𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Codominant autosomal inheritance of polymorphic red cell acid phosphatases of lemurs and some properties of the enzymes

✍ Scribed by George A. Mason; John Buettner-Janusch


Publisher
Springer
Year
1977
Tongue
English
Weight
1023 KB
Volume
15
Category
Article
ISSN
0006-2928

No coin nor oath required. For personal study only.

✦ Synopsis


Red cell acid phosphatase phenotypes of 207 captive animals of the genera Lemur, Hapalemur, and Prophithecus were determined by starch gel electrophoresis and phosphatase-specific staining. In Lemur fulvus, three phenotypes, designated A, B, and AB, were observed. In each of the species L. catta, L. macaco, L. mongoz, and L. variegatus, a single phenotype was observed, In Hapalemur griseus, three phenotypes were found: A,B, and AB. In Propithecus verreauxi, a single phenotype was found. Examination of breeding records in conjunction with the results of the electrophoretic analyses supports the conclusion that the erythrocytic acid phosphatases in this group of nonhuman primates are the products of at least two codominant autosomal alleles. There is a wide range of specific activities of the acid phosphatases as determined by colorimetric assays. The values range from 60.6 micronmoles of p-nitrophenol released per gram of hemoglobin per 30 min in Lemur catta to 429.1 micronmoles in Propithecus verreauxi. The enzymes of L. fulvus and P. vereauxi were purified approximately 400-fold, and Michaelis-Menten constants were determined on the purified preparations. For L. fulvus phenotype A, Km = 0.8 mM; for L. fulvus phenotype B, Km = 0.8 mM; and for P. verreauxi, Km = 0.6 mM; the substrate in each case was p-nitrophenylphosphate.


πŸ“œ SIMILAR VOLUMES


Low voltage isoelectric focusing for the
✍ Dr. Giovanni Destro-Bisol; Dalila Ranalletta πŸ“‚ Article πŸ“… 1988 πŸ› John Wiley and Sons 🌐 English βš– 321 KB

A low voltage isoelectric focusing (IEF) method for typing human red cell acid phosphatase (ACPl) polymorphism is reported. A clear differentiation of the ACPl\*A, ACPl\*B and ACPl\*C allelic products is obtained by minimizing diffusion of the bands during electrophoresis and during enzyme visualiza