The zymotypic variation of rabbit prealbumin esterases is controlled by three autosomal loci, each with two alleles: Est-1 s and Est-1 s, Est-2 v and Est-2 f', Est-3 D and Est-3 d. Est-1 s gives rise to the three S zones possessing the cocainesterase activity, Est-2 v to the three F zones with atrop
Serum esterase genetics in rabbits. I. Phenotypic variation of the prealbumin esterases and classification of atropinesterase and cocainesterase
โ Scribed by L. F. M. Zutphen
- Publisher
- Springer
- Year
- 1974
- Tongue
- English
- Weight
- 833 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0006-2928
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โฆ Synopsis
Rabbit atropinesterase and cocainesterase were studied by starch gel electrophoresis. The enzymes are localized in a region of the gels anodal to the albumins (prealbumin esterases). In this region, three groups of esterase zones ( S, F, and D) can be distinguished. The S and F zones are almost exclusively responsible for the hydrolysis of cocaine and atropine, respectively. There is an interdependence of the S, F, and D zones: the activity of zone D depends on the presence of the three F zones, whereas these F zones are found only in combination with the three S zones, o~-Naphthylacetate as a substrate reveals six different phenotypes; two of these phenotypes are shown to be composed of two subtypes when a supplementary staining procedure is executed. A tropinesterase and cocainesterase are classified as carboxylesterases (E.C. 3.1.1.1.) with a rather wide specificity for both aliphatic and aromatic esters. The ~-naphthol esters are split better than the corresponding fl-naphthol esters. Naphthol esters with an acyl side-chain of three carbon atoms are hydrolyzed optimally by the enzymes.
๐ SIMILAR VOLUMES
Discontinuous starch gel electrophoresis revealed a fourth allele of rabbit pre-albumin serum esterase at locus Est-2. This allele is designated Est-2f and appears to be silent. In addition to the prealbumin serum esterases, another serum esterase system was studied in rabbits. This system is locali
The segregation of rat esterases controlled by loci residing in linkage group V (LGV) has been studied in two backcross series, (LEW/Han ร BN/Han)F1 ร LEW/Han and (LEW/Han x LE/Han)F1 ร LEW/Han. Es-14 (formerly Es-Si) was shown to be closely linked to Es-1. A new esterase locus, Es-15, was described