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Cell-Free Expression System Derived from a Near-Minimal Synthetic Bacterium.


ABSTRACT: Cell-free expression (CFE) systems are fundamental to reconstituting metabolic pathways in vitro toward the construction of a synthetic cell. Although an Escherichia coli-based CFE system is well-established, simpler model organisms are necessary to understand the principles behind life-like behavior. Here, we report the successful creation of a CFE system derived from JCVI-syn3A (Syn3A), the minimal synthetic bacterium. Previously, high ribonuclease activity in Syn3A lysates impeded the establishment of functional CFE systems. Now, we describe how an unusual cell lysis method (nitrogen decompression) yielded Syn3A lysates with reduced ribonuclease activity that supported in vitro expression. To improve the protein yields in the Syn3A CFE system, we optimized the Syn3A CFE reaction mixture using an active machine learning tool. The optimized reaction mixture improved the CFE 3.2-fold compared to the preoptimized condition. This is the first report of a functional CFE system derived from a minimal synthetic bacterium, enabling further advances in bottom-up synthetic biology.

SUBMITTER: Sakai A 

PROVIDER: S-EPMC10278164 | biostudies-literature | 2023 Jun

REPOSITORIES: biostudies-literature

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Cell-Free Expression System Derived from a Near-Minimal Synthetic Bacterium.

Sakai Andrei A   Jonker Aafke J AJ   Nelissen Frank H T FHT   Kalb Evan M EM   van Sluijs Bob B   Heus Hans A HA   Adamala Katarzyna P KP   Glass John I JI   Huck Wilhelm T S WTS  

ACS synthetic biology 20230606 6


Cell-free expression (CFE) systems are fundamental to reconstituting metabolic pathways <i>in vitro</i> toward the construction of a synthetic cell. Although an <i>Escherichia coli</i>-based CFE system is well-established, simpler model organisms are necessary to understand the principles behind life-like behavior. Here, we report the successful creation of a CFE system derived from JCVI-syn3A (Syn3A), the minimal synthetic bacterium. Previously, high ribonuclease activity in Syn3A lysates imped  ...[more]

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