Plasma-activated immobilization of biomolecules onto graphite-encapsulated magnetic nanoparticles

We describe the amino group surface functionalisation of graphite-encapsulated iron compound nanoparticles by radio frequency (RF) plasma processing followed by oxidized dextran immobilization. We have found that surface treatment using plasma represents an important step before biomolecules immobilization. After plasma treatment, the dispersion property of nanoparticles in dextran solution in water was significantly improved. The successful dextran immobilization was confirmed by X-ray photoelectron spectroscopy (XPS) and high resolution-transmission electron microscopy (HR-TEM) analyses followed by amino group derivatization using 4-(trifluoromethyl)-benzaldehyde (TFBA). As an evidence for covalent bonding between nanoparticles and dextran, the area percentage of deconvoluted CN peak at ～389.6 eV increased from 0% to 10.53 ± 1.30% with increasing the dextran concentration. The result is consistent with the evidenced decreasing of the free amino group percentage from 68.09 ± 5.10% to 14.73 ± 5.89% on the nanoparticle surface after dextran immobilization.     

The rapid,living, anionic polymerization of 2‐vinylnaphthalene at ambient temperature: Characterization of an n‐butyllithium/tetrahydrofuran system in 1,2,3,4‐tetrahydronaphthalene

We report the first well‐controlled room temperature anionic polymerization of 2‐vinylnaphthalene (2‐VNP), using alkyllithium (RLi) initiators. The nucleophilicity and solubility of the RLi as well as that of the 2‐vinylnaphthalenyllithium (VNPLi) and poly(2‐vinylnaphthalenyl)lithium (PVNPLi) propagating species were found to be very important factors in this reaction. An initiator system composed of n‐butyllithium (n‐BuLi) with tetrahydrofuran (THF) in 1,2,3,4‐tetrahydronaphthalene (THN) was determined to be the most effective of the various systems examined. The n‐BuLi/THF complex initiates polymerization and the resulting VNPLi/THF and PVNPLi/THF complexes act as propagating species at room temperature. These species offer adequate nucleophilicity and stability without promoting side reactions. As a result, rapid anionic polymerization was achieved. Various poly(2‐VNP) products with well‐defined polymeric chain structures were synthesized by this process at room temperature. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41901.     

Fiber Formation in Medium and Ultra‐High‐Molecular‐Weight Polyhydroxybutyrate Blends under Shear Flow

Summary: Polyhydroxybutyrate (PHB) is an ideal bioplastic, however, this polymer undergoes a severe embrittlement process because of its spherulitic structure, rendering the material brittle. Using a series of in‐situ rheo techniques, we have previously observed only the rapid initial stage of shish formation, we term a partial shish, which existed at high shears in medium‐molecular‐weight PHB, = 360 000. The shish kebab morphology is anticipated to remove or severely lessen this embrittlement process whilst providing new properties and applications. For medium and ultra high‐molecular‐weight (MMWT, = 360 000/UHMWT, = 5 × 10⁶) PHB 99/1 and 99.5/0.5 blends only a partial shish is identified. However, the initial shish formation stage and subsequent stages were observed at 98/2 and 97/3 blend ratios resulting in a complete shish, we term the full shish, and fiber formation was evident. We believe this fiber morphology achieved by high molecular weights is crucial to sustaining the shish kebab structure for an excessive period.

Left: In‐situ rheo‐light scattering micrograph; 97/3 MMWT/UHMWT PHB at 100 s^?1 for 1 s shear shish held at 75 s. Right: In situ rheo‐optical micrograph; PHB fiber morphology observed at 50 s^?1 for 2 s shear 98/2 MMWT/UHMWT PHB after 1 min.     

Lipase-Catalyzed Esterification of Triterpene Alcohols and Phytosterols with Oleic Acid

Oleic acid esters of phytosterols (PSs) and triterpene alcohols (TAs), derived from rice bran, were synthesized using lipases under mild conditions. Some lipases, especially from Candida rugosa, type VII, showed very high substrate specificity towards both PSs and TAs, when a mixture of PS and TA (PS/TA mixture) was used as the substrate source. The maximum yield of PS esters was ca. 80 % in each case; however, the maximum yield of TA esters was much lower when the reaction was continued for 7 days. Due to the difficulty in purifying the esters obtained when the PS/TA mixture was used as source of substrate, free PSs and TAs were separated from the PS/TA mixture by silica-gel and reverse-phase chromatography prior to esterification. The pure PSs or TAs were esterified with oleic acid to obtain the corresponding esters with high purity. Differential scanning calorimetric analysis of the resulting esters revealed that their melting points ranged from 7.0 to 42 °C. These values were at least 100 °C lower than those of the free PSs and TAs.     

Enzymatic synthesis of fructose 1,6-diphosphate with ATP regeneration in a batch reactor and a semibatch reactor using purified enzymes of Bacillus stearothermophilus

The enzymatic synthesis of fructose 1,6-diphosphate (FDP), an important glycolytic intermediate whose applications in the field of medicine have generated a great deal of interest, was performed in a batch reactor and a semibatch reactor. Using the batch reactor, FDP was first synthesized from glucose by three enzymatic reactions and the ATP consumed was regenerated simultaneously using conjugated enzymes, all of which were purified from crude cell extract of thermophilic Bacillus stearothermophilus. The results of the experiments performed using several enzyme concentrations suggest the existence of an optimum concentration for each enzyme at which the maximum FDP yield can be attained. Since the thermal decomposition of acetyl phosphate reduced the yield of FDP in the batch reactor, the use of a semibatch reactor in which acetyl phosphate was fed continuously was examined. The yield of FDP was improved but the time required to complete the reaction was longer, resulting in a lower productivity of FDP. The yields observed in the two reactors using various enzyme and substrate concentrations were in good agreement with the theoretical predictions calculated based on differential equations derived for the system using the rate equations and the kinetic parameters determined previously. This means that these equations can be used for the analysis of the experimental results as well as for determining the optimum experimental conditions.     

Effect of additives on transesterification activity of Rhizopus chinensis lipase

The transesterification activity of powder lipase prepared from the purified lipase of Rhizopus chinensis cells by freeze-drying was quite low compared with that of acetone-dried cells. Additives which could enhance the transesterification activity of the freeze-dried powder lipase were screened. The freeze-dried lipases prepared with certain fatty acid methylesters or certain types of surfactants exhibited high transesterification activity. It was shown that not only the solubility of the freeze-dried lipase in n-hexane but also the organic solvent-stability was enhanced when methyl stearate was added to the lipase solution at the freeze-drying step.     

Numerical simulation of fluid flow and heat transfer in a rotating cylindrical container with a counter-rotating disk at the fluid surface

Fluid flow and heat transfer in a rotating cylindrical container with a counterrotating disk at the fluid surface are numerically investigated. The effects of disk rotation and of Prandtl numbers on the fluid flow and heat transfer in the container are discussed. Flow and temperature fields are obtained for various rotational Reynolds numbers of the disk and for Prandtl numbers of the fluid. Nusselt numbers on the walls are calculated for the temperature fields and are compared with available experimental data. © 1999 Scripta Technica, Heat Trans Asian Res, 28(3): 172–182, 1999     

Performance Analysis of Bidding Policy for Competitive Network Providers

This paper proposes an optimum bidding policy in a competitive network provider's environment, where each network provider can bid for individual connection requests according to its own criteria. The proposed bidding policy is based on the concept of shadow price. In other words, each network provider bids only for connection requests with an expected profit exceeding its shadow price. Because such connection request brings profit in the long term, each network provider can maximize its long-term profit by adopting this bidding policy. In this paper, the optimum bidding policy for network providers is analyzed by means of the policy iteration method derived from the Markov decision theory. The economic efficiency of the bidding policy is evaluated using several numerical examples, in which each network provider adopts fixed pricing and state-dependent pricing, respectively. By adopting the bidding policy in both cases, each network provider can maximize its long-term profit while the total users' consumer surplus is slightly reduced.     

Purification and characterization of organic solvent-stable protease from organic solvent-tolerant Pseudomonas aeruginosa PST-01

An organic solvent-stable protease (PST-01 protease) in a culture broth of organic solvent-tolerant Pseudomonas aeruginosa PST-01 was purified by successive hydrophobic interaction chromatography using Butyl-Toyopearl gels. The purified enzyme was homogeneous as determined by SDS-polyacrylamide gel electrophoresis. PST-01 protease had a molecular mass of 38 kDa. The optimum temperature and pH for casein hydrolysis were 55 degrees C and 8.5, respectively. PST-01 protease was stable at pH 8-12 and below 50 degrees C and was determined to be a metalloprotease which was inhibited by EDTA, 1,10-phenanthroline, and phosphoramidon. PST-01 protease inhibited by EDTA was reactivated completely by the addition of zinc or cobalt ions. The stability of PST-01 protease in solutions containing water-soluble organic solvents or alcohols was higher than that in the absence of organic solvent. Furthermore, in general, PST-01 protease was more stable than commercially available proteases, namely, subtilisin Carlsberg, thermolysin, and alpha-chymotrypsin, in the presence of water-soluble organic solvents or alcohols.