Department of Biochemistry and Microbiology, Cook College, Rutgers University, P. O. Box 231, New Brunswick, New Jersey 08903.
Appl Environ Microbiol. 1990 Nov;56(11):3261-5. doi: 10.1128/aem.56.11.3261-3265.1990.
A double-antibody sandwich enzyme-linked immunosorbent assay was developed for quantifying cellobiohydrolase I (CBH I) in crude preparations of the cellulase complex from Trichoderma reesei. The other enzymes (endoglucanase and beta-glucosidase) in this complex and other ingredients in culture broth did not interfere with this assay. The antibody configuration that resulted in the highest specificity for the assay of CBH I employed a monoclonal antibody to coat wells in polystyrene plates and peroxidase-labeled polyclonal antibody to detect cellobiohydrolase bound to the immobilized monoclonal antibody. Previously, procedures have not been available for the direct assay of CBH I activity in the presence of the other enzymes in the complex, and current indirect procedures are cumbersome and inaccurate. The direct procedure described here is highly specific for CBH I and useful for quantifying this enzyme in the range of 0.1 to 0.8 mug/ml.
建立了一种双抗体夹心酶联免疫吸附测定法,用于定量测定里氏木霉纤维素酶复合体系中粗提的纤维二糖水解酶 I(CBH I)。该复合体系中的其他酶(内切葡聚糖酶和β-葡萄糖苷酶)和培养液中的其他成分不会干扰该测定法。用于 CBH I 测定的抗体构型具有最高的特异性,它采用单克隆抗体包被聚苯乙烯板的孔,并用过氧化物酶标记的多克隆抗体检测与固定化单克隆抗体结合的纤维二糖水解酶。以前,在复合体系中的其他酶存在的情况下,无法直接测定 CBH I 活性,而目前的间接测定方法繁琐且不准确。本文所述的直接测定法对 CBH I 具有高度特异性,可用于定量测定 0.1 至 0.8μg/ml 范围内的这种酶。