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Macromolecular crowding effects on transcription and translation are regulated by free magnesium ion
Author(s) -
Ge Xumeng,
Xu Jianfeng
Publication year - 2019
Publication title -
biotechnology and applied biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.468
H-Index - 70
eISSN - 1470-8744
pISSN - 0885-4513
DOI - 10.1002/bab.1827
Subject(s) - macromolecular crowding , ficoll , macromolecule , transcription (linguistics) , cell free system , protein biosynthesis , in vitro , crowding , intracellular , translation (biology) , biology , transcription factor , microbiology and biotechnology , biochemistry , messenger rna , chemistry , biophysics , gene , neuroscience , peripheral blood mononuclear cell , linguistics , philosophy
Abstract Cell‐free metabolic engineering is an emerging and promising alternative platform for the production of fuels and chemicals. In recent years, macromolecular crowding effect, which is an important function in living cells but ignored in cell‐free systems, has been transferred to cell‐free protein synthesis (CFPS). However, inhibitory effects of crowding agents on CFPS were frequently observed, and the mechanism is unclear. In this study, free Mg 2+ was found to be a key factor that can regulate the macromolecular crowding effect on in vitro transcription, in vitro translation, and coupled transcript/translation. Addition of crowding agents (20% of Ficoll‐70 or Ficoll‐400) enhanced in vitro transcription at an index of free Mg 2+ concentration (IFMC) below 2 mM but inhibited the transcription when the IFMC was higher than 2 mM. Similarly, Ficoll‐400 enhanced in vitro translation and coupled transcription/translation at a lower IFMC (0.1–2 mM) and inhibited the reactions at higher IFMC (>2 mM). Based on the results, CFPS systems could be further optimized by adjusting the content of crowding agents and the IFMC. Besides, the results also indicate that macromolecular crowding effect is important for maintaining the efficiency of in vivo transcription and translation which occur at a low intracellular IFMC (<1 mM).