High Expression of Human Cathepsin S by Recombinant Pichia pastoris with Cod Skin as an Organic Co-Nitrogen Source.

IF 1.2 Q2 Biochemistry, Genetics and Molecular Biology Journal of Molecular Microbiology and Biotechnology Pub Date : 2017-01-01 Epub Date: 2018-02-06 DOI:10.1159/000486395
Guiying Y Li, Man Fu, Mei Qin, Liming M Xue
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引用次数: 1

Abstract

Human cathepsin S production by recombinant Pichia pastoris using cod skin as the co-nitrogen source was investigated in this study. The addition of carbon sources of glycerol in the fed-batch phase and of methanol in the induction stage was also investigated. A new approach to the highly expression of human cathepsin S was developed using 90 g/L of cod skin (wet weight). After 24 h of the initial fermentation, 4% glycerol (v/v, glycerol/culture) was added once to enhance the cell density (OD600) in the cultivation. Then, adding and maintaining methanol at 0.5% (v/v, methanol/cultivation) after about 48 h of fermentation achieved a high expression of human cathepsin S in a 5-L bioreactor. The results demonstrate that the maximum activity of human cathepsin S in the fermentation supernatant reached 7,152 U/L after 96 h of methanol induction. The methylotrophic yeast P. pastoris grown in the medium containing cod skin (90 g/L) as the co-nitrogen source provided a 21% higher cell density (OD600) and 18.3% higher human cathepsin S yield than P. pastoris grown in BMGY medium. For the first time, human cathepsin S was successfully expressed by P. pastoris with cod skin as the co-nitrogen source. The glycerol fed-batch controlling strategy and method of maintaining methanol at a constant concentration of 0.5% (v/v, methanol/cultivation) in the induction stage was efficient for P. pastoris growth and the expression of human cathepsin S.

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以鳕鱼皮为有机共氮源的重组毕赤酵母高效表达人组织蛋白酶S。
本研究以鳕鱼皮为共氮源,对重组毕赤酵母生产人组织蛋白酶S进行了研究。还研究了在进料间歇阶段添加甘油碳源和在诱导阶段添加甲醇碳源。利用90 g/L鳕鱼皮(湿重)建立了一种高表达人组织蛋白酶S的新方法。初始发酵24 h后,添加一次4%甘油(v/v,甘油/培养物),以提高培养中的细胞密度(OD600)。然后,添加0.5% (v/v,甲醇/培养量)的甲醇,发酵约48 h后,在5-L生物反应器中实现了人组织蛋白酶S的高表达。结果表明,甲醇诱导96 h后,发酵上清液中人组织蛋白酶S的活性最高可达7152 U/L。在含鳕鱼皮(90 g/L)共氮源培养基中培养的甲基营养酵母比在BMGY培养基中培养的酵母细胞密度(OD600)高21%,人组织蛋白酶S产量高18.3%。以鳕鱼皮为共氮源,首次成功地表达了人组织蛋白酶S。在诱导阶段,甘油补料分批控制策略和保持甲醇浓度恒定在0.5% (v/v,甲醇/培养)的方法对ppastoris的生长和人组织蛋白酶S的表达是有效的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Molecular Microbiology and Biotechnology
Journal of Molecular Microbiology and Biotechnology 生物-生物工程与应用微生物
CiteScore
3.90
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: We are entering a new and exciting era of microbiological study and application. Recent advances in the now established disciplines of genomics, proteomics and bioinformatics, together with extensive cooperation between academic and industrial concerns have brought about an integration of basic and applied microbiology as never before.
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Contents Front & Back Matter The Life Cycle of Dictyostelium discoideum Is Accelerated via MAP Kinase Cascade by a Culture Extract Produced by a Synthetic Microbial Consortium A Riboflavin Transporter in Bdellovibrio exovorous JSS Front & Back Matter
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