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基因拷贝数和伴侣蛋白共表达对毕赤酵母表达重组疏水蛋白 HFBI 生物表面活性剂产量的影响。

Effect of gene copy number and chaperone coexpression on recombinant hydrophobin HFBI biosurfactant production in Pichia pastoris.

机构信息

Department of Biomedical Engineering, University of Virginia, Thornton Hall, Charlottesville, Virginia.

Department of Chemical Engineering, University of Virginia, Charlottesville, Virginia.

出版信息

Biotechnol Bioeng. 2019 Aug;116(8):2029-2040. doi: 10.1002/bit.26982. Epub 2019 Apr 16.

Abstract

Hydrophobins are small highly surface-active fungal proteins with potential as biosurfactants in a wide array of applications. However, practical implementation of hydrophobins at large scale has been hindered by low recombinant yields. In this study, the effects of increasing hydrophobin gene copy number and overexpressing endoplasmic reticulum resident chaperone proteins Kar2p, Pdi1p, and Ero1p were explored as a means to enhance recombinant yields of the class II hydrophobin HFBI in the eukaryotic expression host Pichia pastoris. One-, 2-, and 3-copy-HFBI strains were attained using an in vitro multimer ligation approach, with strains displaying copy number stability following subsequent transformations as measured by quantitative polymerase chain reaction. Increasing HFBI copy number alone had no effect on increasing HFBI secretion, but increasing copy number in concert with chaperone overexpression synergistically increased HFBI secretion. Overexpression of PDI1 or ERO1 caused insignificant changes in HFBI secretion in 1- and 2-copy strains, but a statistically significant HFBI secretion increase in 3-copy strain. KAR2 overexpression consistently resulted in enhanced HFBI secretion in all copy number strains, with 3-copy-HFBI secreting 22±1.6 fold more than the 1-copy-HFBI/no chaperone strain. The highest increase was seen in 3-copy-HFBI/Ero1p overexpressing strain with 30±4.0 fold increase in HFBI secretion over 1-copy-HFBI/no chaperone strain. This corresponded to an expression level of approximately 330 mg/L HFBI in the 5 ml small-scale format used in this study.

摘要

水蛋白是一种具有表面活性的小型真菌蛋白,具有作为生物表面活性剂在广泛应用中的潜力。然而,由于重组产量低,水蛋白在大规模实际应用中受到了阻碍。在这项研究中,通过增加水蛋白基因拷贝数和过表达内质网驻留伴侣蛋白 Kar2p、Pdi1p 和 Ero1p,探索了提高真核表达宿主毕赤酵母中 II 类水蛋白 HFBI 重组产量的方法。通过体外多聚体连接方法获得了 1 拷贝、2 拷贝和 3 拷贝的 HFBI 菌株,通过定量聚合酶链反应测量,这些菌株在随后的转化中显示出拷贝数的稳定性。单独增加 HFBI 拷贝数对增加 HFBI 分泌没有影响,但与伴侣蛋白过表达协同增加 HFBI 分泌。PDI1 或 ERO1 的过表达在 1 拷贝和 2 拷贝菌株中对 HFBI 分泌没有显著影响,但在 3 拷贝菌株中 HFBI 分泌有统计学意义的增加。KAR2 的过表达在所有拷贝数菌株中均导致 HFBI 分泌增强,3 拷贝-HFBI 比 1 拷贝-HFBI/无伴侣蛋白菌株分泌增加 22±1.6 倍。在 3 拷贝-HFBI/Ero1p 过表达菌株中观察到的增加幅度最大,HFBI 分泌增加了 30±4.0 倍,比 1 拷贝-HFBI/无伴侣蛋白菌株增加了 30±4.0 倍。这对应于本研究中小规模 5ml 格式中约 330mg/L HFBI 的表达水平。

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