4.7 Article

Enhancing isoprenoid synthesis in Yarrowia lipolytica by expressing the isopentenol utilization pathway and modulating intracellular hydrophobicity

Journal

METABOLIC ENGINEERING
Volume 61, Issue -, Pages 344-351

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ymben.2020.07.010

Keywords

Isopentenol utilization pathway; Prenyl phosphates; Isoprenoid sequestration; Lipid content; Lycopene; Yarrowia lipolytica

Funding

  1. U.S. Department of Energy [DE-SC0008744, DE-EE0007531]
  2. DiSTAP Center of the Singapore-MIT Alliance for Research and Technology (SMART)
  3. National Outstanding Youth Foundation [21822806]
  4. National Natural Science Foundation of China [31670095, 31770097]
  5. Fundamental Research Funds for the Central Universities [JUSRP51701A]
  6. Distinguished Professor Project of Jiangsu Province
  7. China Postdoctoral Science Foundation [2020M671466]
  8. Jiangsu Postdoctoral Research Foundation [2020Z115]
  9. Doctor Candidate Foundation of Jiangnan University of China [JUDCF11019]
  10. Jiangnan University Scholarship Fund
  11. Polish Ministry of Education Mobility Plus Fellowship [1284/MOB/IV/2015/0]

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The abundant supply of biosynthetic precursors and product compatibility with the intracellular environment play important roles for microbial isoprenoid production. In this study, we tailor to both of these requirements by introducing the two-step isopentenol utilization pathway (IUP) to augment the native pathway in the oleaginous yeast Yarrowia lipolytica. With shortcut access to the common isoprenoid precursor, isopentenyl pyrophosphate (IPP) and its isomer dimethylallyl pyrophosphate (DMAPP), IUP is capable of elevating IPP + DMAPP levels by 15.7-fold compared to the mevalonate pathway alone. The increase in IPP + DMAPP levels can directly lead to better isoprenoid synthesis, which is illustrated using lycopene as a model compound. Moreover, we also demonstrate that higher lipid contents in the cells correlate with improved intracellular lycopene production, suggesting the importance of having a substantial hydrophobic environment to sequester isoprenoids. Combining these strategies with further genetic and fermentation optimizations, we achieved a final lycopene titer of 4.2 g/ L. Overall, these strategies hold great potential for strengthening the synthesis of long-chain isoprenoids and fatsoluble natural products in microbes.

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