Lüthi E, Jasmat N B, Bergquist P L
Department of Cellular and Molecular Biology, University of Auckland, New Zealand.
Appl Microbiol Biotechnol. 1990 Nov;34(2):214-9. doi: 10.1007/BF00166783.
The xynC gene coding for an acetylxylan esterase from the extreme thermophile "Caldocellum saccharolyticum" was overexpressed in Escherichia coli strain RR28 by cloning the gene downstream from the lacZ promoter region of pUC18 (pNZ1447) or downstream from the temperature-inducible lambda pRpL promoters of pJLA602 (pNZ1600). The protein formed high molecular weight aggregates in induced cells of RR28/pNZ1600 but not in RR28/pNZ1447. The enzyme constituted up to 10% of the total cell protein and was located in the cytoplasmic fraction of RR28/pNZ1447. The acetyl esterase was most active at pH 6.0 and 70-75 degrees C with a half-life of 64 h at 70 degrees C and 30 h at 80 degrees C, respectively.
编码来自嗜热菌“嗜糖栖热放线菌”的乙酰木聚糖酯酶的xynC基因,通过将该基因克隆到pUC18(pNZ1447)的lacZ启动子区域下游,或pJLA602(pNZ1600)的温度诱导型λ pRpL启动子下游,在大肠杆菌RR28菌株中实现了过表达。该蛋白在RR28/pNZ1600的诱导细胞中形成高分子量聚集体,但在RR28/pNZ1447中则没有。该酶占总细胞蛋白的比例高达10%,位于RR28/pNZ1447的细胞质部分。该乙酰酯酶在pH 6.0和70 - 75℃时活性最高,在70℃时半衰期为64小时,在80℃时半衰期为30小时。