School of Environment and Energy, Peking University Shenzhen Graduate School, Shenzhen 518055, China.
Guangdong Engineering Research Centre for Marine Algal Biotechnology, Shenzhen Key Laboratory of Marine Bioresource and Eco-environmental Science, College of Life Sciences and Oceanography, Shenzhen University, Shenzhen 518060, China.
Mar Drugs. 2018 Sep 1;16(9):310. doi: 10.3390/md16090310.
sp. PKU#SW7 is a thraustochytrid strain that was found to exhibit high potential for docosahexaenoic acid (DHA, C22:6n-3) production. In this work, the transcriptome of sp. PKU#SW7 was analyzed for the study of genes involved in basic metabolic functions and especially in the mechanisms of DHA biosynthesis. Sequence annotation and functional analysis revealed that the strain contains components of fatty acid synthesis (FAS) and polyketide synthase (PKS) pathways. Fatty acid desaturases and elongases were identified as components of FAS pathway, whilst key components of PKS pathway were also found in the cDNA library. The relative contribution of the two pathways to the synthesis of DHA was unknown, as both pathways appeared to be lacking full complement of genes for standalone synthesis of DHA. Further analysis of two putative genes encoding the very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase and dehydrase/isomerase involved in FAS and PKS pathways, respectively, revealed that under various salinity conditions, their relative expression levels changed corresponding to the variation of DHA content in sp. Independent knock outs of these genes in sp. resulted in poor cell growth, probably due to little or no intracellular DHA accumulation. Hence, it can be speculated that both genes are engaged in DHA biosynthesis and DHA in sp. could be produced by jointed actions of both FAS and PKS systems.
sp. PKU#SW7 是一种裂殖壶菌菌株,具有生产二十二碳六烯酸(DHA,C22:6n-3)的巨大潜力。在这项工作中,分析了 sp. PKU#SW7 的转录组,以研究参与基本代谢功能的基因,特别是 DHA 生物合成机制的基因。序列注释和功能分析表明,该菌株包含脂肪酸合成(FAS)和聚酮合酶(PKS)途径的成分。鉴定出脂肪酸去饱和酶和延伸酶是 FAS 途径的组成部分,而 PKS 途径的关键成分也在 cDNA 文库中发现。两条途径对 DHA 合成的相对贡献尚不清楚,因为这两条途径似乎都缺乏独立合成 DHA 的完整基因。进一步分析两个编码非常长链(3R)-3-羟酰基辅酶 A 脱水酶和脱水酶/异构酶的假定基因,它们分别参与 FAS 和 PKS 途径,发现这两个基因在不同盐度条件下,其相对表达水平随着 DHA 含量的变化而变化。sp. 中的这些基因的独立敲除导致细胞生长不良,可能是由于细胞内 DHA 积累很少或没有。因此,可以推测这两个基因都参与了 DHA 的生物合成,并且 sp. 中的 DHA 可能是由 FAS 和 PKS 系统的联合作用产生的。