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利用具有磷饥饿诱导型启动子的2型二酰基甘油酰基转移酶增强莱茵衣藻质体外油脂合成

Enhancement of extraplastidic oil synthesis in Chlamydomonas reinhardtii using a type-2 diacylglycerol acyltransferase with a phosphorus starvation-inducible promoter.

作者信息

Iwai Masako, Ikeda Keiko, Shimojima Mie, Ohta Hiroyuki

机构信息

Center for Biological Resources and Informatics, Tokyo Institute of Technology, Midori-ku, Yokohama, Japan; Core Research for Evolutional Science and Technology (CREST), Japan Science and Technology Agency (JST), Chiyoda-ku, Tokyo, Japan.

出版信息

Plant Biotechnol J. 2014 Aug;12(6):808-19. doi: 10.1111/pbi.12210. Epub 2014 Jun 9.

Abstract

When cultivated under stress conditions, many plants and algae accumulate oil. The unicellular green microalga Chlamydomonas reinhardtii accumulates neutral lipids (triacylglycerols; TAGs) during nutrient stress conditions. Temporal changes in TAG levels in nitrogen (N)- and phosphorus (P)-starved cells were examined to compare the effects of nutrient depletion on TAG accumulation in C. reinhardtii. TAG accumulation and fatty acid composition were substantially changed depending on the cultivation stage before nutrient starvation. Profiles of TAG accumulation also differed between N and P starvation. Logarithmic-growth-phase cells diluted into fresh medium showed substantial TAG accumulation with both N and P deprivation. N deprivation induced formation of oil droplets concomitant with the breakdown of thylakoid membranes. In contrast, P deprivation substantially induced accumulation of oil droplets in the cytosol and maintaining thylakoid membranes. As a consequence, P limitation accumulated more TAG both per cell and per culture medium under these conditions. To enhance oil accumulation under P deprivation, we constructed a P deprivation-dependent overexpressor of a Chlamydomonas type-2 diacylglycerol acyl-CoA acyltransferase (DGTT4) using a sulphoquinovosyldiacylglycerol 2 (SQD2) promoter, which was up-regulated during P starvation. The transformant strongly enhanced TAG accumulation with a slight increase in 18 : 1 content, which is a preferred substrate of DGTT4. These results demonstrated enhanced TAG accumulation using a P starvation-inducible promoter.

摘要

在胁迫条件下培养时,许多植物和藻类会积累油脂。单细胞绿色微藻莱茵衣藻在营养胁迫条件下会积累中性脂质(三酰甘油;TAGs)。研究了氮(N)和磷(P)饥饿细胞中TAG水平的时间变化,以比较营养耗竭对莱茵衣藻TAG积累的影响。TAG积累和脂肪酸组成会根据营养饥饿前的培养阶段而发生显著变化。N饥饿和P饥饿时TAG积累的情况也有所不同。稀释到新鲜培养基中的对数生长期细胞在N和P缺乏时均显示出大量的TAG积累。N缺乏会诱导油滴形成,同时伴随着类囊体膜的解体。相反,P缺乏会显著诱导油滴在细胞质中积累,并维持类囊体膜。因此,在这些条件下,P限制使每个细胞和每单位培养基积累了更多的TAG。为了在P缺乏条件下增强油脂积累,我们使用在P饥饿期间上调的磺基喹喔啉二酰基甘油2(SQD2)启动子构建了莱茵衣藻2型二酰基甘油酰基-CoA酰基转移酶(DGTT4)的P缺乏依赖性过表达载体。该转化体强烈增强了TAG积累,同时18:1含量略有增加,18:1是DGTT4的优选底物。这些结果证明了使用P饥饿诱导型启动子可增强TAG积累。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3a5/4160818/e6623828f2e0/pbi0012-0808-f1.jpg

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