This preliminary program is subject to change.

S-Adenosyl Methionine, Cysteine, Tyrosine, Iron, and Sulfide Stimulate in Vitro [FeFe] Hydrogenase Activation in a Heterologous E. Coli System


Jon M. Kuchenreuther, Chemical Engineering, Stanford University, Stanford, CA
James A. Stapleton, Chemical Engineering, Stanford University, Stanford, CA
James R. Swartz, Chemical Engineering, Stanford University, Stanford, CA

[FeFe] hydrogenases are metalloenzymes involved in the anaerobic metabolism of H2. These proteins are distinguished by an active site cofactor known as the H-cluster. This unique [6Fe–6S] complex contains multiple non-protein moieties and requires at least three maturation enzymes for its assembly; the biosynthetic pathways and direct biochemical precursors for which have yet to be elucidated. In this work, we identify small molecules that cooperatively stimulate post-translational [FeFe] hydrogenase activation, providing the first evidence for in vitro synthesis of the H-cluster cofactor. The system is comprised of purified hydrogenase apoprotein; heterologous HydE, HydF, and HydG maturases; and exogenous substrates. Following anaerobic incubation of the Chlamydomonas reinhardtii HydA1 apohydrogenase with ferrous iron, inorganic sulfide, S-adenosyl methionine, cysteine, tyrosine, and the non-purified maturases, hydrogenase activity increased 5-fold relative to incubations without the exogenous small molecules. Moreover, we have begun investigating post-translational hydrogenase activation using purified maturases to further study the biosynthesis of the H-cluster cofactor from a defined set of small molecules. The in vitro system allows for direct assessment of hydrogenase maturation, establishing a robust means to characterize biosynthesis of the H­-cluster cofactor and its non-protein moieties.

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