Saccharomyces yeasts degrade sugars to two-carbon components, in particular ethanol, even in the presence of excess oxygen. This characteristic is called the Crabtree effect and is the background for the 'make–accumulate–consume' life strategy, which in natural habitats helps Saccharomyces yeasts to out-compete other microorganisms. A global promoter rewiring in the Saccharomyces cerevisiae lineage, which occurred around 100 mya, was one of the main molecular events providing the background for evolution of this strategy. Here we show that the Dekkera bruxellensis lineage, which separated from the Saccharomyces yeasts more than 200 mya, also efficiently makes, accumulates and consumes ethanol and acetic acid. Analysis of promoter sequences indicates that both lineages independently underwent a massive loss of a specific cis-regulatory element from dozens of genes associated with respiration, and we show that also in D. bruxellensis this promoter rewiring contributes to the observed Crabtree effect.

Plastic is one of the most commonly produced and used materials in the world due to its outstanding features. However, the worldwide use of plastics and poor waste management have led to negative impacts on ecosystems. Plastic degradation in the environment leads to the generation of plastic particles with a size of <5 mm, which are defined as microplastics (MPs). These represent a global concern due to their wide dispersion in water environments and unclear potential ecotoxicological effects. Different studies have been performed with the aim of evaluating the presence and impacts of MPs in the marine environment. However, the presence of MPs in freshwater systems is still poorly investigated, making data retrieval a difficult task. The purpose of this review is to identify the main aspects concerning MPs pollution sources in lakes and rivers, with a focus on freshwater sediments as a site of accumulation and as the habitat of benthic organisms, which are key components of food webs and play a fundamental role in energy/contaminant transfer processes, but are still poorly considered. Through this review, the sources and fate of MPs in freshwater are analysed, ecotoxicological studies focused on sediments and benthic fauna are exposed, the most frequently used sampling and analysis strategies are reported, and future trends of MPs analysis in this field are proposed.

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Industrial fermentation of lignocellulosic hydrolysates to ethanol requires microorganisms able to utilise a broad range of carbon sources and generate ethanol at high yield and productivity. D. bruxellensis has recently been reported to contaminate commercial ethanol processes, where it competes with Saccharomyces cerevisiae [4, 26]. In this work Brettanomyces/Dekkera yeasts were studied to explore their potential to produce ethanol from renewable sources under conditions suitable for industrial processes, such as oxygen-limited and low-pH conditions. Over 50 strains were analysed for their ability to utilise a variety of carbon sources, and some strains grew on cellobiose and pentoses. Two strains of D. bruxellensis were able to produce ethanol at high yield (0.44 g g(-1) glucose), comparable to those reported for S. cerevisiae. B. naardenensis was shown to be able to produce ethanol from xylose. To obtain ethanol from synthetic lignocellulosic hydrolysates we developed a two-step fermentation strategy: the first step under aerobic conditions for fast production of biomass from mixtures of hexoses and pentoses, followed by a second step under oxygen limitation to promote ethanol production. Under these conditions we obtained biomass and ethanol production on synthetic lignocellulosic hydrolysates, with ethanol yields ranging from 0.2 to 0.3 g g(-1) sugar. Hexoses, xylose and arabinose were consumed at the end of the process, resulting in 13 g l(-1) of ethanol, even in the presence of furfural. Our studies showed that Brettanomyces/Dekkera yeasts have clear potential for further development for industrial processes aimed at production of ethanol from renewable sources.