30 resultados para cheese ripening


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植物激素乙烯作为一种信使分子调节控制果实完熟。ACC合成酶是植物体内乙烯生物合成途径的限速酶,其反义RNA的表达将能有效地抑制乙烯的生物合成而延缓果实完熟,利用反转录PCR技术克隆获得了ACC合成酶多基因家族成员之一LE-ACC2阅读框架约1.7kb的cDNA,经酶切图谱和序列分析鉴定无误后,反向连入植物表达载体pBin437中构建成组成型表达ACC合成酶反义RNA的双元载体。经农杆菌途径转化番茄“丽春”品种,获得了60株抗卡那再生杭株,PCR检测证明有6株为转基因植株,Southern杂交和Northern杂交分析进一步确证了外源基因的插入及其转录活性。反义番茄果实的乙烯释放受到明显抑制,表现出更好的耐储保鲜特性,并且与对照相比,在果实品质上没有明显差别。大田培育Fl和F2代转化番茄植株,反义番茄纯合品系的筛选工作正在进行之中。 同时,本研究利用已经获得的ACC合成酶和PG的cDNA克隆,构建了两个嵌合转化基因载体pPGACC1、pPGACC10,它包括1300bp的ACC合成酶cDNA编码序列,并分别含有反向与正向的250bp的5’端PG基因片断。酶切图谱和序列分析鉴定无误后,以pBin437为植物表达载体构建了双元载体pBPGACC1和pBPGACC10,分别表达PG正义RNA和反义RNA,并均表达ACC合成酶反义RNA。经农杆菌转化番茄子叶,植株的再生培育有待进行。通过对转基因植物的分析,我们期望阐明用单一嵌合基因表达载体通过反义抑制与抑制作用实现对内源两同源基因——PG和ACC合成酶下降调节的可能性,并可望得到具有更好耐储效果且品质优良的番茄品系。

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连续2年对“京秀”ד亚历山大”(编号97-2)杂交后代10个单株和“京秀”ד香妃”(编号97-3)杂交后代10个单株成熟期和延迟采收期的糖酸组分含量进行测定,以了解葡萄浆果延迟采收内在品质的变化差异。第二年 对可长期挂果的亲本“京秀”、“亚历山大”和杂交后代单株“97-2-23”、“97-2-24”成熟期和延迟采收期糖酸组分动态变化进行测定,以了解葡萄浆果糖酸品质延迟采收期的动态变化规律。同时对以上四个单株的浆果中蔗糖代谢相关酶活性和浆果呼吸强度进行测定,以对不同蔗糖表现型的产生原因进行探讨。研究表明: 葡萄延迟采收,浆果内可溶性糖变化可分为积累型和稳定型两种类型。延迟采收3周,糖积累型的8个单株浆果 可溶性糖显著积累,而稳定型的12个单株的糖与成熟时不存在显著差异。浆果主要积累果糖和葡萄糖,这两种糖的 动态变化趋势基本一致,但果糖变化幅度较大。两种类型的有机酸含量在延迟采收期间变化不大,没有显著差异。 糖积累型的“京秀”和“97-2-23”延迟采收期间各蔗糖分解酶(酸性转化酶、中性转化酶、蔗糖合成酶分解方 向)活性持续升高,但糖稳定型的“亚历山大”和“97-2-24”延迟采收第3周时急剧降低。此外,果实成熟和延迟 采收期间两种糖表现型浆果的呼吸速率也存在差异。浆果的蔗糖分解酶活性和呼吸速率存在的差异可能是两种类型 延迟采收期间糖含量存在差异的重要原因。

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For the InAs/GaAs quantum-dot system, the evolution of the wetting layer (WL) with the InAs deposition thickness has been studied by reflectance difference spectroscopy (RDS) in combination with atomic force microscopy and photoluminescence. One transition related to the light hole in the WL has been observed clearly in RDS, from which its transition energy and in-plane optical anisotropy (OA) are determined. The evolution of WL with the InAs dot formation and ripening has been discussed. In addition, the remarkable changes in OA at the onsets of the dot formation and ripening have been observed, implying the mode transitions of atom transport between the WL and the dots.

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本工作用小角激光光散射(SALS)研究了Poly (Styrene -co-acrylontrile)/Poly (methyl methacrylate)共混体系的相分离动力学。通过溶液共混得到的均相混合物淬火到较高温度的热力学不稳区,随着时间增长,体系相区及相区间及相区间的反应逐渐增大,对应SALS的V_v散射环逐渐变小,散射强度逐渐增大;在Cahn-Hilliard线性理论基础上测得体系相分离初期的增长速率及扩散系数,在相分离后期散射峰强Im和峰位qm与时间t满足幂指数关系:Im αt~θ、qm αt~(-θ)且θ ≈ 3φ;光散射积分不变量及相差显微镜观察表明在相分离后其发生了Ostwald Ripening,若减小体系PMMA分子量,相分离速率增大很快。

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本工作从实验和理论上探讨了高分子混合体系不稳相分离动力学机理。用光散射和固体核磁技术研究了苯乙烯一丙烯腈共聚物和聚甲基丙烯酸甲酯混合体系相分离过程。证实了Cahn-Hiuiand线理论适合与描述相分离早期过程;首次用激光散射方法在Cahn-Hiuiard线性理论基础上得到了相分离增长速率存在最大值R(9m);同时阐明了界面目由能对R(q)的影响,澄清了文献多年的争议问题;在Cook线性理论框架中得到了虚结谱因子,探讨了热力对相分离初期的影响,从固体核磁实验中得到了该体系相分离初期相区浓度随相分离时间变化的趋势;探讨了相分离中后期散射峰强I_m,峰位q_m与时间t的标度行为以及结构函数的标度行为;光散射积分不变量表明在相分离后期发生了Q9+wald Ripening;在leibler和kawasaki理论基础上探讨了相分离动力学,得到了一个描述相分离动力学非缘性方程。

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大气CO2浓度升高能够对农田生态系统产生一系列的影响。土壤线虫在农田生态系统腐屑食物网中占有重要的地位,能够对外界环境变化作出较迅速的响应。本文利用江苏省江都市小记镇的稻-麦轮作FACE系统研究平台,在2007-2008年小麦生长季,研究了大气CO2浓度升高和不同氮肥处理(高N和低N)对农田土壤线虫群落的影响。 研究结果表明:高氮肥施用情况下, CO2浓度升高显著降低了麦田土壤铵态氮和硝态氮含量。不同氮肥处理中CO2浓度升高条件下土壤可溶性碳的含量显著低于对照,而土壤总有机碳和微生物量碳含量高于对照。 大气CO2浓度升高条件下,麦田土壤线虫群落组成和多样性与对照相比表现出显著差异。CO2浓度升高显著增加了麦田土壤线虫总数、食细菌线虫、食真菌线虫和植物寄生线虫数量。在小麦拔节期和成熟期,低N和高N施用条件下,FACE处理中土壤线虫多样性指数(H’)、成熟度指数(MI和PPI)均低于对照处理,而结构指数(SI)高于对照处理。线虫生态指数的结果表明,大气CO2浓度升高条件下,土壤线虫群落多样性降低,土壤环境受到一定的干扰,食物网趋于结构化。

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Size modification of Au nanoparticles (NPs), deposited on the Au-thick film surface and irradiated by slow highly charged ions (SHCI) 40Arq+ (3 6 q 6 12) with fixed low dose of 4.3 1011 ions/cm2 and various energy ranging from 74.64 to 290.64 keV at room temperature (293.15 K), was investigated by atomic force microscopy (AFM) and transmission electron microscopy (TEM). The effect of projectile kinetic energy on the modified size of NPs was explored by an appropriate choice of the fixed process parameters such as ion flux, irradiation temperature, incident angle, irradiation time, etc. The morphological changes of NPs were interpreted by models involving collisional mixing, Ostwald ripening (OR) and inverse Ostwald ripening (IOR) of spherical NPs on a substrate. A critical kinetic energy as well as a critical potential energy of the projectile in the Au NPs size modification process were observed.

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以肥熟土垫旱耕人为土为供试土壤,冬小麦(Triticum aestivum L.)小偃22为供试植物,在全生育期人工控制土壤水分条件下,采用分层隔水土柱法研究了与田间土层分布相同土柱不同土层水分、氮、磷组合对冬小麦不同器官氮、磷养分累积及分配的影响.结果表明:(1)冬小麦不同器官氮、磷累积量表现为籽粒茎秆、叶>穗余部>根系.(2)与整体湿润处理相比,上干下湿水分处理可降低小麦各器官氮、磷累积量,但仅籽粒氮、磷累积量所占比例减少,而营养器官氮累积量所占比例均增加.(3)从肥料处理看,单施氮、单施磷和氮磷配施处理的小麦植株各器官氮、磷累积量均比对照增加,但籽粒氮、磷累积量所占比例均减小.(4)施肥层根系氮、磷累积量比对照相对增加,并以0~30cm土层根系氮、磷累积量为最高.(5)单施氮条件下,以0~90cm土层施肥各器官氮、磷累积量最高,0~30cm土层施肥最低;单施磷和氮磷配施时,以0~90cm土层施肥处理籽粒氮、磷累积量最高,其次是0~30cm土层施肥.由于石灰性土壤中肥料氮终产物以硝态氮为主且容易移动,而磷肥不易在土壤中迁移,在生产实践中仍以氮磷配施入0~30cm土层为佳.

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The nucleation and growth kinetics of CdS nanocrystals in a two-phase synthesis system have been investigated. It was found that the nucleation process is quite lengthy and overlapped with the growth process; nevertheless, as formed nanocrystals show extremely narrow size distribution owing to the unique heterogeneous reacting environment and Ostwald ripening growth. The nucleation and growth kinetics of the nanocrystals were also influenced strongly by the monomer concentration, capping agent concentration, and solvent polarity. It was also found that a high monomer concentration, a low capping agent concentration, and low solvent polarity lead to a higher maximum nucleus concentration and nanocrystal concentration, while high polarity solvents are favorable for the formation of nanocrystals with narrower size distribution and higher photoluminescence quantum yield.

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With the assistance of urea, uniform 2D nanoflakes assembled 3D In2S3 microflowers were synthesized via a facile hydrothermal method at relative low temperature. The properties of the as-obtained In2S3 flowers were characterized by various techniques. In this work, the utilization of urea and L-cysteine, as well as the amount of them played important roles in the formation of In2S3 with different nanostructures. Inferred from their morphology evolution, a urea induced precursor-decomposition associated with the Ostwald-ripening mechanism was proposed to interpret these hierarchical structure formation.

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In this contribution, we report a facile, gram-scale, low-cost route to prepare monodisperse superparamagnetic single-crystal magnetite NPs with mesoporous structure (MSSMN) via a very simple solvothermal method. The formation mechanism of MSSMN is also discussed and we think that Ostwald ripening probably plays an important role in this synthesis process. It is also interestingly found that the size and morphology of mesoporous Fe3O4 NPs can be easily controlled by changing the amount of NaOH and 1,2-ethylenediamine (ETH). Most importantly, the MSSMN can be used as an effective drug delivery carrier. A typical anticancer drug, doxorubicin (Dox), is used for drug loading, and the release behaviors of Dox in two different pH solutions are studied. The results indicate that the MSSMN has a high drug loading capacity and favorable release property for Dox; thus, it is very promising for the application in drug delivery.

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Needle-like single crystals of poly(3-octylthiophene) (P3OT) have been prepared by tetrahydrofuran-vapor annealing. The morphology and structure of the crystals were characterized with optical microscopy, scanning electron microscopy, atomic force microscopy, transmission electron microscopy, and wide-angle X-ray diffraction. It is observed that the P3OT molecules are packed with the backbones parallel to the length axis of the crystal and the alkyl side chains perpendicular to the substrate. The field effect transistor based on the P3OT single crystal exhibited a charge carrier mobility of 1.54 x 10(-4) cm(2)/(Vs) and on/off current ratio of 37, and the molecular orientation of the crystal is ascribed to account for the device performance. The time-dependent morphological evolution demonstrated that the crystals underwent Ostwald ripening when annealed.

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Cobalt ferrite one-dimensional nanostructures (nanoribbons and nanofibers) were prepared by electrospinning combined with sol-gel technology. The nanoribbons and nanofibers were formed through assembling magnetic nanoparticles with poly(vinyl pyrrolidone) (PVP) as the structure-directing template. Nanoribbons and nanofibers were obtained after calcining the precursor nanoribbons at different temperatures. Successive Ostwald ripening processes occur during the formation of CoFe2O4 nanoribbons and nanofibers. The sizes of nanoparticles varied with calcination temperatures, which leads to different one-dimensional structures and variable magnetic properties. These novel magnetic one-dimensional structures can potentially be used in nanoelectronic devices, magnetic sensors, and flexible magnets.

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Lysozyme monolayer-protected gold nanoparticles (Au NPs) which are hydrophilic and biocompatible and show excellent colloidal stability at low temperature, ca. 4 degrees C, were synthesized in aqueous medium by chemical reduction of HAuCl4 with NaBH4 in the presence of a familiar small enzyme, lysozyme. UV-vis spectra, transmission electron microscopy (TEM), atomic force microscopy, and X-ray photoelectron spectroscopy characterization of the as prepared nanoparticles revealed the formation of well-dispersed An NPs of ca. 2 nm diameter. Moreover, the color change of the An NP solution as well as UV-vis spectroscopy and TEM measurements have also demonstrated the occurrence of Ostwald ripening of the nanoparticles at low temperature. Further characterization with Fourier transform infrared spectroscopy (FTIR) and dynamic light scattering indicated the formation of a monolayer of lysozyme molecules on the particle surface. FTIR data also indicated the intactness of the protein molecules coated on An NPs. All the characterization results showed that the monodisperse An NPs are well-coated directly with lysozyme. Driven by the dipole-dipole attraction, the protein-stabilized Au NPs self-assembled into network structures and nanowires upon aging under ambient temperature.

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The dynamics of phase separation in a binary polymer blend of poly(vinyl acetate) with poly(methyl methacrylate) was investigated by using a time-resolved light-scattering technique. In the later stages of spinodal decomposition, a simple dynamic scaling law was found for the scattering function S(q, t)(S(q, t) approximately I(q, t)): S(q, t)q(m)-3 S approximately (q/q(m)). The scaling function determined experimentally was in good agreement with that predicted by Furukawa, S approximately (X) approximately X2/(3 + X8) for critical concentration, and approximately in agreement with that predicted by Furukawa, S approximately (X) approximately X2/(3 + X6) for non-critical mixtures. The light-scattering invariant shows that the later stages of the spinodal decomposition were undergoing domain ripening.