Literature DB >> 31915387

A comprehensive guide to dynamic analysis of microbial gene expression using the 3D-printed PFIbox and a fluorescent reporter library.

Shawn French1,2, Amelia Bing Ya Guo1,2, Eric D Brown3,4.   

Abstract

Temporally resolved assays of bacterial gene expression using printed fluorescence imaging boxes (PFIboxes) are non-destructive, inexpensive and simple to prepare. Herein, we describe a full experimental pipeline wherein PFIbox parts are modified and 3D printed, electronics assembled and used to study transcriptional responses of Escherichia coli to chemical stressors. A chemical probe is added to agar growth medium, and a promoter-fluorophore fusion library is arrayed in high density on the agar slab. With high temporal resolution, the reporter library is imaged in PFIboxes, then quantified using promoter activity as a measure of gene expression. PFIboxes have advantages over conventional transcriptomic approaches such as RNA-seq, as the non-destructive nature permits a high-resolution temporal dimension in the data. This results in rapid measurement of transcriptional responses to chemical or physical stimuli. Each time-course gene expression assay costs about US$2 to run, in triplicate, using this method. Printing time depends on printer and settings, but once printed, PFIboxes can be fully assembled, programmed and loaded with samples in less than 1 h. Experimental durations and sampling frequency are set according to user need, but can be run in the duration of a microbial growth curve.

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Year:  2020        PMID: 31915387     DOI: 10.1038/s41596-019-0257-0

Source DB:  PubMed          Journal:  Nat Protoc        ISSN: 1750-2799            Impact factor:   13.491


  1 in total

1.  High-resolution analysis of the pneumococcal transcriptome under a wide range of infection-relevant conditions.

Authors:  Rieza Aprianto; Jelle Slager; Siger Holsappel; Jan-Willem Veening
Journal:  Nucleic Acids Res       Date:  2018-11-02       Impact factor: 16.971

  1 in total

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