Synthesis and structure-activity study of quaternary ammonium functionalized beta-cyclodextrin-carboxymethylcellulose polymers

Carboxymethylcellulose (CMC) and beta-cyclodextrin (beta-CD)-based polymers functionalized with two types of quaternary ammonium compounds (QACs), the alkaquat DMB-451 (N-alkyl (50% C14, 40% C12, 10% C10) dimethylbenzylammonium chloride) (DMD-451) named polymer DMB-451, and FMB 1210-8 (a blend of 32 w% N-alkyl (50% C14, 40% C12, 10% C10) dimethylbenzylammonium chloride and 48 w% of didecyldimethylammonium chloride) named polymer FMB 1210-8, were synthethized and characterized by Fourier transform infrared spectroscopy. The antimicrobial activities of these polymers against Eschericia coli were also evaluated at 25 degrees C in wastewater. The results have indicated that the polymer FMB 1210-8 possesses a high-affinity binding with bacterial cells that induces a rapid disinfection process. Moreover, in the same experimental conditions of disinfection (mixture of 1.0 g of polymer and 100 mL of wastewater), the polymer FMB 1210-8 has a higher antimicrobial efficiency (99.90%) than polymer DMB-451 (92.8%). This phenomenon might be associated to a stronger interaction with bacterial cells due to stronger binding affinity for E. coli cells and greater killing efficiency of the C10 alkyl chains QAC of polymer FMB 1210-8 to disrupt the bacterial cell membrane as compared to N-alkyl (50% C14, 40% C12, 10% C10) dimethylbenzylammonium chloride. Together, these results suggest that the polymer FMB 1210-8 could constitute a good disinfectant against Escherichia coli, which could be advantageously used in wastewater treatments due to the low toxicity of beta-CD and CMC, and moderated toxicity of FMB 1210-8 to human and environment.     

Structural and Functional Characterization of 4-Hydroxyphenylacetate 3-Hydroxylase from Escherichia coli

The hydroxylation of phenols into polyphenols, which are valuable chemicals and pharmaceutical products, is a challenging reaction. The search for green synthetic processes has led to considering microorganisms and pure hydroxylases as catalysts for phenol hydroxylation. Herein, we report the structural and functional characterization of the flavin adenine dinucleotide (FAD)-dependent 4-hydroxyphenylacetate 3-monooxygenase from Escherichia coli, named HpaB. It is shown that this enzyme enjoys a relatively broad substrate specificity, which allows the conversion of a number of non-natural phenolic compounds, such as tyrosol, hydroxymandelic acid, coumaric acid, hydroxybenzoic acid and its methyl ester, and phenol, into the corresponding catechols. The reaction can be performed by using a simple chemical assay based on formate as the electron donor and the organometallic complex [Rh(bpy)Cp*(H₂O)]²⁺ (Cp*: 1,2,3,4,5-pentamethylcyclopentadiene, bpy: 2,2′-bipyridyl) as the catalyst for FAD reduction. The availability of a crystal structure of HpaB in complex with FAD at 1.8 Å resolution opens up the possibility of the rational tuning of the substrate specificity and activity of this interesting class of phenol hydroxylases.     

Borago officinalis oil: Fatty acid fractionation by immobilized Candida rugosa lipase

γ-Linolenic acid (Z,Z,Z-6,9,12-octadecatrienoic acid), a very important polyunsaturated fatty acid is found in the free fatty acid fraction prepared by the hydrolysis of borage oil. Our aim was to enrich this fraction in γ-linolenic acid using selective esterification. Candida rugosa lipase was used as catalyst after immobilization on the following ion-exchange resins: Amberlite IRC50, IRA35, IRA93, and Duolite A7, A368, A568. In every case, immobilization modified the lipae’s specificity: palmitic, stearic, oleic, and linoleic acids were preferentially esterified compared to γ-linolenic acid, thus allowing a γ-linolenic acid enrichment of 3.0.     

Visual signal detection in structured backgrounds. III. Calculation of figures of merit for model observers in statistically nonstationary backgrounds

Models of human visual detection have been successfully used in computer-generated noise. For these backgrounds, which are generally statistically stationary, model performance can be readily calculated by computing the index of detectability d' from the noise power spectrum, the signal profile, and the model template. However, model observers are ultimately needed in more real backgrounds, which may be statistically non-stationary. We investigated different methods to calculate figures of merit for model observers in real backgrounds based on different assumptions about image stationarity. We computed performance of the nonpre-whitening matched-filter observer with an eye filter on mammography and coronary angiography for an additive or a multiplicative signal. Performance was measured either by applying the model template to the images or by computing closed-form expressions with various assumptions about image stationarity. Results show first that the structured backgrounds investigated cannot be considered stationary. Second, traditional closed-form expressions of detectability calculated from the noise power spectra with the assumption of background stationarity lead to erroneous estimates of model performance. Third, the most accurate way of measuring model performances is by directly applying the model template on the images or by computing a closed-form expression that does not assume image stationarity.     

Calibration and testing of a TLD dosemeter for area monitoring

The response of a TLD-600/TLD-700 area dosemeter has been characterized in neutron fields around the 590 MeV cyclotron ring at the Paul Scherrer Institute (PSI). The dosemeter is based on a cylindrical paraffin moderator with three of each type of TLD chip at the centre, and is intended to use for area monitoring around accelerator facilities. The dosemeter is calibrated in terms of ambient dose equivalent using a non-moderated 252Cf neutron source. The ambient dose equivalent response has been tested in five locations where the neutron fields and dose rates have been well characterized by Bonner sphere spectrometer and active neutron monitor measurements. The different spectrum shapes and dose rates in the five locations permit the comparison of the behavior of the active and passive dosemeters in these neutron fields.     

Calibration of dosemeters used in mammography with different X ray qualities: EUROMET project no. 526

The effect of different X ray radiation qualities on the calibration of mammographic dosemeters was investigated within the framework of a EUROMET (European Collaboration in Measurement Standards) project. The calibration coefficients for two ionization chambers and two semiconductor detectors were established in 13 dosimetry calibration laboratories for radiation qualities used in mammography. They were compared with coefficients for other radiation qualities, including those defined in ISO 4037-1, with first half value layers in the mammographic range. The results indicate that the choice of the radiation quality is not crucial for instruments with a small energy dependence of the response. However, the radiation quality has to be chosen carefully if instruments with a marked dependence of their response to the radiation energy are calibrated.     

Evidence of a critical content in Fe(0) on FoCa7 bentonite reactivity at 80 °C

In order to assess the evolution of the confinement properties of clay engineered barriers (EBS) when in contact with metallic canisters containing radioactive wastes, Fe(0)-bentonite interactions need to be assessed. “45 days–80 °C” tests were performed using powdered FoCa7 bentonite and metallic iron. Since one fundamental parameter may be the available quantity of Fe(0), a wide range of Iron/Clay mass ratios (I/C) from 0 to 1/3 is used. The confinement power of clay material results from the swelling properties and the retention capacity. Thus, the major criterion which is chosen to assess the evolution of the confinement properties in this study is the variation of Cation Exchange Capacity (CEC). In parallel, the physico-chemical evolution of bentonite is studied using XRD and EDS-TEM microanalyses. The evolution of the distribution of iron environments is obtained by ⁵⁷Fe Mössbauer spectroscopy.This study evidences that both kaolinite and smectite from the bentonite are altered into SiAlFe gels when in contact with Fe(0). These gels maturates into Fe-rich di-trioctahedral phyllosilicates, whose composition is bounded by the one of odinite and greenalite in a Fe–M⁺–4Si diagram when I/C = 1/3. Most of all, it is evidenced that the reaction depends on the available quantity of Fe(0). When the I/C ratio is between 1/30 and 1/7.5, the exchange capacity of FoCa7 bentonite starts decreasing, the consumption of Fe(0) becomes significant, the alteration of smectites occurs and secondary oxides are formed. The crystallization of Fe-rich phyllosilicates is observable when I/C ratio is higher, from a threshold between 1/7.5 and 1/5. Above I/C = 1/3.75, initial iron oxides are strongly consumed and participate in the incorporation of Fe²⁺ and Fe³⁺ in gels or new phyllosilicates octahedra.These experimental results were used as input data for the prediction of the long-term evolution of the EBS using Crunch reaction-transport model.     

Lipase-based quantitation of triacylglycerols in cellular lipid extracts: Requirement for presence of detergent and prior separation by thin-layer chromatography

A protocol, based on the use of Pseudomonas lipase, is presented to measure quantitatively the amount of triacylglycerols in extracts from cultured cells or tissues. Since the lipase also acts on di- and monoacylglycerols, separation of the extracts by thin-layer chromatography is recommended. In order to allow the lipase-catalyzed hydrolysis to proceed efficiently, lipid extracts or eluates from silica scraping were mixed with the detergent Thesit [dodecylpoly(ethylene glycol ether)], prior to drying. After dissolution of the dried residues in water, the amount of triacylglycerols was quantified using Pseudomonas sp. lipase, glycerol kinase, glycerol-phosphate oxidase, and peroxidase. The activity of the latter enzyme was followed either colorimetrically in the presence of 4-aminoantipyrine and 2,4,6-tribromo-3-hydroxybenzoic acid or fluorimetrically in the presence of homovanillic acid.     

Characterisation of the PSI whole body counter by radiographic imaging

A joint project between the Paul Scherrer Institut (PSI) and the Institute of Radiation Physics was initiated to characterise the PSI whole body counter in detail through measurements and Monte Carlo simulation. Accurate knowledge of the detector geometry is essential for reliable simulations of human body phantoms filled with known activity concentrations. Unfortunately, the technical drawings provided by the manufacturer are often not detailed enough and sometimes the specifications do not agree with the actual set-up. Therefore, the exact detector geometry and the position of the detector crystal inside the housing were determined through radiographic images. X-rays were used to analyse the structure of the detector, and (60)Co radiography was employed to measure the core of the germanium crystal. Moreover, the precise axial alignment of the detector within its housing was determined through a series of radiographic images with different incident angles. The hence obtained information enables us to optimise the Monte Carlo geometry model and to perform much more accurate and reliable simulations.