• DocumentCode
    3322006
  • Title

    Notice of Retraction
    High Cell-Density Fermentation of Recombinant Escherichia coli Expressing PlyCB

  • Author

    Weiqing Chen ; Yang Li ; Mingfeng Shen ; Jiarong Yao

  • Author_Institution
    Coll. of Biol. & Environ. Eng., Zhejiang Shuren Univ., Hangzhou, China
  • fYear
    2011
  • fDate
    10-12 May 2011
  • Firstpage
    1
  • Lastpage
    4
  • Abstract
    Notice of Retraction

    After careful and considered review of the content of this paper by a duly constituted expert committee, this paper has been found to be in violation of IEEE´s Publication Principles.

    We hereby retract the content of this paper. Reasonable effort should be made to remove all past references to this paper.

    The presenting author of this paper has the option to appeal this decision by contacting TPII@ieee.org.

    Lysins are murein hydrolases produced by bacteriophage which can kill bacteria efficiently and specifically. Streptococcus bacteriophage lysin PlyC, constituted by two peptides, PlyCA and PlyCB, can rapidly cleavage pathogenic β hemolytic streptococci in vitro. In order to achieve the objective of high cell-density fermentation and high level expression of the recombinant strain BL21(DE3)/ pET-32a(+)-PlyCB, the fed batch fermentation was carried out in a 5 liter automatic fermentor after flask shaking culture was done to obtain some optimized culture conditions. Results showed that after 12-14 h induction by controlling dissolved oxygen and by pH-stat feeding solution, high cell-density and high protein expression were achieved. Under the established conditions, 42.6 g/ L dry cell weight (DCW) could be obtained, and the expression rate of PlyCB reached 32% of total protein while the final cell density (OD600) achieved 29.0. The study provides a basis for large scale production of this recombinant protein.
  • Keywords
    biochemistry; biological specimen preparation; cellular biophysics; fermentation; macromolecules; microorganisms; molecular configurations; proteins; PlyCA peptide; PlyCB peptide; automatic fermentor; bacteriophage; cell-density fermentation; dissolved oxygen; flask shaking culture; murein hydrolases; pH-stat feeding solution; pathogenic β hemolytic streptococci; protein expression; recombinant escherichia coli; streptococcus bacteriophage lysin PlyC; time 12 h to 14 h; Imaging; Media; Microorganisms; Proteins; Strain; Sugar;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Bioinformatics and Biomedical Engineering, (iCBBE) 2011 5th International Conference on
  • Conference_Location
    Wuhan
  • ISSN
    2151-7614
  • Print_ISBN
    978-1-4244-5088-6
  • Type

    conf

  • DOI
    10.1109/icbbe.2011.5780272
  • Filename
    5780272