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利用裂殖壶菌和三孢布拉氏霉菌将粗甘油转化为二十二碳六烯酸和β-胡萝卜素的纯馏分。

Valorification of crude glycerol for pure fractions of docosahexaenoic acid and β-carotene production by using Schizochytrium limacinum and Blakeslea trispora.

机构信息

Department of Food Science, Life Science Institute, University of Agricultural Sciences and Veterinary Medicine, Cluj-Napoca, Romania.

CENCIRA Agrofood Research and Innovation Centre, Cluj-Napoca, Romania.

出版信息

Microb Cell Fact. 2018 Jun 16;17(1):97. doi: 10.1186/s12934-018-0945-4.

DOI:10.1186/s12934-018-0945-4
PMID:29908562
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6004094/
Abstract

The goal of this research is the investigation of a way to maximize the production of docosahexaenoic acid (DHA) and β-carotene by optimizing the culture conditions of their sources, microalgae Schizochytrium limacinum and fungus Blakeslea trispora respectively, in a fermentation medium. The influencing factors in the fermentation process for producing DHA and β-carotene have proven to be: the concentration of carbon source (different glycerol crude and pure concentrations) for both of them, and in particular temperature for DHA and pH for β-carotene. Testing the effect of these parameters was determined: biomass, DHA and β-carotene concentration. The highest production by S. limacinum was obtained at 25 °C, while using a quantity of 90 g/L of glycerol (crude or pure) as a carbon source. Temperature was the main factor that influenced the biosynthesis of DHA. The quantification of DHA was made by GC-MS chromatography, followed by a purification process, with the end result of DHA in pure phase. The maximum quantities for β-carotene production were obtained with pH 7 and 60 g/L of crude glycerol. The results highlight the possibility of using crude glycerol as a low-cost substrates for growth of microalgae S. limacinum and of fungus B. trispora in order to obtain the crucial molecules: docosahexaenoic acid and β-carotene.

摘要

本研究的目的是通过优化其来源微藻裂殖壶菌和真菌 Blakeslea trispora 的培养条件,分别在发酵培养基中最大程度地生产二十二碳六烯酸 (DHA) 和 β-胡萝卜素。已证明,在发酵过程中影响 DHA 和 β-胡萝卜素生产的因素有:两种生物的碳源浓度(不同浓度的甘油粗品和纯品),特别是 DHA 的温度和 β-胡萝卜素的 pH 值。测试这些参数的效果为:生物量、DHA 和 β-胡萝卜素浓度。在 25°C 下,使用 90g/L 的甘油(粗品或纯品)作为碳源,裂殖壶菌的产量最高。温度是影响 DHA 生物合成的主要因素。通过 GC-MS 色谱法对 DHA 进行定量,然后进行纯化处理,最终得到纯相的 DHA。在 pH 7 和 60g/L 的粗甘油条件下,β-胡萝卜素的产量最高。这些结果突出了使用粗甘油作为微藻裂殖壶菌和真菌 Blakeslea trispora 生长的低成本基质的可能性,以获得关键分子:二十二碳六烯酸和 β-胡萝卜素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a13f/6004094/fd84f37b2959/12934_2018_945_Fig14_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a13f/6004094/fd84f37b2959/12934_2018_945_Fig14_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a13f/6004094/dedfbe91bc7c/12934_2018_945_Fig1_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a13f/6004094/51bb1c77dca8/12934_2018_945_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a13f/6004094/900f3735d15f/12934_2018_945_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a13f/6004094/5c2991e0d3fa/12934_2018_945_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a13f/6004094/fb5ddd4f1bf5/12934_2018_945_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a13f/6004094/bbf079c0229d/12934_2018_945_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a13f/6004094/da2d98c98c72/12934_2018_945_Fig11_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a13f/6004094/d4d08ac99e17/12934_2018_945_Fig12_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a13f/6004094/13db4ea16d7a/12934_2018_945_Fig13_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a13f/6004094/fd84f37b2959/12934_2018_945_Fig14_HTML.jpg

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