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红酵母组成型启动子的挖掘与应用

Mining and application of constitutive promoters from Rhodosporidium toruloides.

作者信息

Guo Xiao, Bai Zhenzhen, Zhang Yang, Zhao Huimin, Shi Shuobo

机构信息

Beijing Advanced Innovation Center for Soft Matter Science and Engineering, College of Life Science and Technology, Beijing University of Chemical Engineering, North Third Ring Road 15, Chaoyang District, Beijing, 100029, China.

CAS Key Laboratory of Microbial Physiological and Metabolic Engineering, State Key Laboratory of Microbial Resources, Institute of Microbiology, Chinese Academy of Sciences, Beijing, 100101, China.

出版信息

AMB Express. 2023 Feb 8;13(1):17. doi: 10.1186/s13568-023-01522-1.

Abstract

Rhodosporidium toruloides is an oleaginous yeast under development with promising industrial applications. Since promoters of different strengths have been demonstrated as an efficient strategy to fine-tune gene expression in synthetic biology, a set of constitutive promoters with strengths varying over 2 orders of magnitude were identified in R. toruloides through transcriptome analysis under different growth conditions. Promoter candidates were first cloned and characterized using an enhanced green fluorescent protein (EGFP) as a reporter under eight conditions, and 31 promoters were identified with strength varied from 0.1 to 19.0 folds of the commonly used strong promoter of the glyceraldehyde-3-phosphate dehydrogenase gene (P). The resultant promoters were then used to optimize the linoleic acid biosynthetic pathway in R. toruloides in different media, including the use of lignocellulosic hydrolysate as the fermentation substrate, and improved the production of linoleic acid by up to 214.2% in minimal medium, with the highest production of 350.3 mg/L in Yeast Peptone Dextrose medium. This work has enriched the promoter library of R. toruloides, and helped develop R. toruloides as a platform organism for applications in biomanufacturing and synthetic biology.

摘要

红酵母是一种正在开发中的产油酵母,具有广阔的工业应用前景。由于不同强度的启动子已被证明是在合成生物学中微调基因表达的有效策略,因此通过在不同生长条件下的转录组分析,在红酵母中鉴定出了一组强度变化超过2个数量级的组成型启动子。首先在八种条件下使用增强型绿色荧光蛋白(EGFP)作为报告基因对启动子候选物进行克隆和表征,鉴定出31个启动子,其强度为常用的甘油醛-3-磷酸脱氢酶基因强启动子(P)的0.1至19.0倍。然后将所得启动子用于优化红酵母在不同培养基中的亚油酸生物合成途径,包括使用木质纤维素水解产物作为发酵底物,并在基本培养基中将亚油酸产量提高了214.2%,在酵母蛋白胨葡萄糖培养基中的最高产量为350.3mg/L。这项工作丰富了红酵母的启动子文库,并有助于将红酵母开发成为用于生物制造和合成生物学应用的平台生物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10df/9908808/e7754102143a/13568_2023_1522_Fig1_HTML.jpg

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