Additivities for Soluble Recombinant Protein Expression in Cytoplasm of Escherichia coli

• Published in: Fermentation (Basel) Vol. 10; no. 3; p. 120
• Main Authors: Atroshenko, Denis L., Sergeev, Egor P., Golovina, Diana I., Pometun, Anastasia A.
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 01-03-2024
• Subjects: Additives; Biotechnology; Cell growth; Cofactors; Cytoplasm; E coli; Enzymes; Escherichia coli; Ethanol; Glucose; Glycerol; Lactose; Optimization; Osmoprotectants; Osmotic stress; Protein expression; Protein synthesis; Proteins; Pyridoxine; Riboflavin; Sorbitol
• ISSN: 2311-5637; 2311-5637
• DOI: 10.3390/fermentation10030120

Recombinant protein expression in Escherichia coli is a fundamental technique in molecular biology and biotechnology. This review provides a comprehensive overview of various additivities to enhance the expression levels of soluble recombinant proteins in E. coli. The discussion encompasses five key aspects. Inducer Optimization: strategies for optimizing the inducer concentration to enhance protein expression. Autoinduction system optimization: the examination of glucose, lactose, and glycerol optimization within autoinduction systems to improve protein production. Osmolytes and osmoprotectants: an analysis of the use of osmolytes and osmoprotectants, such as sorbitol and glycine-betaine, to overcome with ease osmotic stress and enhance protein solubility. Ethanol additives: the impact of ethanol on E. coli physiology and its potential to improve recombinant protein expression. Cofactors and metabolic precursors: insights into the addition of cofactors, such as pyridoxal phosphate, riboflavin, thiamine, and pyridoxine, and the utilization of metabolic precursors to enhance the corresponding protein expression. This review highlights both the successful strategies and challenges in recombinant protein expression and provides insights into potential future research directions. Understanding and optimizing these factors is crucial for the efficient production of recombinant proteins for various applications in biotechnology. Furthermore, based on the analyzed data, we propose a straightforward scheme to optimize the additives in the cultivation medium.