首页> 美国卫生研究院文献>Biomolecules >Transcriptome Mechanism of Utilizing Corn Steep Liquor as the Sole Nitrogen Resource for Lipid and DHA Biosynthesis in Marine Oleaginous Protist Aurantiochytrium sp.
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Transcriptome Mechanism of Utilizing Corn Steep Liquor as the Sole Nitrogen Resource for Lipid and DHA Biosynthesis in Marine Oleaginous Protist Aurantiochytrium sp.

机译:利用玉米浸泡液作为唯一氮源的脂族和DHA生物合成的转录组机制

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摘要

In the current study, corn steep liquor (CSL) is evaluated as an ideal raw agro-material for efficient lipid and docosahexaenoic acid DHA production by sp. Low CSL level in medium (nitrogen deficiency) stimulated the biosynthesis of lipids and DHA while inhibiting cellular growth. The transcriptomic profiles of the sp. cells are analyzed and compared when cultured under high (H group), normal (N group), and low (L group) levels of CSL in the medium. The discriminated transcriptomic profiles from the three groups indicates that changes in CSL level in medium result in a global change in transcriptome of sp. The overall de novo assembly of cDNA sequence data generated 61,163 unigenes, and 18,129 of them were annotated in at least one database. A total of 5105 differently expressed (DE) genes were found in the N group versus the H group, with 2218 downregulated and 2887 upregulated. A total of 3625 DE genes were found in the N group versus the L group, with 1904 downregulated and 1721 upregulated. The analysis and categorization of the DE genes indicates that the regulation mechanism of CSL involved in the perception and transduction of the limited nitrogen signal, the interactions between the transcription factors (TFs) and multiple downstream genes, and the variations in downstream genes and metabolites, in sequence, are illuminated for the first time in the current study.
机译:在当前的研究中,玉米浆(CSL)被评估为通过sp。生产高效脂质和二十二碳六烯酸DHA的理想原料。培养基中低的CSL水平(氮缺乏)刺激了脂质和DHA的生物合成,同时抑制了细胞的生长。 sp。的转录组概况。在高水平(H组),正常水平(N组)和低水平(L组)的培养基中培养细胞时进行分析和比较。从三组中区分出的转录组概况表明,培养基中CSL水平的变化导致sp转录组的整体变化。 cDNA序列数据的整体从头组装产生了61,163个单基因,其中18,129个在至少一个数据库中标注。 N组与H组共发现5105个差异表达(DE)基因,其中2218个下调而2887个上调。与L组相比,N组共发现3625个DE基因,下调1904个,上调1721个。 DE基因的分析和分类表明,CSL的调控机制涉及有限氮信号的感知和转导,转录因子(TFs)与多个下游基因之间的相互作用以及下游基因和代谢产物的变异,按顺序,在本研究中首次被照亮。

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