Protein expression, selective isotopic labeling, and analysis of hyperfine-shifted NMR signals of Anabaena 7120 vegetative [2Fe-2S]ferredoxin

Two alternative T7 RNA promoter/polymerase systems have been employed for the heterologous expression of a plant-type [2Fe-2S]ferredoxin, Anabaena 7120 vegetative ferredoxin, in Escherichia coli at high levels (approximately 20 mg/liter of culture). One system was used when 15N-labeling the ferredoxin uniformly by growing E. coli with 15NH4Cl as the nitrogen source; the other was used in conjunction with auxotrophic host strains to enrich the protein selectively by incorporating 2H-, 13C-, and 15N-labeled amino acids. The labeled ferredoxin samples were studied by 1H, 2H, 13C, and 15N NMR spectroscopy. Results from 1H and 2H NMR studies of samples containing [2H(alpha)]Cys, [2H(beta2,beta3)]Cys, [13C(beta)]Cys, and [15N]Cys have confirmed previous cysteinyl proton resonance assignments (L. Skjeldal, W.M. Westler, B.-H. Oh, A. M. Krezel, H.M., Holden, B.L. Jacobson, I. Rayment, and J.L. Markley (1991) Biochemistry 30, 7363-7368). All four 13C NMR peaks arising from the four cysteinyl beta-carbons and all four 15N NMR peaks from the four cysteinyl nitrogens were resolved in spectra of both the oxidized and reduced ferredoxins. The nitrogen resonance of Cys46, which is located in a unique (Ala-Cys) dipeptide, was assigned by detection of 13C'-15N(i+1) coupling in a ferredoxin sample with incorporated [13C']Ala and [15N]Cys. The nitrogen signal of Cys41 was assigned tentatively on the basis of its chemical shift and T1 relaxation time. The cysteinyl beta-carbon resonances in the reduced state have been assigned to individual residues on the basis of correlations with their (previously assigned) beta-protons. The beta-carbon resonance from Cys46 in the oxidized state has been assigned by its correlation with the corresponding resonance in the reduced state; this was accomplished by following the progressive air oxidation of a protein sample reduced by dithionite in the presence of methyl viologen. The spin-lattice relaxation times of the beta-carbons of the two cysteines coordinated to Fe(III) were similar in the oxidized and reduced states. This suggests that the antiferromagnetic coupling present in the reduced cluster has little influence on the electronic relaxation time of the Fe(III). Studies of the temperature dependence of the 1H, 13C, and 15N signals of the cysteinyl ligands to the [2Fe-2S] cluster show that the slope of the temperature dependence (delta delta/delta T-1) can be different for different atom types within a given residue. For example, in the reduced ferredoxin, although delta delta/delta T-1 is positive for Cys49 1H beta 2 and 1H beta 3, it is negative for Cys49 13C beta. Although delta delta/delta T-1 is negative for protons of cysteines ligated to Fe(II) and positive for protons of cysteines ligated to Fe(III), it is positive for all the cysteinyl nitrogens. Nearly complete assignments for the spin system of Arg42 were derived from NMR studies of three selectively labeled samples: ferredoxin incorporating [U-15N]Arg, [26% U-13C]Arg, and [2H alpha,beta 2,beta 3]Arg. The resonance arising from the backbone amide nitrogen exhibited an unusual chemical shift at 201.6 ppm in the oxidized state but was unresolved in the reduced state. The NMR results indicate that the hydrogen bond observed between the Arg42 backbone nitrogen and a sulfide of the iron-sulfur cluster in the X-ray structure of the oxidized ferredoxin crystal (W. R. Rypsiewski, W. R. Breiter, M. M. Benning, G. Wesenberg, B.-H. Oh, J.L. Markley, I. Rayment, and H. M. Holden (1991) Biochemistry 30, 4126-4131) is present in solution in both the oxidized and reduced forms of the protein. The results show that the noncysteinyl, hyperfine-shifted peak (peak "K") in the spectrum of the reduced ferredoxin does not arise from 1H alpha of Arg42 as previously postulated.