103,670 research outputs found

    Characterization and biodegradation of poly (vinyl alcohol)/cassava starch

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    A series of poly (vinyl alcohol)/cassava starch (PVA/CS) blends at 50, 60, 70 and 80 wt.% cassava starch contents were prepared in one-step compounding process. One step compounding means, all blends were compound together without solely plasticized PVA or cassava starch at beginning. All blends were characterized and testing accordingly. In this research, comparison between one-step compounding and two-step compounding (plasticized PVA/CS at the beginning) were tested by tensile strength. It shows that their tensile strengths were comparatively higher than the two-step compounding process of PVA/CS blends. In term of impact test, it indicates that CS acts as non-reinforcing filler. The compatibility of PVA/CS represents the similarity functional group and possess same polar group. Studies on thermal stability and crystallinity shows, increasing the cassava starch loading in PVA matrix, has reduced the enthalpy of melting point as well as degree of crystallinity. The onset degradation had shifted to a higher temperature when a higher percentage of cassava starch was used in PVA matrix. This is due to cyclic hemiacetal had been introduced into PVA blend by cassava starch. It resist to thermal attack. In biodegradability test, several factors have been determined to evaluate the rate of biodegradation. Increase the humidity as well as increasing the cassava starch loading in PVA matrix will improve the susceptibility contact of microorganism onto the surface of PVA/CS blend. Aspergillus Oryzae had been selected as a good reagent used to degrade the sample of PVA/CS blend compared to Bacillus Amyloliquefaciens and effective microorganism. The biodegradation process of PVA/CS blends in anaerobic condition is much more faster compared to aerobic conditions

    Intramitochondrial sorting of the precursor to yeast cytochrome c oxidase subunit Va.

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    We have continued our studies on the import pathway of the precursor to yeast cytochrome c oxidase subunit Va (pVa), a mitochondrial inner membrane protein. Previous work on this precursor demonstrated that import of pVa is unusually efficient, and that inner membrane localization is directed by a membrane-spanning domain in the COOH-terminal third of the protein. Here we report the results of studies aimed at analyzing the intramitochondrial sorting of pVa, as well as the role played by ancillary factors in import and localization of the precursor. We found that pVa was efficiently imported and correctly sorted in mitochondria prepared from yeast strains defective in the function of either mitochondrial heat shock protein (hsp)60 or hsp70. Under identical conditions the import and sorting of another mitochondrial protein, the precursor to the beta subunit of the F1 ATPase, was completely defective. Consistent with previous results demonstrating that the subunit Va precursor is loosely folded, we found that pVa could be efficiently imported into mitochondria after translation in wheat germ extracts. This results suggests that normal levels of extramitochondrial hsp70 are also not required for import of the protein. The results of this study enhance our understanding of the mechanism by which pVa is routed to the mitochondrial inner membrane. They suggest that while the NH2 terminus of pVa is exposed to the matrix and processed by the matrix metalloprotease, the protein remains anchored to the inner membrane before being assembled into a functional holoenzyme complex

    The preparation and characterization of chitosan/poly (vinyl alcohol) blended films : mechanical, thermal and surface investigations

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    In this study, blends of chitosan (CS) and polyvinyl alcohol (PVA) (CS/PVA) having various proportions were prepared and characterized by universal mechanical tester, the differential scanning calorimetry (DSC) and contact angle measurements. Studying the mechanical properties of the films showed that blending improved the tensile strength, which increased with increasing PVA content up to 40% while the elongation% at break of the blends was decreased compared to that of the pure components. The obtained results of DSC suggested that some interaction between chitosan and PVA mostly took place. Static water contact angle measurements showed an improvement in the wettability of the obtained films

    Cloning, preparation and preliminary crystallographic studies of penicillin V acylase autoproteolytic processing mutants

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    The crystallization of three catalytically inactive mutants of penicillin Vacylase (PVA) from Bacillus sphaericus in precursor and processed forms is reported. The mutant proteins crystallize in different primitive monoclinic space groups that are distinct from the crystal forms for the native enzyme. Directed mutants and clone constructs were designed to study the post-translational autoproteolytic processing of PVA. The catalytically inactive mutants will provide threedimensional structures of precursor PVA forms, plus open a route to the study of enzyme-substrate complexes for this industrially important enzyme

    Zeta Potential of Modified Multi-walled Carbon Nanotubes in Presence of poly (vinyl alcohol) Hydrogel

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    The main objective of this study is investigate the behavior of the Zeta Potential of the MWCNT modified with SDS(Sodium Dodecyl Sulfate) and CTAB(Cetyl Tetraethyl Ammonium Bromide) in presence of PVA. Full hydrolyzed PVA was used. As a result, adding PVA in the CNT solution led to decrease the Zeta Potential. The Zeta Potential of suspended colloid varied from 42.00mV to 6.48mV and -45.00mV to -6.4mV at 1.5% concentration of PVA; according with the changing pH, the Zeta Potential dropped to near zero at pH 3 and 11. The pH and PVA has strong influence in the reduction of ZP of MWCNT solution. MWCNT-PVA solution with 33.30mV, -35.69mV at 0.01% of PVA was exposed under AC field; a uniform coat was obtained, with the SDS-MWCNT-PVA solution.National Natural Science Foundation of China Project (Grant No.51073024), the Royal Society-NSFC international joint project (Grant No.51111130207) and Beijing Municipal Science and Technology Plan Projects (No. Z111103066611005)

    Determination of effective diffusion coefficient of immobilized Baker's yeast invertase in various concentration of PVA-alginate matrix

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    Baker's yeast invertase is immobilized in PVA-alginate matrix using an improved method. PVA beads were prepared by adding calcium alginate to improve its stability, mechanical and chemical properties. Boric acid was used as the cross-linking agent and additional chemicals consisting of 10% boric acid and sodium sulphate solution was used as a treatment solution to harden the PVA-alginate beads. The determination of the effective diffusion of PVA-alginate matrix the vital step in optimizing the preparation of immobilized and water-soluble biocatalyst. In this study the two-level full factorial design was used to investigate the effect of PVA and boric acid concentrations and diffusions coefficient. Diffusion coefficient (De) is one of the factors that significantly affect the mass transport within the immobilization matrix. De value varies for each concentration of PVA and boric acid. The result concluded that both factors significantly affect the De. A maximum De value of 5.0141 x 10(-5) cm2s-1 was obtained at boric acid and PVA concentraion of 7w/v and 10.5 w/v respectively

    Effect of PVA doping on flux pinning in Bulk MgB2

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    The synthesis and characterization of PVA (Poly Vinyl Acetate) doped bulk MgB2 superconductor is reported here. PVA is used as a Carbon source. PVA doping effects made two distinguishable contributions: first enhancement of Jc field performance and second an increase in Hc2 value, both because of carbon incorporation into MgB2 crystal lattice. The susceptibility measurement reveals that Tc decreased from 37 to 36 K. Lattice parameter a decreased from 3.085 A to 3.081 A due to the partial substitution of Carbon at Boron site. PVA doped sample exhibited the Jc values greater than 10^5 A/cm2 at 5 & 10 K at low fields; which is almost 3 times higher than the pure one, while at high fields the Jc is increased by an order of magnitude in comparison to pure MgB2. From R(T)H measurements we found higher Tc values under magnetic field for doped sample; indicating an increase in Hc2. Also the magnetization measurements exhibited a significant enhancement in Hirr value. The improved performance of PVA doped MgB2 can be attributed to the substitution of carbon at boron site in parent MgB2 and the resulting impact on the carrier density and impurity scattering. The improved flux pinning behavior could easily be seen from reduced flux pinning force plots.Comment: 14 Pages of Text + Figs. To appear in Physica

    Electrospun polyvinyl alcohol/carbon dioxide modified polyethyleneimine composite nanofiber scaffolds

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    A novel biocompatible polyvinyl alcohol/carbon dioxide modified polyethyleneimine (PVA/PEI-CO2) composite nanofiber was fabricated by a green and facile protocol, which reduces the cytotoxicity of PEI through the surface modification of the PEI with CO2. The 13C NMR spectrum, elemental analysis, and TGA show that CO2 has been incorporated in the PEI surface resulting in a relatively stable structure. The resulting PVA/PEI-CO2 composite nanofibers have been characterized by attenuated total reflection-Fourier transform infrared spectroscopy (ATR-FTIR), contact angle, and scanning electron microscopy (SEM). The results show that the average diameters of the nanofibers range from 265 ± 53 nm to 423 ± 80 nm. The cytotoxicity of PVA/PEI-CO2 composite nanofibers was assessed by cytotoxicity evaluation using the growth and cell proliferation of normal mice Schwann cells. SEM and the MTT assay demonstrated the promotion of cell growth and proliferation on the PVA/PEI-CO2 composite scaffold. It suggests that PEI-CO2 can have tremendous potential applications in biological material research
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