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Blue-Purple evaluation: Chromoproteins facilitate the identification of BioBrick compatibility. | LitMetric

Blue-Purple evaluation: Chromoproteins facilitate the identification of BioBrick compatibility.

Biotechnol Bioeng

School of Physical Science and Technology, ShanghaiTech University, Shanghai, China.

Published: January 2025

AI Article Synopsis

  • - Synthetic BioBricks enable precise manipulation of genetic information and programming of cellular behavior, but their stability relies on the compatibility of DNA fragments without causing harm to host cells.
  • - The study introduces a new method called BP (Blue/Purple, Ban/Pick) evaluation, which uses chromoproteins to assess BioBrick compatibility efficiently by analyzing the color ratio of E. coli colonies.
  • - Several compatible BioBrick assemblies were identified using this method, indicating its potential to improve the evaluation of BioBricks in biotechnological applications and broaden the use of chromoproteins in synthetic biology.

Article Abstract

Synthetic BioBricks introduce novel capabilities to manipulate genetic information, direct transcription-translation processes, and program cellular behaviors in living organisms. To maintain the stability and functionality of synthetic BioBricks, assembled DNA fragments should be mutually compatible without inducing negative effects such as metabolic burden or cellular toxicity in host cells. However, a simple, rapid, and reliable method to evaluate BioBrick compatibility remains to be developed. In this study, we report BP (Blue/Purple, Ban/Pick) evaluation, a method utilizing chromoproteins to facilitate the identification of BioBrick compatibility in one-pot reactions. By visualizing and quantifying the ratio of blue to purple Escherichia coli (E. coli) colonies on LB-agar plates, we can easily validate the compatibility of desired BioBrick constructions. To demonstrate our design, we characterized BioBrick assemblies with antitoxin-toxin pair ccdA-ccdB, lysis protein E, or heterologous protein sfGFP. Among these, we successfully identified several compatible assemblies. We anticipate that BP evaluation will enhance biotechnological assessments of BioBrick compatibility in vivo and expand the application of chromoproteins in synthetic biology.

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Source
http://dx.doi.org/10.1002/bit.28862DOI Listing

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