| Literature DB >> 34133952 |
Fumihiro Ishikawa1, Sho Konno2, Chiharu Uchida3, Takehiro Suzuki4, Katsuki Takashima3, Naoshi Dohmae4, Hideaki Kakeya2, Genzoh Tanabe5.
Abstract
Much of our current knowledge on nonribosomal peptide synthetases (NRPSs) is based on studies in which the full NRPS system or each protein domain is expressed in heterologous hosts. Consequently, methods to detect the endogenous activity of NRPSs, under natural cellular conditions, are needed for the study of NRPS cell biology. Here, we describe the in vivo activity-based protein profiling (ABPP) for endogenous NRPSs and its applications to the study of their activities in bacteria. Remarkably, in vitro and in vivo ABPP in the context of the surfactin producer Bacillus subtilis enabled the visualization, tracking, and imaging of an endogenous SrfAB-NRPS with remarkable selectivity and sensitivity. Furthermore, in vivo, ABPP allowed the discovery of the degradation processes of the endogenous SrfAB-NRPS in the context of its native producer bacteria. Overall, this study deepens our understanding of the properties of NRPSs that cannot be addressed by conventional methods.Entities:
Keywords: activity-based protein profiling; adenylation domain; cellular imaging; in vitro labeling; in vivo labeling; natural product biosynthesis; nonribosomal peptide synthetase; photoaffinity labeling; protein degradation; proteomics
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Year: 2021 PMID: 34133952 DOI: 10.1016/j.chembiol.2021.05.014
Source DB: PubMed Journal: Cell Chem Biol ISSN: 2451-9448 Impact factor: 8.116