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Precursor-Directed Combinatorial Biosynthesis of Cinnamoyl, Dihydrocinnamoyl, and Benzoyl Anthranilates in Saccharomyces cerevisiae
- Source :
- PloS one, vol 10, iss 10, PLoS ONE, PLoS ONE, Vol 10, Iss 10, p e0138972 (2015), Eudes, A; Benites, VT; Wang, G; Baidoo, EEK; Lee, TS; Keasling, JD; et al.(2015). Precursor-directed combinatorial biosynthesis of cinnamoyl, dihydrocinnamoyl, and benzoyl anthranilates in saccharomyces cerevisiae. PLoS ONE, 10(10). doi: 10.1371/journal.pone.0138972. UC Berkeley: Retrieved from: http://www.escholarship.org/uc/item/5k82n2c2
- Publication Year :
- 2015
- Publisher :
- eScholarship, University of California, 2015.
-
Abstract
- © 2015 Eudes et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Biological synthesis of pharmaceuticals and biochemicals offers an environmentally friendly alternative to conventional chemical synthesis. These alternative methods require the design of metabolic pathways and the identification of enzymes exhibiting adequate activities. Cinnamoyl, dihydrocinnamoyl, and benzoyl anthranilates are natural metabolites which possess beneficial activities for human health, and the search is expanding for novel derivatives that might have enhanced biological activity. For example, biosynthesis in Dianthus caryophyllus is catalyzed by hydroxycinnamoyl/benzoyl-CoA:anthranilate N-hydroxycinnamoyl/ benzoyltransferase (HCBT), which couples hydroxycinnamoyl-CoAs and benzoyl-CoAs to anthranilate. We recently demonstrated the potential of using yeast (Saccharomyces cerevisiae) for the biological production of a few cinnamoyl anthranilates by heterologous co-expression of 4-coumaroyl:CoA ligase from Arabidopsis thaliana (4CL5) and HCBT. Here we report that, by exploiting the substrate flexibility of both 4CL5 and HCBT, we achieved rapid biosynthesis of more than 160 cinnamoyl, dihydrocinnamoyl, and benzoyl anthranilates in yeast upon feeding with both natural and non-natural cinnamates, dihydrocinnamates, benzoates, and anthranilates. Our results demonstrate the use of enzyme promiscuity in biological synthesis to achieve high chemical diversity within a defined class of molecules. This work also points to the potential for the combinatorial biosynthesis of diverse and valuable cinnamoylated, dihydrocinnamoylated, and benzoylated products by using the versatile biological enzyme 4CL5 along with characterized cinnamoyl- CoA- and benzoyl-CoA-utilizing transferases.
- Subjects :
- Spectrometry, Mass, Electrospray Ionization
General Science & Technology
Saccharomyces cerevisiae
lcsh:Medicine
Chemical synthesis
chemistry.chemical_compound
Biosynthesis
Complementary and Alternative Medicine
Complementary and Integrative Health
Combinatorial Chemistry Techniques
ortho-Aminobenzoates
lcsh:Science
chemistry.chemical_classification
DNA ligase
Multidisciplinary
biology
Spectrometry
organic chemicals
lcsh:R
Electrospray Ionization
Mass
biology.organism_classification
Yeast
Metabolic pathway
Enzyme
chemistry
Biochemistry
Generic Health Relevance
biology.protein
Enzyme promiscuity
lcsh:Q
Research Article
Subjects
Details
- Database :
- OpenAIRE
- Journal :
- PloS one, vol 10, iss 10, PLoS ONE, PLoS ONE, Vol 10, Iss 10, p e0138972 (2015), Eudes, A; Benites, VT; Wang, G; Baidoo, EEK; Lee, TS; Keasling, JD; et al.(2015). Precursor-directed combinatorial biosynthesis of cinnamoyl, dihydrocinnamoyl, and benzoyl anthranilates in saccharomyces cerevisiae. PLoS ONE, 10(10). doi: 10.1371/journal.pone.0138972. UC Berkeley: Retrieved from: http://www.escholarship.org/uc/item/5k82n2c2
- Accession number :
- edsair.doi.dedup.....b0b4c25c5b442eabdf398b2bcb4befe7
- Full Text :
- https://doi.org/10.1371/journal.pone.0138972.