4.7 Article

Transcriptome analysis reveals the promoting effect of trisodium citrate on astaxanthin accumulation in Haematococcus pluvialis under high light condition

Journal

AQUACULTURE
Volume 543, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.aquaculture.2021.736978

Keywords

Haematococcus pluvialis; Astaxanthin biosynthesis; Tricarboxylic acid cycle (TCA cycle); Fatty acid biosynthesis; Reactive oxygen species (ROS)

Funding

  1. National Natural Science Foundation of China [31572638, 31701400]
  2. Public Benefit Program of Zhejiang Science and Technology Department [2015C32021]
  3. K. C. Wong Magna Fund in Ningbo University

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The addition of trisodium citrate (TSC) was found to significantly increase astaxanthin accumulation in Haematococcus pluvialis under high light stress by up-regulating the expression of genes involved in TCA cycle, glucose metabolism, astaxanthin biosynthesis, and fatty acids metabolism, as well as changing the expression of genes involved in ROS scavenging and cell wall biosynthesis. These findings provide new insights into the mechanism of TSC-induced astaxanthin biosynthesis in H. pluvialis.
Some organic carbons were able to further promote astaxanthin accumulation in Haematococcus pluvialis under stress conditions. In this study, we demonstrate that adding 0.6 mM trisodium citrate (TSC) into the culture media increased astaxanthin content in the single cell by 2.4 folds and increased astaxanthin yield by 11.9% in H. pluvialis at day 7 under high light stress. In addition, the ROS level, which was highly associated with astaxanthin accumulation, was also increased by TSC. Subsequent comparative transcriptomic analysis revealed the mechanism underlying the promoting effect of trisodium citrate on astaxanthin accumulation. TSC treatment up-regulated significantly the expression of many enzyme encoding genes involved in TCA cycle, glucose metabolism, astaxanthin biosynthesis and fatty acids metabolism. In addition, trisodium citrate treatment significantly changed the expression of genes involved in ROS scavenging and cell wall biosynthesis. Our results indicated that TSC can not only be used as a carbon source but also further increase the ROS level in H. pluvialis under high light stress. Collectively, this study provides a new method that can increase astaxanthin yield, but also insights into the mechanism of trisodium citrate-induced astaxanthin biosynthesis in H. pluvialis under high light.

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