CEReS -Co-processing of Coal Mine & Electronic Wastes: Novel Resources for a Sustainable Future

International audienceMany coal mines produce waste which causes acid mine drainage (AMD) potentially resulting in severe environmental damage. This drainage can be treated, but most wastes will continue to produce such drainage for hundreds of years. Therefore, longer term, permanent solutions are needed. At the same time, the pace of technological development means most electrical and electronic equipment becomes obsolete within a matter of years. This results in the generation of vast and growing quantities of electronic waste (e-waste) every year. Where this cannot be recycled, it must be discarded. CEReS was a 3.2 M€ RFCS-funded project comprising eight partners from five countries. It targeted the development of a co-processing approach to treat these waste streams to produce metals and other valuable products, while eliminating their environmental impact. This brings together two waste streams from opposite ends of the supply chain (for which no alternative treatment option exists); turning each into a novel resource in a single, coherent 'grave-to-cradle' process. This industrial ecology approach is key to supporting a circular economy while securing the sustainable supply of critical raw materials. The project successfully elaborated a novel co-processing flow-sheet comprising: (i) the accelerated weathering of AMD-generating coal production wastes to generate a biolixiviant; (ii) the pyrolysis and catalytic cracking of low-grade PCBs to produce hydrocarbon fuel, a halogen brine a Cu-rich char; (iii) the leaching of base metals from the char using the biolixiviant; (iv) the reuse of the stabilised coal wastes; and (v) the recovery of valuable metal while concentrating precious and critical metals into enriched substrates. These individual process units were demonstrated individually at lab-pilot scale. The data were then used to validate the entire flow-sheet in an integrated process simulator. Finally an LCA approach was used to demonstrate the environmental benefits of the CEReS process over the status quo

Stress-Induced PARP Activation Mediates Recruitment of Drosophila Mi-2 to Promote Heat Shock Gene Expression

Eukaryotic cells respond to genomic and environmental stresses, such as DNA damage and heat shock (HS), with the synthesis of poly-[ADP-ribose] (PAR) at specific chromatin regions, such as DNA breaks or HS genes, by PAR polymerases (PARP). Little is known about the role of this modification during cellular stress responses. We show here that the nucleosome remodeler dMi-2 is recruited to active HS genes in a PARP–dependent manner. dMi-2 binds PAR suggesting that this physical interaction is important for recruitment. Indeed, a dMi-2 mutant unable to bind PAR does not localise to active HS loci in vivo. We have identified several dMi-2 regions which bind PAR independently in vitro, including the chromodomains and regions near the N-terminus containing motifs rich in K and R residues. Moreover, upon HS gene activation, dMi-2 associates with nascent HS gene transcripts, and its catalytic activity is required for efficient transcription and co-transcriptional RNA processing. RNA and PAR compete for dMi-2 binding in vitro, suggesting a two step process for dMi-2 association with active HS genes: initial recruitment to the locus via PAR interaction, followed by binding to nascent RNA transcripts. We suggest that stress-induced chromatin PARylation serves to rapidly attract factors that are required for an efficient and timely transcriptional response

SS18 Together with Animal-Specific Factors Defines Human BAF-Type SWI/SNF Complexes

Contains fulltext : 94049.pdf (publisher's version ) (Open Access

DNA methylation and methyl-CpG binding proteins: developmental requirements and function

DNA methylation is a major epigenetic modification in the genomes of higher eukaryotes. In vertebrates, DNA methylation occurs predominantly on the CpG dinucleotide, and approximately 60% to 90% of these dinucleotides are modified. Distinct DNA methylation patterns, which can vary between different tissues and developmental stages, exist on specific loci. Sites of DNA methylation are occupied by various proteins, including methyl-CpG binding domain (MBD) proteins which recruit the enzymatic machinery to establish silent chromatin. Mutations in the MBD family member MeCP2 are the cause of Rett syndrome, a severe neurodevelopmental disorder, whereas other MBDs are known to bind sites of hypermethylation in human cancer cell lines. Here, we review the advances in our understanding of the function of DNA methylation, DNA methyltransferases, and methyl-CpG binding proteins in vertebrate embryonic development. MBDs function in transcriptional repression and long-range interactions in chromatin and also appear to play a role in genomic stability, neural signaling, and transcriptional activation. DNA methylation makes an essential and versatile epigenetic contribution to genome integrity and function

Utilisation de techniques bactériologiques et biochimiques pour l'étude du biofilm bactérien

La formation d'un voile biologique sur des surfaces métalliques exposées en milieu marin se traduit par une augmentation de la résistance au transfert thermique et à l'écoulement du fluide, mais aussi par un risque d'initiation de corrosion localisée due à la présence et à l'activité métabolique des microorganismes constituant ce biofilm. L'utilisation conjointe des méthodes microbiologiques et biochimiques permet une meilleure compréhension, à la fois des mécanismes de formation de ce biofilm et de la structure de la communauté bactérienne qui le constitue. Ces méthodes ont déjà été utilisées simultanément lors de travaux visant à étudier la corrosion bactérienne, la colonisation bactérienne de surfaces métalliques exposées à une eau de mer circulante ou l'action de biocides sur la formation du biofilm