Michaud P, Belaich A, Courtois B, Courtois J
Laboratoire des Polysaccharides Microbiens et Végétaux, Université de Picardie Jules Verne, IUT d'Amiens, Génie Biologique, Avenue des Facultés, Le Bailly, 80 025 Amiens cedex, France.
Appl Microbiol Biotechnol. 2002 May;58(6):767-71. doi: 10.1007/s00253-002-0953-4. Epub 2002 Mar 19.
The EndS encoding sequence was isolated from Sinorhizobium meliloti M5N1CS DNA. Comparisons between the deduced amino acid sequence of the mature EndS (337 amino acids, molecular mass 36,418 Da, isoelectric point 4.92) and those of published beta-glycanases showed that this enzyme belongs to family 5 of the glycoside hydrolases. The protein was overproduced in Escherichia coli using a T7 expression system. When the purified overexpressed EndS protein was tested on cellulose-type components, the best substrate was CM-cellulose.
EndS编码序列是从苜蓿中华根瘤菌M5N1CS DNA中分离得到的。成熟EndS的推导氨基酸序列(337个氨基酸,分子量36,418 Da,等电点4.92)与已发表的β-聚糖酶的氨基酸序列比较表明,该酶属于糖苷水解酶家族5。使用T7表达系统在大肠杆菌中过量表达该蛋白。当对纯化的过表达EndS蛋白进行纤维素类型成分测试时,最佳底物是羧甲基纤维素。