Abstract Dairy cattle when fed on aflatoxin B1 may excrete aflatoxin M1 in milk as a consequence of dietary exposure. Once AFM1 is excreted in milk, it is present in dairy products such as cheese, yogurt, among others. This mycotoxin is quite resistant to temperature therefore heat treatments like pasteurization and ultra-pasteurization are not enough to inactivate it. In this context, this article provides an overview of the biological decontamination methods on milk and cheese of the last decade, as a contribution to evaluate the evolution of this strategy as well as its efficiency according to their authors. Relevant studies published between January 2009 and May 2019 were selected after a systematic search of the literature in PubMed, Science direct and Google Scholar databases. According with our research in the last decade few studies have been published on these methods and unfortunately none of the published studies tested such methods in cheese. Throughout the research many studies on decontamination methods were found, however, in phosphate buffered saline solution or in culture medium. Further studies on biological decontamination on milk and mainly on cheese are necessary for this technique to be better developed and applied to a large scale in the industries.

Resumo Folhas de oliveira contêm oleuropeína, um composto fenólico conhecido por seu potencial antioxidante, antimicrobiano, anti-inflamatório, entre outros. Este trabalho teve como objetivo estudar a extração da oleuropeína, utilizando solvente hidroalcoólico. Folhas de oliveira (FO) foram maceradas a 25 °C com um solvente (S), formado por uma mistura de etanol e água (70:30 v/v), nas proporções FO:S iguais a 1:8, 1:6 e 1:3, em massa, com ou sem a presença de ácido acético. Observou-se que o maior teor de oleuropeína no extrato liofilizado (18 g/100 g, aproximadamente) foi obtido no procedimento utilizando a razão FO:S = 1:3, com ácido acético. Por fim, foi realizado um teste para verificar o efeito do extrato liofilizado sobre o tempo de indução em amostras de azeite de oliva extravirgem e refinado, verificando-se um aumento de três e duas horas, respectivamente. Concluiu-se que é possível obter extratos de folhas de oliveira utilizando solventes renováveis e que a oleuropeína pode atuar como um antioxidante natural no azeite, melhorando sua estabilidade oxidativa.

Abstract Olive leaves contain oleuropein, a substance known for its antioxidant, antimicrobial and antiinflammatory potentials, amongst others. The objective of this work was to study the extraction of oleuropein using a hydroalcoholic solvent. Olive leaves (OL) were macerated at 25 °C with a solvent (S) consisting of a mixture of ethanol and water (70:30 v/v), with OL:S mass ratios equal to 1:8, 1:6 and 1:3, with or without the presence of acetic acid. The highest oleuropein content found in the freeze dried extract (approximately 18 g/100 g) was obtained from the procedure using an OL:S ratio = 1: 3, in the presence of acetic acid. Finally, a test was carried out to verify the effect of the freeze dried extract on the induction time in samples of extra-virgin and refined olive oil, and increases of 3 and 2 hours, respectively, were observed. It was concluded that it is possible to obtain olive leaf extracts using renewable solvents, and that oleuropein can act as a natural antioxidant in olive oil, improving its oxidative stability.

ABSTRACT This study aimed to investigate the effect of peracetic acid (PAA, 0.5%) on adherent cells of three strains of Listeria monocytogenes strains belonging to serotypes 4b and 1/2b that had been previously isolated from the environment of a Brazilian cheese plant. The assays were conducted using polystyrene microplates and stainless steel coupons and the adhered cells were treated with PAA for 60, 120 and 180 s. On stainless steel, biofilms were partially inactivated by PAA after 60 s and almost 100% of the cells were damaged within 180 s using epifluorescence microscopy with LIVE/DEAD® staining. On polystyrene microplates, PAA decreased (P<0.05) biofilm biomass produced by the three L. monocytogenes isolates at 60 s, when compared with controls (no PAA treatment). However, PAA did not completely eliminate L. monocytogenes cells on polystyrene microplates (decreasing 1.8-2.5 log cycles after treatment with PAA for 180 s). The correct concentration and contact time of PAA is critical for eliminating biofilms formed by L. monocytogenes on stainless steel surfaces, although further studies are needed for defining efficient PAA treatments to remove adherent cells of this pathogen on plastic polymers.