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编码枸杞拟盘多毛孢植酸酶的合成基因在甲基营养型酵母毕赤酵母中的高水平表达。

High level expression of a synthetic gene encoding Peniophora lycii phytase in methylotrophic yeast Pichia pastoris.

作者信息

Xiong Ai-Sheng, Yao Quan-Hong, Peng Ri-He, Zhang Zhen, Xu Fang, Liu Jin-Ge, Han Pei-Lai, Chen Jian-Min

机构信息

Agro-Biotechnology Research Center of Shanghai Academy of Agricultural Sciences, Shanghai Key Laboratory of Agricultural Genetics and Breeding, 2901 Beidi Rd, Shanghai, 201106, PR China.

出版信息

Appl Microbiol Biotechnol. 2006 Oct;72(5):1039-47. doi: 10.1007/s00253-006-0384-8. Epub 2006 Apr 7.

Abstract

Phytase is widespread in nature. It has been used as a cereal feed additive that can enhance the phosphorus and mineral absorption in monogastric animals to reduce the level of phosphorus output in manure. Phytase of Peniophora lycii is a 6'-phytase, which owns high specific activity. To achieve a high expression level of 6'-phytase in Pichia pastoris, the 1,230-bp phytase gene of P. lycii was synthesized and optimized for codon usage, G+C content, as well as mRNA secondary structures. The gene constructs containing wild type or modified phytase gene coding sequences under the control of the highly-inducible alcohol oxidase gene (AOX1) promoter, the synthetic signal peptide (designated MF4I), which is a codon-modified Saccharomyces cerevisiae mating factor alpha-prepro-leader sequence, were used to transform P. pastoris. The P. pastoris strain that expressed the modified phytase gene (phy-pl-sh) with MF4I sequence produced 12.2 g phytase per liter of fluid culture, with the phytase activity of 10,540 U ml(-1). The yield of the modified phytase gene, with bias codon usage and MF4I signal, is 4.4 times higher than that of the wild type gene with MF4I signal and 13.6 times higher than that of the wild type gene with wild type S. cerevisiae signal. The recombinant phytase had one optimum pH (pH 4.5) and an optimum temperature of 50 degrees C. The P. pastoris strain expressed the modified 6-phytase gene, with the MF4I signal peptide showing great potential as a commercial phytase production system.

摘要

植酸酶在自然界中广泛存在。它已被用作谷物饲料添加剂,可提高单胃动物对磷和矿物质的吸收,以降低粪便中磷的排放水平。枸杞拟多孔菌的植酸酶是一种6'-植酸酶,具有较高的比活性。为了在毕赤酵母中实现6'-植酸酶的高表达水平,合成了枸杞拟多孔菌1230 bp的植酸酶基因,并对其密码子使用、G+C含量以及mRNA二级结构进行了优化。含有野生型或修饰的植酸酶基因编码序列的基因构建体,在高度诱导型醇氧化酶基因(AOX1)启动子的控制下,以及合成信号肽(命名为MF4I),它是一种密码子修饰的酿酒酵母交配因子α-前原导序列,用于转化毕赤酵母。表达带有MF4I序列的修饰植酸酶基因(phy-pl-sh)的毕赤酵母菌株,每升液体培养物产生12.2 g植酸酶,植酸酶活性为10540 U ml(-1)。使用偏向密码子和MF4I信号的修饰植酸酶基因的产量,比带有MF4I信号的野生型基因高4.4倍,比带有野生型酿酒酵母信号的野生型基因高13.6倍。重组植酸酶有一个最适pH(pH 4.5)和最适温度50℃。表达带有MF4I信号肽的修饰6-植酸酶基因的毕赤酵母菌株,作为商业植酸酶生产系统具有巨大潜力。

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