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Cloning and Expression of Aspergillus tamarii FS132 Lipase Gene in Pichia pastoris

机译:毕赤酵母毕赤酵母曲霉FS132脂肪酶基因的克隆与表达

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摘要

A lipase gene (atl) was cloned from Aspergillus tamarii FS132 for the first time. The gene was found to have an open reading frame of 1024 base pairs (bp), and the coding region of the gene contained two introns (51 bp and 52 bp). Multi-alignment analysis of the deduced amino acid sequence indicated high homology between the enzyme and mono-and diacylglycerol lipases from fungi Aspergillus. The recombinant lipase was expressed in Pichia pastoris GS115 cells. The recombinant lipase was found to have a molecular mass of 36.7 kDa, and it exhibited lipase activity of 20 U/mL in culture supernatant when tributyrin was used as the substrate.
机译:第一次从tamarii FS132克隆脂肪酶基因(atl)。发现该基因具有1024个碱基对(bp)的开放阅读框,并且该基因的编码区包含两个内含子(51bp和52bp)。推导的氨基酸序列的多比对分析表明该酶与来自曲霉属真菌的单和二酰基甘油脂肪酶之间具有高度同源性。重组脂肪酶在毕赤酵母GS115细胞中表达。发现重组脂肪酶的分子量为36.7kDa,并且当将三丁酸甘油酯用作底物时,其在培养上清液中表现出20U / mL的脂肪酶活性。

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