To elucidate the mechanism of polymorph-selective crystallization of L
-glutamic acid (L-Glu) crystals by the additives, the effects of vario
us L-amino acids, carboxylic acids, and a di-peptide, gamma-L-glutamyl
-L-glutamic acid (gamma-Glu-Glu) on the growth of the {1 0 1}, {0 1 0}
, and {0 0 1}, three dominant faces of the beta-form of L-Glu crystals
have been investigated experimentally and structurally. gamma-Glu-Glu
and L-phenylalanine (L-Phe) showed nearly the same strong inhibitory
effects on the three faces of the P-form in contrast to their differen
t behavior on the two dominant faces of the alpha-form of L-Glu. These
phenomena were explained in terms of the characteristics of the hydro
gen bonds of each face and it was found that the beta-form has less di
scriminating capacity than the alpha-form for the recognition of the m
olecules. Finally, the cause of the polymorph-selective crystallizatio
n by the additives in the L-Glu is attributed mainly to the difference
in the inhibitory effects of the additives on the two dominant faces
of the alpha-form.