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从产油微藻盐泽小球藻中克隆得到的硬脂酰-酰基载体蛋白去饱和酶基因:克隆、鉴定和转录分析。

Stearoyl-acyl carrier protein desaturase gene from the oleaginous microalga Chlorella zofingiensis: cloning, characterization and transcriptional analysis.

机构信息

Institute for Food and Bioresource Engineering, College of Engineering, Peking University, Beijing, China.

出版信息

Planta. 2012 Dec;236(6):1665-76. doi: 10.1007/s00425-012-1718-7. Epub 2012 Aug 2.

DOI:10.1007/s00425-012-1718-7
PMID:22855030
Abstract

The green alga Chlorella zofingiensis can accumulate high level of oleic acid (OA, C18:1△(9)) rich oils in response to stress conditions. To understand the regulation of biosynthesis of fatty acid in particular OA at the molecular level, we cloned and characterized the stearoyl acyl carrier protein (ACP) desaturase (SAD) responsible for OA formation through desaturation of stearic acid (C18:0) from C. zofingiensis. Southern blot indicated that the C. zofingiensis genome contained a single copy of SAD, from which the deduced amino acid sequence shared high identity to the corresponding homologs from other microalgae and higher plants. The desaturation activity of SAD was demonstrated in vitro using C18:0-ACP as a substrate. Stress conditions such as high light (HL), nitrogen deficiency (N(-)), or combination of HL and N(-) (HL + N(-)) drastically up-regulated the transcripts of biotin carboxylase (BC, a subunit of ACCase) and SAD, and therefore induced considerably the cellular accumulation of total fatty acids including OA. Glucose (50 mM) gave rise to the similar up-regulation of the two genes and induction of fatty acid accumulation. The accumulation of intracellular reactive oxygen species was found to be associated with the up-regulation of genes. This is the first report of characterization of Chlorella-derived SAD and the results may contribute to understanding of the mechanisms involved in fatty acid/lipid biosynthesis in microalgae.

摘要

小球藻(Chlorella zofingiensis)能够在应激条件下积累高水平的富含油酸(OA,C18:1△(9))的油脂。为了在分子水平上了解脂肪酸,特别是 OA 的生物合成调控机制,我们通过从小球藻中硬脂酰-ACP 去饱和酶(SAD)将硬脂酸(C18:0)去饱和来克隆和鉴定负责 OA 形成的 SAD。Southern blot 表明,小球藻基因组包含 SAD 的一个单一拷贝,其推导的氨基酸序列与其他微藻和高等植物的相应同源物高度相似。体外使用 C18:0-ACP 作为底物证明了 SAD 的去饱和活性。高光(HL)、氮缺乏(N(-))或 HL 和 N(-)的组合(HL + N(-))等应激条件极大地上调了生物素羧化酶(BC,乙酰辅酶 A 羧化酶的 a 亚基)和 SAD 的转录物,因此大大诱导了包括 OA 在内的总脂肪酸的细胞积累。葡萄糖(50 mM)也导致了这两个基因的相似上调和脂肪酸积累的诱导。发现细胞内活性氧的积累与基因的上调有关。这是首次报道小球藻衍生的 SAD 的特性,研究结果可能有助于理解微藻中脂肪酸/脂质生物合成的机制。

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