacterium would commonly occur. These embrace species from the genus, Aspergillus|fungus genus}, Penicillium, Fusarium and fungus. Aspergillus, Penicillium and Fusarium has been referred to as the producers of mycotoxins, that ar secondary metabolites of fungi accountable mycoticoses in animals and humans. These mycotoxins include: aflatoxins, fumonisins and deoxynivalenol. The study was laboratory primarily based administered on mursik samples collected from households. All mursik samples were processed at phytology laboratory, Center for biology analysis (CMR), KEMRI. 
 Kuiper-Goodman, T., Scott, P. and Watanabe, H., 1987. Risk assessment of the mycotoxin zearalenone. Regulatory toxicology and pharmacology, 7(3), (Web Link)
 Kuiper-Goodman, T. and Scott, P.M., 1989. Risk assessment of the mycotoxin ochratoxin A. Biomedical and environmental sciences: BES, 2(3), (Web Link)
 van der Gaag, B., Spath, S., Dietrich, H., Stigter, E., Boonzaaijer, G., van Osenbruggen, T. and Koopal, K., 2003. Biosensors and multiple mycotoxin analysis. Food control, 14(4), (Web Link)
 Variable protein homeostasis in housekeeping and non-housekeeping pathways under mycotoxins stress
Yu Sun, Jikai Wen, Ruohong Chen & Yiqun Deng
Scientific Reports volume 9, Article number: 7819 (2019) (Web Link)
 Talaam, K. K., Nga’ng’a, Z. W., Lang’at, K. B., Kirui, M. C., Gonoi, T. and Bii, C. C. (2018) “The Presence of Mycotoxins in Kenya’s Kalenjin Traditional Fermented Milk ‘Mursik’”, Journal of Scientific Research and Reports, 21(1), (Web Link)