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作 者:张慧敏[1] 李剑芳[1] 邬敏辰 魏喜换[1] 杨严俊[1]
机构地区:[1]江南大学食品学院,江苏无锡214122 [2]江南大学医药学院,江苏无锡214122
出 处:《食品与生物技术学报》2013年第2期124-128,共5页Journal of Food Science and Biotechnology
基 金:国家自然科学基金项目(31101229);2011年高校博士研究生科研创新计划项目(JUDCF10056)
摘 要:将一种11家族极端耐热木聚糖酶的密码子优化基因Syxyn11克隆到毕赤酵母表达载体pPIC9K中,得到重组质粒pPIC9K-Syxyn11,将其经SalⅠ线性化后转化毕赤酵母(Pichia pastoris)GS115。经G418筛选得到重组工程菌GS115/Syxyn11,用甲醇诱导表达重组木聚糖酶SyXyn11,酶活可达到17.74 U/mL。SDS-PAGE显示,SyXyn11的相对分子质量为31 000。SyXyn11的最适反应温度为85℃,在80℃以下稳定。最适反应pH为6.5,在pH 5.0~7.5范围内稳定。EDTA和大多数金属离子对重组酶的活性影响不大。结果表明Syxyn11成功在P.pastoris GS115中实现表达,而且重组木聚糖酶的耐热性并未改变。A codon-optimized gene encoding a hyperthermostable xylanase belongs to the glycoside hydrolase family 11 (abbreviated as Syxyn11) has been cloned into the expression plasmid pPIC9K (named pPIC9K-Syxyn11). The pPIC9K-Syxyn11 was linearized with SalⅠ and integrated into the genome of Pichia pastoris GS115 by electroporation. The recombinant P. pastoris GS115/Syxyn11 was screened by G418 and then was induced with methanol to express SyXyn11. The SyXyn11 activity expressed by P. pastoris transformant reached 17.74 U/mL. The molecular weight of SyXyn11 was estimated to be 31 000 by SDS-PAGE. The SyXyn11 displayed the highest activity at 85 ℃and pH 6.5. It was highly stable at a temperature of 80 ℃ or below,and at a pH range of 5.0~ 7.5. Its activity was not significantly affected by most of metal ions tested and EDTA. This revealed that Syxyn11 was successfully expressed in P. pastoris and remained the high thermostability.
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