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莱茵衣藻磷脂酰甘油磷酸合酶在集胞藻PCC 6803中的特性分析

Characterization of Chlamydomonas reinhardtii phosphatidylglycerophosphate synthase in Synechocystis sp. PCC 6803.

作者信息

Hung Chun-Hsien, Endo Kaichiro, Kobayashi Koichi, Nakamura Yuki, Wada Hajime

机构信息

Institute of Plant and Microbial Biology, Academia Sinica Taipei, Taiwan.

Department of Life Sciences, Graduate School of Arts and Sciences, The University of Tokyo Tokyo, Japan.

出版信息

Front Microbiol. 2015 Aug 24;6:842. doi: 10.3389/fmicb.2015.00842. eCollection 2015.

Abstract

Phosphatidylglycerol (PG) is an indispensable phospholipid class with photosynthetic function in plants and cyanobacteria. However, its biosynthesis in eukaryotic green microalgae is poorly studied. Here, we report the isolation and characterization of two homologs (CrPGP1 and CrPGP2) of phosphatidylglycerophosphate synthase (PGPS), the rate-limiting enzyme in PG biosynthesis, in Chlamydomonas reinhardtii. Heterologous complementation of Synechocystis sp. PCC 6803 pgsA mutant by CrPGP1 and CrPGP2 rescued the PG-dependent growth phenotype, but the PG level and its fatty acid composition were not fully rescued in the complemented strains. As well, oxygen evolution activity was not fully recovered, although electron transport activity of photosystem II was restored to the wild-type level. Gene expression study of CrPGP1 and CrPGP2 in nutrient-starved C. reinhardtii showed differential response to phosphorus and nitrogen deficiency. Taken together, these results highlight the distinct and overlapping function of PGPS in cyanobacteria and eukaryotic algae.

摘要

磷脂酰甘油(PG)是植物和蓝细菌中具有光合功能的一类不可或缺的磷脂。然而,其在真核绿藻中的生物合成研究较少。在此,我们报告了莱茵衣藻中磷脂酰甘油磷酸合酶(PGPS)(PG生物合成中的限速酶)的两个同源物(CrPGP1和CrPGP2)的分离与鉴定。CrPGP1和CrPGP2对集胞藻PCC 6803 pgsA突变体的异源互补挽救了依赖PG的生长表型,但在互补菌株中PG水平及其脂肪酸组成并未完全恢复。同样,尽管光系统II的电子传递活性恢复到了野生型水平,但放氧活性并未完全恢复。对营养饥饿的莱茵衣藻中CrPGP1和CrPGP2的基因表达研究表明,它们对磷和氮缺乏有不同的反应。综上所述,这些结果突出了PGPS在蓝细菌和真核藻类中的独特和重叠功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8126/4547039/c6cf2d7e7b90/fmicb-06-00842-g001.jpg

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