Paradis F W, Warren R A, Kilburn D G, Miller R C
Department of Microbiology, University of British Columbia, Vancouver, Canada.
Gene. 1987;61(2):199-206. doi: 10.1016/0378-1119(87)90114-4.
The exoglucanase gene (cex) and the endoglucanase A gene (cenA) from Cellulomonas fimi were subcloned into the Escherichia coli/Brevibacterium lactofermentum shuttle vector pBK10. Both genes were expressed to five to ten times higher levels in B. lactofermentum than in E. coli, probably because these genes were expressed from C. fimi promoters. In B. lactofermentum virtually all of the enzyme activities were in the culture supernatant. This system will facilitate analysis of the expression of the C. fimi genes in and secretion of their products from a Gram-positive bacterium.
来自纤维单胞菌(Cellulomonas fimi)的外切葡聚糖酶基因(cex)和内切葡聚糖酶A基因(cenA)被亚克隆到大肠杆菌/乳酸发酵短杆菌穿梭载体pBK10中。这两个基因在乳酸发酵短杆菌中的表达水平比在大肠杆菌中高五到十倍,这可能是因为这些基因是从纤维单胞菌的启动子表达的。在乳酸发酵短杆菌中,几乎所有的酶活性都存在于培养上清液中。该系统将有助于分析纤维单胞菌基因在革兰氏阳性细菌中的表达及其产物的分泌情况。