open access publication

Article, 2024

Complete biosynthesis of QS-21 in engineered yeast

Nature, ISSN 0028-0836, 1476-4687, Volume 629, 8013, Pages 937-944, 10.1038/s41586-024-07345-9

Contributors

Liu Y. 0000-0001-5614-1951 [1] [2] Zhao X. [1] [2] Gan F. 0000-0003-1670-5251 [1] [2] Chen X. [1] [3] [4] Deng K. 0000-0003-2937-8931 [1] [5] Crowe S.A. 0000-0002-9900-5252 [1] [2] [6] Hudson G.A. [1] [2] Belcher M.S. 0000-0003-2352-6817 [1] [3] [4] Schmidt M. 0000-0002-3363-4777 [1] [4] [7] Astolfi M.C.T. 0000-0001-6995-2497 [1] Kosina S.M. 0000-0003-2885-1248 [4] Pang B. 0000-0001-7110-6732 [1] [2] Shao M. [1] [4] Yin J. 0000-0002-0029-5393 [1] [4] Sirirungruang S. 0000-0002-2624-5124 [1] [3] [4] [8] Iavarone A.T. [2] Reed J. 0000-0001-5780-6134 [9] Martin L.B.B. 0000-0002-6921-7246 [9] El-Demerdash A. 0000-0001-6459-2955 [9] Kikuchi S. 0000-0001-9033-6242 [9] Misra R.C. 0000-0001-9594-3789 [9] Liang X. 0000-0003-0180-8450 [1] [4] Cronce M.J. [1] Chen X. [1] [4] Zhan C. 0000-0001-9504-6439 [1] [4] Kakumanu R. [1] [4] Baidoo E.E.K. [1] [4] Chen Y. [1] [4] Petzold C.J. 0000-0002-8270-5228 [1] [4] Northen T.R. 0000-0001-8404-3259 [1] [4] Osbourn A. 0000-0003-2195-5810 [9] Scheller H.V. 0000-0002-6702-3560 [1] [3] [4] Keasling J.D. 0000-0003-4170-6088 (Corresponding author) [1] [2] [4] [6] [10]

Affiliations

  1. [1] Joint BioEnergy Institute
  2. [NORA names: United States; America, North; OECD];
  3. [2] University of California
  4. [NORA names: United States; America, North; OECD];
  5. [3] Department of Plant and Microbial Biology
  6. [NORA names: United States; America, North; OECD];
  7. [4] Lawrence Berkeley National Laboratory
  8. [NORA names: United States; America, North; OECD];
  9. [5] Sandia National Laboratories
  10. [NORA names: United States; America, North; OECD];

Abstract

QS-21 is a potent vaccine adjuvant and remains the only saponin-based adjuvant that has been clinically approved for use in humans. However, owing to the complex structure of QS-21, its availability is limited. Today, the supply depends on laborious extraction from the Chilean soapbark tree or on low-yielding total chemical synthesis. Here we demonstrate the complete biosynthesis of QS-21 and its precursors, as well as structural derivatives, in engineered yeast strains. The successful biosynthesis in yeast requires fine-tuning of the host’s native pathway fluxes, as well as the functional and balanced expression of 38 heterologous enzymes. The required biosynthetic pathway spans seven enzyme families—a terpene synthase, P450s, nucleotide sugar synthases, glycosyltransferases, a coenzyme A ligase, acyl transferases and polyketide synthases—from six organisms, and mimics in yeast the subcellular compartmentalization of plants from the endoplasmic reticulum membrane to the cytosol. Finally, by taking advantage of the promiscuity of certain pathway enzymes, we produced structural analogues of QS-21 using this biosynthetic platform. This microbial production scheme will allow for the future establishment of a structure–activity relationship, and will thus enable the rational design of potent vaccine adjuvants.

Funders

  • Biological and Environmental Research
  • National Institute of Standards and Technology
  • Biotechnology and Biological Sciences Research Council
  • U.S. Department of Commerce
  • National Institutes of Health
  • Office of Science
  • U.S. Department of Energy

Data Provider: Elsevier