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首页> 外文期刊>Plant Cell, Tissue and Organ Culture: An International Journal on in Vitro Culture of Higher Plants >Microprojectile bombardment of Laminaria japonica gametophytes and rapid propagation of transgenic lines within a bubble-column bioreactor.
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Microprojectile bombardment of Laminaria japonica gametophytes and rapid propagation of transgenic lines within a bubble-column bioreactor.

机译:日本海带配子体的微粒轰击和转基因株系在气泡柱生物反应器内的快速繁殖。

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摘要

A human acidic fibroblast growth factor gene, hafgf, was successfully transferred into Laminaria japonica (kelp) gametophytes via microprojectile bombardment using the biolistic PDS-1000/He gene gun. Following phosphinothricin screening, PCR detection and Southern blot analysis, transgenic L. japonica gametophytes were cultivated in an illuminated bubble-column bioreactor to optimize growth conditions. A maximal final dry cell density of 1,695 mg l-1 was obtained in a batch culture having an initial dry cell density of 129.75 mg l-1. This was achieved using an aeration rate of 1.08 l air min-1 l-1 culture in a medium containing 1.5 mM inorganic nitrate and 0.15 mM phosphate. In addition, the relationship between different nitrogen sources and growth of transgenic gametophytes indicated that both urea and sodium nitrate were effective nitrogen sources for cell growth, while ammonium ions inhibited growth of these gametophytes.
机译:使用酸性射弹PDS-1000 / He基因枪,通过微粒轰击成功地将人类酸性成纤维细胞生长因子基因 hafgf 转移到了 Laminaria japonica (海带)配子体中。在膦丝菌素筛选,PCR检测和Southern印迹分析之后,转基因L。在光照的气泡柱生物反应器中培养了粳米配子体,以优化生长条件。在初始干细胞密度为129.75 mg l -1 的分批培养中,最大最终干细胞密度为1,695 mg l -1 。这是通过在包含1.5 mM无机硝酸盐和0.15 mM磷酸盐的培养基中以1.08 l air min -1 l -1 的曝气速率实现的。另外,不同氮源与转基因配子体生长之间的关系表明,尿素和硝酸钠都是细胞生长的有效氮源,而铵离子抑制了这些配子体的生长。

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