Aminov R I, Gribanova L K, Kataeva I A, Golovchenko N P, Tsoĭ T V, Akimenko V K
Genetika. 1990 Aug;26(8):1391-8.
The endoglucanase gene of Clostridium thermocellum F7 was cloned in Escherichia coli cells using pKM4 vector. Both the physical mapping and analysis of the gene products in the E. coli mini-cells system suggest cloning of a new cel gene different from those described earlier. The activity of endoglucanase in E. coli cells is localized in the periplasm, which correlates with secretion of enzymes of this type in C. thermicellum. Apart from 2 major components with Mr 42.5 and 43 kDa, corresponding to mature protein forms, we observed the formation of minor products of various electrophoretic motilities. Cloning of the endoglucanase gene on bhr vector pBS954 controlled by its own regulatory signal yielded high level of the endoglucanase activity in the recombinant strains of Klebsiella pneumoniae, Serratia marcescens and Erwinia carotovora comparable with the level of the gene expression in E. coli cells.
利用pKM4载体在大肠杆菌细胞中克隆了嗜热栖热放线菌F7的内切葡聚糖酶基因。在大肠杆菌微细胞系统中对该基因产物进行的物理图谱分析均表明,克隆得到了一个与先前描述的不同的新cel基因。大肠杆菌细胞中内切葡聚糖酶的活性定位于周质,这与嗜热栖热放线菌中此类酶的分泌情况相关。除了对应于成熟蛋白形式的42.5 kDa和43 kDa这两种主要成分外,我们还观察到了具有不同电泳迁移率的次要产物的形成。将内切葡聚糖酶基因克隆到由其自身调控信号控制的bhr载体pBS954上,在肺炎克雷伯菌、粘质沙雷氏菌和胡萝卜软腐欧文氏菌的重组菌株中产生了高水平的内切葡聚糖酶活性,这与该基因在大肠杆菌细胞中的表达水平相当。