18 research outputs found

    A study on antimicrobial, antioxidant and antimutagenic activities of Elaeagnus Angustifolia L. Leaves

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    Backround: The aim of this work was to investigate the antimicrobial, antioxidant, and antimutagenic potentials of methanol extracts from E. angustifolia.Materials and Methods: Methanol extracts were screened for antimicrobial activity against different species of 4 Gram positive and 3 Gram negative bacteria and one fungus. These bacteria included food pathogens. The leaf extract was tested using disc diffusion assay.Results: The methanol extract of E. angustifolia showed maximum inhibition zone of 16 mm against Yersinia enterocolitica. Whereas, the inhibition zone was not determined by methanol extract against Escherichia coli ATCC 1122 and Candida albicans RSKK 02029. The MIC was evaluated on plant extracts as antimicrobial activity. All of bacterial strains showed the lowest sensitivity to methanol extract of E. angustifolia (3.5 mg/mL), except Yersinia enterocolitica NCTC 11174. In addition, the plant extracts were tested against the stable DPPH (2,2-diphenyl-1- picryl-hydrazyl-hydrate) free-radical. Finally, the methanol extract displayed a strong antioxidant activity (Trolox equivalent = 1.49 mM). Also, E. angustifolia methanol extracts were screened for their antimutagenic activity against sodium azide by Ames test in absence of rat microsomal liver enzyme (-S9). The results showed that E. angustifolia methanol extracts can inhibit mutagenic agents of sodium azide. The plant leaf extracts with the inhibition of 36% sodium azide showed moderate potential in decreasing mutagenic agents in Salmonella typhimurium TA100.Conclusion: E. angustifolia methanol extracts have antimicrobial, antioxidant and antimutagenic potential.Keywords: Elaeagnus, antimicrobial activity, antioxidant activity, antimutagenic activit

    The Antimicrobial Activity of Aliquidambar orientalis mill. Against Food Pathogens and Antioxidant Capacity of Leaf Extracts

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    Background: Medicinal plants are an important source of substances which are claimed to induce antimicrobial, antimutagenic and antioxidanteffects. Many plants have been used due to their antimicrobial treatments. Antimicrobial and antioxidant activities of L. orientalis have not beenreported to the present day. The aim of this work was to investigate of the antimicrobial and antioxidant potentials of different extracts from L.orientalis.Materials and Methods: The extracts were screened for antimicrobial activity against different food pathogens. These bacteria include 4 Grampositive and 3 Gram negative bacteria and one fungi. The leaf extracts of plant were tested by disc diffusion assay. The MIC was evaluated onplant extracts as antimicrobial activity. In addition to, the plant extracts were tested against the stable DPPH (2,2-diphenyl-1-picryl-hydrazylhydrate) free-radical.Results: The acetone, ethanol and methanol extracts of L. orientalis showed maximum inhibition zone of 12 mm against Yersinia enterocolitica,Listeria monocytogenes and Staphylococcus aureus. In addition to, the methanol extract displayed a strong antioxidant activity (trolox equivalent= 2.23 mM).Conclusion: L. orientalis extracts have antimicrobial, and antioxidant potential. Our results support the use of this plant in traditional medicineand suggest that some of the plant extracts possess compounds with good antibacterial properties that can be used as antibacterial agents in thesearch for new drugs.Key words: Antimicrobial activity; Antioxidant activity; L. orientalis

    Hardware/software approaches for reducing the process variation impact on instruction fetches

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    Cataloged from PDF version of article.As technology moves towards finer process geometries, it is becoming extremely difficult to control critical physical parameters such as channel length, gate oxide thickness, and dopant ion concentration. Variations in these parameters lead to dramatic variations in access latencies in Static Random Access Memory (SRAM) devices. This means that different lines of the same cache may have different access latencies. A simple solution to this problem is to adopt the worst-case latency paradigm. While this egalitarian cache management is simple, it may introduce significant performance overhead during instruction fetches when both address translation (instruction Translation Lookaside Buffer (TLB) access) and instruction cache access take place, making this solution infeasible for future high-performance processors. In this study, we first propose some hardware and software enhancements and then, based on those, investigate several techniques to mitigate the effect of process variation on the instruction fetch pipeline stage in modern processors. For address translation, we study an approach that performs the virtual-to-physical page translation once, then stores it in a special register, reusing it as long as the execution remains on the same instruction page. To handle varying access latencies across different instruction cache lines, we annotate the cache access latency of instructions within themselves to give the circuitry a hint about how long to wait for the next instruction to become available

    A STUDY ON ANTIMICROBIAL, ANTIOXIDANT AND ANTIMUTAGENIC ACTIVITIES OF ELAEAGNUS ANGUSTIFOLIA L. LEAVES

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    Backround: The aim of this work was to investigate the antimicrobial, antioxidant, and antimutagenic potentials of methanol extracts from E. angustifolia. Materials and Methods: Methanol extracts were screened for antimicrobial activity against different species of 4 Gram positive and 3 Gram negative bacteria and one fungus. These bacteria included food pathogens. The leaf extract was tested using disc diffusion assay. Results: The methanol extract of E. angustifolia showed maximum inhibition zone of 16 mm against Yersinia enterocolitica. Whereas, the inhibition zone was not determined by methanol extract against Escherichia coli ATCC 1122 and Candida albicans RSKK 02029. The MIC was evaluated on plant extracts as antimicrobial activity. All of bacterial strains showed the lowest sensitivity to methanol extract of E. angustifolia (3.5 mg/mL), except Yersinia enterocolitica NCTC 11174. In addition, the plant extracts were tested against the stable DPPH (2,2-diphenyl-1-picryl-hydrazyl-hydrate) free-radical. Finally, the methanol extract displayed a strong antioxidant activity (Trolox equivalent = 1.49 mM). Also, E. angustifolia methanol extracts were screened for their antimutagenic activity against sodium azide by Ames test in absence of rat microsomal liver enzyme (-S9). The results showed that E. angustifolia methanol extracts can inhibit mutagenic agents of sodium azide. The plant leaf extracts with the inhibition of 36% sodium azide showed moderate potential in decreasing mutagenic agents in Salmonella typhimurium TA100. Conclusion: E. angustifolia methanol extracts have antimicrobial, antioxidant and antimutagenic potential

    Bayesian inference of accurate population sizes and FRET efficiencies from single diffusing biomolecules.

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    It is of significant biophysical interest to obtain accurate intramolecular distance information and population sizes from single-molecule Förster resonance energy transfer (smFRET) data obtained from biomolecules in solution. Experimental methods of increasing cost and complexity are being developed to improve the accuracy and precision of data collection. However, the analysis of smFRET data sets currently relies on simplistic, and often arbitrary methods, for the selection and denoising of fluorescent bursts. Although these methods are satisfactory for the analysis of simple, low-noise systems with intermediate FRET efficiencies, they display systematic inaccuracies when applied to more complex systems. We have developed an inference method for the analysis of smFRET data from solution studies based on rigorous model-based Bayesian techniques. We implement a Monte Carlo Markov chain (MCMC) based algorithm that simultaneously estimates population sizes and intramolecular distance information directly from a raw smFRET data set, with no intermediate event selection and denoising steps. Here, we present both our parametric model of the smFRET process and the algorithm developed for data analysis. We test the algorithm using a combination of simulated data sets and data from dual-labeled DNA molecules. We demonstrate that our model-based method systematically outperforms threshold-based techniques in accurately inferring both population sizes and intramolecular distances.This is the final published version. It's also available from ACS in Analytical Chemistry: http://pubs.acs.org/doi/pdf/10.1021/ac501188r
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