| Literature DB >> 23692082 |
Anurag P Srivastava1, Masakazu Hirasawa, Megha Bhalla, Jung-Sung Chung, James P Allen, Michael K Johnson, Jatindra N Tripathy, Luis M Rubio, Brian Vaccaro, Sowmya Subramanian, Enrique Flores, Masoud Zabet-Moghaddam, Kyle Stitle, David B Knaff.
Abstract
The roles of four conserved basic amino acids in the reaction catalyzed by the ferredoxin-dependent nitrate reductase from the cyanobacterium Synechococcus sp. PCC 7942 have been investigated using site-directed mutagenesis in combination with measurements of steady-state kinetics, substrate-binding affinities, and spectroscopic properties of the enzyme's two prosthetic groups. Replacement of either Lys58 or Arg70 by glutamine leads to a complete loss of activity, both with the physiological electron donor, reduced ferredoxin, and with a nonphysiological electron donor, reduced methyl viologen. More conservative, charge-maintaining K58R and R70K variants were also completely inactive. Replacement of Lys130 by glutamine produced a variant that retained 26% of the wild-type activity with methyl viologen as the electron donor and 22% of the wild-type activity with ferredoxin as the electron donor, while replacement by arginine produces a variant that retains a significantly higher percentage of the wild-type activity with both electron donors. In contrast, replacement of Arg146 by glutamine had minimal effect on the activity of the enzyme. These results, along with substrate-binding and spectroscopic measurements, are discussed in terms of an in silico structural model for the enzyme.Entities:
Mesh:
Substances:
Year: 2013 PMID: 23692082 PMCID: PMC3741069 DOI: 10.1021/bi400354n
Source DB: PubMed Journal: Biochemistry ISSN: 0006-2960 Impact factor: 3.162