Gutschmidt S, Lange U, Riecken E O
Histochemistry. 1980;69(2):189-202. doi: 10.1007/BF00533136.
A quantitative histochemical method to determine the apparent Km and Vmax values of rat intestinal unspecific alkaline phosphatase at different sites of the villi is described. Naphthol-As-Bi-phosphate (0.025-1.5 mM) is employed as substrate and Fast Blue B as coupling reagent, and the resulting azo-dye in the brush border membrane has an absorbance maximum at lambda 550 nm. The ratio between the absorbance at lambda 550 and lambda 500 nm is constant as calculated from automatically recorded spectra at different intense dye deposits. Its absorbance is a linear function of incubation time up to 3 min and thickness of the slices up to 10 micrometers both with medium (0.5 mM) and high (1.5 mM) substrate concentrations. Using the histochemical assay under comparable conditions in test tube experiments with homogenates of intestinal mucosa an app. Km of 0.26 +/- 0.081 mM (weighted regression analysis) and 0.28-0.084 mM (direct linear plotting) is determined, demonstrating an affinity to the histochemical substrate, which is about 10 times higher than for p-Nitro-phenyl-phosphate with the purified enzyme. The results obtained by scanning the total dye deposits along jejunal villi show considerable differences in enzymatic activity between single villi and an increase from the villus base up to the transition between medium and apical villus third. As well in the apical region as at the villus base saturation curves are obtained by determining the relationship between the absorbance and the substrate concentration under standard conditions (slice thickness 10 micrometers, incubation time 3 min, 37 degrees C, pH 8.3). Calculated by weighted regression analysis and direct linear plotting from the absorbance data of six female rats the medium app. kinetic data +/- SD from the jejunal villi read as follows. Apical: Km = 0.81 +/- 0.43 mM, Vmax = 3.99 +/- 1.217 absorbance units (A) and Km = 0.87 +/- 0.428 mM, Vmax = 4.02 +/- 1.191 A, respectively. Basal: Km = 0.82 +/- 0.261 mM, Vmax = 3.26 +/- 0.719 A and Km = 0.77 +/- 0.184 mM, Vmax = 3.04 +/- 0.518 AU, respectively. As demonstrated by factorial analysis of variance only Vmax is influenced by the villus position.
本文描述了一种定量组织化学方法,用于测定大鼠小肠绒毛不同部位非特异性碱性磷酸酶的表观Km值和Vmax值。以萘酚 - As - 二磷酸(0.025 - 1.5 mM)为底物,固蓝B为偶联试剂,刷状缘膜中生成的偶氮染料在550 nm波长处有最大吸光度。根据不同强度染料沉积下自动记录的光谱计算,550 nm和500 nm处的吸光度之比是恒定的。在底物浓度为中等(0.5 mM)和高(1.5 mM)时,其吸光度在孵育时间长达3分钟以及切片厚度达10微米时均为线性函数。在试管实验中,使用肠黏膜匀浆在可比条件下进行组织化学测定,通过加权回归分析测定的表观Km为0.26±0.081 mM,直接线性作图法测定的表观Km为0.28 - 0.084 mM,表明该酶对组织化学底物的亲和力比对纯化酶的对硝基苯磷酸的亲和力高约10倍。沿空肠绒毛扫描总染料沉积获得的结果显示,单个绒毛之间的酶活性存在显著差异,且从绒毛基部到绒毛中部与顶端三分之一交界处酶活性增加。在顶端区域和绒毛基部,通过在标准条件下(切片厚度10微米,孵育时间3分钟,37℃,pH 8.3)测定吸光度与底物浓度之间的关系,均可得到饱和曲线。通过对六只雌性大鼠的吸光度数据进行加权回归分析和直接线性作图计算,空肠绒毛的中等表观动力学数据±标准差如下。顶端:Km = 0.81±0.43 mM,Vmax = 3.99±1.217吸光度单位(A);Km = 0.87±0.428 mM,Vmax = 4.02±1.191 A。基部:Km = 0.82±0.261 mM,Vmax = 3.26±0.719 A;Km = 0.77±0.184 mM,Vmax = 3.04±0.518 AU。方差分析表明,只有Vmax受绒毛位置影响。