Bosco James, Gagliano Emily, Boshae Kassandra L, Statz John P, Wheeler Timothy B, Cuello DeAnna, Sliter Ashlyn, Newby Christian, Lin Bernice, Demeler Aysha, Pierpont C Logan, Yates-Hansen Cindee, Sydor Matthew J, Ferrini Maria E, Kuch Kellie C, Cooper Brandon S, Piggott Beverly J, Certel Sarah J, Hansen Kasper B, Sprang Stephen R, Bowler Bruce, McClelland Levi, Berkmen Mehmet, Voronina Ekaterina
Division of Biological Sciences, Department of Chemistry and Biochemistry, Center for Biomolecular Structure and Dynamics, Center for Structural and Functional Neuroscience, Center for Environmental Health Sciences, University of Montana, Missoula, MT, 59812, USA.
Department of Chemistry and Biochemistry, Alberta RNA Research and Training Institute, University of Lethbridge, Lethbridge, AB, T1K 3M4, Canada.
Sci Rep. 2025 Mar 15;15(1):8936. doi: 10.1038/s41598-025-91954-5.
Protein production using Escherichia coli is a cornerstone of modern biotechnology. In this study, we developed a novel auto-expression medium to maximize protein production. Each E. coli strain tested was capable of auto-expression in response to galactose, including strains in which the endogenous lacZ had been disrupted. This provides key evidence that galactose can regulate the lac operon independent of known lac operon-regulated metabolism. The enhanced capabilities of the novel auto-expression medium were documented across protein production systems including (1) increased yields for routinely expressed proteins (e.g. eGFP), (2) improved expression of human cytochrome c within a dual expression system, (3) robust auto-expression in lacZ-deficient strains producing proteins with challenging disulfide bonds, and (4) reproducible 8-fold increase in SpCas9 yields, at ≥ 95% purity. This novel medium can streamline production and improve yields for routine as well as challenging proteins, accelerating recombinant protein production and creating new opportunities in biotechnology and structural biology.
利用大肠杆菌进行蛋白质生产是现代生物技术的基石。在本研究中,我们开发了一种新型自表达培养基,以最大限度地提高蛋白质产量。测试的每株大肠杆菌都能够响应半乳糖进行自表达,包括内源性lacZ已被破坏的菌株。这提供了关键证据,表明半乳糖可以独立于已知的乳糖操纵子调节的代谢来调节乳糖操纵子。新型自表达培养基的增强能力在多种蛋白质生产系统中得到了证明,包括:(1)常规表达蛋白质(如增强型绿色荧光蛋白)的产量增加;(2)在双表达系统中提高了人细胞色素c的表达;(3)在产生具有挑战性的二硫键的蛋白质的lacZ缺陷菌株中实现了强劲的自表达;(4)SpCas9产量可重复提高8倍,纯度≥95%。这种新型培养基可以简化生产流程,提高常规蛋白质和具有挑战性的蛋白质的产量,加速重组蛋白质的生产,并在生物技术和结构生物学领域创造新的机会。