Metals control activity and expression of the heme biosynthesis enzyme delta-aminolevulinic acid dehydratase in Bradyrhizobium japonicum

The heme biosynthesis enzyme S-aminolevulinic acid dehydratase (AW)) requires magnesium or zinc for activity, depending on the organism, and the heme moiety contains iron. Thus, metals are important for heme formation in at least two different ways, Bradyrhizobium japonicum ALAD(double dagger) is an engineered derivative of wild-type ALAD that requires Zn2+ for activity rather than Mg2+ (S, Chauhan and M. R. O'Brian, J, Biol, Chem. 270:19823-19827, 1995). The pH optimum for ALAD(double dagger) activity was over 3.5 units lower than for that of the wild-type enzyme, and ALAD(double dagger) activity was inhibited by lead and cadmium, as reported for the zinc-containing dehydratases of animals, In addition, ALAD(double dagger) was significantly more thermostable than ALAD; the temperature optima are 50 and 37 degrees C, respectively. These observations strongly suggest that the metal contributes to both catalysis and structure, and this conclusion may be extrapolated to ALADs in general, Although iron did not affect the activity of the preformed protein, enzyme assays and immunoblot analysis demonstrated that the iron concentration in which the cells were grown, had a strong positive effect on ALAD activity and the protein level. RNase protection analysis showed that the transcript quantity of hemB, the gene encoding ALAD, was iron dependent; thus, iron regulates hemB at the mRNA level. Induction of hemB mRNA in response to iron was rapid, suggesting that the factor(s) needed to mediate iron control was present in iron-limited cells and did not need to be synthesized de novo, ALAD protein levels and enzyme activities were similar in cells of the wild type and a heme-defective strain, indicating that control by iron is not an indirect effect of the cellular heme status. We conclude that the heme biosynthetic pathway is coordinated with cellular iron levels and that this control may prevent the accumulation of toxic porphyrin intermediates.