Abstract

Single-cell red microalga Porphyridium cruentum is potentially considered to be the bioresource for biofuel and pharmaceutical production. Nitrogen is a kind of nutrient component for photosynthetic P. cruentum. Meanwhile, nitrogen stress could induce to accumulate some substances such as lipid and phycoerythrin and affect its growth and physiology. However, how marine microalga Porphyridium cruentum respond and adapt to nitrogen starvation remains elusive. Here, acclimation of the metabolic reprogramming to changes in the nutrient environment was studied by high-throughput mRNA sequencing in the unicellular red alga P. cruentum. Firstly, to reveal transcriptional regulation, de novo transcriptome was assembled and 8,244 unigenes were annotated based on different database. Secondly, under nitrogen deprivation, 2100 unigenes displayed differential expression (1134 upregulation and 966 downregulation, respectively) and some pathways including carbon/nitrogen metabolism, photosynthesis, and lipid metabolism would be reprogrammed in P. cruentum. The result demonstrated that nitrate assimilation (with related unigenes of 8–493 fold upregulation) would be strengthen and photosynthesis (with related unigenes of 6–35 fold downregulation) be impaired under nitrogen deprivation. Importantly, compared to other green algae, red microalga P. cruentum presented a different expression pattern of lipid metabolism in response to nitrogen stress. These observations will also provide novel insight for understanding adaption mechanisms and potential targets for metabolic engineering and synthetic biology in P. cruentum.

Highlights

  • Metabolic reprogramming under nitrogen deprivation in Porphyridium cruentum linoleic acid; CT, control; ND, nitrogen depletion; DEGs, differential expression unigenes; GSGOGAT, glutamine synthetase-glutamate synthase; CCM, carbon concentration mechanism; carbonic anhydrases (CA), carbonic anhydrase; PK, pyruvate kinase; DGAT, diacylglycerol acyltransferase; LPAT, lysophosphatidic acid acyltransferase

  • To identify the change of lipid, carbohydrate, protein and delineate their interactions, the physiological responses were tracked under two contrasting culture conditions for P. cruentum: nitrogen repletion (CT: control) and nitrogen deprivation (ND)

  • As for LC-PUFAs, we observed that LA and Arachidonic acid (ARA) were significantly increased under ND condition, while EPA was decreased (Fig 1B)

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Summary

Objectives

We aimed to interrogate transcriptomic change of P. cruentum after the shift from nitrogen repletion to nitrogen depletion by high quality mRNA-Seq data using Illumina NextSeq6000 technology

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Results
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