Department of Chemical and Environmental Engineering, Yale University, 9 Hillhouse Ave, New Haven, CT 06520, USA.
Biotechnol Biofuels. 2012 Sep 24;5(1):74. doi: 10.1186/1754-6834-5-74.
The lack of sequenced genomes for oleaginous microalgae limits our understanding of the mechanisms these organisms utilize to become enriched in triglycerides. Here we report the de novo transcriptome assembly and quantitative gene expression analysis of the oleaginous microalga Neochloris oleoabundans, with a focus on the complex interaction of pathways associated with the production of the triacylglycerol (TAG) biofuel precursor.
After growth under nitrogen replete and nitrogen limiting conditions, we quantified the cellular content of major biomolecules including total lipids, triacylglycerides, starch, protein, and chlorophyll. Transcribed genes were sequenced, the transcriptome was assembled de novo, and the expression of major functional categories, relevant pathways, and important genes was quantified through the mapping of reads to the transcriptome. Over 87 million, 77 base pair high quality reads were produced on the Illumina HiSeq sequencing platform. Metabolite measurements supported by genes and pathway expression results indicated that under the nitrogen-limiting condition, carbon is partitioned toward triglyceride production, which increased fivefold over the nitrogen-replete control. In addition to the observed overexpression of the fatty acid synthesis pathway, TAG production during nitrogen limitation was bolstered by repression of the β-oxidation pathway, up-regulation of genes encoding for the pyruvate dehydrogenase complex which funnels acetyl-CoA to lipid biosynthesis, activation of the pentose phosphate pathway to supply reducing equivalents to inorganic nitrogen assimilation and fatty acid biosynthesis, and the up-regulation of lipases-presumably to reconstruct cell membranes in order to supply additional fatty acids for TAG biosynthesis.
Our quantitative transcriptome study reveals a broad overview of how nitrogen stress results in excess TAG production in N. oleoabundans, and provides a variety of genetic engineering targets and strategies for focused efforts to improve the production rate and cellular content of biofuel precursors in oleaginous microalgae.
由于缺乏油脂微藻的测序基因组,我们对这些生物利用何种机制在细胞内积累甘油三酯(TAG)的认识受到了限制。在此,我们报告了产油微藻 N. oleoabundans 的从头转录组组装和定量基因表达分析,重点研究了与 TAG 生物燃料前体生产相关的复杂途径之间的相互作用。
在氮充足和氮限制条件下生长后,我们定量测定了主要生物分子的细胞含量,包括总脂类、TAG、淀粉、蛋白质和叶绿素。对转录的基因进行测序,从头组装转录组,并通过将读取序列映射到转录组来定量测定主要功能类别、相关途径和重要基因的表达。在 Illumina HiSeq 测序平台上生成了超过 8700 万个、77 个碱基对的高质量读取。基因和途径表达结果支持的代谢物测量表明,在氮限制条件下,碳被分配到 TAG 生产中,比氮充足对照增加了五倍。除了观察到脂肪酸合成途径的过度表达外,氮限制时 TAG 生产还得益于β-氧化途径的抑制、编码丙酮酸脱氢酶复合物的基因上调,该复合物将乙酰辅酶 A 导入脂质生物合成、戊糖磷酸途径的激活以供应还原当量用于无机氮同化和脂肪酸生物合成,以及脂酶的上调——可能是为了重建细胞膜,以便为 TAG 生物合成提供额外的脂肪酸。
我们的定量转录组研究揭示了氮胁迫如何导致 N. oleoabundans 中过量 TAG 产生的广泛概述,并为通过基因工程提高油脂微藻生物燃料前体的产率和细胞含量提供了多种基因工程靶点和策略。