Literature DB >> 12514739

Total biosynthesis of hydrocortisone from a simple carbon source in yeast.

Florence Ménard Szczebara1, Cathy Chandelier, Coralie Villeret, Amélie Masurel, Stéphane Bourot, Catherine Duport, Sophie Blanchard, Agnès Groisillier, Eric Testet, Patricia Costaglioli, Gilles Cauet, Eric Degryse, David Balbuena, Jacques Winter, Tilman Achstetter, Roberto Spagnoli, Denis Pompon, Bruno Dumas.   

Abstract

We report on the production of hydrocortisone, the major adrenal glucocorticoid of mammals and an important intermediate of steroidal drug synthesis, from a simple carbon source by recombinant Saccharomyces cerevisiae strains. An artificial and fully self-sufficient biosynthetic pathway involving 13 engineered genes was assembled and expressed in a single yeast strain. Endogenous sterol biosynthesis was rerouted to produce compatible sterols to serve as substrates for the heterologous part of the pathway. Biosynthesis involves eight mammalian proteins (mature forms of CYP11A1, adrenodoxin (ADX), and adrenodoxin reductase (ADR); mitochondrial forms of ADX and CYP11B1; 3beta-HSD, CYP17A1, and CYP21A1). Optimization involved modulating the two mitochondrial systems and disrupting of unwanted side reactions associated with ATF2, GCY1, and YPR1 gene products. Hydrocortisone was the major steroid produced. This work demonstrates the feasibility of transfering a complex biosynthetic pathway from higher eukaryotes into microorganisms.

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Year:  2003        PMID: 12514739     DOI: 10.1038/nbt775

Source DB:  PubMed          Journal:  Nat Biotechnol        ISSN: 1087-0156            Impact factor:   54.908


  63 in total

Review 1.  Enzymatic functionalization of carbon-hydrogen bonds.

Authors:  Jared C Lewis; Pedro S Coelho; Frances H Arnold
Journal:  Chem Soc Rev       Date:  2010-11-15       Impact factor: 54.564

2.  Construction and engineering of large biochemical pathways via DNA assembler.

Authors:  Zengyi Shao; Huimin Zhao
Journal:  Methods Mol Biol       Date:  2013

3.  Metabolic engineering of the phenylpropanoid pathway in Saccharomyces cerevisiae.

Authors:  Hanxiao Jiang; Karl V Wood; John A Morgan
Journal:  Appl Environ Microbiol       Date:  2005-06       Impact factor: 4.792

4.  Identification of a sterol Delta7 reductase gene involved in desmosterol biosynthesis in Mortierella alpina 1S-4.

Authors:  Shuo Zhang; Eiji Sakuradani; Sakayu Shimizu
Journal:  Appl Environ Microbiol       Date:  2007-01-12       Impact factor: 4.792

5.  Production of benzylisoquinoline alkaloids in Saccharomyces cerevisiae.

Authors:  Kristy M Hawkins; Christina D Smolke
Journal:  Nat Chem Biol       Date:  2008-09       Impact factor: 15.040

Review 6.  Microbial cytochromes P450: biodiversity and biotechnology. Where do cytochromes P450 come from, what do they do and what can they do for us?

Authors:  Steven L Kelly; Diane E Kelly
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2013-01-06       Impact factor: 6.237

Review 7.  Applications of genetically-encoded biosensors for the construction and control of biosynthetic pathways.

Authors:  Joshua K Michener; Kate Thodey; Joe C Liang; Christina D Smolke
Journal:  Metab Eng       Date:  2011-09-18       Impact factor: 9.783

Review 8.  Yeast factories for the production of aromatic compounds: from building blocks to plant secondary metabolites.

Authors:  Miguel Suástegui; Zengyi Shao
Journal:  J Ind Microbiol Biotechnol       Date:  2016-08-31       Impact factor: 3.346

9.  Production of amorphadiene in yeast, and its conversion to dihydroartemisinic acid, precursor to the antimalarial agent artemisinin.

Authors:  Patrick J Westfall; Douglas J Pitera; Jacob R Lenihan; Diana Eng; Frank X Woolard; Rika Regentin; Tizita Horning; Hiroko Tsuruta; David J Melis; Andrew Owens; Scott Fickes; Don Diola; Kirsten R Benjamin; Jay D Keasling; Michael D Leavell; Derek J McPhee; Neil S Renninger; Jack D Newman; Chris J Paddon
Journal:  Proc Natl Acad Sci U S A       Date:  2012-01-12       Impact factor: 11.205

10.  A panel of cytochrome P450 BM3 variants to produce drug metabolites and diversify lead compounds.

Authors:  Andrew M Sawayama; Michael M Y Chen; Palaniappan Kulanthaivel; Ming-Shang Kuo; Horst Hemmerle; Frances H Arnold
Journal:  Chemistry       Date:  2009-11-02       Impact factor: 5.236

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