A plasmid-based genomic screening system for transcriptional regulators of non-adjacent xenobiotic catabolism genes
Autor: | Xing Huang, Feng Chen, Luyao Lu, Ziyu Xing, Jian He, Minggen Cheng |
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Rok vydání: | 2019 |
Předmět: |
0303 health sciences
Reporter gene Bacteria 030306 microbiology Shotgun sequencing Operon Gene Expression Regulation Bacterial Genomics General Medicine Computational biology Biology Applied Microbiology and Biotechnology Genome Xenobiotics 03 medical and health sciences genomic DNA Plasmid Bacterial Proteins Multiple cloning site Gene Genome Bacterial Plasmids Transcription Factors 030304 developmental biology Biotechnology |
Zdroj: | Applied Microbiology and Biotechnology. 104:1163-1174 |
ISSN: | 1432-0614 0175-7598 |
DOI: | 10.1007/s00253-019-10268-5 |
Popis: | Bacteria play an important role in the catabolism of environmental xenobiotics. The study of transcriptional regulation has greatly enhanced our understanding of the molecular mechanisms associated with these processes. However, genes encoding transcription factors (TFs) for xenobiotic catabolism are usually not located in the immediate vicinity of the catabolic genes that they regulate; therefore, functional identification of these TFs is difficult. Significantly modified from a metagenome screening method substrate-induced gene expression (SIGEX), here we propose a synthetic pSRGFP-18 plasmid-based tool as a TF reporter system. In short, two multiple cloning sites (MCS) were designed; one in front of an egfp reporter gene was constructed for promoter insertion, and the other MCS was used for shotgun cloning of genomic DNA. Based on the regulatory relationship between TFs and the promoter of their associated catabolic genes, this approach allowed us to screen for TF genes using a genome shotgun approach. This system performed well when testing the known operons. Following statistical analysis of known catabolic operons in Escherichia coli and Bacillus subtilis, the suggested region of the target promoter for this system was from - 250 to + 150. Furthermore, to broaden the applicability of this plasmid, a series of pSRGFP-18 and pBBR1-based pSRGFP-X plasmids were constructed, which had broad host ranges and contained different antibiotic markers. This study outlines a powerful tool to enable functional identification of TFs for bacterial xenobiotic catabolism. |
Databáze: | OpenAIRE |
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