Lysine 190 Is the Catalytic Base in MenF, the Menaquinone-Specific Isochorismate Synthase from Escherichia coli:  Implications for an Enzyme Family

S Kolappan, J Zwahlen, R Zhou, JJ Truglio… - Biochemistry, 2007 - ACS Publications
S Kolappan, J Zwahlen, R Zhou, JJ Truglio, PJ Tonge, C Kisker
Biochemistry, 2007ACS Publications
Menaquinone biosynthesis is initiated by the conversion of chorismate to isochorismate, a
reaction that is catalyzed by the menaquinone-specific isochorismate synthase, MenF. The
catalytic mechanism of MenF has been probed using a combination of structural and
biochemical studies, including the 2.5 Å structure of the enzyme, and Lys190 has been
identified as the base that activates water for nucleophilic attack at the chorismate C2
carbon. MenF is a member of a larger family of Mg2+ dependent chorismate binding …
Menaquinone biosynthesis is initiated by the conversion of chorismate to isochorismate, a reaction that is catalyzed by the menaquinone-specific isochorismate synthase, MenF. The catalytic mechanism of MenF has been probed using a combination of structural and biochemical studies, including the 2.5 Å structure of the enzyme, and Lys190 has been identified as the base that activates water for nucleophilic attack at the chorismate C2 carbon. MenF is a member of a larger family of Mg2+ dependent chorismate binding enzymes catalyzing distinct chorismate transformations. The studies reported here extend the mechanism recently proposed for this enzyme family by He et al.:  He, Z., Stigers Lavoie, K. D., Bartlett, P. A., and Toney, M. D. (2004) J. Am. Chem. Soc. 126, 2378−85.
ACS Publications
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