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Complete biosynthesis of QS-21 in engineered yeast.
Liu, Yuzhong; Zhao, Xixi; Gan, Fei; Chen, Xiaoyue; Deng, Kai; Crowe, Samantha A; Hudson, Graham A; Belcher, Michael S; Schmidt, Matthias; Astolfi, Maria C T; Kosina, Suzanne M; Pang, Bo; Shao, Minglong; Yin, Jing; Sirirungruang, Sasilada; Iavarone, Anthony T; Reed, James; Martin, Laetitia B B; El-Demerdash, Amr; Kikuchi, Shingo; Misra, Rajesh Chandra; Liang, Xiaomeng; Cronce, Michael J; Chen, Xiulai; Zhan, Chunjun; Kakumanu, Ramu; Baidoo, Edward E K; Chen, Yan; Petzold, Christopher J; Northen, Trent R; Osbourn, Anne; Scheller, Henrik; Keasling, Jay D.
Afiliação
  • Liu Y; California Institute of Quantitative Biosciences (QB3), University of California, Berkeley, Berkeley, CA, USA.
  • Zhao X; Joint BioEnergy Institute, Emeryville, CA, USA.
  • Gan F; California Institute of Quantitative Biosciences (QB3), University of California, Berkeley, Berkeley, CA, USA.
  • Chen X; Joint BioEnergy Institute, Emeryville, CA, USA.
  • Deng K; California Institute of Quantitative Biosciences (QB3), University of California, Berkeley, Berkeley, CA, USA.
  • Crowe SA; Joint BioEnergy Institute, Emeryville, CA, USA.
  • Hudson GA; Joint BioEnergy Institute, Emeryville, CA, USA.
  • Belcher MS; Department of Plant and Microbial Biology, University of California, Berkeley, Berkeley, CA, USA.
  • Schmidt M; Environmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA.
  • Astolfi MCT; Joint BioEnergy Institute, Emeryville, CA, USA.
  • Kosina SM; Department of Biomaterials and Biomanufacturing, Sandia National Laboratories, Livermore, CA, USA.
  • Pang B; California Institute of Quantitative Biosciences (QB3), University of California, Berkeley, Berkeley, CA, USA.
  • Shao M; Joint BioEnergy Institute, Emeryville, CA, USA.
  • Yin J; Department of Chemical and Biomolecular Engineering, University of California, Berkeley, Berkeley, CA, USA.
  • Sirirungruang S; California Institute of Quantitative Biosciences (QB3), University of California, Berkeley, Berkeley, CA, USA.
  • Iavarone AT; Joint BioEnergy Institute, Emeryville, CA, USA.
  • Reed J; Joint BioEnergy Institute, Emeryville, CA, USA.
  • Martin LBB; Department of Plant and Microbial Biology, University of California, Berkeley, Berkeley, CA, USA.
  • El-Demerdash A; Environmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA.
  • Kikuchi S; Joint BioEnergy Institute, Emeryville, CA, USA.
  • Misra RC; Division of Biological Systems and Engineering, Lawrence Berkeley National Laboratory, Berkeley, CA, USA.
  • Liang X; Institute of Applied Microbiology, Aachen Biology and Biotechnology, RWTH Aachen University, Aachen, Germany.
  • Cronce MJ; Joint BioEnergy Institute, Emeryville, CA, USA.
  • Chen X; Department of Bioengineering, University of California, Berkeley, Berkeley, CA, USA.
  • Zhan C; Environmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA.
  • Kakumanu R; California Institute of Quantitative Biosciences (QB3), University of California, Berkeley, Berkeley, CA, USA.
  • Baidoo EEK; Joint BioEnergy Institute, Emeryville, CA, USA.
  • Chen Y; Joint BioEnergy Institute, Emeryville, CA, USA.
  • Petzold CJ; Division of Biological Systems and Engineering, Lawrence Berkeley National Laboratory, Berkeley, CA, USA.
  • Northen TR; Joint BioEnergy Institute, Emeryville, CA, USA.
  • Osbourn A; Division of Biological Systems and Engineering, Lawrence Berkeley National Laboratory, Berkeley, CA, USA.
  • Scheller H; Joint BioEnergy Institute, Emeryville, CA, USA.
  • Keasling JD; Department of Plant and Microbial Biology, University of California, Berkeley, Berkeley, CA, USA.
Nature ; 629(8013): 937-944, 2024 May.
Article em En | MEDLINE | ID: mdl-38720067
ABSTRACT
QS-21 is a potent vaccine adjuvant and remains the only saponin-based adjuvant that has been clinically approved for use in humans1,2. 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 synthesis3,4. 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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Saccharomyces cerevisiae / Saponinas / Adjuvantes Imunológicos / Engenharia Metabólica Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Saccharomyces cerevisiae / Saponinas / Adjuvantes Imunológicos / Engenharia Metabólica Idioma: En Ano de publicação: 2024 Tipo de documento: Article