通过下调MGD1抑制单半乳糖二酰基甘油合成,导致莱茵衣藻膜脂重塑和三酰基甘油生物合成增强。

Jun-Woo Lee, Min-Woo Lee, Chun-Zhi Jin, Hee-Mock Oh, EonSeon Jin, Hyung-Gwan Lee
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引用次数: 1

摘要

背景:膜脂重塑涉及调节细胞膜的物理化学修饰,以对抗非生物应激或衰老,它可能是中性脂含量增加的触发因素。在藻类和高等植物中,单半乳糖二酰基甘油(MGDG)占总膜脂的比例最高,并且在几种非生物胁迫下作为膜脂重塑反应的一部分被高度降低。然而,微藻中MGDG合成的遗传调控及其对脂质合成的影响尚未得到研究。为了培育一株通过促进膜脂重塑而具有高三酰甘油(TAG)积累能力的工业微藻菌株,研究了莱茵衣藻(Chlamydomonas reinhardtii) MGDG合成酶1 (MGD1)下调突变体(Cr-mgd1),并对其作为生物柴油原料的适用性进行了评价。结果:Cr-mgd1 CrMGD1基因表达水平降低65%,MGDG含量降低22%,二酰基甘油三甲基同丝氨酸(DGTS)和TAG含量分别升高1.39倍和5.40倍。大部分与MGDG(质体半乳糖甘油脂降解1)分解和TAG代谢相关的基因(二酰基甘油o -酰基转移酶1、磷脂:二酰基甘油酰基转移酶和主要脂滴蛋白)表达水平升高。Cr-mgd1中DGDG/MGDG比例失衡导致光合电子传递减少,光能利用率降低,活性氧水平升高。此外,DGTS水平升高可引起内质网应激。因此,细胞应激增加和脂质重塑刺激了Cr-mgd1中TAG的加速积累。在强光(400µmol光子/m2/s)下,Cr-mgd1-HL的TAG产率为1.99 mg/L/d,是野生型WT-HL的2.71倍。此外,在氮饥饿和强光下,脂质(124.55 mg/L/d)、TAG (20.03 mg/L/d)和最大中性脂质(56.13 mg/L/d)产量最高。结论:该突变体通过调控mgd1基因表达诱导脂质重塑,不仅中性脂含量高,而且在强光和氮饥饿条件下培养,中性脂产量达到最大,具有较好的生物质性能,最适合生产优质生物柴油。因此,该突变体可能有助于了解MGD1在衣藻脂质合成中的作用,并可能用于产生大量的TAG。
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Inhibition of monogalactosyldiacylglycerol synthesis by down-regulation of MGD1 leads to membrane lipid remodeling and enhanced triacylglycerol biosynthesis in Chlamydomonas reinhardtii.

Background: Membrane lipid remodeling involves regulating the physiochemical modification of cellular membranes against abiotic stress or senescence, and it could be a trigger to increase neutral lipid content. In algae and higher plants, monogalactosyldiacylglycerol (MGDG) constitutes the highest proportion of total membrane lipids and is highly reduced as part of the membrane lipid remodeling response under several abiotic stresses. However, genetic regulation of MGDG synthesis and its influence on lipid synthesis has not been studied in microalgae. For development of an industrial microalgae strain showing high accumulation of triacylglycerol (TAG) by promoting membrane lipid remodeling, MGDG synthase 1 (MGD1) down-regulated mutant of Chlamydomonas reinhardtii (Cr-mgd1) was generated and evaluated for its suitability for biodiesel feedstock.

Results: The Cr-mgd1 showed a 65% decrease in CrMGD1 gene expression level, 22% reduction in MGDG content, and 1.39 and 5.40 times increase in diacylglyceryltrimethylhomoserines (DGTS) and TAG, respectively. The expression levels of most genes related to the decomposition of MGDG (plastid galactoglycerolipid degradation1) and TAG metabolism (diacylglycerol O-acyltransferase1, phospholipid:diacylglycerol acyltransferase, and major lipid droplet protein) were increased. The imbalance of DGDG/MGDG ratio in Cr-mgd1 caused reduced photosynthetic electron transport, resulting in less light energy utilization and increased reactive oxygen species levels. In addition, endoplasmic reticulum stress was induced by increased DGTS levels. Thus, accelerated TAG accumulation in Cr-mgd1 was stimulated by increased cellular stress as well as lipid remodeling. Under high light (HL) intensity (400 µmol photons/m2/s), TAG productivity in Cr-mgd1-HL (1.99 mg/L/d) was 2.71 times higher than that in wild type (WT-HL). Moreover, under both nitrogen starvation and high light intensity, the lipid (124.55 mg/L/d), TAG (20.03 mg/L/d), and maximum neutral lipid (56.13 mg/L/d) productivity were the highest.

Conclusions: By inducing lipid remodeling through the mgd1 gene expression regulation, the mutant not only showed high neutral lipid content but also reached the maximum neutral lipid productivity through cultivation under high light and nitrogen starvation conditions, thereby possessing improved biomass properties that are the most suitable for high quality biodiesel production. Thus, this mutant may help understand the role of MGD1 in lipid synthesis in Chlamydomonas and may be used to produce high amounts of TAG.

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