4.6 Article

A Two-Stage Adaptive Laboratory Evolution Strategy to Enhance Docosahexaenoic Acid Synthesis in Oleaginous Thraustochytrid

期刊

FRONTIERS IN NUTRITION
卷 8, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fnut.2021.795491

关键词

adaptive laboratory evolution; thraustochytrid Aurantiochytrium; docosahexaenoic acid; heavy-ion irradiation; lipid accumulation

资金

  1. National Key Research and Development Program [2019YFD0901904]
  2. National Natural Science Foundation of China [42006114, 42106108, 32001053]
  3. Shandong Province Natural Science Foundation [ZR2020QD099]
  4. Key Deployment Project of Centre for Ocean Mega-Research of Science, Chinese Academy of Sciences [COMS2019J07]
  5. Qingdao independent innovation major project [21-1-2-23-hz]
  6. QIBEBT [QIBEBT I201933]
  7. Dalian National Laboratory for Clean Energy (DNL), CAS

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This study employed a two-stage adaptive laboratory evolution (ALE) strategy to enhance the DHA production in Thraustochytrid Aurantiochytrium sp., resulting in the successful obtaining of the end-point strain E-81 with high DHA content. The increased lipid accumulation and DHA content in E-81 strain were attributed to the up-regulated expression of key enzymes involved in lipid accumulation and polyunsaturated fatty acid synthase, respectively.
Thraustochytrid is a promising algal oil resource with the potential to meet the demand for docosahexaenoic acid (DHA). However, oils with high DHA content produced by genetic modified thraustochytrids are not accepted by the food and pharmaceutical industries in many countries. Therefore, in order to obtain non-transgenic strains with high DHA content, a two-stage adaptive laboratory evolution (ALE) strategy was applied to the thraustochytrid Aurantiochytrium sp. Heavy-ion irradiation technique was first used before the ALE to increase the genetic diversity of strains, and then two-step ALE: low temperature based ALE and ACCase inhibitor quizalofop-p-ethyl based ALE were employed in enhancing the DHA production. Using this strategy, the end-point strain E-81 with a DHA content 51% higher than that of the parental strain was obtained. The performance of E-81 strain was further analyzed by component analysis and quantitative real-time PCR. The results showed that the enhanced in lipid content was due to the up-regulated expression of key enzymes in lipid accumulation, while the increase in DHA content was due to the increased transcriptional levels of polyunsaturated fatty acid synthase. This study demonstrated a non-genetic approach to enhance lipid and DHA content in non-model industrial oleaginous strains.

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