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Journal article

Escherichia coli Data-Driven Strain Design Using Aggregated Adaptive Laboratory Evolution Mutational Data

From

Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark1

Reconstruction, Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark2

Computational Biology, Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark3

Strain Design Teams, Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark4

University of California at San Diego5

ALE Development & Operation (DTU), Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark6

Software Engineering, Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark7

Data Engineering, Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark8

Analytics, Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark9

Microbes are being engineered for an increasingly large and diverse set of applications. However, the designing of microbial genomes remains challenging due to the general complexity of biological systems. Adaptive Laboratory Evolution (ALE) leverages nature's problem-solving processes to generate optimized genotypes currently inaccessible to rational methods.

The large amount of public ALE data now represents a new opportunity for data-driven strain design. This study describes how novel strain designs, or genome sequences not yet observed in ALE experiments or published designs, can be extracted from aggregated ALE data and demonstrates this by designing, building, and testing three novel Escherichia coli strains with fitnesses comparable to ALE mutants.

These designs were achieved through a meta-analysis of aggregated ALE mutations data (63 Escherichia coli K-12 MG1655 based ALE experiments, described by 93 unique environmental conditions, 357 independent evolutions, and 13 957 observed mutations), which additionally revealed global ALE mutation trends that inform on ALE-derived strain design principles.

Such informative trends anticipate ALE-derived strain designs as largely gene-centric, as opposed to noncoding, and composed of a relatively small number of beneficial variants (approximately 6). These results demonstrate how strain design efforts can be enhanced by the meta-analysis of aggregated ALE data.

Language: English
Publisher: American Chemical Society
Year: 2021
Pages: 3379-3395
ISSN: 21615063
Types: Journal article
DOI: 10.1021/acssynbio.1c00337
ORCIDs: Feist, Adam M , Johnsen, Josefin , Yang, Lei , Kim, Se Hyeuk , Schulz, Sebastian , Ozdemir, Emre , Lennen, Rebecca M and Palsson, Bernhard O

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