28 research outputs found

    Cassava genome from a wild ancestor to cultivated varieties

    Get PDF
    Cassava is a major tropical food crop in the Euphorbiaceae family that has high carbohydrate production potential and adaptability to diverse environments. Here we present the draft genome sequences of a wild ancestor and a domesticated variety of cassava and comparative analyses with a partial inbred line. We identify 1,584 and 1,678 gene models specific to the wild and domesticated varieties, respectively, and discover high heterozygosity and millions of single-nucleotide variations. Our analyses reveal that genes involved in photosynthesis, starch accumulation and abiotic stresses have been positively selected, whereas those involved in cell wall biosynthesis and secondary metabolism, including cyanogenic glucoside formation, have been negatively selected in the cultivated varieties, reflecting the result of natural selection and domestication. Differences in microRNA genes and retrotransposon regulation could partly explain an increased carbon flux towards starch accumulation and reduced cyanogenic glucoside accumulation in domesticated cassava. These results may contribute to genetic improvement of cassava through better understanding of its biology

    Influence of thermocouple angles and wire distance on temperature measurement

    No full text
    When a thermocouple is used to measure gas temperature, the measured temperature, i.e., the thermocouple bead temperature, is not equal to the gas temperature. The bead temperature results from the bead energy balance. The positioning angles such as the pitch angle and the roll angle and the wire distance of the thermocouple will influence the convection heat transfer of the thermocouple, causing the bead temperature variation. Two S type thermocouples are used to measure the temperature of the H2/air Hencken flame with the equivalence ratio 0.7. The maximum measurement temperature changes are 52 K and 79 K for the pitch angle variation and the roll angle variation, respectively. CFD simulations are carried out to simulate the experimental phenomena. The differences between the simulated and measured bead temperatures are less than 20.4 K. With 90° roll angle, the bead temperature increases first then decreases with the pitch angle. With 90° pitch angle, the bead temperature increases first then decreases with the roll angle. With 0° pitch angle, the bead temperature increases monotonically with the wire distance. The background physical mechanisms of the phenomena are analyzed with the detailed CFD results

    Thermocouple Effective Length under Sinusoidal Gas Temperature Condition

    No full text
    When a thermocouple is used to measure gas temperature, the measured temperature is the thermocouple bead temperature, which is not equal to the gas temperature. The bead temperature results from its energy balance. Through the wire convection and conduction, the temperature of the bead is related to the gas temperature within a certain geometric range around it, and this range is quantified by the effective length. Under the sinusoidal incoming gas temperature condition, the analytical expression for the effective length is deduced, and its accuracy is validated by the one-dimensional numerical solution. The differences between the analytical and numerical effective lengths are less than 10.5% for the test cases. Similar to that under the uniform incoming gas temperature condition, the effective length under the sinusoidal gas temperature condition increases with the thermal conductivity and the diameter of the wire and decreases with the heat transfer coefficient of the wire. The influence of the amplitude, wavelength and phase of the gas temperature on the effective length are very weak, meaning that the theoretical expression under the uniform gas temperature can calculate the effective length under the non-uniform gas temperature with good accuracy

    Microencapsulation of coupled folate and chitosan nanoparticles for targeted delivery of combination drugs to colon

    Full text link
    Folate-chitosan nanoparticles, co-loaded with 5-fluourouacil (5-FU) and leucovorin (LV) and prepared by ionic gelation technology were physically microencapsulated by enteric polymer using a solvent evaporation method. Average particle size of the microencapsulated particles was in the range of 15 to 35 µm. High drug encapsulation efficiency was obtained for both 5-FU and LV in the microencapsulated particles. Both drugs were in amorphous state in the microencapsulated particles. By enteric coating, excellent pH-dependent release profile was achieved and no drug release was observed in simulated gastric and intestinal fluids. However, when the pH value reached the soluble threshold of Eudragit S-100, a constant and slow drug release was observed. The results indicated that these microencapsulated particles are a promising vehicle for selectively targeting drugs to colon in the chemotherapy of colon cancer

    Optimization of Enzymatic Process for Vanillin Extraction Using Response Surface Methodology

    No full text
    Vanillin was extracted from vanilla beans using pretreatment with cellulase to produce enzymatic hydrolysis, and response surface methodology (RSM) was applied to optimize the processing parameters of this extraction. The effects of heating time, enzyme quantity and temperature on enzymatic extraction of vanillin were evaluated. Extraction yield (mg/g) was used as the response value. The results revealed that the increase in heating time and the increase in enzyme quantity (within certain ranges) were associated with an enhancement of extraction yield, and that the optimal conditions for vanillin extraction were: Heating time 6 h, temperature 60 °C and enzyme quantity 33.5 mL. Calculated from the final polynomial functions, the optimal response of vanillin extraction yield was 7.62 mg/g. The predicted results for optimal reaction conditions were in good agreement with experimental values

    A critical role of CDKN3 in Bcr-Abl-mediated tumorigenesis.

    Get PDF
    CDKN3 (cyclin-dependent kinase inhibitor 3), a dual specificity protein phosphatase, dephosphorylates cyclin-dependent kinases (CDKs) and thus functions as a key negative regulator of cell cycle progression. Deregulation or mutations of CDNK3 have been implicated in various cancers. However, the role of CDKN3 in Bcr-Abl-mediated chronic myelogenous leukemia (CML) remains unknown. Here we found that CDKN3 acts as a tumor suppressor in Bcr-Abl-mediated leukemogenesis. Overexpression of CDKN3 sensitized the K562 leukemic cells to imanitib-induced apoptosis and dramatically inhibited K562 xenografted tumor growth in nude mouse model. Ectopic expression of CDKN3 significantly reduced the efficiency of Bcr-Abl-mediated transformation of FDCP1 cells to growth factor independence. In contrast, depletion of CDKN3 expression conferred resistance to imatinib-induced apoptosis in the leukemic cells and accelerated the growth of xenograph leukemia in mice. In addition, we found that CDKN3 mutant (CDKN3-C140S) devoid of the phosphatase activity failed to affect the K562 leukemic cell survival and xenografted tumor growth, suggesting that the phosphatase of CDKN3 was required for its tumor suppressor function. Furthermore, we observed that overexpression of CDKN3 reduced the leukemic cell survival by dephosphorylating CDK2, thereby inhibiting CDK2-dependent XIAP expression. Moreover, overexpression of CDKN3 delayed G1/S transition in K562 leukemic cells. Our results highlight the importance of CDKN3 in Bcr-Abl-mediated leukemogenesis, and provide new insights into diagnostics and therapeutics of the leukemia

    Optimized Production of Vanillin from Green Vanilla Pods by Enzyme-Assisted Extraction Combined with Pre-Freezing and Thawing

    Get PDF
    Production of vanillin from natural green vanilla pods was carried out by enzyme-assisted extraction combined with pre-freezing and thawing. In the first step the green vanilla pods were pre-frozen and then thawed to destroy cellular compartmentation. In the second step pectinase from Aspergillus niger was used to hydrolyze the pectin between the glucovanillin substrate and β-glucosidase. Four main variables, including enzyme amount, reaction temperature, time and pH, which were of significance for the vanillin content were studied and a central composite design (CCD) based on the results of a single-factor tests was used. Response surface methodology based on CCD was employed to optimize the combination of enzyme amount, reaction temperature, time, and pH for maximum vanillin production. This resulted in the optimal condition in regards of the enzyme amount, reaction temperature, time, and pH at 84.2 mg, 49.5 °C, 7.1 h, and 4.2, respectively. Under the optimal condition, the experimental yield of vanillin was 4.63% ± 0.11% (dwb), which was in good agreement with the value predicted by the model. Compared to the traditional curing process (1.98%) and viscozyme extract (2.36%), the optimized method for the vanillin production significantly increased the yield by 133.85% and 96%, respectively
    corecore