Soluble methane monooxygenase (sMMO) from methane-oxidizing bacteria is a multicomponent nonheme oxygenase that naturally oxidizes methane to methanol and can also cooxidize a wide range of adventitious substrates, including mono-and diaromatic hydrocarbons. Leucine 110, at the mouth of the active site in the ␣ subunit of the hydroxylase component of sMMO, has been suggested to act as a gate to control the access of substrates to the active site. Previous crystallography of the wild-type sMMO has indicated at least two conformations of the enzyme that have the "leucine gate" open to different extents, and mutagenesis of homologous enzymes has indicated a role for this residue in the control of substrate range and regioselectivity with aromatic substrates. By further refinement of the system for homologous expression of sMMO that we developed previously, we have been able to prepare a range of site-directed mutations at position 110 in the ␣ subunit of sMMO. All the mutants (with Gly, Cys, Arg, and Tyr, respectively, at this position) showed relaxations of regioselectivity compared to the wild type with monoaromatic substrates and biphenyl, including the appearance of new products arising from hydroxylation at the 2-and 3-positions on the benzene ring. Mutants with the larger Arg and Trp residues at position 110 also showed shifts in regioselectivity during naphthalene hydroxylation from the 2-to the 1-position. No evidence that mutagenesis of Leu 110 could allow very large substrates to enter the active site was found, however, since the mutants (like the wild type) were inactive toward the triaromatic hydrocarbons anthracene and phenanthrene. Thus, our results indicate that the "leucine gate" in sMMO is more important in controlling the precision of regioselectivity than the sizes of substrates that can enter the active site.Soluble methane monooxygenase (sMMO) is one of two enzyme systems via which methane-oxidizing bacteria catalyze the oxygenation of methane to methanol, which is the particularly challenging first step in the metabolism of the kinetically unreactive methane molecule (28). sMMO is a multicomponent enzyme encoded by the six-gene operon mmoXYBZDC, in which the active binuclear iron center (8,45) that is the site of methane oxidation resides within the ␣ subunit of the hydroxylase component, encoded by mmoX (5). It may be because methane is a small and unfunctionalized substrate that the hydrophobic pocket on the hydroxylase component of sMMO that has evolved to bind methane is also able to accommodate a very wide range of hydrocarbons and other molecules. Indeed, sMMO, whose known substrates number over 100, range in size from methane to naphthalene (2) and biphenyl (23), and also include carbon monoxide and ammonia (37), must surely be among the most catalytically versatile of all known enzymes.The unusual catalytic versatility of sMMO has led to interest in its potential as a biocatalyst for bioremediation and synthetic chemistry as well as an interest in how the structure of the enzyme facil...