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从 PKVL7422 中分离和鉴定盐诱导启动子。

Isolation and Characterization of a Salt Inducible Promoter from PKVL7422.

机构信息

School of Marine and Fisheries Sciences, Pukyong National University, Busan 46241, Republic of Korea.

Department of Biological Sciences, Kongju National University, Kongju 32588, Republic of Korea.

出版信息

J Microbiol Biotechnol. 2023 Jul 28;33(7):955-963. doi: 10.4014/jmb.2304.04005. Epub 2023 Apr 28.

Abstract

is a eukaryotic organism that can be used as an industrial host to produce recombinant proteins. In this study, a salt-inducible promoter (SIP) was isolated from the freshwater species PKVL7422 from the screening of genes that were upregulated after salt treatment. Several -acting elements, including stress response elements, were identified in the isolated SIP. Moreover, the Gaussia luciferase gene was cloned after the SIP and transformed into to test the inducibility of this promoter. Reexamination of transcriptome of revealed that genes involved in the synthesis of methyl jasmonic acid (MeJA), gibberellin (GA), and abscisic acid (ABA) were upregulated when was treated with salt. Furthermore, the expression level of recombinant luciferase increased when the transformed was treated with salt and MeJA, GA, and ABA. This study represents the first report of the SIP and highlights how transformed microalgae could be used for robust expression of recombinant proteins.

摘要

是一种真核生物,可用作生产重组蛋白的工业宿主。在这项研究中,从盐处理后上调表达的基因中筛选到一种来自淡水物种 PKVL7422 的盐诱导启动子(SIP)。在分离的 SIP 中鉴定到了几种顺式作用元件,包括应激反应元件。此外,在 SIP 后克隆了 Gaussia 荧光素酶基因,并将其转化到 中,以测试该启动子的诱导能力。对 转录组的重新检测表明,当用盐处理时,与茉莉酸甲酯(MeJA)、赤霉素(GA)和脱落酸(ABA)合成有关的基因上调。此外,当转化的 用盐、MeJA、GA 和 ABA 处理时,重组荧光素酶的表达水平增加。本研究首次报道了 SIP,并强调了转化微藻如何用于重组蛋白的稳健表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e9b/10394332/d6cb5e8b5f53/jmb-33-7-955-f1.jpg

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