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首页> 外文期刊>Applied biochemistry and biotechnology, Part A. enzyme engineering and biotechnology >Development of Flow Cytometric Protocol for Nuclear DNA Content Estimation and Determination of Chromosome Number in Pongamia pinnata L., a Valuable Biodiesel Plant
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Development of Flow Cytometric Protocol for Nuclear DNA Content Estimation and Determination of Chromosome Number in Pongamia pinnata L., a Valuable Biodiesel Plant

机译:流式细胞仪协议的发展,用于有价值的生物柴油植物Pongamia pinnata L.核DNA含量估计和染色体数目的确定

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摘要

The potentiality of Pongamia pinnata L. as a sustainable source of feedstock for the biodiesel industry is dependent on an extensive knowledge of the genome structure of the plant. Flow cytometry, with propidium iodide (PI) as the DNA stain, was used to estimate the nuclear DNA content of P. pinnata, with respect to Zea mays 'CE-777' as standard. The internal and pseudo-internal standardization was followed on account of the inhibitory effect of secondary compounds on PI intercalation. The antioxidants (PVP-40 and β-mercaptoethanol) were added to the nuclear isolation buffer for the reduction of inhibitory effect of P. pinnata cytosol. Nuclear DNA content estimation was done for P. pinnata leaves from different altitudes (37–117 m height from sea level) of Assam. Flow cytometry analysis indicated that the nuclear DNA content of P. pinnata is 2.66 pg with predicted 1C value of 1,300Mb using Z. mays as standard. Coefficient of variation in flow cytometric analysis was within the limit of 5 % indicating that the results were reliable. Somatic chromosome numbers were counted from root–tip cells and was found to be 2n=22 corresponding to the diploid level (x=11). A decreasing trend in the nuclear DNA content was observed for the species of different altitudes.
机译:Pongamia pinnata L.作为生物柴油行业可持续原料的潜力取决于对植物基因组结构的广泛了解。以碘化丙啶(PI)为DNA染色剂的流式细胞仪,以玉米Ze'CE-777'为标准,用于估计北美假单胞菌的核DNA含量。由于次要化合物对PI嵌入具有抑制作用,因此进行了内部和拟内部标准化。将抗氧化剂(PVP-40和β-巯基乙醇)添加到核分离缓冲液中,以降低对P.pinnata胞质溶胶的抑制作用。对来自阿萨姆邦不同高度(海拔37-117 m)的P. pinnata叶子进行了核DNA含量估算。流式细胞仪分析表明,以玉米Z(Z。mays)为标准,P。pinnata的核DNA含量为2.66 pg,其1C预测值为1300 Mb。流式细胞仪分析的变异系数在5%的范围内,表明结果可靠。从根尖细胞计数体细胞染色体数,发现其2n = 22与二倍体水平相对应(x = 11)。对于不同高度的物种,观察到核DNA含量下降的趋势。

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