On the asymmetric representatives formulation for the vertex coloring problem

We consider the vertex coloring problem, which can be stated as the problem of minimizing the number of labels that can be assigned to the vertices of a graph G such that each vertex receives at least one label and the endpoints of every edge are assigned different labels. In this work, the 0-1 integer programming formulation based on representative vertices is revisited to remove symmetry. The previous polyhedral study related to the original formulation is adapted and generalized. New versions of facets derived from substructures of G are presented, including cliques, odd holes and anti-holes and wheels. In addition, a new class of facets is derived from independent sets of G. Finally, a comparison with the independent sets formulation is provided.     

Structural assessment under uncertain parameters via interval analysis

An efficient health monitoring system for damage detection in civil engineering structures using on-line monitoring data is being developed to identify any possible damage in short time. The present work is based on the treatment of uncertainties, which is one of the basic common difficulties faced when modelling structures. A methodology, based on interval analysis (IA) theory [R.E. Moore, Interval Analysis, Prentice-Hall, Englewood Cliffs, NJ, 1966] applied to a numerical constraint satisfaction problem (CSP) [J.R. Casas, J.C. Matos, J.A. Figueiras, J. Vehí, O. García, P. Herrero, Bridge monitoring and assessment under uncertainty via interval analysis, in: Ninth International Conference On Structural Safety And Reliability—ICOSSAR2005, 2005. pp. 487–494], is implemented in the damage detection [J.R. Casas, J.C. Matos, J.A. Figueiras, J. Vehí, O. García, P. Herrero, Bridge monitoring and assessment under uncertainty via interval analysis, in: Ninth International Conference On Structural Safety And Reliability—ICOSSAR2005, 2005. pp. 487–494] and modelling system of a long-term monitoring project in order to achieve such an objective. An algorithm is being developed for using such methodology with the obtained data.     

A Validated RP–LC Method for Simultaneous Determination of Losartan Potassium and Amlodipine Besilate in Pharmaceutical Preparations

A simple RP–LC method for simultaneous quantification of losartan and amlodipine and separation of their degradation products has been developed. For this purpose we tested appropriated mobile phase pH range, flow rate, temperature and different columns. The method was validated with an ODS column. A gradient of acetonitrile and phosphate pH 3.0 buffer was utilized as mobile phase. The linearity was determined at 50–150% level. Individual recoveries at 70–130% level ranged from 98.8 to 100.5% for losartan and 96.4–101.2% for amlodipine. The robustness was also evaluated. Although losartan has much higher quantities than amlodipine in commercial tablets, this method allowed simultaneous quantification for both drugs.     

A multipotential hydrolytic reactor using the yeast strainKluyveromyces marxianus

In previous publications, we described the continuous production of D-fructose from enzymatic hydrolysis of inulin with immobilized permeabiliized cells ofKluyveromyces marxianus and the increase of productivity obtained by using a mutant selected by NTG action on the wild-type strain. By improving reactor performance, it has been possible to reach 2000 g/L/d of liberated sugar from an inulin solution with the mutant strain.

In addition, it has been shown that the KF 28 mutant was an invertase and pectinase hyperproducer. These enzymatic activities are also secreted by the speciesKluyveromyces marxianus. Therefore, we investigated the possibility of using immobilized cells of this yeast as a multipotential hydrolysis reactor. A sucrose hydrolysis reactor and a pectin hydrolysis reactor were set up. It is shown here that the majority of the optimized parameters from the inulin hydrolysis reactor can be transported directly to the other reactors. However, some parameters have to be adapted, especially for pectin hydrolysis.

     

Need for food reference material in Latin America

Summary Even if some Latin American countries still need to extend their capacity for food quality control, many do have good control laboratories and high quality research institutions. That makes the need for reference material in Latin America similar to that of other parts of the world.The region has special problems related to mail and shipment delays, and to the lack of information on available reference material. It is recommended that additional reference material being made available for vitamins in food, for polar and non-polar organophosphorus pesticides in vegetables, for organophosphorus pesticide and veterinary drugs in meat etc.Reference material should simulate real samples as closely as possible; reference samples for water should contain phthalates which in environmental samples interfere with organochlorines and reference material for organophosphates in vegetables should contain metabolites and degradation products.It is also recommended that commercial standards for trace metals should have the production date and the guaranteed stability printed on the label. Information on reference material should be included in the methods published by AOAC, AOCS and similar publications.     

Determination of total arsenic in seawater by hydride generation atomic fluorescence spectrometry

In this work, the determination of total As in seawater by hydride generation atomic fluorescence spectrometry was studied. The influence of the chemical, flow and instrumental parameters were investigated and optimized. The pre-reduction of As(V) to As(III) was performed using KI plus ascorbic acid in 3.5 mol L^− 1 HCl medium. No multiplicative interference was present and external aqueous calibration could be used. The limit of detection was 36 ng L^− 1, while the repeatability was 2% (n = 10), at a 500 ng L^− 1 concentration level. The sample throughput was 15 h^− 1 if triplicate measurements were made. The accuracy was assessed by the analysis of a seawater certified reference material and excellent agreement between the obtained and certified values was verified. The procedure was used for the analysis of seawater offshore samples collected at the Brazilian coast and results ranging from 860 to 1200 ng L^− 1 were found.     

Optimization and validation of an LC-fLD method for biotin in infant formula, infant cereals, cocoa-malt beverages, and clinical nutrition products

A fast and simple chromatographic method to determine biotin in foods is presented. Biotin is extracted using papain (60 degrees C, 1 h). After pH adjustment and filtration, biotin is determined by LC with fluorescence detection using postcolumn reagent avidin-FITC (avidin labeled with fluorescein isothiocyanate). The method has been validated in a large range of products: milk- and soy-based infant formulas, cereals, cocoa-malt beverages, and clinical nutrition products. The method showed recovery rates of 98.1 +/- 5.7% (average +/- SD) in a large range of concentrations. Biotin concentrations determined in infant formula standard reference materials 1846 and 1849 were in agreement with reference values. RSD of repeatability (RSDr) varied from 2.0 to 4.5%, and intermediate reproducibility (RSD(iR)) from 5.8 to 9.4%. LOD and LOQ were 3.0 and 5.0 microg/100 g, respectively. The proposed method is suitable for routine analysis of biotin in fortified foods (infant formulas, infant cereals, cocoa-malt beverages, and clinical nutrition products). It can be used as a faster, more selective, and precise alternative to the classical microbiological determination, and is easily transferable among laboratories.     

Chromatin supraorganization, mitotic abnormalities and proliferation in cells with increased or down-regulated lox expression: Indirect evidence of a LOX-histone H1 interaction in vivo

Lysyl oxidases (LOXs) are enzymes that permit the covalent crosslinking of the component chains of collagen and elastin. These enzymes are present inside the nuclei of certain mammalian cells. Previous studies have proposed LOX binding to histone H1 in vitro, and histone H1 is known to control global chromatin compaction and mitotic chromosome architecture. Therefore, in the present study, we analyzed chromatin supraorganizational changes, mitotic abnormalities, mitotic indices and cell death ratios in COS-7 and NRK-49F cells with high and low lox expression levels, respectively. The objective was to support biochemical data of LOX-H1 interaction, by providing evidence of chromatin remodeling in vivo, under different lox expressions. Chromatin decondensation assessed by image analysis was observed in COS-7 cells with increased lox expression. This decondensation is suggested to be promoted by LOX actions on histone H1, which loosens the DNA-H1 complex. In NRK-49F cells transfected with antisense lox or subjected to treatment with beta-aminopropionitrile (BAPN), chromatin condensation and nuclear phenotypic variability were found, which may be due to reduced LOX-H1 interaction. When lox expression was increased in COS-7 cells, the frequency of irregular chromosome plates was not affected, but cell proliferation decreased and "cell death preceded by multinucleation" increased. In NRK-49F cells there was accelerated proliferation induced by transfection with the antisense lox, and confirmed when cells were treated with BAPN. Apoptosis increased in NRK-49F cells only with BAPN treatment whereas cell death preceded by multinucleation increased only after antisense lox transfection. The data presented herein regarding chromatin remodeling indirectly support the hypothesis that LOX binds to histone H1 in vivo. Cell proliferation in COS-7 and NRK-49F cells and cell death at least in COS-7 cells agree with predicted effects of LOX interference in these processes.