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Large quantities of recombinantly overproduced Fe-S cluster-containing proteins are necessary for their in-depth biochemical characterization. Commercially available E. coli strain BL21(DE3) and its derivatives have a mutation that inactivates the function of one of the two native pathways (Suf pathway) responsible for cluster biogenesis. Correction of the mutation, combined with sequence changes that elevate Suf protein levels, can increase yield and cluster occupancy of Fe-S cluster-containing enzymes, facilitating the biochemical analysis of this fascinating group of proteins.
Corless et al. (Mon,) studied this question.