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氧化还原伙伴的共表达提高了在表达CYP11B1的裂殖酵母粟酒裂殖酵母中氢化可的松(皮质醇)的生产效率。

Coexpression of redox partners increases the hydrocortisone (cortisol) production efficiency in CYP11B1 expressing fission yeast Schizosaccharomyces pombe.

作者信息

Hakki Tarek, Zearo Silvia, Drăgan Călin-Aurel, Bureik Matthias, Bernhardt Rita

机构信息

Institute of Biochemistry, P.O. Box 151150, Saarland University, D-66041 Saarbrücken, Germany.

出版信息

J Biotechnol. 2008 Feb 1;133(3):351-9. doi: 10.1016/j.jbiotec.2007.06.022. Epub 2007 Jul 14.

Abstract

Cytochromes P450 play a vital role in the steroid biosynthesis pathway of the adrenal gland. An example of an essential P450 cytochrome is the steroid 11beta-hydroxylase CYP11B1, which catalyses the conversion of 11-deoxycorticol to hydrocortisone. However, despite its high biotechnological potential, this enzyme has so far been unsuccessfully employed in present-day biotechnology due to a poor expression yield and inherent protein instability. In this study, CYP11B1 was biotransformed into various strains of the yeast Schizosaccharomyces pombe, all of which also expressed the electron transfer proteins adrenodoxin and/or adrenodoxin reductase - central components of the mitochondrial P450 system - in order to maximise hydrocortisone production efficiency in our proposed model system. Site-directed mutagenesis of CYP11B1 at positions 52 and 78 was performed in order to evaluate the impact of altering the amino acids at these sites. It was found that the presence of an isoleucine at position 78 conferred the highest 11beta-hydroxylation activity of CYP11B1. Coexpression of adrenodoxin and adrenodoxin reductase appeared to further increase the 11beta-hydroxylase activity of the enzyme (3.4 fold). Adrenodoxin mutants which were found to significantly enhance enzyme efficiency in other cytochromes in previous studies were also tested in our system. It was found that, in this case, the wild type adrenodoxin was more efficient. The new fission yeast strain TH75 coexpressing the wild type Adx and AdR displays high hydrocortisone production efficiency at an average of 1mM hydrocortisone over a period of 72h, the highest value published to date for this biotransformation. Finally, our research shows that pTH2 is an ideal plasmid for the coexpression of the mitochondrial electron transfer counterparts, adrenodoxin and adrenodoxin reductase, in Schizosaccharomyces pombe, and so could serve as a convenient tool for future biotechnological applications.

摘要

细胞色素P450在肾上腺的类固醇生物合成途径中起着至关重要的作用。一种重要的P450细胞色素是类固醇11β-羟化酶CYP11B1,它催化11-脱氧皮质醇转化为氢化可的松。然而,尽管该酶具有很高的生物技术潜力,但由于其表达产量低和蛋白质固有的不稳定性,迄今为止在现代生物技术中尚未成功应用。在本研究中,CYP11B1被生物转化到裂殖酵母的各种菌株中,所有这些菌株也表达电子传递蛋白肾上腺铁氧还蛋白和/或肾上腺铁氧还蛋白还原酶——线粒体P450系统的核心成分——以便在我们提出的模型系统中最大化氢化可的松的生产效率。对CYP11B1的52位和78位进行定点诱变,以评估改变这些位点氨基酸的影响。结果发现,78位存在异亮氨酸时,CYP11B1的11β-羟化活性最高。肾上腺铁氧还蛋白和肾上腺铁氧还蛋白还原酶的共表达似乎进一步提高了该酶的11β-羟化酶活性(3.4倍)。在我们的系统中还测试了在先前研究中发现能显著提高其他细胞色素酶效率的肾上腺铁氧还蛋白突变体。结果发现,在这种情况下,野生型肾上腺铁氧还蛋白更有效。共表达野生型Adx和AdR的新裂殖酵母菌株TH75在72小时内平均产生1mM氢化可的松,显示出高氢化可的松生产效率,这是该生物转化迄今为止公布的最高值。最后,我们的研究表明,pTH2是在裂殖酵母中共表达线粒体电子传递对应物肾上腺铁氧还蛋白和肾上腺铁氧还蛋白还原酶的理想质粒,因此可作为未来生物技术应用的便捷工具。

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