4.7 Article

Development of an auto-inducible expression system by nitrogen sources switching based on the nitrogen catabolite repression regulation

Journal

MICROBIAL CELL FACTORIES
Volume 21, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12934-022-01794-5

Keywords

Gene expression system; Auto-inducible; Nitrogen catabolite repression; Aspergillus nidulans

Funding

  1. International S&T Innovation Cooperation Key Project [2017YFE0129600]
  2. National Natural Science Foundation of China [32101014, 21878125]
  3. Natural Sciences Foundation of Jiangsu [BK20200624, BK20210470]
  4. China Postdoctoral Science Foundation [2021M701461]
  5. Priority Academic Program Development of Jiangsu Higher Education Institutions
  6. 111 Project [111-2-06]
  7. Jiangsu Province Collaborative Innovation Center for Advanced Industrial Fermentation Industry Development Program
  8. First-Class Discipline Program of Light Industry Technology and Engineering [LITE2018-04]

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An efficient auto-inducible protein expression system based on nitrogen catabolite regulation was constructed in this study. The system successfully expressed glycosylated and secretory proteins, providing a new option for protein production in laboratory and industrial applications.
Background The construction of protein expression systems is mainly focused on carbon catabolite repression and quorum-sensing systems. However, each of these regulatory modes has an inherent flaw, which is difficult to overcome. Organisms also prioritize using different nitrogen sources, which is called nitrogen catabolite repression. To date, few gene regulatory systems based on nitrogen catabolite repression have been reported. Results In this study, we constructed a nitrogen switching auto-inducible expression system (NSAES) based on nitrogen catabolite regulation and nitrogen utilization in Aspergillus nidulans. The P-niaD promoter that is highly induced by nitrate and inhibition by ammonia was used as the promoter. Glucuronidase was the reporter protein. Glucuronidase expression occurred after ammonium was consumed in an ammonium and nitrate compounding medium, achieving stage auto-switching for cell growth and gene expression. This system maintained a balance between cell growth and protein production to maximize stress products. Expressions of glycosylated and secretory proteins were successfully achieved using this auto-inducible system. Conclusions We described an efficient auto-inducible protein expression system based on nitrogen catabolite regulation. The system could be useful for protein production in the laboratory and industrial applications. Simultaneously, NSAES provides a new auto-inducible expression regulation mode for other filamentous fungi.

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