green microalga
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2022 ◽  
Vol 61 ◽  
pp. 102599
Author(s):  
Yu Wang ◽  
Jing Jia ◽  
Qinglei Chi ◽  
Yanhua Li ◽  
Hongxia Wang ◽  
...  

Cells ◽  
2021 ◽  
Vol 10 (12) ◽  
pp. 3571
Author(s):  
Tatiana Yu. Plyusnina ◽  
Sergei S. Khruschev ◽  
Polina V. Fursova ◽  
Alexei E. Solovchenko ◽  
Taras K. Antal ◽  
...  

Using a mathematical simulation approach, we studied the dynamics of the green microalga Chlorella vulgaris phosphate metabolism response to shortage and subsequent replenishing of inorganic phosphate in the medium. A three-pool interaction model was used to describe the phosphate uptake from the medium, its incorporation into the cell organic compounds, its storage in the form of polyphosphates, and culture growth. The model comprises a system of ordinary differential equations. The distribution of phosphorous between cell pools was examined for three different stages of the experiment: growth in phosphate-rich medium, incubation in phosphate-free medium, and phosphate addition to the phosphorus-starving culture. Mathematical modeling offers two possible scenarios for the appearance of the peak of polyphosphates (PolyP). The first scenario explains the accumulation of PolyP by activation of the processes of its synthesis, and the decline in PolyP is due to its redistribution between dividing cells during growth. The second scenario includes a hysteretic mechanism for the regulation of PolyP hydrolysis, depending on the intracellular content of inorganic phosphate. The new model of the dynamics of P pools in the cell allows one to better understand the phenomena taking place during P starvation and re-feeding of the P-starved microalgal cultures with inorganic phosphate such as transient PolyP accumulation. Biotechnological implications of the observed dynamics of the polyphosphate pool of the microalgal cell are considered. An approach enhancing the microalgae-based wastewater treatment method based on these scenarios is proposed.


Author(s):  
Christian Kleinert ◽  
Carola Griehl

AbstractIn situ extraction or “milking” of microalgae is a promising approach to reduce downstream costs in order to produce low-value substances such as lipids from microalgae in an economical way. Due to its ability to secrete high amounts of long-chain hydrocarbons to an extracellular matrix, the green microalga Botryococcus braunii is suitable for the process of in situ extraction as the cost intensive steps of harvesting, dewatering, and cell disruption could be omitted. Based on a previous study investigating various B. braunii strains in terms of growth, lipid accumulation, and solvent compatibility, the B. braunii strains Showa and Bot22 (both B race) were identified as potential candidates for the process of in situ extraction. In order to prove the suitability of these two strains for the process of in situ extraction, this study first determined the optimal extraction time using short-term in situ extraction over 7 days at different starting biomass concentrations of 1.5 and 2.5 g L−1. Furthermore, both strains were treated applying the optimal extraction time in long-term in situ extractions for 30 days to confirm the results from the short-term extractions. The results indicate a strain-dependent optimal extraction time of 300 min day−1 for strain Showa and 200 min day−1 for strain Bot22. During long-term in situ extraction for 30 days, hydrocarbon productivity was 16.99 mg L−1 day−1 (10.53 mg gDW−1 day−1) for strain Showa and 14.53 mg L−1 day−1 (10.48 mg gDW−1 day−1) for strain Bot22. Furthermore, a direct correlation between hydrocarbon productivity achieved by in situ extraction and the hydrocarbon concentration in the biomass of the respective strain could be established. It could be shown that the consideration of the effective extraction time and the phase boundary area is required to calculate an extraction system independent value for the comparison of different extraction setups.


Marine Drugs ◽  
2021 ◽  
Vol 19 (11) ◽  
pp. 648
Author(s):  
Guillaume Tanguy ◽  
Aline Legat ◽  
Olivier Gonçalves ◽  
Luc Marchal ◽  
Benoît Schoefs

Biocompatible extraction emerges recently as a means to reduce costs of biotechnology processing of microalgae. In this frame, this study aimed at determining how specific culture conditions and the associated cell morphology impact the biocompatibility and the extraction yield of β-carotene from the green microalga Dunaliella salina using n-decane. The results highlight the relationship between the cell disruption yield and cell volume, the circularity and the relative abundance of naturally permeabilized cells. The disruption rate increased with both the cell volume and circularity. This was particularly obvious for volume and circularity exceeding 1500 µm3 and 0.7, respectively. The extraction of β-carotene was the most biocompatible with small (600 µm3) and circular cells (0.7) stressed in photobioreactor (30% of carotenoids recovery with 15% cell disruption). The naturally permeabilized cells were disrupted first; the remaining cells seems to follow a gradual permeabilization process: reversibility (up to 20 s) then irreversibility and cell disruption. This opens new carotenoid production schemes based on growing robust β-carotene enriched cells to ensure biocompatible extraction.


Plants ◽  
2021 ◽  
Vol 10 (11) ◽  
pp. 2413
Author(s):  
Biljana Todorović ◽  
Veno Jaša Grujić ◽  
Andreja Urbanek Krajnc ◽  
Roman Kranvogl ◽  
Jana Ambrožič-Dolinšek

Haematococcus pluvialis, a unicellular green microalga that produces a secondary metabolite under stress conditions, bears one of the most potent antioxidants, namely xanthophyll astaxanthin. The aim of our study was to determine the content of astaxanthin and its esterified forms using three different solvents—methyl tert-butyl ether (MTBE), hexane isopropanol (HEX -IPA) and acetone (ACE)—and to identify them by using high performance liquid chromatography coupled with diode array detection and the quadrupole time-of-flight mass spectrometry (HPLC-DAD and LC-QTOF-MS) technique. We identified eleven astaxanthin monoesters, which accounted for 78.8% of the total astaxanthin pool, six astaxanthin diesters (20.5% of total), while free astaxanthin represented the smallest fraction (0.7%). Astaxanthin monoesters (C16:2, C16:1, C16:0), which were the major bioactive compounds in the H. pluvialis samples studied, ranged from 10.2 to 11.8 mg g−1 DW. Astaxanthin diesters (C18:4/C18:3, C18:1/C18:3) were detected in the range between 2.3 and 2.6 mg g−1 DW. All three solvents were found to be effective for extraction, but MTBE and hexane-isopropanol extracted the greatest amount of free bioactive astaxanthin. Furthermore, MTBE extracted more low-chain astaxanthin monoesters (C16), and hexane-isopropanol extracted more long-chain monoesters (C18 and above) and more diesters. We can conclude that MTBE is the solvent of choice for the extraction of monoesters and hexane-isopropanol for diesters.


2021 ◽  
Vol 59 ◽  
pp. 102434
Author(s):  
Ester Mazepa ◽  
Barbara V. Malburg ◽  
Gilda Mógor ◽  
Amanda C. de Oliveira ◽  
Juliana O. Amatussi ◽  
...  

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