Chlamydomonas cells transition through distinct Fe nutrition stages within 48 h of transfer to Fe-free medium.

IF 2.9 3区 生物学 Q2 PLANT SCIENCES Photosynthesis Research Pub Date : 2024-09-01 Epub Date: 2024-07-17 DOI:10.1007/s11120-024-01103-8
Helen W Liu, Eugen I Urzica, Sean D Gallaher, Stefan Schmollinger, Crysten E Blaby-Haas, Masakazu Iwai, Sabeeha S Merchant
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Abstract

Low iron (Fe) bioavailability can limit the biosynthesis of Fe-containing proteins, which are especially abundant in photosynthetic organisms, thus negatively affecting global primary productivity. Understanding cellular coping mechanisms under Fe limitation is therefore of great interest. We surveyed the temporal responses of Chlamydomonas (Chlamydomonas reinhardtii) cells transitioning from an Fe-rich to an Fe-free medium to document their short and long-term adjustments. While slower growth, chlorosis and lower photosynthetic parameters are evident only after one or more days in Fe-free medium, the abundance of some transcripts, such as those for genes encoding transporters and enzymes involved in Fe assimilation, change within minutes, before changes in intracellular Fe content are noticeable, suggestive of a sensitive mechanism for sensing Fe. Promoter reporter constructs indicate a transcriptional component to this immediate primary response. With acetate provided as a source of reduced carbon, transcripts encoding respiratory components are maintained relative to transcripts encoding components of photosynthesis and tetrapyrrole biosynthesis, indicating metabolic prioritization of respiration over photosynthesis. In contrast to the loss of chlorophyll, carotenoid content is maintained under Fe limitation despite a decrease in the transcripts for carotenoid biosynthesis genes, indicating carotenoid stability. These changes occur more slowly, only after the intracellular Fe quota responds, indicating a phased response in Chlamydomonas, involving both primary and secondary responses during acclimation to poor Fe nutrition.

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衣藻细胞在转移到无铁培养基后的 48 小时内经历了不同的铁营养阶段。
铁(Fe)生物利用率低会限制含铁蛋白质的生物合成,而光合生物体内的含铁蛋白质尤其丰富,从而对全球初级生产力产生负面影响。因此,了解铁限制下的细胞应对机制非常重要。我们调查了衣藻(Chlamydomonas reinhardtii)细胞从富含铁的培养基过渡到不含铁的培养基时的时间反应,以记录它们的短期和长期调整。虽然在无铁培养基中生长缓慢、叶绿素减少和光合作用参数降低等现象只有在一天或多天后才会明显出现,但在细胞内铁含量发生明显变化之前,一些转录本(如编码铁同化转运体和酶的基因)的丰度在几分钟内就发生了变化,这表明存在着一种对铁敏感的感知机制。启动子报告构建物表明,这种直接的主要反应具有转录成分。在提供醋酸盐作为还原碳源的情况下,相对于编码光合作用和四吡咯生物合成成分的转录本,编码呼吸作用成分的转录本保持不变,这表明呼吸作用的代谢优先于光合作用。与叶绿素的损失相反,尽管类胡萝卜素生物合成基因的转录本减少,但类胡萝卜素的含量在铁限制条件下得以维持,这表明类胡萝卜素具有稳定性。这些变化发生得较慢,只有在细胞内铁配额做出反应之后才会发生,这表明衣藻在适应铁营养不良的过程中会做出分阶段的反应,包括初级反应和次级反应。
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来源期刊
Photosynthesis Research
Photosynthesis Research 生物-植物科学
CiteScore
6.90
自引率
8.10%
发文量
91
审稿时长
4.5 months
期刊介绍: Photosynthesis Research is an international journal open to papers of merit dealing with both basic and applied aspects of photosynthesis. It covers all aspects of photosynthesis research, including, but not limited to, light absorption and emission, excitation energy transfer, primary photochemistry, model systems, membrane components, protein complexes, electron transport, photophosphorylation, carbon assimilation, regulatory phenomena, molecular biology, environmental and ecological aspects, photorespiration, and bacterial and algal photosynthesis.
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