The final step in the biosynthesis of the plant hormone ethylene is catalyzed by the non-heme iron-containing enzyme 1-aminocyclopropane-1-carboxylic acid (ACC) oxidase (ACCO). ACC is oxidized at the expense of O2 to yield ethylene, HCN, CO2, and two waters. Continuous turnover of ACCO requires the presence of ascorbate and HCO3- (or an alternative form), but the roles played by these reagents, the order of substrate addition, and the mechanism of oxygen activation are controversial. Here these issues are addressed by development of the first functional single turnover system for ACCO. It is shown that 0.35 mol ethylene/mol Fe(II)ACCO is produced when the enzyme is combined with ACC and O2 in the presence of HCO3- but in the absence of ascorbate. Thus, ascorbate is not required for O2 activation or product formation. Little product is observed in the absence of HCO 3-, demonstrating the essential role of this reagent. By monitoring the EPR spectrum of the sample during single turnover, it is shown that the active site Fe(II) oxidizes to Fe(III) during the single turnover. This suggests that the electrons needed for catalysis can be derived from a fraction of the initial Fe(II)ACCO instead of ascorbate. Addition of ascorbate at 10% of its Km value significantly accelerates both iron oxidation and ethylene formation, suggesting a novel high-affinity effector role for this reagent. This role can be partially mimicked by a nonredox-active ascorbate analog. A mechanism is proposed that begins with ACC and O2 binding, iron oxidation, and one-electron reduction to form a peroxy intermediate. Breakdown of this intermediate, perhaps by HCO3--mediated proton transfer, is proposed to yield a high-valent iron species, which is the true oxidizing reagent for the bound ACC.
Bibliographical noteFunding Information:
Acknowledgements This work was supported by NIH Grants GM24689 (to J.D.L.) and GM33162 (to L.Q.). A.M.R. was supported in part by Training Grant GM08277
- 1-Aminocyclopropane-1-carboxylic acid
- Ethylene forming enzyme
- Oxygen activation