von Deimling O H, Gaa A, Simon M M
Abteilung für Chemische Pathologie Universität Freiburg, F.R.G.
Biochem Genet. 1988 Oct;26(9-10):617-29. doi: 10.1007/BF02399606.
This study describes the biochemical characterization, genetic variation, and linkage of a codominantly inherited murine esterase, termed ES-18. The enzyme was identified by isoelectric focusing of supernatants obtained after centrifugation of tissue homogenates and subsequent staining for esterase using either alpha-naphthyl acetate or 4-methylumbelliferyl elaidate as substrate. ES-18 exhibited an organ-specific variation of the intensity pattern of bands as seen in kidney, spleen, and macrophages, respectively. Its activity was highly sensitive to inhibition by 1 mmol.liter-1 p-chloromercuriphenylsulfonate but was resistant to bis-p-nitrophenyl phosphate. Four allozymes could be distinguished in kidney supernatants obtained from the inbred strains C57BL/10Sn (ES-18A), MOLF/Ei (ES-18B), WLL/BrA (ES-18C), and CAST/Ei (ES-18D). The enzyme is shown to be controlled by a structural locus, Es-18, which resides on chromosome 19. The gene order Ly-1 - Got-1 - 4.7 +/- 1.6 - Es-18 is suggested.
本研究描述了一种共显性遗传的小鼠酯酶ES-18的生化特性、遗传变异及连锁关系。该酶通过对组织匀浆离心后获得的上清液进行等电聚焦,并以α-萘乙酸或4-甲基伞形酮基反油酸酯作为底物进行酯酶染色来鉴定。ES-18在肾脏、脾脏和巨噬细胞中分别呈现出条带强度模式的器官特异性差异。其活性对1 mmol·L⁻¹对氯汞苯磺酸盐的抑制高度敏感,但对双对硝基苯基磷酸酯具有抗性。在从近交系C57BL/10Sn(ES-18A)、MOLF/Ei(ES-18B)、WLL/BrA(ES-18C)和CAST/Ei(ES-18D)获得的肾脏上清液中可区分出四种同工酶。该酶由位于19号染色体上的一个结构基因座Es-18控制。推测基因顺序为Ly-1 - Got-1 - 4.7 ± 1.6 - Es-18。