アカタラセミア,ヒポカタラセミアマウスの赤血球カタラーゼの均一性およびSDS,LISに対する安定性について

Behavior of hemoglobin in the erythrocytes to the addition of H(2)O(2) in saline was examined to be confirmed the equal distribution of catalase in erythrocyte population from acatalasemic heterozygote mouse (Cs(a)Cs(b)) which showed the half of normal (Cs(a)Cs(a)) catalase activity. When H(2)O(2) was added in the suspension mixed erythrocytes with Cs(a)Cs(a) and acatalasemia (Cs(b)Cs(b)), the color changed immediately from red to brownish red with emitting a little buble of O(2). One population of erythrocyte lacking catalase activity should be caused the methemoglobin formation. In fact, rapid spectrophotometric scanning proved that the wave length of maximum absorbance were 500nm and 630nm. When H(2)O(2) was added in the erythrocyte suspension from Cs(a)Cs(b), the color unchanged, remained red, with emitting bubles of O(2). This result was the same as in the erythrocyte suspension from Cs(a)Cs(a). Data indicated that erythrocyte from heterozygote (Cs(a)Cs(b)) is consist of one population and is not two populations of Cs(a)Cs(a) and Cs(b)Cs(b). The nature of blood catalase by stability to the surfactant (SDS and LIS) was compared among normal (Cs(a)Cs(a)), acatalasemic homozygote and heterozygote (Cs(b)Cs(b) and Cs(a)Cs(b)), and hypocatalasemic homozygote and heterozygote (Cs(c)Cs(c) and Cs(a)Cs(c)) mice. In both respects of SDS and LIS stability, Cs(a)Cs(a) was most stable and two heterozygotes (Cs(a)Cs(b) and Cs(a)Cs(c)) were less stable than Cs(a)Cs(a). Cs(c)Cs(c) and Cs(b)Cs(b), namely Cs(b)Cs(b) were of least stability to SDS and to LIS. It was demonstrated that blood catalase molecule of acatalasemic and hypocatalasemic heterozygote (Cs(a)Cs(b) and Cs(a)Cs(c)) differs from that of both parents (Cs(a)(Cs(a), Cs(b)Cs(b) and Cs(a)Cs(c)). It was concluded that 5 sorts of blood catalase were different each other and consist of a single molecular species and suggested that since catalase was a tetramer, the combination of subunits was different each other.