The cloned cDNA sequence of rice (Oryza sativa L.Cpslo17) chitinase gene Oschi was cloned, (which was registered in GenBank, the accession number: EU045451) ligated with the expression vector pGEX-4T-1, and transformed into E.coli BL21(DE3). The expression of Oschi was induced by IPTG, and the conditions were optimized. After purification the in vitro activity of Oschi chitinase was analyzed, and the results indicated that it could efficiently degrade chitin.
陈爱葵,俞陆军,樊剑鸣,冯冬茹,王金发. 水稻几丁质酶基因在大肠杆菌中的表达、纯化与活性分析[J]. Chinese Journal of Biotechnology, 2008, 24(2): 188-192
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