4.5 Article

The Effects of Plant Growth Regulators on Cell Growth, Protein, Carotenoid, PUFAs and Lipid Production of Chlorella pyrenoidosa ZF Strain

Journal

ENERGIES
Volume 10, Issue 11, Pages -

Publisher

MDPI
DOI: 10.3390/en10111696

Keywords

Chlorella pyrenoidosa; plant growth regulators; secondary metabolites; gene expression; lipid

Categories

Funding

  1. Key research and development program of Shandong Province [2016GSF121030, 2017GSF21105, 2017CXGC0309]
  2. National Natural Science Foundation of China [31170279, 41106124]
  3. Natural Science Foundation of Shandong province [ZR2011DM006, ZR2011CQ010]
  4. Project of Shandong Province Higher Educational Science and Technology Program [J17KA132]
  5. Supporting Project for Young Teachers in Shandong University of Technology [4072-114021]

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In the present study, eight kinds plant growth regulators-salicylic acid (SA), 1-naphthaleneacetic acid (NAA), gibberellic acid (GA(3)), 6-benzylaminopurine (6-BA), 2, 4-epi-brassinolide (EBR), abscisic acid (ABA), ethephon (ETH), and spermidine (SPD)-were used to investigate the impact on microalgal biomass, lipid, total soluble protein, carotenoids, and polyunsaturated fatty acids (PUFAS) production of Chlorella pyrenoidosa ZF strain. The results showed the quickest biomass enhancement was induced by 50 mg.L-1 NAA, with a 6.3-fold increase over the control; the highest protein content was increased by 0.005 mg.L-1 ETH, which produced 3.5-fold over the control; total carotenoids content was induced most effectively by 1 mg.L-1 NAA with 3.6-fold higher production than the control; the most efficient elicitor for lipid production was 5 mg.L-1 GA(3) at 1.9-fold of the control; 0.2 mg.L-1 ETH induced the abundant production of 1.82 +/- 0.23% linoleic acid; 0.65 +/- 0.01% linolenic acid was induced by 1 mg.L-1 NAA; 2.53 +/- 0.15% arachidonic acid and 0.44 +/- 0.05% docosahexaenoic acid were induced by 5 mg.L-1 GA3. Transcriptional expression levels of seven lipid-related genes, including ACP, BC, FAD, FATA, KAS, MCTK, and SAD, were studied by real-time RT-q-PCR. 5 mg.L-1 GA3 was the most effective regulator for transcriptional expressions of these seven genes, producing 23-fold ACP, 31-fold BC, 25-fold FAD, 6-fold KAS, 12-fold MCTK compared with the controls, respectively.

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