Optimized expression and purification for high-activity preparations of algal [FeFe]-hydrogenase

PLoS One. 2012;7(4):e35886. doi: 10.1371/journal.pone.0035886. Epub 2012 Apr 26.

Abstract

Background: Recombinant expression and purification of metallo-enzymes, including hydrogenases, at high-yields is challenging due to complex, and enzyme specific, post-translational maturation processes. Low fidelities of maturation result in preparations containing a significant fraction of inactive, apo-protein that are not suitable for biophysical or crystallographic studies.

Principal findings: We describe the construction, overexpression and high-yield purification of a fusion protein consisting of the algal [2Fe2S]-ferredoxin PetF (Fd) and [FeFe]-hydrogenase HydA1. The maturation of Fd-HydA1 was optimized through improvements in culture conditions and media components used for expression. We also demonstrated that fusion of Fd to the N-terminus of HydA1, in comparison to the C-terminus, led to increased expression levels that were 4-fold higher. Together, these improvements led to enhanced HydA1 activity and improved yield after purification. The strong binding-affinity of Fd for DEAE allowed for two-step purification by ion exchange and StrepTactin affinity chromatography. In addition, the incorporation of a TEV protease site in the Fd-HydA1 linker allowed for the proteolytic removal of Fd after DEAE step, and purification of HydA1 alone by StrepTactin. In combination, this process resulted in HydA1 purification yields of 5 mg L(-1) of culture from E. coli with specific activities of 1000 U (U = 1 µmol hydrogen evolved mg(-1) min(-1)).

Significance: The [FeFe]-hydrogenases are highly efficient enzymes and their catalytic sites provide model structures for synthetic efforts to develop robust hydrogen activation catalysts. In order to characterize their structure-function properties in greater detail, and to use hydrogenases for biotechnological applications, reliable methods for rapid, high-yield expression and purification are required.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Chlamydomonas reinhardtii / enzymology
  • Endopeptidases / metabolism
  • Escherichia coli / metabolism
  • Factor Xa / metabolism
  • Ferredoxins / genetics
  • Ferredoxins / metabolism
  • Hydrogenase / genetics
  • Hydrogenase / isolation & purification
  • Hydrogenase / metabolism*
  • Iron-Sulfur Proteins / genetics
  • Iron-Sulfur Proteins / isolation & purification
  • Iron-Sulfur Proteins / metabolism*
  • Plasmids / genetics
  • Plasmids / metabolism
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / isolation & purification
  • Recombinant Fusion Proteins / metabolism

Substances

  • Ferredoxins
  • Iron-Sulfur Proteins
  • Recombinant Fusion Proteins
  • iron hydrogenase
  • Hydrogenase
  • Endopeptidases
  • TEV protease
  • Factor Xa