scholarly journals Effects of osmolarity, ions and compatible osmolytes on cell-free protein synthesis

2003 ◽  
Vol 369 (2) ◽  
pp. 369-374 ◽  
Author(s):  
Maurizio BRIGOTTI ◽  
Pier Giorgio PETRONINI ◽  
Domenica CARNICELLI ◽  
Roberta R. ALFIERI ◽  
Mara A. BONELLI ◽  
...  

To mimic what might happen in cells exposed to hypertonicity, the effects of increased osmolarity and ionic strength on cell-free protein synthesis have been examined. Translation of globin mRNA by rabbit reticulocyte lysate decreased by 30—60% when osmolality was increased from 0.35 to 0.53osmol/kg of water by the addition of NaCl, KCl, CH3CO2Na or CH3CO2K. In contrast, equivalent additions of the compatible osmolytes betaine or myo-inositol caused a 40—50% increase in the rate of translation, whereas amino acids (50—135mM) that are transported via system A had no significant effect. Addition of 75mM KCl caused a dramatic fall in the amount of the 43S pre-initiation complex, whereas it was totally preserved when osmolarity was similarly increased by the addition of 150mM betaine. The formation of a non-enzymic initiation complex between rabbit [3H]Phe-tRNA, poly(U) and the 80S ribosomes was unaffected by the addition of 75mM NaCl or KCl, but translation of the complex decreased by 70%. Density-gradient centrifugation of reticulocyte extracts translating endogenous mRNA revealed that addition of 150mM betaine had no effect, whereas addition of 75mM KCl caused a marked decrease in the polysome peak, concomitant with an increase in the proportion of 80S ribosomes and ribosomal subunits, even when elongation was inhibited with fragment A of diphtheria toxin. These results are consistent with the notion that both initiation and elongation are inhibited by unusually high concentrations of inorganic ions, but not by the compatible osmolytes betaine or myo-inositol.

RSC Advances ◽  
2020 ◽  
Vol 10 (66) ◽  
pp. 40588-40596
Author(s):  
Tony Köhler ◽  
Thomas Heida ◽  
Sandra Hoefgen ◽  
Niclas Weigel ◽  
Vito Valiante ◽  
...  

We describe a bottom-up approach towards functional enzymes utilizing microgels as carriers for genetic information that enable cell-free protein synthesis, in situ immobilization, and utilization of functional deGFP-MatB.


AIChE Journal ◽  
2021 ◽  
Author(s):  
Carlos A. Duran‐Villalobos ◽  
Olotu Ogonah ◽  
Beatrice Melinek ◽  
Daniel G. Bracewell ◽  
Trevor Hallam ◽  
...  

2021 ◽  
Author(s):  
Takeshi Tabuchi ◽  
Yohei Yokobayashi

Synthetic riboswitches can be used as chemical gene switches in cell-free protein synthesis systems. We provide a current perspective on the state of cell-free riboswitch technologies and their future directions.


2021 ◽  
Vol 8 (1) ◽  
Author(s):  
Liyuan Zhang ◽  
Xiaomei Lin ◽  
Ting Wang ◽  
Wei Guo ◽  
Yuan Lu

AbstractCell-free protein synthesis (CFPS) systems have become an ideal choice for pathway prototyping, protein production, and biosensing, due to their high controllability, tolerance, stability, and ability to produce proteins in a short time. At present, the widely used CFPS systems are mainly based on Escherichia coli strain. Bacillus subtilis, Corynebacterium glutamate, and Vibrio natriegens are potential chassis cells for many biotechnological applications with their respective characteristics. Therefore, to expand the platform of the CFPS systems and options for protein production, four prokaryotes, E. coli, B. subtilis, C. glutamate, and V. natriegens were selected as host organisms to construct the CFPS systems and be compared. Moreover, the process parameters of the CFPS system were optimized, including the codon usage, plasmid synthesis competent cell selection, plasmid concentration, ribosomal binding site (RBS), and CFPS system reagent components. By optimizing and comparing the main influencing factors of different CFPS systems, the systems can be optimized directly for the most influential factors to further improve the protein yield of the systems. In addition, to demonstrate the applicability of the CFPS systems, it was proved that the four CFPS systems all had the potential to produce therapeutic proteins, and they could produce the receptor-binding domain (RBD) protein of SARS-CoV-2 with functional activity. They not only could expand the potential options for in vitro protein production, but also could increase the application range of the system by expanding the cell-free protein synthesis platform.


2021 ◽  
Vol 29 ◽  
pp. e00583
Author(s):  
Nawal Abd El-Baky ◽  
Maie Ahmed Elkhawaga ◽  
Eman Shawky Abdelkhalek ◽  
Mona Mohammed Sharaf ◽  
Elrashdy Mustafa Redwan ◽  
...  

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