ArticleJournal of industrial microbiology & biotechnology2011
Simultaneous production and partitioning of heterologous polyketide and isoprenoid natural products in an Escherichia coli two-phase bioprocess.
Article in Journal of industrial microbiology & biotechnology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed, 15 citations in OpenAlex.
- Whole-Cell Production of Patchouli Oil Sesquiterpenes inACS omega · 2020Article
- Improved Production and In Situ Recovery of Sesquiterpene (+)-Zizaene from Metabolically-EngineeredMolecules (Basel, Switzerland) · 2019Article
- Identification, characterization and molecular adaptation of class I redox systems for the production of hydroxylated diterpenoids.Microbial cell factories · 2016Article
- Identification of reproducible drug-resistance-related dysregulated genes in small-scale cancer cell line experiments.Scientific reports · 2015Article
- Computational identification of gene over-expression targets for metabolic engineering of taxadiene production.Applied microbiology and biotechnology · 2012Article
Corrections and comments
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Authors and funding
4 authors at 1 institution in 2 countries.
Funding
Abstract
Natural products have long served as rich sources of drugs possessing a wide range of pharmacological activities. The discovery and development of natural product drug candidates is often hampered by the inability to efficiently scale and produce a molecule of interest, due to inherent qualities of the native producer. Heterologous biosynthesis in an engineering and process-friendly host emerged as an option to produce complex natural products. Escherichia coli has previously been utilized to produce complex precursors to two popular natural product drugs, erythromycin and paclitaxel. These two molecules represent two of the largest classes of natural products, polyketides and isoprenoids, respectively. In this study, we have developed a platform E. coli strain capable of simultaneous production of both product precursors at titers greater than 15 mg l(-1). The utilization of a two-phase batch bioreactor allowed for very strong in situ separation (having a partitioning coefficient of greater than 5,000), which would facilitate downstream purification processes. The system developed here could also be used in metagenomic studies to screen environmental DNA for natural product discovery and preliminary production experiments.
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Registered trials
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