ENVIRONMENTAL ASSESSMENT OF AN INNOVATIVE PLANT FOR THE WASTEWATER PURIFICATION IN THE BEVERAGE INDUSTRY

Nowadays, efforts to reduce the resource depletion and environmental emissions from the anthropic activities, are mandatory for sustainable development pattern. Among the key resources to save, pure water is as important as critic due to its scarcity and its essential role for life and growth. Furthermore, during the last decades, rising attention from institutions and industries is toward solutions for the water intensity decrease and wastewater recovery. This paper proposes the environmental assessment of an innovative wastewater collection and purification plant tailored to a mid-size beverage industry aiming at locally closing the loop of the water chain, allowing its recirculation and local reuse. After the description of the functional module features, sizes and design, based on a prototype actually working in Italy, the paper follows the ISO 14040 standards to develop an environmental assessment of the industrial system, quantifying the impact rising from the manufacturing and the assembly phases

The effects of two gold-N-heterocyclic carbene (NHC) complexes in ovarian cancer cells: a redox proteomic study

Purpose: Ovarian cancer is the fifth leading cause of cancer-related deaths in women. Standard treatment consists of tumor debulking surgery followed by platinum and paclitaxel chemotherapy; yet, despite the initial response, about 70-75% of patients develop resistance to chemotherapy. Gold compounds represent a family of very promising anticancer drugs. Among them, we previously investigated the cytotoxic and pro-apoptotic properties of Au(NHC) and Au(NHC)2PF6, i.e., a monocarbene gold(I) complex and the corresponding bis(carbene) complex. Gold compounds are known to alter the redox state of cells interacting with free cysteine and selenocysteine residues of several proteins. Herein, a redox proteomic study has been carried out to elucidate the mechanisms of cytotoxicity in A2780 human ovarian cancer cells. Methods: A biotinylated iodoacetamide labeling method coupled with mass spectrometry was used to identify oxidation-sensitive protein cysteines. Results: Gold carbene complexes cause extensive oxidation of several cellular proteins; many affected proteins belong to two major functional classes: carbohydrate metabolism, and cytoskeleton organization/cell adhesion. Among the affected proteins, Glyceraldehyde-3-phosphate dehydrogenase inhibition was proved by enzymatic assays and by ESI-MS studies. We also found that Au(NHC)2PF6 inhibits mitochondrial respiration impairing complex I function. Concerning the oxidized cytoskeletal proteins, gold binding to the free cysteines of actin was demonstrated by ESI-MS analysis. Notably, both gold compounds affected cell migration and invasion. Conclusions: In this study, we deepened the mode of action of Au(NHC) and Au(NHC)2PF6, identifying common cellular targets but confirming their different influence on the mitochondrial function

Cell instructive Liquid Crystalline Networks for myotube formation

Development of biological tissues in vitro is not a trivial task and requires the correct maturation of the selected cell line. To this aim, many attempts were done mainly by mimicking the biological environment using micro/nanopatterned or stimulated scaffolds. However, the obtainment of functional tissues in vitro is still far from being achieved. In contrast with the standard methods, we here present an easy approach for the maturation of myotubes toward the reproduction of muscular tissue. By using liquid crystalline networks with different stiffness and molecular alignment, we demonstrate how the material itself can give favorable interactions with myoblasts helping a correct differentiation. Electrophysiological studies demonstrate that myotubes obtained on these polymers have more adult-like morphology and better functional features with respect to those cultured on standard supports. The study opens to a platform for the differentiation of other cell lines in a simple and scalable way

Evaluation of SCO1 deletion on Saccharomyces cerevisiae metabolism through a proteomic approach

The Saccharomyces cerevisiae gene SCO1 has been shown to play an essential role in copper delivery to cytochrome c oxidase. Biochemical studies demonstrated specific transfer of copper from Cox17p to Sco1p, and physical interactions between the Sco1p and Cox2p. Deletion of SCO1 yeast gene results in a respiratory deficient phenotype. This study aims to gain a more detailed insight on the effects of SCO1 deletion on S. cerevisiae metabolism. We compared, using a proteomic approach, the protein pattern of SCO1 null mutant strain and wild-type BY4741 strain grown on fermentable and on nonfermentable carbon sources. The analysis showed that on nonfermentable medium, the SCO1 mutant displayed a protein profile similar to that of actively fermenting yeast cells. Indeed, on 3% glycerol, this mutant displayed an increase of some glycolytic and fermentative enzymes such as glyceraldehyde-3-phosphate dehydrogenase 1, enolase 2, pyruvate decarboxylase 1, and alcohol dehydrogenase 1. These data were supported by immunoblotting and enzyme activity assay. Moreover, the ethanol assay and the oxygen consumption measurement demonstrated a fermentative activity in SCO1 mutant on respiratory medium. Our results suggest that on nonfermentable carbon source, the lack of Sco1p causes a metabolic shift from respiration to fermentation

2D-DIGE analysis of ovarian cancer cell responses to cytotoxic gold compounds

Cytotoxic gold compounds hold today great promise as new pharmacological agents for treatment of human ovarian carcinoma; yet, their mode of action is still largely unknown. To shed light on the underlying molecular mechanisms, we performed 2D-DIGE analysis to identify differential protein expression in a cisplatin-sensitive human ovarian cancer cell line (A2780/S) following treatment with two representative gold(III) complexes that are known to be potent antiproliferative agents, namely AuL12 and Au2Phen. Software analysis using DeCyder was performed and few differentially expressed protein spots were visualized between the three examined settings after 24h exposure to the cytotoxic compounds, implying that cellular damage at least during the early phases of exposure is quite limited and selective reflecting the attempts of the cell to repair damage and to survive the insult. The potential of novel proteomic methods to disclose mechanistic details of cytotoxic metallodrugs is herein further highlighted. Different patterns of proteomic changes were highlighted for the two metallodrugs with only a few perturbed protein spots in common. Using MALDI-TOF MS and ESI-Ion trap MS/MS, several differentially expressed proteins were identified. Two of these were validated by western blotting: Ubiquilin-1, responsible for inhibiting degradation of protein such as p53 and NAP1L1, a candidate marker identified in primary tumors. In conclusion, we performed a comprehensive analysis of proteins regulated by AuL12 and Au2Phen, providing a useful insight into their mechanisms of action

GEOSTAR, an observatory for deep sea geophysical and oceanographic researches: characteristics, first scientific mission and future activity

GEOSTAR (GEophysical and Oceanographic STation for Abyssal Research) is a project funded by in the 4th Framework Programme of the European Commission, with the aim of developing an innovative deep sea benthic observatory capable of carrying out long-term (up to 1 year) scientific observations at abyssal depths. The configuration of the observatory, conceived to be a node of monitoring networks, is made up of two main subsystems: the Bottom Station, which in addition to the acquisition and power systems and all the sensors also hosts the communications systems; and the Mobile Docker, a dedicated tool for surface-assisted deployment and recovery. At present the Bottom Station is equipped with a triaxial broad-band seismometer, two magnetometers (fluxgate and scalar), CTD, transmissometer, ADCP, but it can easily host other sensors for different experiments. The first phase of the project, started in November 1995, was concluded with the demonstration mission in Adriatic Sea at shallow water depth (42 m) in August - September 1998. Some preliminary results of this first scientific experiment are presented and discussed. The second phase, started in 1999, will end with a long-term deep sea scientific mission, scheduled during 2000 for 6-8 months at 3400 m.w.d. in the southern Tyrrhenian bathyal plain.Published491-4973A. Ambiente MarinoN/A or not JCRrestricte

Mission results from the first GEOSTAR observatory (Adriatic Sea, 1998)

We assess the first mission of the GEOSTAR (GEophysical and Oceanographic STation for Abyssal Research) deep-sea multidisciplinary observatory for its technical capacity, performance and quality of recorded data. The functioning of the system was verified by analyzing oceanographic, seismological and geomagnetic measurements. Despite the mission’s short duration (21 days), its data demonstrated the observatory’s technological reliability and scientific value. After analyzing the oceanographic data, we found two different regimes of seawater circulation and a sharp and deepening pycnocline, linked to a down-welling phenomenon. The reliability of the magnetic and seismological measurements was evaluated by comparison with those made using on-land sensors. Such comparison of magnetic signals recorded by permanent land geomagnetic stations and GEOSTAR during a “quiet” day and one with a magnetic storm confirmed the correct functioning of the sensor and allowed us to estimate the seafloor observatory’s orientation. The magnitudes of regional seismic events recorded by our GEOSTAR seismometer agreed with those computed from land stations. GEOSTAR has thus proven itself reliable for integrating other deep-sea observation systems, such as modular observatories, arrays, and instrumented submarine cablesPublished361-373ope