Genetic transformation of Vitreoscilla sp

Of all the methods customarily used to transform E. coli we found only electroporation to be effective for transformation of the Gram-negative bacterium Vitreoscilla, yielding 5.10(5) transformants/microgram of plasmid DNA. The conditions used were close to those described for E. coli E. coli plasmids are stably maintained in Vitreoscilla. This is the first report of exogenous DNA transfer in Vitreoscilla which opens the way for the application of recombinant-DNA techniques to study this unique group of organisms.     

Single units and conscious vision

Figures that can be seen in more than one way are invaluable tools for the study of the neural basis of visual awareness, because such stimuli permit the dissociation of the neural responses that underlie what we perceive at any given time from those forming the sensory representation of a visual pattern. To study the former type of responses, monkeys were subjected to binocular rivalry, and the response of neurons in a number of different visual areas was studied while the animals reported their alternating percepts by pulling levers. Perception-related modulations of neural activity were found to occur to different extents in different cortical visual areas. The cells that were affected by suppression were almost exclusively binocular, and their proportion was found to increase in the higher processing stages of the visual system. The strongest correlations between neural activity and perception were observed in the visual areas of the temporal lobe. A strikingly large number of neurons in the early visual areas remained active during the perceptual suppression of the stimulus, a finding suggesting that conscious visual perception might be mediated by only a subset of the cells exhibiting stimulus selective responses. These physiological findings, together with a number of recent psychophysical studies, offer a new explanation of the phenomenon of binocular rivalry. Indeed, rivalry has long been considered to be closely linked with binocular fusion and stereopsis, and the sequences of dominance and suppression have been viewed as the result of competition between the two monocular channels. The physiological data presented here are incompatible with this interpretation. Rather than reflecting interocular competition, the rivalry is most probably between the two different central neural representations generated by the dichoptically presented stimuli. The mechanisms of rivalry are probably the same as, or very similar to, those underlying multistable perception in general, and further physiological studies might reveal much about the neural mechanisms of our perceptual organization.     

Multi-objective GA with fuzzy decision making for security enhancement in power system

Power system security enhancement is a major concern in the operation of power system. In this paper, the task of security enhancement is formulated as a multi-objective optimization problem with minimization of fuel cost and minimization of FACTS device investment cost as objectives. Generator active power, generator bus voltage magnitude and the reactance of Thyristor Controlled Series Capacitors (TCSC) are taken as the decision variables. The probable locations of TCSC are pre-selected based on the values of Line Overload Sensitivity Index (LOSI) calculated for each branch in the system. Multi-objective genetic algorithm (MOGA) is applied to solve this security optimization problem. In the proposed GA, the decision variables are represented as floating point numbers in the GA population. The MOGA emphasize non-dominated solutions and simultaneously maintains diversity in the non-dominated solutions. A fuzzy set theory-based approach is employed to obtain the best compromise solution over the trade-off curve. The proposed approach has been evaluated on the IEEE 30-bus and IEEE 118-bus test systems. Simulation results show the effectiveness of the proposed approach for solving the multi-objective security enhancement problem.     

Optical detection of CA 15.3 breast cancer antigen using CdS quantum dot

The present study focus on optical sensing of breast cancer antigen 15.3 (CA 15.3) using cadmium sulphide quantum dot (CdS‐QD) in saline and serum samples spiked with antigen. The surface of CdS‐QD was modified by cysteamine capping followed by tagging of CA 15.3 antibody. The samples were characterised using UV‐visible absorption spectroscopy (UV‐VIS Spectroscopy), Fourier transform infrared spectroscopy (FTIR), high‐resolution transmission electron microscopy (HRTEM) attached with energy‐dispersive X‐ray spectroscopy, phase contrast inverted epi‐fluorescence microscopy and photoluminescence (PL) spectrophotometry (EDS). The CdS‐QD showed a mean diameter of 3.02 ± 0.6 nm. The complex formed after antigen‐antibody interaction resulted in distinguishable optical and fluorescence intensity with respect to varying concentration of antigen. The PL study revealed that CA 15.3 antibody labelled CdS QD can detect CA 15.3 tumour marker even at very low concentration of 0.002 KU/L with a constant response time of 15 min. This study clearly indicates that detection of CA 15.3 at low concentration is possible using surface modified CdS QD in serum samples and can find immense applications in biosensor development for detection of breast cancer marker similar to various automated detection kits available in market.Inspec keywords: semiconductor quantum dots, cadmium compounds, II‐VI semiconductors, wide band gap semiconductors, cancer, tumours, optical sensors, biosensors, biomedical equipment, visible spectra, ultraviolet spectra, Fourier transform infrared spectra, transmission electron microscopy, X‐ray chemical analysis, fluorescence, optical microscopy, photoluminescence, proteins, molecular biophysics, nanosensors, nanomedicine, nanoparticlesOther keywords: optical detection, CA 15.3 breast cancer antigen, optical sensing, cadmium sulphide quantum dot, saline samples, serum samples, cysteamine capping, CA 15.3 antibody, UV‐visible absorption spectroscopy, Fourier transform infrared spectroscopy, high‐resolution transmission electron microscopy, energy dispersive X‐ray spectroscopy, phase contrast inverted epifluorescence microscopy, photoluminescence spectrophotometry, antigen‐antibody interaction, fluorescence intensity, optical intensity, CA 15.3 tumour marker, surface modified CdS QD, biosensor development, time 15 min, CdS     

Design of fuzzy expert system for microarray data classification using a novel Genetic Swarm Algorithm

Knowledge gained through classification of microarray gene expression data is increasingly important as they are useful for phenotype classification of diseases. Different from black box methods, fuzzy expert system can produce interpretable classifier with knowledge expressed in terms of if-then rules and membership function. This paper proposes a novel Genetic Swarm Algorithm (GSA) for obtaining near optimal rule set and membership function tuning. Advanced and problem specific genetic operators are proposed to improve the convergence of GSA and classification accuracy. The performance of the proposed approach is evaluated using six gene expression data sets. From the simulation study it is found that the proposed approach generated a compact fuzzy system with high classification accuracy for all the data sets when compared with other approaches.     

An energy flow analysis in a paper-based industry

Industrial sector is the largest user of energy in India and many parts of the world. More than half of the total energy is used in industries to operate various energy-using machineries. Energy conservation is a cost-effective approach in any energy optimization program that can be implemented in industrial activities. Energy-intensive industries in developing economies offer significant energy-saving potential owing to the technology gap as well as lower operating efficiency. A detailed energy flow analysis was conducted in a paper carton manufacturing unit in India to quantify the energy-saving potential. The study revealed that the compressed air leakage is responsible for about 50% of the total energy loss. The specific electrical and thermal energy consumption was estimated and found to be 91.85?kWh/ton and 1,619?MJ/ton of biomass, respectively. Annual energy saving potential was found to be 5.9% of the total annual energy consumption. The cost of DG power is found to be 389% higher than the grid power. The share of self-generated DG power is estimated to be 41% of the total power consumed. Electrical energy intensity of the plant could be reduced by 6.36% implementing energy conservation measures proposed in this study.     

Lymphatic Transport of α-Linolenic Acid and Its Conversion to Long Chain n-3 Fatty Acids in Rats Fed Microemulsions of Linseed Oil

In the present study we evaluated the uptake of ALA and its conversion to EPA + DHA in rats given linseed oil (LSO) in native form or as a microemulsion in whey protein or in lipoid. In a single oral dose study in which rats maintained on rodent pellets deficient in ω-3 fatty acids were intubated with 0.35 g LSO in lipoid, the amount of ALA present in lymph was increased reaching a maximum concentration of 16.23 mg/ml at 2.5 h. The amount of ALA present in lymph was increased to a maximum level of 10.95 mg/ml at 4 h in rats given LSO as a microemulsion in whey protein. When LSO was given without emulsification, the amount of ALA present in lymph was found to reach a maximum level of 7.08 mg/ml at 6 h. A similar result was observed when weaning rats were intubated with 0.15 g of LSO per day for a period of 60 days. Higher levels of ALA by 41 and 103 % were observed in lymph lipids of rats given microemulsions of LSO in whey protein and in lipoid respectively as compared to rats given LSO without pre-emulsification. Very little conversion of ALA to EPA and DHA was observed in lymph lipids but higher amounts of EPA + DHA was observed in liver and serum of rats given LSO in microemulsion form. This study indicated that ALA concentration in lymph lipids was increased when LSO was given in microemulsion form in lipoid and further conversion to EPA and DHA was facilitated in liver and serum.