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. 2008 Aug 12;105(33):11679–11684. doi: 10.1073/pnas.0803576105

Table 1.

Mobilization of molybdenum from NifQ under conditions of FeMo-co synthesis

Protein Molybdenum, mol
NifQ
    Before incubation (as isolated) 0.36 ± 0.03
    After incubation with NifEN 0.28 ± 0.02
    After incubation with NifH 0.29 ± 0.01
    After incubation with NifEN and NifH 0.11 ± 0.01
    After incubation with NifEN, NifH and apo-NifDK 0.15 ± 0.02
NifEN
    Before incubation (as isolated) 0.24 ± 0.03
    After incubation with NifQ 0.19 ± 0.02
    After incubation with NifQ and NifH 0.45 ± 0.06
NifH
    Before incubation (as isolated) 0.009 ± 0.002
    After incubation with NifQ 0.013 ± 0.001
    After incubation with NifQ and NifEN 0.060 ± 0.010

Purified as-isolated NifQ was incubated with purified (i) NifH, (ii) NifEN, (iii) NifH and NifEN, or (iv) NifH, NifEN and apo-NifDK in reaction mixtures that also contained Mg-ATP, DTH, and homocitrate. No external source of molybdenum was added to the mixtures. NifQ, NifH, and NifEN proteins were reisolated by chromatography after incubation. Molybdenum content was quantified by ICP-OES and is shown in mol of molybdenum per mol of protein (i.e. NifQ monomer, NifH dimer, or NifEN tetramer). Values are the average of at least two independent determinations ± SD.