Expression of PPDK from Microbispora rosea subsp. aerata in Escherichia. coli and Its Application in Pyrosequencing
DOI:
CSTR:
Author:
Affiliation:

Clc Number:

Fund Project:

the National Nature Science Foundation of China (No. 30470454) and Central Research Laboratory of Hitachi, Japan.

  • Article
  • |
  • Figures
  • |
  • Metrics
  • |
  • Reference
  • |
  • Related
  • |
  • Cited by
  • |
  • Materials
  • |
  • Comments
    Abstract:

    Pyruvate phosphate dikinase (PPDK; EC 2.7.9.1) is found in certain microorganisms and plants, and catalyzes the conversion of AMP, PPi and phosphoenolpyruvate (PEP) to ATP, Pi and pyruvate. Using the genomic DNA of Microbispora rosea subsp. aerata as the template, a DNA fragment encoding the gene PPDK was amplified by PCR and inserted into the expression vector pET28a(+), yielding pET28a (+)-PPDK. The E. coli BL21 (DE3) was transformed with the pET28a (+)-PPDK. After inducing with IPTG, the E. coli BL21 (DE3) [pET28a (+)-PPDK] expressed recombinant PPDK fused to an N-terminal sequence of 6-His Tag. The molecular weight of PPDK was estimated to be 101 kD by SDS-PAGE. The PPDK was purified by His ? Bind Resin affinity chromatography and ultrafiltration using 10 kD cut-off membrane. The successful application of PPDK in pyrosequencing was also demonstrated.

    Reference
    Related
    Cited by
Get Citation

邹秉杰,陈之遥,周国华. 热玫瑰小双孢菌来源的丙酮酸磷酸双激酶的表达及应用[J]. Chinese Journal of Biotechnology, 2008, 24(4): 679-683

Copy
Share
Article Metrics
  • Abstract:
  • PDF:
  • HTML:
  • Cited by:
History
  • Received:August 04,2007
  • Revised:
  • Adopted:
  • Online:
  • Published:
Article QR Code