4.6 Article

Harnessing Interactional Sensory Genes for Rationally Reprogramming Chaotic Metabolism

Journal

RESEARCH
Volume 2022, Issue -, Pages -

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.34133/research.0017

Keywords

-

Funding

  1. National Key Research and Development Program of China [2018YFA0903600]
  2. National Natural Science Foundation of China [22138007, 31870088, 32170105]

Ask authors/readers for more resources

Rationally controlling cellular metabolism is challenging due to its complex and chaotic nature. In this study, a global metabolic reprogramming platform was developed using sensory proteins and gene interference technology. The platform enables the decoding of gene interactions and has been shown to effectively reduce antibiotic resistance and increase metabolite production in bacteria. A web-based service platform has also been provided for easy implementation of this strategy in various cells.
Rationally controlling cellular metabolism is of great importance but challenging owing to its highly complex and chaotic nature. Natural existing sensory proteins like histidine kinases (HKs) are understood as sensitive nodes of biological networks that can trigger disruptive metabolic reprogramming (MRP) upon perceiving environmental fluctuation. Here, the sensitive node genes were adopted to devise a global MRP platform consisting of a CRISPR interference-mediated dual-gene combinational knockdown toolbox and survivorship-based metabolic interaction decoding algorithm. The platform allows users to decode the interfering effects of nxn gene pairs while only requiring the synthesis of n pairs of primers. A total of 35 HK genes and 24 glycine metabolic genes were selected as the targets to determine the effectiveness of our platform in a Vibrio sp. FA2. The platform was applied to decode the interfering impact of HKs on antibiotic resistance in strain FA2. A pattern of combined knockdown of HK genes (sasA_8 and 04288) was demonstrated to be capable of reducing antibiotic resistance of Vibrio by 108-fold. Patterns of combined knockdown of glycine pathway genes (e.g., gcvT and ltaE) and several HK genes (e.g., cpxA and btsS) were also revealed to increase glycine production. Our platform may enable an efficient and rational approach for global MRP based on the elucidation of high-order gene interactions. A web-based 1-stop service (https://smrp.sjtu.edu.cn) is also provided to simplify the implementation of this smart strategy in a broad range of cells.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available