An automated Design-Build-Test-Learn pipeline for enhanced microbial production of fine chemicals

Автоматизированный конвейер «Проектирование–Конструирование–Тестирование–Обучение» для повышения эффективности микробного производства тонких химических продуктов
Pablo Carbonell, Adrian J. Jervis, Christopher Robinson, Cunyu Yan, Mark S. Dunstan, Neil Swainston, María Vinaixa, Katherine A. Hollywood, Andrew Currin, Nicholas J. W. Rattray, Sandra Taylor, Reynard Spiess, Rehana Sung, Alan Williams, Donal Fellows, Natalie Stanford, Paul Mulherin, Rosalind Le Feuvre, Perdita E. Barran, Royston Goodacre, Nicholas J. Turner, Carole Goble, George Guo-Qiang Chen, Douglas B. Kell, Jason Micklefield, Rainer Breitling, Eriko Takano, Jean‐Loup Faulon, Nigel S. Scrutton
2018-06-04

(2S)-pinocembrinDesign-Build-Test-Learn pipelineEscherichia colibiosynthetic pathway optimizationmicrobial production
Abstract The microbial production of fine chemicals provides a promising biosustainable manufacturing solution that has led to the successful production of a growing catalog of natural products and high-value chemicals. However, development at industrial levels has been hindered by the large resource investments required. Here we present an integrated Design–Build-Test–Learn (DBTL) pipeline for the discovery and optimization of biosynthetic pathways, which is designed to be compound agnostic and automated throughout. We initially applied the pipeline for the production of the flavonoid (2 S )-pinocembrin in Escherichia coli , to demonstrate rapid iterative DBTL cycling with automation at every stage. In this case, application of two DBTL cycles successfully established a production pathway improved by 500-fold, with competitive titers up to 88 mg L −1 . The further application of the pipeline to optimize an alkaloids pathway demonstrates how it could facilitate the rapid optimization of microbial strains for production of any chemical compound of interest.
1
An integrated Design–Build–Test–Learn pipeline was developed for automated, compound-agnostic discovery and optimization of microbial biosynthetic pathways.
2
Application to an alkaloid pathway demonstrated the pipeline’s potential for rapidly optimizing microbial strains for diverse chemical products.
3
Applied to (2S)-pinocembrin production in Escherichia coli, two DBTL cycles improved the production pathway 500-fold.
4
The optimized pinocembrin-producing strain achieved competitive titers of up to 88 mg L−1.
5
The pipeline enables rapid iterative DBTL cycling with automation across every stage of pathway development.

Automated microbial production systems for fine chemicals, demonstrated using engineered Escherichia coli producing (2S)-pinocembrin and an alkaloid

Automated Design–Build–Test–Learn pathway discovery and optimization, including iterative improvement of production pathways and microbial strain titers

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2018-06-04
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Authors
Pablo Carbonell
Adrian J. Jervis
Christopher Robinson
Cunyu Yan
Mark S. Dunstan
Neil Swainston
María Vinaixa
Katherine A. Hollywood
Andrew Currin
Nicholas J. W. Rattray
Sandra Taylor
Reynard Spiess
Rehana Sung
Alan Williams
Donal Fellows
Natalie Stanford
Paul Mulherin
Rosalind Le Feuvre
Perdita E. Barran
Royston Goodacre
Nicholas J. Turner
Carole Goble
George Guo-Qiang Chen
Douglas B. Kell
Jason Micklefield
Rainer Breitling
Eriko Takano
Jean‐Loup Faulon
Nigel S. Scrutton
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