普通小球藻
脱落酸
重组DNA
茉莉酸
荧光素酶
生物
基因
生物化学
转录组
分子生物学
基因表达
植物
藻类
转染
作者
Minjeong Kim,Suhyun Kim,Najib Abdellaoui,Tae‐Jin Choi
出处
期刊:Journal of Microbiology and Biotechnology
[Journal of Microbiology and Biotechnology]
日期:2023-04-28
卷期号:33 (7): 955-963
被引量:3
标识
DOI:10.4014/jmb.2304.04005
摘要
Chlorella 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 Chlorella vulgaris PKVL7422 from the screening of genes that were upregulated after salt treatment. Several cis-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 C. vulgaris to test the inducibility of this promoter. Reexamination of transcriptome of C. vulgaris revealed that genes involved in the synthesis of methyl jasmonic acid (MeJA), gibberellin (GA), and abscisic acid (ABA) were up-regulated when C. vulgaris was-treated with salt. Furthermore, the expression level of recombinant luciferase increased when the transformed C. vulgaris was treated with salt and MeJA, GA, and ABA. This study represents the first report of the C. vulgaris SIP and highlights how transformed microalgae could be used for robust expression of recombinant proteins.
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