Literature DB >> 35294193

Engineered Production of Strictosidine and Analogues in Yeast.

Joshua Misa1, John M Billingsley1, Kanji Niwa1, Rachel K Yu1, Yi Tang1,2.   

Abstract

Monoterpene indole alkaloids (MIAs) are an expansive class of plant natural products, many of which have been named on the World Health Organization's List of Essential Medicines. Low production from native plant hosts necessitates a more reliable source of these drugs to meet global demand. Here, we report the development of a yeast-based platform for high-titer production of the universal MIA precursor, strictosidine. Our fed-batch platform produces ∼50 mg/L strictosidine, starting from the commodity chemicals geraniol and tryptamine. The microbially produced strictosidine was purified to homogeneity and characterized by NMR. Additionally, our approach enables the production of halogenated strictosidine analogues through the feeding of modified tryptamines. The MIA platform strain enables rapid access to strictosidine for reconstitution and production of downstream MIA natural products.

Entities:  

Keywords:  metabolic engineering; monoterpene indole alkaloids; strictosidine; synthetic biology; yeast

Mesh:

Substances:

Year:  2022        PMID: 35294193      PMCID: PMC9171786          DOI: 10.1021/acssynbio.2c00037

Source DB:  PubMed          Journal:  ACS Synth Biol        ISSN: 2161-5063            Impact factor:   5.249


  49 in total

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Journal:  FEBS Lett       Date:  2001-11-16       Impact factor: 4.124

2.  Evaluation of the Saccharomyces cerevisiae ADH2 promoter for protein synthesis.

Authors:  K Michael Lee; Nancy A DaSilva
Journal:  Yeast       Date:  2005-04-30       Impact factor: 3.239

3.  Strictosidine synthase from Rauvolfia serpentina: analysis of a gene involved in indole alkaloid biosynthesis.

Authors:  D Bracher; T M Kutchan
Journal:  Arch Biochem Biophys       Date:  1992-05-01       Impact factor: 4.013

4.  Engineering the biocatalytic selectivity of iridoid production in Saccharomyces cerevisiae.

Authors:  John M Billingsley; Anthony B DeNicola; Joyann S Barber; Man-Cheng Tang; Joe Horecka; Angela Chu; Neil K Garg; Yi Tang
Journal:  Metab Eng       Date:  2017-09-20       Impact factor: 9.783

5.  Controlling heterologous gene expression in yeast cell factories on different carbon substrates and across the diauxic shift: a comparison of yeast promoter activities.

Authors:  Bingyin Peng; Thomas C Williams; Matthew Henry; Lars K Nielsen; Claudia E Vickers
Journal:  Microb Cell Fact       Date:  2015-06-26       Impact factor: 5.328

6.  Integrating carbon-halogen bond formation into medicinal plant metabolism.

Authors:  Weerawat Runguphan; Xudong Qu; Sarah E O'Connor
Journal:  Nature       Date:  2010-11-03       Impact factor: 49.962

7.  Engineering yeast for high-level production of stilbenoid antioxidants.

Authors:  Mingji Li; Konstantin Schneider; Mette Kristensen; Irina Borodina; Jens Nielsen
Journal:  Sci Rep       Date:  2016-11-11       Impact factor: 4.379

8.  An alternative route to cyclic terpenes by reductive cyclization in iridoid biosynthesis.

Authors:  Fernando Geu-Flores; Nathaniel H Sherden; Vincent Courdavault; Vincent Burlat; Weslee S Glenn; Cen Wu; Ezekiel Nims; Yuehua Cui; Sarah E O'Connor
Journal:  Nature       Date:  2012-11-21       Impact factor: 69.504

9.  Engineering biosynthesis of the anticancer alkaloid noscapine in yeast.

Authors:  Yanran Li; Christina D Smolke
Journal:  Nat Commun       Date:  2016-07-05       Impact factor: 14.919

10.  Biosynthesis of medicinal tropane alkaloids in yeast.

Authors:  Prashanth Srinivasan; Christina D Smolke
Journal:  Nature       Date:  2020-09-02       Impact factor: 49.962

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