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. 1998 Aug;64(8):2844–2852. doi: 10.1128/aem.64.8.2844-2852.1998

TABLE 4.

Kinetic constants for amidase-catalyzed acyl transfer reactions with l-enantiomers, d-enantiomers, and racemic mixtures of several α-substituted amides

Compound Structural formula kcat (s−1) Kmamide (mM) KmNH2OH (mM) pH
l-Methioninamide graphic file with name am08801540t4.jpg 245 5.4 36 8
dl-Methioninamide 180 6.4 75 8
l-Leucinamide 63 1.3 39 8
dl-Leucinamide 24 2.4 187 8
l-Phenylalaninamide 8.1 0.8 19 8
dl-Phenylalaninamide 6.2 1.1 19 8
l-Lactamide 67 33 41 7
dl-Lactamide 426 51 507 7
d-Lactamide 2,504 270 2,923 7
l-Alaninamide 66 12 25 8
d-Alaninamide 3,353 379 1,939 8