Volume 3, Issue 2 pp. 45-54
Review

Facilitate Collaborations among Synthetic Biology, Metabolic Engineering and Machine Learning

Stephen Gang Wu

Stephen Gang Wu

Department of Energy, Environmental and Chemical Engineering (EECE), Washington University in St. Louis, One Brookings, 63130 St. Louis, MO, U.S.

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Kazuyuki Shimizu

Kazuyuki Shimizu

Institute of Advanced Biosciences, Keio University, Mizukami 246-2, Kakuganji, Tsuruoka City 997-0052, Yamagata, Japan.

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Joseph Kuo-Hsiang Tang

Joseph Kuo-Hsiang Tang

The Biodesign Institute, Arizona State University, 1001 S McAllister Ave, Tempe, AZ 85281, U.S.

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Yinjie J. Tang

Corresponding Author

Yinjie J. Tang

Department of Energy, Environmental and Chemical Engineering (EECE), Washington University in St. Louis, One Brookings, 63130 St. Louis, MO, U.S.

Department of Energy, Environmental and Chemical Engineering (EECE), Washington University in St. Louis, One Brookings, 63130 St. Louis, MO, U.S.Search for more papers by this author
First published: 04 March 2016
Citations: 14

Abstract

Metabolic engineering (ME) and synthetic biology (SynBio) are two intersecting fields with different focal points. While SynBio focuses more on genomic aspects to build novel cell devices, ME emphasizes the phenotypic outputs (e.g., production). SynBio has the potential to revolutionize the bio-productions; however, the introduction of synthetic devices/pathways often consumes significant cellular resources and incurs fitness costs. Currently, SynBio applications still lack guidelines in re-allocating cellular carbon and energy fluxes. To resolve this, ME principles may help the SynBio community. First, 13C MFA (metabolic flux analysis) can characterize the burdens of genetic infrastructures and reveal optimal strategies for distributing cellular resources. Second, novel microbial chassis should be explored to employ their unique metabolic features for product synthesis. Third, standardization and classification of bio-production papers will not only improve the communication between ME and SynBio, but also facilitate text mining and machine learning to harness information for rational strain design. Ultimately, the data-driven modeling and 13C MFA will be integral components of the SynBio design-build-test-learn cycle for generating novel microbial cell factories.

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