Iwasaki A, Kishida H, Okanishi M
J Antibiot (Tokyo). 1986 Jul;39(7):985-93. doi: 10.7164/antibiotics.39.985.
The gene for an extracellular xylanase from Streptomyces sp. No. 36a was cloned into Streptomyces lividans TK21 using pIJ702 as a vector plasmid. The smallest DNA fragment encoding the xylanase gene and its possible promotor was determined to be a 1.04 kb Sph I-Sac I fragment by sub-cloning studies. This xylanase gene fragment was transferred into the pSK2 series of plasmids and introduced into Streptomyces kasugaensis G3 protoplasts. The cloned xylanase gene was expressed in both S. lividans TK21 and S. kasugaensis G3, and these clones produced and secreted high yields of xylanase into the culture medium. The xylanase production was not detected when a foreign DNA fragment was inserted into the Bcl I site locating in the xylanase gene fragment.
将来自链霉菌属36a号菌株的一种胞外木聚糖酶基因,以pIJ702作为载体质粒克隆到变铅青链霉菌TK21中。通过亚克隆研究确定,编码木聚糖酶基因及其可能启动子的最小DNA片段是一个1.04 kb的Sph I-Sac I片段。该木聚糖酶基因片段被转移到pSK2系列质粒中,并导入春日链霉菌G3原生质体。克隆的木聚糖酶基因在变铅青链霉菌TK21和春日链霉菌G3中均有表达,并且这些克隆株在培养基中产生并分泌了高产的木聚糖酶。当将一个外源DNA片段插入位于木聚糖酶基因片段中的Bcl I位点时,未检测到木聚糖酶的产生。