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不同的构建策略通过关键基因的转录分析对高表达脂肪酶的巴斯德毕赤酵母菌株的生理学产生了影响。

Different construction strategies affected on the physiology of Pichia pastoris strains highly expressed lipase by transcriptional analysis of key genes.

机构信息

a Key Laboratory for Biotechnology on Medicinal Plants of Jiangsu Province, School of Life Sciences , Jiangsu Normal University , Xuzhou , P. R. China.

b State Key Laboratory of Agrobiotechnology and MOA Key Laboratory of Soil Microbiology , College of Biological Sciences, China Agricultural University , Beijing , P. R. China.

出版信息

Bioengineered. 2019 Dec;10(1):150-161. doi: 10.1080/21655979.2019.1614422.

Abstract

We demonstrated previously that expression of Rhizomucor miehei lipase (RML) in Pichia pastoris could be significantly increased by addition of gene propeptide, optimized signal peptide codons and manipulation of gene dosage. In this study, effects of various strategies on the protein synthesis and secretion pathways were analyzed. Using nine strains previously constructed, we evaluated cell culture properties, enzymatic activities, and analyzed transcriptional levels of nine genes involved in protein synthesis and secretion pathways by qPCR. We observed that (i) Addition of propeptide decreased lipase folding stress by down-regulated four UPR-related genes. (ii) Signal peptide codons optimization had no effect on host with no change in the nine detected genes. (iii) Folding stress and limited transport capacity produced when rml gene dosage exceed 2. Different limiting factors on lipase expression in strains with different construction strategies were identified. This study provides a theoretical basis for further improving RML by transforming host.

摘要

我们之前的研究表明,在毕赤酵母中表达里氏木霉脂肪酶(RML)时,添加基因前肽、优化信号肽密码子和操纵基因剂量可以显著提高 RML 的表达量。在本研究中,我们分析了各种策略对蛋白质合成和分泌途径的影响。利用之前构建的九个菌株,我们评估了细胞培养特性、酶活性,并通过 qPCR 分析了参与蛋白质合成和分泌途径的九个基因的转录水平。我们观察到:(i)添加前肽通过下调四个 UPR 相关基因降低了脂肪酶折叠应激。(ii)信号肽密码子优化对宿主没有影响,九个检测基因没有变化。(iii)当 rml 基因剂量超过 2 时,会产生折叠应激和有限的运输能力。不同的构建策略菌株中脂肪酶表达的限制因素不同。本研究为进一步通过转化宿主来提高 RML 的表达提供了理论依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdbd/6527059/7a5c97c558fa/kbie-10-01-1614422-g002.jpg

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