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81.
The viscoelastic properties of soybean curd (tofu) as affected by soymilk concentration and type of coagulant 总被引:1,自引:0,他引:1
Yongqiang Cheng Naoto Shimizu & Toshinori Kimura 《International Journal of Food Science & Technology》2005,40(4):385-390
The viscoelastic properties of different types of tofu were investigated. Soymilk concentrations were 5, 6, 7, 8 and 9%. Coagulants used were 30 mm CaSO4 or 30 mm glucono‐delta‐lactone (GDL). As the concentration of soymilk was increased viscosity and handling difficulties increased. A high concentration of soymilk in tofu gave a high break stress and produced hard tofu. The four‐element Burgers model fitted the creep behaviour and both viscous and elastic parameters could be acquired from model analysis, reflecting changes in elasticity and viscosity of tofu. The constant viscous parameter in the model increased with increasing soymilk concentration. The viscous parameters of viscoelastic materials like tofu gel, obtained from small deformation tests, seemed to correlate, to some extent, with the break stress obtained from large deformation tests. For hard tofu production increasing the soymilk concentration within a certain range and the partial replacement of calcium sulphate coagulant by GDL could be effective options. 相似文献
82.
The regulatory mechanism for poly-3-hydroxybutyrate (PHB) biosynthesis in recombinant Escherichia coli is markedly different from that of Ralstonia eutropha (formerly, Alcaligenes eutrophus) since the former efficiently synthesizes PHB during growth without any nutrient limitation. To analyze how the central metabolic pathways should be balanced with pathways necessary for cell growth and PHB formation, a stoichiometric model was developed to predict the theoretical maximum PHB production capacity for different metabolic variants. Flux analysis results illustrated the importance of the availability of acetyl-CoA and NADPH for achieving the maximum yield of PHB. In order to examine whether the increased availability of the above substances can enhance PHB synthesis in recombinant E. coli, both genetic and environmental perturbations were attempted. Several E. coli K12 derivatives, namely, HMS174, TA3516 (pta-/ack-), and DF11 (pgi-), were transformed with a plasmid which contains the native phb operon. The fermentation characteristics of these recombinant strains were studied and compared. In this study we examined the effects of intracellular acetyl-CoA accumulation, which may promote PHB synthesis in vivo, by perturbations induced from attenuation of acetate kinase and phosphotransacetylase (TA3516, blocked in the acetate pathway) and by cultivation of E. coli HMS174 on gluconate; it can convert gluconate to acetyl-CoA at a higher rate. The effects of intracellular accumulation of NADPH were investigated by introducing a perturbation induced from attenuation of phosphoglucose isomerase, which redirects the carbon flow to the pentose-phosphate (PP) pathway. Results from the analyses of these perturbations indicate that intracellular buildup of acetyl-CoA may not be able to promote PHB synthesis in vivo. On the other hand, since the biosynthesis of PHB in the pgi- mutant strain can utilize the NADPH overproduced through the PP pathway, the growth of the pgi- mutant on glucose was recovered, indicating that the overproduction of NADPH might be able to enhance PHB synthesis. 相似文献
83.
Tetsuya Nanba Asima Sultana Shouichi Masukawa Masaaki Haneda Junko Uchisawa Akira Obuchi Hideaki Hamada 《Topics in Catalysis》2009,52(13-20):1766-1770
Selective catalytic reduction of NO x by NH3 over Cu–FER and Cu–ZSM-5 in the presence of n-decane and SO2 was investigated. NO x conversion over Cu–ZSM-5 decreased in the presence of n-decane, owing to inhibition of the active sites by coke formation. In contrast, coke formation was negligible over Cu–FER, which maintained its NO x conversion activity even in the presence of decane. Coke formation was negligible over H–ZSM-5 and H–FER supports, which suggests that Cu species were involved in coke formation. Temperature-programmed reduction by H2 and electron spin resonance spectroscopy indicated that [Cu–O–Cu]2+ was probably the Cu species involved in coke formation over Cu–ZSM-5. 相似文献
84.
Masaaki Haneda Ohki Houshito Hiromitsu Takagi Kiyoshi Shinoda Yuunosuke Nakahara Kazumi Hiroe Tadahiro Fujitani Hideaki Hamada 《Topics in Catalysis》2009,52(13-20):1868-1872
The activity of Rh/CeO2 for NO reduction by C3H6 was gradually deceased by mixing with ZrO2 until 68 mol%. Rh supported on CeO2–ZrO2 with higher OSC was found to show lower catalytic activity. High OSC of CeO2–ZrO2 would probably stabilize the surface of Rh in oxidized state, resulting in low activity and low efficiency of C3H6 utilization for NO reduction. In situ FT-IR spectroscopy suggested that mononitrosyl species such as Rh(NO)δ? and Rh(NO)δ+ are reaction intermediates in the NO–C3H6–O2 reaction over Rh/CeO2–ZrO2 catalysts. 相似文献
85.
This paper demonstrates two simple ways to increase 5-hydroxymethylfurfural (HMF) yield (selectivity) in fructose dehydration with various solid acid catalysts. One is a water removal from the reaction mixture by a mild evacuation at 0.97 × 105 Pa; it increases HMF yield for various catalysts (heteropoly acid, zeolite, and acidic resin). The removal of water suppresses two undesired reactions: the hydrolysis of HMF to levulinic acid and the reaction of partially dehydrated intermediates to condensation products. The other method is a decrease in the particle (bead) size of the resin (Amberlyst-15). The crushed and sieved Amberlyst-15 powder in a size of 0.15–0.053 mm shows 100% HMF yield at high fructose concentration (50 wt.% in DMSO), which is to our knowledge the highest yield to date. Near-infrared spectroscopic characterization of adsorbed water suggests that the enhanced yield can be caused by an improved removal of adsorbed water in a small-size resin particle. 相似文献
86.
Regiospecific analysis by ethanolysis of oil with immobilized <Emphasis Type="Italic">Candida antarctica</Emphasis> lipase 总被引:1,自引:1,他引:1
Shimada Y Ogawa J Watanabe Y Nagao T Kawashima A Kobayashi T Shimizu S 《Lipids》2003,38(12):1281-1286
A mixture of oil/ethanol (1∶3, w/w) was shaken at 30°C with 4% immobilized Candida antarctica lipase by weight of the reaction mixture. The reaction regiospecifically converted FA at the 1- and 3-positions to FA ethyl
esters, and the lipase acted on C14−C24 FA to a similar degree. The content of 2-MAG reached a maximum after 4 h; the content was 28–29 mol% based on the total amount
of FA in the reaction mixture at 59–69% ethanolysis. Only 2-MAG were present in the reaction mixture during the first 4 h,
and 1(3)-MAG were detected after 7 h. After removal of ethanol from the 4-h reaction mixture by evaporation, 2-MAG were fractionated
by silica gel column chromatography. The contents of FA in the 2-MAG obtained by ethanolysis of several oils coincided well
with FA compositions at the 2-position, which was analyzed by Grignard degradation. It was shown that ethanolysis of oil with
C. antarctica lipase can be applied to analysis of FA composition at the 2-position in TAG. 相似文献
87.
Tetsuro Hori Naoki Fukuoka Tetsuya Masuda Yasuo Miyake Hiroyuki Yoshida Akihiko Fujii Yo Shimizu Masanori Ozaki 《Solar Energy Materials & Solar Cells》2011,95(11):3087-3092
Bulk heterojunction solar cells utilizing soluble phthalocyanine derivative, 1,4,8,11,15,18,22,25-octahexylphthalocyanine (C6PcH2) have been investigated. The active layer was fabricated by spin-coating the mixed solution of C6PcH2 and 1-(3-methoxy-carbonyl)-propyl-1-1-phenyl-(6,6)C61 (PCBM). The photovoltaic properties of the solar cell with bulk heterojunction of C6PcH2 and PCBM demonstrated the strong dependence of active layer thickness, and the optimized active layer thickness was clarified to be 120 nm. By inserting MoO3 hole transport buffer layer between the positive electrode and active layer, the FF and energy conversion efficiency were improved to be 0.50 and 3.2%, respectively. The tandem organic thin-film solar cell has also been studied by utilizing active layer materials of C6PcH2 and poly(3-hexylthiophene) and the interlayer of LiF/Al/MoO3 structure, and a high Voc of 1.27 V has been achieved. 相似文献
88.
Masaaki Hirayama Noriyuki Sonoyama Takeshi Abe Machiko Minoura Masumi Ito Daisuke Mori Atsuo Yamada Ryoji Kanno Takahito Terashima Mikio Takano Kazuhisa Tamura Jun’ichiro Mizuki 《Journal of power sources》2007
A new experimental technique was developed for detecting structure changes at electrode/electrolyte interface of lithium cell using X-ray reflectometry and two-dimensional model electrodes with a restricted lattice-plane. The electrodes were constructed with an epitaxial film of LiCoO2 synthesized by pulsed laser deposition method. The orientation of the epitaxial film depends on the substrate plane; the 2D layer of LiCoO2 is parallel to the SrTiO3 (1 1 1) substrate ((0 0 3)LiCoO2//(1 1 1)SrTiO3), while the 2D layer is perpendicular to the SrTiO3 (1 1 0) substrate ((1 1 0)LiCoO2//(1 1 0)SrTiO3). The anisotropic properties were confirmed by electrochemical measurements. Ex situ X-ray reflectivity measurements indicated that the impurity layer existed on the as-grown LiCoO2 was dissolved and a new SEI layer with lower density was formed after soaking into the electrolyte. In situ X-ray reflectivity measurements indicated that the surface roughness of the intercalation (1 1 0) plane increased with applying voltages, while no significant changes in surface morphology were observed for the intercalation non-active (0 0 3) plane during the pristine stage of the charge–discharge process. 相似文献
89.
90.
Wada M Kawabata H Yoshizumi A Kataoka M Nakamori S Yasohara Y Kizaki N Hasegawa J Shimizu S 《Journal of Bioscience and Bioengineering》1999,87(2):144-148
Multiple ethyl 4-chloro-3-oxobutanoate (COBE)-reducing enzymes were isolated from a cell-free extract of Candida magnoliae. A NADPH-dependent COBE-reducing enzyme, distinct from the carbonyl reductase and aldehyde reductase previously reported, was purified to homogeneity using five steps, including polyethylene glycol treatment. The relative molecular mass of the enzyme was estimated to be 86,000 on high performance gel-permeation chromatography and 29,000 on sodium dodecyl sulfate polyacrylamide gel electrophoresis. The enzyme catalyzed the reduction of COBE to the corresponding (S)-alcohol with a 51% enantiomeric excess. The substrate specificity of the enzyme was different from those of the other COBE-reducing enzymes of the same strain. The partial amino acid sequences of the enzyme showed that it belongs to the short chain alcohol dehydrogenase/reductase (SDR) family. This is the first report of multiple COBE-reducing enzymes with various stereoselectivities occurring in the same strain but belonging to different (super)families. 相似文献