History-Driven Genetic Modification Design Technique Using a Domain-Specific Lexical Model for the Acceleration of DBTL Cycles for Microbial Cell Factories

The development of microbes for conducting bioprocessing via synthetic biology involves design–build–test–learn (DBTL) cycles. To aid the designing step, we developed a computational technique that suggests next genetic modifications on the basis of relatedness to the user’s design history of geneti...

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Veröffentlicht in:ACS synthetic biology 2021-09, Vol.10 (9), p.2308-2317
Hauptverfasser: Nakazawa, Shiori, Imaichi, Osamu, Kogure, Takahisa, Kubota, Takeshi, Toyoda, Koichi, Suda, Masako, Inui, Masayuki, Ito, Kiyoto, Shirai, Tomokazu, Araki, Michihiro
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container_end_page 2317
container_issue 9
container_start_page 2308
container_title ACS synthetic biology
container_volume 10
creator Nakazawa, Shiori
Imaichi, Osamu
Kogure, Takahisa
Kubota, Takeshi
Toyoda, Koichi
Suda, Masako
Inui, Masayuki
Ito, Kiyoto
Shirai, Tomokazu
Araki, Michihiro
description The development of microbes for conducting bioprocessing via synthetic biology involves design–build–test–learn (DBTL) cycles. To aid the designing step, we developed a computational technique that suggests next genetic modifications on the basis of relatedness to the user’s design history of genetic modifications accumulated through former DBTL cycles conducted by the user. This technique, which comprehensively retrieves well-known designs related to the history, involves searching text for previous literature and then mining genes that frequently co-occur in the literature with those modified genes. We further developed a domain-specific lexical model that weights literature that is more related to the domain of metabolic engineering to emphasize genes modified for bioprocessing. Our technique made a suggestion by using a history of creating a Corynebacterium glutamicum strain producing shikimic acid that had 18 genetic modifications. Inspired by the suggestion, eight genes were considered by biologists for further modification, and modifying four of these genes proved experimentally efficient in increasing the production of shikimic acid. These results indicated that our proposed technique successfully utilized the former cycles to suggest relevant designs that biologists considered worth testing. Comprehensive retrieval of well-tested designs will help less-experienced researchers overcome the entry barrier as well as inspire experienced researchers to formulate design concepts that have been overlooked or suspended. This technique will aid DBTL cycles by feeding histories back to the next genetic design, thereby complementing the designing step.
doi_str_mv 10.1021/acssynbio.1c00234
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subjects Corynebacterium glutamicum - genetics
Corynebacterium glutamicum - metabolism
Glucose - metabolism
Metabolic Engineering - methods
Metabolic Networks and Pathways - genetics
Multigene Family
Research Design
Shikimic Acid - metabolism
Synthetic Biology - methods
title History-Driven Genetic Modification Design Technique Using a Domain-Specific Lexical Model for the Acceleration of DBTL Cycles for Microbial Cell Factories
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