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Integration of a Galdieria plasma membrane sugar transporter enables heterotrophic growth of the obligate photoautotrophic red alga Cynanidioschyzon merolae

机译:Galdieria质膜糖转运蛋白的整合可实现专性光自养红藻Cynanidioschyzon merolae的异养生长

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摘要

The unicellular thermoacidophilic red alga Cyanidioschyzon merolae is an emerging model organism of photosynthetic eukaryotes. Its relatively simple genome (16.5 Mbp) with very low‐genetic redundancy and its cellular structure possessing one chloroplast, mitochondrion, peroxisome, and other organelles have facilitated studies. In addition, this alga is genetically tractable, and the nuclear and chloroplast genomes can be modified by integration of transgenes via homologous recombination. Recent studies have attempted to clarify the structure and function of the photosystems of this alga. However, it is difficult to obtain photosynthesis‐defective mutants for molecular genetic studies because this organism is an obligate autotroph. To overcome this issue in C. merolae, we expressed a plasma membrane sugar transporter, GsSPT1, from Galdieria sulphuraria, which is an evolutionary relative of C. merolae and capable of heterotrophic growth. The heterologously expressed GsSPT1 localized at the plasma membrane. GsSPT1 enabled C. merolae to grow mixotrophically and heterotrophically, in which cells grew in the dark with glucose or in the light with a photosynthetic inhibitor 3‐(3,4‐dichlorophenyl)‐1,1‐dimethylurea (DCMU) and glucose. When the GsSPT1 transgene multiplied on the C. merolae chromosome via the URA Cm‐Gs selection marker, which can multiply itself and its flanking transgene, GsSPT1 protein level increased and the heterotrophic and mixotrophic growth of the transformant accelerated. We also found that GsSPT1 overexpressing C. merolae efficiently formed colonies on solidified medium under light with glucose and DCMU. Thus, GsSPT1 overexpresser will facilitate single colony isolation and analyses of photosynthesis‐deficient mutants produced either by random or site‐directed mutagenesis. In addition, our results yielded evidence supporting that the presence or absence of plasma membrane sugar transporters is a major cause of difference in trophic properties between C. merolae and G. sulphuraria.
机译:单细胞热嗜酸红藻Cyanidioschyzon merolae是光合真核生物的新兴模型生物。它的相对简单的基因组(16.5 Mbp)具有极低的遗传冗余,并且其细胞结构具有一个叶绿体,线粒体,过氧化物酶体和其他细胞器,从而促进了研究。此外,该藻类在遗传上是易处理的,并且可以通过同源重组整合转基因来修饰核和叶绿体基因组。最近的研究试图阐明这种藻类的光系统的结构和功能。但是,由于这种生物是专性自养生物,因此很难获得用于分子遗传研究的光合作用缺陷型突变体。为了克服C.merolae中的这个问题,我们表达了一种来自Galdieria sulfuraria的质膜糖转运蛋白GsSPT1,它是C.merolae的进化亲缘种,能够异养生长。异源表达的GsSPT1位于质膜上。 GsSPT1使C.merolae能够混合营养和异养生长,其中的细胞在黑暗中与葡萄糖或在光下与光合抑制剂3-(3,4-二氯苯基)-1,1-二甲基脲(DCMU)和葡萄糖一起生长。当GsSPT1转基因通过URA Cm-Gs选择标记在美人鱼染色体上繁殖时,可以自身和其侧翼转基因繁殖,GsSPT1蛋白水平增加,转化体的异养和杂养增长加速。我们还发现,在葡萄糖和DCMU的光照下,过表达Cs.merolae的GsSPT1在凝固的培养基上有效形成菌落。因此,GsSPT1过表达将促进单菌落的分离和对随机或定点诱变产生的光合作用缺陷型突变体的分析。此外,我们的研究结果提供了证据,证明存在或不存在质膜糖转运蛋白是美耐克罗氏菌和硫杆菌之间营养特性差异的主要原因。

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