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. 2008 Nov 14;283(46):31719–31725. doi: 10.1074/jbc.M802169200

FIGURE 1.

FIGURE 1.

The FAS-II pathway. The FAS-II pathway in M. tuberculosis extends the C18+-CoA products of the FAS-I pathway to C54–C56 fatty acids. The β-ketoacyl synthase FabH condenses the C18+ acyl group with malonyl-AcpM to form a β-ketoacyl-AcpM. This is subsequently reduced, dehydrated, and reduced by the actions of the NADPH-dependent β-ketoacyl reductase MabA, a dehydrase, and the NADH-dependent enoyl reductase InhA, respectively. The β-ketoacyl synthases KasA and KasB initiate additional cycles of elongation by catalyzing the condensation of the growing acyl-AcpM and malonyl-AcpM.