Successful Aging

This issue's Works in Progress department presents six abstracts for projects that are developing interesting solutions to the elderly's quality of life challenges. The first two abstracts discuss projects that will help provide the elderly with freedom and independence by instrumenting their environments with supportive technology. The next two abstracts discuss projects building specialized user interfaces for addressing some of the challenges associated with aging, such as vision impairment. The final two abstracts present projects that will aid independence for the elderly by providing remote monitoring and assistance.     

Flow and Flow Decay of Refractory Castables

Installation of refractory castables depend not only on flow,but also on how soon the flow is lost because of setting.The loss of flow(flow decay)has always been one of the main problems of refractory castable manufacturers,a problem that has not been too well described in literature.The flow decay has been studied for a castable system based on alumina,pointing out some general trends.The flow decay was found very temperature sensitive,being strongly accelerated by temperature increases.To compensate for excessive flow loss,a retarder like citric acid may be used.Thus flow decay was measured as a function of citric acid(retarder) addition at 35℃.     

A dual-affinity gene fusion system to express small recombinant proteins in a soluble form: expression and characterization of protein A deletion mutants

A novel gene fusion system to express and purify small recombinantproteins in Escherichia coli has been constructed. The conceptallows for affinity purification of soluble gene products bysequential albumin- and Zn²+-affinity chromatography. The dual-affinitysystem is well suited for expression of unstable proteins asonly full-length protein is obtained after purification andproteins gain proteolytic stability in the fusion protein. Herewe show that the dual-affinity approach can be used for theexpression of various unstable derivatives of a single IgG-bindingdomain based on staphylococcal protein A. Analysis of the proteolyticstabilities and the IgG-binding properties of the differentmutant proteins suggest that the model for the structure ofan IgG-binding domain must be re-evaluated.     

Microalgae growth for nutrient recovery from sludge liquor and production of renewable bioenergy

Proof-of-concept has been demonstrated for a process that will utilize nutrients from sludge liquor, natural light, and CO2 from biogas to grow microalgae at wastewater treatment plants. This process will reduce the impact of returning side-streams to the head of the plant. The produced algae will be fed to anaerobic digesters for increased biogas production. Dewatering of anaerobically digested sludge in centrifuges produces reject water with extremely low transmittance of light. A pretreatment procedure was developed that improved light transmittance for reject water from the FREVAR, Norway, wastewater treatment plant from 0.1% T to 77% T (670 nm, 1 cm path). Chlorella sp. microalgae were found to be suitable for growth in this pre-treated reject water. Typical nitrogen removal was 80-90 g N/kg TSS of produced microalgae. The microalgae were successfully harvested by chemically assisted flocculation followed by straining through a 33 microm sieve cloth, achieving up to 99% recovery. Harvested algae were anaerobically co-digested with wastewater sludge. The specific methane gas production (mL CH4/g VS fed) for the algae varied from less than 65% to 90% of the specific methane gas production for the wastewater sludge, depending on digester temperature, retention time and pre-treatment of the algae biomass.     

Kinetic study on the alkaline degradation of cotton hydrocellulose

The kinetics of alkaline degradation of cotton hydrocellulose were determined in 5% NaOH at various temperatures. An activation energy of 24 kcal./mole was found for the endwise degradation reaction, while that of termination to a stable m-saccharinic acid endunit is 32 kcal./mole. Consequently, the DP_n of the degradable chain length is highly dependent on the reaction temperature, being 1000 at 65°C. and 140 at 132°C. At lower temperatures, the majority of degrading chains terminate to a normal reducing endgroup at the crystalline–amorphous transition region. From the data, the D P_n of cellulose chain segments participating in the amorphous regions of the original cotton fibril was calculated to be 143. This result strongly supports the classical micellar fibril structure over the folded model proposed by Manley.     

Iterative voting for inference of structural saliency and characterization of subcellular events.

Saliency is an important perceptual cue that occurs at different levels of resolution. Important attributes of saliency are symmetry, continuity, and closure. Detection of these attributes is often hindered by noise, variation in scale, and incomplete information. This paper introduces the iterative voting method, which uses oriented kernels for inferring saliency as it relates to symmetry. A unique aspect of the technique is the kernel topography, which is refined and reoriented iteratively. The technique can cluster and group nonconvex perceptual circular symmetries along the radial line of an object's shape. It has an excellent noise immunity and is shown to be tolerant to perturbation in scale. The application of this technique to images obtained through various modes of microscopy is demonstrated. Furthermore, as a case example, the method has been applied to quantify kinetics of nuclear foci formation that are formed by phosphorylation of histone gammaH2AX following ionizing radiation. Iterative voting has been implemented in both 2-D and 3-D for multi image analysis.     

A RAPID METHOD FOR DETERMINING BIOTIN ACTIVITY IN RAW MATERIALS FOR FERMENTATION

The biotin activity of a raw material towards yeast may consist of the sum of the activities of biotin, desthiobiotin, oxybiotin, biocytin and possibly other factors. Some of these substances only stimulate certain strains of yeast; on the other hand, the strains of lactobacilli generally used for estimation of biotin activity utilize only D-biotin. It is thus desirable to have a method available in which a manufacturer's own strain of yeast is used as test organism for biotin activity. A simple method for biotin determination based on the cup plate assay is described. Biotin-free agar is inoculated with yeast and a series of standard solutions of D-biotin and a series of dilutions of the raw material under investigation are placed in holes cut in the agar. After incubation, the zones of growth are measured and from their diameters the biotin activity can be calculated.