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Overexpression of Fusarium solani lipase in Pichia pastoris and its application in lipid degradation

机译:枯萎病中枯萎镰刀菌脂肪酶的过表达及其在脂质降解中的应用

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ABSTRACT Fusarium solani NAN103 lipase was successfully overexpressed in Pichia pastoris using inducible expression system and constitutive expression system under the control of alcohol oxidase 1 promoter (p AOX1 ) and glyceraldehyde-3-phosphate dehydrogenase promoter (p GAP ), respectively. Lipase obtained using the constitutive promoter showed the highest activity of 18.8 U/mg in 3????days of cultivation time. Optimal lipase activity was observed at pH 7.0 and 35 ???°C using p -nitrophenyl laurate as the substrate. Lipase activity was enhanced by Mn 2+ , Ba 2+ , Li + , Ca 2+ , Ni 2+ , CHAPS and Triton X-100 but was inhibited by Hg 2+ , Ag + and SDS. The addition of 10% v/v of octanol, p -xylene, hexane and isopropanol increased lipase activity. Cultivation of lipase-expressing P. pastoris under p GAP in synthetic wastewater containing 1% w/v palm oil resulted in degradation of 87% of the oil within 72????h. P. pastoris expressing F. solani lipase from constitutive expression system has the potential to be used as an alternative microorganism for lipid degradation.
机译:摘要在醇氧化酶1启动子(p AOX1)和甘油醛-3-磷酸脱氢酶启动子(p GAP)的控制下,诱导型表达系统和组成型表达系统分别成功地在啤酒毕赤酵母中成功表达了枯萎镰刀菌NAN103脂肪酶。用组成型启动子获得的脂肪酶在3-6天的培养时间内显示出最高的活性18.8U / mg。以月桂酸对硝基苯酯为底物,在pH 7.0和35℃下观察到最佳的脂肪酶活性。脂肪酶活性被Mn 2+,Ba 2+,Li +,Ca 2+,Ni 2+,CHAPS和Triton X-100增强,但被Hg 2+,Ag +和SDS抑制。加入10%v / v的辛醇,对二甲苯,己烷和异丙醇可提高脂肪酶活性。在含有1%w / v棕榈油的合成废水中,在p GAP下培养表达脂肪酶的巴斯德毕赤酵母会导致72%?h内87%的油脂降解。从组成型表达系统表达茄形毕赤酵母脂肪酶的巴斯德毕赤酵母有潜力用作脂质降解的替代微生物。

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