4.2 Article

Enhancement of a high efficient autoinducible expression system in Bacillus subtilis by promoter engineering

Journal

PROTEIN EXPRESSION AND PURIFICATION
Volume 127, Issue -, Pages 81-87

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.pep.2016.07.008

Keywords

Promoter; Expression system; Autoinducible; Overexpression

Funding

  1. National High Technology Research and Development Program of China (863 Program) [2014AA021304]
  2. Fundamental Research Funds for the Central Universities [JUSRP51411B]
  3. National Natural Science Foundation of China [31400058]
  4. Natural Science Foundation of Jiangsu Province [BK20130139]
  5. Public Project for Key Laboratory of Industrial Biotechnology, Ministry of Education [KLIB-KF201306]
  6. Priority Academic Program Development of Jiangsu Higher Education Institutions
  7. 111 Project [111-2-06]
  8. Jiangsu province Collaborative Innovation Center for Advanced Industrial Fermentation industry development program

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Quorum-sensing related promoter srfA (P-srfA) was used to construct autoinducible expression system for production of recombinant proteins in Bacillus subtilis. PsrfA was prominent in the unique property of inducer-free activity that is closely correlated with cell density. Here, using green fluorescent protein (GFP) as the reporter protein, P-srfA was optimized by shortening its sequences and changing the nucleotides at the conserved regions of 35 15 and 10 regions, obtaining a library of P-srfA derivatives varied in the strength of GFP production. Among all the promoter mutants, the strongest promoter P10 was selected and the strength in GFP expression was 150% higher than that of P-srfA. Heterologous protein of aminopeptidase and nattokinase could be overexpressed by P10, the activities of which were 360% and 50% higher than that of P-srfA, respectively. These results suggested that the enhanced promoter P10 could be used to develop autoinducible expression system for overexpression of heterologous proteins in B. subtilis. (C) 2016 Published by Elsevier Inc.

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