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1.
Nat Methods ; 15(5): 387-393, 2018 05.
Article in English | MEDLINE | ID: mdl-29578536

ABSTRACT

Cells use feedback regulation to ensure robust growth despite fluctuating demands for resources and differing environmental conditions. However, the expression of foreign proteins from engineered constructs is an unnatural burden that cells are not adapted for. Here we combined RNA-seq with an in vivo assay to identify the major transcriptional changes that occur in Escherichia coli when inducible synthetic constructs are expressed. We observed that native promoters related to the heat-shock response activated expression rapidly in response to synthetic expression, regardless of the construct. Using these promoters, we built a dCas9-based feedback-regulation system that automatically adjusts the expression of a synthetic construct in response to burden. Cells equipped with this general-use controller maintained their capacity for native gene expression to ensure robust growth and thus outperformed unregulated cells in terms of protein yield in batch production. This engineered feedback is to our knowledge the first example of a universal, burden-based biomolecular control system and is modular, tunable and portable.


Subject(s)
Escherichia coli/physiology , Gene Expression Regulation, Bacterial/physiology , Synthetic Biology , Escherichia coli/genetics , High-Throughput Nucleotide Sequencing , Plasmids , Promoter Regions, Genetic , Sequence Analysis, RNA , Transcription, Genetic
2.
Nat Commun ; 15(1): 1817, 2024 Feb 28.
Article in English | MEDLINE | ID: mdl-38418817

ABSTRACT

Plants and microbes communicate to collaborate to stop pests, scavenge nutrients, and react to environmental change. Microbiota consisting of thousands of species interact with each other and plants using a large chemical language that is interpreted by complex regulatory networks. In this work, we develop modular interkingdom communication channels, enabling bacteria to convey environmental stimuli to plants. We introduce a "sender device" in Pseudomonas putida and Klebsiella pneumoniae, that produces the small molecule p-coumaroyl-homoserine lactone (pC-HSL) when the output of a sensor or circuit turns on. This molecule triggers a "receiver device" in the plant to activate gene expression. We validate this system in Arabidopsis thaliana and Solanum tuberosum (potato) grown hydroponically and in soil, demonstrating its modularity by swapping bacteria that process different stimuli, including IPTG, aTc and arsenic. Programmable communication channels between bacteria and plants will enable microbial sentinels to transmit information to crops and provide the building blocks for designing artificial consortia.


Subject(s)
Arabidopsis , Microbiota , Pseudomonas putida , Solanum tuberosum , Arabidopsis/genetics , Crops, Agricultural
3.
Methods Mol Biol ; 2229: 313-330, 2021.
Article in English | MEDLINE | ID: mdl-33405229

ABSTRACT

RNA-seq enables the analysis of gene expression profiles across different conditions and organisms. Gene expression burden slows down growth, which results in poor predictability of gene constructs and product yields. Here, we describe how we applied RNA-seq to study the transcriptional profiles of Escherichia coli when burden is elicited during heterologous gene expression. We then present how we selected early responsive promoters from our RNA-seq results to design sensors for gene expression burden. Finally, we describe how we used one of these sensors to develop a burden-driven feedback regulator to improve cellular fitness in engineered E. coli.


Subject(s)
Escherichia coli Proteins/genetics , Escherichia coli/genetics , Gene Expression Profiling/methods , Cell Engineering , Gene Expression Regulation, Bacterial , Sequence Analysis, RNA , Synthetic Biology
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