The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Apr. 04, 2017

Filed:

Nov. 23, 2012
Applicant:

Protein Design Lab, Ltd., Beijing, CN;

Inventor:

Xiaoqing Qiu, Beijing, CN;

Assignee:
Attorney:
Primary Examiner:
Int. Cl.
CPC ...
C12N 15/62 (2006.01); C07K 19/00 (2006.01); C07K 14/00 (2006.01); C12N 15/70 (2006.01); C07K 14/245 (2006.01); C07K 14/31 (2006.01); C12P 21/02 (2006.01); C12N 1/20 (2006.01);
U.S. Cl.
CPC ...
C07K 14/001 (2013.01); C07K 14/245 (2013.01); C07K 14/31 (2013.01); C12N 1/20 (2013.01); C12N 15/62 (2013.01); C12N 15/70 (2013.01); C12P 21/02 (2013.01); C07K 2319/01 (2013.01); C07K 2319/035 (2013.01);
Abstract

Provided are methods for highly expressing recombinant protein of engineering bacteria and the use thereof. The method comprises the following steps: (1) engineering bacteria ofwith pET system are transfected with recombinant mutated plasmid to obtain positive monoclonal colonies; (2) the positive monoclonal colonies are enriched to obtain a seed bacteria solution, and the seed bacteria solution is induced to enrichment and growth in a large amount; and (3) the bacteria supernatant containing the recombinant protein as the expression target is separated, and then the recombinant protein in the bacteria supernatant is extracted and purified. The method is characterized in that the engineering bacteria ofwith pET system areB834 (DE3). The components of the mass enrichment medium and the protein purification steps are also optimized such that a significant improvement in the yield and purity of the protein is achieved and the method is suitable for applying to the large-scale production of recombinant protein expressed by the engineering bacteria of


Find Patent Forward Citations

Loading…